HeLa-cell adherence patterns and actin aggregationof enteropathogenic Escherichia coli (EPEC)and Shiga-toxin-producing E. coli (STEC) strainscarrying different eae and tir alleles
Int. microbiol
; 12(4): 243-251, dic. 2009. tab
Article
en En
| IBECS
| ID: ibc-77877
Biblioteca responsable:
ES1.1
Ubicación: BNCS
ABSTRACT
A collection of 69 eae-positive strains expressing 29 different intimin types and eight tir alleles was characterized with respect to their adherence patterns to HeLa cells, ability to promote actin accumulation in vitro, the presence of bfpA alleles in positive strains, and bundle-forming pilus (BFP) expression. All of the nine typical enteropathogenic Escherichia coli (tEPEC) studied harbored the enteropathogenic E. coli adherence factor (EAF) plasmid, as shown by PCR and/or EAF probe results. In addition, they were positive for bfpA, as shown by PCR, and BFP expression, as confirmed by immunofluorescence (IFL) and/or immunoblotting (IBL) assays. Localized adherence (LA) was exclusively displayed by those nine tEPEC, while localized-adherence-like (LAL) was the most frequent pattern among atypical EPEC (aEPEC) and Shiga-toxinproducing E. coli (STEC). All LA and LAL strains were able to cause attaching and effacing (AE) lesions, as established by means of the FAS test. There was a significant association between the presence of tir allele alpha1 and bfpA-positive strains, and consequently, with the LA pattern. However, intimin type or bfpA was not associated with the adherence pattern displayed in HeLa cells. Among the eight bfpA alleles detected, a new type (beta10; accession number FN391178) was identified in a strain of serotype O157H45, and a truncated variant (beta3.2-t; accession number FN 391181) in four strains belonging to different pathotypes (AU)
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Colección:
06-national
/
ES
Base de datos:
IBECS
Asunto principal:
Adhesión Bacteriana
/
Actinas
/
Escherichia coli Enteropatógena
/
Escherichia coli Shiga-Toxigénica
Tipo de estudio:
Prognostic_studies
Límite:
Humans
Idioma:
En
Revista:
Int. microbiol
Año:
2009
Tipo del documento:
Article