Cargando…
Ozone exposure disrupts insect sexual communication
Insect sexual communication often relies upon sex pheromones. Most insect pheromones, however, contain carbon-carbon double bonds and potentially degrade by oxidation. Here, we show that frequently reported increased levels of Anthropocenic ozone can oxidize all described male-specific pheromones of...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014992/ https://www.ncbi.nlm.nih.gov/pubmed/36918554 http://dx.doi.org/10.1038/s41467-023-36534-9 |
_version_ | 1784907118818623488 |
---|---|
author | Jiang, Nan-Ji Chang, Hetan Weißflog, Jerrit Eberl, Franziska Veit, Daniel Weniger, Kerstin Hansson, Bill S. Knaden, Markus |
author_facet | Jiang, Nan-Ji Chang, Hetan Weißflog, Jerrit Eberl, Franziska Veit, Daniel Weniger, Kerstin Hansson, Bill S. Knaden, Markus |
author_sort | Jiang, Nan-Ji |
collection | PubMed |
description | Insect sexual communication often relies upon sex pheromones. Most insect pheromones, however, contain carbon-carbon double bonds and potentially degrade by oxidation. Here, we show that frequently reported increased levels of Anthropocenic ozone can oxidize all described male-specific pheromones of Drosophila melanogaster, resulting in reduced amounts of pheromones such as cis-Vaccenyl Acetate and (Z)−7-Tricosene. At the same time female acceptance of ozone-exposed males is significantly delayed. Interestingly, groups of ozone-exposed males also exhibit significantly increased levels of male-male courtship behaviour. When repeating similar experiments with nine other drosophilid species, we observe pheromone degradation and/or disrupted sex recognition in eight of them. Our data suggest that Anthropocenic levels of ozone can extensively oxidize double bonds in a variety of insect pheromones, thereby leading to deviations in sexual recognition. |
format | Online Article Text |
id | pubmed-10014992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100149922023-03-16 Ozone exposure disrupts insect sexual communication Jiang, Nan-Ji Chang, Hetan Weißflog, Jerrit Eberl, Franziska Veit, Daniel Weniger, Kerstin Hansson, Bill S. Knaden, Markus Nat Commun Article Insect sexual communication often relies upon sex pheromones. Most insect pheromones, however, contain carbon-carbon double bonds and potentially degrade by oxidation. Here, we show that frequently reported increased levels of Anthropocenic ozone can oxidize all described male-specific pheromones of Drosophila melanogaster, resulting in reduced amounts of pheromones such as cis-Vaccenyl Acetate and (Z)−7-Tricosene. At the same time female acceptance of ozone-exposed males is significantly delayed. Interestingly, groups of ozone-exposed males also exhibit significantly increased levels of male-male courtship behaviour. When repeating similar experiments with nine other drosophilid species, we observe pheromone degradation and/or disrupted sex recognition in eight of them. Our data suggest that Anthropocenic levels of ozone can extensively oxidize double bonds in a variety of insect pheromones, thereby leading to deviations in sexual recognition. Nature Publishing Group UK 2023-03-14 /pmc/articles/PMC10014992/ /pubmed/36918554 http://dx.doi.org/10.1038/s41467-023-36534-9 Text en © The Author(s) 2023 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jiang, Nan-Ji Chang, Hetan Weißflog, Jerrit Eberl, Franziska Veit, Daniel Weniger, Kerstin Hansson, Bill S. Knaden, Markus Ozone exposure disrupts insect sexual communication |
title | Ozone exposure disrupts insect sexual communication |
title_full | Ozone exposure disrupts insect sexual communication |
title_fullStr | Ozone exposure disrupts insect sexual communication |
title_full_unstemmed | Ozone exposure disrupts insect sexual communication |
title_short | Ozone exposure disrupts insect sexual communication |
title_sort | ozone exposure disrupts insect sexual communication |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014992/ https://www.ncbi.nlm.nih.gov/pubmed/36918554 http://dx.doi.org/10.1038/s41467-023-36534-9 |
work_keys_str_mv | AT jiangnanji ozoneexposuredisruptsinsectsexualcommunication AT changhetan ozoneexposuredisruptsinsectsexualcommunication AT weißflogjerrit ozoneexposuredisruptsinsectsexualcommunication AT eberlfranziska ozoneexposuredisruptsinsectsexualcommunication AT veitdaniel ozoneexposuredisruptsinsectsexualcommunication AT wenigerkerstin ozoneexposuredisruptsinsectsexualcommunication AT hanssonbills ozoneexposuredisruptsinsectsexualcommunication AT knadenmarkus ozoneexposuredisruptsinsectsexualcommunication |