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Microneme Rhomboid Protease TgROM1 Is Required for Efficient Intracellular Growth of Toxoplasma gondii

微核 生物 弓形虫 细胞生物学 菱形 跨膜蛋白 细胞内寄生虫 跨膜结构域 高尔基体 蛋白酵素 细胞内 顶复亚门 遗传学 恶性疟原虫 生物化学 内质网 免疫学 受体 疟疾 抗体
作者
Fabien Brossier,G. Lucas Starnes,Wandy L. Beatty,L. David Sibley
出处
期刊:Eukaryotic Cell [American Society for Microbiology]
卷期号:7 (4): 664-674 被引量:50
标识
DOI:10.1128/ec.00331-07
摘要

Rhomboids are serine proteases that cleave their substrates within the transmembrane domain. Toxoplasma gondii contains six rhomboids that are expressed in different life cycle stages and localized to different cellular compartments. Toxoplasma rhomboid protein 1 (TgROM1) has previously been shown to be active in vitro, and the orthologue in Plasmodium falciparum processes the essential microneme protein AMA1 in a heterologous system. We investigated the role of TgROM1 to determine its role during in vitro growth of T. gondii. TgROM1 was localized in the secretory pathway of the parasite, including the Golgi apparatus and micronemes, which contain adhesive proteins involved in invasion of host cells. However, unlike other micronemal proteins, TgROM1 was not released onto the parasite surface during cell invasion, suggesting it does not play a critical role in cell invasion. Suppression of TgROM1 using the tetracycline-regulatable system revealed that ROM1-deficient parasites were outcompeted by wild-type T. gondii. ROM1-deficient parasites showed only modest decrease in invasion but replicated more slowly than wild-type cells. Collectively, these results indicate that ROM1 is required for efficient intracellular growth by T. gondii.

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