Kumari Sarita, Kumar Rajiv Ranjan, Mendiratta Sanjod Kumar, Kumar Deepak, Rana Preeti, Kumar Dhananjay, Jawla Jyoti
Department of Livestock Products Technology, PGIVER, RAJUVAS, Jaipur, India.
2Division of Livestock Products Technology, Indian Veterinary Research Institute, Izatnagar, Bareilly, 243122 India.
3 Biotech. 2019 Mar;9(3):69. doi: 10.1007/s13205-019-1595-x. Epub 2019 Feb 5.
The present study was carried out with the objective of development of species-specific loop-mediated isothermal amplification (LAMP) assay for identification of tissue of cattle origin. The cattle-specific LAMP primer set was designed by targeting mitochondrial D-loop gene. The conditions for LAMP reaction for amplification of template DNA from cattle using designed cattle-specific primer set were optimized for the components of mixture and temperature of reaction. Amplified products were analysed using SYBR Green I dye and by agarose gel electrophoresis. The developed species-specific LAMP assay was evaluated for its specificity, sensitivity and validated in laboratory on samples from known, coded, binary meat admixture with other than cattle at relative percentage of 20%, 10%, 5% and 1%, Phire tissue direct PCR master mix treated tissues of cattle and on species-specific polymerase chain reaction assay positive samples. The developed LAMP assay using self-designed primer set was highly specific, amplifying the DNA template exclusively from cattle tissue under the optimized LAMP reaction conditions. The sensitivity assay using serially diluted DNA templates revealed lowest level of detection as 0.01 ng of absolute DNA from target species. Laboratory validation substantiated the accuracy of assay in known/unknown (coded) samples and up to the 1% level of admixture in binary meat sample. DNA present in supernatant of Phire Animal tissue kit treated samples were also amplified successfully eliminating the extra step of extraction of genomic DNA. The developed assays exhibited comparable results with previously established species-specific PCR assay taken as gold standards. Thus, it was concluded that developed species-specific loop-mediated isothermal amplification assay was effective in identification of tissue of cattle origin.
本研究旨在开发用于鉴定牛源组织的种特异性环介导等温扩增(LAMP)检测方法。通过靶向线粒体D-loop基因设计了牛特异性LAMP引物组。针对混合物成分和反应温度,优化了使用设计的牛特异性引物组从牛中扩增模板DNA的LAMP反应条件。使用SYBR Green I染料和琼脂糖凝胶电泳分析扩增产物。对所开发的种特异性LAMP检测方法进行特异性、灵敏度评估,并在实验室中对已知编码的二元肉混合物样本(牛与其他物种的相对比例分别为20%、10%、5%和1%)、经Phire组织直接PCR预混液处理的牛组织样本以及种特异性聚合酶链反应检测呈阳性的样本进行验证。使用自行设计的引物组开发的LAMP检测方法具有高度特异性,在优化的LAMP反应条件下仅从牛组织中扩增DNA模板。使用系列稀释的DNA模板进行的灵敏度检测显示,目标物种的最低检测水平为0.01 ng绝对DNA。实验室验证证实了该检测方法在已知/未知(编码)样本以及二元肉样本中高达1%混合水平时的准确性。Phire动物组织试剂盒处理样本上清液中的DNA也成功扩增,省去了基因组DNA提取的额外步骤。所开发的检测方法与作为金标准的先前建立的种特异性PCR检测方法结果相当。因此,得出结论,所开发的种特异性环介导等温扩增检测方法可有效鉴定牛源组织。