Abstract
The isolation and identification of Listeria monocytogenes in processed meat samples by a combined cultural-molecular method is described. It allows the identification of Listeria strains by means of a hybridization technique with a specific DNA probe directed to the listerial internalin gene. The specificity of this method was found to be 100% and sensitivity was as low as 1 CFU/2.5 g of food sample. A total of 278 meat samples were tested in comparison with PCR and conventional cultural assays. A total of 42 (15.4%) L. monocytogenes were detected. PCR analysis gave 3 false negative results and culture failed to detect the Listeria in 5 cases. With this cultural-molecular method the identification and quantitative detection of L. monocytogenes were achieved within 36 hours and no false positive or negative tests were obtained, thus fitting most food industry requirements. © 2007 Science Publications.
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Ingianni, A., Quartuccio, M., Madeddu, M. A., Sanna, A., Dessi, S., & Pompei, R. (2007). Isolation and identification of Listeria monocytogenes in processed meat by a combined cultural-molecular method. American Journal of Infectious Diseases, 3(3), 159–164. https://doi.org/10.3844/ajidsp.2007.159.164
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