Department of Medical Microbiology, Radboudumc Center for Infectious Diseases, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, Netherlands.
Faculty of Veterinary Medicine, Experimental Parasitology, Ludwig Maximilian University, Munich, Germany.
mBio. 2021 Aug 31;12(4):e0140921. doi: 10.1128/mBio.01409-21. Epub 2021 Aug 24.
Apicomplexan parasites, such as Toxoplasma gondii and Plasmodium falciparum, are the cause of many important human and animal diseases. While T. gondii tachyzoites replicate through endodyogeny, during which two daughter cells are formed within the parental cell, P. falciparum replicates through schizogony, where up to 32 parasites are formed in a single infected red blood cell and even thousands of daughter cells during mosquito- or liver-stage development. These processes require a tightly orchestrated division and distribution over the daughter parasites of one-per-cell organelles such as the mitochondrion and apicoplast. Although proper organelle segregation is highly essential, the molecular mechanism and the key proteins involved remain largely unknown. In this review, we describe organelle dynamics during cell division in T. gondii and P. falciparum, summarize the current understanding of the molecular mechanisms underlying organelle fission in these parasites, and introduce candidate fission proteins.
顶复门寄生虫,如刚地弓形虫和疟原虫,是许多重要的人类和动物疾病的病原体。刚地弓形虫速殖子通过内二分裂进行复制,在此过程中,两个子细胞在亲代细胞内形成,而疟原虫通过裂殖生殖进行复制,在单个受感染的红细胞中可形成多达 32 个寄生虫,在蚊媒或肝期发育过程中甚至可形成数千个子细胞。这些过程需要对一个细胞中的细胞器(如线粒体和顶质体)进行精细的分裂和分配给子虫体。尽管适当的细胞器分离是非常必要的,但分子机制和涉及的关键蛋白仍知之甚少。在这篇综述中,我们描述了刚地弓形虫和疟原虫细胞分裂过程中的细胞器动态,总结了目前对这些寄生虫中细胞器分裂分子机制的理解,并介绍了候选分裂蛋白。