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恶性疟原虫感染中极低寄生虫密度下配子体生成的起始

Initiation of gametocytogenesis at very low parasite density in Plasmodium falciparum infection.

作者信息

Farid Ryan, Dixon Matthew W, Tilley Leann, McCarthy James S

机构信息

QIMR Berghofer Medical Research Institute and University of Queensland, Brisbane, Australia; and.

Department of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute, University of Melbourne, Victoria, Australia.

出版信息

J Infect Dis. 2017 Apr 1;215(7):1167-1174. doi: 10.1093/infdis/jix035.

Abstract

The recent focus on the elimination of malaria has led to an increased interest in the role of sexual stages in its transmission. We introduce Plasmodium falciparum gametocyte exported protein-5 (PfGEXP5) transcript analysis as an important tool for evaluating the earliest (ring) stage sexual gametocytes in the blood of infected individuals. We show that gametocyte rings are detected in the peripheral blood immediately following establishment of asexual infections-without the need for triggers such as high-density asexual parasitemia or drug treatment. Committed gametocytes are refractory to the commonly used drug piperaquine, and mature gametocytes reappear in the bloodstream 10 days after the initial appearance of gametocyte rings. A further wave of commitment is observed following recrudescent asexual parasitemia, and these gametocytes are again refractory to piperaquine treatment. This work has implications for monitoring gametocyte and transmission dynamics and responses to drug treatment.

摘要

近期对疟疾消除的关注引发了人们对疟原虫有性阶段在传播中作用的更多兴趣。我们引入恶性疟原虫配子体输出蛋白5(PfGEXP5)转录本分析,作为评估受感染个体血液中最早(环状)阶段有性配子体的重要工具。我们发现,无性感染建立后,外周血中立即就能检测到配子体环状体,无需诸如高密度无性疟原虫血症或药物治疗等触发因素。已确定的配子体对常用药物哌喹具有抗性,成熟配子体在配子体环状体首次出现10天后重新出现在血液中。在无性疟原虫血症复发后观察到另一波配子体确定过程,这些配子体同样对哌喹治疗具有抗性。这项工作对监测配子体及传播动态以及药物治疗反应具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cf0/5426372/f5fff34f29b7/jix03501.jpg

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