2008
DOI: 10.1128/aem.01459-08
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TaqMan-Based Real-Time PCR Method for Detection of Yersinia pseudotuberculosis in Food

Abstract: A sensitive and specific assay for detection of food-borne pathogenic Yersinia pseudotuberculosis was developed. The primer-probe set was designed to target a 157-bp sequence of the chromosomally located gene ail. The complete method, including an internal amplification control, was evaluated for several different food items.

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Cited by 37 publications
(15 citation statements)
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“…Yersinia enterocolitica was detected with the amplification of the ail gene [ 13 ], using a previously described procedure [ 12 ]. To detect all the Y. pseudotuberculosis serotypes, the wzz and ail genes were amplified in two independent reactions [ 12 , 14 , 15 ]. Amplification of the ail gene detects all serotypes but O:11 and O:12, and amplification of the wzz gene detects all serotypes but O:6 and O:7 [ 14 , 15 ].…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Yersinia enterocolitica was detected with the amplification of the ail gene [ 13 ], using a previously described procedure [ 12 ]. To detect all the Y. pseudotuberculosis serotypes, the wzz and ail genes were amplified in two independent reactions [ 12 , 14 , 15 ]. Amplification of the ail gene detects all serotypes but O:11 and O:12, and amplification of the wzz gene detects all serotypes but O:6 and O:7 [ 14 , 15 ].…”
Section: Methodsmentioning
confidence: 99%
“…To detect all the Y. pseudotuberculosis serotypes, the wzz and ail genes were amplified in two independent reactions [ 12 , 14 , 15 ]. Amplification of the ail gene detects all serotypes but O:11 and O:12, and amplification of the wzz gene detects all serotypes but O:6 and O:7 [ 14 , 15 ]. A sample was considered positive for Y. enterocolitica or Y. pseudotuberculosis when at least one positive result was obtained in the direct reaction or after enrichment in any of the three rt-PCRs used.…”
Section: Methodsmentioning
confidence: 99%
“…Milk, milk filter and bovine faecal samples were analysed at the Finnish Food Safety Authority Evira. Screening of environmental samples for YP, pathogenic Yersinia enterocolitica and STEC was conducted by real-time PCR [9][10][11]. For Y. enterocolitica detection, we followed the technical specification ISO/WD 10273 [12] and for STEC detection we followed ISO/TS 13136 [11], where presumptive STEC is defined as real-time PCR detection of (i) the stx gene, (ii) stx and eae genes or (iii) stx and eae genes as well as genes associated with one of the serogroups O157, O111, O26, O103 or O145.…”
Section: Traceback and Microbiological Investigationmentioning
confidence: 99%
“…The remaining BHI suspensions were supplemented with 15% glycerol before storage in −80°C for subsequent analysis. Duallabelled probe real-time PCR was performed for Salmonella [14], Y. enterocolitica [15] and Y. pseudotuberculosis [16] on the DNA extracts. Any sample with a threshold cycle (C t ) < 35 was considered positive.…”
Section: Pcr Analysis and Isolation Of Pathogensmentioning
confidence: 99%