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Two regulatory factors of Vibrio cholerae activating the mannose-sensitive haemagglutinin pilus expression is important for biofilm formation and colonization in mice.

Abstract
Vibrio cholerae the causative agent of cholera, uses a large number of coordinated transcriptional regulatory events to transition from its environmental reservoir to the host intestine, which is its preferred colonization site. Transcription of the mannose-sensitive haemagglutinin pilus (MSHA), which aids the persistence of V. cholerae in aquatic environments, but causes its clearance by host immune defenses, was found to be regulated by a yet unknown mechanism during the infection cycle of V. cholerae. In this study, genomic expression library screening revealed that two regulators, VC1371 and VcRfaH, are able to positively activate the transcription of MSHA operon. VC1371 is localized and active in the cell membrane. Deletion of vc1371 or VcrfaH genes in V. cholerae resulted in less MshA protein production and less efficiency of biofilm formation compared to that in the wild-type strain. An adult mouse model showed that the mutants with vc1371 or VcrfaH deletion colonized less efficiently than the wild-type; the VcrfaH deletion mutant showed less colonization efficiency in the infant mouse model. The findings strongly suggested that the two regulators, namely VC1371 and VcRfaH, which are involved in the regulation of MSHA expression, play an important role in V. cholerae biofilm formation and colonization in mice.
AuthorsMengting Shi, Yue Zheng, Xianghong Wang, Zhengjia Wang, Menghua Yang
JournalMicrobiology (Reading, England) (Microbiology (Reading)) Vol. 167 Issue 10 (10 2021) ISSN: 1465-2080 [Electronic] England
PMID34665117 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Bacterial Proteins
  • Mannose-Binding Lectin
  • MshA protein, Vibrio cholerae
  • Fimbriae Proteins
Topics
  • Animals
  • Bacterial Proteins (genetics, metabolism)
  • Biofilms (growth & development)
  • Cell Membrane (metabolism)
  • Cholera (microbiology)
  • Fimbriae Proteins (genetics, metabolism)
  • Gene Expression Regulation, Bacterial
  • Mannose-Binding Lectin (genetics, metabolism)
  • Mice
  • Mutation
  • Operon
  • Promoter Regions, Genetic
  • Vibrio cholerae (genetics, metabolism, pathogenicity)
  • Virulence (genetics)

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