Gripenberg-Lerche C, Skurnik M, Zhang L, Söderström K O, Toivanen P
Department of Medical Microbiology, Turku University, Finland.
Infect Immun. 1994 Dec;62(12):5568-75. doi: 10.1128/iai.62.12.5568-5575.1994.
Outer membrane protein YadA, the Yersinia adhesin, is one of the plasmid-encoded virulence factors of yersiniae. To evaluate the role of YadA in the pathogenesis of reactive arthritis experimentally, we used YadA- strain YeO8-116, a kanamycin GenBlock insertion mutant derived from Yersinia enterocolitica O:8 wild-type strain 8081. As control strains, a plasmid-cured derivative (8081-c) of 8081 and a YopH- mutant (8081-yoph) were used. In addition, YeO8-116, with the yadA mutation transcomplemented with plasmid pMW10, was used. YeO8-116 induced arthritis to a considerably lesser extent than did wild-type strain 8081 when inoculated intravenously into Lewis rats. In rats surviving for over 14 days after the bacterial inoculation, the arthritis incidences were 6% (4 of 72) among those inoculated with the yadA mutant and 51% (33 of 65) among those inoculated with wild-type strain 8081. When the yadA gene was transcomplemented back to YeO8-116, YeO8-116/pMW10 induced arthritis in 47% (9 of 19) of the inoculated rats. Plasmid-cured strain 8081-c did not induce arthritis in any of the 24 inoculated rats, whereas YopH- mutant 8081-yoph induced arthritis in 20% (5 of 25) of the rats inoculated. Although the 50% lethal dose of YeO8-116 was about sixfold higher than that of 8081, the kinetics of bacterial elimination from the spleen and mesenteric lymph nodes were about the same with both strains. Antibody responses in rats infected with the two strains were also indistinguishable. Our results indicate that YadA contributes to the arthritogenicity of Y. enterocolitica in the rat model.
外膜蛋白YadA是耶尔森氏菌粘附素,是耶尔森氏菌中一种由质粒编码的毒力因子。为了通过实验评估YadA在反应性关节炎发病机制中的作用,我们使用了YadA缺陷菌株YeO8 - 116,它是一株来自小肠结肠炎耶尔森氏菌O:8野生型菌株8081的卡那霉素基因阻断插入突变体。作为对照菌株,使用了8081的质粒消除衍生物(8081 - c)和YopH缺陷突变体(8081 - yoph)。此外,还使用了通过质粒pMW10对yadA突变进行反式互补的YeO8 - 116。当静脉注射到Lewis大鼠体内时,YeO8 - 116诱导关节炎的程度比野生型菌株8081小得多。在细菌接种后存活超过14天的大鼠中,接种yadA突变体的大鼠关节炎发病率为6%(72只中有4只),接种野生型菌株8081的大鼠关节炎发病率为51%(65只中有33只)。当yadA基因反式互补回YeO8 - 116时,YeO8 - 116/pMW10在47%(19只中有9只)的接种大鼠中诱导了关节炎。质粒消除菌株8081 - c在24只接种大鼠中均未诱导关节炎,而YopH缺陷突变体8081 - yoph在20%(25只中有5只)的接种大鼠中诱导了关节炎。尽管YeO8 - 116的半数致死剂量比8081高约6倍,但两种菌株从脾脏和肠系膜淋巴结中清除细菌的动力学大致相同。感染这两种菌株的大鼠的抗体反应也没有区别。我们的结果表明,YadA在大鼠模型中对小肠结肠炎耶尔森氏菌的致关节炎性有贡献。