Kang Soo Ji, Jang Chan Song, Son Ji Min, Hong Kwang Won
Department of Food Science and Biotechnology, College of Life Science and Biotechnology, Dongguk University, Goyang 10326, Korea.
Food Sci Anim Resour. 2021 Jan;41(1):85-94. doi: 10.5851/kosfa.2020.e80. Epub 2021 Jan 1.
A pig-specific real-time PCR assay based on the mitochondrial gene was developed to detect porcine material in food and other products. To optimize the performance of assay, seven commercial TaqMan master mixes and two real-time PCR platforms (Applied Biosystems StepOnePlus and Bio-rad CFX Connect) were used to evaluate the limit of detection (LOD) as well as the PCR efficiency and specificity. The LODs and PCR efficiencies for the seven master mixes on two platforms were 0.5-5 pg/reaction and 84.96%-108.80%, respectively. Additionally, non-specific amplifications of DNA from other animal samples (human, dog, cow, and chicken) were observed for four master mixes. These results imply that the sensitivity and specificity of a real-time PCR assay may vary depending on master mix and platform used. The best combination of master mix and real-time PCR platform can accurately detect 0.5 pg porcine DNA, with a PCR efficiency of 100.49%.
开发了一种基于线粒体基因的猪特异性实时荧光定量PCR检测方法,用于检测食品和其他产品中的猪源性物质。为优化该检测方法的性能,使用了七种商业TaqMan预混试剂和两个实时荧光定量PCR平台(Applied Biosystems StepOnePlus和Bio-rad CFX Connect)来评估检测限(LOD)以及PCR效率和特异性。两个平台上七种预混试剂的检测限和PCR效率分别为0.5-5 pg/反应和84.96%-108.80%。此外,观察到四种预混试剂对其他动物样本(人类样本、犬类样本、牛类样本和鸡类样本)的DNA存在非特异性扩增。这些结果表明,实时荧光定量PCR检测方法的灵敏度和特异性可能会因所使用的预混试剂和平台而异。预混试剂和实时荧光定量PCR平台的最佳组合能够准确检测出0.5 pg猪源DNA,PCR效率为100.49%。