Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/28165
Title: Citrobacter rodentium lifA/efa1 is essential for colonic colonization and crypt cell hyperplasia in vivo
Authors: Klapproth, Jan Michel A
Sasaki, Maiko
Sherman, Melaine
Babbin, Brian
Donnenberg, Michael S.
Fernandes, Paula J.
Scaletsky, Isabel CA [UNIFESP]
Kalman, Daniel
Nusrat, Asma
Williams, Ifor R.
Emory Univ
Univ Maryland
Universidade Federal de São Paulo (UNIFESP)
Issue Date: 1-Mar-2005
Publisher: Amer Soc Microbiology
Citation: Infection and Immunity. Washington: Amer Soc Microbiology, v. 73, n. 3, p. 1441-1451, 2005.
Abstract: Previously, we have identified a large gene (lifA, for lymphocyte inhibitory factor A) in enteropathogenic Escherichia coli (EPEC) encoding a protein termed lymphostatin that suppresses cytokine expression in vitro. This protein also functions as an adhesion factor for enterohemorrhagic E. coli (EHEC) and Shiga toxin-producing E. coli and is alternatively known as efa1 (EHEC factor for adherence 1). the lifA/efa1 gene is also present in Citrobacter rodentium, an enteric pathogen that causes a disease termed transmissible murine colonic hyperplasia (TMCH), which induces colitis and massive crypt cell proliferation, in mice. To determine if lifA/efa1 is required for C. rodentium-induced colonic pathology in vivo, three in-frame mutations were generated, disrupting the glycosyltransferase (GIM12) and protease (PrMC31) motifs and a domain in between that does not encode any known activity (EID3). in contrast to infection with wild-type C. rodentium, that with any of the lifA/efa1 mutant strains did not induce weight loss or TMCH. Enteric infection with motif mutants GIM12 and PrM31 resulted in significantly reduced colonization counts during the entire 20-day course of infection. in contrast, EID3 was indistinguishable from the wild type during the initial colonic colonization, but cleared rapidly after day 8 of the infection. the colonic epithelium of all infected mice displayed increased epithelial regeneration. However, significantly increased regeneration was observed by day 20 only in mice infected with the wild-type in comparison to those infected with lifA/efa1 mutant EID3. in summary, lifA/efa1 is a critical gene outside the locus for enterocyte effacement that regulates bacterial colonization, crypt cell proliferation, and epithelial cell regeneration.
URI: http://repositorio.unifesp.br/handle/11600/28165
ISSN: 0019-9567
Other Identifiers: http://dx.doi.org/10.1128/IAI.73.3.1441-1451.2005
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