Toward an international standard for PCR-based detection of Escherichia coli O157 -: Part 1.: Assay development and multi-center validation

被引:18
作者
Abdulmawjood, A
Bülte, M
Cook, N
Roth, S
Schönenbrücher, H
Hoorfar, J
机构
[1] Danish Vet Inst, DK-1790 Copenhagen V, Denmark
[2] Univ Giessen, Inst Vet Food Sci, D-35392 Giessen, Germany
[3] DEFRA, Cent Sci Lab, York YO14 1LZ, N Yorkshire, England
关键词
Escherichia coli O157; rfbE gene; validation; standard;
D O I
10.1016/j.mimet.2003.08.012
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
As part of a major European research project, a diagnostic PCR assay, including an internal amplification control, was developed and validated in a collaborative trial for the detection of Escherichia coli O157. The assay is based on amplification of sequences of the rJbE O157 gene. The collaborative trial, including 12 international laboratories, was carried out in two phases: phase (a) was performed with identical PCR reagents, including the internal control, provided by the sending laboratory; phase (b) was performed on the same samples and internal control but using in-house PCR reagents of own choice. Phase (a) showed an inclusivity (detection of target strains) of 96.8% and the exclusivity (negative response from nontarget strains) was 100%. The overall performance resulted of phase (a) in an accordance of 98.8, concordance of 98.6, and a concordance odds ratio of 1.11. Phase (b) results showed an accuracy of 100% with all partners and by using different polymerase types and thermocycler models. This indicates that the assay, under consideration as an international standard, was just as reproducible between laboratories, as repeatable within a laboratory. The assay is taken further for validation on carcass-rinse samples. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:775 / 786
页数:12
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