Stringent factor and proteolysis control of sigma factor RpoS expression in Vibrio cholerae

• Published in: International journal of medical microbiology Vol. 307; no. 3; pp. 154 - 165
• Main Authors: Wurm, Philipp, Tutz, Sarah, Mutsam, Beatrice, Vorkapic, Dina, Heyne, Barbara, Grabner, Claudia, Kleewein, Katharina, Halscheidt, Anja, Schild, Stefan, Reidl, Joachim
• Format: Journal Article
• Language: English
• Published: Germany Elsevier GmbH 01.04.2017
• Subjects: Bacterial Proteins - metabolism; Chemotaxis; Culture Media - chemistry; Endopeptidase Clp - metabolism; Gene Expression Regulation, Bacterial; GTP Pyrophosphokinase - metabolism; Humans; Infectious Disease; Medical Education; Proteolysis; Sigma Factor - metabolism; Vibrio cholerae - genetics; Vibrio cholerae - growth & development; Vibrio cholerae - metabolism
• ISSN: 1438-4221; 1618-0607
• DOI: 10.1016/j.ijmm.2017.01.006

Abstract Vibrio cholerae can colonize the gastrointestinal track of humans and cause the disease cholera. During colonization, the alternative sigma factor, RpoS, controls a process known as “mucosal escape response,” defining a specific spatial and temporal response and effecting chemotaxis and motility. In this report, the expression and proteolytic control of RpoS in V. cholerae was characterized. To date, aspects of proteolysis control, the involved components, and proteolysis regulation have not been addressed for RpoS in V. cholerae . Similar to Escherichia coli , we find that the RpoS protein is subjected to regulated intracellular proteolysis, which is mediated by homologues of the proteolysis-targeting factor RssB and the protease complex ClpXP. As demonstrated, RpoS expression transiently peaks after cells are shifted from rich to minimal growth medium. This peak level is dependent on (p)ppGpp-activated rpoS transcription and controlled RpoS proteolysis. The RpoS peak level also correlates with induction of a chemotaxis gene, encoding a methyl-accepting chemotaxis protein, earlier identified to belong to the mucosal escape response pathway. These results suggest that the RpoS expression peak is linked to (p)ppGpp alarmone increase, leading to enhanced motility and chemotaxis, and possibly contributing to the mucosal escape response.