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Luciferase-Based, High-Throughput Assay for Screening and Profiling Transmission-Blocking Compounds against Plasmodium falciparum Gametocytes

机译:基于萤光素酶的高通量分析,用于筛选和分析恶性疟原虫配子细胞的传导阻滞化合物

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摘要

The discovery of new antimalarial drugs able to target both the asexual and gametocyte stages of Plasmodium falciparum is critical to the success of the malaria eradication campaign. We have developed and validated a robust, rapid, and cost-effective high-throughput reporter gene assay to identify compounds active against late-stage (stage IV and V) gametocytes. The assay, which is suitable for testing compound activity at incubation times up to 72 h, demonstrates excellent quality and reproducibility, with average Z′ values of 0.85 ± 0.01. We used the assay to screen more than 10,000 compounds from three chemically diverse libraries. The screening outcomes highlighted the opportunity to use collections of compounds with known activity against the asexual stages of the parasites as a starting point for gametocytocidal activity detection in order to maximize the chances of identifying gametocytocidal compounds. This assay extends the capabilities of our previously reported luciferase assay, which tested compounds against early-stage gametocytes, and opens possibilities to profile the activities of gametocytocidal compounds over the entire course of gametocytogenesis.
机译:发现能够针对恶性疟原虫的无性和配子期阶段的新抗疟药,对于消除疟疾运动的成功至关重要。我们已经开发并验证了一种可靠,快速且具有成本效益的高通量报道基因测定法,以鉴定对晚期(IV和V期)配子细胞具有活性的化合物。该测定法适合在长达72小时的孵育时间测试化合物活性,证明了卓越的质量和可重复性,平均Z'值为0.85±0.01。我们使用该测定法从三个化学不同的文库中筛选了10,000多种化合物。筛选结果突显了机会,可以利用对寄生虫无性阶段具有已知活性的化合物收集物作为杀灭杀虫剂活性检测的起点,以最大程度地确定杀灭杀虫剂化合物的机会。该测定法扩展了我们先前报道的萤光素酶测定法的功能,该方法测试了化合物对抗早期配子细胞的作用,并开辟了在整个配子生成过程中对杀线菌剂化合物的活性进行分析的可能性。

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