Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Corvallis, Oregon, USA.
Department of Microbiology, Oregon State University, Corvallis, Oregon, USA.
Infect Immun. 2014 Jul;82(7):2788-801. doi: 10.1128/IAI.01292-13. Epub 2014 Apr 14.
Vibrio cholerae, an etiological agent of cholera, circulates between aquatic reservoirs and the human gastrointestinal tract. The type II secretion (T2S) system plays a pivotal role in both stages of the lifestyle by exporting multiple proteins, including cholera toxin. Here, we studied the kinetics of expression of genes encoding the T2S system and its cargo proteins. We have found that under laboratory growth conditions, the T2S complex was continuously expressed throughout V. cholerae growth, whereas there was growth phase-dependent transcriptional activity of genes encoding different cargo proteins. Moreover, exposure of V. cholerae to different environmental cues encountered by the bacterium in its life cycle induced transcriptional expression of T2S. Subsequent screening of a V. cholerae genomic library suggested that σ(E) stress response, phosphate metabolism, and the second messenger 3',5'-cyclic diguanylic acid (c-di-GMP) are involved in regulating transcriptional expression of T2S. Focusing on σ(E), we discovered that the upstream region of the T2S operon possesses both the consensus σ(E) and σ(70) signatures, and deletion of the σ(E) binding sequence prevented transcriptional activation of T2S by RpoE. Ectopic overexpression of σ(E) stimulated transcription of T2S in wild-type and isogenic ΔrpoE strains of V. cholerae, providing additional support for the idea that the T2S complex belongs to the σ(E) regulon. Together, our results suggest that the T2S pathway is characterized by the growth phase-dependent expression of genes encoding cargo proteins and requires a multifactorial regulatory network to ensure appropriate kinetics of the secretory traffic and the fitness of V. cholerae in different ecological niches.
霍乱弧菌是霍乱的病原体,它在水生储层和人类胃肠道之间循环。II 型分泌(T2S)系统在生活方式的两个阶段都发挥着关键作用,它可以输出多种蛋白质,包括霍乱毒素。在这里,我们研究了编码 T2S 系统及其货物蛋白的基因表达的动力学。我们发现,在实验室生长条件下,T2S 复合物在整个霍乱弧菌生长过程中持续表达,而编码不同货物蛋白的基因则存在生长阶段依赖性的转录活性。此外,霍乱弧菌暴露于其生命周期中遇到的不同环境线索会诱导 T2S 的转录表达。随后对霍乱弧菌基因组文库的筛选表明,σ(E)应激反应、磷酸盐代谢和第二信使 3',5'-环二鸟苷酸(c-di-GMP)参与调节 T2S 的转录表达。我们关注σ(E),发现 T2S 操纵子的上游区域同时具有σ(E)和σ(70)的保守序列,并且删除σ(E)结合序列会阻止 RpoE 对 T2S 的转录激活。σ(E)的异位过表达刺激了野生型和同源 rpoE 缺失菌株中 T2S 的转录,这为 T2S 复合物属于σ(E)调控子的观点提供了额外的支持。总之,我们的结果表明,T2S 途径的特点是货物蛋白编码基因的表达具有生长阶段依赖性,并且需要一个多因素调控网络来确保分泌途径的适当动力学和霍乱弧菌在不同生态位中的适应性。