Patiño Belén, González-Salgado Amaia, González-Jaén M Teresa, Vázquez Covadonga
Departamento de Microbiología III, Universidad Complutense de Madrid, Spain.
Int J Food Microbiol. 2005 Oct 15;104(2):207-14. doi: 10.1016/j.ijfoodmicro.2005.02.011.
Two PCR assays have been developed to detect Aspergillus carbonarius and Aspergillus ochraceus, considered the main sources of ochratoxin A (OTA) contaminating commodities, particularly grapes, coffee and derivatives, in warm climates. The species specific primers have been designed on the basis of ITS (internal transcribed spacers of rDNA units) sequence comparisons obtained from Aspergillus strains and have been tested in a number of strains from different origins and hosts. These PCR assays, based on multi-copy sequences, are highly sensitive and specific and represent a good tool for an early detection of OTA-producing Aspergillus species and to prevent OTA entering the food chain.
已开发出两种聚合酶链反应(PCR)检测方法,用于检测炭黑曲霉和赭曲霉,这两种曲霉被认为是在温暖气候下污染商品(尤其是葡萄、咖啡及其衍生物)的赭曲霉毒素A(OTA)的主要来源。物种特异性引物是根据从曲霉菌株获得的ITS(核糖体DNA单位的内部转录间隔区)序列比较设计的,并已在许多来自不同来源和宿主的菌株中进行了测试。这些基于多拷贝序列的PCR检测方法具有高度的敏感性和特异性,是早期检测产OTA曲霉物种以及防止OTA进入食物链的良好工具。