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编码磷酸结合蛋白PstS1和PstS2的基因发生破坏的结核分枝杆菌在磷酸盐摄取方面存在缺陷,并表现出体内毒力降低。

Mycobacterium tuberculosis with disruption in genes encoding the phosphate binding proteins PstS1 and PstS2 is deficient in phosphate uptake and demonstrates reduced in vivo virulence.

作者信息

Peirs Priska, Lefèvre Philippe, Boarbi Samira, Wang Xiao-Ming, Denis Olivier, Braibant Martine, Pethe Kevin, Locht Camille, Huygen Kris, Content Jean

机构信息

Pasteur Institute of Brussels, Engelandstraat 642, B-1180-Brussels, Belgium.

出版信息

Infect Immun. 2005 Mar;73(3):1898-902. doi: 10.1128/IAI.73.3.1898-1902.2005.

Abstract

By measuring phosphate uptake by Mycobacterium tuberculosis strains with the pstS1 and pstS2 genes genetically inactivated, we showed that these pstS genes encode high-affinity phosphate binding proteins. In a mouse infection model, both mutants were attenuated in virulence, suggesting that M. tuberculosis encounters limiting phosphate concentrations during its intracellular life span.

摘要

通过测量基因敲除pstS1和pstS2基因的结核分枝杆菌菌株对磷酸盐的摄取,我们发现这些pstS基因编码高亲和力磷酸盐结合蛋白。在小鼠感染模型中,两种突变体的毒力均减弱,这表明结核分枝杆菌在其细胞内存活期间会遇到磷酸盐浓度受限的情况。

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