Evaluation of IS200-PCR and comparison with other molecular markers to trace Salmonella enterica subsp enterica serotype typhimurium bovine isolates from farm to meat
Y. Millemann et al., Evaluation of IS200-PCR and comparison with other molecular markers to trace Salmonella enterica subsp enterica serotype typhimurium bovine isolates from farm to meat, J CLIN MICR, 38(6), 2000, pp. 2204-2209
A procedure that uses an original molecular marker (IS200-PCR) and that is
based on the amplification of DNA with outward-facing primers complementary
to each end of IS200 has been evaluated with a collection of 85 Salmonella
enterica subsp. enterica serotype Typhimurium isolates. These strains were
isolated from a group of 10 cows at different stages: during transportatio
n between the farm and the slaughterhouse, on the slaughter line, from the
environment, and from the final product (ground beef). The 85 isolates were
characterized by their antibiotic resistance patterns and were compared by
IS200-PCR and by use of four other genotypic markers. Those markers includ
ed restriction profiles for 16S and 23S rRNA (ribotypes) and amplification
profiles obtained by different approaches: random amplified polymorphic DNA
analysis, enterobacterial repetitive intergenic consensus PCR, and PCR rib
otyping. The results of the IS200-PCR were in accordance with those of othe
r molecular typing methods for this collection of isolates. Five different
genotypes were found, which made it possible to refine the hypotheses on tr
ansmission obtained from phenotypic results, The genotyping results indicat
ed the massive contamination of the whole group of animals and of the envir
onment by one clonal strain originally recovered from one cow that excreted
the strain. On the other hand, a few animals and their environment appeare
d to be simultaneously contaminated with genetically different strains.