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Chemosensory sensitivity reflects reproductive status in the ant Harpegnathos saltator
Insects communicate with pheromones using sensitive antennal sensilla. Although trace amounts of pheromones can be detected by many insects, context-dependent increased costs of high sensitivity might lead to plasticity in sensillum responsiveness. We have functionally characterized basiconic sensil...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473913/ https://www.ncbi.nlm.nih.gov/pubmed/28623371 http://dx.doi.org/10.1038/s41598-017-03964-7 |
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author | Ghaninia, Majid Haight, Kevin Berger, Shelley L. Reinberg, Danny Zwiebel, Laurence J. Ray, Anandasankar Liebig, Jürgen |
author_facet | Ghaninia, Majid Haight, Kevin Berger, Shelley L. Reinberg, Danny Zwiebel, Laurence J. Ray, Anandasankar Liebig, Jürgen |
author_sort | Ghaninia, Majid |
collection | PubMed |
description | Insects communicate with pheromones using sensitive antennal sensilla. Although trace amounts of pheromones can be detected by many insects, context-dependent increased costs of high sensitivity might lead to plasticity in sensillum responsiveness. We have functionally characterized basiconic sensilla of the ant Harpegnathos saltator for responses to general odors in comparison to cuticular hydrocarbons which can act as fertility signals emitted by the principal reproductive(s) of a colony to inhibit reproduction by worker colony members. When released from inhibition workers may become reproductive gamergates. We observed plasticity in olfactory sensitivity after transition to reproductive status with significant reductions in electrophysiological responses to several long-chained cuticular hydrocarbons. Although gamergates lived on average five times longer than non-reproductive workers, the shift to reproductive status rather than age differences matched the pattern of changes in olfactory sensitivity. Decreasing sensillum responsiveness to cuticular hydrocarbons could potentially reduce mutually inhibitory or self-inhibitory effects on gamergate reproduction. |
format | Online Article Text |
id | pubmed-5473913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54739132017-06-21 Chemosensory sensitivity reflects reproductive status in the ant Harpegnathos saltator Ghaninia, Majid Haight, Kevin Berger, Shelley L. Reinberg, Danny Zwiebel, Laurence J. Ray, Anandasankar Liebig, Jürgen Sci Rep Article Insects communicate with pheromones using sensitive antennal sensilla. Although trace amounts of pheromones can be detected by many insects, context-dependent increased costs of high sensitivity might lead to plasticity in sensillum responsiveness. We have functionally characterized basiconic sensilla of the ant Harpegnathos saltator for responses to general odors in comparison to cuticular hydrocarbons which can act as fertility signals emitted by the principal reproductive(s) of a colony to inhibit reproduction by worker colony members. When released from inhibition workers may become reproductive gamergates. We observed plasticity in olfactory sensitivity after transition to reproductive status with significant reductions in electrophysiological responses to several long-chained cuticular hydrocarbons. Although gamergates lived on average five times longer than non-reproductive workers, the shift to reproductive status rather than age differences matched the pattern of changes in olfactory sensitivity. Decreasing sensillum responsiveness to cuticular hydrocarbons could potentially reduce mutually inhibitory or self-inhibitory effects on gamergate reproduction. Nature Publishing Group UK 2017-06-16 /pmc/articles/PMC5473913/ /pubmed/28623371 http://dx.doi.org/10.1038/s41598-017-03964-7 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Ghaninia, Majid Haight, Kevin Berger, Shelley L. Reinberg, Danny Zwiebel, Laurence J. Ray, Anandasankar Liebig, Jürgen Chemosensory sensitivity reflects reproductive status in the ant Harpegnathos saltator |
title | Chemosensory sensitivity reflects reproductive status in the ant Harpegnathos saltator |
title_full | Chemosensory sensitivity reflects reproductive status in the ant Harpegnathos saltator |
title_fullStr | Chemosensory sensitivity reflects reproductive status in the ant Harpegnathos saltator |
title_full_unstemmed | Chemosensory sensitivity reflects reproductive status in the ant Harpegnathos saltator |
title_short | Chemosensory sensitivity reflects reproductive status in the ant Harpegnathos saltator |
title_sort | chemosensory sensitivity reflects reproductive status in the ant harpegnathos saltator |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473913/ https://www.ncbi.nlm.nih.gov/pubmed/28623371 http://dx.doi.org/10.1038/s41598-017-03964-7 |
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