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一种用于恶性疟原虫成熟配子体的简单且具有预测性的表型高内涵成像分析方法,以鉴定疟疾传播阻断化合物。

A simple and predictive phenotypic High Content Imaging assay for Plasmodium falciparum mature gametocytes to identify malaria transmission blocking compounds.

作者信息

Lucantoni Leonardo, Silvestrini Francesco, Signore Michele, Siciliano Giulia, Eldering Maarten, Dechering Koen J, Avery Vicky M, Alano Pietro

机构信息

Discovery Biology, Eskitis Institute for Drug Discovery, Griffith University, 4111 Nathan, Queensland, Australia.

Dipartimento di Malattie Infettive, Parassitarie ed Immunomediate, Istituto Superiore di Sanità, Viale Regina Elena n. 299, 00161 Roma, Italy.

出版信息

Sci Rep. 2015 Nov 10;5:16414. doi: 10.1038/srep16414.

Abstract

Plasmodium falciparum gametocytes, specifically the mature stages, are the only malaria parasite stage in humans transmissible to the mosquito vector. Anti-malarial drugs capable of killing these forms are considered essential for the eradication of malaria and tools allowing the screening of large compound libraries with high predictive power are needed to identify new candidates. As gametocytes are not a replicative stage it is difficult to apply the same drug screening methods used for asexual stages. Here we propose an assay, based on high content imaging, combining "classic" gametocyte viability readout based on gametocyte counts with a functional viability readout, based on gametocyte activation and the discrimination of the typical gamete spherical morphology. This simple and rapid assay has been miniaturized to a 384-well format using acridine orange staining of wild type P. falciparum 3D7A sexual forms, and was validated by screening reference antimalarial drugs and the MMV Malaria Box. The assay demonstrated excellent robustness and ability to identify quality hits with high likelihood of confirmation of transmission reducing activity in subsequent mosquito membrane feeding assays.

摘要

恶性疟原虫配子体,特别是成熟阶段,是人类疟疾寄生虫中唯一可传播给蚊媒的阶段。能够杀死这些形态的抗疟药物被认为是根除疟疾所必需的,并且需要具有高预测能力的工具来筛选大型化合物库以识别新的候选药物。由于配子体不是复制阶段,因此难以应用用于无性阶段的相同药物筛选方法。在此,我们提出了一种基于高内涵成像的检测方法,将基于配子体计数的“经典”配子体活力读数与基于配子体激活和典型配子球形形态辨别的功能活力读数相结合。这种简单快速的检测方法已使用野生型恶性疟原虫3D7A有性形态的吖啶橙染色小型化为384孔板形式,并通过筛选参考抗疟药物和MMV疟疾盒进行了验证。该检测方法显示出优异的稳健性,并且能够识别在随后的蚊媒膜饲试验中极有可能确认具有传播减少活性的优质命中物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ae9/4639769/7d86bf7c55ca/srep16414-f1.jpg

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