On point identification of species origin of food animals by recombinase polymerase amplification-lateral flow (RPA-LF) assay targeting mitochondrial gene sequences

被引:15
|
作者
Kumar, Dhananjay [1 ]
Kumar, Rajiv Ranjan [1 ]
Rana, Preeti [2 ]
Mendiratta, S. K. [1 ]
Agarwal, R. K. [1 ]
Singh, Praveen [3 ]
Kumari, Sarita [4 ]
Jawla, Jyoti [5 ]
机构
[1] Indian Vet Res Inst, Div Livestock Prod Technol, Bareilly 243122, Uttar Pradesh, India
[2] DUVASU, CVASc, Dept Livestock Prod Technol, Mathura, India
[3] Indian Vet Res Inst, Div Vet Biotechnol, Bareilly, Uttar Pradesh, India
[4] RAJUVAS, Dept Livestock Prod Technol, PGIVER, Jaipur, Rajasthan, India
[5] GADVASU, Div Livestock Prod Technol, Ludhiana, Punjab, India
来源
关键词
Meat speciation; RPA-LFA; Meat admixture; Mitochondrial gene; RAPID DETECTION; MEAT; STRIP; DEER; PCR; DNA;
D O I
10.1007/s13197-020-04637-6
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The present study was aimed to develop and standardize Recombinase polymerase amplification-lateral flow (RPA-LF) assays for on point identification of species origin of food animals viz: cattle, buffalo and pig. Species specific RPA primers sets for cattle, buffalo and pig were designed by homology comparisons of the sequences of mitochondrial cytochrome b gene and d-loop region from common food species viz: cattle, buffalo, sheep, goat, pig and chicken. The RPA assays for designed primers sets were optimized using the reaction components from Twist Amp basic kit and instructions in its manual. Endpoint detection of species specific amplified RPA products were made by gel electrophoresis and designed species specific RPA-LFA strips. The developed assays were evaluated for their specificity, diagnostic sensitivity, and validated on coded samples and binary meat admixtures with relative percentage of 20, 10, 5 & 1% target species. The developed RPA assays resulted in amplification of DNA template exclusively of cattle, buffalo and pig origin to product sizes of 294, 405 and 283 bp respectively. The diagnostic sensitivities of developed assays were up to 10 pg of genomic DNA and highly correlated with species specific PCR assays taken as gold standard. Developed species specific RPA assays also identified the target species in coded samples and binary meat admixture up to 1%.
引用
收藏
页码:1286 / 1294
页数:9
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