Bechtsi D P, Waters A P
Institute of Infection, Immunity and Inflammation, College of Medical Veterinary & Life Sciences, Sir Graham Davies Building, University of Glasgow, 120 University Place, Glasgow, G12 8TA Scotland, UK.
Institute of Infection, Immunity and Inflammation, College of Medical Veterinary & Life Sciences, Sir Graham Davies Building, University of Glasgow, 120 University Place, Glasgow, G12 8TA Scotland, UK.
Int J Parasitol. 2017 Jun;47(7):425-434. doi: 10.1016/j.ijpara.2017.03.002. Epub 2017 Apr 26.
Malaria is the disease caused by the apicomplexan parasites belonging to the genus Plasmodium. Expanding our arsenal to include transmission-blocking agents in our fight against malaria is becoming increasingly important. Such an implementation requires detailed understanding of the biology of the Plasmodium life cycle stages that are transmissible. Plasmodium gametocytes are the only parasite stage that can be transmitted to the mosquito vector and are the product of sexual development in a small percentage of parasites that continually proliferate in host blood. The critical decision made by asexual erythrocytic stages to cease further proliferation and differentiate into gametocytes, as well as the first steps they take into maturity, have long remained unknown. Recent studies have contributed to a breakthrough in our understanding of this branch point in development. In this review, we will discuss the findings that have allowed us to make this major leap forward in our knowledge of sexual commitment in Plasmodium. We will further propose a model for the mechanism triggering the switch to sexual development, constructed around the proteins currently known to regulate this process. Further insight into sexual commitment and gametocyte development will help identify targets for the development of transmission-blocking malaria therapies.
疟疾是由属于疟原虫属的顶复门寄生虫引起的疾病。在抗击疟疾的斗争中,扩充我们的武器库以纳入传播阻断剂正变得越来越重要。这样的实施需要详细了解疟原虫生命周期中可传播阶段的生物学特性。疟原虫配子体是唯一可传播给蚊媒的寄生虫阶段,是一小部分在宿主血液中持续增殖的寄生虫进行有性发育的产物。无性红细胞阶段做出停止进一步增殖并分化为配子体的关键决定,以及它们走向成熟的最初步骤,长期以来一直不为人知。最近的研究为我们对这一发育分支点的理解带来了突破。在这篇综述中,我们将讨论那些使我们在疟原虫有性发育知识方面取得这一重大进展的研究发现。我们还将围绕目前已知调控这一过程的蛋白质构建一个触发向有性发育转变机制的模型。对有性发育和配子体发育的进一步深入了解将有助于确定传播阻断性疟疾疗法的开发靶点。