Development and validation of a rapid real-time PCR based method for the specific detection of Salmonella on fresh meat

被引:55
作者
McGuinness, Sheila [1 ]
McCabe, Evonne [3 ]
O'Regan, Edel [4 ]
Dolan, Anthony [3 ]
Duffy, Geraldine [3 ]
Burgess, Catherine [3 ]
Fanning, Seamus [4 ]
Barry, Thomas [1 ,2 ]
O'Grady, Justin [1 ]
机构
[1] Natl Univ Ireland Galway, Natl Ctr Biomed Engn Sci, Mol Diagnost Res Grp, Galway, Ireland
[2] Natl Univ Ireland Galway, Sch Nat Sci, Galway, Ireland
[3] Ashtown Food Res Ctr, Food Safety Dept, Dublin, Ireland
[4] Univ Coll Dublin, Sch Agr Food Sci & Vet Med, Dublin 2, Ireland
关键词
Salmonella; Real-time PCR; ssrA Gene; IAC; Fresh meat; Detection; DIAGNOSTIC PCR; LISTERIA-MONOCYTOGENES; FOOD SAMPLES; TO-EAT; ENTERICA; SYSTEM; ASSAYS; SPP; GENE; RAW;
D O I
10.1016/j.meatsci.2009.07.004
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
In this study, a combined enrichment/real-time PCR method for the rapid detection of Salmonella on fresh meat carcasses, was designed, developed and validated in-house following requirements outlined in ISO 16140:2003. The method included an 18 h non-selective enrichment in buffered peptone water (BPW) and a 6 h selective enrichment in Rappaport Vasilliadis Soya (RVS) broth, based on the traditional culture method, ISO 6579:2002. The real-time PCR assay included an internal amplification control (IAC), was 100% specific and was sensitive to one cell equivalent. The alternative method was validated against the traditional culture method and relative accuracy of 94.9%, sensitivity of 94.7% and specificity of 100% were determined using 150 fresh meat carcass swabs. This alternative method had a detection limit of 1-10 CFU/100 cm(2) for fresh meat carcass swabs and was performed in 26 h. Following further inter-laboratory Studies, this alternative method could be suitable for implementation in testing laboratories for the analysis of carcass swabs. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:555 / 562
页数:8
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