Aix-Marseille Université et CNRS, Laboratoire d'Ingénierie des Systèmes Macromoléculaires, UMR7255, 13402 Marseille cedex 20, France.
J Biol Chem. 2012 Aug 3;287(32):27095-105. doi: 10.1074/jbc.M112.376368. Epub 2012 Jun 4.
The genome of Pseudomonas aeruginosa PAO1 contains three type VI secretion systems (T6SSs) called H1-, H2-, and H3-T6SS. The H1-T6SS secretes three identified toxins that target other bacteria, providing a fitness advantage for P. aeruginosa, and likely contributes to bacterial pathogenesis in chronic infections. However, no specific substrates or defined roles have been described for the two other systems. Here, we demonstrate that the expression of H2-T6SS genes of strain PAO1 is up-regulated during the transition from exponential to stationary phase growth and regulated by the Las and Rhl quorum sensing systems. In addition, we identify two putative Fur boxes in the promoter region and find that H2-T6SS transcription is negatively regulated by iron. We also show that the H2-T6SS system enhances bacterial uptake into HeLa cells (75% decrease in internalization with a H2-T6SS mutant) and into lung epithelial cells through a phosphatidylinositol 3-kinase-dependent pathway that induces Akt activation in the host cell (50% decrease in Akt phosphorylation). Finally, we show that H2-T6SS plays a role in P. aeruginosa virulence in the worm model. Thus, in contrast to H1-T6SS, H2-T6SS modulates interaction with eukaryotic host cells. Together, T6SS can carry out different functions that may be important in establishing chronic P. aeruginosa infections in the human host.
铜绿假单胞菌 PAO1 的基因组包含三个类型 VI 分泌系统(T6SS),分别称为 H1-、H2-和 H3-T6SS。H1-T6SS 分泌三种已鉴定的毒素,这些毒素靶向其他细菌,为铜绿假单胞菌提供了适应性优势,可能有助于慢性感染中的细菌发病机制。然而,其他两个系统没有特定的底物或明确的作用。在这里,我们证明了 PAO1 菌株的 H2-T6SS 基因的表达在从指数生长期到静止期生长的转变过程中上调,并受到 Las 和 Rhl 群体感应系统的调节。此外,我们在启动子区域识别出两个假定的 Fur 盒,并发现 H2-T6SS 转录受铁的负调控。我们还表明,H2-T6SS 系统通过一种依赖于磷脂酰肌醇 3-激酶的途径增强细菌进入 HeLa 细胞(H2-T6SS 突变体的内化减少 75%)和肺上皮细胞的摄取,该途径诱导宿主细胞中 Akt 的激活(Akt 磷酸化减少 50%)。最后,我们表明 H2-T6SS 在虫模型中发挥了铜绿假单胞菌毒力的作用。因此,与 H1-T6SS 相反,H2-T6SS 调节与真核宿主细胞的相互作用。总之,T6SS 可以执行不同的功能,这些功能可能在建立人类宿主中慢性铜绿假单胞菌感染中很重要。