Chouikha Iman, Hinnebusch B Joseph
Laboratory of Zoonotic Pathogens, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840
Laboratory of Zoonotic Pathogens, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840.
Proc Natl Acad Sci U S A. 2014 Dec 30;111(52):18709-14. doi: 10.1073/pnas.1413209111. Epub 2014 Dec 1.
The arthropod-borne transmission route of Yersinia pestis, the bacterial agent of plague, is a recent evolutionary adaptation. Yersinia pseudotuberculosis, the closely related food-and water-borne enteric species from which Y. pestis diverged less than 6,400 y ago, exhibits significant oral toxicity to the flea vectors of plague, whereas Y. pestis does not. In this study, we identify the Yersinia urease enzyme as the responsible oral toxin. All Y. pestis strains, including those phylogenetically closest to the Y. pseudotuberculosis progenitor, contain a mutated ureD allele that eliminated urease activity. Restoration of a functional ureD was sufficient to make Y. pestis orally toxic to fleas. Conversely, deletion of the urease operon in Y. pseudotuberculosis rendered it nontoxic. Enzymatic activity was required for toxicity. Because urease-related mortality eliminates 30-40% of infective flea vectors, ureD mutation early in the evolution of Y. pestis was likely subject to strong positive selection because it significantly increased transmission potential.
鼠疫的病原体——鼠疫耶尔森菌通过节肢动物传播的途径是一种近期的进化适应。假结核耶尔森菌是一种与鼠疫耶尔森菌密切相关的食源和水源性肠道菌种,鼠疫耶尔森菌在不到6400年前从该菌种分化而来,它对鼠疫的跳蚤传播媒介具有显著的口服毒性,而鼠疫耶尔森菌则没有。在本研究中,我们确定耶尔森菌脲酶为造成口服毒性的毒素。所有鼠疫耶尔森菌菌株,包括那些在系统发育上最接近假结核耶尔森菌祖先的菌株,都含有一个突变的ureD等位基因,该等位基因消除了脲酶活性。恢复功能性ureD足以使鼠疫耶尔森菌对跳蚤产生口服毒性。相反,在假结核耶尔森菌中缺失脲酶操纵子使其无毒。毒性需要酶活性。由于与脲酶相关的死亡率消除了30%-40%的感染性跳蚤传播媒介,鼠疫耶尔森菌进化早期的ureD突变可能受到强烈的正选择,因为它显著提高了传播潜力。