Duplex PCR-ELONA for the detection of pork adulteration in meat products

被引:25
|
作者
Skouridou, Vasso [1 ]
Tomaso, Herbert [2 ]
Rau, Joerg [3 ]
Bashammakh, Abdulaziz S. [4 ]
El-Shahawi, Mohammad S. [4 ]
Alyoubi, Abdulrahman O. [4 ]
O'Sullivan, Ciara K. [1 ,5 ]
机构
[1] Univ Rovira & Virgili, Interfibio Nanobiotechnol & Bioanal Grp, Dept Engn Quim, Avinguda Paisos Catalans 26, E-43007 Tarragona, Spain
[2] Friedrich Loeffler Inst, Inst Bacterial Infect & Zoonoses, Naumburger Str 96a, D-07743 Jena, Germany
[3] Chem & Vet Invest Off Stuttgart, Schaflandstr 3-2, D-70736 Fellbach, Germany
[4] King Abdulaziz Univ, Fac Sci, Dept Chem, POB 80203, Jeddah 21589, Saudi Arabia
[5] ICREA, Passeig Lluis Companys 23, Barcelona 08010, Spain
关键词
Food authentication; Pork adulteration; Duplex PCR; Enzyme Linked Oligonucleotide Assay; Species-specific tailed primers; REAL-TIME PCR; MULTIPLEX PCR; SPECIES IDENTIFICATION; SENSITIVE DETECTION; FOOD; AUTHENTICATION; DNA; HALAL; MIXTURES; HORSE;
D O I
10.1016/j.foodchem.2019.02.095
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In this work, a duplex PCR-Enzyme Linked Oligonucleotide Assay (ELONA) is reported for the sensitive and reliable detection of pork adulteration in beef and chicken products, two of the most widely consumed meat types in the world. The strategy relies on the use of species-specific tailed primers for duplex amplification and simple dilution of the PCR reactions for direct colorimetric detection via hybridization, eliminating the need for any other post-amplification steps. A high sensitivity was achieved, with as low as 71-188 pg of genomic DNA able to be detected using mixtures of control DNA from each species. The strategy was validated using DNA add-mixtures as well as DNA extracted from raw meat mixtures and 0.5-1% w/w pork could be easily detected when mixed with beef or chicken. The proposed approach is simple, sensitive and cost-effective compared to equivalent commercial kits suitable for detecting adulterant pork levels in meat products.
引用
收藏
页码:354 / 362
页数:9
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