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Social transmission of bacterial symbionts homogenizes the microbiome within and across generations of group-living spiders

Disentangling modes and fidelity of symbiont transmission are key for understanding host–symbiont associations in wild populations. In group-living animals, social transmission may evolve to ensure high-fidelity transmission of symbionts, since non-reproducing helpers constitute a dead-end for verti...

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Autores principales: Rose, Clémence, Lund, Marie B., Søgård, Andrea M., Busck, Mette M., Bechsgaard, Jesper S., Schramm, Andreas, Bilde, Trine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276852/
https://www.ncbi.nlm.nih.gov/pubmed/37330540
http://dx.doi.org/10.1038/s43705-023-00256-2
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author Rose, Clémence
Lund, Marie B.
Søgård, Andrea M.
Busck, Mette M.
Bechsgaard, Jesper S.
Schramm, Andreas
Bilde, Trine
author_facet Rose, Clémence
Lund, Marie B.
Søgård, Andrea M.
Busck, Mette M.
Bechsgaard, Jesper S.
Schramm, Andreas
Bilde, Trine
author_sort Rose, Clémence
collection PubMed
description Disentangling modes and fidelity of symbiont transmission are key for understanding host–symbiont associations in wild populations. In group-living animals, social transmission may evolve to ensure high-fidelity transmission of symbionts, since non-reproducing helpers constitute a dead-end for vertical transmission. We investigated symbiont transmission in the social spider Stegodyphus dumicola, which lives in family groups where the majority of females are non-reproducing helpers, females feed offspring by regurgitation, and individuals feed communally on insect prey. Group members share temporally stable microbiomes across generations, while distinct variation in microbiome composition exists between groups. We hypothesized that horizontal transmission of symbionts is enhanced by social interactions, and investigated transmission routes within (horizontal) and across (vertical) generations using bacterial 16S rRNA gene amplicon sequencing in three experiments: (i) individuals were sampled at all life stages to assess at which life stage the microbiome is acquired. (ii) a cross-fostering design was employed to test whether offspring carry the microbiome from their natal nest, or acquire the microbiome of the foster nest via social transmission. (iii) adult spiders with different microbiome compositions were mixed to assess whether social transmission homogenizes microbiome composition among group members. We demonstrate that offspring hatch symbiont-free, and bacterial symbionts are transmitted vertically across generations by social interactions with the onset of regurgitation feeding by (foster)mothers in an early life stage. Social transmission governs horizontal inter-individual mixing and homogenization of microbiome composition among nest mates. We conclude that temporally stable host–symbiont associations in social species can be facilitated and maintained by high-fidelity social transmission.
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spelling pubmed-102768522023-06-19 Social transmission of bacterial symbionts homogenizes the microbiome within and across generations of group-living spiders Rose, Clémence Lund, Marie B. Søgård, Andrea M. Busck, Mette M. Bechsgaard, Jesper S. Schramm, Andreas Bilde, Trine ISME Commun Article Disentangling modes and fidelity of symbiont transmission are key for understanding host–symbiont associations in wild populations. In group-living animals, social transmission may evolve to ensure high-fidelity transmission of symbionts, since non-reproducing helpers constitute a dead-end for vertical transmission. We investigated symbiont transmission in the social spider Stegodyphus dumicola, which lives in family groups where the majority of females are non-reproducing helpers, females feed offspring by regurgitation, and individuals feed communally on insect prey. Group members share temporally stable microbiomes across generations, while distinct variation in microbiome composition exists between groups. We hypothesized that horizontal transmission of symbionts is enhanced by social interactions, and investigated transmission routes within (horizontal) and across (vertical) generations using bacterial 16S rRNA gene amplicon sequencing in three experiments: (i) individuals were sampled at all life stages to assess at which life stage the microbiome is acquired. (ii) a cross-fostering design was employed to test whether offspring carry the microbiome from their natal nest, or acquire the microbiome of the foster nest via social transmission. (iii) adult spiders with different microbiome compositions were mixed to assess whether social transmission homogenizes microbiome composition among group members. We demonstrate that offspring hatch symbiont-free, and bacterial symbionts are transmitted vertically across generations by social interactions with the onset of regurgitation feeding by (foster)mothers in an early life stage. Social transmission governs horizontal inter-individual mixing and homogenization of microbiome composition among nest mates. We conclude that temporally stable host–symbiont associations in social species can be facilitated and maintained by high-fidelity social transmission. Nature Publishing Group UK 2023-06-17 /pmc/articles/PMC10276852/ /pubmed/37330540 http://dx.doi.org/10.1038/s43705-023-00256-2 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
Rose, Clémence
Lund, Marie B.
Søgård, Andrea M.
Busck, Mette M.
Bechsgaard, Jesper S.
Schramm, Andreas
Bilde, Trine
Social transmission of bacterial symbionts homogenizes the microbiome within and across generations of group-living spiders
title Social transmission of bacterial symbionts homogenizes the microbiome within and across generations of group-living spiders
title_full Social transmission of bacterial symbionts homogenizes the microbiome within and across generations of group-living spiders
title_fullStr Social transmission of bacterial symbionts homogenizes the microbiome within and across generations of group-living spiders
title_full_unstemmed Social transmission of bacterial symbionts homogenizes the microbiome within and across generations of group-living spiders
title_short Social transmission of bacterial symbionts homogenizes the microbiome within and across generations of group-living spiders
title_sort social transmission of bacterial symbionts homogenizes the microbiome within and across generations of group-living spiders
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276852/
https://www.ncbi.nlm.nih.gov/pubmed/37330540
http://dx.doi.org/10.1038/s43705-023-00256-2
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