摘要
利用肠毒索性大肠杆菌(ETEC)的LT-A、ST-1毒素基因和肠沙门菌的iroB基因设计3对引物,建立能同时检测ETEC和肠沙门菌的多重PCR方法.结果:多重PCR扩增出了预计的PCR产物,本方法的特异性为100%、灵敏度达10102 CFU/mL,用建立的多重PCR方法对30份临床可疑腹泻样品进行检测并与生化试验比较,结果两种方法检出大肠杆菌和沙门菌的阳性符合率达100%.
The objective of this study was to use LT-A, ST-1 enterotoxigenic genes of ETEC and iroB gene of Salmonella ente-ria to design three different pairs of oligonucleotide primers in order to establish a multiplex PCR detection method which both si-muhaneously detected ETEC and Salmonella enteria. Results:The expected PCR products were amplified, respectively. 30 meatspecimens from suspicious and diarrheal swine were examined using this muhiplux PCR and biochemical test, with the specificityreaching 100% and the sensitivity 10-llY bacteria/mho. The positive detection rates of Escherichia coli and Salmonella using twokinds of methods showed 100% conformity.
出处
《中国兽医杂志》
CAS
北大核心
2015年第4期79-82,共4页
Chinese Journal of Veterinary Medicine
基金
河南省教育厅计划项目
项目(12A230010)
关键词
肠毒素性大肠杆菌
肠沙门菌
多重PCR
Enterotoxingenic Eschefichia Coli
Salmonella enteria
Muhiplux PCR