TNO Defence, Security and Safety, 2280 AA, Rijswijk, the Netherlands.
Folia Microbiol (Praha). 2011 Mar;56(2):95-102. doi: 10.1007/s12223-011-0027-z. Epub 2011 Apr 6.
We determined the role of Yersinia pestis virulence markers in an animal model of pneumonic plague. Eleven strains of Y. pestis were characterized using PCR assays to detect the presence of known virulence genes both encoded by the three plasmids as well as chromosomal markers. The virulence of all Y. pestis strains was compared in a mouse model for pneumonic plague. The presence of all known virulence genes correlated completely with virulence in the Balb/c mouse model. Strains which lacked HmsF initially exhibited visible signs of disease whereas all other strains (except wild-type strains) did not exhibit any disease signs. Forty-eight hours post-infection, mice which had received HmsF(-) strains regained body mass and were able to control infection; those infected with strains possessing a full complement of virulence genes suffered from fatal disease. The bacterial loads observed in the lung and other tissues reflected the observed clinical signs as did the cytokine changes measured in these animals. We can conclude that all known virulence genes are required for the establishment of pneumonic plague in mammalian animal models, the role of HmsF being of particular importance in disease progression.
我们在肺鼠疫动物模型中确定了鼠疫耶尔森氏菌毒力标记物的作用。使用 PCR 检测方法对 11 株鼠疫耶尔森氏菌进行了特征分析,以检测三种质粒以及染色体标记物上编码的已知毒力基因的存在情况。在用于肺鼠疫的小鼠模型中比较了所有鼠疫耶尔森氏菌菌株的毒力。所有已知毒力基因的存在与巴尔通体小鼠模型中的毒力完全相关。最初缺乏 HmsF 的菌株表现出明显的疾病迹象,而所有其他菌株(野生型菌株除外)均未出现任何疾病迹象。感染后 48 小时,接受 HmsF(-) 菌株感染的小鼠恢复了体重并能够控制感染;而感染具有完整毒力基因的菌株的小鼠则患有致命疾病。在肺部和其他组织中观察到的细菌负荷与观察到的临床症状以及在这些动物中测量的细胞因子变化相吻合。我们可以得出结论,在哺乳动物动物模型中建立肺鼠疫需要所有已知的毒力基因,HmsF 的作用在疾病进展中尤为重要。