期刊论文详细信息
PLoS Pathogens
acr-23 Encodes a Monepantel-Sensitive Channel in Caenorhabditis elegans
Dominique A. Glauser1  Roland Baur1  Jacques Bouvier1  Samantha Rey2  Alessandro Puoti2  Nicola Bedoni3  Erwin Sigel3  Robin Beech4  Lucien Rufener4 
[1] Department of Biology, University of Fribourg, Fribourg, Switzerland;Institute for Biochemistry and Molecular Medicine, University of Bern, Bern, Switzerland;Institute of Parasitology, Macdonald College, McGill University, Ste Anne de Bellevue, Quebec, Canada;Novartis Centre de Recherche Santé Animale, St. Aubin, Switzerland
关键词: Cholines;    Caenorhabditis elegans;    Xenopus oocytes;    Nicotinic acetylcholine receptors;    Embryos;    Polymerase chain reaction;    Acetylcholine;    Transgenic engineering;   
DOI  :  10.1371/journal.ppat.1003524
学科分类:生物科学(综合)
来源: Public Library of Science
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【 摘 要 】

Monepantel is a member of the recently identified class of anthelmintics known as the amino-acetonitrile derivatives (AADs). Monepantel controls all major gastro-intestinal nematodes in sheep including those that are resistant to the classical anthelmintics. Previous studies have shown that the Caenorhabditis elegans acr-23 and the Haemonchus contortus Hco-mptl-1 genes may be prominent targets of monepantel. With this discovery it became possible to investigate the mode of action of monepantel in nematodes at the molecular level. In the present study, we show that a C. elegans mutant acr-23 strain is fully rescued by expressing the wild-type acr-23 gene. Moreover, we present a new mutant allele, and characterize acr-23 alleles genetically. We also show that acr-23 is expressed in body wall muscle cells, and provide therefore a possible explanation for the paralysis caused by monepantel. Furthermore, genetic evidence suggests that the chaperone RIC-3 is required for expression of full monepantel resistance. Finally, we present reconstitution of the C. elegans ACR-23 receptor in Xenopus laevis oocytes and provide direct evidence of its modulation by monepantel. Conversely, co-injection of the chaperone RIC-3 had no impact for channel reconstitution in X. laevis oocytes. These results reinforce the involvement of the ACR-23 family in the mode of action of monepantel and advance our understanding of this new class of anthelmintics.

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