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Unraveling the Biology of a Fungal Meningitis Pathogen Using Chemical Genetics
Author(s) -
Jessica C. S. Brown,
Justin Nelson,
Benjamin VanderSluis,
Raamesh Deshpande,
Arielle Butts,
Sarah Kagan,
Itzhack Polacheck,
Damian J. Krysan,
Chad L. Myers,
Hiten D. Madhani
Publication year - 2014
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2014.10.044
Subject(s) - biology , cryptococcus neoformans , antifungal drug , genetics , pathogen , genetic screen , virulence , gene , genome , human pathogen , computational biology , phenotype , candida albicans
The fungal meningitis pathogen Cryptococcus neoformans is a central driver of mortality in HIV/AIDS. We report a genome-scale chemical genetic data map for this pathogen that quantifies the impact of 439 small-molecule challenges on 1,448 gene knockouts. We identified chemical phenotypes for 83% of mutants screened and at least one genetic response for each compound. C. neoformans chemical-genetic responses are largely distinct from orthologous published profiles of Saccharomyces cerevisiae, demonstrating the importance of pathogen-centered studies. We used the chemical-genetic matrix to predict novel pathogenicity genes, infer compound mode of action, and to develop an algorithm, O2M, that predicts antifungal synergies. These predictions were experimentally validated, thereby identifying virulence genes, a molecule that triggers G2/M arrest and inhibits the Cdc25 phosphatase, and many compounds that synergize with the antifungal drug fluconazole. Our work establishes a chemical-genetic foundation for approaching an infection responsible for greater than one-third of AIDS-related deaths.

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