Bellagamba Federica, Comincini Sergio, Ferretti Luca, Valfrè Franco, Moretti Vittorio M
Dipartimento di Scienze e Tecnologie Veterinarie per la Sicurezza Alimentare (VSA), Facoltà di Medicina Veterinaria, Università degli Studi di Milano, Italy.
J Food Prot. 2006 Apr;69(4):891-6. doi: 10.4315/0362-028x-69.4.891.
This study describes a method for quantitative and species-specific detection of animal DNA from different species (cattle, sheep, goat, swine, and chicken) in animal feed and feed ingredients, including fish meals. A quantitative real-time PCR approach was carried out to characterize species-specific sequences based on the amplification of prion-protein sequence. Prion-protein species-specific primers and TaqMan probes were designed, and amplification protocols were optimized in order to discriminate the different species with short PCR amplicons. The real-time quantitative PCR approach was also compared to conventional species-specific PCR assays. The real-time quantitative assay allowed the detection of 10 pg of ruminant, swine, and poultry DNA extracted from meat samples processed at 130 degrees C for 40 min, 200 kPa. The origin of analyzed animal meals was characterized by the quantitative estimation of ruminant, swine, and poultry DNA. The TaqMan assay was used to quantify ruminant DNA in feedstuffs with 0.1% of meat and bone meal. In conclusion, the proposed molecular approach allowed the detection of species-specific DNA in animal meals and feedstuffs.
本研究描述了一种用于定量和特异性检测动物饲料及饲料原料(包括鱼粉)中不同物种(牛、羊、山羊、猪和鸡)动物DNA的方法。采用定量实时PCR方法,基于朊病毒蛋白序列的扩增来鉴定物种特异性序列。设计了朊病毒蛋白物种特异性引物和TaqMan探针,并优化了扩增方案,以便用短PCR扩增子区分不同物种。还将实时定量PCR方法与传统的物种特异性PCR检测进行了比较。实时定量检测能够检测出在130℃、200 kPa条件下处理40分钟的肉样中提取的10 pg反刍动物、猪和家禽DNA。通过对反刍动物、猪和家禽DNA的定量估计来确定所分析动物饲料的来源。TaqMan检测法用于定量含有0.1%肉骨粉的饲料中的反刍动物DNA。总之,所提出的分子方法能够检测动物饲料和饲料原料中的物种特异性DNA。