Department of Biotechnology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.
FEMS Microbiol Lett. 2010 Feb;303(2):190-6. doi: 10.1111/j.1574-6968.2009.01876.x. Epub 2009 Dec 3.
Nitrate reduction is believed to be vital for the survival of tubercle bacteria under hypoxic/anaerobic conditions that are thought to prevail within granulomas. Nitrate reductase activity is rapidly induced in Mycobacterium tuberculosis (M. tb) under hypoxic conditions and is attributed to the induced expression of the nitrate/nitrite transporter gene, narK2. By contrast, Mycobacterium bovis (M. bovis) and M. bovis BCG (BCG) do not support the hypoxic induction of either nitrate reductase activity or narK2. Here, we show that the induction defect in the narK2X operon in M. bovis and BCG is caused by a -6T/C single nucleotide polymorphism (SNP) in the -10 promoter element essential for narK2X promoter activity. Complementation of M. bovis with both narGHJI and narK2X genes from M. tb failed to restore nitrate reductase activity in M. bovis, suggesting the involvement of additional genes/regulatory mechanisms for nitrate reduction that are absent in M. bovis. The -6T/C promoter-linked SNP enabled clear differentiation of M. tb from the other members of the M. tb complex, including M. bovis, BCG, Mycobacterium africanum and Mycobacterium microti, through a PCR-RFLP assay.
硝酸盐还原被认为对结核分枝杆菌在缺氧/厌氧条件下的生存至关重要,这些条件被认为在肉芽肿内普遍存在。在缺氧条件下,结核分枝杆菌(M. tb)中的硝酸盐还原酶活性迅速诱导,这归因于硝酸盐/亚硝酸盐转运基因 narK2 的诱导表达。相比之下,牛分枝杆菌(M. bovis)和牛分枝杆菌卡介苗(BCG)不支持硝酸盐还原酶活性或 narK2 的缺氧诱导。在这里,我们表明,牛分枝杆菌和 BCG 中 narK2X 操纵子的诱导缺陷是由 -10 启动子元件中一个对 narK2X 启动子活性至关重要的 -6T/C 单核苷酸多态性(SNP)引起的。用来自结核分枝杆菌的 narGHJI 和 narK2X 基因对牛分枝杆菌进行互补未能恢复牛分枝杆菌中的硝酸盐还原酶活性,这表明硝酸盐还原涉及其他基因/调节机制,而这些机制在牛分枝杆菌中不存在。-6T/C 启动子相关 SNP 通过 PCR-RFLP 分析能够清晰地区分结核分枝杆菌与结核分枝杆菌复合群的其他成员,包括牛分枝杆菌、卡介苗、非洲分枝杆菌和微小分枝杆菌。