A Robust and Poisson Validated Quantitative 5′ Nuclease TaqMan® Real-Time PCR Assay Targeting fimA for the Rapid Detection of Salmonella spp. in Food

被引:10
|
作者
Mann, E. [1 ]
Hein, I. [1 ]
Mester, P. [2 ]
Stessl, B. [1 ]
Rossmanith, P. [1 ,2 ]
Wagner, M. [1 ]
Dzieciol, M. [1 ]
机构
[1] Univ Vet Med, Inst Milk Hyg Milk Technol & Food Sci IMMF, Dept Farm Anim & Vet Publ Hlth, A-1210 Vienna, Austria
[2] Univ Vet Med, Christian Doppler Lab Mol Food Analyt, Dept Farm Anim & Vet Publ Hlth, A-1210 Vienna, Austria
关键词
fimA; IAC; qPCR; Quantitative; Salmonella; LISTERIA-MONOCYTOGENES; GENE; AMPLIFICATION; TYPHIMURIUM; SEQUENCE; QUALITY; MEAT;
D O I
10.1007/s12161-012-9534-z
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
A newly designed TaqManA (R) probe and an internal amplification control were implemented in a conventional PCR system targeting the major fimbrial subunit encoding gene fimA. This assay has an inclusivity and exclusivity of 100 % (n = 126). The limit of detection (LOD) and the absolute quantification limit, both determined by advanced Poisson analyses, were three bacterial cell equivalents per quantitative real-time PCR reaction. The fimA assay achieved 100 % accuracy and performed very robustly, producing reproducible, reliable data for quantification of Salmonella spp., even at the LOD.
引用
收藏
页码:991 / 995
页数:5
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