| Literature DB >> 26394644 |
Tomotaka Tanabe1, Katsushiro Miyamoto2, Hiroshi Tsujibo2, Shigeo Yamamoto3, Tatsuya Funahashi3.
Abstract
The cytotoxicity of Vibrio parahaemolyticus has been related to the type III secretion system 1 effector protein VP1680, which is secreted and translocated into host cells with the help of the specific chaperone protein, VP1682. This study sought to confirm the in silico analysis, which predicted that a small regulatory RNA (Spot 42) could base pair with the region encompassing the ribosomal-binding site and initiation codon of the vp1682 mRNA. Electrophoresis mobility shift assays indicated that Spot 42 could bind to the vp1682 mRNA with the help of Hfq. Consistent with these results, the translation of the vp1682 mRNA was inhibited when both Hfq and Spot 42 were added to the in vitro translation reaction. The cytotoxic activity against infected Caco-2 cells was significantly increased in the Spot 42 deletion mutant (Δspf) at 4 h after infection as compared with the parental strain. Additionally, we observed that both VP1682 and VP1680 were more highly expressed in Δspf mutants than in the parental strain. These results indicate that Spot 42 post-transcriptionally regulates the expression of VP1682 in V. parahaemolyticus, which contributes to cytotoxicity in vivo. © FEMS 2015. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.Entities:
Keywords: Spot 42; Vibrio parahaemolyticus; chaperone; effector; small RNA; type III secretion system
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Year: 2015 PMID: 26394644 DOI: 10.1093/femsle/fnv173
Source DB: PubMed Journal: FEMS Microbiol Lett ISSN: 0378-1097 Impact factor: 2.742