Title: | Reduction of stress responses in honey bees by synthetic ligands targeting an allatostatin receptor |
Author(s): | Sanchez-Morales A; Gigoux V; Matsoukas MT; Perez-Benito L; Fourmy D; Alibes R; Busque F; Cordomi A; Devaud JM; |
Address: | "Departament de Quimica, Universitat Autonoma de Barcelona, Bellaterra, 08193, Barcelona, Spain. Centre de Recherches en Cancerologie de Toulouse (CRCT), INSERM Unite Mixte de Recherche UMR-1037, CNRS Equipe de Recherche Labellisee ERL5294, Universite de Toulouse, Toulouse, France. Unitat de Bioestadistica, Universitat Autonoma de Barcelona, Bellaterra, 08193, Barcelona, Spain. Computational Chemistry, Janssen Research & Development, Janssen Pharmaceutica N. V., Turnhoutseweg 30, B-2340, Beerse, Belgium. Departament de Quimica, Universitat Autonoma de Barcelona, Bellaterra, 08193, Barcelona, Spain. Felix.Busque@uab.cat. Unitat de Bioestadistica, Universitat Autonoma de Barcelona, Bellaterra, 08193, Barcelona, Spain. arnau.cordoni@esci.upf.edu. Bioinformatics, ESCI-Universitat Pompeu Fabra, Passeig Pujades 1, 08003, Barcelona, Spain. arnau.cordoni@esci.upf.edu. Centre de Recherches Sur La Cognition Animale (CRCA), Centre de Biologie Integrative, 9 (CBI), Universite de Toulouse, CNRS, Toulouse, France. jean-marc.devaud@univ-tlse3.fr" |
DOI: | 10.1038/s41598-022-20978-y |
ISSN/ISBN: | 2045-2322 (Electronic) 2045-2322 (Linking) |
Abstract: | "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" |
Keywords: | Animals Bees *Neuropeptides/metabolism Pheromones/chemistry *Pollination; |
Notes: | "MedlineSanchez-Morales, Adria Gigoux, Veronique Matsoukas, Minos-Timotheos Perez-Benito, Laura Fourmy, Daniel Alibes, Ramon Busque, Felix Cordomi, Arnau Devaud, Jean-Marc eng Research Support, Non-U.S. Gov't England 2022/10/07 Sci Rep. 2022 Oct 6; 12(1):16760. doi: 10.1038/s41598-022-20978-y" |