MODIFIED ARTHROPOD AND METHOD OF USE
A modified arthropod, an arthropod-modifying bacterium, and use thereof as an agent for control of diseases transmitted by arthropods, particularly mosquitoes, is provided. More specifically, an isolated arthropod-adapted Wolbachia bacterium capable of modifying one or more biological properties of a mosquito host is provided. The modified arthropod may be characterized as having a shortened life-span, a reduced ability to transmit disease, a reduced susceptibility to a pathogen, a reduced fecundity, and/or a reduced ability to feed from a host, when compared to a corresponding wild-type arthropod.
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This patent application claims the benefit of U.S. Provisional Patent Application No. 61/187,805, filed Jun. 17, 2009, and Australian Patent Application No. 2009222557, filed Oct. 2, 2009, which are incorporated by reference herein.
INCORPORATION-BY-REFERENCE OF MATERIAL SUBMITTED ELECTRONICALLYIncorporated by reference in its entirety herein is a computer-readable nucleotide/amino acid sequence listing submitted concurrently herewith and identified as follows: One 9,489 Byte ASCII (Text) file named “706551_ST25.TXT,” created on Jun. 17, 2010.
FIELD OF THE INVENTIONTHIS INVENTION relates to arthropods and arthropod-transmitted diseases. More particularly, this invention relates to a modified arthropod, an arthropod-modifying bacterium, and use thereof as an agent for control of diseases transmitted by arthropods, particularly mosquitoes.
BACKGROUND OF THE INVENTIONArthropods are a source of, or transmit, many diseases and conditions in humans and other animals. Some arthropods may simply cause localized irritation of the skin without transmission of disease, such as occurs with mites and ticks, or by transmission of disease-causing pathogens such as arboviruses, protozoa, bacteria and nematodes. These disease-causing pathogens are responsible for a variety of different diseases of humans and other animals including malaria, Dengue fever, Eastern Equine encephalitis, Western Equine encephalitis, Venezuelan equine encephalitis, Japanese encephalitis, Murray Valley encephalitis, West Nile fever, Yellow fever, LaCrosse encephalitis Asian spotted fever, Q fever, Lymphatic filariasis (Elephantiasis), Chikungunya fever, Ross river fever and Chagas disease.
Most pathogens that are transmitted by mosquitoes share a common property; they have to undergo a significant period of development in their insect vector before they can be transmitted to a new host. After a female mosquito ingests an infectious blood-meal, parasites or arboviruses, such as dengue, penetrate the mosquito's midgut and replicate in various tissues before infecting the salivary glands, where they are transmitted to a new host during subsequent blood-feeding. This time period from pathogen ingestion to potential infectivity is termed the extrinsic incubation period (EIP), and lasts approximately two weeks for both dengue (Siler et al., 1926; Watts et al., 1987) and malaria (Gilles et al., 2002). A female mosquito must survive longer than its initial non-feeding period (usually less than 2 days) plus the EIP to successfully contribute to pathogen transmission. Mosquito survival is therefore considered a critical component of a vector population's capacity for pathogen transmission (Dye, 1992). Interventions that aim to reduce the daily survivorship of adult mosquitoes, such as the spraying of residual insecticides in houses and insecticide-treated bednets for malaria control, yield large reductions in pathogen transmission rates (Masabo et al., 2004; Schellenberg et al., 2001) because of the sensitive relationship between mosquito survival and vectorial capacity (Garrett-Jones, 1964; MacDonald, 1957).
The control of diseases such as dengue primarily targets Aedes aegypti, a domesticated mosquito that prefers to live in and around human habitation (Gubler et al., 1997). With few exceptions, dengue management strategies have been complicated by the inability to completely eradicate A. aegypti from urban settings, and the ineffective application of long lasting vector control programs (Morrison et al., 2008). This has led to a worldwide resurgence of dengue, and highlighted the urgent need for novel and sustainable disease control strategies.
A strain of the obligate intracellular bacterium Wolbachia pipientis, wMelPop, has been described that reduces adult lifespan of its natural fruit fly host Drosophila melanogaster (Min and Benzer, 1997). Wolbachia are maternally-inherited bacteria that use mechanisms such as cytoplasmic incompatibility (CI), a type of embryonic lethality that results from crosses between infected males with uninfected females, to rapidly spread into insect populations (Hoffmann and Turelli, 1997).
However, life-shortening Wolbachia strains do not occur in mosquitoes naturally and experimental transfer of Wolbachia between host species (transinfection) has lacked success (Van Meer and Stouthamer, 1999). In some cases, transferred strains can be stable and maternally inherited, primarily when Wolbachia is transferred within or between closely related species in a family or genus (Boyle et al., 1993; Xi et al., 2005; Zabalou et al., 2004). In other cases, the new infection appears poorly adapted to its new host, showing fluctuating infection densities and variable degrees of transovarial transmission. The result is often loss of infection within a few host generations. Wolbachia infections tend to be more susceptible to loss when they have been transferred between phylogenetically distant hosts (Kang et al., 2003; Riegler et al., 2004). Similarly, those species that do not naturally harbour Wolbachia have proven refractory to transinfection (Curtis and Sinkins, 1998; Rigaud et al., 2001).
SUMMARY OF THE INVENTIONMost pathogens require a relatively long incubation period in their arthropod host before they can be transmitted to a new host. Thus, it has been proposed that a life-shortening Wolbachia bacterium may be used to reduce disease transmission by arthropod hosts that do not naturally harbour Wolbachia.
However, despite significant efforts, researchers have been unable to achieve colonization of Wolbachia in distantly related arthropod species due to the inability of Wolbachia to quickly adapt to new intra-cellular environments. To overcome this problem, the inventors have identified a need for a modified bacterium that can be easily introduced into populations of disease-transmitting arthropod vectors and reduce transmission of pathogens such as dengue virus and malaria.
The invention therefore arises from the inventors' unexpected finding that long-term serial passage of Wolbachia in an arthropod cell line resulted in the production of an arthropod-adapted bacterium that can be successfully transferred into, and maintained in, an arthropod and populations thereof. Furthermore, the inventors surprisingly discovered that arthropods harbouring this arthropod-adapted bacterium have a shorter lifespan, a reduced fecundity, altered feeding behaviour, and/or are less susceptible to pathogens, including viruses, fungi, worms, protozoans, and bacteria, than their wild-type counterparts.
In a first aspect, the invention provides an isolated arthropod-adapted bacterium capable of modifying one or more biological properties of an arthropod host, wherein said arthropod-adapted bacterium does not normally colonize, inhabit, reside in, or infect said arthropod host.
In a preferred embodiment, said arthropod-adapted bacterium is of the genus Wolbachia.
In another preferred embodiment, said isolated arthropod-adapted bacterium is of a species of Wolbachia pipientis.
In one particularly preferred embodiment, said isolated arthropod-adapted bacterium is wMelPop-CLA.
In a second aspect, the invention provides a method of producing an arthropod-adapted bacterium capable of modifying one or more biological properties of an arthropod host, said method including the step of culturing a bacterium with one or more arthropod cells, optionally with one or more differentiating agents, to thereby produce said arthropod-adapted bacterium, wherein said arthropod-adapted bacterium does not normally colonize, inhabit, reside in, or infect said arthropod host.
In one particular embodiment, the isolated arthropod-adapted bacterium of the first aspect or the arthropod-adapted bacterium produced according to the method of the second aspect, comprises one or more genetic modifications compared to a wild-type counterpart.
In certain particular embodiments, said one or more genetic modifications correspond to one or more nucleotide sequence deletions, insertions, substitutions or mutations.
In one preferred embodiment, said arthropod-adapted bacterium is of the genus Wolbachia.
In another preferred embodiment, said arthropod-adapted bacterium is of a species of Wolbachia pipientis.
In one particularly preferred embodiment, said arthropod-adapted bacterium is wMelPop-CLA.
Preferably, said arthropod-adapted bacterium is cultured outside its native host for at least 6 months.
More preferably, said arthropod-adapted bacterium is cultured outside its native host between 1.5 to 5 years.
Even more preferably, said arthropod-adapted bacterium is cultured outside its native host for 2 to 4 years.
In one embodiment, the isolated arthropod-adapted bacterium of the first aspect or the arthropod-adapted bacterium produced according to the method of the second aspect shortens a life-span of an arthropod.
In another embodiment, the isolated arthropod-adapted bacterium of the first aspect or the arthropod-adapted bacterium produced according to the method of the second aspect reduces a susceptibility of an arthropod to a pathogen.
In yet another embodiment, the isolated arthropod-adapted bacterium of the first aspect or the arthropod-adapted bacterium produced according to the method of the second aspect reduces a fecundity of an arthropod.
In still another embodiment, the isolated arthropod-adapted bacterium of the first aspect or the arthropod-adapted bacterium produced according to the method of the second aspect reduces a desiccation tolerance of eggs produced by the arthropod.
In still yet another embodiment, the isolated arthropod-adapted bacterium of the first aspect or the arthropod-adapted bacterium produced according to the method of the second aspect reduces the ability of the arthropod to feed from a host.
In a third aspect, the invention provides an arthropod comprising the isolated arthropod-adapted bacterium of the first aspect, or the arthropod-adapted bacterium produced according to the method of the second aspect.
Suitably, said arthropod-adapted bacterium does not normally colonize, inhabit, reside in, or infect said arthropod.
Preferably, said arthropod is selected from the group consisting of an insect, an arachnid and a crustacean.
In one embodiment, said arthropod is an insect.
In another embodiment, said arthropod is a mosquito.
In one preferred embodiment, a wild-type of said arthropod is a disease-transmitting mosquito.
In another preferred embodiment, said arthropod is a mosquito of the genus selected from the group consisting of Culex, Aedes and Anopheles.
In one particularly preferred embodiment, said arthropod is a mosquito of a species selected from the group consisting of Aedes aegypti, and Anopheles gambiae.
In a fourth aspect, the invention provides a method of producing an arthropod comprising the isolated arthropod-adapted bacterium of the first aspect, or the arthropod-adapted bacterium produced according to the method of the second aspect.
In one embodiment, the arthropod of the third aspect or the arthropod produced according to the method of the fourth aspect has a reduced life-span.
Typically, according to this embodiment, said reduced life-span is shorter than an average life-span of a wild-type of said arthropod.
In another embodiment, the arthropod of the third aspect, or the arthropod produced according to the method of the fourth aspect, has a reduced susceptibility to a pathogen.
Preferably, the arthropod of the third aspect, or the arthropod produced according to the method of the fourth aspect, has improved protection against, or resistance to, a pathogen compared to a wild-type counterpart.
Typically, according to this embodiment, said pathogen is selected from the group consisting of a virus, a fungus, a worm, a protozoan, and a bacterium.
In yet another embodiment, the arthropod of the third aspect, or the arthropod produced according to the method of the fourth aspect has a reduced fecundity.
In still another embodiment, the arthropod of the third aspect, or the arthropod produced according to the method of the fourth aspect has a reduced ability to feed from a host.
In a fifth aspect, the invention provides a method of modifying an arthropod population, said method including the step of introducing the arthropod of the third aspect, or the arthropod produced according to the method of the fourth aspect, into said arthropod population, to thereby modify one or more biological properties of said arthropod population.
In one embodiment of the fifth aspect, the invention provides a method of reducing pathogen transmission by an arthropod population, said method including the step of introducing the arthropod of the third aspect, or the arthropod produced according to the method of the fourth aspect, into said arthropod population, to thereby reduce, decrease, or mitigate pathogen transmission by said arthropod population.
In another embodiment of the fifth aspect, the invention provides a method of reducing a susceptibility to a pathogen in an arthropod population, said method including the step of introducing the arthropod of the third aspect, or the arthropod produced according to the method of the fourth aspect, into said arthropod population, to thereby reduce, decrease, or mitigate the susceptibility to said pathogen in said arthropod population.
Preferably, said pathogen is selected from the group consisting of a virus, a fungus, a worm, a protozoan, and a bacterium.
In yet another embodiment of the fifth aspect, the invention provides a method of reducing an average life-span of an arthropod population, said method including the step of introducing the arthropod of the third aspect, or the arthropod produced according to the method of the fourth aspect, into said arthropod population, to thereby reduce, lower, shorten or decrease said average life-span of said arthropod population.
In still another embodiment of the fifth aspect, the invention provides a method of reducing a fecundity of an arthropod population, said method including the step of introducing the arthropod of the third aspect, or the arthropod produced according to the method of the fourth aspect, into said arthropod population, to thereby reduce, lower, or decrease said fecundity of said arthropod population.
In still yet another embodiment of the fifth aspect, the invention provides a method of reducing an ability of an arthropod population to feed from a host, said method including the step of introducing the arthropod of the third aspect, or the arthropod produced according to the method of the fourth aspect, into said arthropod population, to thereby reduce, lower, or decrease said ability of said arthropod population to feed from a host.
Throughout this specification, unless otherwise indicated, “comprise”, “comprises” and “comprising” are used inclusively rather than exclusively, so that a stated integer or group of integers may include one or more other non-stated integers or groups of integers.
The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.
The present invention has arisen from the inventors' unexpected discovery that long-term serial passage of a Wolbachia bacterium in an arthropod cell line resulted in the production of an arthropod-adapted bacterium that can be successfully transferred into an arthropod which does not naturally harbour Wolbachia. The inventors have also surprisingly found that arthropods harbouring the arthropod-adapted bacterium, and populations thereof, have a shorter life-span, a reduced fecundity, altered feeding behaviour, and/or a lower susceptibility to pathogens such as viruses, fungi, worms (e.g. nematodes), protozoans, and bacteria.
This invention therefore provides an arthropod-adapted bacterium, and an arthropod comprising the same, for use in the reduction of arthropod-borne diseases such as, but not limited to, dengue fever, malaria and lymphatic filariasis.
For the purposes of this invention, by “isolated” is meant material that has been removed from its natural state or otherwise been subjected to human manipulation. Isolated material may be substantially or essentially free from components that normally accompany it in its natural state, or may be manipulated so as to be in an artificial state together with components that normally accompany it in its natural state.
As used herein, the term “arthropod” refers to an invertebrate animal that is characterized by a chitinous exoskeleton and a segmented body with paired, jointed appendages (e.g. legs or feet). Accordingly, an arthropod may be an insect (e.g. a mosquito or a fly), a crustacean (e.g. a prawn, a crab, or a lobster), or an arachnid (e.g. a tick or a mite), although without limitation thereto. As also used herein, the terms “arthropod vector” or “arthropod vector population” refer to an arthropod, or a population thereof, that is capable of transmitting a pathogen from one host to another.
Arthropods preferably include insects, arachnids and crustaceans.
Insects include insects of orders such as Diptera (e.g. mosquitoes, horseflies, midges, stableflies and tsetse flies), Phthiraptera (e.g. lice), Siphonaptera (e.g. fleas) and Hemiptera (e.g. bedbugs and triatomine bugs).
An example of an arachnid is a tick or mite (e.g of the families Argasida, Trombidiidae and Ixodidae). These can simply cause localized irritation of the skin or transmit pathogens such as bacteria (e.g. Rickettsia and Coxiella) and viruses (typically Flaviviruses) which cause diseases such as Asian spotted fever, North American or Rocky Mountain spotted fever, American mountain fever or Colorado tick fever, Q fever, Russian spring-summer encephalitis and tick paralysis. Spider mites, which are members of the Acari (mite) family Tetranychidae, may also spread disease by transferring pathogens (e.g. fungus) between plants.
An example of a crustacean is a prawn or a crab (e.g. of the families Peneidae and Coenobitidae). Most cultured penaeid prawns (e.g. Penaeus monodon, Marsupenaeus japonicus and Litopenaeus vannamei) carry and transfer the DNA viruses of the species White Spot Syndrome Baculovirus Complex, which cause White Spot Syndrome in crustaceans such as prawns, lobsters and crabs.
In one aspect, the invention provides an isolated arthropod-adapted bacterium capable of modifying one or more biological properties of an arthropod host.
By “arthropod-adapted” bacterium is meant a bacterium (e.g. of the genus Wolbachia) that has been taken out of its native host environment and adapted to a new arthropod host environment, in which environment said bacterium does not naturally reside. Accordingly, a non-limiting example of an arthropod-adapted bacterium is a Wolbachia bacterium that has been isolated from its native host (e.g. Drosophila melanogaster) and adapted to a new host (e.g. Aedes aegyptii or Anopheles gambiae).
It will be appreciated that the term arthropod-adapted bacterium encompasses any bacterium that is capable of colonizing, infecting, or residing in an arthropod host within which it does not normally reside.
In a preferred embodiment, said isolated arthropod-adapted bacterium is of the genus Wolbachia.
Wolbachia includes strains such as wMel, wMelPop, wMelPop-CLA, wMelCS, wAu, wRi, wNo, wHa, wMau, and wCer2, although without limitation thereto.
In one particular embodiment, said isolated arthropod-adapted bacterium is Wolbachia pipientis.
In one particularly preferred embodiment, said isolated arthropod-adapted bacterium is wMelPop-CLA.
As used herein, the term “wMelPop-CLA” refers to a particularly preferred arthropod-adapted wMelPop.
In one embodiment, said isolated arthropod-adapted bacterium shortens a life-span of an arthropod.
In another embodiment, said isolated arthropod-adapted bacterium reduces a susceptibility of an arthropod to a pathogen.
As used herein, an arthropod that has a “reduced susceptibility” to a pathogen is less likely to become infected by, carry and/or transmit a pathogen than a wild-type counterpart.
As referred to herein, a pathogen may be a virus, a fungus, a protozoan, a worm or a bacterium.
Non-limiting examples of virus pathogens include arboviruses such as Alphaviruses (e.g. Chikungunya virus, Eastern Equine Encephalitis virus, Western Equine Encephalitis virus), Flaviviruses (e.g. dengue virus, West Nile virus, Yellow Fever virus), and Bunyaviruses (e.g. La Crosse virus, Rift Valley fever virus, Colorado tick fever virus).
An example of a protozoan parasite is a malaria parasite of the Plasmodium genus such as, but not limited to, Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale, Plasmodium malariae, Plasmodium berghei, Plasmodium gallinaceum, and Plasmodium knowlesi.
Non-limiting examples of worm pathogens include nematodes, inclusive of filarial nematodes such as Wuchereria bancrofti, Brugia malayi, Brugia pahangi, Brugia timori, and Dirofilaria immitis.
A pathogen may also be a bacterium, inclusive of a Gram negative and Gram positive bacterium.
It will be appreciated that non-limiting examples of pathogenic bacteria include spirochetes (e.g. Borrelia), actinomycetes (e.g. Actinomyces), mycoplasmas, Rickettsias, Gram negative aerobic rods, Gram negative aerobic cocci, Gram negatively facultatively anaerobic rods (e.g. Erwinia and Yersinia), Gram-negative cocci, Gram negative coccobacilli, Gram positive cocci (e.g. Staphylococcus and Streptococcus), endospore-forming rods, and endospore-forming cocci.
By way of example only, pathogenic bacteria include Yersinia pestis, Borellia spp, Rickettsia spp, and Erwinia carotovora.
In yet another embodiment, said isolated arthropod-adapted bacterium introduces a reproductive abnormality in an arthropod host such as, but not limited to, parthenogenesis, feminization, male killing, and cytoplasmic incompatibility (CI).
Typically, according to this embodiment, said reproductive abnormality reduces a fecundity within an arthropod vector population.
As used herein, the term “fecundity” refers to the ability of an arthropod, or a population thereof, to reproduce.
In another aspect, the invention provides a method of producing an arthropod-adapted bacterium capable of modifying one or more biological properties of an arthropod host, said method including the step of culturing a bacterium with one or more arthropod cells, optionally with one or more differentiating agents, to thereby produce said arthropod-adapted bacterium.
Suitably, said arthropod-adapted bacterium does not normally colonize, inhabit, reside in, or infect said arthropod host.
In a preferred embodiment, said arthropod-adapted bacterium is of the genus Wolbachia.
Wolbachia includes strains such as wMel, wMelPop, wMelPop-CLA, wMelCS, wAu, wRi, wNo, wHa, wMau, and wCer2, although without limitation thereto.
In one particular embodiment, said isolated arthropod-adapted bacterium is Wolbachia pipientis.
In one particularly preferred embodiment, said arthropod-adapted Wolbachia bacterium is wMelPop-CLA.
Preferably, said arthropod-adapted bacterium is cultured outside its native host for at least 6 months.
More preferably, said arthropod-adapted bacterium is cultured outside its native host between 1.5 to 5 years.
Accordingly, it will be appreciated that said arthropod may be cultured outside its native host for about 2 years, 2.5 years, 3 years, 3.5 years, 4 years, 4.5 years, and up to about 5 years.
Even more preferably, said arthropod-adapted bacterium is cultured outside its native host for 2 to 4 years.
In one particular embodiment, said native host is of the genus Drosophila.
In another particular embodiment, said native host is of a species of Drosophila melanogaster.
In yet another particular embodiment, said native host is of a species of Drosophila simulans.
In one embodiment, said one or more arthropod cells are of an arthropod of the genus selected from the group consisting of Aedes and Anopheles.
In another embodiment, said one or more arthropod cells are of an arthropod of a species selected from the group consisting of Aedes albopictus, Aedes aegypti, and Anopheles gambiae.
Accordingly, a non-limiting exemplary method of producing the arthropod-adapted bacterium according to this aspect comprises the steps of (i) isolating a bacterium (e.g. wMelPop) from an arthropod host (e.g. Drosophila melanogaster), (ii) establishing the isolated bacterium in a first culture of one or more arthropod cells (e.g. of a species of Aedes albopictus); (iii) culturing the first culture for a period of time (e.g. 2-3 years); (iv) isolating the bacterium from the first culture; (v) introducing the bacterium from the first culture into a second culture of one or more arthropod cells (e.g. of a species of Aedes aegyptii or Anopheles gambiae), and (vi) culturing the second culture for a period of time (e.g. 3-12 months), to thereby produce the arthropod-adapted bacterium (e.g. wMelPop-CLA) according to this aspect.
A skilled person will appreciate that the bacterium which is to be adapted to a new arthropod host may be isolated from an arthropod during different developmental stages of their life-cycle and from different tissues such as, an embryo, a cytoplasm, or a hemolymph, although without limitation thereto.
Non-limiting methods for introducing an isolated bacterium into an uninfected arthropod host, or cells thereof, may be selected from the group consisting of a shell vial technique, and a microinjection.
In yet another embodiment, the arthropod-adapted bacterium reduces the ability of an arthropod to feed from a host.
Typically, according to this embodiment, the arthropod (e.g. a mosquito) may have a reduced ability to obtain, ingest, or otherwise acquire blood from an arthropod host (e.g. a human) compared to a corresponding wild-type arthropod.
In some embodiments, the arthropod-adapted bacterium (e.g. wMelPop-CLA) comprises one or more genetic modifications when compared to a corresponding wild-type counterpart (e.g. wMelPop).
Such genetic modifications may be selected from the group consisting of a nucleotide sequence insertion, a deletion, a single nucleotide polymorphism (SNP), a mutation, a frame-shift, a chromosomal rearrangement, or a transposition, although without limitation thereto.
In some embodiments, said genetic modifications relate to the modification of one or more nucleotide sequences as set forth in Table 7.
In another aspect, the invention provides an arthropod comprising the isolated arthropod-adapted bacterium.
An arthropod comprising the isolated arthropod-adapted bacterium of the aforementioned aspects may be referred to as a “modified arthropod”.
Suitably, a wild-type of said modified arthropod is an arthropod vector that carries and transfers a pathogen from one “host” to another.
A “host” may be any animal or plant upon which an arthropod feeds and/or to which an arthropod is capable of transmitting a disease-causing pathogen. Non-limiting examples of hosts are plants (e.g. flowers, vegetables, fruits, and crops), mammals such as humans, domesticated pets (e.g. dogs and cats), wild animals (e.g. monkeys, rodents and wild cats) livestock animals (e.g. sheep, pigs, cattle, and horses), avians such as poultry (e.g. chickens, turkeys and ducks) and other animals such as crustaceans (e.g. prawns and lobsters).
It will be appreciated that an arthropod vector may act as a carrier of a pathogen that is harmful to a host (e.g. a human) and not to the arthropod vector itself.
A non-limiting example of vector-borne pathogen transmission is by blood-feeding arthropods (e.g. mosquitoes). The pathogen (e.g. a dengue virus) multiplies within the arthropod vector, and the pathogen is transmitted from the arthropod vector to an animal host (e.g. a human) when the arthropod takes a blood meal. Mechanical transmission of pathogens may occur when arthropods physically carry pathogens from one place or host to another, usually on body parts.
It will also be appreciated that an arthropod vector may transmit disease within an arthropod group. A non-limiting example is the transmission of the viral pathogens that cause White Spot Syndrome in crustaceans from one arthropod (e.g. a prawn) to another.
An arthropod may also facilitate pathogen transmission between plants. A non-limiting example is the transfer of yeast pathogens to grapes by mites.
While in certain embodiments, arthropod-adapted bacteria may be useful for creating modified arthropod vectors (e.g. mosquitoes) having reduced capacity to transmit disease-causing pathogens (e.g. malaria), in other embodiments, the invention provides arthropods that have “beneficial traits” or uses which are enhanced or improved by arthropod-adapted bacteria. Non-limiting examples include insects such as honey-bees and crustaceans such as prawns, lobsters and crabs having reduced susceptibility to pathogens.
Preferably, said arthropod is selected from the group consisting of an insect, an arachnid and a crustacean.
In one particular embodiment, said arthropod is an insect.
In another particular embodiment, said arthropod is a mosquito.
In one particular embodiment, a wild-type of said arthropod is a disease-transmitting mosquito.
As used herein “mosquito” and “mosquitoes” include insects of the family Culicidae. Preferably, mosquitoes are of the sub-families Anophelinae and Culicinae. Even more preferably, mosquitoes are capable of transmitting disease-causing pathogens, including viruses, protozoa, worms (e.g. nematodes) and bacteria. Non-limiting examples include species of the genus Anopheles which transmit malaria pathogens, species of the genus Culex, and species of the genus Aedes (e.g. Aedes aegypti, Aedes albopictus and Aedes polynesiensis) which transmit nematode worm pathogens, arbovirus pathogens such as Alphaviruses (e.g. Eastern Equine encephalitis, Western Equine encephalitis, Venezuelan equine encephalitis), Flavivirus pathogens that cause diseases such as Japanese encephalitis, Murray Valley Encephalitis, West Nile fever, Yellow fever, Dengue fever, and Bunyavirus pathogens that cause diseases such as LaCrosse encephalitis, Rift Valley Fever, and Colorado tick fever, although without limitation thereto. Non-limiting examples of worm pathogens include nematodes (e.g. filarial nematodes such as Wuchereria bancrofti, Brugia malayi, Brugia pahangi or Brugia timori), which may be transmitted by mosquitoes.
Disease-causing pathogens transmitted by mosquitoes also include bacteria (e.g. Yersinia pestis, Borellia spp, Rickettsia spp, and Erwinia carotovora).
Non-limiting examples of pathogens that may be transmitted by Aedes aegypti are dengue virus, Yellow fever virus, Chikungunya virus and heartworm (Dirofilaria immitis).
Examples of pathogens that may be transmitted by Aedes albopictus include West Nile Virus, Yellow fever virus, St. Louis Encephalitis, dengue virus, and Chikungunya fever although without limitation thereto.
Pathogens frequently transmitted by the mosquito vector Anopheles gambiae include malaria parasites of the genus Plasmodium such as, but not limited to, Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale, Plasmodium malariae, Plasmodium berghei, Plasmodium gallinaceum, and Plasmodium knowlesi.
In one particularly preferred embodiment, said arthropod is a mosquito of the genus selected from the group consisting of Culex, Aedes and Anopheles.
In another particularly preferred embodiment, said arthropod is a mosquito of a species selected from the group consisting of Aedes aegypti, Aedes albopictus, and Anopheles gambiae.
In another aspect, the invention provides a method of producing the modified arthropod.
In one embodiment, the modified arthropod has a reduced susceptibility to a pathogen.
Typically, according to this embodiment, said pathogen is selected from the group consisting of a virus, a fungus, a protozoan, a nematode, and a bacterium.
In another embodiment, the modified arthropod has a reduced life-span.
Typically, according to this embodiment, said “reduced life-span” is shorter than an average life-span of a wild-type of said modified arthropod. Accordingly, said reduced life-span may be 10%, 20%, 30%, 40%, 50%, or up to 80% shorter than the average life-span of a wild-type of said arthropod.
It will be appreciated that the modified arthropod may be less likely to transmit a pathogen than its wild-type counterpart, since most pathogens have to undergo a relatively long incubation period in an arthropod vector before they can be transmitted to a new host.
In yet another embodiment, the modified arthropod has a reduced fecundity.
In one particular embodiment, said reduced fecundity may result in a loss of progeny following a cross between a modified male arthropod and a wild-type female arthropod.
In another particular embodiment, the modified arthropod (e.g. a mosquito) may be used in a method for controlling the growth of an arthropod population during the dry period since eggs from a modified arthropod (e.g. a female mosquito) have a reduced tolerance to desiccation and a shorter life-span compared to eggs from a wild-type arthropod.
As used herein, “reduced tolerance to desiccation” refers to a reduced, diminished or decreased ability of eggs from an arthropod to withstand or endure extreme dryness or drought-like conditions.
According to this particular embodiment, the life-span of eggs from a modified arthropod (e.g. a mosquito) may be at least 4 weeks, at least 8 weeks, at least 12 weeks, and up to at least 18 weeks shorter than eggs from said wild-type arthropod.
In another aspect, the invention provides a method of modifying an arthropod population, said method including the step of introducing the modified arthropod into said arthropod population, to thereby modify one or more biological properties of said arthropod population.
Preferably, said arthropod population is an insect vector population.
More preferably, said arthropod population is a mosquito vector population.
Even more preferably, said arthropod population is a disease-transmitting mosquito vector population.
In one embodiment, this aspect provides a method of mitigating, reducing, or decreasing pathogen transmission by said arthropod population.
In another embodiment, this aspect provides a method of reducing, mitigating, or decreasing a susceptibility to a pathogen in said arthropod population.
Typically, according to this embodiment, said pathogen is selected from the group consisting of a virus, a fungus, a worm, a protozoan, and a bacterium.
In one particular embodiment, said pathogen is a protozoan of the genus Plasmodium.
In another particular embodiment, said pathogen is of a species selected from the group consisting of Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale, Plasmodium malariae, Plasmodium berghei, Plasmodium gallinaceum, and Plasmodium knowlesi.
In yet another particular embodiment, said pathogen is a virus of the genus Flavivirus (e.g., a dengue virus).
Accordingly, in a non-limiting example, an arthropod population (e.g. a population of Aedes aegypti) comprising one or more modified arthropods may have a reduced susceptibility to a pathogen (e.g. a malaria parasite or a dengue virus), compared to a corresponding wild-type arthropod population.
In yet another embodiment, this aspect of the invention provides a method of reducing, lowering, shortening, or decreasing an average life-span of said arthropod population.
It will be appreciated that an arthropod population with a reduced average life-span compared to a corresponding wild-type arthropod population may have a reduced capacity to transmit pathogens, such as viruses, fungi, worms, parasites, and bacteria, since a pathogen must undergo a significant period of development in their arthropod vector before it can be transmitted to a new host. Accordingly, a reduction of the average life-span of a disease-transmitting mosquito population may help reduce transmission of vector-borne diseases such as, but not limited to, malaria, dengue fever, and lymphatic filariasis.
In yet another embodiment, this aspect of the invention provides a method of reducing, lowering or decreasing an average fecundity of said arthropod population.
In one particular embodiment, said reduced average fecundity results in a loss of progeny following a cross between a modified male arthropod and a wild-type female arthropod.
In another particular embodiment, said reduced average fecundity results in a reduced life-span of eggs from a modified female arthropod.
In still yet another embodiment, this aspect of the invention provides a method of reducing an ability of an arthropod population to feed from a host.
It will also be appreciated that the methods of this aspect may be used together with other agents that reduce an average life-span of an arthropod population. Such agents include entomopathogenic fungi and mosquito densoviruses, although without limitation thereto.
So that the invention may be fully understood and put into practical effect, the skilled reader is directed to the following non-limiting detailed Examples.
EXAMPLES Example 1 Host Adaptation of Wolbachia after Long-Term Serial Passage in Mosquito Cell Lines Materials and Methods Cell Lines and MaintenanceThree cell lines were used in this study: (i) Aa23.T derived from Ae. albopictus embryos (O'Neill et al., 1997) (ii) RML-12 derived from Ae. aegypti larvae (C. E. Yunker; personal communication) (Kuno, 1983) and (iii) MOS-55 derived from An. gambiae larvae (Marhoul and Pudney, 1972). All these cell lines were confirmed as negative for Wolbachia infection prior to this study by PCR as outlined below. Aa23.T and RML-12 cell lines were maintained in growth medium consisting of equal volumes of Mitsuhashi-Maramorosch (Mitsuhashi and Maramorosch, 1964) (1 mM CaCl2, 0.2 mM MgCl2, 2.7 mM KCl, 120 mM NaCl, 1.4 mM NaHCO3, 1.3 mM NaH2PO4, 22 mM D (+) glucose, 6.5 g/L lactalbumin hydrolysate, and 5.0 g/L yeast extract) and Schneider's Insect Medium (Sigma-Aldrich, St Louis, Mo.) supplemented with 10% heat-inactivated fetal bovine serum (HIFBS). MOS-55 was maintained in Schneider's Insect Medium supplemented with 20% HIFBS. Both media also contained penicillin (50 U/mL) and streptomycin (50 μg/mL). For routine maintenance, cells were grown in 25 cm2 plastic tissue culture flasks containing 5 mL of medium at 26° C. without CO2 incubation. Cells were passed every 3-4 days by vigorous shaking of the flask, and seeding a new flask with 20% of the resuspended cells with 5 mL fresh media.
Establishment of wMelPop Infected Cell Lines
wMelPop was purified from D. melanogaster w1118 embryos (Min and Benzer, 1997) and established in an uninfected Ae. albopictus cell line (Aa23.T) using the shell vial technique (Dobson et al., 2002). Embryos were collected every 45 min on molasses agar plates covered with live yeast paste and dechorionated using freshly prepared 50%-diluted bleach (White King, Victoria, Australia) (2.1% sodium hypochlorite final concentration) for 2 min. Embryos were then rinsed several times in sterile dH2O, immersed in 70% ethanol for 15 sec, and rinsed three times in sterile PBS, pH 7.4. Approximately 20 mg of surface sterilized embryos (˜50-100 μL of packed embryos) were then transferred to a mini Dounce tissue homogenizer (Wheaton, USA) and suspended in 400 μL of PBS. Embryos were then homogenized for 2-3 min with a tight pestle. 200 μL of homogenate was then overlaid separately onto two 80% confluent wells of Aa23.T cells prepared 24 hr earlier in a 12-well cell culture plate. The plate was then centrifuged at 2000 g for 1 hr at 15° C. Cells were then incubated at 26° C. for 24 hr and the contents of each well transferred to individual 25 cm2 cell culture flasks with 5 mL of fresh media. After a confluent monolayer had formed, cells were split 1:5 and passaged as usual.
To establish the infection in Ae. aegypti RML-12 and An. gambiae, MOS-55 cell lines, wMelPop, was purified from Aa23 cells as described below and introduced into these cell lines using the shell vial technique.
Characterization of wMelPop in Cell Lines
Wolbachia infections were characterized in cell lines using (i) PCR screening and sequencing, and (ii) electron microscopy. For each assay naturally uninfected or tetracycline-cured derivatives of each cell line were used as negative controls.
(i) PCR Screening and SequencingTo monitor infection status of cells, DNA was extracted from cultures as previously described (Dobson et al., 2002) and amplified using the general Wolbachia surface protein (wsp) primers 81F and 691R, or the diagnostic wsp primer set for wMelPop, 308F and 691R (Zhou et al., 1998). To confirm the presence of wMelPop in these three cell lines, fragments of the Wolbachia 16S rRNA and wsp gene were PCR-amplified, cloned and sequenced. DNA was extracted from cells using a DNeasy Tissue kit (Qiagen) and amplified as previously described using the diagnostic primers 99F and 994R for the Wolbachia 16S rRNA gene (O'Neill et al., 1992), and the primers 81F and 691R for the wsp gene (Zhou et al., 1998). Total DNA from cell lines was also PCR-amplified using the general eubacterial 16S rRNA primers 10F/1507R (Mateos et al., 2006) and 968F/R1401R (Nubel et al., 1996). The resulting PCR products were cloned into the pGEM-T easy vector (Promega) and four clones from each infected cell line randomly picked and sequenced for each product. The presence of wMelPop and no other contaminating bacteria in cell lines was verified by denaturing gradient gel electrophoresis (DGGE), using a general primer set targeting eubacterial 16S rRNA genes (F-968-GC and R-1401) (Nubel et al., 1996), using previously described methods (Pittman et al., 2008).
(ii) Electron MicroscopyInsect cells were washed in PBS and rapidly fixed with microwave processing in 2.5% glutaraldehyde solution containing 0.1% CaCl2 and 1% sucrose in 0.1 M Na cacodylate, enrobed in 2% agarose, and postfixed in 1% osmium tetroxide in 0.1 M Na cacodylate buffer. Samples were then dehydrated in a sequence of increasing ethanol concentration and in a final step in acetone (100%), and then embedded in epoxy resin (Epon 812) using microwave processing (Feinberg et al., 2001; O'Neill et al., 1997). Ultra-thin sections (50-80 nm) prepared on a Leica Ultracut T ultramicrotome (Leica Inc.) were then placed on copper grids and stained with 2% uranyl acetate followed by Reynolds lead citrate. The sections were then examined in a JEOL-1010 electron microscope operated at 80 kV.
Purification of Wolbachia from Cell Culture for Embryonic Microinjection
Insect cells from the confluent monolayers of two 175 cm2 flasks were harvested and centrifuged in 50 mL conical flasks at 1000 g for 5 min at 4° C. and the cell culture media discarded. The cellular pellet was then washed in SPG buffer (218 mM sucrose, 3.8 mM KH2PO4, 7.2 mM K2HPO4, and 4.9 mM L-glutamate, pH 7.2) and the centrifugation and wash steps repeated. After washing, the pellet was resuspended in 5 mL SPG and sonicated twice on ice for 10 sec at 12.5 W with a Fisher Scientific model 60 Sonic Dismembranator (3 mm microtip diameter) to lyse the cells. This suspension was then centrifuged at 1,000 g for 5 min at 4° C. to pellet cellular debris. The supernatant was then passed through a 5 μM Acrodisc syringe filter (Pall Life Sciences) and the filtrate collected in 1.5 mL microcentrifuge tubes. These were then centrifuged at 12,000 g for 15 min at 4° C. to pellet Wolbachia. The supernatant was then discarded, pellets were combined and resuspended in 400 μL SPG buffer and centrifuged at 300 g for 5 min to remove any remaining debris (Xi and Dobson, 2005). The supernatant was then transferred into a clean tube and stored on ice until used for injection (<3 hr).
Embryonic MicroinjectionPurified Wolbachia from RML-12 was microinjected into embryos of the D. melanogaster line w1118.T (Min and Benzer, 1997). Prior to microinjection, this line was confirmed to be free of Wolbachia by PCR using primers specific for the wMelPop IS5 repeat: IS5-FWD1 (5′-GTATCCAACAGATCTAAGC) (SEQ ID NO: 1) and IS5-REV1 (5′-ATAACCCTACTCATAGCTAG) (SEQ ID NO: 2). IS5 is a multi-copy insertion element, and as such a much more sensitive target for determining infection status than single copy genes such as wsp. For microinjection, early (pre-blastoderm) stage embryos were collected every 30 min using molasses agar plates with live yeast paste. Purified Wolbachia was microinjected into the posterior pole of embryos within 30 min of collection using standard techniques (Ashburner, 1989; Boyle et al., 1993; Xi and Dobson, 2005). After hatching, larvae were transferred to a standard cornmeal based Drosophila rearing medium (Ashburner and Roote, 2000) and incubated at 24° C.
Drosophila Rearing and PCR Screening for Infection StatusVirgin females resulting from injected embryos (generation 0 [G0]) were placed in vials with three w1118.T males to establish isofemale lines. After egg laying G0 females were sacrificed and DNA extracted using the Holmes-Bonner DNA extraction protocol (Holmes and Bonner, 1973). Wolbachia was detected in samples using PCR primers specific for the IS5 repeat element in wMelPop. The quality of the insect DNA was assessed using the primer set 12SA1 and 12SB1 that amplifies the D. melanogaster 12S ribosomal RNA gene (O'Neill et al., 1992). Amplification of DNA was carried out in a 20 μL reaction volume which included: 2.0 μL of 10× buffer (New England Biolabs, Beverly, Mass.), 25 μM of dNTPs, 0.5 μM of forward and reverse primer, 0.75 U of Taq polymerase (New England Biolabs, Beverly, Mass.), and 1.0 μL of DNA template. PCR conditions were as follows; denaturation at 94° C. for 3 min; 35 cycles of denaturation at 94° C. for 30 sec, annealing at 55° C. for 30 secs, and extension at 72° C. for 1 min; followed by a final 10 min extension step at 72° C.
To select for a stable infection, only offspring from females that tested positive for Wolbachia by PCR screening were used as parental stock. Each generation, 25-50 females from each line were isolated as virgins, placed into individual vials and outcrossed to three w1118.T males. Females that tested negative for Wolbachia were discarded along with their progeny. This selection regime was maintained for three generations after which the lines were closed. The two resulting lines, wMelPopCLA-1 and wMelPopCLA-2, were then monitored periodically by PCR to confirm infection status. The selection regime was again repeated at G14 due to fluctuations in infection frequencies in both lines.
Lifespan AssaysThe lifespan of wMelPopCLA-1, wMelPopCLA-2 and wMelPop lines was compared to tetracycline-cured derivatives of each line created by the addition of tetracycline into the adult diet (3 mg/mL) according to standard methods (Hoffmann et al., 1986). Treated flies were reared on tetracycline for two generations, and then transferred to a normal diet for a minimum of five generations before being used in experiments. To reduce genetic drift effects that may have occurred in these lines during tetracycline treatment, 100 females from each fly line (including infected lines) were backcrossed with 100 males from the same w1118.T stock line and the progeny combined to form the next generation. This was repeated for five generations (G23-G28). Longevity assays were then conducted at G31, G33 and G35. To control for any crowding effects or size variability, the larval density of each stock bottle used to obtain flies was standardized (200 larvae/bottle) prior to longevity assays. Stock bottles were kept at 24° C. until adult eclosion 9-10 days later, when flies were sexed as virgins and separated. In each assay, six vials of 20 flies for each sex were maintained at 29° C. in standard cornmeal food vials without additional live yeast. Each day the number of new deaths were recorded. Flies were moved to fresh food vials every five days. Survival curves for the various treatment groups were compared using a mixed effects Cox Proportional Hazard (coxme) model of survival analysis using the kinship package of the R suite of statistical software (www.r-project.org).
Cytoplasmic Incompatibility (CI) TestsCI tests were conducted at G36 and G38 post-transinfection using the previously backcrossed lines. To standardize rearing conditions for CI tests, fly stock bottles were grown under low-density conditions (n=150-200) at 24° C. with a 12 hr light/dark cycle. To obtain offspring for CI crosses, stock bottles were seeded with a set density of 200 eggs per 40 mL of diet. After eclosion, flies were sexed and separated as virgins and aged until CI tests. Male flies were collected on day 2 of emergence and were used within 24 hr of eclosion (Reynolds et al., 2003; Yamada et al., 2007). The female flies used were 5-7 days old. For each cross, single mating pairs (n=40) were introduced to plastic bottles with molasses plate lids. Pairs were given 24 hr to mate, then the males were removed and the females allowed to lay eggs. Eggs were collected every 24 hr on molasses agar plates dotted with live yeast suspension for three days. Females that laid <50 eggs total across the three plates were discarded from the experiment. The plates were then placed at 24° C. for a further 36-48 hr, and then the number of total and unhatched eggs were counted. Statistical significance of hatch rates for various crosses was determined using a Mann-Whitney U-Test. A Bonferroni correction was used to compensate for multiple comparisons.
Quantitative PCR and Density DeterminationTo examine if the density of Wolbachia in D. melanogaster had changed after long-term serial passage in mosquito cell lines, infection densities were monitored in head tissues of w1118 flies carrying the wMelPopCLA-1, wMelPopCLA-2 or wMelPop strain over their lifespan using quantitative PCR (qPCR). Heads were selected for qPCR as wMelPop infection densities had previously been shown to rapidly increase in nervous tissue with adult age (McGraw et al., 2002; Min and Benzer, 1997). Density of the closely-related non-virulent Wolbachia strain wMel was also examined after introgression for three generations from yw67c23 into the w1118 genetic background. qPCR assays were conducted at G46 post-transinfection. Flies reared as described for lifespan assays were collected at four-day intervals (from 4-32 days) until all the flies in a line were dead, and stored at −80° C. before analysis. Total DNA was extracted from dissected head tissues using the DNeasy tissue kit protocol (Qiagen). To estimate the relative abundance of Wolbachia in each sample, we compared abundance of the single-copy Wolbachia ankyrin repeat gene WD0550 to the single-copy D. melanogaster gene Act88F. The following primers were used to amplify a 74 bp amplicon from WD0550 (For 5′-CAGGAGTTGCTGTGGGTATATTAGC (SEQ ID NO: 3) and Rev 5′-TGCAGGTAATGCAGTAGCGTAAA (SEQ ID NO: 4)); and a 78 bp amplicon from Act88F (For 5′-ATCGAGCACGGCATCATCAC (SEQ ID NO: 5) and Rev 5′-CACGCGCAGCTCGTTGTA (SEQ ID NO: 6)). 12 biological replicates were examined per time point for each treatment. For each sample, qPCR amplification of DNA was performed in triplicate using a Rotor-Gene 6000 (Corbett Research, Australia). Amplification was carried out in a 10 μL reaction volume which included: 5 μL Platinum SYBR Green I Supermix (Invitrogen, CA), 1 μM of forward and reverse primer and 1 ng DNA template. The PCR conditions were 50° C. for 2 min; 95° C. for 2 min; 40 cycles of 95° C. for 5 sec, 60° C. for 5 sec and 72° C. for 10 sec; followed by a melt curve from 67° C. to 95° C. A standard calibrator was used to normalise between qPCR runs; and the specificity of PCR products was determined by melt-curve analysis. Crossing threshold (Ct) and amplification efficiency values for each sample were calculated using Corbett Rotor-Gene (Version 1.7.75) software. The relative abundance of Wolbachia in each sample was then determined using the method discussed by Pfaffl (Pfaffl, 2001). Regression analysis was used to detect trends in density of Wolbachia over the lifetime of individual fly lines. ANCOVA was then employed to examine the relationship between density and the covariates age and strain. All abundance data were log transformed prior to analysis. A Bonferroni correction was used to compensate for multiple comparisons.
ResultsSeveral initial attempts to establish wMelPop in the Ae. albopictus embryonic cell line Aa23 were unsuccessful. Typically infection was lost after several passages, or lines were discontinued due to a complete loss of confluence or growth of mosquito cells. This situation mirrors that observed when wMelPop purified from Drosophila is injected into mosquitoes, with large fluctuations in infection density eventually leading to loss of infection (EAM and SLO unpublished data). In total, only 2 out of 68 (3%) independent attempts to establish the wMelPop infection in Aa23 cells were successful.
Once established in Aa23, wMelPop was serially passaged for 237 passages (˜2.5 years) before being transferred to the Ae. aegypti cell line RML-12 and the An. gambiae cell line MOS-55. Stable establishment of wMelPop in these two cell lines occurred much more easily than the initial infection of Aa23, with 2 out of 2 independent attempts for each cell line forming stable wMelPop infections. Partial sequences of the Wolbachia 16S rRNA and wsp genes from the three cell lines used were all identical to the sequence from wMelPop, confirming that infections were not the result of contamination with other strains. Infection in mosquito cells was also confirmed using transmission electron microscopy (TEM). TEM micrographs of the three infected mosquito cell lines show that representative cells from each line were heavily infected by wMelPop (
The infection frequency in wMelPopCLA lines was then monitored periodically over time (
To assess the effect of continuous cell line culture on the ability of this Wolbachia strain to colonize Drosophila, we compared infection densities in flies that contained wMelPopCLA with those carrying the original wMelPop infection by qPCR. Since it is known that wMelPop densities increase rapidly in adult flies when held at 29° C., we assessed Wolbachia densities across the adult lifespan. As populations of flies aged, Wolbachia densities in head tissue rapidly increased in wMelPop infected flies (
To test whether the ability of wMelPop to induce the life-shortening phenotype had changed during long-term serial passage, we conducted a series of longevity assays at G31, G33 and G35 post-transinfection. For these experiments, the survival of infected flies from wMelPopCLA-1, wMelPopCLA-2 and wMelPop lines was compared with uninfected tetracycline-treated lines of each strain at 29° C. Survival curves for males and females of each treatment group were measured independently. In all assays, male and female flies from the wMelPop-infected line demonstrated the most pronounced lifespan reduction when compared to flies from the wMelPopCLA lines and tetracycline-treated controls (
In order to examine effects of long-term cell culture on CI expression we established test crosses between uninfected and infected flies and examined hatch rates of the resulting eggs. Results from incompatible test crosses indicated that wMelPop.T females mated with wMelPop males produced embryos with a mean hatch rate of 24%, which was significantly lower than the same cross with wMelPopCLA-1 males or wMelPopCLA-2 males (Mann Whitney, P<0.001) (
The naturally uninfected JCU strain of Aedes aegypti was established from A. aegypti eggs that were field-collected from Cairns (Queensland, Australia) in 2005. For routine maintenance, eggs were hatched under vacuum for 30 min, and larvae reared at a set density of ˜150 larvae in 3 L of distilled water in plastic trays (30×40×8 cm). Larvae were fed with 150 mg (½ tablet) fish food per pan per day (Tetramin Tropical Tablets, Tetra, Germany) until pupation. Adult mosquitoes were maintained in screened 30×30×30 cm cages enclosed within transparent plastic bags, with damp cotton wool to maintain elevated humidity (25±1° C., ˜80% relative humidity (RH), 12:12 h light:dark). Adults were provided with constant access to 10% sucrose solution, and females (5 day old) supplied with a human blood source for egg production. PGYP1 and PGYP2 lines were maintained continuously without prolonged desiccation of eggs.
Embryonic MicroinjectionMethods used for embryo injections were based upon those successfully used for the transfer of Wolbachia to both Drosophila and A. aegypti (Example 1; Xi et al., 2005). To collect eggs for microinjection, approximately ten gravid JCU females (˜5 days post-blood meal) were placed in a Drosophila vial with a wet filter paper funnel, and the vial moved to a dark place to promote oviposition. Embryos were collected after allowing females to oviposit for ≦90 min. Pre-blastoderm stage embryos (grey in colour) (Lobo et al., 2006) were aligned on double-sided tape (Scotch 665, St. Paul, Minn.), briefly desiccated, and covered with water-saturated halocarbon 700 oil (Sigma-Aldrich) (Xi et al., 2005). Embryos were then microinjected in the posterior pole with wMelPop, purified as previously described from the Aedes cell line RML-12 (see Example 1), using an IM-200 micro-injector (Narishige, Tokyo, Japan). Microinjection needles were prepared from borosilicate microcapillaries (#30-0038, Harvard Apparatus, Kent, UK) using a PC-10 micropipette puller (Narishige, Tokyo, Japan). After injection, embryos were incubated at 80% RH and 25° C. for approximately 40 min, after which time excess oil was removed and embryos transferred to wet filter paper. Embryos were then allowed to develop for 4-5 days, before being hatched and reared to adulthood using the standard maintenance procedures outlined above.
Isofemale Line Rearing and Selection for Stable InfectionFemales (G0) resulting from microinjected embryos were isolated as pupae to assure virginity, and subsequently mated with JCU males. Following blood feeding and oviposition, G0 females were sacrificed and DNA extracted using the DNeasy protocol (Qiagen). Wolbachia was detected in samples using PCR primers specific for the IS5 repeat element in wMelPop (see Example 1). G0 females that tested negative for Wolbachia were discarded along with their progeny. Offspring from females that tested positive for Wolbachia by PCR screening were used as parental stock to select for stable infections. PGYP1 females were outcrossed with JCU males for three generations (G0-G2), after which time this line was closed and infected females and males allowed to interbreed. Typically 50 JCU males and 50 virgin PGYP1 females were used in an outcross. Experimental selection to increase infection frequencies was applied to this line from G0-G3 (
PGYP1 and PGYP2 lines were cleared of wMelPop infection at G8 and G11 respectively, by introducing a 1 mg/ml tetracycline solution (final concentration)—dissolved in 10% sucrose—into adult cages (Dobson and Rattanadechakul, 2001). Lines were treated with tetracycline for two generations (with a 14 day course of tetracycline) and then allowed to recover for at least two generations before being used in experiments. Tetracycline-treated lines were confirmed to be cured of wMelPop by PCR as described above. The tetracycline-cleared mosquito strains, designated PGYP1.tet and PGYP2.tet, were also re-colonized with resident gut microflora by adding 100 ml water used to rear untreated JCU larvae to the larval water of treated lines for two generations after tetracycline treatment had ceased.
Lifespan AssaysThree different experimental designs were used for lifespan assays: First, the lifespan of G6 PGYP1 mosquitoes was compared with those from the naturally uninfected JCU strain at two different temperatures. For these assays, larvae were hatched and reared at 25° C. or 30° C. using the standard method described above. After emergence, adult mosquitoes were maintained in 2.2 L plastic buckets at their treatment temperature; with 80% RH and a 12:12 h light:dark cycle in a controlled growth chamber (Model 620RHS, Contherm Scientific, New Zealand). For each strain at each temperature, six buckets of 50 mosquitoes (25 of each sex) were maintained and checked daily. Cotton balls soaked in 2% sucrose solution as a carbohydrate source were placed inside each cage and changed daily. Second, the lifespan of G9 PGYP1 and JCU mosquitoes was compared under fluctuating abiotic conditions designed to simulate a summer day in Cairns, North Queensland, Australia. Mosquitoes were exposed to a diurnal cycle of 12 h light, 32° C., and 50% RH; and a nocturnal cycle 12 h dark, 25° C. and 80% RH in a controlled growth chamber as above. For this experiment a cohort of 300 adult mosquitoes (150 of each sex) from each strain were maintained in 30×30×30 cm cages. A sugar cube suspended 10 cm below the top of each cage was provided to necessitate flight to obtain a carbohydrate source. A human blood meal was provided to females in each cage daily for 15 min, in addition to a water-filled cup lined with filter paper as an oviposition substrate. Third, larger lifespan assays were conducted to compare survivorship of PGYP1, PGYP2, JCU and tetracycline-cleared strains. These assays were conducted at G13 and G15 for PGYP1 and PGYP2 lines respectively. For each strain, three replicate 30×30×30 cm cages of 200 mosquitoes (100 of each sex) were maintained at 25±1° C., 70-90% RH, 12:12 h light:dark in a temperature-controlled insectary, with 2% sucrose changed daily. For all three classes of experiments, the number of new deaths was recorded each day until all mosquitoes in the cages were dead. Mosquito survival was analysed using Kaplan-Meier Survival analysis, and log rank tests were used to determine the equality of the survival distributions between treatments.
Cytoplasmic Incompatibility (CI) TestsMass crosses were conducted between 35 virgin individuals (3 d old) of each sex from G9 PGYP1 and JCU strains; G13 PGYP1 and PGYP1.tet; and G16 PGYP2 and PGYP2.tet strains to assess CI levels. Groups were allowed to mate for 2 days before females were blood-fed and isolated individually for oviposition. Eggs were hatched 120 hours after oviposition by submersion in nutrient-infused deoxygenated water (75 mg Tetramin/L) for 48 hr. To hatch any remaining eggs, egg papers were dried briefly and then resubmerged for a further 5 days before the final numbers of hatched larvae were recorded. All females used in crosses were checked for insemination by dissection of spermathecae followed by direct observation of sperm by light microscopy. CI expression was determined by comparing the percentage of hatched eggs from each of the crosses. Statistical significance of hatch rates for various crosses was determined using a Mann-Whitney U-Test. A Bonferroni correction was used to compensate for multiple comparisons. To examine the role of male age on CI, virgin G17 PGYP1 and PGYP1.tet males were aged to 3, 10 and 17 d old prior to mating with 3 d old PGYP1.tet virgin females.
Maternal TransmissionThe proportion of Wolbachia-infected progeny derived from the first and third reproductive cycles of G17 PGYP1 females was assessed to provide an estimate of maternal transmission over lifespan. Cohorts of virgin PGYP1 females and uninfected wild-type JCU males were mass-mated. Five days after mating, females were blood-fed, and 72-96 hour post-blood meal, eggs were collected for three days. PGYP1 females were 9 days old at the time of oviposition for the first cycle, and 23 days old for the third cycle. After development, eggs were hatched and DNA extracted from larval offspring using the DNeasy protocol (Qiagen). In total, 515 larvae collected from 31 females (˜17 larvae per female); and 527 larvae collected from five cohorts of 20 females (˜105 larvae per cohort), were screened from the first and third reproductive cycles respectively. To establish the presence or absence of Wolbachia, PCR analysis was performed on individual larvae using IS5 repeat primers as previously described (see Example 1). To ensure that Wolbachia negative results were not a result of low quality DNA template, samples were also tested with primers specific for the single-copy A. aegypti gene, Ribosomal protein S17 (RpS17) (Cook et al., 2006): Forward 5′-CACTCCCAGGTCCGTGGTAT (SEQ ID NO: 7), Reverse 5′-GGACACTTCCGGCACGTAGT (SEQ ID NO: 8). If samples that were initially negative for Wolbachia tested positive for host DNA, they were screened once again with IS5 primers on a range of DNA template concentrations before infection status was finally assigned.
ResultsTo facilitate the transfer of the life-shortening Wolbachia strain wMelPop that infects D. melanogaster (Min and Benzer, 1997) into the mosquito A. aegypti, we adapted the bacteria by continuous serial passage in mosquito cell culture for three years. A consequence of this culturing was a reduction in growth rates and associated virulence when transferred back into Drosophila (see Example 1). We purified the mosquito cell-line adapted isolate of wMelPop and microinjected it into naturally uninfected A. aegypti embryos (JCU strain). Surviving adult females were isolated, blood-fed, and after egg laying were assayed for Wolbachia infection using diagnostic PCR (see Example 1; Materials and Methods). Eight independent isofemale lines carrying the wMelPop infection were generated. Six of these lines were lost from G1-G3 (See Materials and Methods), and the remaining two lines formed stable associations. These two lines, ‘PGYP1’ and ‘PGYP2’ were chosen for further characterization, and after a period of experimental selection have remained persistently infected by wMelPop (100% infection frequency) until G33 and G30 respectively, when last assayed (
In Drosophila species, wMelPop shortens the lifespan of adult flies by up to 50% (Min and Benzer, 1997; McGraw et al., 2002). We performed several lifespan assays in A. aegypti for a range of experimental conditions. As wMelPop-induced early death in Drosophila is temperature sensitive (Min and Benzer, 1997); Reynolds et al., 2003), we compared the lifespan of the newly generated wMelPop-infected PGYP1 line to the naturally uninfected JCU strain at 25° C. and 30° C. (
In contrast to Drosophila, where the life-shortening phenotype is weakly expressed at 25° C. and strongly at 30° C., rapid mortality of PGYP1 mosquitoes (G6) relative to the uninfected parental JCU strain was observed at both temperatures. Under lab conditions at 25° C. and 80% RH (
To examine the effect of the wMelPop infection under more biologically realistic conditions, we exposed a cohort of PGYP1 (G9) and JCU strains to a fluctuating temperature and humidity regime, and provided female mosquitoes with daily access to a human blood meal (
To exclude the possibility that observed reductions in lifespan resulted from genetic drift during the establishment of the PGYP1 strain, we generated an uninfected strain from PGYP1 (PGYP1.tet) by addition of the antibiotic tetracycline to the adult diet (Dobson and Rattanadechakul, 2001). After antibiotic curing of the wMelPop infection (Materials and Methods), no significant differences in the rate of mortality were observed between females or males of uninfected PGYP1.tet and JCU strains (e.g. females, log-rank statistic=1.23, P=0.2191). Both females and males from the PGYP1 (G13) strain had significantly reduced lifespan when compared to those from the PGYP1.tet strain (e.g. females, log-rank statistic=13.70, P=<0.0001), indicative of wMelPop-induced life-shortening (
To test for CI we made crosses between the PGYP1 and wild-type JCU and PGYP1.tet strains and measured egg hatch rates. Consistent with the induction of strong CI in A. aegypti (Xi et al., 2005), no eggs hatched from more than 2500 embryos obtained from crosses between male PGYP1 (G9) and uninfected JCU females (
In its natural D. melanogaster host wMelPop infection induces CI that quickly diminishes with male age (Reynolds et al., 2003). This effect could slow the invasion of the strain into natural populations. Crosses between uninfected A. aegypti females and wMelPop-infected males up to 17 days old resulted in a complete absence of egg hatch from more than 9500 embryos (Table 1), indicating wMelPop infection induced CI that is insensitive to male age.
Overall, no significant differences in fecundity between PGYP1, PGYP1.tet or JCU strains were observed at G13 post-transinfection (
High maternal inheritance of Wolbachia from infected females to their progeny is a key parameter for successful population invasion. The maternal transmission rate predicts stable prevalence of the infection once it has invaded a population under the action of CI (Hoffmann and Turelli, 1997). To estimate maternal transmission rates of wMelPop over the lifespan of A. aegypti, we used the polymerase chain reaction to determine the proportion of Wolbachia-infected progeny derived from the first and third reproductive cycles of PGYP1 females (G17) mated with uninfected wild-type JCU males. Of the 515 larvae screened from 31 females (˜17 larvae sampled per female) from the first reproductive cycle (females aged 9 days old), 99.74±0.26% were infected. This estimate of maternal inheritance was not significantly different from that obtained from the third reproductive cycle (females aged 23 days old) in which 527 larvae were screened from five cohorts of 20 females (˜105 larvae sampled per cohort) and were 99.45±0.37% infected (Mann Whitney, P=0.208).
Example 3 Increased Locomotor Activity and Metabolism of Aedes Aegypti Infected with a Life-Shortening Strain of Wolbachia Pipientis Materials and Methods Experimental OrganismsThe wMelPop-infected Aedes aegypti line (PGYP1) used in this study was generated as previously described (see Example 2). In brief, the Wolbachia strain, wMelPop, native to Drosophila melanogaster (Min and Benzer, 1997) was transferred into Ae. aegypti by embryonic microinjection. Descendants of this isofemale line were outcrossed for several generations to the original recipient line of mosquitoes and selected for stable infection before closing the colony. At generations 8 & 9 post-transinfection, an aposymbiotic control line was created by antibiotic treatment of the Wolbachia infected line (see Example 2). All experiments reported here were carried out on mosquitoes at generations 14-16 post trans-infection (i.e. 4-6 generations post treatment), with replicates representing different generations. Mosquitoes were reared under standard conditions (25° C., 12:12 LD, 80% RH) (Gerberg et al., 1994). Larvae were reared in plastic trays at a density of 150 per three litres of water and supplied with a daily dose of 0.15 g TetraMin aquarium fish food (Tetra, Germany). Adults were separated by sex and maintained as virgins in cages (30×30×30 cm) of ˜150 individuals. Adults were supplied with a basic diet of 10% sucrose solution administered through cotton pledgets. The adult ages of 3, 15, and 25 days of age were selected to represent the periods when 100%, ˜90%, and ˜20% of the wMelPop infected population was still surviving, respectively (see Example 2).
Videorecording of Mosquito LocomotionOur locomotor assay was based on several previously published models (Allemand et al., 1994; Bonatz et al., 1987; Grobbelaar et al., 1967; Kawada and Takagi, 2004; Liseichikov and Zakharevskii, 1978; Mankin, 1994; Reynolds and Riley, 2002; Rowley et al., 1987; Sbalzarini and Koumoutsakos, 2005), but was most heavily influenced by Williams and Kokkinn (Williams and Kokkinn, 2005). Mosquitoes were placed in an observation chamber during experiments and their motion captured via a video camera. The observation chamber was constructed using white (sides and back) and transparent Perspex (front pane) and contained distinct cells that allowed for the simultaneous observation of 10 individual mosquitoes, one per cell. Mosquitoes were provided with 10% sucrose solution ad libitum during observation periods dispensed through dental cotton wicks (1×ø0.5 cm). The wicks placed in each observation cell also provided constant humidity (80-85% RH). Mosquitoes were transferred from rearing cages to observation chambers 20 min prior to recording of activity to allow them to adapt to the new environment. Recording began daily at 14:30 pm, was paused during the hours of darkness (21:00-07:00) and was completed at 12:30 the following day to allow time to transfer in the next set of mosquitoes. After each observation period mosquitoes were aspirated out of the chamber and sacrificed. The chambers were cleaned with ethanol (80%) and food supply replaced prior to subsequent observation periods. No mosquito mortality was observed during the observations. A total of three replicates each of 10 mosquitoes were studied per sex×strain×age per study chamber.
A two-color camera (DR2-13S2 m/C-CS, Point Grey Research, Vancouver, BC, Canada) was fitted with a CCTV lens (12VM412ASIR, Tamron, Commack, N.Y., USA) and fixed on a mounting bracket 110 cm from the chamber. The distance of the camera to the object, the zoom, and the focus and iris aperture were optimized to reduce barreling and distortion of images. A flat light source emitting light intensity was placed 10 cm behind the chamber, which provided sufficient lighting for the camera sensor to capture high quality images but did not increase ambient temperatures. The light source power switch was synchronized with the room lights using a timer. The entire experimental setup was enclosed in cardboard to minimise intrusion of additional stimuli.
The file format used for recording, Audio Video Interleave (AVI), is limited to a maximum size of 2 GB, which amounted to approximately 8 min of video footage. To obtain a continuous video recording, we developed a program called Mossiecap that recorded multiple sequential 1.5 GB AVI files. This file size captured six minutes of video (i.e. 10 files=60 min) at 12 frame s−1. Each day's footage (˜420 GB) was recorded onto an external hard drive connected to a desktop computer. The contents of each hard drive were then transferred to the hierarchical storage management (HSM) system at The University of Queensland. Video files stored on the HSM were then evenly distributed to local disks on 20 workstations located in the Visualization and Advanced Computing (ViSAC) laboratories at The University of Queensland. Mossiefly, a custom program developed in Matlab (The MathWorks, Inc, Natick, Mass.) was used to process videos for motion detection and tracking. This program detected and tracked movement (walking and flying separately) of individual mosquitoes and digitised the coordinates and time for each movement. The files containing data from movement detection were then analysed using Mossiestat, a program developed in Matlab that summarised the movement data captured with Mossiefly into numerical values used for statistical analysis. A total measure of activity (summation of time spent flying and walking) reported per hour was used for all subsequent statistical analysis as it was more informative than examining the variables independently.
Metabolic RateClosed-system respirometry was used to measure CO2 production (VYCO2) in the mosquitoes. CO2 production has been shown extensively to be an accurate measure of the metabolism for small and highly aerobic organisms such as insects (Lighton, 1991; Lighton and Duncan, 2002; Van Voorhies et al., 2004). Our experiment was designed to determine whether metabolic rate was significantly different between wMelPop-infected and -uninfected mosquitoes in each of two, day time intervals lasting 4 hours. Fifteen individual mosquitoes were measured for each sex×strain×age×interval combination. These measurements were replicated 3 times. Mosquitoes were discarded after the recording interval and replaced with fresh mosquitoes from the same rearing cage.
An ADInstruments gas analyzer (ML205) and a PowerLab (85P) analog-to-digital converter connected to a computer running data acquisition software (ADInstruments, Chart 5) were used to measure CO2 production from mosquitoes. Before each experiment, the gas analyser was calibrated with gas of a known CO2 content. Individual mosquitoes were loaded into 25 ml syringes, mounted with a three-way valve stopcock. Before closing the three-way valve the syringe was carefully flushed with room air to remove possible CO2 traces. Immediately after closing the 15 syringes, a separate syringe was filled with air and kept as a control sample for initial room air CO2 concentration. After the 4 h interval, the syringes were injected into the gas analyser at 2 ml s−1 until 5 ml of air remained. The gas concentrations for each mosquito were used to calculate mosquito metabolic rate. The dry mass of each mosquito was obtained after freezing them for 48 h at −20° C. and desiccating the tissue in a dry vacuum pump. Dry mass was measured with an electronic balance (Sartorius BP211D) to the closest 0.01 of a milligram. Mosquitoes were not weighed before metabolic rate experiments because immobilisation methods (i.e. CO2 asphyxiation) may alter metabolic rates.
The following formulas based on (Bartholomew et al., 1985) were used for calculations of metabolic rates:
VYCO2(mlCO2h−1)=Va*Vb*t−1
where Va was the increase in volume of carbon dioxide in the samples (calculated from the difference between final and initial CO2 fractional concentrations), Vb was the effective volume in the syringe (25 ml minus the mosquito volume, estimated as 1.01 * body mass), and t was the elapsed time in hours. Due to variation in mass between male and female, mosquitoes metabolic rate was allometrically scaled using the following formula based on (Fuery et al., 1998):
Scaled MR (mlCO2h−1)=((
where
Transformations (square root) of the activity measures and the scaled metabolic rate were necessary to generate normal distributions. General linear models were then constructed in Statistica Release 8 (StatSoft) for each of the sexes separately to explore the effects of age, infection status, time of day and replicate on each of the activity and metabolic rate datasets separately. T-tests were then employed to specifically test for differences in metabolic rates between infected and uninfected mosquitoes at each of the three ages.
Results Mosquito ActivityOn average, Wolbachia infected individuals were more active during the day than their uninfected counterparts at each of the three adult ages examined (
Metabolic rate was measured for separate sets of mosquitoes during two daytime windows, 07:30-11:30 and 11:30-15:30. The data from the two windows were combined after they were shown not to differ from one another using a general linear model (data not shown). In females (
All fly lines were maintained on standard cornmeal diet at a constant temperature of 25° C. with a 12 hour light/dark cycle. The Oregon RC (ORC) line was obtained from the Bloomington Drosophila stock centre at Indiana University in 2004, whereas the Oregon R(OR) and w1118 lines have been maintained long term in the O'Neill lab. The Champetières (Champ) stock was obtained in 2005 from the Drosophila Genetic Resource Centre at Kyoto Institute of Technology (stock number 103403) and maintained in the Johnson lab.
Drosophila C virus isolate EB (Johnson and Christian, 1998) was plaque purified, passaged in Drosophila (DL2) cells and purified by centrifugation through a 10-40% sucrose gradient as previously described (Hedges and Johnson, 2008). The cricket paralysis virus (CrPV) (Johnson and Christian, 1996) and the Flock House virus (FHV) isolate we previously described (Johnson et al., 2001) were used in the current study. DL2 cells were infected with either CrPV or FHV and cells harvested two days post infection. Cells were lysed by two rounds of freeze thawing and lysates were clarified by centrifugation for 20 min at 5000 g. Virus was pelleted through a 20% sucrose cushion by centrifugation at 100000 g for 3 hours. Virus was resuspended in 50 mM Tris, pH 7.4, aliquoted and stored at −80° C. A fresh aliquot was thawed for each experiment.
The concentration of tissue culture infectious units (IU) of each virus preparation was determined essentially as previously described (Scotti, 1980). Briefly, 50 μl of a suspension of DL2 cells (1×106 cells/ml) was transferred to individual wells of a flat bottomed 96 well tissue culture tray and cells were allowed to attach for at least 1 hour. A ten-fold dilution series was prepared in standard cell culture medium for titration. Each virus dilution was used to inoculate 8 wells (50 μl per well). The plates were incubated at 27° C. for 4-5 days before scoring for cytopathic effects (CPE) and the concentration of IU in the virus sample calculated as described previously (Scotti, 1980).
Survival AssaysFor survival assays 4-6 day old adult male Drosophila were infected by micro-injection of virus into the upper lateral part of the abdomen. For negative controls flies were injected with PBS. Samples were injected into flies anaesthetised with carbon dioxide, using needles pulled from borosilicate glass capillaries and a pulse pressure micro-injector. Virus was diluted to a standard concentration (DCV 1.8×108 IU/ml, CrPV 1.8×108 IU/ml and 1.8×108 IU/ml FHV) in PBS and approximately 100 nl was injected into each fly. For each fly line assayed, three groups of 15 flies were injected with virus and one group of 15 flies were injected with PBS. Flies were maintained in vials at a constant temperature of 25° C. with a 12 h light/dark cycle and mortality was recorded daily. Mortality that occurred within 2 days of injection was deemed to be due to injury. Negligible mortality (<10% in all cases) was observed in negative controls (data not shown). Each experiment was repeated in triplicate. Survival curves were compared using Kaplan-Meier analysis (Statview).
Diagnosis of Wolbachia and DCV InfectionFive flies were pooled from each fly line and genomic DNA was extracted using the previously described STE method (O'Neill et al., 1992). The DNA was PCR screened for presence of Wolbachia using the diagnostic wsp primer set 81F and 691R (Zhou et al., 1998) and the integrity of the DNA was confirmed using the 12S primer set 12SA1 and 12SB1 (Simon et al., 1994). All fly stocks were confirmed to be DCV free (data not shown).
Tetracycline TreatmentAll Wolbachia infected fly lines used were treated with 0.03% tetracycline (Hoffmann et al., 1986) to generate uninfected fly lines. Following the tetracycline treatment flies (designated ORCT or w1118 T) were held for more than five generations to recover before being used for experiments.
RT-qPCR Analysis of VirusRNA concentration in flies Flies from the ORC and ORCT lines injected with DCV as described above were harvested immediately following injection (0 day time point), 2 days or 7 days post infection. Four flies were pooled, RNA extracted, random primed cDNA synthesised and the amount of DCV RNA quantified using the primers DCV-rt-fw1 5′ AGGCTGTGTTTGCGCGAAG 3′ (SEQ ID NO: 9) and DCV-rt-rv1 5′AATGGCAAGCGCACACAATTA3′ (SEQ ID NO: 10) as previously described (Hedges and Johnson, 2008). For each time point shown four pools flies were independently assayed.
ResultsWe compared the survival of flies infected with DCV in the presence or absence of Wolbachia infection (
Plaque purified DCV isolate EB (Hedges and Johnson, 2008) and FHV (Johnson et al., 2001) were propagated and purified from DL2 cells (Schneider, 1972). DL2 cells were maintained in Schneider's media supplemented with 10% FBS, 1× glutamine and 1× penstrep (Invitrogen) at 27.5° C. Cells grown in 75 cm2 flasks were infected with either DCV or FHV at a low multiplicity of infection (<1) and harvested at 4-5 dpi. Cells were lysed by two rounds of freeze-thawing and cell debris removed by centrifugation at 5,000 rpm for 5 min. The virus was purified from the supernatant by pelleting through a 6 ml 10% sucrose cushion at 27,000 rpm at 12° C. for 3 hours in a SW28 swing bucket rotor (Beckman). The resuspended virus was layered onto a continuous 10-40% w/v sucrose gradient and centrifuged at 27,000 rpm at 12° C. for 3 hours in a SW41 swing bucket rotor (Beckman). The virus-containing fractions were harvested, diluted in 50 mM Tris pH 7.4 and virus was pelleted by centrifugation at 27,000 rpm, 12° C. for 3 hours. The virus was resuspended in 50 mM Tris pH 7.4 at 4° C. overnight, aliquoted and stored at −20° C. The concentration of tissue culture infectious units (IU) of each virus preparation was determined by replicate TCID50 analysis on two separate frozen aliquots, as previously described (see Example 4).
Flies and WolbachiaAll Wolbachia infected fly lines were obtained from the culture collection in the O'Neill lab and were maintained on standard cornmeal diet at a constant temperature of 25° C. with a 12-hour light/dark cycle. The D. simulans fly line Me29 is infected with wMel. The wMel infection was established by injection of Wolbachia containing cytoplasm from D. melanogaster Wien 5 embryos into D. simulans NHaTC embryos (Poinsot et al., 1998). The other D. simulans lines are naturally infected with Wolbachia strains as previously described and are listed in Table 2 (Hoffman et al., 1986; Mercot and Poinsot, 1998; O'Neill and Karr, 1990; and Hoffman et al., 1996).
Preparation of Wolbachia- and Virus-Free Fly LinesVirus-free populations of each of the Wolbachia containing fly line were prepared essentially as previously described (Brun and Plus, 1980). Briefly, flies were aged for at least 20 days, transferred to fresh media (supplemented with dry yeast) and allowed to lay eggs for up to 16 hours. The eggs were collected from the surface of the media and treated for 4 minutes in 1.7% (w/v) sodium hypochlorite solution to remove the chorion. After treatment the eggs were thoroughly rinsed with water, transferred to moist filter paper and placed on fresh virus-free media. Virus-free flies were maintained separately from untreated stocks.
To generate fly lines free of Wolbachia each virus-free Wolbachia infected fly line was treated with 0.03% tetracycline (Hoffman et al., 1986). Following the tetracycline treatment flies were held for more than four generations to recover before being used for experiments.
Survival BioassaysDrosophila were infected with DCV, FHV or mock infected by microinjection of virus or PBS into the upper lateral part of the abdomen. Samples were injected using needles pulled from borosilicate glass capillaries and a pulse pressure micro-injector into 4-7 day old male flies that were anaesthetised with carbon dioxide. For each fly line assayed, three groups of 15 flies were injected with virus and one group of 15 flies were injected with PBS. After injection flies were maintained in vials at a constant temperature of 25° C. with a 12 h light/dark cycle and mortality was recorded daily. Mortality that occurred within one day of injection was deemed to be due to injury. Each experiment was replicated using independent cohorts of flies. Survival curves were compared using Kaplan-Meier analysis and log-rank statistics reported (GraphPad Prism). For each assay described in this paper a fresh aliquot of either DCV or FHV was defrosted and diluted to 1×108 IU/ml before use.
Virus Accumulation AssaysThe accumulation of infectious DCV particles in both Wolbachia infected and uninfected flies was measured. For each of the five fly lines, groups of flies with and without Wolbachia were injected with DCV as for survival bioassays. At designated times post injection, two pools of four live DCV injected flies were collected and frozen at −20° C. Flies from all Wolbachia infected and uninfected fly lines were collected at 2 dpi. For Me29, DSR and CO flies infected with Wolbachia samples were also collected at 10 days post injection; for N7NO and DSH containing Wolbachia and all tet-treated lines there were not enough live flies remaining at 10 days for collection. For CO-Wolbachia flies an additional collection was included at 30 dpi.
Each pool of four flies was homogenised in 100 μl of PBS with two 3 mm beads (Sigma-Aldrich) using a Mini BeadBeater-96 (Biospec Products) for 60 seconds. The homogenates were clarified by centrifuging at 14 K for 8 minutes. The virus—containing supernatant was aliquoted and stored at −20° C. Virus titre was determined using the TCID50 assay as previously described (see Example 4). The two replicates for each fly population were assayed on different days to control for between-day variation in TCID50 assays. Statistical analysis of the data was done using unpaired t tests to compare the geometric means of the duplicate samples between flies of each line with and without Wolbachia at 2 dpi (GraphPad Prism).
Analysis of Wolbachia DensityFor each fly line 200 eggs were collected and incubated on fresh food with a constant temperature of 25° C. for 10 days. Freshly emerged flies were collected for 8 hours, aged to 4 days old and then five male flies from a single collection were pooled. For each fly line a total of 10 pools of flies were collected from independent bottles and the DNA extracted using a DNeasy Blood and Tissue Kit as per the Manufacturer's instructions (Qiagen). The relative ratio of Wolbachia to fly genomic DNA was determined by quantitative PCR. Each 10 μL qPCR reaction included 5 μL of Sybr Green qPCR Supermix-UDG (Invitrogen), 1 μL of DNA template and 1 μM each of the forward and reverse primers. Primers for Wolbachia were designed from an alignment of the sequence of the WSP genes from all five Wolbachia strains (wspFQALL 5′ GCATTTGGTTAYAAAATGGACGA 3′ (SEQ ID NO: 11) and wspRQALL 5′ GGAGTGATAGGCATATCTTCAAT 3′) (SEQ ID NO: 12) and for the host gene RPS17 (Dmel.rps17F 5′ CACTCCCAGGTGCGTGGTAT 3′ (SEQ ID NO: 13) and Dmel.rps17R 5′ GGAGACGGCCGGGACGTAGT 3′ (SEQ ID NO: 14)). Reactions were done in duplicate in a Rotor-gene thermal cycler (Corbett Life Sciences) with the following conditions: one cycle of 50° C. 2 min, 95° C. 2 min, followed by 40 cycles of 95° C. 5 sec, 60° C. 5 sec, 72° C. 10 sec. A third technical replicate was done where necessary and DNA extracted from flies without Wolbachia was used as a negative control. Ratios were calculated in Qgene and statistical analysis included Mann-Whitney t test to compare differences of the means.
Accession NumbersEF423761 wsp wRi; DQ235409 wsp wAu; AF020074 wsp wNo; AF020073 wsp wHa; NM—079278 RPS17
Results Wolbachia strain wMel can protect D. simulans from DCVWolbachia strains closely related to wMel have previously been shown to protect their natural host D. melanogaster from accumulation of DCV particles and DCV-induced mortality (Teixeira et al., 2008; see also Example 4). To establish whether wMel can protect D. simulans from DCV, we assayed Me29, a D. simulans line that was transinfected with wMel (Poinsot et al., 1998) (Table 2). Me29 flies infected with wMel and the genetically paired population that had been cured of Wolbachia infection were challenged with DCV and mortality was recorded for 15 days (
The accumulation of infectious DCV particles was assayed in Me29 flies with and without wMel. The titre of infectious virus in homogenates from flies collected 2 dpi was significantly different in flies with and without wMel (p<0.002;
D. simulans Wolbachia strains and protection from DCV induced mortality
D. simulans populations are naturally infected with a range of Wolbachia strains. To analyse whether diverse strains could protect from DCV induced mortality we assayed four D. simulans lines CO, DSR, DSH and N7NO, which are naturally infected with wAu, wRi, wHa and wNo, respectively (Table 2). Each of the four fly lines was treated with tetracycline to produce a genetically paired line without Wolbachia infection. Flies with and without Wolbachia were challenged by injection with DCV or mock infected with PBS (
Not all Wolbachia strains protected flies from DCV induced mortality. The median survival time of DSH and N7NO flies challenged with DCV was 4 days regardless of Wolbachia infection status for fly lines infected by wHa or wNo, respectively (
Accumulation of DCV in Flies with and without Wolbachia
DCV accumulation was assayed in each D. simulans line in the presence or absence of Wolbachia (
D. simulans Wolbachia strains and protection from FHV induced mortality
Having identified that some but not all Wolbachia strains mediate protection against DCV in the D. simulans lines tested, we next investigated whether antiviral protection was consistent across different viruses. Flies with and without Wolbachia were challenged by injection with FHV or mock infected with PBS (
Not all of the fly lines were protected from FHV-induced mortality by Wolbachia infection. The median survival time of DSH flies challenged with FHV was 6 days regardless of the presence or absence of wHa (
To investigate whether virus protection correlated with the density of the Wolbachia in the fly lines, we utilized quantitative PCR to determine Wolbachia density from pools of 5 male flies from each fly line. Estimates of abundance for a single copy Wolbachia gene were determined and then normalized against abundance of a single copy host gene to determine relative abundance of Wolbachia (
Dengue Interference by wMel and wMelPop in Mosquitoes
As shown in
Five different A. aegypti lines were used including the original inbred wMelPop-CLA infected line (PGYP1) and its tetracycline-cured counterpart PGYP1.tet (see Example 2). A genetically diverse line derived from PGYP1, named PGYP1.out was generated by backcrossing PGYP1 for three generations to F1 males of 52 independent field-collected isofemale lines from Cairns, Australia. A further two generations of backcrossing were conducted with F2 field-collected material before the colony was used in experiments. This backcrossing scheme is expected to replace 96.9% of the original inbred genotype. A tetracycline-cured counterpart (PGYP1.out.tet, −Wolb) was generated by antibiotic treatment of backcrossed adults, followed by two generations of recovery and recolonization with gut bacteria as previously described (see Example 2). A genetically diverse wild type line was also generated at the same time from field-collected material sourced from 245 ovitraps across seven suburbs of Cairns, Australia in late 2008 and named Cairns3. For the malaria experiments, a susceptible A. fluviatilis strain (Rodrigues et al., 2008) was used in parallel with PGYP1.out (+Wolb) and PGYP1.out.tet (−Wolb) A. aegypti mosquitoes. Insects were kept in a controlled environment insectary at 25 C, ˜80% RH and a 12 hour light regime. Larvae were maintained with fish food pellets (Tetramin, Tetra) and adults were offered 10% sucrose solution, ad libitum. Adult females were bloodfed on human volunteers for egg production. Three to five day old female mosquitoes were used for the DENV and malaria infection experiments. Seven day old females were used for the CHIKV experiments.
Viruses Dengue VirusDengue virus serotype 2 (DENV-2) (92T) was isolated from human serum collected from a patient from Townsville, Australia, in 1992. Virus stocks were passaged five times in Aedes albopictus cell line (C6/36) grown in RPMI 1640 medium supplemented with 10% fetal calf serum (FCS), penicillin (100 μg/ml), streptomycin (100 μg/ml), and 1× glutamax (Invitrogen), and maintained at 28° C. Supernatants were collected 5 days after infection, separated into 0.5 ml aliquots, and then frozen at −80° C. Virus used in microinjection experiments was obtained from thawed stocks of above and had a titer of 107.6 CClD50 per ml. To prepare the DENV-2 for oral feeding, the frozen virus stock was passaged once more through C6/36 cells and the supernatant was harvested at 5 days and then mixed directly with blood to formulate a bloodmeal for feeding. Virus solution with higher titer (108.85 CClD50/ml) was obtained by harvesting the viral supernatant and the intracellular virus from cell lysates.
Chikungunya VirusCHIKV strain 06113879, isolated from a viremic traveler returning from Mauritius to Victoria, Australia in 2006 was provided by the Victorian Infectious Diseases Research Laboratory, Melbourne, Australia. Cultures were grown at 37° C. in Vero (African green monkey kidney) cells for 4 days before the supernatant was harvested and frozen at −80° C. This CHIKV stock was passaged once more in Vero cells and the virus was concentrated from 1.8 L of infected culture supernatant via ultracentrifugation at 10 000 g for 17 hrs at 4° C. Pelleted virus was resuspended in 20 ml of Opti-MEMO reduced serum medium (Gibco BRL®, Invitrogen, California) supplemented with 10% FCS before aliquots of the prepared virus were frozen at −80° C. The stock concentration had a final viral titer of 108.0 CClD50/ml.
Exposure of Mosquitoes to VirusesIntrathoracic Injection with DENV-2
Female mosquitoes were briefly anesthetized with CO2 and placed on a glass plate over ice. Insects were handled with forceps under a dissecting scope and injected into their thorax (pleural membrane) with a pulled glass capillary and a handheld microinjector (Nanoject II, Drummond Sci.). Sixty-nine nanolitres of DENV-2 stock was injected into each mosquito, which corresponds to approx. 2,750 virus particles/mosquito. After injection mosquitoes were transferred to 1 L plastic cages within polystyrene boxes and these boxes were maintained inside an environmentally controlled incubator 12:12 (L:D) h, 27° C. and 70% RH. Sucrose solution and apple slices were provided on top of each cage. Mosquitoes were collected from each cage 5 and 14 days after infection and 5 dpi (days postinfection) samples were dissected into abdomen and thorax plus head. Samples were placed on dry ice and then transferred to −80° C. until RNA extraction (see below). Fourteen days after thoracic injection eight mosquitoes were collected from each cage, briefly anesthetized with CO2 and placed on a glass plate over ice. Wings and legs were removed with forceps and their mouthparts were introduced into a 1 cm piece of polypropylene tubing (0.61×0.28 mm, Microtube Extrusions, NSW, Australia) filled with light mineral oil (Novak et al., 1995). Females were allowed to salivate into these capillaries for 5 minutes at room temperature, and then the capillaries were rinsed into 20 μl of fetal calf serum with a Hamilton syringe. Samples were centrifuged at 14,000 g for 2 minutes and kept frozen (−80° C.) for further virus detection using a cell culture enzyme immunoassay (CCEIA). Mosquito whole bodies were frozen on dry ice and kept at −80° C. for quantitative PCR virus detection.
Oral Feeding with DENV-2 and CHIKV
Mosquitoes were starved for 24 hrs and then transferred to 1 L or 2.5 L plastic feeding containers. Prior to feeding, DENV-2 was harvested from C6/36 cell culture supernatant and diluted 1:5 in defibrinated sheep's blood. For the CHIKV experiments, frozen aliquots of stock virus were rapidly thawed, and diluted in washed defibrinated sheep blood and 1% sucrose. Blood-virus mixtures were maintained at 37° C. for 1 h and 4 h for DENV-2 and CHIKV, respectively, using membrane feeders (Rutledge et al., 1964) and covered with a porcine intestine as the membrane. After feeding, mosquitoes were anesthetized using CO2 and partially and non-engorged mosquitoes were discarded. Fully engorged mosquitoes were maintained on a 15% sucrose solution at 12:12 (L:D) h, 27-28° C. and 70% RH. To determine DENV-2 infection and dissemination rates, up to 40 mosquitoes were processed separately at 7 and 14 d post-exposure. To follow the replication and dissemination of CHIKV, 10-30 mosquitoes were processed on days 0, 2, 4, 7, 10 and 14 post-exposure. Mosquitoes were anesthetized using CO2, and the legs (for DENV-2) and legs and wings (for CHIKV) from each mosquito were removed, and these and the remaining body and head were stored separately at −80° C. Samples were processed using the CCEIA method (DENV-2) or qRT-PCR(CHIKV) described below. Differences in the frequency of DENV-2 infection and dissemination between mosquito lines were analyzed using chisquare goodness of fit tests after the 7 or 14 d extrinsic incubation period for DENV-2 and at 14 d for CHIKV (Zar, 1999).
Cell Culture Enzyme ImmunoassaysTitration of DENV-2 and CHIKV stocks and blood/virus mixtures was performed using a CCEIA method similar to that previously described (Broom et al., 1998). For DENV-2, C6/36 cell monolayers (60-90% confluent) in 96-well plates were inoculated with 50 μl/well of virus dilutions and plates were incubated at 28° C. with 5% CO2 for 5 d. Cell monolayers then were fixed and examined for DENV-2 antigens using a cocktail of flavivirus cross-reactive monoclonal antibodies (4G4 and 4G2) (Hall et al., 1991). For CHIKV, all titrations were performed in Vero cells, which were incubated at 37° C. with 5% CO2. After 7 d plates were examined for cytopathic effect (CPE), which was confirmed using the CCEIA and the broadly reactive alphavirus monoclonal antibody, B 10.
Plasmodium gallinaceum
Two to three day-old White Leghorn chickens were infected through intraperitoneal or intradermal injection of Plasmodium gallinaceum 8A strain parasitized blood (Rodrigues et al., 2008). Parasitemia was determined every other day through Giemsa-stained blood smears. Ten microscopic fields were examined under immersion oil to count one hundred red blood cells and determine the ratio of infected cells. Presence of gametocytes and rising parasitemia was ensured in order to enhance the chance of mosquito infection. Before infection mosquitoes were deprived of sugar solution overnight and on the next morning chickens were placed on top of the cages and mosquitoes were fed for about 45 minutes. Only bloodfed female mosquitoes were kept for further observations. Four independent experiments were performed with independent cohorts. Seven days after bloodfeeding mosquitoes had their midguts dissected in 1×PBS and after staining the midguts with 0.2% Mercurochrome solution oocysts were counted under a microscope (DIC, 100×). Fifteen days after infection mosquitoes were collected and DNA was extracted (Qiagen Blood & Tissue kit) for Plasmodium detection. For P. gallinaceum detection around 1 ng of genomic DNA was used in quantitative PCR reactions as described below. Primers for the Plasmodium spp. 18S ssu rRNA gene (Schneider and Shahabuddin, 2000) were used for the parasite sequence amplification and A. aegypti Actin primers were used as a host control gene (see primer sequences in Table 6). Analyses were performed with qGENE (Joehanes and Nelson, 2008) and Mann Whitney-U tests (STATISTICA V8, StatSoft, Inc.) to compare relative abundance between lines.
Quantitative DENV PCR AnalysisIndividual frozen mosquito whole bodies or body parts were placed into 2 ml screw cap vials with a glass bead (2 mm diameter, Sigma-Aldrich). 200 μl of Trizol (Invitrogen) was added and the sample homogenized for 150 s using a Mini BeadBeater (Biospec Products). Tubes were incubated at room temperature for 5 min, 40 μl of chloroform was added to each tube and samples were thoroughly vortexed for 10 s. Tubes were centrifuged for 15 min at 14,000 g at 4° C. and the supernatant containing the RNA was transferred to new tubes. RNA was precipitated by adding 40 μl of isopropanol and incubated at −20° C. overnight. Samples were centrifuged at 12,000 g for 10 min at 4° C. to pellet the RNA. Pellets were washed with 200 μL of 70% ethanol and after centrifugation (7,500×g for 5 min at 4° C.) ethanol was removed and pellets were dried for 10 min in a fume hood. RNA was resuspended in 25 μL of RNAse-free milli-Q water and tubes were incubated for 10 min at 56° C. Samples were maintained at −80° C. until further analysis. cDNA synthesis was based on the protocol described by Richardson (Richardson et al., 2006), which allowed us to determine both the genomic (+RNA) and replicative (anti-genomic) virus forms (−RNA). Briefly, 0.5 ng of each RNA (2 μg for saliva samples) was mixed with 0.625 μM of either the DENV-2 NS5 forward or reverse primer (see Table 6) plus 0.2 mM dNTPs in separate cDNA reactions. Samples were incubated at 86° C. for 15 min and 5 min on ice, then 5× first strand buffer and 100 U of Superscript III (Invitrogen) was added to a total volume of 20 Samples were incubated at 25° C. for 10 min, followed by 42° C. for 50 min and 10 min at 95° C. to inactivate the transcriptase. Negative controls (no template) were included in each reaction. For DENV-2 detection, cDNA samples were diluted 1:10 with milli-Q water. The qPCR reaction consisted of 2 μl of the diluted cDNAs, 5 μl of Sybr Green mix (Invitrogen) and 1 μM of each primer (see above), in 10 μl total volume. Reactions were performed in duplicate in a Rotor-gene thermal cycler (Corbett Life Sciences) with the following conditions: 50° C. 2 min, 95° C. 2 min, 45 cycles (95° C. 5 s, 60° C. 5 s, 72° C. 10 s) followed by the melting curve (68° C. to 95° C.). Melting curves for each sample were analyzed after each run to check specificity. A standard curve was created by cloning the DENV-2 NS5 fragment into pGEM®T-Easy (Promega). After linearization with Pst I the plasmid was serially diluted into known concentrations and run in parallel, in order to determine the absolute number of DENV-2 copies contained in each sample. Mann-Whitney U tests were employed (STATISTICA V8, StatSoft, Inc.) to examine the effect of Wolbachia infection on dengue number for each for each paired strain combination (PGYP1×PGYP1.tet; PGYP1.out×PGYP1.out.tet)×body part (whole, abdomen, thorax)×age (5 or 14 d) post inoculation. The tests were based on the means from each of 4 independently replicated experiments.
CHIKV qRT-PCR Analysis
Individual frozen mosquito bodies and heads or legs and wings were homogenized for 3 min in 1 ml of Opti-MEM® reduced serum medium respectively using glass beads and a mechanical homogenizer (Spex Industries, Edison, N.J.). The supernatant from each sample was removed for potential virus isolation and stored at −80° C. The remaining mosquito pellet from each sample was resuspended in equal volumes (200 μl) of Opti-MEM® reduced serum medium and TRIzol® LS reagent (Invitrogen Life Technologies, California) and homogenized again as described above. After incubation at room temperature for 5 min and addition of 40 μl of chloroform, the entire homogenate for each sample was then vortexed for 15 sec and transferred to a pre-spun Phase Lock Gel™ Heavy tube (5 Prime, GmbH, Germany). The lysed contents of each tube were allowed to settle for 5 min at room temperature and organic and aqueous phases were separated by centrifugation at 16 000 g for 10 min at room temperature. Aqueous phases were recovered from each tube before total RNA was extracted at room temperature using a modification of the RNeasy Mini Kit protocol (Qiagen, Australia) and on column-DNase treatment. RNA was eluted from the column with 30 μl of RNasefree H2O and a final centrifugation step for 1 min. All RNA samples were stored at −80° C. prior to analysis by qRT-PCR. RNA standards were produced for the relative quantification of CHIKV RNA copy numbers normalized to RNA levels of the ribosomal A. aegypti housekeeping gene RpS17 (see Table 6).
Immune GenesPGYP1.out and PGYP1.out.tet mosquitoes were analyzed by RT-qPCR for a selection of immune genes. Two biologically independent cohorts often sugar-fed, 5-6 day old, female mosquitoes were collected and analyzed from each mosquito line. Total RNA was extracted from whole mosquitoes using TRI REAGENT (Molecular Research Center, Inc.) or RiboZol (AMRESCO). The RNA samples were DNase treated (Promega) and reverse transcribed using random primers and SuperScript III Reverse Transcriptase (Invitrogen). Quantitative PCR was carried out as per Platinum SYBR Green protocol (Invitrogen). The sequences of the primers used for qPCR are detailed in Table 6. Primer sequences for REL1, REL2, CECG and DEFC were obtained elsewhere (Xi et al., 2008) and the other primers were designed using gene sequences obtained from VectorBase. The temperature profile of the qPCR was 95° C. for 2 min, 50° C. for 2 min and 40 cycles of 95° C. for 10 s, 60° C. for 10 s and 72° C. for 20s. The house-keeping gene RpS17 (Cook et al., 2006) was used to normalize expression. Target gene to house-keeping gene ratios were obtained for each biological replicate using QGene 4.2 (Joehanes and Nelson, 2008). Treatment effects on the expression ratios were examined using Mann Whitney-U tests in STATISTICA V8 (StatSoft, Inc.) and fold change was calculated by the REST method (Pfaffl et al., 2002).
ImmunofluorescenceFollowing the removal of legs and wings, 14 dpi mosquitoes were fixed overnight at 4° C. in 4% (w/v) paraformaldehyde in PBS, containing 0.5% (v/v) Triton X-100. Fixed mosquitoes were dehydrated in an ethanol series of 50, 70, 90, 95, 100% ethanol, followed by two toluene treatments and then infiltrated with paraffin wax (Paraplast-Xtra, McCormick Scientific) at 60° C. Paraffin-embedded mosquitoes were sectioned using a rotary microtome to obtain 8 μm sections that were adhered to superfrost plus slides (Menzel-Gläser). Slides were dried, deparaffinated in 100% xylene, rehydrated in an ethanol series and then washed in PBS-T before being blocked overnight in 2% (w/v) bovine serum albumin (BSA) in PBS-T at 4 C. Sections were then incubated simultaneously for 1 hour with antirabbit WSP (1:100) and anti-dengue (1:10) 4G4 or anti-Plasmodium CSP (Krettli et al., 1988) antibodies (1:100) (both monoclonal, developed in mouse), diluted in blocking solution. Tissue sections were washed twice with PBS-T and the slides were then incubated simultaneously with Alexa-conjugated secondary antibodies (Alexa-488 developed in rabbit or Alexa-594, developed in mice, respectively, Molecular Probes, Invitrogen) diluted 1:1000 each in blocking solution for 1 h at room temperature. After two washes in PBS-T, the slides were incubated in DAPI for 10 min, rinsed in PBS-T and then mounted using an antifading reagent (ProLong, Invitrogen). Immunostaining was analyzed with a Zeiss Axio Imager II epifluorescence microscope equipped with an Axiocam camera, using the same exposure conditions for each filter channel. Photos are representative of at least 10 mosquitoes of each treatment.
Fluorescence In Situ HybridizationFISH was done using a modified protocol adapted from GeneDetect.com. Briefly, paraffin-embedded mosquitoes were sectioned and de-paraffinated as described above. Sections were then dehydrated in an ethanol series and hybridised overnight at 37° C. in a hybridization buffer containing 4×SSC, 50% formamide, 250 mg/ml dextran sulfate, 250 μg/ml poly(A), 250 μg/ml tRNA, 250 ug/ml salmon sperm DNA, 100 mM DTT and 0.5×Denhardt's solution and 200 ng of Wolbachia specific 16S rRNAprobes (W2: 5′-CTTCTGTGAGTACCGTCATTATC-3′ (SEQ ID NO: 15) and W3: 5′-AACCGACCCTATCCCTTCGAATA-3′ (SEQ ID NO: 16)) labelled at the 3′ end with rhodamine. Both probes are 100% homologous to both wMelPop and wFlu. Following overnight hybridizations, sections were washed twice in 1×SSC containing 10 mM DTT and twice in 0.5×SSC containing 10 mM DTT for 15 min each at 55° C., followed by a 10 min wash at 0.5×SSC containing 10 mM DTT and 1 μg/ml DAPI. Slides were briefly rinsed in water, mounted using an antifading reagent (ProLong, Invitrogen) and observed and photographed as described in the immunofluorescence method.
Western Blot AnalysisTotal protein from 5 mosquitoes of each treatment was extracted using protein lysis buffer containing 50 mM Tris pH 7.4, 140 mM NaCl, 0.5% (v/v) Triton X-100, 1.5 μg/ml DNAseI and protease inhibitors (Roche). Samples were boiled for 10 min in the presence of protein loading buffer, run on a 12% Laemmli SDS gel and transferred to a nitrocellulose membrane (Immobilon-P, Millipore) through the semidry Transblot SD (BioRad). Because the 4G4 antidengue antibody recognizes a conformational epitope, -mercaptoethanol was omitted from the sample loading buffer. Membranes were blocked with 5% non-fat dried milk in TBS-T overnight at 4 C, and then probed with antiwsp polyclonal antibody (Braig et al., 1998) (diluted 1:1,000 in 5% (w/v) skim milk in TBS-T) or anti-dengue (4G4) monoclonal antibody (1:100 dilution) for 1 h at room temperature. After 3 washes in TBS-T, membranes were incubated with anti-rabbit or anti-mouse IgG alkaline phosphatase conjugated antibody (Sigma) (1:4,000) for 1 h, respectively. Following washing in TBS-T blots were developed with NBT/BCIP (Promega). Western blots on Wolbachia-infected mosquitoes revealed a single band around 26 kDa that corresponds with the correct molecular weight of wsp (25540 Da) (Braig et al., 1998), whereas the 4G4 antibody revealed a band of around 50 kDa in dengue-positive mosquitoes.
Wolbachia Density in Aedes spp. Mosquitoes
A standard curve was created by cloning a Wolbachia wsp gene fragment (Braig et al., 1998) into pGEM T-Easy (Promega). After linearization with Pst I the plasmid was serially diluted into known concentrations and run in parallel, in order to determine the absolute number of Wolbachia copies contained in each mosquito sample. Mann-Whitney U tests were employed (STATISTICA V8, StatSoft, Inc.) to examine the density of Wolbachia in both mosquito species.
PCR Amplification of Wolbachia Sequences from A. fluviatilis
The Wolbachia surface protein gene wsp was amplified using the primers 81F and 691R that amplify a wide range of Wolbachia strains (Braig et al., 1998). PCR cycling conditions were as follows: 94° C. 3 min, (94° C. 30 s, 52° C. 30 s, 68° C. 90 s)×35 cycles, then 68° C. 10 mM. The reaction mixture contained 625 nM of each primer, 125 μM dNTPs, 1.5 mM MgSO4, 20 ng of mosquito DNA and 0.5 μL of proof-reading Elongase enzyme mix (Invitrogen) in a final volume of 25 PCR products were separated in 1% agarose gels and stained with ethidium bromide. Six independent PCR amplicons were cloned into the pGEM T Easy vector (Promega) and six clones were sequenced with T7 and M13R universal primers using the AB Big Dye terminator Version 3.1 kit with fluorescent sequencing (FS), AmpliTaq DNA polymerase (Perkin-Elmer) and analysed on (AB) 3730xl-96 capillary sequencer. Sequencing was done at the Australian Genome Research Facility (AGRF). Sequence similarity searches were performed using the BLAST algorithm (Altschul et al., 1997) at NCBI, and a phylogenetic tree was constructed using DNAstar (Lasergene). A partial wsp gene sequence from wFlu has been deposited in GenBank (Accession number GQ917108).
Relative Quantification of CHIKV RNA Copy NumbersRNA standards were produced for the relative quantification of CHIKV RNA copy numbers normalized to RNA levels of the ribosomal A. aegypti housekeeping gene RpS17. Firstly, a CHIKV RNA synthetic transcript was produced by RT-PCR amplification of a 588 bp fragment from the CHIKV strain 06113879 using primers designed from its deduced partial E1 structural gene sequence (GenBank accession number EU404186) (see Table 6). The one-step RT-PCR was performed using the Superscript® III One-Step RT-PCR System with Platinum® Taq High Fidelity (Invitrogen Life Technologies, California) according to the manufacturer's instructions with 400 nM of each primer and 5 μl of CHIKV RNA in a final reaction volume of 50 Amplification was performed in an Eppendorf Mastercycler epgradient S (Eppendorf, Germany) and included one cycle at 50° C. for 15 min for reverse transcription, an inactivation step at 94° C. for 2 min, 40 cycles of 94° C. for 2 min, 59° C. for 30 sec and 68° C. for 2.5 min and final extension at 68° C. for 5 min. Amplicon DNA was purified using the QIAquick Gel Extraction Kit (Qiagen, Australia) and supplied instructions and then cloned into the plasmid vector pGEM®-T Easy (Promega). After the presence and orientation of the insert DNA was verified by nucleotide sequencing, the plasmid was linearized for in vitro RNA transcription by digestion with SpeI. Synthetic RNA transcripts were then prepared using the Riboprobe® T7 System (Promega) before multiple treatments with DNase 1 (RQ1 RNase-Free DNase; Promega Corporation, WI, USA). The final CHIKV transcript of 654 bp was stored in single use aliquots at −80° C. and RNA levels were determined by spectrophotometry immediately prior to use. For the housekeeping gene RpS17 RNA standard, total RNA from whole A. aegypti mosquitoes was extracted as before with the exception that on-column DNase treatment was omitted. In this instance, RNA was DNase treated and stored as described for the CHIKV RNA transcript. To enable a direct comparison of CHIKV RNA copy numbers in prepared mosquito body plus head, and legs plus wings samples, two specific one-step qRT-PCR real-time TaqMan® assays were developed targeting the CHIKV E1 and A. aegypti RpS17 genes respectively. Both were performed using the ABI 7500 Fast Real-Time PCR System (PE Applied Biosystems, Foster City, Calformia) and all reaction mixes, amplification parameters, result analysis and CHIKV primer and probe sequences were used as previously reported. Primers and dual labelled probe (5′-FAMCAGGAGGAGGAACGTGAGCGCAG-TAMRA-3′) (SEQ ID NO: 17) for the RpS17 housekeeping assay were derived from the A. aegypti RpS17 gene sequence—GenBank accession number AY927787. Standard curves for qRT-PCRs were generated using triplicate 15-fold serial dilutions of either the CHIKV T7 RNA transcript or the prepared RpS17 reference RNA. Equivalent CHIKV RNA copy numbers normalized to reference RpS17 RNA levels were then calculated for the CHIKV infected mosquito samples by comparing threshold cycle numbers (Ct) with the respective standards.
Results Wolbachia and Dengue virusWe tested the effect of Wolbachia on vector competence in two mosquito genetic backgrounds: the original inbred PGYP1 line, which was stably transinfected with wMelPop-CLA (see Example 2) and the same strain after 5 generations of backcrossing to the F1 progeny of wild-caught A. aegypti, collected in Cairns, Australia and named PGYP1.out. These mosquito strains were compared to tetracycline-treated counterparts that were genetically identical but lacked the Wolbachia infection, named PGYP1.tet and PGYP1.out.tet, respectively. In addition, a wild-type strain of A. aegypti established from field-collected material in Cairns, Australia (Cairns3) was used as an additional negative control.
Mosquitoes were fed an artificial blood meal spiked with DENV-2 in four independent experiments to examine possible interactions with Wolbachia. The presence of DENV-2 in whole mosquito bodies was examined 7 and 14 days post exposure using a cell culture enzyme immunoassay (CCEIA) (Knox et al., 2003). In three separate experiments no Wolbachia-infected mosquitoes (PGYP1.out) tested positive for DENV-2, but DENV-2 infection rates in Wolbachia-uninfected mosquitoes (PGYP1.out.tet and Cairns3) ranged from 30-100% (Table 3, Exp 1-3). The body viral infection rates in PGYP1.out.tet mosquitoes ranged from 30-100% after 7 d and 48-97% after 14 d, while the body viral infection rates in Cairns3 ranged from 50-95% after 7 d and 57-95% after 14 d. The disseminated viral infection rates measured through the presence of virus in mosquito legs in tetracycline-treated A. aegypti ranged from 10-23 and 37-43% after 7 and 14 d respectively. Disseminated infections in Wolbachia-free wildtype Cairns3 strain of A. aegypti ranged from 5-13% and 20-33% after 7 and 14 d, respectively (Table 3) (P<0.001, chi-square). In one experiment (Table 3, Exp 4) when mosquitoes were fed the highest titer (107.8 Logs) of DENV-2 a small number of Wolbachia-infected mosquitoes tested positive for DENV-2 at both 7 and 14 days post infection (5 and 8%, respectively) but this was significantly fewer than Wolbachia uninfected controls (63-78% and 70-75%, respectively) (P<0.001, chi-square). To provide a more conservative test of Wolbachia-mediated interference, mosquitoes were intrathoracically injected with DENV-2. These experiments circumvented the midgut barrier to infection (Woodring et al., 1996) and allowed for the delivery of a repeatable inoculating dose (around 2,750 infectious particles/mosquito) of DENV-2 that produced consistent high-titre infections in control mosquitoes. Accumulation of genomic (+RNA) and anti-genomic (−RNA) RNA strands was assessed at 5 and 14 d post-injection by quantitative real time PCR using DENV-2 specific primers (Richardson et al., 2006). At both time points, the amount of DENV-2 RNA present was reduced by up to 4 logs in both the PGYP1 and PGYP1.out Wolbachia-infected strains compared to their paired tetracycline treated counterparts (
We then went on to determine if the virus interference phenotype would extend to the alphavirus CHIKV. The virus strain used in the experiments contained the alanine to valine mutation in the membrane fusion glycoprotein E1 gene (E1-A226V), which has been linked to increased infectivity in A. albopictus. An Australian population of A. aegypti was recently shown to also be a highly efficient laboratory vector of this virus strain. Mosquitoes were exposed to a blood/virus mixture containing 106.4 CClD50/ml of CHIKV, and at various timepoints post exposure, mosquitoes were processed for quantification of the number of viral RNA copies using qPCR and CHIKV-specific primers and probes. Immediately after feeding, the number of CHIKV genomic (+RNA) RNA copies in the body and head were comparable for all three lines, suggesting that they imbibed similar amounts of virus (Table 4). The median number of copies then decreased in all three lines on days 2, prior to it increasing in the PGYP1.out.tet and Cairns3 mosquitoes to its highest level at day 14-post exposure. The day 14 infection rates were 87% and 79% for the PGYP1.out.tet and Cairns3 controls and 17% for the Wolbachia infected PGYP1.out line (P<0.001, chi-square). In all three groups, CHIKV RNA was detected in the legs and wings immediately after feeding, as percentage of dissemination (Table 4). This may represent either direct contact between the legs and/or wings and the blood/virus mixture or a rupture of the mesenteron, which released virus directly in the hemolymph (Turell, 1988). After day 0, CHIKV was not detected in the legs and wings of any PGYP1.out (+Wolb) mosquitoes. In contrast, on all days post exposure, virus was detected in the legs and wings of PGYP.out.tet and Cairns3 control mosquitoes (−Wolb) and by day 14, the virus was detected in the legs and wings of 100% and 90%, respectively, of mosquitoes which had positive bodies and heads (P=0.125, chi-square).
Wolbachia and PlasmodiumConsidering that the viral interference effect appeared robust for two unrelated arboviruses we then went on to test for the effect on the protozoan parasite P. gallinaceum. While not a human pathogen, this species of malaria parasite is known to be able to infect A. aegypti mosquitoes in the laboratory. Wolbachia infected and uninfected A. aegypti mosquitoes (PGYP1.out and PGYP1.out.tet strains) as well as a susceptible strain of Aedes fluviatilis were fed in parallel on P. gallinaceum infected chickens. A. fluviatilis has a broad geographical distribution in Latin America and has been used in the laboratory as a safe avian malaria (P. gallinaceum) model vector, as it does not naturally transmit DENV or yellow fever virus (Tason de Camargo and Krettli, 1981). Seven days post-feeding on infected chickens, mosquito midguts were dissected and the number of Plasmodium oocysts counted. The presence of wMelPop-CLA Wolbachia significantly reduced the oocyst load in A. aegypti mosquitoes (P<0.0001, Mann-Whitney U test) (
When we incubated the mosquito sections with an anti-Wolbachia (wsp) antibody we serendipitously discovered a Wolbachia infection in A. fluviatilis mosquitoes indicating that this species of mosquito was naturally infected with Wolbachia. PCR using Wolbachia general wsp primers (Braig et al., 1998; Zhou et al., 1998) amplified a fragment from all A. fluviatilis tested. Sequence of the amplified DNA indicated that this Wolbachia strain (named wFlu) belongs to the Wolbachia B supergroup and is distantly related to wMelPop-CLA. qPCR analysis revealed that the density of wFlu in A. fluviatilis is about 20-fold lower than the density of wMelPop-CLA in A. aegypti (
To examine whether resistance of Wolbachia infected mosquitoes to pathogen infection may be related to stimulation or priming of the mosquito innate immune system, we quantified the expression of a sample of immune genes. It was recently demonstrated that some immune genes are differentially regulated in A. aegypti mosquitoes infected with dengue virus (Xi et al., 2008). Interestingly, regulation of the immune pathway genes in these mosquitoes was also stimulated by their natural gut microbiota and rearing mosquitoes aseptically, and so depleting their bacterial flora, resulted in a 2-fold increase of dengue virus in the midgut (Xi et al., 2008). We chose a subset of the genes that were shown to be upregulated upon dengue virus infection to assess the effect of Wolbachia infection on the mosquito immune system.
The expression levels of eleven immune pathway genes in the wMelPop-CLA infected PGYP1.out and its uninfected control line were compared for two independently reared cohorts of mosquitoes (
wMelPop-infected PGYP1 and tetracycline-cleared PGYP1.tet strains of Aedes aegypti (see Example 2) were maintained at 25° C., 75-85% relative humidity, with a 12:12 h light:dark photoperiod. Larvae were reared in plastic trays (30×40×8 cm) at a set density of 150 larvae in 3 L distilled water, and fed 150 mg fish food (TetraMin Tropical Tablets, Tetra, Germany) per pan every day until pupation. Adults were kept in screened 30×30×30 cm cages, and provided with constant access to 10% sucrose solution and water. Females (5 days old) were blood-fed using human blood for egg production. For routine colony maintenance, eggs from PGYP1 were hatched 5-7 days post-oviposition (i.e. without prolonged desiccation) to initiate the next generation. All fitness experiments with PGYP1 were conducted at G20 to G22 post transinfection.
Pre-Imaginal Development and SurvivorshipEggs (120 h old) from PGYP1 and PGYP1.tet strains were hatched synchronously in nutrient-infused deoxygenated water for 1 h. After hatching, individual first instar larvae (n=156 per strain) were placed into separate plastic 30 mL plastic cups with 20 mL of water, and fed 1 mg powdered TetraMin suspended in distilled water each day until pupation. The number of days spent in each pre-imaginal life stage (i.e., 1st, 2nd, 3rd and 4th instars, pupae), mortality at each stage, and sex of eclosing adults were recorded every 24 h. Stage-specific development and eclosion times for each strain were compared using Mann-Whitney U (MWU) tests conducted in Statistica Version 8 (StatSoft, Tulsa, Okla.).
Adult Wing Length MeasurementsAs an indicator of adult body size, wing lengths of PGYP1 and PGYP1.tet mosquitoes (n=50 of each sex) derived from the pre-imaginal development time assay were measured (Nasci, 1986). Wing lengths of males and females from each strain were compared using MWU tests.
Viability of Quiescent Embryos Over TimePGYP1 and PGYP1.tet females were blood-fed on human blood, and 96 h post-blood meal isolated individually for oviposition in plastic Drosophila vials with wet filter paper funnels. After oviposition, egg papers were kept wet for 48 h, after which time they were removed from vials, wrapped individually in paper towel, and conditioned for a further 72 h at 25° C. and 75-85% relative humidity. Egg batches were then moved to their respective storage temperature of 18° C., or 25° C. in glass desiccator jars; maintained at a constant relative humidity of 85% with a saturated KCl solution (Winston and Bates 1960). For each temperature, 20 oviposition papers from each strain were hatched at seven time points at 7 day-intervals (5 to 47 days post-oviposition) by submersion in nutrient-infused deoxygenated water for 48 h. To hatch any remaining eggs, oviposition papers were dried briefly then submersed for a further 5 days and before the final number of hatched larvae was recorded. Regression analysis was used to detect trends in the viability of eggs from each strain over time. MWU tests were used to compare viability of eggs between strains at the same storage age.
Lifetime Productivity MeasurementsReplicate 30×30×30 cm cages containing 200 individuals of each sex from PGYP1 and PGYP1.tet strains were maintained over multiple gonotrophic cycles, with ad libitum access to 10% sucrose solution and water, for the duration of their lifespan. During each cycle, females were provided with a human blood meal for 2×10 min periods on consecutive days, and 96 h post-blood meal a random sample of females (n=48) was collected from each cage and isolated individually for oviposition. Following a set 24 h period for oviposition, females were returned to their respective cages and the proportion of females laying eggs determined. Eggs were conditioned and hatched 120 h post-oviposition as described above, and the total number of eggs (fecundity) and hatched larvae (fertility) from each female were recorded. To ensure that gravid females not sampled for oviposition could also lay eggs every cycle, oviposition cups were introduced into each stock cage (96 h post-blood meal) for a period of 48 h. Females were then blood fed to initiate the next gonotrophic cycle.
Cages were sampled until all females in the population were dead, which occurred after 7 and 16 gonotrophic cycles for PGYP1 and PGYP1.tet strains respectively. To ensure PGYP1.tet females did not become depleted of sperm, young males (3 days old) were supplemented to this cage after 8 gonotrophic cycles. An analysis of covariance (ANCOVA) was used to examine the relationship between mosquito fecundity/fertility and the covariates mosquito age and infection status. Regression analysis was used to detect trends in fecundity/fertility of mosquitoes from each strain over their lifespan. Student's t-test was used to compare the fecundity/fertility of mosquitoes from both strains of the same age.
Results Pre-Imaginal Development and Adult SizeNo significant differences in development times for larval stages of wMelPop-infected PGYP1 or tetracycline-cleared PGYP1.tet males (
A comparison of the wing lengths of newly emerged adults from both strains revealed a minor, yet statistically significant adult size cost to wMelPop infection for both sexes (
The viability of quiescent embryos from the wMelPop-infected PGYP1 strain decreased over time at 25° C. and 18° C., whereas viability of embryos from of the tetracycline-treated PGYP1.tet strain was relatively stable at both storage temperatures (
Reproductive Output over Lifespan
PGYP1 and PGYP1.tet females had similar reproductive outputs in terms of the number of eggs oviposited and the number of viable larvae hatched per female during their first gonotrophic cycle (
For all experiments two laboratory lines of Aedes aegypti were used, the Aedes aegypti PGYP1 line, previously generated by transinfection with wMelPop and its Wolbachia cured control line, PGYP1.tet (see Example 2). Mosquitoes were reared at 26±2° C., RH 75% with 12 h:12 h light/dark cycle. Larvae were fed 0.1 mg/larvae of TetraMin Tropical Tablets once per day. Females were separated from males at the pupal stage and placed into 300 mm3 cages for emergence at a density of 400 individuals per cage. The females were fed 10% sucrose solution ad libitum until the day before feeding trials.
Confirmation of Infection StatusMosquito lines were screened to confirm presence (PGYP1) or absence (PGYP1.tet) of infection every two generations using a PCR based assay. Five days after eclosion, DNA was extracted from 10 females using DNeasy spin columns (QIAGEN, Australia), following the Manufacturer's protocol. PCR was then carried out using primers for the IS5 transposable element present in Wolbachia (see Example 1). Reaction conditions were as follows: 0.01-0.09 μg of each DNA sample, 2 μl of 10×Buffer, 0.5 μl mM dNTPs, 0.5 μl of 20 μM IS5 primers, 0.15 μl Taq DNA polymerase and water up to 20 μl. Samples were denatured for three minutes at 94° C. then cycled 34 times for 30 seconds at 94° C., 30 seconds at 55° C. and one minute at 72° C. This cycle was followed by a final 10-minute extension at 72° C. in a MJ Research PTC-200 Peltier Thermal Cycler (Geneworks Pty Ltd, SA). Presence of the expected size product was then confirmed by agarose gel electrophoresis.
Preparation for Feeding TrialsExperiments were conducted with five, 26 and 35-day-old adult mosquitoes. Behaviours were measured in either small populations (proportion of population fed, number and length of attempted bites) or for single mosquitoes depending on feasibility (response time to human, blood-meal weight). The afternoon prior to each trial the required number of mosquitoes were removed from their rearing cages and stored in mesh-covered holding buckets at a density of five mosquitoes per bucket. At the same time an additional population of five mosquitoes were set aside to replace any mosquitoes that died during the starvation period. Mosquitoes were starved of sucrose but given access to water for ˜16 hours until trials began the next morning. Prior to each trial, mosquitoes were transferred from holding buckets into a 645 cm3 cage and allowed to acclimate for 5 minutes. All human volunteers cleaned both of their forearms with 70% isopropyl alcohol wipes, rinsed their forearms with distilled water and dried them with paper towel, and placed latex gloves on both their hands before feeding.
Population TrialsAll population trials were carried out in two cages placed next to one another. One cage contained five PGYP1 mosquitoes and the adjacent cage contained five PGYP1.tet mosquitoes. The position (left or right) of the two lines was randomised throughout the experiment. Volunteers inserted their left and right arms into the respectively into the two cages and rested their hands on buckets placed within each cage. Both the volunteer and an external assistant monitored the number of attempted bites each mosquito made on the volunteer's forearm. An attempted bite was recorded when a mosquito landed and actively attempted to probe the volunteer's skin at a location. A single mosquito could probe multiple times at a single location, but if a mosquito moved to a new position and attempted to probe again this new location was recorded as another attempted bite. Mosquitoes in both cages were monitored for 15 minutes before the volunteer shook their arms and withdrew both arms from the cages. Mosquito abdomens were examined for presence of a blood meal and the proportion of the population that imbibed a blood meal was recorded. This experiment was replicated with six volunteers (3 female, 3 male)×4 replicate trials for each of the three adult mosquito age classes.
Individual TrialsA single mosquito from each line was separately aspirated into on a pre-weighed 1.5 ml Eppendorf tube and weighted on a Satorius BP211D balance (Selby Biolabs). Each mosquito was then released simultaneously into the adjacent 645 mm3 cages. Randomisation of cage position, mosquito settlement time and trial length were as per population trials. The volunteer inserted his arms into the cage and the times at which mosquito's made their first attempted bite (host-seeking time) were recorded by the volunteer into a voice recorder (Olympus VN-1100). After the trial, mosquitoes were transferred back into the tubes they were originally weighed in and the tubes were re-weighed. The weight of the blood-meal imbibed by each mosquito was then calculated. The volunteer (male) hosted four groups of 10 mosquitoes from each of the three age classes.
Statistical AnalysisAll analysis was conducted using STATISTICA v8 (StatSoft, Inc). The variables, host-seeking time and blood-meal weight were normally distributed. The number of attempted bites was transformed by square root to achieve normality. The role of infection and age on these variables was examined using general linear mixed models. The role of human volunteer was not examined as there were only 6 replicate individuals and they were internally controlled. When infection status was significant, t-tests were then used to further identify specific differences between infected and uninfected lines within each of the three age classes. The proportion of mosquitoes obtaining a blood meal did not respond to transformation and so non-parametric Mann Whitney U-tests tests were employed instead of linear models to examine differences between infected and uninfected mosquitoes for all three ages.
Results Host SeekingIf the Wolbachia infected mosquitoes were hungrier than uninfected counterparts they might be more rapid in their response to an offered human forearm. Over the short distances in a laboratory cage environment, infected mosquitoes were no different to uninfected controls (F=0.10, df=1, P=0.77) in the time it took them to land on the human volunteer and initiate an “attempted bite” (
The number of “attempted bites” made by infected mosquitoes was examined as a possible indicator of hunger. As per our methods, an attempted bite included both probing and attempted probing in a particular region on the arm. Given the cage sizes and numbers of mosquitoes involved we could not visually differentiate between a probing event that broke the skin and one that did not. See the subsequent associated study by Moreira et al. for dissection of biting behaviour into successful and unsuccessful probing events (see Example 9). Infection status (F=13.37, df=1, P=0.014), age of mosquitoes (F=5.72, df=2, P=0.021), and the interaction between age and infection status (F=5.76, df=2, P=0.021) were significant determinants in the number of attempted bites made. In particular, Wolbachia-infected mosquitoes at 26 (t=−3.70, df=238, P<0.001) and 35 days of age (t=−5.35, df=235, P<0.001) attempted to bite more than their uninfected counterparts (
Blood-meal weight (
Normally during biting a mosquito may probe unsuccessfully, but will ultimately insert its stylet into a host. In this study, infected mosquitoes were observed in which the proboscis repeatedly bent as the mosquito pushed its head towards the skin while probing. This phenotype appeared to be correlated with old age and poor ability to obtain a blood meal. Due to its correlation with old age, the behaviour was not observed in the study until much of the other work was completed, hence its quantification and correlation with biting success is reported in another study (see Example 9).
Example 9 Human Probing Behaviour of Aedes Aegypti when Infected with a Life-Shortening Strain of Wolbachia Materials and Methods MosquitoesAedes aegypti mosquitoes, wMelPop infected (PGYP1) and its Tetracycline-cured counterpart (PGYP1.tet) (see Example 2), were kept in a controlled environment insectary at 25° C. and 80% RH. Larvae were maintained with fish food pellets (Tetramin, Tetra) and adults were offered 10% sucrose solution, ad libitum. Adult females were fed on human blood for egg production and eggs were dried for at least 96 h prior to hatching.
Behaviour AssaysFertilized and non-blood fed females of different ages (5, 15, 26 and 35 days old) were used in all behaviour experiments. Sucrose solutions were removed from cages on the night before the experiments. Forty females were used per age and per infectious status. Single mosquitoes were transferred to a transparent Perspex cage (25 cm3) and filmed through a digital camera with 6 mm Microlens (IEEE-1394, Point Grey Research) mounted on a tripod. Mosquitoes were given about five minutes to settle within the cage before a human gloved-hand was inserted into the cage. A window of about 15 cm2 was cut of the upper part of the latex glove in order to delineate the probing field.
Movies were recorded (QuickTime Player) for a maximum of 10 minutes or until blood was seen within the mosquito midgut and subsequentially watched for time calculations. Two electronic timers were used, one for recording pre-probing time and the second for probing time. Pre-probing time was defined and the time since the mosquito has landed on the bare hand area until the insertion of mouthparts into the human skin. Probing time is defined as the initial insertion of insect mouthparts until blood can be seen within the mosquito midgut through the abdominal pleura (Ribeiro et al., 1984). Timing stopped when mosquitoes left the bare hand area or withdrew their mouthparts before taking blood and began again when the mosquito came back or after subsequent stylet penetration. If blood was not found by the end of 10 minutes, we defined this case as unsuccessful probing and it was measured as a proportion. Movies were also used to visualize additional abnormal phenotypes as the jittering action of mosquito body while landed on top of the human hand, and named “shaky”. Furthermore, the inability of mosquitoes to insert their mouthparts due to a bendy proboscis (Example 8) was also analysed.
Mosquito Saliva CollectionMosquitoes of different ages (5, 26 and 35-days-old) and infectious status were starved overnight (without sucrose solution or water). On the following morning mosquitoes were briefly anesthetized with CO2 and placed on a glass plate over ice. Wings and legs were removed with forceps and their proboscis introduced into a 1 cm piece of polypropylene tubing (0.61×0.28 mm, Microtube Extrusions, NSW, Australia) (see Ribeiro et al., 1984). Females were allowed to salivate for 5 minutes and then the diameter of the saliva droplets was measured through an ocular micrometer at 40× magnification. Volumes were calculated via the sphere formula (Novak et al., 1995). Saliva was then collected into 20 μL of 0.05 mM Tris-HCl pH 7.5 by attaching the needle of a 10 μL Hamilton syringe and rinsing the tubing content a few times. Samples were centrifuged at 14,000 g for 2 minutes and kept frozen (−80° C.) in 20 μL of 0.05 mM Tris-HCl, pH 7.5 for enzymatic assay (see below).
Apyrase AssaySaliva samples (8 μL) were transferred, in duplicates, into individual wells of a plastic 96-well ELISA plate (NUNC Maxisorp). For the blank, 8 μL of the 0.05 mM Tris buffer was added to the wells. To each well, 100 μL was added of a mixture containing 100 mM NaCl, 50 mM Tris-HCl (pH 8.95), 5 mM CaCl2, 2 mM ATP and 20 mM B-Mercapthanol. The plate was incubated at 37° C. for 10 mM and then the reaction was immediately stopped, by adding 25 uL of acid molybdate solution (1.25% ammonium molybdate in 2.5 mM H2SO4). Immediately after termination of the reaction, 2 μL of a reducing solution (0.11 mM NaHSO3, 0.09 mM Na2SO3 and 8 mM 1-amino-2-naphthol-4-sulphonic acid) was added to each well and the plate was incubated at 37° C. for 20 min (Novak et al., 1995). Plates were read at a FLUOstar OPTIMA ELISA plate reader (BMG Technologies) at 660 nm. Readings were quantified by comparison with an inorganic phosphate standard curve (1, 0.5, 0.25, 0.125, 0.06125, 0.03125, 0.015625 mM of sodium phosphate).
PCR Confirmation of Mosquito Infection Status and Saliva ScreeningWolbachia infection was confirmed through PCR to detect both mosquito (apyrase gene: ApyF: 5′-TTTCGACGGAAGAGCTGAAT-3′ (SEQ ID NO: 18) and ApyR: 5′-TCCGTTGGTATCCTCGTTTC-3′ (SEQ ID NO: 19)) and Wolbachia (IS5-F: 5′-CTGAAATTTTAGTACGGGGTAAAG-3′ (SEQ ID NO: 20) and IS5-R: 5′-CAAGCATATTCCCTCTTTAAC-3′ (SEQ ID NO: 21)) sequences. Saliva screening to check the presence of Wolbachia was done via PCR (with IS5 primers) using saliva samples of infected and non-infected mosquitoes. Mosquito sequences in this case were detected with primers for the ribosomal protein gene RpS17 (Cook et al., 2006).
Statistical AnalysisIn all cases, general linear models were employed to examine the effects of the variables age and infection status and their interaction with one another. Models demonstrating significance for the variable infection status were then followed by individual t-tests examining the differences between infected and uninfected mosquitoes for each age class. The proportion of infected and uninfected mosquitoes that obtained blood meals were examined using Mann-Whitney U tests instead of linear models, given the deviation of the data from normality. Chi-square 2×2 contingency tests were employed to examine the relationship between observed behavioural traits and lack of feeding success. The correlation between these traits was quantified using a cox-proportional hazards model for age, with the behavioural traits and lack of blood meal success covariates. All statistical analyses were carried out in STATISTICA v8 (StatSoft, Inc. Tulsa, Okla.).
Results Pre-Probing TimeWe measured the time mosquitoes spent from first contact with a human volunteer until the insertion of the insect's mouthparts as a measure of pre-probing time. All feeding trials were carried out with individual mosquitoes, which had been starved prior to the assay, at four adult ages (5, 15, 26 and 35-days-old). Mosquitoes that never successfully achieved a blood meal were excluded from this analysis. Overall both age (df=3, F=13.73, P<0.0001) and infection status (df=1, F=23.18, P<0.0001) had a significant effect on the length of pre-probing time. On average infected mosquitoes spend more time pre-probing especially as they age (
In the same feeding trials described above, the length of time between insertion of mouthparts and the first visible sign of blood in the abdominal pleura (Ribeiro et al., 1984) was recorded as probing time for the mosquitoes. As with pre-probing time, the variables of age (df=3, F=11.36, P<0.0001), infection status (df=1, F=29.46, P<0.0001) and the interaction (df=3, F=10.56, P<0.0001) between these two variables were highly significant. Infected and uninfected mosquitoes did not differ in their probing time (˜33 sec) at 5 (df=78, t=−0.46, P=0.64) and 15 (df=75, t=1.43, P=0.15) days of age (
In the assays detailed above we then compared the ability of infected and uninfected mosquitoes to obtain blood meals (
It is important to note that as infected mosquitoes aged, the frequency of events where they pierced the skin did not increase despite failed attempts at feeding (FIG. 43). A general linear model revealed that age (df=3, F=20.47, P<0.0001), infection (df=3, F=29.12, P<0.0001) and age X infection (df=3, F=27.18, P<0.0001) were significant determinants of the number of probings. Subsequent t-tests comparing the number of probings between infected and uninfected mosquitoes at each of the age points (data not shown), however, demonstrated that only 35 day old (df=1, t=−8.44, P<0.0001) mosquitoes differed. In this case, uninfected females probed more on average per session (1.05±0.05) than wMelPop infected mosquitoes (0.3±0.073). This is due to other behaviours, which impaired the infected mosquitoes to feed (see below).
Additional Behavioural PhenotypesIn other work we have reported the appearance of a “bendy” proboscis in association with wMelPop, which was the inability of the mosquito to properly orient its mouthparts and insert the stylet into the skin (Example 8). During the feeding trials in this study we quantified the occurrence of this trait. The bendy proboscis was never observed in any of the uninfected mosquitoes regardless of age, nor was it present in 5 day-old infected mosquitoes. The trait first appeared at a low level (2.5%) in 15 day-old mosquitoes and rose to a frequency of 65% by 35 days of age (
To check whether the probing behaviour and the additional phenotypes we observed were due to differences in saliva volume and salivary gland apyrase activity we measured both traits in infected and uninfected mosquitoes at three adult ages. Apyrase activity (
In an attempt to interpret the effects of Wolbachia on host-feeding behaviour we tested for the presence of Wolbachia in the saliva and salivary glands of infected mosquitoes. PCR amplification of the Wolbachia wsp gene or mosquito apyrase has shown only the presence of Wolbachia in salivary glands, but not in saliva (
We have recently sequenced the complete wMelPop and wMelPop-CLA genomes and we have identified, by using a comparative genomics approach, a series of mutations that have occurred during the 3 years in cell culture. These mutations are part of the wMelPop-CLA strain present in the transinfected Aedes aegypti mosquitoes.
The wMelPop-CLA strain has at least 5 major genetic differences with the original wMelPop strain. These differences include gene insertions, deletions and single nucleotide polymorphisms (SNPs). The combination of these 5 elements is unique to wMelPop-CLA and can be used to differentiate this strain from any other Wolbachia strain, including very closely related strains such as wMelCS. As a result of these genetic differences, the wMelPop-CLA genome is approximately 20952 bp smaller that wMelPop (1247197 bp vs 1268149 bp).
wMelPop-CLA Unique Genetic Features
SNP in Gene WD0200The gene WD0200 encodes for a hypothetical protein, according to the wMel genome annotation (Wu et al., 2004). During the adaptation of wMelPop to mosquito cell culture in our laboratory, the sequence of this gene has mutated resulting in the substitution of a C residue for a T in wMelPop-CLA (
Gene WD0413 encodes an aspartyl-tRNA synthetase (aspS) [6.1.1.12] involved in protein biosynthesis. Following the sequencing of wMelPop and wMelPop-CLA WD0413 we have identified a 10 bp deletion in wMelPop-CLA that was not present prior to cell culture adaptation (
This 10 bp deletion occurs just before the TGA stop codon and creates a frameshift that extends the wMelPop-CLA encoded protein by an extra 10 aminoacids before a new stop codon is read (
IS5 insertion elements are common transposable elements identified in several Wolbachia genomes. The IS5 insertion element is 918 bp long and is constituted by two ORFs (OrfA and B), flanked by a terminal inverted repeat. The closely related wMel Wolbachia genome, (Wu et al., 2004), contains 13 identical IS5 elements. wMelPop also contains 13 IS5 elements, although 2 of them have translocated when compared to wMel.
The novel IS5 insertion present in the wMelPop-CLA strain is located in the intergenic region between the genes WD0765 and WD0766 (
The wMelPop-CLA strain contains a 21.6 Kb deletion when compared to the original wMelPop strain (
We have also identified WD0513 as a potential candidate for horizontal gene transfer between mosquitoes and Wolbachia (Woolfit et al., 2009).
Insertion of a G in Gene WD0758Gene WD0758 encodes for a glutaredoxin family protein. This gene contains an extra G at position 196 in wMelPop-CLA when compared with its counterpart in wMelPop. This mutation creates a premature stop codon in wMelPop-CLA and as a consequence, the WD0758 protein is 46 residues shorter in wMelPop-CLA than in wMelPop (
PCR Characterization of Unique wMelPop-CLA Features
Three of the 5 described genetic features that distinguish wMelPop-CLA from its predecessor wMelPop can be easily identified and diagnosed by PCR, as shown in
The use of an in vitro cell culture system provided an ideal means to examine the adaptation of Wolbachia to a novel host environment. This approach contrasts with directly transferring Wolbachia between insects, where selective forces are presumably different and more complex, and where longer insect generation times, vertical transmission, and the labour intensive nature of rearing live insects make selection for transinfected lines challenging.
The initial difficulty in establishing wMelPop infection in the Aedes albopictus cell line Aa23 demonstrated that wMelPop was not naturally pre-adapted for growth in mosquito cells. Following stable infection of Aa23 and serial passage for several years, wMelPop was successfully established in Aedes aegypti RML-12 and Anopheles gambiae MOS-55 cell lines, two species that are not naturally infected by Wolbachia (Curtis and Sinkins, 1998; Kittayapong et al., 2000; Rasgon and Scott, 2004; Ricci et al., 2002; Tsai et al., 2004).Transfer of wMelPop between Aa23 and these two mosquito cell lines occurred much more readily than the initial transfer from D. melanogaster to Aa23, potentially due to (i) a higher infective dose of wMelPop purified from Aa23 and used for transfer; and (ii) a smaller divergence in intracellular environments among these mosquito cell lines as opposed to the initial transfer from Drosophila. The cell line-adapted Wolbachia displayed reduced infectivity and maternal transmission when injected back into its original Drosophila host. It grew to lower densities and showed phenotypic shifts for both life-shortening and CI expression. Taken together, these results provide evidence for the active genetic adaptation of wMelPop to mosquito cell lines during long-term serial passage.
A comparison of results from this study, with simulations from recent theoretical models that examine the potential of life-shortening Wolbachia to modify mosquito population age structure (Brownstein et al., 2003; Rasgon et al., 2003), suggests that wMelPop should be able to initiate a population invasion of A aegypti. Given the relationship that exists between mosquito survival and vectorial capacity (Garett, 1964; MacDonald, 1957), if the longevity of adults A aegypti can be approximately halved under field conditions, as observed in our laboratory experiments, then the introduction of life-shortening Wolbachia strains would be predicted to reduce pathogen transmission and the incidence of human disease.
Vertically inherited parasites like Wolbachia are predicted to evolve towards reduced virulence over time (Lipsitch and Moxon, 1997). Unlike chemical insecticides, biological agents that induce mortality in late life, such as wMelPop or entomopathogenic fungi, are expected to impose relatively weak selection pressures for the evolution of resistance (Thomas and Reed, 2007). This is because the majority of individuals in the population are able to initiate several reproductive cycles prior to death, minimizing costs to reproductive output. Moreover, since the initial description of wMelPop in D. melanogaster over ten years ago, no signs of resistance to life-shortening have emerged in laboratory stocks.
Furthermore, our finding that the wMelPop Wolbachia infection eliminates the ability of dengue virus to establish a productive infection has significant implications for any future control measure based on the use of life-shortening Wolbachia. Life-shortening effects on mosquitoes would become secondary and only act on any rare individuals that might escape the direct interference effect. We could also presume that because of the observed effects on dengue virus accumulation that any mosquitoes that did escape the interference effect despite the presence of Wolbachia would likely have extended extrinsic incubation periods. This in turn would act synergistically with the life-shortening effect to eliminate dengue virus transmission.
Our recent studies have also revealed that, as A. aegypti infected with wMelPop-CLA age, they show increasing difficulty in completing the process of blood feeding effectively and efficiently. These effects on blood feeding behaviour may reduce vectorial capacity and point to underlying physiological changes in Wolbachia-infected mosquitoes.
Thus, the ability of Wolbachia to spread into A aegypti and A. anopheles populations and persist over time may provide an inexpensive approach to dengue and malaria control, particularly in urban areas that are less amenable to conventional control strategies. Given the ability of wMelPop to induce life-shortening, cytoplasmic incompatibility, altered feeding behaviour, and reduced pathogen susceptibility in a range of insect hosts, this strategy may be broadly applicable to reduce pathogen transmission by other insect disease vectors of medical or agricultural importance.
The fact that many insect species are infected with Wolbachia raises the possibility that Wolbachia-mediated antiviral protection could be a widespread phenomenon. To test the generality of Wolbachia-mediated antiviral protection further, the inventors used D. simulans and its naturally occurring Wolbachia infections.
Wolbachia strains vary both between host species and within a host species (see for example Casiraghi et al., 2005). Naturally occurring Wolbachia strains in D. melanogaster ubiquitously protect against DCV (see Example 4 and Teixeira et al., 2008), however these strains are very closely related (Riegler et al., 2005). Wolbachia is maternally inherited and therefore has a close association with its host. Using D. simulans fly lines that are naturally infected by different Wolbachia strains we showed that some strains did not mitigate virus-induced mortality. Strains wAu and wRi protected the CO and DSH host flies respectively. In contrast, neither wHa nor wNo protected their host lines from DCV induced mortality. Phylogenetic analysis indicates that the D. simulans Wolbachia strains wAu and wRi are most similar to wMel. Whereas of the phylogenetic supergroup A strains, wHa is the most divergent to wMel, and wNo belongs to supergroup B (Zhou et al., 1998; Casiraghi et al., 2005). This may suggest that there is a Wolbachia feature involved in antiviral protection, which is conserved among strains more closely related to wMel.
With the exception of the Me29 flies infected by wMel, natural host-Wolbachia combinations were used. The D. simulans Wolbachia strains are known to be associated with different mitochondrial haplotypes (Ballard, 2000) and we did not control for host nuclear genetic background which can have an impact on virus infection (Teixeira et al., 2008). As a consequence it is not possible to rule out that intrinsic variability in susceptibility to virus that is linked to the host background has an influence on the outcome of Wolbachia-mediated protection in our experiments. Indeed there is variation in the time to death of Wolbachia-free D. simulans lines used in this study when challenged with DCV (see
Since protection against DCV was not seen in all the fly lines infected with the Wolbachia strains, we tested whether there is specificity in protection against different viruses. Infection of D. melanogaster by Wolbachia protected the flies from all RNA viruses tested (see Example 4 and Teixeira et al., 2008). Although each of these viruses was a non-enveloped, positive sense RNA virus, the viruses come from a broad spectrum of virus families. Compared to DCV the most divergent of these viruses is FHV. DCV is a member of the Dicistroviridae family and has a single genomic RNA that is not capped but is polyadenylated (Christian et al., 2005). The genome is a bicistronic mRNA from which the structural and non-structural polyproteins are translated via internal ribosome entry sites (Wilson et al., 2000; Johnson and Christian, 1998; Sasaki and Nakashima, 1999). DCV RNA replication occurs on membranes derived from the golgi (Cherry et al., 2006). In contrast, the nodavirus FHV genome comprises two mRNA sense RNAs which are capped but not polyadenylated and a third subgenomic RNA is synthesised during replication (Ball and Johnson, 1998). FHV genome replication occurs on mitochondrial membranes (Kopek et al., 2007; Miller et al., 2001). Interestingly, although DCV and FHV have distinct infection cycles the same Wolbachia strains protected D. simulans lines from both DCV and FHV induced mortality. This suggests that the mechanism of protection from virus-induced mortality may be common across diverse viruses, although it is not currently known what the mechanism of viral pathogenesis is in flies infected with either DCV or FHV. It remains to be seen whether the same host-Wolbachia combinations that do or do not protect against DCV and FHV have similar outcomes for other viruses, or indeed other types of pathogens.
Concurrent with protection from virus induced mortality in D. melanogaster was a delay in accumulation of DCV (see Example 4). Here a similar result was seen with wMel protection in D. simulans, the amount of infectious virus accumulated 2 dpi was significantly lower in Wolbachia infected flies. By 10 dpi the DCV titre in Wolbachia infected flies was similar to the day 2 titre for Wolbachia-free flies. This may suggest that the resistance to DCV accumulation protects the flies from DCV induced mortality, however, the results observed with the D. simulans Wolbachia strains complicate this interpretation. The CO flies infected with wAu survived DCV infection beyond 30 dpi, whereas the Wolbachia-free flies were clearly susceptible to DCV-induced mortality. wAu infected flies had by 10 dpi accumulated high titres of DCV and the virus titre remained high at 30 dpi. This shows that wAu infected flies were tolerant of DCV infection, that is the virus accumulated but did not cause mortality (Schneider and Ayres, 2008). Interestingly, although wRi-infected DSR flies were protected from DCV induced mortality, at 2 dpi there was no difference in virus accumulation in flies with and without wRi. We cannot rule out that accumulation was delayed in wRi-infected flies earlier than 2 dpi.
Taken together our results indicate that Wolbachia-mediated antiviral protection could arise in flies in two ways. Wolbachia can interfere with the virus infection cycle to delay virus accumulation, that is, it can induce resistance to virus infection in the host. In addition Wolbachia infection can protect flies from the pathogenesis associated with virus infection, that is, it can increase host tolerance to virus infection. The processes or mechanisms involved in resistance and tolerance may be the same, independent or overlap. Our results show that Wolbachia strains can induce both resistance and tolerance to DCV infection, but importantly prolonged resistance is not a requirement for protection against DCV-induced mortality. These results are consistent with those reported for FHV in Wolbachia infected D. melanogaster, where there was no difference in FHV accumulation 6 dpi but Wolbachia infection protected flies from FHV induced mortality (Teixeira et al., 2008).
The strains of Wolbachia that mediate antiviral protection were anticipated to be present at higher density in infected flies (Giordano et al., 1995; Sinkins et al., 1995). We confirmed the density of Wolbachia in the particular fly lines used in this study correlated with protection. The density of Wolbachia was assayed in whole flies as previous assays have shown that in addition to reproductive tissues somatic tissues are commonly infected with Wolbachia (Dobson et al., 1999; Ijichi et al., 2002). Further experiments controlling the density of a single strain are required to determine if high Wolbachia density is a pre-requisite for antiviral protection.
The mechanisms or processes by which Wolbachia protects the host from virus are not yet understood. The correlation of high bacterial density of the strains that protect the host suggests that Wolbachia density may be important for antiviral protection. Potentially protection may require a threshold of Wolbachia density to be exceeded, which would be consistent with protection being a consequence of competition between the two intracellular microbes for limited host resources. Antiviral protection may also be dependent on the distribution of Wolbachia between tissue or cell types. Wolbachia have been identified in a range of somatic and reproductive tissues in insects and are known to display variable tissue tropism depending on infecting strain and host combination (Dobson et al., 1999; Ijichi et al., 2002; Miller and Riegler, 2006). Late in infection DCV is widely distributed in Drosophila tissues including both reproductive and somatic tissues (Cherry and Perrimon, 2004; Jousset et al., 1972; Lautié-Harivel and Thomas-Orillard, 1990), giving abundant opportunity for overlap with Wolbachia distribution. However, little is known about the spread of virus from the initial infection site or if replication of the virus is equivalent in all of the susceptible tissues. It is possible that there are tissues or cell types that are critical to virus replication or pathogenesis and that Wolbachia-mediated protection occurs by exclusion or regulation of virus in these tissues. In addition, if particular tissues are critical for pathogenesis, tolerance may be a result of protection of those tissues.
The relatively close phylogenetic relationships of the strains that do confer antiviral protection compared to non-protective strains, suggests that other features of the Wolbachia strains could determine the outcome of virus infection. Protection via both resistance and tolerance could be induced by modulation of host antiviral responses by Wolbachia. For example, proteins from the ankyrin family, which can play a role in innate immune pathways, vary considerably both in number and sequence between Wolbachia strains (Duron et al., 2007; Iturbe-Ormaetxe et al., 2005; Walker et al., 2007). Interestingly defence against bacterial infection in flies via the melanisation response has been shown to involve both resistance and tolerance effects (Ayres and Schneider, 2008).
Wolbachia are able to rapidly invade host populations and are often maintained at high prevalence in these populations (Turelli and Hoffmann, 1991). In many cases this is achieved at least in part by Wolbachia manipulation of host reproductive systems to increase the prevalence of infected individuals in the host population. For example the Wolbachia strains wRi, wHa and wNo used in this study induce cytoplasmic incompatibility in D. simulans. However, wAu does not manipulate host reproductive systems (Hoffmann et al., 1986; Mercot and Poinsot, 1998; O'Neill and Karr, 1990; Turelli and Hoffmann, 1995). In the absence of strong reproductive parasitism, theory predicts that to be maintained in a host population Wolbachia must provide a fitness advantage to the female host (see for example review by Haine, 2008). Wolbachia-mediated protection from viruses and other pathogens (Panteleev et al., 2007) may confer this fitness advantage. It is therefore likely that the interactions between Wolbachia and viruses such as DCV impact on the distribution of both microbes in insect populations.
Throughout the specification the aim has been to describe the preferred embodiments of the invention without limiting the invention to any one embodiment or specific collection of features. It will therefore be appreciated by those of skill in the art that, in light of the instant disclosure, various modifications and changes can be made in the particular embodiments exemplified without departing from the scope of the present invention.
All computer programs, algorithms, patent and scientific literature referred to herein is incorporated herein by reference.
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Claims
1. An isolated arthropod-adapted bacterium capable of modifying one or more biological properties of an arthropod host, wherein said arthropod-adapted bacterium does not normally colonize, inhabit, reside in, or infect said arthropod host.
2. The isolated arthropod-adapted bacterium of claim 1, wherein said arthropod-adapted bacterium is of the genus Wolbachia.
3. The isolated arthropod-adapted bacterium of claim 2, wherein said isolated arthropod-adapted bacterium is of a species of Wolbachia pipientis.
4. The isolated arthropod-adapted bacterium of claim 1, wherein said isolated arthropod-adapted bacterium is wMelPop-CLA.
5. A method of producing an arthropod-adapted bacterium capable of modifying one or more biological properties of an arthropod host, said method including the step of culturing a bacterium with one or more arthropod cells, optionally with one or more differentiating agents, to thereby produce said arthropod-adapted bacterium, wherein said arthropod-adapted bacterium does not normally colonize, inhabit, reside in, or infect said arthropod host.
6. The method of claim 5, wherein said arthropod-adapted bacterium is of the genus Wolbachia.
7. The method of claim 6, wherein said arthropod-adapted bacterium is of a species of Wolbachia pipientis.
8. The method of claim 5, wherein said arthropod-adapted bacterium is wMelPop-CLA.
9. The isolated arthropod-adapted bacterium of claim 1, wherein said arthropod-adapted bacterium comprises one or more genetic modifications.
10. The isolated arthropod-adapted bacterium of claim 9, wherein said one or more genetic modifications are in a gene selected from the group of genes designated WD0200, WD0413, WD0765-WD0766, WD0758, WD0506, WD0507, WD0508, WD0509, WD0510, WD0511, WD0512, WD0513, WD0514, WD0515, WD0516, WD0517, and WD0518.
11. An arthropod comprising the isolated arthropod-adapted bacterium of claim 1.
12. A method of producing an arthropod comprising the isolated arthropod-adapted bacterium of claim 1.
13. The arthropod of claim 11, wherein said arthropod is selected from the group consisting of an insect, an arachnid and a crustacean.
14. The arthropod of claim 13, wherein said arthropod is an insect.
15. The arthropod of claim 14, wherein said insect is a mosquito.
16. The arthropod of claim 15, wherein said mosquito is of the genus selected from the group consisting of Culex, Aedes and Anopheles.
17. The arthropod of claim 16, wherein said mosquito is of a species selected from the group consisting of Aedes aegypti, and Anopheles gambiae.
18. The arthropod of claim 11, wherein one or more eggs from said arthropod has a reduced desiccation tolerance.
19. The arthropod of claim 11, wherein said arthropod has a reduced ability to feed from a host when compared to a corresponding wild-type arthropod.
20. The arthropod of claim 11, wherein said arthropod has improved protection against, or resistance to, a pathogen.
21. The arthropod of claim 20, wherein said pathogen is selected from the group consisting of a virus, a protozoan, a worm, a bacterium, and a fungus.
22. The arthropod of claim 21, wherein said virus is an arbovirus selected from the group consisting of an alphavirus, a flavivirus, and a bunyavirus.
23. The arthropod of claim 22, wherein said alphavirus is a Chikungunya virus.
24. The arthropod of claim 22, wherein said flavivirus is selected from the group consisting of a dengue virus, a West Nile virus, and a Yellow Fever virus.
25. The arthropod of claim 21, wherein said protozoan is a malaria parasite of the genus Plasmodium.
26. The arthropod of claim 25, wherein said malaria parasite is of a species of Plasmodium selected from the group consisting of Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale, Plasmodium malariae, Plasmodium berghei, Plasmodium gallinaceum, and Plasmodium knowlesi.
27. The arthropod of claim 21, wherein said worm is a nematode.
28. The arthropod of claim 27, wherein said nematode is a filarial nematode.
29. The arthropod of claim 21, wherein said bacterium is selected from the group consisting of a Gram negative and a Gram positive bacterium.
30. A method of modifying an arthropod population, said method including the step of introducing the arthropod of claim 11 into said arthropod population, to thereby modify one or more biological properties of said arthropod population.
31. The method of claim 30, wherein said method reduces, decreases, or mitigates pathogen transmission by said arthropod population.
32. The method of claim 30, wherein said method reduces, decreases, or mitigates a susceptibility to a pathogen in said arthropod population.
33. The method of claim 30, wherein said method reduces, lowers, shortens or decreases an average life-span of said arthropod population.
34. The method of claim 30, wherein said method reduces, lowers, or decreases a fecundity of said arthropod population.
35. The method of claim 30, wherein said method reduces an ability of an arthropod population to feed from a host.
36. The method of claim 31 or 32, wherein said pathogen is selected from the group consisting of a virus, a protozoan, a worm, a bacterium, and a fungus.
37. The method of claim 36, wherein said virus is an arbovirus selected from the group consisting of an alphavirus, a flavivirus, and a bunyavirus.
38. The method of claim 37, wherein said alphavirus is a Chikungunya virus.
39. The method of claim 37, wherein said flavivirus is selected from the group consisting of a dengue virus, a West Nile virus, and a Yellow Fever virus.
40. The method of claim 36, wherein said protozoan is a malaria parasite of the genus Plasmodium.
41. The method of claim 40, wherein said malaria parasite is of a species of Plasmodium selected from the group consisting of Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale, Plasmodium malariae, Plasmodium berghei, Plasmodium gallinaceum, and Plasmodium knowlesi.
42. The method of claim 36, wherein said worm is a nematode.
43. The method of claim 42, wherein said nematode is a filarial nematode.
44. The method of claim 36, wherein said bacterium is selected from the group consisting of a Gram-negative and a Gram-positive bacterium.
Type: Application
Filed: Jun 17, 2010
Publication Date: Jun 16, 2011
Applicant: The University of Queensland (St. Lucia)
Inventor: Scott Leslie O'Neill (Paddington)
Application Number: 12/817,933
International Classification: A01K 67/033 (20060101); C12N 1/20 (20060101); C12N 1/36 (20060101); A01N 63/00 (20060101); A01P 7/00 (20060101); A01P 7/04 (20060101);
