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Specificity of a novel TaqMan PCR method for detection of poultry DNA
被引:7
|作者:
Scholtens, Ingrid M. J.
[1
]
Prins, Theo W.
[1
]
van Raamsdonk, Leo W. D.
[1
]
机构:
[1] RIKILT Wageningen UR, Akkermaalsbos 2,POB 230, NL-6708 WB Wageningen, Netherlands
来源:
关键词:
Poultry;
Species-to-species ban;
Feed;
Processed Animal Protein (PAP);
Transmissible Spongiform Encephalopathy (TSE);
Bovine Spongiform Encephalopathy (BSE);
REAL-TIME PCR;
PROCESSED ANIMAL PROTEINS;
SPECIES IDENTIFICATION;
MEAT;
VALIDATION;
CHICKEN;
TURKEY;
ASSAYS;
DUCK;
QUANTIFICATION;
D O I:
10.1016/j.foodcont.2016.08.045
中图分类号:
TS2 [食品工业];
学科分类号:
0832 ;
摘要:
After the Bovine Spongiform Encephalopathy (BSE) crisis emerged in 1985/1986, all processed animal proteins (PAPs) were finally banned for use in animal feed in the European Union. To partially lift this feed ban, paths for re-introduction of PAPs from species other than ruminants e.g. pig and poultry, are described in the Transmissible Spongiform Encephalopathies (TSE) Roadmap 2. Cannibalism, however, is still not allowed. Specific detection methods for pig and poultry meal and PAPs are prerequisites for reintroduction of pig and poultry processed animal proteins into animal feed. Developing a sensitive PCR method that specifically detects the taxonomically diverse and therefore artificial group 'poultry' and that does not detect other birds at the same time is a challenge. Here, a novel TaqMan PCR method for poultry detection is presented. The specificity of the poultry method against target and non-target species has been extensively investigated. The efficiency, linearity and sensitivity was tested using dilution series of chicken, turkey, duck and goose DNA isolated from meat and autoclaved meat as a model system for PAPs. (C) 2016 Elsevier Ltd. All rights reserved.
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页码:532 / 539
页数:8
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