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acr-23 Encodes a Monepantel-Sensitive Channel in Caenorhabditis elegans
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 Caen...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738477/ https://www.ncbi.nlm.nih.gov/pubmed/23950710 http://dx.doi.org/10.1371/journal.ppat.1003524 |
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author | Rufener, Lucien Bedoni, Nicola Baur, Roland Rey, Samantha Glauser, Dominique A. Bouvier, Jacques Beech, Robin Sigel, Erwin Puoti, Alessandro |
author_facet | Rufener, Lucien Bedoni, Nicola Baur, Roland Rey, Samantha Glauser, Dominique A. Bouvier, Jacques Beech, Robin Sigel, Erwin Puoti, Alessandro |
author_sort | Rufener, Lucien |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3738477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37384772013-08-15 acr-23 Encodes a Monepantel-Sensitive Channel in Caenorhabditis elegans Rufener, Lucien Bedoni, Nicola Baur, Roland Rey, Samantha Glauser, Dominique A. Bouvier, Jacques Beech, Robin Sigel, Erwin Puoti, Alessandro PLoS Pathog Research Article 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. Public Library of Science 2013-08-08 /pmc/articles/PMC3738477/ /pubmed/23950710 http://dx.doi.org/10.1371/journal.ppat.1003524 Text en © 2013 Rufener et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Rufener, Lucien Bedoni, Nicola Baur, Roland Rey, Samantha Glauser, Dominique A. Bouvier, Jacques Beech, Robin Sigel, Erwin Puoti, Alessandro acr-23 Encodes a Monepantel-Sensitive Channel in Caenorhabditis elegans |
title |
acr-23 Encodes a Monepantel-Sensitive Channel in Caenorhabditis elegans
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title_full |
acr-23 Encodes a Monepantel-Sensitive Channel in Caenorhabditis elegans
|
title_fullStr |
acr-23 Encodes a Monepantel-Sensitive Channel in Caenorhabditis elegans
|
title_full_unstemmed |
acr-23 Encodes a Monepantel-Sensitive Channel in Caenorhabditis elegans
|
title_short |
acr-23 Encodes a Monepantel-Sensitive Channel in Caenorhabditis elegans
|
title_sort | acr-23 encodes a monepantel-sensitive channel in caenorhabditis elegans |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738477/ https://www.ncbi.nlm.nih.gov/pubmed/23950710 http://dx.doi.org/10.1371/journal.ppat.1003524 |
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