恶性疟原虫和动质体科无性期己糖转运

S. Krishna , C.J. Woodrow , R.J.S. Burchmore , K.J. Saliba , K. Kirk
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引用次数: 41

摘要

己糖葡萄糖是大多数生物体的重要能量来源,也是恶性疟原虫无性阶段的必需营养物。着丝质体生物(如锥虫和利什曼原虫)在其生命周期的某些关键阶段也需要葡萄糖。尽管在系统发育上不相关,但这些生物在寄生生命周期的哺乳动物阶段有许多共同的挑战,并且具有可以使用类似方法研究的己糖摄取机制。确定己糖进入寄生虫的途径可能会暴露出一个阿喀琉斯之踵,这是抗疾病和抗寄生虫措施都可以瞄准的。了解葡萄糖的进入模式也为多室系统的底物获取提供了一个很好的通用模型。在这篇综述中,Sanjeev Krishna及其同事总结了目前对恶性疟原虫己糖转运过程的理解,并提供了与着丝质体获得的数据的比较。
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Hexose Transport in Asexual Stages of Plasmodium falciparum and Kinetoplastidae

The hexose sugar, glucose, is a vital energy source for most organisms and an essential nutrient for asexual stages of Plasmodium falciparum. Kinetoplastid organisms (e.g. Trypanosoma and Leishmania spp) also require glucose at certain critical stages of their life cycles. Although phylogenetically unrelated, these organisms share many common challenges during the mammalian stages of a parasitic life cycle, and possess hexose uptake mechanisms that are amenable to study using similar methods. Defining hexose permeation pathways into parasites might expose an Achilles’ heel at which both antidisease and antiparasite measures can be aimed. Understanding the mode of entry of glucose also presents a good general model for substrate acquisition in multicompartment systems. In this review, Sanjeev Krishna and colleagues summarize current understanding of hexose transport processes in P. falciparum and provide a comparison with data obtained from kinetoplastids.

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Websites of interest Neosporosis. Seeking new targets for antiparasitic agents Response from A. Serero et al. Parasitology nomenclature – a recommendation Implications for neonatal HIV/AIDS and TB of sensitization in utero to helminths
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