Hoffmann B, Strauch E, Gewinner C, Nattermann H, Appel B
Robert Koch-Institut, Fachbereich Genetik/Gentechnik, Berlin, Germany.
Syst Appl Microbiol. 1998 Jun;21(2):201-11. doi: 10.1016/S0723-2020(98)80024-6.
The aim of our study was to find out if plasmids of foodborne Yersinia enterocolitica biogroup 1A strains harbour genes related to the virulence genes located on the virulence plasmid pYV of Yersinia enterocolitica. The foodborne strains were isolated from pork, as pigs are considered as an important reservoir for enteropathogenic Y. enterocolitica 0:3 and 0:9 strains. The plasmids of the foodborne strains were characterized by restriction enzyme analysis and hybridized to the virulence plasmid pYV of pathogenic Y. enterocolitica strains (0:3 biogroup 4; 0:9 biogroup 2). In several cases the plasmids of the foodborne strains showed homologies to parts of the pYV plasmid. Analysis of the hybridizing regions revealed that genes involved in replication, sequences of transposable elements and an endonuclease gene caused the observed hybridization to the virulence plasmid. In cause of the study also a remnant of a Tn3-like transposon was shown to be present adjacent to the yadA gene on the pYV plasmid. Although there is evidence that at least some strains of Y. enterocolitica biogroup 1A might possess pathogenic properties none of the well known plasmid encoded virulence genes were present on the plasmids of the investigated foodborne biogroup 1A strains.
我们研究的目的是确定食源性小肠结肠炎耶尔森菌生物群1A菌株的质粒是否携带与位于小肠结肠炎耶尔森菌毒力质粒pYV上的毒力基因相关的基因。食源性菌株是从猪肉中分离出来的,因为猪被认为是肠道致病性小肠结肠炎耶尔森菌0:3和0:9菌株的重要宿主。通过限制性内切酶分析对食源性菌株的质粒进行了鉴定,并与致病性小肠结肠炎耶尔森菌菌株(0:3生物群4;0:9生物群2)的毒力质粒pYV进行杂交。在一些情况下,食源性菌株的质粒与pYV质粒的部分区域显示出同源性。对杂交区域的分析表明,参与复制的基因、转座元件序列和一个内切核酸酶基因导致了观察到的与毒力质粒的杂交。在该研究中还发现,pYV质粒上yadA基因附近存在一个Tn3样转座子的残余部分。尽管有证据表明至少一些小肠结肠炎耶尔森菌生物群1A菌株可能具有致病特性,但在所研究的食源性生物群1A菌株的质粒上未发现任何已知的由质粒编码的毒力基因。