The narrow-spectrum anthelmintic oxantel is a potent agonist of a novel acetylcholine receptor subtype in whipworms
In the absence of efficient alternative strategies, the control of parasitic nematodes, impacting human and animal health, mainly relies on the use of broad-spectrum anthelmintic compounds. Unfortunately, most of these drugs have a limited single-dose efficacy against infections caused by the whipwo...
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description | In the absence of efficient alternative strategies, the control of parasitic nematodes, impacting human and animal health, mainly relies on the use of broad-spectrum anthelmintic compounds. Unfortunately, most of these drugs have a limited single-dose efficacy against infections caused by the whipworm, Trichuris. These infections are of both human and veterinary importance. However, in contrast to a wide range of parasitic nematode species, the narrow-spectrum anthelmintic oxantel has a high efficacy on Trichuris spp. Despite this knowledge, the molecular target(s) of oxantel within Trichuris is still unknown. In the distantly related pig roundworm, Ascaris suum, oxantel has a small, but significant effect on the recombinant homomeric Nicotine-sensitive ionotropic acetylcholine receptor (N-AChR) made up of five ACR-16 subunits. Therefore, we hypothesized that in whipworms, a putative homolog of an ACR-16 subunit, can form a functional oxantel-sensitive receptor. Using the pig whipworm T. suis as a model, we identified and cloned a novel ACR-16-like subunit and successfully expressed the corresponding homomeric channel in Xenopus laevis oocytes. Electrophysiological experiments revealed this receptor to have distinctive pharmacological properties with oxantel acting as a full agonist, hence we refer to the receptor as an O-AChR subtype. Pyrantel activated this novel O-AChR subtype moderately, whereas classic nicotinic agonists surprisingly resulted in only minor responses. We observed that the expression of the ACR-16-like subunit in the free-living nematode Caenorhabditis elegans conferred an increased sensitivity to oxantel of recombinant worms. We demonstrated that the novel Tsu-ACR-16-like receptor is indeed a target for oxantel, although other receptors may be involved. These finding brings new insight into the understanding of the high sensitivity of whipworms to oxantel, and highlights the importance of the discovery of additional distinct receptor subunit types within Trichuris that can be used as screening tools to evaluate the effect of new synthetic or natural anthelmintic compounds. |
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Unfortunately, most of these drugs have a limited single-dose efficacy against infections caused by the whipworm, Trichuris. These infections are of both human and veterinary importance. However, in contrast to a wide range of parasitic nematode species, the narrow-spectrum anthelmintic oxantel has a high efficacy on Trichuris spp. Despite this knowledge, the molecular target(s) of oxantel within Trichuris is still unknown. In the distantly related pig roundworm, Ascaris suum, oxantel has a small, but significant effect on the recombinant homomeric Nicotine-sensitive ionotropic acetylcholine receptor (N-AChR) made up of five ACR-16 subunits. Therefore, we hypothesized that in whipworms, a putative homolog of an ACR-16 subunit, can form a functional oxantel-sensitive receptor. Using the pig whipworm T. suis as a model, we identified and cloned a novel ACR-16-like subunit and successfully expressed the corresponding homomeric channel in Xenopus laevis oocytes. Electrophysiological experiments revealed this receptor to have distinctive pharmacological properties with oxantel acting as a full agonist, hence we refer to the receptor as an O-AChR subtype. Pyrantel activated this novel O-AChR subtype moderately, whereas classic nicotinic agonists surprisingly resulted in only minor responses. We observed that the expression of the ACR-16-like subunit in the free-living nematode Caenorhabditis elegans conferred an increased sensitivity to oxantel of recombinant worms. We demonstrated that the novel Tsu-ACR-16-like receptor is indeed a target for oxantel, although other receptors may be involved. These finding brings new insight into the understanding of the high sensitivity of whipworms to oxantel, and highlights the importance of the discovery of additional distinct receptor subunit types within Trichuris that can be used as screening tools to evaluate the effect of new synthetic or natural anthelmintic compounds.</description><identifier>ISSN: 1553-7374</identifier><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1008982</identifier><identifier>PMID: 33544769</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acetylcholine receptors ; Albendazole ; Amino acids ; Animals ; Anthelmintic agents ; Antinematodal Agents - pharmacology ; Antiparasitic agents ; Biology and Life Sciences ; Caenorhabditis elegans - drug effects ; Cloning ; Female ; Gametocytes ; Helminth Proteins - antagonists & inhibitors ; Helminth Proteins - classification ; Helminth Proteins - metabolism ; Human health and pathology ; Infectious diseases ; Isoforms ; Life Sciences ; Livestock ; Male ; Medicine and Health Sciences ; Microbiology and Parasitology ; Nematodes ; Oocytes ; Parasites ; Parasitology ; Peptides ; Pharmaceutical sciences ; Pharmacology ; Phylogenetics ; Proteins ; Pyrantel - analogs & derivatives ; Pyrantel - pharmacology ; Receptors ; Receptors, Cholinergic - chemistry ; Receptors, Cholinergic - classification ; Receptors, Cholinergic - metabolism ; Research and Analysis Methods ; Swine ; Trichuriasis - drug therapy ; Trichuriasis - metabolism ; Trichuriasis - parasitology ; Trichuris - drug effects ; Worms ; Xenopus laevis ; Xenopus laevis - metabolism</subject><ispartof>PLoS pathogens, 2021-02, Vol.17 (2), p.e1008982-e1008982</ispartof><rights>2021 Hansen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Unfortunately, most of these drugs have a limited single-dose efficacy against infections caused by the whipworm, Trichuris. These infections are of both human and veterinary importance. However, in contrast to a wide range of parasitic nematode species, the narrow-spectrum anthelmintic oxantel has a high efficacy on Trichuris spp. Despite this knowledge, the molecular target(s) of oxantel within Trichuris is still unknown. In the distantly related pig roundworm, Ascaris suum, oxantel has a small, but significant effect on the recombinant homomeric Nicotine-sensitive ionotropic acetylcholine receptor (N-AChR) made up of five ACR-16 subunits. Therefore, we hypothesized that in whipworms, a putative homolog of an ACR-16 subunit, can form a functional oxantel-sensitive receptor. Using the pig whipworm T. suis as a model, we identified and cloned a novel ACR-16-like subunit and successfully expressed the corresponding homomeric channel in Xenopus laevis oocytes. Electrophysiological experiments revealed this receptor to have distinctive pharmacological properties with oxantel acting as a full agonist, hence we refer to the receptor as an O-AChR subtype. Pyrantel activated this novel O-AChR subtype moderately, whereas classic nicotinic agonists surprisingly resulted in only minor responses. We observed that the expression of the ACR-16-like subunit in the free-living nematode Caenorhabditis elegans conferred an increased sensitivity to oxantel of recombinant worms. We demonstrated that the novel Tsu-ACR-16-like receptor is indeed a target for oxantel, although other receptors may be involved. These finding brings new insight into the understanding of the high sensitivity of whipworms to oxantel, and highlights the importance of the discovery of additional distinct receptor subunit types within Trichuris that can be used as screening tools to evaluate the effect of new synthetic or natural anthelmintic compounds.</description><subject>Acetylcholine receptors</subject><subject>Albendazole</subject><subject>Amino acids</subject><subject>Animals</subject><subject>Anthelmintic agents</subject><subject>Antinematodal Agents - pharmacology</subject><subject>Antiparasitic agents</subject><subject>Biology and Life Sciences</subject><subject>Caenorhabditis elegans - drug effects</subject><subject>Cloning</subject><subject>Female</subject><subject>Gametocytes</subject><subject>Helminth Proteins - antagonists & inhibitors</subject><subject>Helminth Proteins - classification</subject><subject>Helminth Proteins - metabolism</subject><subject>Human health and pathology</subject><subject>Infectious diseases</subject><subject>Isoforms</subject><subject>Life Sciences</subject><subject>Livestock</subject><subject>Male</subject><subject>Medicine and Health Sciences</subject><subject>Microbiology and Parasitology</subject><subject>Nematodes</subject><subject>Oocytes</subject><subject>Parasites</subject><subject>Parasitology</subject><subject>Peptides</subject><subject>Pharmaceutical sciences</subject><subject>Pharmacology</subject><subject>Phylogenetics</subject><subject>Proteins</subject><subject>Pyrantel - analogs & derivatives</subject><subject>Pyrantel - pharmacology</subject><subject>Receptors</subject><subject>Receptors, Cholinergic - chemistry</subject><subject>Receptors, Cholinergic - classification</subject><subject>Receptors, Cholinergic - metabolism</subject><subject>Research and Analysis Methods</subject><subject>Swine</subject><subject>Trichuriasis - drug therapy</subject><subject>Trichuriasis - metabolism</subject><subject>Trichuriasis - parasitology</subject><subject>Trichuris - drug effects</subject><subject>Worms</subject><subject>Xenopus laevis</subject><subject>Xenopus laevis - metabolism</subject><issn>1553-7374</issn><issn>1553-7366</issn><issn>1553-7374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNptUsFu1DAUjBCIlsIfILDEBQ672GvHdi6VqgpopZW4lLPlJM8brxI72M4u-_d42bRqK062n2fmvTeaonhP8JJQQb5u_RSc7pfjqNOSYCwruXpRnJOypAtBBXv56H5WvIlxizEjlPDXxRmlJWOCV-dFvOsAOR2C3y_iCE0K04C0Sx30g3XJNsj_yU_okY1Io9EncAnpjXc2JuRNrjm_y9-6gXTom8731gEK0MCYfEBxqtNhBGQd2nd23PswxLfFK6P7CO_m86L49f3b3fXNYv3zx-311XrRlBynhWHCVHVFWyCYCGIYlC1UXNSlqUUpW2mqigJpGyM5qTXFteAM17Bqa82NwfSi-HjSHXsf1exXVKsSEylXDNOMuD0hWq-3agx20OGgvLbqX8GHjdIhm9CD4oauuGSUccOZJExS0YLUomKU0toctS7nblM9QNtkn4Lun4g-_XG2Uxu_U0JWeb3juF9OAt0z2s3VWh1rmOa2JZc7krGf52bB_54gJjXY2EDfawd-yjsyKUhZMVJl6Kdn0P87wU6oJvgYA5iHCQhWx7zds9Qxb2rOW6Z9eLz0A-k-YPQvhY7VOw</recordid><startdate>20210201</startdate><enddate>20210201</enddate><creator>Hansen, Tina V A</creator><creator>Cirera, Susanna</creator><creator>Neveu, Cédric</creator><creator>Courtot, Elise</creator><creator>Charvet, Claude L</creator><creator>Calloe, Kirstine</creator><creator>Klaerke, Dan A</creator><creator>Martin, Richard J</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-2744-3093</orcidid><orcidid>https://orcid.org/0000-0001-8105-1579</orcidid><orcidid>https://orcid.org/0000-0002-0596-6598</orcidid><orcidid>https://orcid.org/0000-0002-1777-7938</orcidid><orcidid>https://orcid.org/0000-0003-4314-1850</orcidid><orcidid>https://orcid.org/0000-0003-0937-6218</orcidid></search><sort><creationdate>20210201</creationdate><title>The narrow-spectrum anthelmintic oxantel is a potent agonist of a novel acetylcholine receptor subtype in whipworms</title><author>Hansen, Tina V A ; Cirera, Susanna ; Neveu, Cédric ; Courtot, Elise ; Charvet, Claude L ; Calloe, Kirstine ; Klaerke, Dan A ; Martin, Richard J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c560t-f47f9b93de10171f4e5de967b5fb758d8f993e1dcf861ba30b7640be2dba6ff03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acetylcholine receptors</topic><topic>Albendazole</topic><topic>Amino acids</topic><topic>Animals</topic><topic>Anthelmintic agents</topic><topic>Antinematodal Agents - 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Unfortunately, most of these drugs have a limited single-dose efficacy against infections caused by the whipworm, Trichuris. These infections are of both human and veterinary importance. However, in contrast to a wide range of parasitic nematode species, the narrow-spectrum anthelmintic oxantel has a high efficacy on Trichuris spp. Despite this knowledge, the molecular target(s) of oxantel within Trichuris is still unknown. In the distantly related pig roundworm, Ascaris suum, oxantel has a small, but significant effect on the recombinant homomeric Nicotine-sensitive ionotropic acetylcholine receptor (N-AChR) made up of five ACR-16 subunits. Therefore, we hypothesized that in whipworms, a putative homolog of an ACR-16 subunit, can form a functional oxantel-sensitive receptor. Using the pig whipworm T. suis as a model, we identified and cloned a novel ACR-16-like subunit and successfully expressed the corresponding homomeric channel in Xenopus laevis oocytes. Electrophysiological experiments revealed this receptor to have distinctive pharmacological properties with oxantel acting as a full agonist, hence we refer to the receptor as an O-AChR subtype. Pyrantel activated this novel O-AChR subtype moderately, whereas classic nicotinic agonists surprisingly resulted in only minor responses. We observed that the expression of the ACR-16-like subunit in the free-living nematode Caenorhabditis elegans conferred an increased sensitivity to oxantel of recombinant worms. We demonstrated that the novel Tsu-ACR-16-like receptor is indeed a target for oxantel, although other receptors may be involved. These finding brings new insight into the understanding of the high sensitivity of whipworms to oxantel, and highlights the importance of the discovery of additional distinct receptor subunit types within Trichuris that can be used as screening tools to evaluate the effect of new synthetic or natural anthelmintic compounds.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>33544769</pmid><doi>10.1371/journal.ppat.1008982</doi><orcidid>https://orcid.org/0000-0002-2744-3093</orcidid><orcidid>https://orcid.org/0000-0001-8105-1579</orcidid><orcidid>https://orcid.org/0000-0002-0596-6598</orcidid><orcidid>https://orcid.org/0000-0002-1777-7938</orcidid><orcidid>https://orcid.org/0000-0003-4314-1850</orcidid><orcidid>https://orcid.org/0000-0003-0937-6218</orcidid><oa>free_for_read</oa></addata></record> |
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source | Public Library of Science (PLoS) Journals Open Access; MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access |
subjects | Acetylcholine receptors Albendazole Amino acids Animals Anthelmintic agents Antinematodal Agents - pharmacology Antiparasitic agents Biology and Life Sciences Caenorhabditis elegans - drug effects Cloning Female Gametocytes Helminth Proteins - antagonists & inhibitors Helminth Proteins - classification Helminth Proteins - metabolism Human health and pathology Infectious diseases Isoforms Life Sciences Livestock Male Medicine and Health Sciences Microbiology and Parasitology Nematodes Oocytes Parasites Parasitology Peptides Pharmaceutical sciences Pharmacology Phylogenetics Proteins Pyrantel - analogs & derivatives Pyrantel - pharmacology Receptors Receptors, Cholinergic - chemistry Receptors, Cholinergic - classification Receptors, Cholinergic - metabolism Research and Analysis Methods Swine Trichuriasis - drug therapy Trichuriasis - metabolism Trichuriasis - parasitology Trichuris - drug effects Worms Xenopus laevis Xenopus laevis - metabolism |
title | The narrow-spectrum anthelmintic oxantel is a potent agonist of a novel acetylcholine receptor subtype in whipworms |
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