Wang Wenjun, Wei Tiean, Shi Manna, Han Yu, Shen Yang, Zhou Xiang, Liu Bang
Key Laboratory of Agricultural Animal Genetics, Breeding, and Reproduction of Ministry of Education, Hongshan Laboratory, Huazhong Agricultural University, Wuhan 430070, China.
College of Animal Science and Technology, Hebei Agricultural University, Baoding 071000, China.
Foods. 2023 Jan 31;12(3):594. doi: 10.3390/foods12030594.
Adulteration of meat with carnivorous animals (such as cats, dogs, foxes, and minks) can cause ethical problems and lead to disease transmission; however, DNA quantitative methods for four carnivorous species in one tube reaction are still rare. In this study, a carnivore-specific nuclear DNA sequence that is conserved in carnivorous animals but has base differences within the sequence was used to design universal primers for its conserved region and corresponding species-specific probes for the hypervariable region. A novel universal primer multiplex real-time PCR (UP-M-rtPCR) approach was developed for the specific identification and quantitation of cat, dog, fox, and mink fractions in a single reaction, with a 0.05 ng absolute limit of detection (LOD) and 0.05% relative LOD. This approach simplifies the PCR system and improves the efficiency of simultaneous identification of multiple animal-derived ingredients in meat. UP-M-rtPCR showed good accuracy (0.48-7.04% relative deviation) and precision (1.42-13.78% relative standard deviation) for quantitative analysis of cat, dog, fox, and mink DNA as well as excellent applicability for the evaluation of meat samples.
用食肉动物(如猫、狗、狐狸和水貂)的肉掺假会引发伦理问题并导致疾病传播;然而,能在一个管反应中对四种食肉动物物种进行DNA定量分析的方法仍然很少见。在本研究中,利用一种在食肉动物中保守但序列内存在碱基差异的食肉动物特异性核DNA序列,为其保守区域设计通用引物,并为高变区域设计相应的物种特异性探针。开发了一种新型通用引物多重实时PCR(UP-M-rtPCR)方法,用于在单一反应中特异性鉴定和定量猫、狗、狐狸和水貂成分,绝对检测限(LOD)为0.05 ng,相对LOD为0.05%。该方法简化了PCR系统,提高了同时鉴定肉类中多种动物源性成分的效率。UP-M-rtPCR在猫、狗、狐狸和水貂DNA的定量分析中显示出良好的准确性(相对偏差为0.48 - 7.04%)和精密度(相对标准偏差为1.42 - 13.78%),并且在肉类样品评估中具有出色的适用性。