Department of Biomedical Sciences, Iowa State University, Ames, Iowa, United States of America.
Department of Microbiology and Immunology, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York, United States of America.
PLoS Pathog. 2021 Apr 1;17(4):e1009394. doi: 10.1371/journal.ppat.1009394. eCollection 2021 Apr.
Obligate intracellular malaria parasites reside within a vacuolar compartment generated during invasion which is the principal interface between pathogen and host. To subvert their host cell and support their metabolism, these parasites coordinate a range of transport activities at this membrane interface that are critically important to parasite survival and virulence, including nutrient import, waste efflux, effector protein export, and uptake of host cell cytosol. Here, we review our current understanding of the transport mechanisms acting at the malaria parasite vacuole during the blood and liver-stages of development with a particular focus on recent advances in our understanding of effector protein translocation into the host cell by the Plasmodium Translocon of EXported proteins (PTEX) and small molecule transport by the PTEX membrane-spanning pore EXP2. Comparison to Toxoplasma gondii and other related apicomplexans is provided to highlight how similar and divergent mechanisms are employed to fulfill analogous transport activities.
专性内共生疟原虫生活在入侵过程中产生的一种空泡隔室中,该隔室是病原体与宿主之间的主要界面。为了颠覆宿主细胞并支持其代谢,这些寄生虫在这个膜界面上协调一系列运输活动,这些活动对寄生虫的生存和毒力至关重要,包括营养物质的输入、废物的排出、效应蛋白的输出以及宿主细胞质的摄取。在这里,我们回顾了我们目前对疟原虫在血液和肝期发育过程中空泡中运输机制的理解,特别关注了我们对 Plasmodium Translocon of EXported proteins (PTEX) 将效应蛋白转运入宿主细胞以及 EXP2 转运小分子的理解方面的最新进展。与刚地弓形虫和其他相关的顶复门生物进行比较,突出了类似的运输活动是如何采用相似和不同的机制来完成的。