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Peptidomics of Haemonchus contortus

[Image: see text] The nematode Haemonchus contortus (the barber’s pole worm) is an endoparasite infecting wild and domesticated ruminants worldwide. Widespread anthelmintic resistance of H. contortus requires alternative strategies to control this parasite. Neuropeptide signaling represents a promis...

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Autores principales: Buzy, Armelle, Allain, Camille, Harrington, John, Lesuisse, Dominique, Mikol, Vincent, Bruhn, David F., Maule, Aaron G., Guillemot, Jean-Claude
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153747/
https://www.ncbi.nlm.nih.gov/pubmed/34056183
http://dx.doi.org/10.1021/acsomega.1c00650
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author Buzy, Armelle
Allain, Camille
Harrington, John
Lesuisse, Dominique
Mikol, Vincent
Bruhn, David F.
Maule, Aaron G.
Guillemot, Jean-Claude
author_facet Buzy, Armelle
Allain, Camille
Harrington, John
Lesuisse, Dominique
Mikol, Vincent
Bruhn, David F.
Maule, Aaron G.
Guillemot, Jean-Claude
author_sort Buzy, Armelle
collection PubMed
description [Image: see text] The nematode Haemonchus contortus (the barber’s pole worm) is an endoparasite infecting wild and domesticated ruminants worldwide. Widespread anthelmintic resistance of H. contortus requires alternative strategies to control this parasite. Neuropeptide signaling represents a promising target for anthelmintic drugs. Identification and relative quantification of nematode neuropeptides are, therefore, required for the development of such therapeutic targets. In this work, we undertook the profiling of the whole H. contortus larvae at different stages for the direct sequencing of the neuropeptides expressed at low levels in these tissues. We set out a peptide extraction protocol and a peptidomic workflow to biochemically characterize bioactive peptides from both first-stage (L1) and third-stage larvae (L3) of H. contortus. This work led to the identification and quantification at the peptidomic level of more than 180 mature neuropeptides, including amidated and nonamidated peptides, arising from 55 precursors of H. contortus. The differential peptidomic approach provided evidence that both life stages express most FMRFamide-like peptides (FLPs) and neuropeptide-like proteins (NLPs). The H. contortus peptidome resource, established in this work, could add the discovery of neuropeptide system-targeting drugs for ruminants.
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spelling pubmed-81537472021-05-27 Peptidomics of Haemonchus contortus Buzy, Armelle Allain, Camille Harrington, John Lesuisse, Dominique Mikol, Vincent Bruhn, David F. Maule, Aaron G. Guillemot, Jean-Claude ACS Omega [Image: see text] The nematode Haemonchus contortus (the barber’s pole worm) is an endoparasite infecting wild and domesticated ruminants worldwide. Widespread anthelmintic resistance of H. contortus requires alternative strategies to control this parasite. Neuropeptide signaling represents a promising target for anthelmintic drugs. Identification and relative quantification of nematode neuropeptides are, therefore, required for the development of such therapeutic targets. In this work, we undertook the profiling of the whole H. contortus larvae at different stages for the direct sequencing of the neuropeptides expressed at low levels in these tissues. We set out a peptide extraction protocol and a peptidomic workflow to biochemically characterize bioactive peptides from both first-stage (L1) and third-stage larvae (L3) of H. contortus. This work led to the identification and quantification at the peptidomic level of more than 180 mature neuropeptides, including amidated and nonamidated peptides, arising from 55 precursors of H. contortus. The differential peptidomic approach provided evidence that both life stages express most FMRFamide-like peptides (FLPs) and neuropeptide-like proteins (NLPs). The H. contortus peptidome resource, established in this work, could add the discovery of neuropeptide system-targeting drugs for ruminants. American Chemical Society 2021-04-07 /pmc/articles/PMC8153747/ /pubmed/34056183 http://dx.doi.org/10.1021/acsomega.1c00650 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Buzy, Armelle
Allain, Camille
Harrington, John
Lesuisse, Dominique
Mikol, Vincent
Bruhn, David F.
Maule, Aaron G.
Guillemot, Jean-Claude
Peptidomics of Haemonchus contortus
title Peptidomics of Haemonchus contortus
title_full Peptidomics of Haemonchus contortus
title_fullStr Peptidomics of Haemonchus contortus
title_full_unstemmed Peptidomics of Haemonchus contortus
title_short Peptidomics of Haemonchus contortus
title_sort peptidomics of haemonchus contortus
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153747/
https://www.ncbi.nlm.nih.gov/pubmed/34056183
http://dx.doi.org/10.1021/acsomega.1c00650
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