Laboratoire d'Ingénierie des Systèmes Macromoléculaires (UMR7255), CNRS & Aix-Marseille Univ, Marseille, France.
PLoS One. 2013 Oct 21;8(10):e76030. doi: 10.1371/journal.pone.0076030. eCollection 2013.
Three Type VI Secretion System (T6SS) loci called H1- to H3-T6SS coexist in Pseudomonas aeruginosa. H1-T6SS targets prokaryotic cells whereas H2-T6SS mediates interactions with both eukaryotic and prokaryotic host cells. Little is known about the third system, except that it may be connected to H2-T6SS during the host infection. Here we show that H3-T6SS is required for P. aeruginosa PAO1 virulence in the worm model. We demonstrate that the two putative H3-T6SS operons, called "left" and "right", are coregulated with H2-T6SS by the Las and Rhl Quorum Sensing systems. Interestingly, the RpoN σ54 factor has divergent effects on the three operons. As for many T6SSs, RpoN activates the expression of H3-T6SS left. However, RpoN unexpectedly represses the expression of H3-T6SS right and also H2-T6SS. Sfa2 and Sfa3 are putative enhancer binding proteins encoded on H2-T6SS and H3-T6SS left. In other T6SSs EBPs can act as σ54 activators to promote T6SS transcription. Strikingly, we found that the RpoN effects of H3-T6SS are Sfa-independent while the RpoN mediated repression of H2-T6SS is Sfa2-dependent. This is the first example of RpoN repression of a T6SS being mediated by a T6SS-encoded EBP.
在铜绿假单胞菌中存在三个称为 H1-T6SS 至 H3-T6SS 的 VI 型分泌系统 (T6SS) 基因座。H1-T6SS 靶向原核细胞,而 H2-T6SS 介导与真核和原核宿主细胞的相互作用。人们对第三个系统知之甚少,只知道它在宿主感染期间可能与 H2-T6SS 有关。在这里,我们表明 H3-T6SS 是铜绿假单胞菌 PAO1 在蠕虫模型中毒力所必需的。我们证明了两个假定的 H3-T6SS 操纵子,称为“左”和“右”,通过 Las 和 Rhl 群体感应系统与 H2-T6SS 共调控。有趣的是,RpoN σ54 因子对三个操纵子有不同的影响。对于许多 T6SS 而言,RpoN 激活 H3-T6SS 左的表达。然而,RpoN 出人意料地抑制了 H3-T6SS 右和 H2-T6SS 的表达。Sfa2 和 Sfa3 是编码在 H2-T6SS 和 H3-T6SS 左的假定增强子结合蛋白。在其他 T6SS 中,EBPs 可以作为 σ54 激活因子促进 T6SS 转录。引人注目的是,我们发现 H3-T6SS 的 RpoN 效应与 Sfa 无关,而 H2-T6SS 的 RpoN 介导的抑制作用依赖于 Sfa2。这是 RpoN 介导的 T6SS 抑制作用被 T6SS 编码的 EBP 介导的第一个例子。