Department of Animal Science, Division of Microbiology and Animal Hygiene, Georg-August-University of Goettingen, Goettingen, Germany.
TwistDx(TM) Limited, Cambridge, United Kingdom.
Food Chem. 2020 Aug 30;322:126759. doi: 10.1016/j.foodchem.2020.126759. Epub 2020 Apr 6.
Detection of animal species in meat product is crucial to prevent adulterated and unnecessary contamination during processing. Gold standard is the real-time PCR assays, which can be conducted at highly equipped laboratories. Toward the development of point-of-need test, two rapid molecular assays based on recombinase polymerase amplification (RPA) for the detection of pork and horse DNA were established. Target genes are the porcine mitochondrial ND2 and equine ATP 6-8 genes. The pork and horse_RPA assays detected 16 and one DNA molecules/µl in eleven to six minutes, respectively. The myoglobin in the meat did not influence the assays performances, while the presence of high background-DNA induced a one log decrease in the sensitivity. Both assays are highly specific and identify down to 0.1% of their target DNA in meat mixtures. Both RPA assays could be used on-site as a rapid and mobile detection system to determine contamination of meat products.
检测肉类产品中的动物物种对于防止加工过程中的掺假和不必要的污染至关重要。金标准是实时聚合酶链反应(PCR)检测方法,可以在高度配备的实验室中进行。为了开发现场即时检测方法,我们建立了两种基于重组酶聚合酶扩增(RPA)的快速分子检测方法,用于检测猪肉和马 DNA。目标基因是猪线粒体 ND2 和马 ATP6-8 基因。猪肉和马_RPA 检测方法分别在 11 到 6 分钟内检测到 16 个和 1 个 DNA 分子/µl。肉中的肌红蛋白不会影响检测方法的性能,而高背景 DNA 的存在会使灵敏度降低一个对数级。两种检测方法都具有高度特异性,可在肉混合物中识别出低至 0.1%的目标 DNA。两种 RPA 检测方法都可以现场使用,作为一种快速、移动的检测系统,用于确定肉类产品的污染情况。