College of Animal Science and Technology, College of Veterinary Medicine, Zhejiang A&F University, Hangzhou, Zhejiang, China.
State Key Laboratory of Subtropical Silviculture, Zhejiang A&F University, Hangzhou, Zhejiang, China.
Appl Environ Microbiol. 2022 Apr 26;88(8):e0007222. doi: 10.1128/aem.00072-22. Epub 2022 Apr 6.
Vibrio cholerae is the causative agent of cholera, a life-threatening diarrheal disease in humans. The ability of V. cholerae to colonize the intestine of different animals is a key factor for its fitness and transmissibility between hosts. Many virulence factors, including the ToxT regulon, have been identified to be the major components allowing V. cholerae to colonize the small intestine of suckling mice; however, the mechanism of V. cholerae colonization in the adult mammalian intestine is unclear. In this study, using the streptomycin-treated adult mouse animal model, we characterized the role of the ToxT regulon in V. cholerae colonization in adult mammalian intestine. We first found that the activity of TcpP regulating ToxT regulon expression was attenuated by intestinal reactive oxygen species (ROS). We then found that V. cholerae containing a deletion of the ToxT regulon showed a competition advantage in colonizing adult mice; however, a mutant containing a constitutively active ToxT regulon showed a significant defect in colonizing adult mice. Constitutively producing the virulence factors in the ToxT regulon causes a V. cholerae competition defect in nutrient-limiting conditions. The results of this study demonstrate that modulating the activity of the ToxT regulon through ROS sensed by TcpP is critical for V. cholerae to enhance its colonization in the intestine of adult mice. Vibrio cholerae can inhabit both marine and freshwater ecosystems and can also enter and proliferate in the intestine of different animals which consume contaminated food or water. To successfully colonize the intestines of different hosts, V. cholerae coordinates its gene expression in response to different environments. Here, we describe how V. cholerae modulates the activity of the ToxT regulon by TcpP sensing ROS signals in the intestine of adult mice to better survive in this environment. We found that the constitutively active ToxT regulon causes V. cholerae growth retardation and colonization defect in adult mice. Our work highlights the distinctive role that regulating the activity of the ToxT regulon plays for V. cholerae to achieve full survival fitness in the adult mammalian intestine.
霍乱弧菌是霍乱的病原体,霍乱是一种危及生命的人类腹泻病。霍乱弧菌在不同动物肠道中定殖的能力是其在宿主间适应性和传染性的关键因素。许多毒力因子,包括 ToxT 调控子,已被确定为允许霍乱弧菌在哺乳期小鼠小肠中定殖的主要成分;然而,霍乱弧菌在成年哺乳动物肠道中的定殖机制尚不清楚。在这项研究中,我们使用链霉素处理的成年小鼠动物模型,研究了 ToxT 调控子在霍乱弧菌成年哺乳动物肠道定殖中的作用。我们首先发现,调节 ToxT 调控子表达的 TcpP 的活性受到肠道活性氧 (ROS) 的抑制。然后,我们发现,含有 ToxT 调控子缺失的霍乱弧菌在成年小鼠中定殖具有竞争优势;然而,含有组成型激活 ToxT 调控子的突变体在成年小鼠中定殖明显缺陷。组成型产生 ToxT 调控子中的毒力因子会导致霍乱弧菌在营养限制条件下竞争缺陷。这项研究的结果表明,通过 TcpP 感知 ROS 调节 ToxT 调控子的活性对于霍乱弧菌增强其在成年小鼠肠道中的定殖能力至关重要。
霍乱弧菌可以栖息在海洋和淡水生态系统中,也可以进入并在食用受污染食物或水的不同动物的肠道中增殖。为了成功定殖不同宿主的肠道,霍乱弧菌会根据不同的环境协调其基因表达。在这里,我们描述了霍乱弧菌如何通过 TcpP 感知肠道中的 ROS 信号来调节 ToxT 调控子的活性,从而更好地在这种环境中生存。我们发现,组成型激活的 ToxT 调控子导致霍乱弧菌在成年小鼠中生长迟缓和定殖缺陷。我们的工作强调了调节 ToxT 调控子活性对于霍乱弧菌在成年哺乳动物肠道中实现完全生存适应性的独特作用。