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Real-time PCR method based on single-copy nuclear DNA sequences for the quantitative detection of pork adulteration in processed beef products

文献类型: 外文期刊

作者: Chang, Lijuan 1 ; Huang, Ping 1 ; Liu, Jikai 2 ; Fu, Chengping 1 ; Liu, Wenjuan 3 ; Gao, Yongfeng 2 ; Li, Yuanhong 1 ; Liu, Yongling 1 ; Long, Ailin 1 ;

作者机构: 1.Sichuan Acad Agr Sci, Inst Remote Sensing & Digital Agr, Chengdu 610066, Sichuan, Peoples R China

2.Southwest Univ Sci & Technol, Sch Life Sci & Engn, Mianyang 621010, Sichuan, Peoples R China

3.Sichuan Acad Agr Sci, Inst Qual Stand & Testing Technol Agroprod, Chengdu 610066, Sichuan, Peoples R China

关键词: Food safety; Real-time polymerase chain reaction; Pork; Beef; Meat adulteration; Quantification method

期刊名称:FOOD CONTROL ( 影响因子:6.0; 五年影响因子:5.8 )

ISSN: 0956-7135

年卷期: 2024 年 163 卷

页码:

收录情况: SCI

摘要: Meat adulteration, which adversely impacts food safety, economy, and religious beliefs, has come to be considered as a matter of global concern. The lack of a standard method that can be employed to quantitatively detect the pork content in processed meat products has led to demands for an accurate and sensitive method capable of detecting the proportion of pork in processed beef products. In this study, we aimed to develop a realtime PCR-based method to accurately and quantitatively detect pork adulteration in processed beef. We used bovine and porcine species -specific sequences to design primers and probes that specifically amplified bovine and porcine genes. Our real-time PCR method was evaluated via quantitative detection of reference samples and found to be highly accurate. Sensitivity analyses indicated that the limit of detection for beef as well as for pork was as low as five copies, while the limit of quanti fi cation for beef and for pork was 0.1%. To compare qualitative and quantitative results, beef samples cross -contaminated with pork were analyzed using both quantitative and standard qualitative methods. No undeclared meat components were found among the 25 processed meat products that were analyzed to evaluate the applicability of the quantitative method. However, the beef content in some processed beef products was very low, even approaching zero. This real-time PCR method may be reliably applied for quantitatively detect pork adulteration in processed beef products. Thus, this method of ours may help promote healthy and sustainable development of meat products.

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