Clark Clifford G, Johnson Shelley T, Easy Russell H, Campbell Jennifer L, Rodgers Frank G
National Laboratory for Enteric Pathogens, National Microbiology Laboratory, Canadian Science Centre for Human and Animal Health, Winnipeg, Manitoba, Canada.
J Clin Microbiol. 2002 Jul;40(7):2671-4. doi: 10.1128/JCM.40.7.2671-2674.2002.
A PCR assay that uses primers whose sequences were obtained from the published sequence of the cdt-III gene was developed to determine the frequencies of the cdt-I, cdt-II, and cdt-III genes in Escherichia coli isolates from humans and animals. E. coli isolates producing cytolethal distending toxin (CDT) were infrequently detected. The cdt-I gene was preferentially detected in strains with the cnf1 gene, while the cdt-III gene was found in strains carrying the cnf2 gene. The cdt-III genotype was more prevalent in animal isolates, while the cdt-I and cdt-II genotypes were more evident in human isolates. The presence of further cdt gene variants was indicated by the presence of toxin activity in cell culture in the absence of PCR amplification of the cdt-I, cdt-II, or cdt-III gene.
开发了一种聚合酶链反应(PCR)检测方法,该方法使用从已发表的cdt-III基因序列中获取序列的引物,以确定从人和动物分离的大肠杆菌中cdt-I、cdt-II和cdt-III基因的频率。很少检测到产生细胞致死性扩张毒素(CDT)的大肠杆菌分离株。cdt-I基因在携带cnf1基因的菌株中优先被检测到,而cdt-III基因在携带cnf2基因的菌株中被发现。cdt-III基因型在动物分离株中更为普遍,而cdt-I和cdt-II基因型在人类分离株中更为明显。在没有cdt-I、cdt-II或cdt-III基因的PCR扩增的情况下,细胞培养中毒素活性的存在表明存在其他cdt基因变体。