Cargando…
Social communication of predator-induced changes in Drosophila behavior and germ line physiology
Behavioral adaptation to environmental threats and subsequent social transmission of adaptive behavior has evolutionary implications. In Drosophila, exposure to parasitoid wasps leads to a sharp decline in oviposition. We show that exposure to predator elicits both an acute and learned oviposition d...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456452/ https://www.ncbi.nlm.nih.gov/pubmed/25970035 http://dx.doi.org/10.7554/eLife.07423 |
_version_ | 1782374842738147328 |
---|---|
author | Kacsoh, Balint Z Bozler, Julianna Ramaswami, Mani Bosco, Giovanni |
author_facet | Kacsoh, Balint Z Bozler, Julianna Ramaswami, Mani Bosco, Giovanni |
author_sort | Kacsoh, Balint Z |
collection | PubMed |
description | Behavioral adaptation to environmental threats and subsequent social transmission of adaptive behavior has evolutionary implications. In Drosophila, exposure to parasitoid wasps leads to a sharp decline in oviposition. We show that exposure to predator elicits both an acute and learned oviposition depression, mediated through the visual system. However, long-term persistence of oviposition depression after predator removal requires neuronal signaling functions, a functional mushroom body, and neurally driven apoptosis of oocytes through effector caspases. Strikingly, wasp-exposed flies (teachers) can transmit egg-retention behavior and trigger ovarian apoptosis in naive, unexposed flies (students). Acquisition and behavioral execution of this socially learned behavior by naive flies requires all of the factors needed for primary learning. The ability to teach does not require ovarian apoptosis. This work provides new insight into genetic and physiological mechanisms that underlie an ecologically relevant form of learning and mechanisms for its social transmission. DOI: http://dx.doi.org/10.7554/eLife.07423.001 |
format | Online Article Text |
id | pubmed-4456452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-44564522015-06-05 Social communication of predator-induced changes in Drosophila behavior and germ line physiology Kacsoh, Balint Z Bozler, Julianna Ramaswami, Mani Bosco, Giovanni eLife Cell Biology Behavioral adaptation to environmental threats and subsequent social transmission of adaptive behavior has evolutionary implications. In Drosophila, exposure to parasitoid wasps leads to a sharp decline in oviposition. We show that exposure to predator elicits both an acute and learned oviposition depression, mediated through the visual system. However, long-term persistence of oviposition depression after predator removal requires neuronal signaling functions, a functional mushroom body, and neurally driven apoptosis of oocytes through effector caspases. Strikingly, wasp-exposed flies (teachers) can transmit egg-retention behavior and trigger ovarian apoptosis in naive, unexposed flies (students). Acquisition and behavioral execution of this socially learned behavior by naive flies requires all of the factors needed for primary learning. The ability to teach does not require ovarian apoptosis. This work provides new insight into genetic and physiological mechanisms that underlie an ecologically relevant form of learning and mechanisms for its social transmission. DOI: http://dx.doi.org/10.7554/eLife.07423.001 eLife Sciences Publications, Ltd 2015-05-13 /pmc/articles/PMC4456452/ /pubmed/25970035 http://dx.doi.org/10.7554/eLife.07423 Text en © 2015, Kacsoh et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Kacsoh, Balint Z Bozler, Julianna Ramaswami, Mani Bosco, Giovanni Social communication of predator-induced changes in Drosophila behavior and germ line physiology |
title | Social communication of predator-induced changes in Drosophila behavior and germ line physiology |
title_full | Social communication of predator-induced changes in Drosophila behavior and germ line physiology |
title_fullStr | Social communication of predator-induced changes in Drosophila behavior and germ line physiology |
title_full_unstemmed | Social communication of predator-induced changes in Drosophila behavior and germ line physiology |
title_short | Social communication of predator-induced changes in Drosophila behavior and germ line physiology |
title_sort | social communication of predator-induced changes in drosophila behavior and germ line physiology |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456452/ https://www.ncbi.nlm.nih.gov/pubmed/25970035 http://dx.doi.org/10.7554/eLife.07423 |
work_keys_str_mv | AT kacsohbalintz socialcommunicationofpredatorinducedchangesindrosophilabehaviorandgermlinephysiology AT bozlerjulianna socialcommunicationofpredatorinducedchangesindrosophilabehaviorandgermlinephysiology AT ramaswamimani socialcommunicationofpredatorinducedchangesindrosophilabehaviorandgermlinephysiology AT boscogiovanni socialcommunicationofpredatorinducedchangesindrosophilabehaviorandgermlinephysiology |