Bouffartigues Emeline, Si Hadj Mohand Ishac, Maillot Olivier, Tortuel Damien, Omnes Jordane, David Audrey, Tahrioui Ali, Duchesne Rachel, Azuama Cecil Onyedikachi, Nusser Michael, Brenner-Weiss Gerald, Bazire Alexis, Connil Nathalie, Orange Nicole, Feuilloley Marc G J, Lesouhaitier Olivier, Dufour Alain, Cornelis Pierre, Chevalier Sylvie
Laboratoire de Microbiologie Signaux et Microenvironnement (LMSM) EA 4312, Normandie Université, Université de Rouen Normandie, Centre de Sécurité Sanitaire de Normandie, Evreux, France.
Institute of Functional Interfaces, Karlsruhe Institute of Technology, Karlsruhe, Germany.
Front Microbiol. 2020 Oct 21;11:579495. doi: 10.3389/fmicb.2020.579495. eCollection 2020.
is a highly adaptable Gram-negative opportunistic pathogen, notably due to its large number of transcription regulators. The extracytoplasmic sigma factor (ECFσ) AlgU, responsible for alginate biosynthesis, is also involved in responses to cell wall stress and heat shock via the RpoH alternative σ factor. The SigX ECFσ emerged as a major regulator involved in the envelope stress response via membrane remodeling, virulence and biofilm formation. However, their functional interactions to coordinate the envelope homeostasis in response to environmental variations remain to be determined. The regulation of the putative operon located directly upstream was investigated by applying sudden temperature shifts from 37°C. We identified a SigX- and an AlgU- dependent promoter region upstream of and , respectively. We show that expression is increased upon heat shock through an AlgU-dependent but RpoH independent mechanism. In addition, the ECFσ SigX is activated in response to valinomycin, an agent altering the membrane structure, and up-regulates transcription in response to cold shock. Altogether, these data provide new insights into the regulation exerted by SigX and networks that are involved in maintaining envelope homeostasis.
是一种高度适应性的革兰氏阴性机会致病菌,特别是由于其大量的转录调节因子。负责藻酸盐生物合成的胞外sigma因子(ECFσ)AlgU,也通过RpoH替代σ因子参与对细胞壁应激和热休克的反应。SigX ECFσ作为一种主要调节因子出现,通过膜重塑、毒力和生物膜形成参与包膜应激反应。然而,它们在响应环境变化时协调包膜稳态的功能相互作用仍有待确定。通过从37°C突然改变温度,研究了直接位于上游的假定操纵子的调控。我们分别在和的上游鉴定出一个依赖SigX和一个依赖AlgU的启动子区域。我们表明,在热休克时,通过依赖AlgU但不依赖RpoH的机制,表达增加。此外,ECFσ SigX在响应缬氨霉素(一种改变膜结构的试剂)时被激活,并在冷休克时上调转录。总之,这些数据为SigX和参与维持包膜稳态的网络所施加的调控提供了新的见解。