Oyofo B A, Mohran Z S, el-Etr S H, Wasfy M O, Peruski L F
Enteric Microbiology Branch, U.S. Naval Medical Research Unit No. 3, Cairo, Egypt.
J Diarrhoeal Dis Res. 1996 Sep;14(3):207-10.
Three oligonucleotide primers were used in a polymerase chain reaction (PCR) assay for the simultaneous amplification of regions of the invasive plasmid antigen (ipaH) of Shigella spp., flagellin gene (flaA) of Campylobacter spp., and heat-labile enterotoxin (LT) of enterotoxigenic Escherichia coli (ETEC). The multiplex assay was performed using DNA extracted by a chaotropic method directly from diarrhoeal stools. The diagnostic efficacy of the assay was analyzed by agarose gel electrophoresis. This assay shows a novel approach for the diagnosis of diarrhoea caused by Shigella spp., ETEC, and Campylobacter spp.
在聚合酶链反应(PCR)分析中使用了三种寡核苷酸引物,用于同时扩增志贺氏菌属的侵袭性质粒抗原(ipaH)区域、弯曲杆菌属的鞭毛蛋白基因(flaA)以及产肠毒素大肠杆菌(ETEC)的不耐热肠毒素(LT)。多重分析使用通过离液序列高的方法直接从腹泻粪便中提取的DNA进行。通过琼脂糖凝胶电泳分析该分析方法的诊断效力。该分析方法展示了一种诊断由志贺氏菌属、ETEC和弯曲杆菌属引起的腹泻的新方法。