Detection of Salmonella species in foodstuffs.

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Abstract

Conventional methods to detect Salmonella spp. in foodstuffs may take up to 1 wk. Methods for pathogen detection are required. Real-time detection of Salmonella spp. will broaden our ability to screen large number of samples in a short time. This chapter describes a step-by-step procedure using an oligonucleotide probe that becomes fluorescent upon hybridization to the target DNA (Molecular Beacon; MB) in a real-time polymerase chain reaction (PCR) assay. The capability of the assay to detect Salmonella species from artificially inoculated fresh- and fresh-cut produce as well as ready-to-eat meats is demonstrated. The method uses internal positive and negative controls which enable researchers to detect false-negative PCR results. The procedure uses the buffered peptone water for the enrichment of Salmonella spp. and successfully detects the pathogen at low level of contamination (2-4 cells/25 g) in <24 h.

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Bhagwat, A. A., Patel, J., Chua, T., Chan, A., Cruz, S. R., & Aguilar, G. A. G. (2008). Detection of Salmonella species in foodstuffs. Methods in Molecular Biology (Clifton, N.J.), 429, 33–43. https://doi.org/10.1007/978-1-60327-040-3_3

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