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Plasmodium vivax liver stage development and hypnozoite persistence in human liver-chimeric mice

机译:人肝嵌合体小鼠间日疟原虫肝阶段发育和次子体持久性

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摘要

Plasmodium vivax malaria is characterized by periodic relapses of symptomatic blood stage parasite infections likely initiated by activation of dormant liver stage parasites -hypnozoites. The lack of tractable animal models for P. vivax constitutes a severe obstacle to investigate this unique aspect of its biology and to test drug efficacy against liver stages. We show that the FRG KO huHep liver-humanized mice support P. vivax sporozoite infection, development of liver stages, and the formation of small non-replicating hypnozoites. Cellular characterization of P. vivax liver stage development in vivo demonstrates complete maturation into infectious exo-erythrocytic merozoites and continuing persistence of hypnozoites. Primaquine prophylaxis or treatment prevents and eliminates liver stage infection. Thus, the P. vivax/FRG KO huHep mouse infection model constitutes an important new tool to investigate the biology of liver stage development and dormancy and might aid in the discovery of new drugs for the prevention of relapsing malaria.
机译:间日疟原虫疟疾的特征在于有症状的血液阶段寄生虫感染的周期性复发可能是由休眠的肝阶段寄生虫-次生子的活化引起的。间日疟原虫缺乏可处理的动物模型,这是严重的障碍,无法研究其生物学的这一独特方面并测试针对肝脏阶段的药物疗效。我们显示,FRG KO huHep肝脏人源化小鼠支持间日疟原虫子孢子感染,肝脏发育阶段以及小的非复制性次生子的形成。体内间日疟原虫肝阶段发育的细胞特征表明,其完全成熟为感染性外红细胞裂殖子,并且持续存在着次裂殖子。预防或治疗Primaquine可以预防和消除肝阶段感染。因此,间日疟原虫/ FRG KO huHep小鼠感染模型构成了研究肝脏阶段发育和休眠生物学的重要新工具,并可能有助于发现预防复发性疟疾的新药。

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