Gebru Tamirat, Mordmüller Benjamin, Held Jana
Institute of Tropical Medicine, Eberhard Karls University, Tübingen, Germany German Centre for Infection Research, Partner Site Tübingen, Tübingen, Germany Department of Medical Laboratory Sciences, College of Health and Medical Sciences, Haramaya University, Haramaya, Ethiopia.
Institute of Tropical Medicine, Eberhard Karls University, Tübingen, Germany Centre de Recherches Médicales de Lambaréné, Lambaréné, Gabon German Centre for Infection Research, Partner Site Tübingen, Tübingen, Germany.
Antimicrob Agents Chemother. 2014 Dec;58(12):7398-404. doi: 10.1128/AAC.03772-14. Epub 2014 Sep 29.
Plasmodium falciparum gametocytes are not associated with clinical symptoms, but they are responsible for transmitting the pathogen to mosquitoes. Therefore, gametocytocidal interventions are important for malaria control and resistance containment. Currently available drugs and vaccines are not well suited for that purpose. Several dyes have potent antimicrobial activity, but their use against gametocytes has not been investigated systematically. The gametocytocidal activity of nine synthetic dyes and four control compounds was tested against stage V gametocytes of the laboratory strain 3D7 and three clinical isolates of P. falciparum with a bioluminescence assay. Five of the fluorescent dyes had submicromolar 50% inhibitory concentration (IC50) values against mature gametocytes. Three mitochondrial dyes, MitoRed, dihexyloxacarbocyanine iodide (DiOC6), and rhodamine B, were highly active (IC(50)s < 200 nM). MitoRed showed the highest activity against gametocytes, with IC(50)s of 70 nM against 3D7 and 120 to 210 nM against clinical isolates. All compounds were more active against the laboratory strain 3D7 than against clinical isolates. In particular, the endoperoxides artesunate and dihydroartemisinin showed a 10-fold higher activity against 3D7 than against clinical isolates. In contrast to all clinically used antimalarials, several fluorescent dyes had surprisingly high in vitro activity against late-stage gametocytes. Since they also act against asexual blood stages, they shall be considered starting points for the development of new antimalarial lead compounds.
恶性疟原虫配子体与临床症状无关,但它们负责将病原体传播给蚊子。因此,杀配子体干预措施对于疟疾控制和耐药性遏制至关重要。目前可用的药物和疫苗并不完全适用于此目的。几种染料具有强大的抗菌活性,但它们对配子体的作用尚未得到系统研究。使用生物发光测定法测试了九种合成染料和四种对照化合物对实验室菌株3D7的V期配子体以及恶性疟原虫的三个临床分离株的杀配子体活性。五种荧光染料对成熟配子体的50%抑制浓度(IC50)值在亚微摩尔范围内。三种线粒体染料,MitoRed、二己基氧杂羰花青碘化物(DiOC6)和罗丹明B,具有高活性(IC50<200 nM)。MitoRed对配子体显示出最高活性,对3D7的IC50为70 nM,对临床分离株的IC50为120至210 nM。所有化合物对实验室菌株3D7的活性均高于对临床分离株的活性。特别是,青蒿琥酯和双氢青蒿素这两种过氧化物对3D7的活性比对临床分离株的活性高10倍。与所有临床使用的抗疟药不同,几种荧光染料对晚期配子体具有惊人的高体外活性。由于它们也作用于无性血液阶段,因此应被视为开发新型抗疟先导化合物的起点。