Quality and Safety Department, Nestlé Research Center, PO Box 44, 1000 Lausanne 26, Switzerland.
J Dairy Sci. 2011 Aug;94(8):3787-93. doi: 10.3168/jds.2011-4195.
Asian countries are major producers of cow and buffalo milk. For quality and authenticity purposes, a multiplex real-time PCR assay was developed to specifically and simultaneously detect DNA from these 2 bovine species. Targeting the cytochrome b gene of mitochondrial DNA, common PCR primers amplified a 105-bp fragment, and 2 fluorescent probes specific to either cow or buffalo were designed for their identification. Specificity was successfully tested on 6 other species, including sheep and goat, and sensitivity reached 1% of cow DNA in buffalo DNA and vice versa. As an evaluation, the method was tested using 119 freeze-dried Asian milk samples from regional industrial milk facilities. Although these samples did not cover the entire Asian zone, the multiplex assay indicated that approximately 20% of the samples (mainly from India) showed high levels of cross-contamination of cow milk by buffalo milk, and vice versa. Fast, sensitive, and straightforward, this method is fit-for-purpose for the authenticity control of Asian milk.
亚洲国家是奶牛和水牛奶的主要生产国。为了保证质量和真实性,开发了一种多重实时 PCR 检测方法,用于特异性和同时检测这两种牛科动物的 DNA。该方法针对线粒体 DNA 的细胞色素 b 基因,使用通用的 PCR 引物扩增出 105bp 的片段,并且设计了 2 种针对牛或水牛的荧光探针用于鉴定。该方法在其他 6 个物种(包括绵羊和山羊)上的特异性检测得到了成功验证,灵敏度达到了在水牛 DNA 中检测 1%的牛 DNA 和反之亦然。作为评估,该方法使用来自地区性工业牛奶加工设施的 119 份冷冻干燥的亚洲牛奶样本进行了测试。尽管这些样本没有涵盖整个亚洲地区,但多重检测方法表明,大约 20%的样本(主要来自印度)显示出了牛奶中牛和水牛奶的高度交叉污染,反之亦然。该方法快速、灵敏、直接,非常适合亚洲牛奶的真实性控制。