Courtot Elise, Charvet Claude L, Beech Robin N, Harmache Abdallah, Wolstenholme Adrian J, Holden-Dye Lindy, O'Connor Vincent, Peineau Nicolas, Woods Debra J, Neveu Cedric
INRA, UMR1282 Infectiologie et Santé Publique, Nouzilly, France.
Université de François Rabelais de Tours, UMR1282 Infectiologie et Santé Publique, Tours, France.
PLoS Pathog. 2015 Dec 1;11(12):e1005267. doi: 10.1371/journal.ppat.1005267. eCollection 2015 Dec.
Acetylcholine receptors are pentameric ligand-gated channels involved in excitatory neuro-transmission in both vertebrates and invertebrates. In nematodes, they represent major targets for cholinergic agonist or antagonist anthelmintic drugs. Despite the large diversity of acetylcholine-receptor subunit genes present in nematodes, only a few receptor subtypes have been characterized so far. Interestingly, parasitic nematodes affecting human or animal health possess two closely related members of this gene family, acr-26 and acr-27 that are essentially absent in free-living or plant parasitic species. Using the pathogenic parasitic nematode of ruminants, Haemonchus contortus, as a model, we found that Hco-ACR-26 and Hco-ACR-27 are co-expressed in body muscle cells. We demonstrated that co-expression of Hco-ACR-26 and Hco-ACR-27 in Xenopus laevis oocytes led to the functional expression of an acetylcholine-receptor highly sensitive to the anthelmintics morantel and pyrantel. Importantly we also reported that ACR-26 and ACR-27, from the distantly related parasitic nematode of horses, Parascaris equorum, also formed a functional acetylcholine-receptor highly sensitive to these two drugs. In Caenorhabditis elegans, a free-living model nematode, we demonstrated that heterologous expression of the H. contortus and P. equorum receptors drastically increased its sensitivity to morantel and pyrantel, mirroring the pharmacological properties observed in Xenopus oocytes. Our results are the first to describe significant molecular determinants of a novel class of nematode body wall muscle AChR.
乙酰胆碱受体是五聚体配体门控通道,参与脊椎动物和无脊椎动物的兴奋性神经传递。在 nematodes 中,它们是胆碱能激动剂或拮抗剂驱虫药物的主要靶点。尽管 nematodes 中存在大量不同的乙酰胆碱受体亚基基因,但到目前为止,只有少数受体亚型得到了表征。有趣的是,影响人类或动物健康的寄生 nematodes 拥有该基因家族的两个密切相关成员,acr - 26 和 acr - 27,而在自由生活或植物寄生物种中基本不存在。以反刍动物的致病性寄生 nematode捻转血矛线虫为模型,我们发现Hco - ACR - 26和Hco - ACR - 27在体肌细胞中共同表达。我们证明,Hco - ACR - 26和Hco - ACR - 27在非洲爪蟾卵母细胞中的共同表达导致了对驱虫药莫仑太尔和噻嘧啶高度敏感的乙酰胆碱受体的功能性表达。重要的是,我们还报告说,来自远缘相关的马寄生线虫马副蛔虫的ACR - 26和ACR - 27也形成了对这两种药物高度敏感的功能性乙酰胆碱受体。在自由生活的模式线虫秀丽隐杆线虫中,我们证明了捻转血矛线虫和马副蛔虫受体的异源表达极大地增加了其对莫仑太尔和噻嘧啶的敏感性,这反映了在非洲爪蟾卵母细胞中观察到的药理学特性。我们的结果首次描述了一类新型线虫体壁肌肉AChR的重要分子决定因素。