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Please use this identifier to cite or link to this item: http://hdl.handle.net/11019/246

Title: Development of a real-time multiplex PCR assay for the detection of multiple Salmonella serotypes in chicken samples.
Authors: O'Regan, Edel
McCabe, Evonne
Burgess, Catherine M
McGuinness, Sheila
Barry, Thomas
Duffy, Geraldine
Whyte, Paul
Fanning, Seamus
Keywords: Real-time multiplex PCR assay
Salmonella serotypes
Issue Date: 21-Sep-2008
Publisher: Biomed Central
Citation: Edel O'Regan, Evonne McCabe, Catherine Burgess, Sheila McGuinness, Thomas Barry, Geraldine Duffy, Paul Whyte and Seamus Fanning. Development of a real-time multiplex PCR assay for the detection of multiple Salmonella serotypes in chicken samples. BMC Microbiology 2008, 8:156. DOI:10.1186/1471-2180-8-156
Series/Report no.: BMC Microbiology
Abstract: Background: A real-time multiplex PCR assay was developed for the detection of multiple Salmonella serotypes in chicken samples. Poultry-associated serotypes detected in the assay include Enteritidis, Gallinarum, Typhimurium, Kentucky and Dublin. The traditional cultural method according to EN ISO 6579:2002 for the detection of Salmonella in food was performed in parallel. The real-time PCR based method comprised a pre-enrichment step in Buffered Peptone Water (BPW) overnight, followed by a shortened selective enrichment in Rappaport Vasilliadis Soya Broth (RVS) for 6 hours and subsequent DNA extraction. Results: The real-time multiplex PCR assay and traditional cultural method showed 100% inclusivity and 100% exclusivity on all strains tested. The real-time multiplex PCR assay was as sensitive as the traditional cultural method in detecting Salmonella in artificially contaminated chicken samples and correctly identified the serotype. Artificially contaminated chicken samples resulted in a detection limit of between 1 and 10 CFU per 25 g sample for both methods. A total of sixty-three naturally contaminated chicken samples were investigated by both methods and relative accuracy, relative sensitivity and relative specificity of the real-time PCR method were determined to be 89, 94 and 87%, respectively. Thirty cultures blind tested were correctly identified by the real-time multiplex PCR method. Conclusion: Real-time PCR methodology can contribute to meet the need for rapid identification and detection methods in food testing laboratories.
Description: peer-reviewed
URI: http://hdl.handle.net/11019/246
http://dx.doi.org/10.1186/1471-2180-8-156
Appears in Collections:Food Safety
Teagasc publications in Biomed Central

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