Guan Feng, Jin Yu-Ting, Zhao Jin, Xu Ai-Chun, Luo Yuan-Yuan
College of Life Sciences, China Jiliang University, Hangzhou 310018, China.
J Anal Methods Chem. 2018 Feb 5;2018:5890140. doi: 10.1155/2018/5890140. eCollection 2018.
There are many PCR-based methods for animal species identification; however, their detection numbers are limited or could not identify unknown species. We set out to solve this problem by developing a universal primer PCR assay for simultaneous identification of eight animal species, including goat, sheep, deer, buffalo, cattle, yak, pig, and camel. In this assay, the variable lengths of mitochondrial DNA were amplified using a pair of universal primers. PCR amplifications yielded 760 bp, 737 bp, 537 bp, 486 bp, 481 bp, 464 bp, 429 bp, and 359 bp length fragments for goat, sheep, deer, buffalo, cattle, yak, pig, and camel, respectively. This primer pair had no cross-reaction with other common domestic animals and fish. The limit of detection varied from 0.01 to 0.05 ng of genomic DNA for eight animal species in a 20 l PCR mixture. Each PCR product could be further digested into fragments with variable sizes and qualitative analysis by I restriction enzyme. This developed PCR-RFLP assay was sufficient to distinguish all targeted species. Compared with the previous published related methods, this approach is simple, with high throughput, fast processing rates, and more cost-effective for routine identification of meat in foodstuffs.
有许多基于聚合酶链式反应(PCR)的方法用于动物物种鉴定;然而,它们的检测种类有限,或者无法鉴定未知物种。我们着手通过开发一种通用引物PCR检测方法来解决这个问题,该方法可同时鉴定八种动物物种,包括山羊、绵羊、鹿、水牛、牛、牦牛、猪和骆驼。在该检测方法中,使用一对通用引物扩增线粒体DNA的可变长度。PCR扩增分别产生了长度为760 bp、737 bp、537 bp、486 bp、481 bp、464 bp、429 bp和359 bp的片段,对应山羊、绵羊、鹿、水牛、牛、牦牛、猪和骆驼。该引物对与其他常见家畜和鱼类无交叉反应。在20 μl PCR混合物中,八种动物物种的基因组DNA检测限为0.01至0.05 ng。每个PCR产物都可以用I型限制性内切酶进一步消化成大小可变的片段并进行定性分析。这种开发的PCR-限制性片段长度多态性(RFLP)检测方法足以区分所有目标物种。与先前发表的相关方法相比,该方法简单、高通量、处理速度快,并且在食品中肉类的常规鉴定方面更具成本效益。