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Competition-based screening helps to secure the evolutionary stability of a defensive microbiome

BACKGROUND: The cuticular microbiomes of Acromyrmex leaf-cutting ants pose a conundrum in microbiome biology because they are freely colonisable, and yet the prevalence of the vertically transmitted bacteria Pseudonocardia, which contributes to the control of Escovopsis fungus garden disease, is nev...

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Autores principales: Worsley, Sarah F., Innocent, Tabitha M., Holmes, Neil A., Al-Bassam, Mahmoud M., Schiøtt, Morten, Wilkinson, Barrie, Murrell, J. Colin, Boomsma, Jacobus J., Yu, Douglas W., Hutchings, Matthew I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8444595/
https://www.ncbi.nlm.nih.gov/pubmed/34526023
http://dx.doi.org/10.1186/s12915-021-01142-w
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author Worsley, Sarah F.
Innocent, Tabitha M.
Holmes, Neil A.
Al-Bassam, Mahmoud M.
Schiøtt, Morten
Wilkinson, Barrie
Murrell, J. Colin
Boomsma, Jacobus J.
Yu, Douglas W.
Hutchings, Matthew I.
author_facet Worsley, Sarah F.
Innocent, Tabitha M.
Holmes, Neil A.
Al-Bassam, Mahmoud M.
Schiøtt, Morten
Wilkinson, Barrie
Murrell, J. Colin
Boomsma, Jacobus J.
Yu, Douglas W.
Hutchings, Matthew I.
author_sort Worsley, Sarah F.
collection PubMed
description BACKGROUND: The cuticular microbiomes of Acromyrmex leaf-cutting ants pose a conundrum in microbiome biology because they are freely colonisable, and yet the prevalence of the vertically transmitted bacteria Pseudonocardia, which contributes to the control of Escovopsis fungus garden disease, is never compromised by the secondary acquisition of other bacterial strains. Game theory suggests that competition-based screening can allow the selective recruitment of antibiotic-producing bacteria from the environment, by providing abundant resources to foment interference competition between bacterial species and by using Pseudonocardia to bias the outcome of competition in favour of antibiotic producers. RESULTS: Here, we use RNA-stable isotope probing (RNA-SIP) to confirm that Acromyrmex ants can maintain a range of microbial symbionts on their cuticle by supplying public resources. We then used RNA sequencing, bioassays, and competition experiments to show that vertically transmitted Pseudonocardia strains produce antibacterials that differentially reduce the growth rates of other microbes, ultimately biassing the bacterial competition to allow the selective establishment of secondary antibiotic-producing strains while excluding non-antibiotic-producing strains that would parasitise the symbiosis. CONCLUSIONS: Our findings are consistent with the hypothesis that competition-based screening is a plausible mechanism for maintaining the integrity of the co-adapted mutualism between the leaf-cutting ant farming symbiosis and its defensive microbiome. Our results have broader implications for explaining the stability of other complex symbioses involving horizontal acquisition. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01142-w.
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spelling pubmed-84445952021-09-17 Competition-based screening helps to secure the evolutionary stability of a defensive microbiome Worsley, Sarah F. Innocent, Tabitha M. Holmes, Neil A. Al-Bassam, Mahmoud M. Schiøtt, Morten Wilkinson, Barrie Murrell, J. Colin Boomsma, Jacobus J. Yu, Douglas W. Hutchings, Matthew I. BMC Biol Research Article BACKGROUND: The cuticular microbiomes of Acromyrmex leaf-cutting ants pose a conundrum in microbiome biology because they are freely colonisable, and yet the prevalence of the vertically transmitted bacteria Pseudonocardia, which contributes to the control of Escovopsis fungus garden disease, is never compromised by the secondary acquisition of other bacterial strains. Game theory suggests that competition-based screening can allow the selective recruitment of antibiotic-producing bacteria from the environment, by providing abundant resources to foment interference competition between bacterial species and by using Pseudonocardia to bias the outcome of competition in favour of antibiotic producers. RESULTS: Here, we use RNA-stable isotope probing (RNA-SIP) to confirm that Acromyrmex ants can maintain a range of microbial symbionts on their cuticle by supplying public resources. We then used RNA sequencing, bioassays, and competition experiments to show that vertically transmitted Pseudonocardia strains produce antibacterials that differentially reduce the growth rates of other microbes, ultimately biassing the bacterial competition to allow the selective establishment of secondary antibiotic-producing strains while excluding non-antibiotic-producing strains that would parasitise the symbiosis. CONCLUSIONS: Our findings are consistent with the hypothesis that competition-based screening is a plausible mechanism for maintaining the integrity of the co-adapted mutualism between the leaf-cutting ant farming symbiosis and its defensive microbiome. Our results have broader implications for explaining the stability of other complex symbioses involving horizontal acquisition. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01142-w. BioMed Central 2021-09-15 /pmc/articles/PMC8444595/ /pubmed/34526023 http://dx.doi.org/10.1186/s12915-021-01142-w Text en © The Author(s) 2021 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
Worsley, Sarah F.
Innocent, Tabitha M.
Holmes, Neil A.
Al-Bassam, Mahmoud M.
Schiøtt, Morten
Wilkinson, Barrie
Murrell, J. Colin
Boomsma, Jacobus J.
Yu, Douglas W.
Hutchings, Matthew I.
Competition-based screening helps to secure the evolutionary stability of a defensive microbiome
title Competition-based screening helps to secure the evolutionary stability of a defensive microbiome
title_full Competition-based screening helps to secure the evolutionary stability of a defensive microbiome
title_fullStr Competition-based screening helps to secure the evolutionary stability of a defensive microbiome
title_full_unstemmed Competition-based screening helps to secure the evolutionary stability of a defensive microbiome
title_short Competition-based screening helps to secure the evolutionary stability of a defensive microbiome
title_sort competition-based screening helps to secure the evolutionary stability of a defensive microbiome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8444595/
https://www.ncbi.nlm.nih.gov/pubmed/34526023
http://dx.doi.org/10.1186/s12915-021-01142-w
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