Rohr Claudia M, Park Sang-Kyu, Aguiar-Martins Kelsilandia, Anderson Timothy J C, Berger Duncan J, Berriman Matthew, Buddenborg Sarah K, Bustinduy Amaya L, Chevalier Frédéric D, Cotton James A, Crellen Thomas, Doyle Stephen R, Emery Aidan M, Smith Julien Kincaid, Kinung'hi Safari, Lamberton Poppy H L, Le Clec'h Winka, Ndombi Eric, Pennance Tom, Rowel Candia, Summers Shannan S, Tushabe John Vianney, Walker Martin, Webster Bonnie L, Webster Joanne P, Wilson Shona, Marchant Jonathan S
Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, WI, USA.
Department of Pathobiology and Population Sciences, Royal Veterinary College, University of London, Herts, UK.
bioRxiv. 2025 Aug 27:2025.08.27.671753. doi: 10.1101/2025.08.27.671753.
The anthelmintic praziquantel (PZQ) has been used for decades as the clinical therapy for schistosomiasis, and remains the only available drug. As a cheap and effective drug therapy for all human disease-causing species, usage of PZQ underpins mass drug administration strategies aimed at eliminating schistosomiasis as a public health problem by 2030. Concern over the potential emergence of resistance to PZQ is therefore warranted, as it would constitute a major threat to this approach. In terms of molecular adaptations conferring PZQ resistance, variation in the sequence and/or expression of the drug target is an obvious mechanism and should be a priority for surveillance efforts. The target of PZQ is a transient receptor potential ion channel, TRPM, which is established as a locus that regulates schistosome sensitivity to PZQ. Here, we describe the establishment of a community resource, 'TRPtracker', which coalesces data on TRPM natural variants together with measurements of individual variant sensitivity to PZQ. A compendium of laboratory-generated mutants in TRPM is also compiled in TRPtracker to map regions within TRPM critical for PZQ sensitivity. Aggregation of data from multiple research groups into TRPtracker permits rapid community-wide exchange of data, cataloguing which TRPM variants have been functionally profiled, where geographically these variants have been found, their frequency within populations and their potential impact on PZQ sensitivity.
驱虫药吡喹酮(PZQ)已作为血吸虫病的临床治疗药物使用了数十年,并且仍然是唯一可用的药物。作为针对所有人类致病物种的廉价且有效的药物疗法,PZQ的使用是旨在到2030年将血吸虫病作为公共卫生问题消除的群体药物给药策略的基础。因此,对PZQ潜在耐药性出现的担忧是有道理的,因为这将对该方法构成重大威胁。就赋予PZQ耐药性的分子适应性而言,药物靶点序列和/或表达的变化是一种明显的机制,应该是监测工作的重点。PZQ的靶点是一种瞬时受体电位离子通道TRPM,它已被确定为调节血吸虫对PZQ敏感性的位点。在这里,我们描述了一个社区资源“TRPtracker”的建立,它将TRPM自然变异的数据与单个变异对PZQ敏感性的测量结果整合在一起。TRPtracker中还汇编了TRPM实验室生成突变体的简编,以绘制TRPM中对PZQ敏感性至关重要的区域。将多个研究小组的数据汇总到TRPtracker中,可以在社区范围内快速交换数据,编目哪些TRPM变异体已进行功能分析、在哪些地理区域发现了这些变异体、它们在群体中的频率以及它们对PZQ敏感性的潜在影响。