Between February and May 2000, 279 meat samples were collected from 136 ret
ail stores in Gualeguaychu City, Argentina. Samples were assayed for Escher
ichia coli O157:H7 by selective enrichment in modified EC broth containing
novobiocin, followed by immunomagnetic separation (IMS) and plating onto bo
th sorbitol MacConkey agar supplemented with cefixime and potassium telluri
te and a chromogenic medium. Eleven E. coli O157:H7 isolates were detected
in 6 (3.8%) of 160 ground beef samples, in 4 (4.8%) of 83 fresh sausages, a
nd in 1 (3.3%) of 30 dry sausages. E. coli O157:H7 was not isolated from fi
ve hamburger patties or one barbecue-type fresh sausage assayed. The isolat
es were tested for virulence-related genes. Ten additional Shiga toxin-prod
ucing E. coli (STEC) O157:H7 isolates of food origin, recovered from differ
ent locations in Argentina, were included for comparison purposes. All 21 i
solates harbored both eae and EHEC-hlyA genes, and 12 (57.1%) encoded stx2/
stx2vh-a. The isolates were of phage types 87 (seven strains), 14 (four str
ains), 4 (three strains), and 26 (one strain). Six strains were nontypable
by phage typing. Pulsed-field gel electrophoresis (PFGE) revealed 19 XbaI-P
FGE profiles. Fifteen (71%) strains were grouped in four clusters. which sh
ared more than 80% of DNA restriction fragments. The enrichment culture met
hod with IMS was a sensitive procedure to detect E. coli O157:H7 strains in
retail meats. Some of the isolates from different stores presented a high
clonal relatedness, as determined by XbaI-PFGE and phage typing, and harbor
ed the virulence factors associated with human illness.