Cargando…

Memory of social experience affects female fecundity via perception of fly deposits

BACKGROUND: Animals can exhibit remarkable reproductive plasticity in response  to their social surroundings, with profound fitness consequences. The presence of same-sex conspecifics can signal current or future expected competition for resources or mates. Plastic responses to elevated sexual compe...

Descripción completa

Detalles Bibliográficos
Autores principales: Fowler, E. K., Leigh, S., Rostant, W. G., Thomas, A., Bretman, A., Chapman, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620669/
https://www.ncbi.nlm.nih.gov/pubmed/36310170
http://dx.doi.org/10.1186/s12915-022-01438-5
_version_ 1784821375955894272
author Fowler, E. K.
Leigh, S.
Rostant, W. G.
Thomas, A.
Bretman, A.
Chapman, T.
author_facet Fowler, E. K.
Leigh, S.
Rostant, W. G.
Thomas, A.
Bretman, A.
Chapman, T.
author_sort Fowler, E. K.
collection PubMed
description BACKGROUND: Animals can exhibit remarkable reproductive plasticity in response  to their social surroundings, with profound fitness consequences. The presence of same-sex conspecifics can signal current or future expected competition for resources or mates. Plastic responses to elevated sexual competition caused by exposure to same-sex individuals have been well-studied in males. However, much less is known about such plastic responses in females, whether this represents sexual or resource competition, or if it leads to changes in investment in mating behaviour and/or reproduction. Here, we used Drosophila melanogaster to measure the impact of experimentally varying female exposure to other females prior to mating on fecundity before and after mating. We then deployed physical and genetic methods to manipulate the perception of different social cues and sensory pathways and reveal the potential mechanisms involved. RESULTS: The results showed that females maintained in social isolation prior to mating were significantly more likely to retain unfertilised eggs before mating, but to show the opposite and lay significantly more fertilised eggs in the 24h after mating. More than 48h of exposure to other females was necessary for this social memory response to be expressed. Neither olfactory nor visual cues were involved in mediating fecundity plasticity—instead, the relevant cues were perceived through direct contact with the non-egg deposits left behind by other females. CONCLUSIONS: The results demonstrate that females show reproductive plasticity in response to their social surroundings and can carry this memory of their social experience forward through mating. Comparisons of our results with previous work show that the nature of female plastic reproductive responses and the cues they use differ markedly from those of males. The results emphasise the deep divergence in how each sex realises its reproductive success. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01438-5.
format Online
Article
Text
id pubmed-9620669
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-96206692022-11-01 Memory of social experience affects female fecundity via perception of fly deposits Fowler, E. K. Leigh, S. Rostant, W. G. Thomas, A. Bretman, A. Chapman, T. BMC Biol Research Article BACKGROUND: Animals can exhibit remarkable reproductive plasticity in response  to their social surroundings, with profound fitness consequences. The presence of same-sex conspecifics can signal current or future expected competition for resources or mates. Plastic responses to elevated sexual competition caused by exposure to same-sex individuals have been well-studied in males. However, much less is known about such plastic responses in females, whether this represents sexual or resource competition, or if it leads to changes in investment in mating behaviour and/or reproduction. Here, we used Drosophila melanogaster to measure the impact of experimentally varying female exposure to other females prior to mating on fecundity before and after mating. We then deployed physical and genetic methods to manipulate the perception of different social cues and sensory pathways and reveal the potential mechanisms involved. RESULTS: The results showed that females maintained in social isolation prior to mating were significantly more likely to retain unfertilised eggs before mating, but to show the opposite and lay significantly more fertilised eggs in the 24h after mating. More than 48h of exposure to other females was necessary for this social memory response to be expressed. Neither olfactory nor visual cues were involved in mediating fecundity plasticity—instead, the relevant cues were perceived through direct contact with the non-egg deposits left behind by other females. CONCLUSIONS: The results demonstrate that females show reproductive plasticity in response to their social surroundings and can carry this memory of their social experience forward through mating. Comparisons of our results with previous work show that the nature of female plastic reproductive responses and the cues they use differ markedly from those of males. The results emphasise the deep divergence in how each sex realises its reproductive success. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01438-5. BioMed Central 2022-10-31 /pmc/articles/PMC9620669/ /pubmed/36310170 http://dx.doi.org/10.1186/s12915-022-01438-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Fowler, E. K.
Leigh, S.
Rostant, W. G.
Thomas, A.
Bretman, A.
Chapman, T.
Memory of social experience affects female fecundity via perception of fly deposits
title Memory of social experience affects female fecundity via perception of fly deposits
title_full Memory of social experience affects female fecundity via perception of fly deposits
title_fullStr Memory of social experience affects female fecundity via perception of fly deposits
title_full_unstemmed Memory of social experience affects female fecundity via perception of fly deposits
title_short Memory of social experience affects female fecundity via perception of fly deposits
title_sort memory of social experience affects female fecundity via perception of fly deposits
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620669/
https://www.ncbi.nlm.nih.gov/pubmed/36310170
http://dx.doi.org/10.1186/s12915-022-01438-5
work_keys_str_mv AT fowlerek memoryofsocialexperienceaffectsfemalefecundityviaperceptionofflydeposits
AT leighs memoryofsocialexperienceaffectsfemalefecundityviaperceptionofflydeposits
AT rostantwg memoryofsocialexperienceaffectsfemalefecundityviaperceptionofflydeposits
AT thomasa memoryofsocialexperienceaffectsfemalefecundityviaperceptionofflydeposits
AT bretmana memoryofsocialexperienceaffectsfemalefecundityviaperceptionofflydeposits
AT chapmant memoryofsocialexperienceaffectsfemalefecundityviaperceptionofflydeposits