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Toxoplasma gondii Targets a Protein Phosphatase 2C to the Nuclei of Infected Host Cells

机译:弓形虫将蛋白磷酸酶2C靶向感染宿主细胞的核

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摘要

Intracellular pathogens have evolved a wide array of mechanisms to invade and co-opt their host cells for intracellular survival. Apicomplexan parasites such as Toxoplasma gondii employ the action of unique secretory organelles named rhoptries for internalization of the parasite and formation of a specialized niche within the host cell. We demonstrate that Toxoplasma gondii also uses secretion from the rhoptries during invasion to deliver a parasite-derived protein phosphatase 2C (PP2C-hn) into the host cell and direct it to the host nucleus. Delivery to the host nucleus does not require completion of invasion, as evidenced by the fact that parasites blocked in the initial stages of invasion with cytochalasin D are able to target PP2C-hn to the host nucleus. We have disrupted the gene encoding PP2C-hn and shown that PP2C-hn-knockout parasites exhibit a mild growth defect that can be rescued by complementation with the wild-type gene. The delivery of parasite effector proteins via the rhoptries provides a novel mechanism for Toxoplasma to directly access the command center of its host cell during infection by the parasite.
机译:细胞内病原体已经进化出多种机制来入侵并共同选择其宿主细胞进行细胞内存活。蚜虫寄生虫(例如弓形虫)利用称为rhoptries的独特分泌细胞器作用,将寄生虫内在化并在宿主细胞内形成专门的生态位。我们证明弓形虫也使用入侵期间从rhoptries的分泌物,将寄生虫来源的蛋白磷酸酶2C(PP2C-hn)传递到宿主细胞中,并将其定向到宿主细胞核。递送到宿主核不需要入侵的完成,这一事实证明,在细胞松弛素D侵袭初期被阻断的寄生虫能够将PP2C-hn靶向宿主核。我们已经破坏了编码PP2C-hn的基因,并显示PP2C-hn敲除寄生虫表现出轻度的生长缺陷,可以通过与野生型基因互补来挽救。寄生虫效应蛋白通过杂种的传递为弓形虫在被寄生虫感染期间直接进入其宿主细胞的指挥中心提供了新的机制。

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