Institut Pasteur, Biologie des Bactéries Intracellulaires, 75724 Paris Cedex 15, France.
J Bacteriol. 2010 Jan;192(2):446-55. doi: 10.1128/JB.00610-09. Epub 2009 Nov 13.
The bacterial pathogen Legionella pneumophila responds to environmental changes by differentiation. At least two forms are well described: replicative bacteria are avirulent; in contrast, transmissive bacteria express virulence traits and flagella. Phenotypic analysis, Western blotting, and electron microscopy of mutants of the regulatory genes encoding RpoN, FleQ, FleR, and FliA demonstrated that flagellin expression is strongly repressed and that the mutants are nonflagellated in the transmissive phase. Transcriptome analyses elucidated that RpoN, together with FleQ, enhances transcription of 14 out of 31 flagellar class II genes, which code for the basal body, hook, and regulatory proteins. Unexpectedly, FleQ independent of RpoN enhances the transcription of fliA encoding sigma 28. Expression analysis of a fliA mutant showed that FliA activates three out of the five remaining flagellar class III genes and the flagellar class IV genes. Surprisingly, FleR does not induce but inhibits expression of at least 14 flagellar class III genes on the transcriptional level. Thus, we propose that flagellar class II genes are controlled by FleQ and RpoN, whereas the transcription of the class III gene fliA is controlled in a FleQ-dependent but RpoN-independent manner. However, RpoN and FleR might influence flagellin synthesis on a posttranscriptional level. In contrast to the commonly accepted view that enhancer-binding proteins such as FleQ always interact with RpoN to fullfill their regulatory functions, our results strongly indicate that FleQ regulates gene expression that is RpoN dependent and RpoN independent. Finally, FliA induces expression of flagellar class III and IV genes leading to the complete synthesis of the flagellum.
细菌病原体嗜肺军团菌通过分化来响应环境变化。至少有两种形式得到了很好的描述:复制细菌是无毒的;相比之下,传播细菌表达毒力特征和鞭毛。对编码 RpoN、FleQ、FleR 和 FliA 的调节基因的突变体进行表型分析、Western blot 和电子显微镜检查表明,鞭毛蛋白的表达受到强烈抑制,并且在传播阶段突变体是非鞭毛的。转录组分析阐明了 RpoN 与 FleQ 一起增强了 31 个鞭毛 II 类基因中的 14 个的转录,这些基因编码基体、钩和调节蛋白。出乎意料的是,FleQ 独立于 RpoN 增强了编码 sigma 28 的 fliA 的转录。对 fliA 突变体的表达分析表明,FliA 激活了五个剩余的鞭毛 III 类基因中的三个和鞭毛 IV 类基因。令人惊讶的是,FleR 没有诱导但在转录水平上抑制了至少 14 个鞭毛 III 类基因的表达。因此,我们提出鞭毛 II 类基因受 FleQ 和 RpoN 控制,而 fliA 编码的 III 类基因的转录受 FleQ 依赖性但 RpoN 独立性控制。然而,RpoN 和 FleR 可能在转录后水平上影响鞭毛蛋白的合成。与增强子结合蛋白(如 FleQ)总是与 RpoN 相互作用以充分发挥其调节功能的普遍观点相反,我们的结果强烈表明 FleQ 调节 RpoN 依赖性和 RpoN 非依赖性基因表达。最后,FliA 诱导鞭毛 III 类和 IV 类基因的表达,导致鞭毛的完全合成。