Bottero M T, Dalmasso I A, Nucera D, Turi R M, Rosati S, Squadrone S, Goria M, Civera T
Dipartimento di Patologia Animale, Università degli Studi di Torino, via Leonardo da Vinci 44 10095 Grugliasco, Torino, Italy.
J Food Prot. 2003 Dec;66(12):2307-12. doi: 10.4315/0362-028x-66.12.2307.
The European Community ban on use of meat and bone meal in ruminant feed, as a consequence of the spread of bovine spongiform encephalopathy in Europe, has prompted a number of investigations about the possibility of detecting animal tissues in feedstuff. In this paper, a study on vertebrate primers, designed in the 16S rRNA gene of mitochondrial DNA, is described. These primers were able to amplify fragments that contained between 234 and 265 bp. The fragments were specific for bovine, porcine, goat, sheep, horse, rabbit, chicken, trout, and European pilchard and were confirmed by sequence analysis amplicons. The primers were used in a PCR assay applied to five samples of meat and blood meals of different species and subjected to severe rendering treatments (134.4 to 141.9 degrees C and 3.03 to 4.03 bar for 24 min). The presence of vertebrate tissues was detected in all samples. The assay proved to be rapid and sensitive (detection limit 0.0625%). It can be used as a routine method to detect animal-derived ingredients in animal feedstuff.
由于牛海绵状脑病在欧洲的传播,欧洲共同体禁止在反刍动物饲料中使用肉骨粉,这引发了一系列关于检测饲料中动物组织可能性的调查。本文描述了一项针对线粒体DNA的16S rRNA基因设计的脊椎动物引物的研究。这些引物能够扩增出长度在234至265 bp之间的片段。这些片段对牛、猪、山羊、绵羊、马、兔、鸡、鳟鱼和欧洲沙丁鱼具有特异性,并通过扩增子序列分析得到证实。这些引物被用于一项聚合酶链反应(PCR)检测,该检测应用于五个不同物种的肉粉和血粉样本,并经过了严格的炼制处理(134.4至141.9摄氏度,3.03至4.03巴,持续24分钟)。在所有样本中都检测到了脊椎动物组织的存在。该检测方法被证明快速且灵敏(检测限为0.0625%)。它可以用作检测动物饲料中动物源性成分的常规方法。