Kumar Dhananjay, Kumar Rajiv Ranjan, Rana Preeti, Mendiratta S K, Agarwal R K, Singh Praveen, Kumari Sarita, Jawla Jyoti
Division of Livestock Products Technology, Indian Veterinary Research Institute, Izatnagar, Bareilly, 243122 India.
Department of Livestock Products Technology, CVASc, DUVASU, Mathura, India.
J Food Sci Technol. 2021 Apr;58(4):1286-1294. doi: 10.1007/s13197-020-04637-6. Epub 2020 Jul 16.
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%.
本研究旨在开发并标准化重组酶聚合酶扩增-侧向流动(RPA-LF)检测方法,用于现场鉴定食用动物(即牛、水牛和猪)的物种来源。通过对常见食用动物(牛、水牛、绵羊、山羊、猪和鸡)线粒体细胞色素b基因和d环区域序列进行同源性比较,设计了牛、水牛和猪的物种特异性RPA引物组。使用Twist Amp basic试剂盒中的反应成分及其手册中的说明,对设计的引物组进行RPA检测优化。通过凝胶电泳和设计的物种特异性RPA-LFA试纸条对物种特异性扩增的RPA产物进行终点检测。对所开发的检测方法进行特异性、诊断敏感性评估,并在编码样品和目标物种相对比例为20%、10%、5%和1%的二元肉类混合物上进行验证。所开发的RPA检测方法分别仅扩增出牛、水牛和猪来源的DNA模板,产物大小分别为294、405和283 bp。所开发检测方法的诊断敏感性高达10 pg基因组DNA,与作为金标准的物种特异性PCR检测方法高度相关。所开发的物种特异性RPA检测方法还能在编码样品和二元肉类混合物中鉴定出高达1%的目标物种。