摘要
针对产志贺毒素大肠杆菌的stx2、wzy、hlyA的保守序列,设计特异性的引物,建立一种新的多重PCR检验方法。结果显示,该方法特异性强,扩增结果与各参考菌株基因型一致,并能良好的区分出O157菌株和非O157型产志贺毒素大肠杆菌。该方法能用于食品样品的检测和流行病学分离株的快速鉴定。
Specific primers were designed according to the conserved loci of stx2,wzy and hlyA genes of Shiga toxin-producing Escherichia coli(STEC).A Multiplex PCR method was then developed.The result demonstrated that this method was highly specific.It detected the presence of the three target genes in a manner consistent with the known genotype of each reference strain.O157 and non-O157 STEC strains could also be well distinguished.The multiplex PCR developed in this study could be used for mass screening of food samples,and identification of clinical STEC isolates.
出处
《食品研究与开发》
CAS
北大核心
2010年第11期161-163,共3页
Food Research and Development