Fratamico Pina M, Briggs Connie E, Needle Danielle, Chen Chin-Yi, DebRoy Chitrita
Eastern Regional Research Center, Agricultural Research Service, U.S. Department of Agriculture, Wyndmoor, Pennsylvania 19038, USA.
J Clin Microbiol. 2003 Jul;41(7):3379-83. doi: 10.1128/JCM.41.7.3379-3383.2003.
The DNA sequence of the 15,155-bp O-antigen gene cluster of Escherichia coli O121 was determined, and 14 open reading frames were identified (all had the same transcriptional direction). Analyses of results indicated that the wzx (O-antigen flippase) and wzy (O-antigen polymerase) genes were E. coli O121 specific, so regions in these two genes were chosen for development of PCR assays. The PCR assays using DNA from 99 E. coli O121 strains, strains representative of non-O121 E. coli serogroups, and strains of other bacterial genera and PCR assays using DNA from seven enrichments of swine fecal samples naturally contaminated with E. coli O121 showed specificity for E. coli O121. Thus, the PCR assay can be employed to reliably identify E. coli O121 and to potentially detect the organism in food, fecal, and environmental samples.
测定了大肠杆菌O121的15155 bp O抗原基因簇的DNA序列,鉴定出14个开放阅读框(均具有相同的转录方向)。结果分析表明,wzx(O抗原翻转酶)和wzy(O抗原聚合酶)基因是大肠杆菌O121特有的,因此选择这两个基因中的区域用于开发PCR检测方法。使用来自99株大肠杆菌O121菌株、非O121大肠杆菌血清群代表菌株以及其他细菌属菌株的DNA进行的PCR检测,以及使用来自七份自然污染大肠杆菌O121的猪粪便样本富集物的DNA进行的PCR检测,均显示出对大肠杆菌O121的特异性。因此,该PCR检测方法可用于可靠地鉴定大肠杆菌O121,并有可能检测食品、粪便和环境样本中的该微生物。