A multiplex PCR method for detection of five animal species in processed meat products using novel species-specific nuclear DNA sequences

被引:11
|
作者
Wang, Wenjun [1 ]
Wang, Xiaokang [1 ]
Zhang, Qingde [2 ]
Liu, Zuhong [1 ]
Zhou, Xiang [1 ]
Liu, Bang [1 ]
机构
[1] Huazhong Agr Univ, Key Lab Agr Anim Genet Breeding & Reprod, Minist Educ, Wuhan 430070, Hubei, Peoples R China
[2] Huazhong Agr Univ, Coll Vet Med, Lab Anim Ctr, Wuhan 430070, Hubei, Peoples R China
关键词
Species-specific nuclear DNA sequence; Multiplex PCR; Meat products; Species identification; REAL-TIME PCR; MITOCHONDRIAL-DNA; DIGITAL PCR; IDENTIFICATION; CHICKEN; PORK; QUANTIFICATION; RABBIT; DUCK; AUTHENTICATION;
D O I
10.1007/s00217-020-03494-z
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The continuous development of fast and simple new methods to identify animal-derived ingredients is very important for the authentication of meat products. This study intended to develop a multiplex PCR method using new species-specific nuclear DNA (nDNA) sequences for the detection of ingredients derived from sheep/goat, bovine, chicken, duck and pig in meat products. Sequence alignment analysis in 53 species showed high specificity of species-specific nDNA. Species-specific primers were designed on the conservative region of each species-specific nDNA sequence. The specificity and conservation of the sequences and primers were verified by PCR reaction and sequencing with the limit of detection down to 0.5 ng. Then, a species-specific multiplex PCR method was developed and optimized to simultaneously detect sheep/goat (237 bp), bovine (223 bp), chicken (192 bp), duck (168 bp) and pig (154 bp) in one reaction. Various processed meat products containing one or more animal-derived ingredients were detected by the developed multiplex PCR method, and the results were consistent with their labeled meat species. Our study provides a fast and simple detection method for regulating labeling of animal-derived ingredients in meat products.
引用
收藏
页码:1351 / 1360
页数:10
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