Neubauer H, Hensel A, Aleksic S, Meyer H
Institute of Microbiology, German Armed Forces Medical Academy, Munich.
Syst Appl Microbiol. 2000 Apr;23(1):58-62. doi: 10.1016/S0723-2020(00)80046-6.
In this report we describe a PCR strategy for the unambigous identification of biochemically presumptive typed Yersinia (Y.) enterocolitica. A total of 269 isolates belonging to ten species of the genus Yersinia were investigated. In a first PCR only isolates classified as Y. enterocolitica (n = 113) gave rise to a specific amplification resulting in a sensitivity and a specificity of 100%. By sequencing the 269 amplicons of a second pan-Yersinia PCR spanning a distinct 16S rRNA gene region, 20 different sequence clusters could be identified within the genus. By this, Y. enterocolitica isolates of American and European origin could be distinguished safely and already described sequence clusters of the species Y. frederiksenii were confirmed. New 16S rRNA gene sequence clusters were detected for the species Y. frederiksenii, Y. intermedia, Y. mollaretii, Y. aldovae, Y. kristensenii, and Y. rohdei.
在本报告中,我们描述了一种用于明确鉴定生化推定分型的小肠结肠炎耶尔森菌(Yersinia enterocolitica)的PCR策略。共研究了属于耶尔森菌属十个物种的269株分离株。在首次PCR中,仅归类为小肠结肠炎耶尔森菌的分离株(n = 113)产生特异性扩增,灵敏度和特异性均为100%。通过对跨越一个独特16S rRNA基因区域的第二次全耶尔森菌PCR的269个扩增子进行测序,在该属内可鉴定出20个不同的序列簇。由此,可以安全地区分美国和欧洲来源的小肠结肠炎耶尔森菌分离株,并且已确认了弗氏耶尔森菌(Y. frederiksenii)物种的已描述序列簇。还检测到了弗氏耶尔森菌、中间耶尔森菌(Y. intermedia)、莫氏耶尔森菌(Y. mollaretii)、奥尔森耶尔森菌(Y. aldovae)、克里斯滕森耶尔森菌(Y. kristensenii)和罗德耶尔森菌(Y. rohdei)物种的新16S rRNA基因序列簇。