Department of Molecular Microbiology, Washington University School of Medicine, St Louis, Missouri, United States of America.
PLoS Pathog. 2012;8(11):e1002992. doi: 10.1371/journal.ppat.1002992. Epub 2012 Nov 8.
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.
分泌多态丝氨酸/苏氨酸激酶控制弓形虫在小鼠中的发病机制。遗传研究表明,拟激酶 ROP5 对于急性毒力是必需的,但并未揭示其作用机制。本文作者证明 ROP5 通过阻断激活的巨噬细胞中 IFN-γ 介导的清除作用来控制毒力。ROP5 对于活性 S/T 激酶 ROP18 的催化活性是必需的,ROP18 磷酸化宿主免疫相关 GTP 酶(IRG)并保护寄生虫免受清除。ROP5 在体外直接调节 ROP18 的活性,并且这两种蛋白对于避免巨噬细胞中 IRG 的募集和清除都是必需的。在缺乏 Irgm3 的巨噬细胞中,Δrop5 和 Δrop18 突变体的清除作用被逆转,而 Irgm3 是 IRG 功能所必需的,在 Irgm3(-/-) 小鼠中,毒力缺陷得到完全恢复。这些发现确立了拟激酶 ROP5 控制 ROP18 的活性,从而阻断了巨噬细胞中 IRG 介导的清除作用。此外,ROP5 还具有其他功能,这些功能也依赖于 Irgm3 和 IFN-γ,表明它在调节阻断免疫的毒力因子方面发挥着一般作用。