Pajuelo David, Lee Chung-Te, Roig Francisco J, Lemos Manuel L, Hor Lien-I, Amaro Carmen
Department of Microbiology and Ecology, University of Valencia, Valencia, Spain.
Infect Immun. 2014 Feb;82(2):731-44. doi: 10.1128/IAI.01117-13. Epub 2013 Dec 2.
The zoonotic serovar of Vibrio vulnificus (known as biotype 2 serovar E) is the etiological agent of human and fish vibriosis. The aim of the present work was to discover the role of the vulnibactin- and hemin-dependent iron acquisition systems in the pathogenicity of this zoonotic serovar under the hypothesis that both are host-nonspecific virulence factors. To this end, we selected three genes for three outer membrane receptors (vuuA, a receptor for ferric vulnibactin, and hupA and hutR, two hemin receptors), obtained single and multiple mutants as well as complemented strains, and tested them in a series of in vitro and in vivo assays, using eels and mice as animal models. The overall results confirm that hupA and vuuA, but not hutR, are host-nonspecific virulence genes and suggest that a third undescribed host-specific plasmid-encoded system could also be used by the zoonotic serovar in fish. hupA and vuuA were expressed in the internal organs of the animals in the first 24 h of infection, suggesting that they may be needed to achieve the population size required to trigger fatal septicemia. vuuA and hupA were sequenced in strains representative of the genetic diversity of this species, and their phylogenies were reconstructed by multilocus sequence analysis of selected housekeeping and virulence genes as a reference. Given the overall results, we suggest that both genes might form part of the core genes essential not only for disease development but also for the survival of this species in its natural reservoir, the aquatic environment.
创伤弧菌的人畜共患病血清型(即生物型2血清型E)是人类和鱼类弧菌病的病原体。本研究的目的是在假定嗜铁素和血红素依赖性铁摄取系统均为非宿主特异性毒力因子的前提下,探究它们在这种人畜共患病血清型致病性中的作用。为此,我们选择了编码三种外膜受体的三个基因(vuuA,一种嗜铁嗜铁素受体,以及hupA和hutR,两种血红素受体),获得了单突变体、多突变体以及互补菌株,并以鳗鱼和小鼠作为动物模型,在一系列体外和体内试验中对它们进行了测试。总体结果证实,hupA和vuuA而非hutR是宿主非特异性毒力基因,并表明一种尚未描述的宿主特异性质粒编码系统也可能被这种人畜共患病血清型用于感染鱼类。hupA和vuuA在感染后最初24小时内在动物的内脏中表达,这表明它们可能是触发致命败血症所需达到的种群规模所必需的。对代表该物种遗传多样性的菌株中的vuuA和hupA进行了测序,并通过对选定的管家基因和毒力基因进行多位点序列分析来重建它们的系统发育,作为参考。鉴于总体结果,我们认为这两个基因可能不仅是疾病发展所必需的核心基因的一部分,也是该物种在其自然宿主水生环境中生存所必需的核心基因的一部分。