Martín I, García T, Fajardo V, López-Calleja I, Rojas M, Pavón M A, Hernández P E, González I, Martín R
Departamento de Nutrición, Bromatología y Tecnología de los Alimentos, Facultad de Veterinaria, Universidad Complutense de Madrid, 28040 Madrid, Spain.
J Anim Sci. 2007 Feb;85(2):452-8. doi: 10.2527/jas.2006-350.
PCR method was applied for the qualitative identification of chicken (Gallus gallus), turkey (Meleagris gallipavo), duck (Anas platyrhynchos x Cairina muschata), and goose (Anser anser) tissues in feed-stuffs, on an individual basis. The assay uses oligonucleotide primers that are specific for each avian species, targeting the 12S rRNA mitochondrial gene. The primers designed generated amplicons of 95, 122, 64, and 98 bp length for chicken, turkey, duck, and goose, respectively. The specificity of the primers was tested against 29 animal species including mammals, birds, and fish, as well as 8 plant species. Analysis of experimental feedstuffs demonstrated the detection of each target species in the range of 0.1 to 100%. The performance of this method was not affected by prolonged heat-treatment (up to 133 degrees C for 20 min at 300 kPa), and consequently, it could be very useful for the accurate identification of tissues from these 4 avian species in products submitted to denaturing technologies, for which other methods cannot be applied.
采用聚合酶链反应(PCR)方法对饲料中鸡(家鸡)、火鸡 (火鸡)、鸭(绿头鸭×疣鼻栖鸭)和鹅(鸿雁)的组织进行个体定量鉴定。该检测方法使用针对每种禽类的寡核苷酸引物,靶向线粒体12S rRNA基因。所设计的引物分别扩增出长度为95bp、122bp、64bp和98bp的鸡、火鸡、鸭和鹅的扩增产物。针对包括哺乳动物、鸟类和鱼类在内的29种动物以及8种植物测试了引物的特异性。对实验饲料的分析表明,每种目标物种的检测范围为0.1%至100%。该方法的性能不受长时间热处理(在300kPa下133摄氏度持续20分钟)的影响,因此,对于提交到变性技术的产品中源自这四种禽类的组织的准确鉴定非常有用,而其他方法无法用于该类产品。