Griffiths Kate R, McLaughlin Jacob L H, Hall Felicity, Partis Lina, Hansen Samuel C, Tulloch Rachel, Burke Daniel G
Bioanalysis Section, National Measurement Institute, Lindfield, Sydney, NSW 2070, Australia.
Foods. 2023 Oct 20;12(20):3839. doi: 10.3390/foods12203839.
Laboratory testing methods to confirm the identity of meat products and eliminate food fraud regularly rely on PCR amplification of extracted DNA, with most published assays detecting mitochondrial sequences, providing sensitive presence/absence results. By targeting single-copy nuclear targets instead, relative quantification measurements are achievable, providing additional information on the proportions of meat species detected. In this Methods paper, new assays for horse, donkey, duck, kangaroo, camel, water buffalo and crocodile have been developed to expand the range of species that can be quantified, and a previously published reference assay targeting the myostatin gene has been modified to include marsupials and reptiles. The accuracy of this ratio measurement approach was demonstrated using dPCR with mixtures of meat DNA down to 0.1%. However, the limit of detection (LOD) of this approach is not just determined by the assay targets, but by the samples themselves, with food or feed ingredients and processing impacting the DNA yield and integrity. In routine testing settings, the myostatin assay can provide multiple quality control roles, including monitoring the yield and purity of extracted DNA, identifying the presence of additional meats not detected by the suite of species-specific assays and potentially estimating a sample-specific LOD based on measured copy numbers of the myostatin target. In addition to the myostatin positive control assay, a synthetic DNA reference material (RM) has been designed, containing PCR targets for beef, pork, sheep, chicken, goat, kangaroo, horse, water buffalo and myostatin, to be used as a positive template control. The availability of standardised measurement methods and associated RMs significantly improves the reliability, comparability and transparency of laboratory testing, leading to greater confidence in results.
用于确认肉类产品身份并消除食品欺诈的实验室检测方法通常依赖于对提取的DNA进行PCR扩增,大多数已发表的检测方法检测线粒体序列,可提供灵敏的存在/不存在结果。通过靶向单拷贝核靶标,可实现相对定量测量,从而提供有关检测到的肉类物种比例的额外信息。在本方法论文中,已开发出针对马、驴、鸭、袋鼠、骆驼、水牛和鳄鱼的新检测方法,以扩大可定量的物种范围,并且对先前发表的靶向肌生成抑制素基因的参考检测方法进行了修改,以纳入有袋动物和爬行动物。使用含有低至0.1%肉类DNA混合物的数字PCR证明了这种比率测量方法的准确性。然而,这种方法的检测限不仅取决于检测靶标,还取决于样品本身,食品或饲料成分以及加工过程会影响DNA产量和完整性。在常规检测环境中,肌生成抑制素检测可发挥多种质量控制作用,包括监测提取DNA的产量和纯度、识别特定物种检测套件未检测到的其他肉类的存在,并可能根据肌生成抑制素靶标的测量拷贝数估计样品特异性检测限。除了肌生成抑制素阳性对照检测外,还设计了一种合成DNA参考物质(RM),包含牛肉、猪肉、绵羊、鸡肉、山羊、袋鼠、马、水牛和肌生成抑制素的PCR靶标,用作阳性模板对照。标准化测量方法和相关参考物质的可用性显著提高了实验室检测的可靠性、可比性和透明度,从而增强了对结果的信心。