State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, China.
State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, China; Shanghai Collaborative Innovation Center for Biomanufacturing Technology, 130 Meilong Road, Shanghai 200237, China; Shanghai Engineering Research Center of Maricultured Animal Vaccines, Shanghai 200237, China.
Microbiol Res. 2020 Oct;239:126528. doi: 10.1016/j.micres.2020.126528. Epub 2020 Jun 27.
Edwardsiella piscicida is a notorious pathogen infecting diverse kinds of fish and causes substantial economic losses in the global aquaculture industries. The EsrA-EsrB two-component system plays a critical role in the regulation of virulence genes expression, including type III and type VI secretion systems (T3/T6SSs). In this study, the putative regulators of esrB were screened by the transposon insertion sequencing (TIS) technology. As a result, MviN, a lipid II flippase, was identified as a modulator to upregulate esrB and downstream T3/T6SS gene expression in the earlier growth phases while downregulate esrB at the later stages. Complement or overexpression of the mviN restored the esrB as well as T3/T6SS expression in the ΔmviN mutant strain. Moreover, MviN also mediated the regulation of environmental osmotic pressure on the expression of esrB. MviN was also found to significantly influence the in vivo colonization of E. piscicida in turbot. Collectively, this study enhanced our understanding of pathogenesis and virulence regulatory network of E. piscicida.
杀鲑爱德华氏菌是一种感染多种鱼类的著名病原体,给全球水产养殖业造成了巨大的经济损失。EsrA-EsrB 双组分系统在毒力基因表达的调控中起着关键作用,包括 III 型和 VI 型分泌系统(T3/T6SS)。在本研究中,通过转座子插入测序(TIS)技术筛选了 esrB 的假定调控因子。结果表明,脂 II 翻转酶 MviN 是上调 esrB 及其下游 T3/T6SS 基因表达的调节剂,在早期生长阶段上调,而在后期下调 esrB。mviN 的互补或过表达恢复了 ΔmviN 突变株中 esrB 以及 T3/T6SS 的表达。此外,MviN 还介导了环境渗透压对 esrB 表达的调节。还发现 MviN 显著影响了杀鲑爱德华氏菌在大菱鲆体内的定殖。总之,本研究增进了我们对杀鲑爱德华氏菌发病机制和毒力调控网络的理解。