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IL-1 beta expression in Int407 is induced by flagellin of Vibrio cholerae through TLR5 mediated pathway

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Title IL-1 beta expression in Int407 is induced by flagellin of Vibrio cholerae through TLR5 mediated pathway
 
Creator Bandyopadhaya, A
Sarkar, M
Chaudhuri, K
 
Subject Immunology; Microbiology
 
Description Vibrio cholerae, a noninvasive enteric bacterium, causing inflammatory diarrheal disease cholera. is associated with the secretion of proinflamammatory cytokines including IL-1 beta ill Cultured epithelial cells. Incubation of Int407 with live V. cholerae resulted in increased IL-1 beta mRNA expression as early as 2h of infection, reached a peak at similar to 3.5 h and decreased thereafter. The identity of the effector molecule(s) is large unknown. The bacterial culture supernatant showed IL-1 beta stimulating activity. An engineered aflagellate V. cholerae flaA mutant (O395FLAN) resulted in highly reduced level of IL-1 beta; expression in Int407. The crude flagellar protein of V. cholerae as well as recombinant FlaA induced IL-1 beta expression in Int407. Infection of Toll-like receptor 5 (TLR5) transfected HeLa cells with O395FLAN showed reduced expression of IL-1 beta; compared to wild-type. Unlike wild-type V. cholerae, O395FLAN did not activate the NF-kappa B while the recombinant Ha elfin Could activate NF-kappa B. Finally. the mitogen activated protein kinases(ERK1 and 2. p38) were phosphorylated in wild-type and recombinant flagellin treated Int407 cells and inhibition of the p38 and ERK pathways significantly decreased the IL-1 beta response induced by wild-type V. cholerae as well as recombinant flagellin. Our data clearly indicate that flagellin of V. cholerae could induce IL-1 beta expression by recognizing TLR5 that activate NF-kappa B and MAP kinase in Int407. (C) 2008 Elsevier Ltd. All rights reserved.
 
Publisher ACADEMIC PRESS LTD ELSEVIER SCIENCE LTDLONDON24-28 OVAL RD, LONDON NW1 7DX, ENGLAND
 
Date 2011-09-20T12:12:44Z
2011-09-20T12:12:44Z
2008
 
Type Article
 
Identifier MICROBIAL PATHOGENESIS
0882-4010
http://hdl.handle.net/123456789/14401
 
Language English