TaqMan probe real-time polymerase chain reaction assay for the quantification of canine DNA in chicken nugget

被引:6
|
作者
Rahman, Md. Mahfujur [1 ]
Abd Hamid, Sharifah Bee [1 ]
Basirun, Wan Jefrey [1 ,2 ]
Bhassu, Subha [3 ,4 ]
Rashid, Nur Raifana Abdul [1 ]
Mustafa, Shuhaimi [5 ]
Desa, Mohd Nasir Mohd [5 ]
Ali, Md. Eaqub [1 ]
机构
[1] Univ Malayaob, Nanotechnol & Catalysis Res Ctr, Kuala Lumpur, Malaysia
[2] Univ Malaya, Dept Chem, Kuala Lumpur 59100, Malaysia
[3] Univ Malaya, Inst Biol Sci, Kuala Lumpur, Malaysia
[4] Univ Malaya, CEBAR Lab, Kuala Lumpur, Malaysia
[5] Univ Putra Malaysia, Inst Halal Prod Res, Serdang 43400, Malaysia
关键词
qPCR assay; canine species; nugget formulation; halal meat; food adulteration; CYTOCHROME-B GENE; DOG MEAT ADULTERATION; SPECIES IDENTIFICATION; PORK ADULTERATION; PCR ASSAY; SEQUENCE; PRODUCTS; POSITION; CAT;
D O I
10.1080/19440049.2015.1104558
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This paper describes a short-amplicon-based TaqMan probe quantitative real-time PCR (qPCR) assay for the quantitative detection of canine meat in chicken nuggets, which are very popular across the world, including Malaysia. The assay targeted a 100-bp fragment of canine cytb gene using a canine-specific primer and TaqMan probe. Specificity against 10 different animals and plants species demonstrated threshold cycles (Ct) of 16.13 +/- 0.12 to 16.25 +/- 0.23 for canine DNA and negative results for the others in a 40-cycle reaction. The assay was tested for the quantification of up to 0.01% canine meat in deliberately spiked chicken nuggets with 99.7% PCR efficiency and 0.995 correlation coefficient. The analysis of the actual and qPCR predicted values showed a high recovery rate (from 87%+/- 28% to 112%+/- 19%) with a linear regression close to unity (R-2=0.999). Finally, samples of three halal-branded commercial chicken nuggets collected from different Malaysian outlets were screened for canine meat, but no contamination was demonstrated.
引用
收藏
页码:10 / 18
页数:9
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