Serotypes, intimin variants and other virulence factors of eae positive Escherichia coli strains isolated from healthy cattle in Switzerland. Identification of a new intimin variant gene (eae-η2)
Open Access
- 9 May 2005
- journal article
- Published by Springer Nature in BMC Microbiology
- Vol. 5 (1), 23
- https://doi.org/10.1186/1471-2180-5-23
Abstract
Enteropathogenic Escherichia coli (EPEC) and Shigatoxin-producing Escherichia coli (STEC) share the ability to introduce attaching-and-effacing (A/E) lesions on intestinal cells. The genetic determinants for the production of A/E lesions are located on the locus of enterocyte effacement (LEE), a pathogenicity island that also contains the genes encoding intimin (eae). This study reports information on the occurrence of eae positive E. coli carried by healthy cattle at the point of slaughter, and on serotypes, intimin variants, and further virulence factors of isolated EPEC and STEC strains. Of 51 eae positive bovine E. coli strains, 59% were classified as EPEC and 41% as STEC. EPEC strains belonged to 18 O:H serotypes, six strains to typical EPEC serogroups. EPEC strains harbored a variety of intimin variants with eae-beta1 being most frequently found. Moreover, nine EPEC strains harbored astA (EAST1), seven bfpA (bundlin), and only one strain was positive for the EAF plasmid. We have identified a new intimin gene (eta2) in three bovine bfpA and astA-positive EPEC strains of serotype ONT:H45. STEC strains belonged to seven O:H serotypes with one serotype (O103:H2) accounting for 48% of the strains. The majority of bovine STEC strains (90%) belonged to five serotypes previously reported in association with hemolytic uremic syndrom (HUS), including one O157:H7 STEC strain. STEC strains harbored four intimin variants with eae-epsilon1 and eae-gamma1 being most frequently found. Moreover, the majority of STEC strains carried only stx1 genes (13 strains), and was positive for ehxA (18 strains) encoding for Enterohemolysin. Four STEC strains showed a virulence pattern characteristic of highly virulent human strains (stx2 and eae positive). Our data confirm that ruminants are an important source of serologically and genetically diverse intimin-harboring E. coli strains. Moreover, cattle have not only to be considered as important asymptomatic carriers of O157 STEC but can also be a reservoir of EPEC and eae positive non-O157 STEC, which are described in association with human diseases.Keywords
This publication has 66 references indexed in Scilit:
- Typing of Intimin ( eae ) Genes in Attaching and Effacing Escherichia coli Strains from MonkeysJournal of Clinical Microbiology, 2004
- Characterization of Shiga Toxin-Producing Escherichia coli Strains Isolated from Human Patients in Germany over a 3-Year PeriodJournal of Clinical Microbiology, 2004
- Serotypes, Virulence Genes, and Intimin Types ofShiga Toxin (Verotoxin)-Producing Escherichia coli Isolatesfrom Cattle in Spain and Identification of a New Intimin VariantGene( eae- ξ)Journal of Clinical Microbiology, 2004
- Characterization of Atypical Enteropathogenic Escherichia coli Strains Harboring the astA Gene That Were Associated with a Waterborne Outbreak of Diarrhea in JapanJournal of Clinical Microbiology, 2003
- Genetic Profiling of Enterohemorrhagic Escherichia coli Strains in Relation to Clonality and Clinical Signs of InfectionJournal of Clinical Microbiology, 2002
- Escherichia coliHarboring Shiga Toxin 2 Gene Variants: Frequency and Association with Clinical SymptomsThe Journal of Infectious Diseases, 2002
- The United States National Prospective Hemolytic Uremic Syndrome Study: Microbiologic, Serologic, Clinical, and Epidemiologic FindingsThe Journal of Infectious Diseases, 2001
- Isolation and virulence factors of vero cyto toxinproducing Escherichia coli in human stool samplesClinical Microbiology & Infection, 1997
- Prevalence and Clinical Significance of Vero‐cytotoxin‐producing Escherichia coli (VTEC) isolated from Cattle in Herds with and without Calf DiarrhoeaJournal of Veterinary Medicine, Series B, 1995
- CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choiceNucleic Acids Research, 1994