A novel regulator controls Clostridium difficile sporulation, motility and toxin production

被引:60
|
作者
Edwards, Adrianne N. [1 ]
Tamayo, Rita [2 ]
McBride, Shonna M. [1 ]
机构
[1] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[2] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC USA
基金
美国国家卫生研究院;
关键词
PROTEIN ASPARTATE PHOSPHATASES; QUORUM-SENSING SYSTEM; BACILLUS-SUBTILIS; OLIGOPEPTIDE PERMEASE; COMPETENCE DEVELOPMENT; TRANSPORT-SYSTEM; GENE-EXPRESSION; VIRULENCE; RESISTANCE; INITIATION;
D O I
10.1111/mmi.13361
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Clostridium difficile is an anaerobic pathogen that forms spores which promote survival in the environment and transmission to new hosts. The regulatory pathways by which C. difficile initiates spore formation are poorly understood. We identified two factors with limited similarity to the Rap sporulation proteins of other spore-forming bacteria. In this study, we show that disruption of the gene CD3668 reduces sporulation and increases toxin production and motility. This mutant was more virulent and exhibited increased toxin gene expression in the hamster model of infection. Based on these phenotypes, we have renamed this locus rstA, for regulator of sporulation and toxins. Our data demonstrate that RstA is a bifunctional protein that upregulates sporulation through an unidentified pathway and represses motility and toxin production by influencing sigD transcription. Conserved RstA orthologs are present in other pathogenic and industrial Clostridium species and may represent a key regulatory protein controlling clostridial sporulation.
引用
收藏
页码:954 / 971
页数:18
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