蛋白酶体
一氧化氮
突变体
结核分枝杆菌
微生物学
生物
基因
活性氮物种
化学
生物化学
肺结核
医学
内分泌学
病理
作者
K. Heran Darwin,Sabine Ehrt,José-Carlos Gutierrez-Ramos,Nadine Weich,Carl Nathan
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2003-12-11
卷期号:302 (5652): 1963-1966
被引量:537
标识
DOI:10.1126/science.1091176
摘要
The production of nitric oxide and other reactive nitrogen intermediates (RNI) by macrophages helps to control infection by Mycobacterium tuberculosis (Mtb). However, the protection is imperfect and infection persists. To identify genes that Mtb requires to resist RNI, we screened 10,100 Mtb transposon mutants for hypersusceptibility to acidified nitrite. We found 12 mutants with insertions in seven genes representing six pathways, including the repair of DNA (uvrB) and the synthesis of a flavin cofactor (fbiC). Five mutants had insertions in proteasome-associated genes. An Mtb mutant deficient in a presumptive proteasomal adenosine triphosphatase was attenuated in mice, and exposure to proteasomal protease inhibitors markedly sensitized wild-type Mtb to RNI. Thus, the mycobacterial proteasome serves as a defense against oxidative or nitrosative stress.
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