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A duplex polymerase chain reaction (PCR) for detection of Salmonella based on species- and serogroup-specific primers was compared with traditional plate culture methods. The influence of various sample matrices and mechanical agitation conditions on detection of Salmonella and their effect on the performance of the duplex PCR was studied. A duplex PCR was performed on sterile and non-sterile chicken breast samples (n=195) artificially inoculated with Salmonella typhimurium. The types of antimicrobial preservatives used (sodium azide, sodium benzoate, potassium sorbate) were also investigated. Contamination rates were 13% for plate culture and 0% for duplex PCR. Higher rates of detection of Salmonella were seen in chicken breast samples that had been pasteurized than raw samples. The technique was also more sensitive for detection of Salmonella in samples with low levels of contamination. Mechanical agitation resulted in higher rates of detection, but were less sensitive. These findings demonstrate the potential of the developed duplex PCR for identification of Salmonella in chicken breast samples.Chemically-induced mutagenesis in Saccharomyces cerevisiae. A new tool for the analysis of cytotoxic effects.
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