Clonal structure and virulence factors in strains of Escherichia coli of the classic serogroup O55

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Abstract

Virulence properties and genetic variation as determined by multilocus enzyme electrophoresis were studied in 70 strains of Escherichia coli O55, a common serogroup of enteropathogenic E. coli (EPEC), a major cause of infantile diarrhea in developing countries. Nearly 40% of the strains were originally isolated in Brazil and represented serotypes O55:H6, O55:H7, and O55:H51 and nonmotile (O55:H-) strains. The analysis of electrophoretic variants of 20 enzymes defined seven distinct electrophoretic types (ETs). ET1 was represented by 41% of the strains, including strains which usually hybridized with DNA probes for the intimin gene (eaeA), the EPEC adherence plasmid (EAF), and the gene for the pilin subunit of the bundle-forming pilus (bfpA). The ET I strains were also typically serotype O55:H6, displayed localized adherence (LA) in tissue culture assays, and were positive in the fluorescent-actin staining test for intimate cell adherence. These same characteristics were observed in the closely related ETs 2 to 4, which clustered in the same branch as ET 1. No known virulence marker could be identified in ET 6. ET 5 included 23 strains, all of which carried the eaeA gene but otherwise displayed a striking array of distinct virulence traits. This ET was represented by O55:H7 strains with phenotypes as diverse as the simultaneous expression of LA and diffuse adherence and the ability to form a newly described adherence pattern, called LA-like adherence. The results suggest that ET 5 marks a special pathogenic clone with a propensity to acquire virulence factors which may facilitate the emergence of new pathogenic strains.

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Rodrigues, J., Scaletsky, I. C. A., Campos, L. C., Gomes, T. A. T., Whittam, T. S., & Trabulsi, L. R. (1996). Clonal structure and virulence factors in strains of Escherichia coli of the classic serogroup O55. Infection and Immunity, 64(7), 2680–2686. https://doi.org/10.1128/iai.64.7.2680-2686.1996

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