Department of Biochemistry and Molecular Biology, Monash University, Clayton Campus, VIC 3800, Australia.
Infect Immun. 2011 Sep;79(9):3659-64. doi: 10.1128/IAI.01351-10. Epub 2011 Jul 18.
Burkholderia pseudomallei, the causal agent of melioidosis, employs a number of virulence factors during its infection of mammalian cells. One such factor is the type three secretion system (TTSS), which is proposed to mediate the transport and secretion of bacterial effector molecules directly into host cells. The B. pseudomallei genome contains three TTSS gene clusters (designated TTSS1, TTSS2, and TTSS3). Previous research has indicated that neither TTSS1 nor TTSS2 is involved in B. pseudomallei virulence in a hamster infection model. We have characterized a B. pseudomallei mutant lacking expression of the predicted TTSS1 ATPase encoded by bpscN. This mutant was significantly attenuated for virulence in a respiratory melioidosis mouse model of infection. In addition, analyses in vitro showed diminished survival and replication in RAW264.7 cells and an increased level of colocalization with the autophagy marker protein LC3 but an unhindered ability to escape from phagosomes. Taken together, these data provide evidence that the TTSS1 bpscN gene product plays an important role in the intracellular survival of B. pseudomallei and the pathogenesis of murine infection.
类鼻疽伯克霍尔德菌是类鼻疽病的病原体,在感染哺乳动物细胞的过程中会使用多种毒力因子。其中一种因子是 III 型分泌系统(TTSS),该系统被认为介导细菌效应分子直接转运和分泌到宿主细胞中。类鼻疽伯克霍尔德菌基因组包含三个 TTSS 基因簇(分别命名为 TTSS1、TTSS2 和 TTSS3)。先前的研究表明,TTSS1 和 TTSS2 均不参与仓鼠感染模型中的类鼻疽伯克霍尔德菌毒力。我们已经对一种缺乏预测的由 bpscN 编码的 TTSS1 ATP 酶表达的类鼻疽伯克霍尔德菌突变体进行了特征描述。该突变体在呼吸道类鼻疽病感染的小鼠模型中,其毒力显著减弱。此外,体外分析表明,该突变体在 RAW264.7 细胞中的存活和复制能力下降,与自噬标志物蛋白 LC3 的共定位水平增加,但逃避吞噬体的能力不受影响。综合这些数据表明,TTSS1 bpscN 基因产物在类鼻疽伯克霍尔德菌的细胞内存活和小鼠感染发病机制中发挥重要作用。