MlrA, a MerR family regulator in Vibrio cholerae, senses the anaerobic signal in the small intestine of the host to promote bacterial intestinal colonization

Gut Microbes. 2022 Jan-Dec;14(1):2143216. doi: 10.1080/19490976.2022.2143216.

Abstract

Vibrio cholerae (V. cholerae), one of the most important bacterial pathogens in history, is a gram-negative motile bacterium that causes fatal pandemic disease in humans via oral ingestion of contaminated water or food. This process involves the coordinated actions of numerous regulatory factors. The MerR family regulators, which are widespread in prokaryotes, have been reported to be associated with pathogenicity. However, the role of the MerR family regulators in V. cholerae virulence remains unknown. Our study systematically investigated the influence of MerR family regulators on intestinal colonization of V. cholerae within the host. Among the five MerR family regulators, MlrA was found to significantly promote the colonization capacity of V. cholerae in infant mice. Furthermore, we revealed that MlrA increases bacterial intestinal colonization by directly enhancing the expression of tcpA, which encodes one of the most important virulence factors in V. cholerae, by binding to its promoter region. In addition, we revealed that during infection, mlrA is activated by anaerobic signals in the small intestine of the host through Fnr. In summary, our findings reveal a MlrA-mediated virulence regulation pathway that enables V. cholerae to sense environmental signals at the infection site to precisely activate virulence gene expression, thus providing useful insights into the pathogenic mechanisms of V. cholerae.

Keywords: MerR family regulator; MlrA; Vibrio cholerae; pathogenicity; toxin-coregulated pilus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anaerobiosis
  • Animals
  • Bacterial Proteins / metabolism
  • Cholera* / microbiology
  • Gastrointestinal Microbiome*
  • Gene Expression Regulation, Bacterial
  • Humans
  • Intestine, Small / metabolism
  • Mice
  • Vibrio cholerae* / metabolism

Substances

  • Bacterial Proteins

Grants and funding

This study was supported by the National Key R&D Program of China (2022YFC2305302), the National Natural Science Foundation of China (NSFC) Program (grant no. 32100144, 32070130, 81772148, 31820103002, 31770144, 31970084, 32170086), Distinguished Young Scholar of Tianjin (grant no. 20JCJQJC00180), the Natural Science Foundation (Key Project) of Tianjin (grant no. 20JCZDJC00820) and the Fundamental Research Funds for the Central Universities.