DebRoy Chitrita, Roberts Elisabeth, Kundrat James, Davis Michael A, Briggs Connie E, Fratamico Pina M
Gastroenteric Disease Center, Department of Veterinary Science, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.
Appl Environ Microbiol. 2004 Mar;70(3):1830-2. doi: 10.1128/AEM.70.3.1830-1832.2004.
PCR-based assays for detecting enterohemorrhagic Escherichia coli serogroups O26 and O113 were developed by targeting the wzx (O-antigen flippase) and the wzy (O-antigen polymerase) genes found in the O-antigen gene cluster of each organism. The PCR assays were specific for the respective serogroups, as there was no amplification of DNA from non-O26 and non-O113 E. coli serogroups or from other bacterial genera tested. Using the PCR assays, we were able to detect the organisms in seeded apple juice inoculated at concentration levels as low as < or =10 CFU/ml. The O26- and O113-specific PCR assays can potentially be used for typing E. coli O26 and O113 serogroups; these assays will offer an advantage to food and environmental microbiology laboratories in terms of identifying these non-O157 serogroups by replacing antigen-based serotyping.
通过靶向每种生物体O抗原基因簇中的wzx(O抗原翻转酶)和wzy(O抗原聚合酶)基因,开发了用于检测肠出血性大肠杆菌O26和O113血清型的基于PCR的检测方法。这些PCR检测方法对各自的血清型具有特异性,因为来自非O26和非O113大肠杆菌血清型或所测试的其他细菌属的DNA没有扩增。使用这些PCR检测方法,我们能够在接种浓度低至≤10 CFU/ml的接种苹果汁中检测到这些生物体。O26和O113特异性PCR检测方法有可能用于对大肠杆菌O26和O113血清型进行分型;这些检测方法将通过取代基于抗原的血清分型,在鉴定这些非O157血清型方面为食品和环境微生物学实验室提供优势。