首页> 外文期刊>PLoS Biology >Phosphorylation of Mouse Immunity-Related GTPase (IRG) Resistance Proteins Is an Evasion Strategy for Virulent Toxoplasma gondii
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Phosphorylation of Mouse Immunity-Related GTPase (IRG) Resistance Proteins Is an Evasion Strategy for Virulent Toxoplasma gondii

机译:小鼠免疫相关的GTPase(IRG)抗性蛋白的磷酸化是一种强毒弓形虫的规避策略。

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Virulence of complex pathogens in mammals is generally determined by multiple components of the pathogen interacting with the functional complexity and multiple layering of the mammalian immune system. It is most unusual for the resistance of a mammalian host to be overcome by the defeat of a single defence mechanism. In this study we uncover and analyse just such a case at the molecular level, involving the widespread intracellular protozoan pathogen Toxoplasma gondii and one of its most important natural hosts, the house mouse (Mus musculus). Natural polymorphism in virulence of Eurasian T. gondii strains for mice has been correlated in genetic screens with the expression of polymorphic rhoptry kinases (ROP kinases) secreted into the host cell during infection. We show that the molecular targets of the virulent allelic form of ROP18 kinase are members of a family of cellular GTPases, the interferon-inducible IRG (immunity-related GTPase) proteins, known from earlier work to be essential resistance factors in mice against avirulent strains of T. gondii. Virulent T. gondii strain ROP18 kinase phosphorylates several mouse IRG proteins. We show that the parasite kinase phosphorylates host Irga6 at two threonines in the nucleotide-binding domain, biochemically inactivating the GTPase and inhibiting its accumulation and action at the T. gondii parasitophorous vacuole membrane. Our analysis identifies the conformationally active switch I region of the GTP-binding site as an Achilles' heel of the IRG protein pathogen-resistance mechanism. The polymorphism of ROP18 in natural T. gondii populations indicates the existence of a dynamic, rapidly evolving ecological relationship between parasite virulence factors and host resistance factors. This system should be unusually fruitful for analysis at both ecological and molecular levels since both T. gondii and the mouse are widespread and abundant in the wild and are well-established model species with excellent analytical tools available.
机译:哺乳动物中复杂病原体的毒力通常取决于病原体的多种成分与哺乳动物免疫系统的功能复杂性和多层性相互作用。哺乳动物宿主的抵抗力被单一防御机制的破坏所克服是最不寻常的。在这项研究中,我们在分子水平上发现并分析了这种情况,涉及广泛的细胞内原生动物病原体弓形虫及其最重要的自然宿主之一,家鼠(Mus musculus)。欧亚弓形虫对小鼠的毒力中的自然多态性已在遗传筛选中与感染过程中分泌到宿主细胞中的多态rhoptry激酶(ROP激酶)的表达相关。我们显示ROP18激酶的强毒等位基因形式的分子靶标是细胞GTP酶家族的成员,GTP酶是干扰素诱导的IRG(免疫相关GTPase)蛋白,从早期工作中已知是小鼠对无毒株的基本抗性因子T. gondii。强大的弓形虫菌株ROP18激酶使几种小鼠IRG蛋白磷酸化。我们显示,该寄生虫激酶在核苷酸结合结构域的两个苏氨酸上磷酸化了Irga6宿主,生物化学失活了GTPase,并抑制了其在T. gondii寄生虫液泡膜上的积累和作用。我们的分析确定了GTP结合位点的构象活​​性开关I区是IRG蛋白病原体抵抗机制的致命弱点。弓形虫天然种群中ROP18的多态性表明,寄生虫毒力因子和宿主抗性因子之间存在动态,快速发展的生态关系。该系统在生态和分子水平上都应具有异常丰富的分析能力,因为刚地弓形虫和小鼠均在野外分布广泛且丰富,并且是建立良好的模型物种,并具有出色的分析工具。

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