The localized adherence pattern of an atypical enteropathogenic Escherichia coli is mediated by intimin omicron and unexpectedly promotes HeLa cell invasion.

Autor: Hernandes RT; Departamento de Microbiologia, Imunologia e Parasitologia da Universidade Federal de São Paulo, Escola Paulista de Medicina, São Paulo, Brazil., Silva RM, Carneiro SM, Salvador FA, Fernandes MC, Padovan AC, Yamamoto D, Mortara RA, Elias WP, da Silva Briones MR, Gomes TA
Jazyk: angličtina
Zdroj: Cellular microbiology [Cell Microbiol] 2008 Feb; Vol. 10 (2), pp. 415-25. Date of Electronic Publication: 2007 Oct 02.
DOI: 10.1111/j.1462-5822.2007.01054.x
Abstrakt: Enteropathogenic Escherichia coli (EPEC) forms attaching and effacing lesions in the intestinal mucosa characterized by intimate attachment to the epithelium by means of intimin (an outer membrane adhesin encoded by eae). EPEC is subgrouped into typical (tEPEC) and atypical (aEPEC); only tEPEC carries the EAF (EPEC adherence factor) plasmid that encodes the bundle-forming pilus (BFP). Characteristically, after 3 h of incubation, tEPEC produces localized adherence (LA) (with compact microcolonies) in HeLa/HEp-2 cells by means of BFP, whereas most aEPEC form looser microcolonies. We have previously identified nine aEPEC strains displaying LA in extended (6 h) assays (LA6). In this study, we analysed the kinetics of LA6 pattern development and the role of intimin in the process. Transmission electron microscopy and confocal laser microscopy showed that the invasive process of strain 1551-2 displays a LA phenotype. An eae-defective mutant of strain 1551-2 prevented the invasion although preserving intense diffused adherence. Sequencing of eae revealed that strain 1551-2 expresses the omicron subtype of intimin. We propose that the LA phenotype of aEPEC strain 1551-2 is mediated by intimin omicron and hypothesize that this strain expresses an additional novel adhesive structure. The present study is the first to report the association of compact microcolony formation and an intense invasive ability in aEPEC.
Databáze: MEDLINE