Preston Sarah, Jiao Yaqing, Jabbar Abdul, McGee Sean L, Laleu Benoît, Willis Paul, Wells Timothy N C, Gasser Robin B
Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, Victoria, 3010, Australia.
Metabolic Research Unit, Metabolic Reprogramming Laboratory, School of Medicine, Faculty of Health, Deakin University, Waurn Ponds, Victoria, 3216, Australia.
Int J Parasitol Drugs Drug Resist. 2016 Dec;6(3):329-334. doi: 10.1016/j.ijpddr.2016.07.004. Epub 2016 Jul 28.
There is a substantial need to develop new medicines against parasitic diseases via public-private partnerships. Based on high throughput phenotypic screens of largely protozoal pathogens and bacteria, the Medicines for Malaria Venture (MMV) has recently assembled an open-access 'Pathogen Box' containing 400 well-curated chemical compounds. In the present study, we tested these compounds for activity against parasitic stages of the nematode Haemonchus contortus (barber's pole worm). In an optimised, whole-organism screening assay, using exsheathed third-stage (xL3) and fourth-stage (L4) larvae, we measured the inhibition of larval motility, growth and development of H. contortus. We also studied the effect of the 'hit' compound on mitochondrial function by measuring oxygen consumption. Among the 400 Pathogen Box compounds, we identified one chemical, called tolfenpyrad (compound identification code: MMV688934) that reproducibly inhibits xL3 motility as well as L4 motility, growth and development, with IC values ranging between 0.02 and 3 μM. An assessment of mitochondrial function showed that xL3s treated with tolfenpyrad consumed significantly less oxygen than untreated xL3s, which was consistent with specific inhibition of complex I of the respiratory electron transport chain in arthropods. Given that tolfenpyrad was developed as a pesticide and has already been tested for absorption, distribution, excretion, biotransformation, toxicity and metabolism, it shows considerable promise for hit-to-lead optimisation and/or repurposing for use against H. contortus and other parasitic nematodes. Future work should assess its activity against hookworms and other pathogens that cause neglected tropical diseases.
通过公私合作开发抗寄生虫病新药的需求十分迫切。基于对大量原生动物病原体和细菌的高通量表型筛选,疟疾药物事业(MMV)最近组装了一个开放获取的“病原体盒”,其中包含400种精心挑选的化合物。在本研究中,我们测试了这些化合物对捻转血矛线虫(捻转胃虫)寄生阶段的活性。在一项优化的全生物体筛选试验中,我们使用脱鞘第三期(xL3)和第四期(L4)幼虫,测量了捻转血矛线虫幼虫运动、生长和发育的抑制情况。我们还通过测量氧气消耗研究了“命中”化合物对线粒体功能的影响。在400种病原体盒化合物中,我们鉴定出一种名为唑虫酰胺(化合物识别码:MMV688934)的化学物质,它能可重复地抑制xL3的运动以及L4的运动、生长和发育,IC值在0.02至3μM之间。线粒体功能评估表明,用唑虫酰胺处理的xL3消耗的氧气明显少于未处理的xL3,这与节肢动物呼吸电子传递链复合体I的特异性抑制一致。鉴于唑虫酰胺是作为一种杀虫剂开发的,并且已经进行了吸收、分布、排泄、生物转化、毒性和代谢测试,它在针对捻转血矛线虫和其他寄生线虫的命中到先导优化和/或重新利用方面显示出相当大的前景。未来的工作应该评估其对钩虫和其他导致被忽视热带病的病原体的活性。