Institut Pasteur, Biologie et Génétique du Paludisme, 75724 Paris, France.
Mol Microbiol. 2011 Sep;81(5):1343-57. doi: 10.1111/j.1365-2958.2011.07767.x. Epub 2011 Aug 4.
Transmission of Plasmodium species from a mammalian host to the mosquito vector requires the uptake, during an infected blood meal, of gametocytes, the precursor cells of the gametes. Relatively little is known about the molecular mechanisms involved in the developmental switch from asexual development to sexual differentiation or the maturation and survival of gametocytes. Here, we show that a gene coding for a novel putative transporter, NPT1, plays a crucial role in the development of Plasmodium berghei gametocytes. Parasites lacking NPT1 are severely compromised in the production of gametocytes and the rare gametocytes produced are unable to differentiate into fertile gametes. This is the earliest block in gametocytogenesis obtained by reverse genetics and the first to demonstrate the role of a protein with a putative transport function in sexual development. These results and the high degree of conservation of NPT1 in Plasmodium species suggest that this protein could be an attractive target for the development of novel drugs to block the spread of malaria.
从哺乳动物宿主向蚊子传播媒介传播疟原虫物种需要在受感染的血液餐中摄取配子体,配子体是配子的前体细胞。关于涉及从无性发育到性分化的发育开关的分子机制或配子体的成熟和存活的相对了解甚少。在这里,我们表明编码新型假定转运蛋白 NPT1 的基因在疟原虫伯氏疟原虫配子体的发育中起着至关重要的作用。缺乏 NPT1 的寄生虫在配子体的产生中受到严重损害,并且产生的罕见配子体无法分化为可育配子。这是通过反向遗传学获得的配子发生的最早阻断,也是首次证明具有推定运输功能的蛋白质在性发育中的作用。这些结果以及 NPT1 在疟原虫物种中的高度保守性表明,该蛋白可能是开发新型药物以阻止疟疾传播的有吸引力的靶标。