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The Polymorphic Pseudokinase ROP5 Controls Virulence in Toxoplasma gondii by Regulating the Active Kinase ROP18

机译:多态性假激酶ROP5通过调节活性激酶ROP18控制弓形虫的毒力。

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摘要

Secretory polymorphic serine/threonine kinases control pathogenesis of Toxoplasma gondii in the mouse. Genetic studies show that the pseudokinase ROP5 is essential for acute virulence, but do not reveal its mechanism of action. Here we demonstrate that ROP5 controls virulence by blocking IFN-γ mediated clearance in activated macrophages. ROP5 was required for the catalytic activity of the active S/T kinase ROP18, which phosphorylates host immunity related GTPases (IRGs) and protects the parasite from clearance. ROP5 directly regulated activity of ROP18 in vitro, and both proteins were necessary to avoid IRG recruitment and clearance in macrophages. Clearance of both the Δrop5 and Δrop18 mutants was reversed in macrophages lacking Irgm3, which is required for IRG function, and the virulence defect was fully restored in Irgm3−/− mice. Our findings establish that the pseudokinase ROP5 controls the activity of ROP18, thereby blocking IRG mediated clearance in macrophages. Additionally, ROP5 has other functions that are also Irgm3 and IFN-γ dependent, indicting it plays a general role in governing virulence factors that block immunity.
机译:分泌型多态丝氨酸/苏氨酸激酶控制着小鼠弓形虫的发病机理。遗传研究表明,假激酶ROP5对于急性毒力必不可少,但没有揭示其作用机理。在这里,我们证明ROP5通过阻止激活的巨噬细胞中的IFN-γ介导的清除来控制毒力。 ROP5是活性S / T激酶ROP18的催化活性所必需的,ROP18可使宿主免疫相关的GTPases(IRGs)磷酸化并保护寄生虫免于清除。 ROP5在体外直接调节ROP18的活性,这两种蛋白都是避免IRG募集和清除巨噬细胞所必需的。在缺少Irgm3的巨噬细胞中,Δrop5和Δrop18突变体的清除率都被逆转了,这是IRG功能所必需的,毒力缺陷在Irgm3 -/-小鼠中得以完全恢复。我们的发现建立了假激酶ROP5控制ROP18的活性,从而阻断了巨噬细胞中IRG介导的清除。此外,ROP5还具有Irgm3和IFN-γ依赖性的其他功能,这表明ROP5在控制阻断免疫力的毒力因子中起一般作用。

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