Stx2 subtyping of shiga toxin-producing Escherichia coli isolated from cattle in France: Detection of a new Stx2 subtype and correlation with additional virulence factors

Citation
Y. Bertin et al., Stx2 subtyping of shiga toxin-producing Escherichia coli isolated from cattle in France: Detection of a new Stx2 subtype and correlation with additional virulence factors, J CLIN MICR, 39(9), 2001, pp. 3060-3065
Citations number
28
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Microbiology
Journal title
JOURNAL OF CLINICAL MICROBIOLOGY
ISSN journal
00951137 → ACNP
Volume
39
Issue
9
Year of publication
2001
Pages
3060 - 3065
Database
ISI
SICI code
0095-1137(200109)39:9<3060:SSOSTE>2.0.ZU;2-J
Abstract
At least 11 Stx2 variants produced by Shiga toxin-producing Escherichia col i (STEC) isolated from patients and animals have been described. The Stx2 s ubtyping of STEC isolated from healthy cows positive for stx(2) (n=104) or stx(2) and stx(1) (n=63) was investigated. Stx2vh-b, Stx2 (renamed Stx2-EDL 933), and Stx2vh-a were the subtypes mostly detected among the bovine isola tes (39.5, 39, and 25.5%, respectively). Stx2e was not present, and subtype s included in the Stx2d group (Stx2d-OX3a, Stx2d-O111, and Stx2d-Ount) were found infrequently among. the isolates examined (8.5%). A combination of t wo distinct Stx2 subtypes was observed among 23.5% of the strains. For the first time, a combination of three subtypes (Stx2-EDL933/Stx2vh-b/Stx2d and Stx2vh-a/Stx2vh-b/Stx2d) was detected (3.5% of the isolates). In addition, bovine STEC harboring stx(1) and one or two stx(2) genes appeared highly c ytotoxic toward Vero cells. A new Stx2 subtype (Stx2-NV206), present among 14.5% of the isolates, showed high cytotoxicity for Vero cells. Two amino a cid residues (Ser-291 and Glu-297) important for the activation of Stx2 by human intestinal mucus were conserved on the Stx2-NV206 A subunit. The gene encoding Ehx enterohemolysin was prominent among STEC harboring stx(2)-EDL 933 alone (78%) or a combination of stx(2)-EDL933 and stx(2)vh-b (85%). In addition, Stx2-EDL933 and/or Stx2vh-b subtypes were highly associated with other putative virulence factors such as Stx1 and EspP extracellular serine protease, but not with EAST1 enterotoxin.