Functional Characterization of the Oxantel-Sensitive Acetylcholine Receptor from Trichuris muris
AuthorsHansen, Tina V. A.; orcid: 0000-0002-2744-3093; email: firstname.lastname@example.org
Grencis, Richard K.; email: email@example.com
Issouf, Mohamed; orcid: 0000-0003-4964-8492; email: firstname.lastname@example.org
Neveu, Cédric; email: email@example.com
Charvet, Claude L.; orcid: 0000-0002-0596-6598; email: firstname.lastname@example.org
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AbstractThe human whipworm, Trichuris trichiura, is estimated to infect 289.6 million people globally. Control of human trichuriasis is a particular challenge, as most anthelmintics have a limited single-dose efficacy, with the striking exception of the narrow-spectrum anthelmintic, oxantel. We recently identified a novel ACR-16-like subunit from the pig whipworm, T. suis which gave rise to a functional acetylcholine receptor (nAChR) preferentially activated by oxantel. However, there is no ion channel described in the mouse model parasite T. muris so far. Here, we have identified the ACR-16-like and ACR-19 subunits from T. muris, and performed the functional characterization of the receptors in Xenopus laevis oocytes using two-electrode voltage-clamp electrophysiology. We found that the ACR-16-like subunit from T. muris formed a homomeric receptor gated by acetylcholine whereas the ACR-19 failed to create a functional channel. The subsequent pharmacological analysis of the Tmu-ACR-16-like receptor revealed that acetylcholine and oxantel were equally potent. The Tmu-ACR-16-like was more responsive to the toxic agonist epibatidine, but insensitive to pyrantel, in contrast to the Tsu-ACR-16-like receptor. These findings confirm that the ACR-16-like nAChR from Trichuris spp. is a preferential drug target for oxantel, and highlights the pharmacological difference between Trichuris species.
CitationPharmaceuticals, volume 14, issue 7, page e698
DescriptionFrom MDPI via Jisc Publications Router
History: accepted 2021-07-16, pub-electronic 2021-07-20
Publication status: Published
Funder: Wellcome Trust; Grant(s): Z10661/Z/18/Z
Funder: Wellcome Trust Centre for Cell Matrix Research; Grant(s): Z03128/Z/16/Z
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