| Literature DB >> 31871097 |
Hang-Hang Jiang1,2,3, Yitian Zhou3, Ming Liu4, Jessie Larios-Valencia3, Zachariah Lee3, Hui Wang4, Xing-Hua Gao5, Jun Zhu6.
Abstract
Like many other pathogens, Vibrio cholerae, the causative agent of cholera, can modulate its gene expression to combat stresses encountered in both aquatic and host environments, including stress posed by reactive oxygen species (ROS). We previously reported that the virulence activator AphB in V. cholerae is involved in ROS resistance. In this study, we found that another key virulence regulator, ToxR, was important for V. cholerae resistance to hydrogen peroxide. Through a genome-wide transposon screen, we discovered that a deletion in mneA, which encodes a manganese exporter, restored ROS resistance of the toxR mutant. We then showed that ToxR did not affect mneA transcription but that the ToxR-regulated major porin OmpU was critical for ROS resistance. The addition of manganese in culture medium restored ROS resistance in both the toxR and ompU mutants. Furthermore, elemental analysis indicated that the intracellular concentration of manganese in both the toxR and ompU mutants was reduced. This may result in intracellular ROS accumulation in these mutants. Our data suggest that ToxR plays an important role in the resistance to reactive oxygen species through the regulation of manganese transport.Entities:
Keywords: Mn; ROS; ToxR; Vibrio choleraezzm321990; manganese transport; porin
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Year: 2020 PMID: 31871097 PMCID: PMC7035944 DOI: 10.1128/IAI.00944-19
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441