Abstract: Embodiments of the present invention illustrate methods of treating and preventing infection due to a pathogen such as a fungal pathogen. In particular, the present invention relates to compositions and methods for vaccinations against or treatment for a fungal organism in a non-immunocompromised or immunocompromised subject.
Abstract: The present invention provides methods for simultaneously assessing microbial phosphoglucose isomerase, ketol-isomerase and glucosamine-6-phosphate acetyltransferase activities, by measuring the production of Coenzyme A (CoA). The present invention finds use in the isolation of new classes of antifungal drugs, wherein the compounds have the ability to inhibit fungal glucose utilization.
Type:
Grant
Filed:
August 10, 2001
Date of Patent:
June 1, 2004
Assignees:
MycoLogics, Inc., Toyama Chemical Co., Ltd.
Inventors:
Claude P. Selitrennikoff, Mitsunori Nakata
Abstract: The present invention relates to methods to assay 2-amino-2-deoxy-D-glucose-6-phosphate ketol-isomerase activity. The present invention also relates to methods for drug screening to identify compounds having antimicrobial activity, wherein the compounds have the ability to inhibit the enzymatic activity of a microbial ketol-isomerase. In other embodiments, methods are provided for the identification of compounds that selectively inhibit microbial ketol-isomerase activity compared to the ketol-isomerase activity of the subject being treated for an infection.
Type:
Grant
Filed:
May 25, 2001
Date of Patent:
May 4, 2004
Assignee:
Mycologics, Inc.
Inventors:
Claude P. Selitrennikoff, Mitsunori Nakata
Abstract: The present invention provides methods for simultaneously assessing microbial phosphoglucose isomerase, ketol-isomerase and glucosamine-6-phosphate acetyltransferase activities, by measuring the production of Coenzyme A (CoA). The present invention finds use in the isolation of new classes of antifungal drugs, wherein the compounds have the ability to inhibit fungal glucose utilization.
Type:
Application
Filed:
August 10, 2001
Publication date:
October 16, 2003
Applicant:
MycoLogics, Inc.
Inventors:
Claude P. Selitrennikoff, Mitsunori Nakata
Abstract: The novel compositions and methods of the subject invention can be used in antifugal applications. The antifugal agents of the subject invention can be used in the treatment of an animal or human having a fugal infection. In a further embodiment the compounds can be used to treat plant fugal infections, disinfect surfaces, and prevent spoilage of organic compositions such as food and cosmetics.
Type:
Grant
Filed:
July 20, 2001
Date of Patent:
February 18, 2003
Assignees:
Harbor Branch Oceanographic Institution, Inc., Mycologics, Inc.
Inventors:
Ying Chen, Katherine Chilson, Keith Brian Killday, Dedra Harmody, Peter J. McCarthy, Shirley A. Pomponi, Rebecca Schimoler, Claude Selitrennikoff, Amy E. Wright
Abstract: A novel antifungal compound, “CAY-1”, was isolated from the dried fruit of Capsicum frutescens (cayenne pepper), purified to homogeneity, and characterized as a novel sterol glycoside (a saponin) with a molecular mass of 1243.35 Da. CAY-1 demonstrates antifungal activity against a large variety of fungal organisms associated with diseases in plants, animals and humans including, but not limited to, Aspergillus flavus, A. fumigatus, A. parasiticus, A. niger, Pneumocystis carnii and Candida albicans, but has minimal toxic effects on mammalian cells.
Type:
Grant
Filed:
September 14, 2000
Date of Patent:
October 30, 2001
Assignees:
The United States of America as represented by the Secretary
of Agriculture, Mycologics, Inc.
Inventors:
Anthony J. De Lucca, II, John M. Bland, Craig B. Vigo, Claude P. Selitrennikoff
Abstract: A method and device for performing comparative assay of binding and bindable substances such as antibodies and antigens. The device includes a circulation conduit for continuously conveying a carrier fluid between a support zone therein and a detection zone therein. A competitive binding substance is fixed in the support zone and is capable of competitively binding a test substance and an analytical detection substance such that changes in concentration of the test substance in the carrier fluid responsively cause changes of concentration of analytical detection substance in the carrier fluid. Each of the analytical detection substance (antigen-fluorochrome, for example) and the test substance (antigen, for example) are bound to the binding substance (monoclonal antibody, for example) in proportion to the concentration of the test substance in the carrier fluid.