Zhang Yiquan, Gao He, Osei-Adjei George, Zhang Ying, Yang Wenhui, Yang Huiying, Yin Zhe, Huang Xinxiang, Zhou Dongsheng
School of Medicine, Jiangsu University, Zhenjiang, China.
State Key Laboratory for Infectious Disease Prevention and Control, National Institute for Communicable Disease Control and Prevention, Chinese Centre for Disease Control and Prevention, Beijing, China.
Front Microbiol. 2017 Oct 16;8:2005. doi: 10.3389/fmicb.2017.02005. eCollection 2017.
, the leading cause of seafood-associated gastroenteritis, harbors two separate T6SSs on chromosomes 1 and 2, i.e., T6SS1 (VP1386-1420) and T6SS2 (VPA1025-1046). T6SS1 contains at least 7 putative operons: VP1386-1387, VP1388-1390, VP1392-1391, VP1393-1406, VP1400-1406, VP1409-1407, and VP1410-1420. AphA and OpaR are the two master regulators of quorum sensing (QS) system that are highly expressed at low cell density and high cell density, respectively. ToxR is a membrane-bound virulence regulatory protein conserved across the family. In the present work, we show that ToxR coordinates with AphA and OpaR to repress T6SS1 expression in . OpaR binds to the promoters of VP1388-1390, VP1400-1406, and VP1409-1407 to repress their transcription, but it appears to negatively regulate VP1393-1406 transcription in an indirect manner. By contrast, AphA negatively regulated the above four T6SS1 operons in an indirect manner. In addition, ToxR binds to the promoters of VP1400-1406 and VP1409-1407 to inhibit their transcription, but it presents an indirect interaction with VP1388-1390 and VP1393-1406 promoters. Notably, the expression of ToxR also manifested in a QS-dependent manner and the highest expression occurred at LCD. Meanwhile, the highest expression of T6SS1 occurred at an OD value of 0.6 to 0.8 due to the tight regulation of ToxR and QS, suggesting T6SS1 functions only during the mid-logarithmic growth phase. These observations provide significant insight into the molecular mechanism of T6SS1 gene regulation by QS and ToxR in .
作为海鲜相关性肠胃炎的主要病因,在染色体1和2上含有两个独立的VI型分泌系统(T6SS),即T6SS1(VP1386 - 1420)和T6SS2(VPA1025 - 1046)。T6SS1至少包含7个假定的操纵子:VP1386 - 1387、VP1388 - 1390、VP1392 - 1391、VP1393 - 1406、VP1400 - 1406、VP1409 - 1407和VP1410 - 1420。AphA和OpaR是群体感应(QS)系统的两个主要调节因子,分别在低细胞密度和高细胞密度时高表达。ToxR是一种跨家族保守的膜结合毒力调节蛋白。在本研究中,我们表明ToxR与AphA和OpaR协同作用以抑制霍乱弧菌中T6SS1的表达。OpaR与VP1388 - 1390、VP1400 - 1406和VP1409 - 1407的启动子结合以抑制它们的转录,但它似乎以间接方式负调节VP1393 - 1406的转录。相比之下,AphA以间接方式负调节上述四个T6SS1操纵子。此外,ToxR与VP1400 - 1406和VP1409 - 1407的启动子结合以抑制它们的转录,但它与VP1388 - 1390和VP1393 - 1406启动子存在间接相互作用。值得注意的是,ToxR的表达也以群体感应依赖的方式表现,并且在低细胞密度时表达最高。同时,由于ToxR和群体感应的严格调控,T6SS1在OD值为0.6至0.8时表达最高,这表明T6SS1仅在对数中期生长阶段发挥作用。这些观察结果为霍乱弧菌中群体感应和ToxR对T6SS1基因调控的分子机制提供了重要见解。