Manganelli Riccardo, Cioetto-Mazzabò Laura, Segafreddo Greta, Boldrin Francesca, Sorze Davide, Conflitti Marta, Serafini Agnese, Provvedi Roberta
Department of Molecular Medicine, University of Padova, Padova, Italy.
Department of Biology, University of Padova, Padova, Italy.
Front Microbiol. 2023 Mar 7;14:1075143. doi: 10.3389/fmicb.2023.1075143. eCollection 2023.
The Extracellular function (ECF) sigma factor SigE is one of the best characterized out of the 13 sigma factors encoded in the chromosome. SigE is required for blocking phagosome maturation and full virulence in both mice and guinea pigs. Moreover, it is involved in the response to several environmental stresses as surface stress, oxidative stress, acidic pH, and phosphate starvation. Underscoring its importance in physiology, SigE is subjected to a very complex regulatory system: depending on the environmental conditions, its expression is regulated by three different sigma factors (SigA, SigE, and SigH) and a two-component system (MprAB). SigE is also regulated at the post-translational level by an anti-sigma factor (RseA) which is regulated by the intracellular redox potential and by proteolysis following phosphorylation from PknB upon surface stress. The set of genes under its direct control includes other regulators, as SigB, ClgR, and MprAB, and genes involved in surface remodeling and stabilization. Recently SigE has been shown to interact with PhoP to activate a subset of genes in conditions of acidic pH. The complex structure of its regulatory network has been suggested to result in a bistable switch leading to the development of heterogeneous bacterial populations. This hypothesis has been recently reinforced by the finding of its involvement in the development of persister cells able to survive to the killing activity of several drugs.
细胞外功能(ECF)σ因子SigE是染色体编码的13种σ因子中特征最明确的因子之一。在小鼠和豚鼠中,SigE是阻断吞噬体成熟和实现完全毒力所必需的。此外,它还参与对多种环境应激的反应,如表面应激、氧化应激、酸性pH值和磷酸盐饥饿。SigE受到非常复杂的调控系统的作用,这突出了其在生理学中的重要性:根据环境条件,其表达受三种不同的σ因子(SigA、SigE和SigH)和一个双组分系统(MprAB)调控。SigE在翻译后水平还受到抗σ因子(RseA)的调控,RseA受细胞内氧化还原电位以及表面应激时PknB磷酸化后的蛋白水解作用调控。其直接控制的基因集包括其他调控因子,如SigB、ClgR和MprAB,以及参与表面重塑和稳定的基因。最近研究表明,SigE在酸性pH条件下与PhoP相互作用以激活一部分基因。其调控网络的复杂结构被认为会导致双稳态开关,从而导致细菌群体的异质性发展。最近发现它参与了能够在多种药物的杀伤活性下存活的持留细胞的形成,这一假设得到了进一步加强。