Functional Characterization of a Novel Class of Morantel-Sensitive Acetylcholine Receptors in Nematodes
Author(s) -
Élise Courtot,
Claude Charvet,
Robin N. Beech,
Abdallah Harmache,
Adrian J. Wolstenholme,
Lindy HoldenDye,
Vincent O’Connor,
Nicolas Peineau,
Debra J. Woods,
Cédric Neveu
Publication year - 2015
Publication title -
plos pathogens
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.719
H-Index - 206
eISSN - 1553-7374
pISSN - 1553-7366
DOI - 10.1371/journal.ppat.1005267
Subject(s) - acetylcholine receptor , receptor , acetylcholine , biology , chemistry , biochemistry , pharmacology
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.
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