Dual role of CsrA in regulating the hemolytic activity of Escherichia coli O157:H7

Bibliographic Details
Title: Dual role of CsrA in regulating the hemolytic activity of Escherichia coli O157:H7
Authors: Zhibin Sun, Ning Zhou, Wenting Zhang, Yan Xu, Yu-Feng Yao
Source: Virulence, Vol 13, Iss 1, Pp 859-874 (2022)
Publisher Information: Taylor & Francis Group, 2022.
Publication Year: 2022
Collection: LCC:Infectious and parasitic diseases
Subject Terms: Escherichia coli O157:H7, hemolysis, CsrA/RsmA, virulence, protein–RNA interaction, Infectious and parasitic diseases, RC109-216
More Details: Post-transcriptional global carbon storage regulator A (CsrA) is a sequence-specific RNA-binding protein involved in the regulation of multiple bacterial processes. Hemolysin is an important virulence factor in the enterohemorrhagic Escherichia coli O157:H7 (EHEC). Here, we show that CsrA plays a dual role in the regulation of hemolysis in EHEC. CsrA significantly represses plasmid-borne enterohemolysin (EhxA)-mediated hemolysis and activates chromosome-borne hemolysin E (HlyE)-mediated hemolysis through different mechanisms. RNA structure prediction revealed a well-matched stem-loop structure with two potential CsrA binding sites located on the 5' untranslated region (UTR) of ehxB, which encodes a translocator required for EhxA secretion. CsrA inhibits EhxA secretion by directly binding to the RNA leader sequence of ehxB to repress its expression in two different ways: CsrA either binds to the Shine–Dalgarno sequence of ehxB to block ribosome access or to ehxB transcript to promote its mRNA decay. The predicted CsrA-binding site 1 of ehxB is essential for its regulation. There is a single potential CsrA-binding site at the 5'-end of the hlyE transcript, and its mutation completely abolishes CsrA-dependent activation. CsrA can also stabilize hlyE mRNA by directly binding to its 5' UTR. Overall, our results indicate that CsrA acts as a hemolysis modulator to regulate pathogenicity under certain conditions.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 21505594
2150-5608
2150-5594
Relation: https://doaj.org/toc/2150-5594; https://doaj.org/toc/2150-5608
DOI: 10.1080/21505594.2022.2073023
Access URL: https://doaj.org/article/a9e70a1361464c0e861c3ae553768da2
Accession Number: edsdoj.9e70a1361464c0e861c3ae553768da2
Database: Directory of Open Access Journals
More Details
ISSN:21505594
21505608
DOI:10.1080/21505594.2022.2073023
Published in:Virulence
Language:English