| Literature DB >> 26599913 |
Andrei Sorin Bolocan1, Anca Ioana Nicolau2, Avelino Alvarez-Ordóñez3, Daniela Borda2, Elena Alexandra Oniciuc2, Beatrix Stessl4, Leontina Gurgu2, Martin Wagner4, Kieran Jordan5.
Abstract
This study determined the colonisation scenario of Listeria monocytogenes in a newly-opened ready-to-eat meat processing facility using a combination of classical microbiology and molecular biology techniques. Samples (n=183), including food contact surfaces, non-food contact surfaces, raw materials and food samples, collected on four sampling occasions, were analysed for L. monocytogenes by the ISO 11290:1996 standard method and by real-time PCR applied to the second enrichment broth from the ISO method. No L. monocytogenes were detected on the first sampling occasion, but by the second sampling occasion a persistent clone had colonised the facility. Analysis of the second enrichment of the ISO method by real-time PCR was more sensitive for the detection of L. monocytogenes than the ISO method alone. In order to reduce the risk of cross contamination and the public health risk, awareness and proactive measures are required to control L. monocytogenes from the first days of production in a newly opened meat processing facility.Entities:
Keywords: Benzalkonium chloride (PubChem CID: 15865); Colonisation; Hydrogen peroxide (PubChem CID: 784); Hygiene; Listeria monocytogenes; Meat processing environment; Peracetic acid (PubChem CID: 6585); Prevalence
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Year: 2015 PMID: 26599913 DOI: 10.1016/j.meatsci.2015.10.016
Source DB: PubMed Journal: Meat Sci ISSN: 0309-1740 Impact factor: 5.209