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Reduction of stress responses in honey bees by synthetic ligands targeting an allatostatin receptor

Honey bees are of great economic and ecological importance, but are facing multiple stressors that can jeopardize their pollination efficiency and survival. Therefore, understanding the physiological bases of their stress response may help defining treatments to improve their resilience. We took an...

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Autores principales: Sánchez-Morales, Adrià, Gigoux, Véronique, Matsoukas, Minos-Timotheos, Perez-Benito, Laura, Fourmy, Daniel, Alibes, Ramón, Busqué, Félix, Cordomí, Arnau, Devaud, Jean-Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537510/
https://www.ncbi.nlm.nih.gov/pubmed/36202961
http://dx.doi.org/10.1038/s41598-022-20978-y
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author Sánchez-Morales, Adrià
Gigoux, Véronique
Matsoukas, Minos-Timotheos
Perez-Benito, Laura
Fourmy, Daniel
Alibes, Ramón
Busqué, Félix
Cordomí, Arnau
Devaud, Jean-Marc
author_facet Sánchez-Morales, Adrià
Gigoux, Véronique
Matsoukas, Minos-Timotheos
Perez-Benito, Laura
Fourmy, Daniel
Alibes, Ramón
Busqué, Félix
Cordomí, Arnau
Devaud, Jean-Marc
author_sort Sánchez-Morales, Adrià
collection PubMed
description Honey bees are of great economic and ecological importance, but are facing multiple stressors that can jeopardize their pollination efficiency and survival. Therefore, understanding the physiological bases of their stress response may help defining treatments to improve their resilience. We took an original approach to design molecules with this objective. We took advantage of the previous identified neuropeptide allatostatin A (ASTA) and its receptor (ASTA-R) as likely mediators of the honey bee response to a biologically relevant stressor, exposure to an alarm pheromone compound. A first series of ASTA-R ligands were identified through in silico screening using a homology 3D model of the receptor and in vitro binding experiments. One of these (A8) proved also efficient in vivo, as it could counteract two behavioral effects of pheromone exposure, albeit only in the millimolar range. This putative antagonist was used as a template for the chemical synthesis of a second generation of potential ligands. Among these, two compounds showed improved efficiency in vivo (in the micromolar range) as compared to A8 despite no major improvement in their affinity for the receptor in vitro. These new ligands are thus promising candidates for alleviating stress in honey bees.
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spelling pubmed-95375102022-10-08 Reduction of stress responses in honey bees by synthetic ligands targeting an allatostatin receptor Sánchez-Morales, Adrià Gigoux, Véronique Matsoukas, Minos-Timotheos Perez-Benito, Laura Fourmy, Daniel Alibes, Ramón Busqué, Félix Cordomí, Arnau Devaud, Jean-Marc Sci Rep Article Honey bees are of great economic and ecological importance, but are facing multiple stressors that can jeopardize their pollination efficiency and survival. Therefore, understanding the physiological bases of their stress response may help defining treatments to improve their resilience. We took an original approach to design molecules with this objective. We took advantage of the previous identified neuropeptide allatostatin A (ASTA) and its receptor (ASTA-R) as likely mediators of the honey bee response to a biologically relevant stressor, exposure to an alarm pheromone compound. A first series of ASTA-R ligands were identified through in silico screening using a homology 3D model of the receptor and in vitro binding experiments. One of these (A8) proved also efficient in vivo, as it could counteract two behavioral effects of pheromone exposure, albeit only in the millimolar range. This putative antagonist was used as a template for the chemical synthesis of a second generation of potential ligands. Among these, two compounds showed improved efficiency in vivo (in the micromolar range) as compared to A8 despite no major improvement in their affinity for the receptor in vitro. These new ligands are thus promising candidates for alleviating stress in honey bees. Nature Publishing Group UK 2022-10-06 /pmc/articles/PMC9537510/ /pubmed/36202961 http://dx.doi.org/10.1038/s41598-022-20978-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Sánchez-Morales, Adrià
Gigoux, Véronique
Matsoukas, Minos-Timotheos
Perez-Benito, Laura
Fourmy, Daniel
Alibes, Ramón
Busqué, Félix
Cordomí, Arnau
Devaud, Jean-Marc
Reduction of stress responses in honey bees by synthetic ligands targeting an allatostatin receptor
title Reduction of stress responses in honey bees by synthetic ligands targeting an allatostatin receptor
title_full Reduction of stress responses in honey bees by synthetic ligands targeting an allatostatin receptor
title_fullStr Reduction of stress responses in honey bees by synthetic ligands targeting an allatostatin receptor
title_full_unstemmed Reduction of stress responses in honey bees by synthetic ligands targeting an allatostatin receptor
title_short Reduction of stress responses in honey bees by synthetic ligands targeting an allatostatin receptor
title_sort reduction of stress responses in honey bees by synthetic ligands targeting an allatostatin receptor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537510/
https://www.ncbi.nlm.nih.gov/pubmed/36202961
http://dx.doi.org/10.1038/s41598-022-20978-y
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