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The Plasmodium falciparum rhoptry protein RhopH3 plays essential roles in host cell invasion and nutrient uptake

机译:恶性疟原虫rhophory蛋白RhopH3在宿主细胞侵袭和营养吸收中起重要作用

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摘要

Merozoites of the protozoan parasite responsible for the most virulent form of malaria, Plasmodium falciparum, invade erythrocytes. Invasion involves discharge of rhoptries, specialized secretory organelles. Once intracellular, parasites induce increased nutrient uptake by generating new permeability pathways (NPP) including a Plasmodium surface anion channel (PSAC). RhopH1/Clag3, one member of the three-protein RhopH complex, is important for PSAC/NPP activity. However, the roles of the other members of the RhopH complex in PSAC/NPP establishment are unknown and it is unclear whether any of the RhopH proteins play a role in invasion. Here we demonstrate that RhopH3, the smallest component of the complex, is essential for parasite survival. Conditional truncation of RhopH3 substantially reduces invasive capacity. Those mutant parasites that do invade are defective in nutrient import and die. Our results identify a dual role for RhopH3 that links erythrocyte invasion to formation of the PSAC/NPP essential for parasite survival within host erythrocytes.>DOI:
机译:原生动物寄生虫的裂殖子入侵了疟疾的最致命形式,恶性疟原虫侵入红细胞。入侵涉及排泄物,专门的分泌细胞器。进入细胞内后,寄生虫通过产生包括疟原虫表面阴离子通道(PSAC)在内的新的通透性途径(NPP)来诱导增加的养分吸收。 RhopH1 / Clag3是三种蛋白质的RhopH复合物之一,对PSAC / NPP活性很重要。但是,尚不清楚RhopH复合物中其他成员在PSAC / NPP建立中的作用,目前尚不清楚任何RhopH蛋白是否在入侵中发挥作用。在这里,我们证明了RhopH3(复合物的最小成分)对于寄生虫生存至关重要。有条件地截断RhopH3会大大降低侵袭能力。那些确实入侵的突变寄生虫在营养输入和死亡方面存在缺陷。我们的结果确定了RhopH3的双重作用,该作用将红细胞入侵与宿主红细胞内寄生虫生存所必需的PSAC / NPP形成联系起来。> DOI:

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