Abrahamsen Mitchell S, Templeton Thomas J, Enomoto Shinichiro, Abrahante Juan E, Zhu Guan, Lancto Cheryl A, Deng Mingqi, Liu Chang, Widmer Giovanni, Tzipori Saul, Buck Gregory A, Xu Ping, Bankier Alan T, Dear Paul H, Konfortov Bernard A, Spriggs Helen F, Iyer Lakshminarayan, Anantharaman Vivek, Aravind L, Kapur Vivek
Department of Veterinary and Biomedical Science, College of Veterinary Medicine, University of Minnesota, St. Paul, MN 55108, USA.
Science. 2004 Apr 16;304(5669):441-5. doi: 10.1126/science.1094786. Epub 2004 Mar 25.
The apicomplexan Cryptosporidium parvum is an intestinal parasite that affects healthy humans and animals, and causes an unrelenting infection in immunocompromised individuals such as AIDS patients. We report the complete genome sequence of C. parvum, type II isolate. Genome analysis identifies extremely streamlined metabolic pathways and a reliance on the host for nutrients. In contrast to Plasmodium and Toxoplasma, the parasite lacks an apicoplast and its genome, and possesses a degenerate mitochondrion that has lost its genome. Several novel classes of cell-surface and secreted proteins with a potential role in host interactions and pathogenesis were also detected. Elucidation of the core metabolism, including enzymes with high similarities to bacterial and plant counterparts, opens new avenues for drug development.
顶复门的微小隐孢子虫是一种肠道寄生虫,可感染健康的人类和动物,并在免疫功能低下的个体(如艾滋病患者)中引发持续感染。我们报告了微小隐孢子虫II型分离株的完整基因组序列。基因组分析确定了极其简化的代谢途径以及对宿主营养物质的依赖。与疟原虫和弓形虫不同,该寄生虫缺乏顶质体及其基因组,并且拥有一个已失去基因组的退化线粒体。还检测到几类在宿主相互作用和发病机制中可能起作用的新型细胞表面和分泌蛋白。对核心代谢的阐明,包括与细菌和植物对应酶高度相似的酶,为药物开发开辟了新途径。