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Unraveling the Biology of a Fungal Meningitis Pathogen Using Chemical Genetics

机译:使用化学遗传学揭示真菌性脑膜炎病原体的生物学

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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, O_2M, 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.
机译:真菌性脑膜炎病原体新隐球菌是导致HIV / AIDS死亡的主要因素。我们报告了这种病原体的基因组规模化学遗传数据图,该图量化了439个小分子挑战对1,448个基因敲除的影响。我们确定了83%的突变体的化学表型,并为每种化合物确定了至少一种遗传反应。 C. neoformans的化学遗传反应在很大程度上与啤酒酵母的直系同源文献有所不同,证明了以病原体为中心的研究的重要性。我们使用化学遗传矩阵预测新的致病性基因,推断复合作用模式,并开发了预测抗真菌协同作用的算法O_2M。这些预测已通过实验验证,从而确定了毒性基因,触发G2 / M阻滞并抑制Cdc25磷酸酶的分子以及与抗真菌药fluconazole协同作用的许多化合物。我们的工作为应对导致三分之一以上与艾滋病相关的死亡的感染建立了化学遗传基础。

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