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A polymerase chain reaction (PCR) assay with two nested pairs of primers selected from conserved sequences within a 2·3 kb randomly cloned DNA fragment from the Salmonella typhimurium chromosome was developed. The nested PCR assay correctly identified 128 of a total of 129 Salmonella strains belonging to subspecies I, II, IIIb and IV. One strain of Salm. arizona (ssp. IIIa) tested negative. No PCR products were obtained from any of the 31 non‐Salmonella strains examined. The sensitivity of the assay was 2 cfu, as determined by analysis of proteinase K‐treated boiled lysates of Salm. typhimurium. The performance of the assay was evaluated for environmental water, sewage and food samples spiked with Salm. typhimurium. Water and sewage samples were filtered and filters were enriched overnight in a non‐selective medium. Prior to PCR, the broth cultures were subjected to a rapid and simple preparation procedure consisting of centrifugation, proteinase K treatment and boiling. This assay enabled detection of 10 cfu 100 ml−1 water with background levels of up to 8700 heterotrophic organisms ml−1 and 10 000 cfu of coliform organisms 100 ml−1 water. Spiked food samples were analysed with and without overnight enrichment in a non‐selective medium using the same assay as above. Nested PCR performed on enriched broths enabled detection of < 10 cfu g−1 food. Variable results were obtained for food samples examined without prior enrichment and most results were negative. This rapid and simple assay provides a sensitive and specific means of screening drinking water or environmental water samples, as well as food samples, for the presence of Salmonella spp.

A two-step polymerase chain reaction (PCR) procedure with two nested pairs of primers specific for theyad4 gene of Yersinia enterocolitica was developed. The PCR assay identified all common pathogenic serogroups

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