The use of DNA probes for rapid identification of foodborne pathogens
is an emerging field. We have standardized a method for the detection
of Salmonella in food samples by using a specific insertion sequence (
IS-200) of Salmonella chromosomal DNA as the probe. The procedure for
colony hybridization, and washing conditions for the stringency were e
stablished. All the ten Salmonella strains, belonging to various serot
ypes tested were positive while 18 other bacterial cultures, mainly be
longing to the family Enterobacteriaceae such as E. coli Shigella, Pro
teus etc., were negative in colony hybridization. The sensitivity of t
he detection was found to be 10(5) cfu using P-32-labeled probe. We su
rveyed 16 chicken and 6 fish samples from local market using IS-200 pr
obe after preenrichment and selective enrichment. All the samples test
ed were found positive with DNA probe. The major strains of Salmonella
isolared from these samples were S. gallinarum, S. typhimurium, S. en
teritidis, S. choleraesuis and S. paratyphi A. These results were conf
irmed by standard Salmonella identification method.