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Immune challenge reduces gut microbial diversity and triggers fertility-dependent gene expression changes in a social insect

BACKGROUND: The gut microbiome can influence life history traits associated with host fitness such as fecundity and longevity. In most organisms, these two life history traits are traded-off, while they are positively linked in social insects. In ants, highly fecund queens can live for decades, whil...

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Autores principales: Negroni, Matteo Antoine, Segers, Francisca H. I. D., Vogelweith, Fanny, Foitzik, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682046/
https://www.ncbi.nlm.nih.gov/pubmed/33225893
http://dx.doi.org/10.1186/s12864-020-07191-9
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author Negroni, Matteo Antoine
Segers, Francisca H. I. D.
Vogelweith, Fanny
Foitzik, Susanne
author_facet Negroni, Matteo Antoine
Segers, Francisca H. I. D.
Vogelweith, Fanny
Foitzik, Susanne
author_sort Negroni, Matteo Antoine
collection PubMed
description BACKGROUND: The gut microbiome can influence life history traits associated with host fitness such as fecundity and longevity. In most organisms, these two life history traits are traded-off, while they are positively linked in social insects. In ants, highly fecund queens can live for decades, while their non-reproducing workers exhibit much shorter lifespans. Yet, when fertility is induced in workers by death or removal of the queen, worker lifespan can increase. It is unclear how this positive link between fecundity and longevity is achieved and what role the gut microbiome and the immune system play in this. To gain insights into the molecular regulation of lifespan in social insects, we investigated fat body gene expression and gut microbiome composition in workers of the ant Temnothorax rugatulus in response to an experimental induction of fertility and an immune challenge. RESULTS: Fertile workers upregulated several molecular repair mechanisms, which could explain their extended lifespan. The immune challenge altered the expression of several thousand genes in the fat body, including many immune genes, and, interestingly, this transcriptomic response depended on worker fertility. For example, only fertile, immune-challenged workers upregulated genes involved in the synthesis of alpha-ketoglutarate, an immune system regulator, which extends the lifespan in Caenorhabditis elegans by down-regulating the TOR pathway and reducing oxidant production. Additionally, we observed a dramatic loss in bacterial diversity in the guts of the ants within a day of the immune challenge. Yet, bacterial density did not change, so that the gut microbiomes of many immune challenged workers consisted of only a single or a few bacterial strains. Moreover, the expression of immune genes was linked to the gut microbiome composition, suggesting that the ant host can regulate the microbiome in its gut. CONCLUSIONS: Immune system flare-ups can have negative consequence on gut microbiome diversity, pointing to a previously underrated cost of immunity. Moreover, our results provide important insights into shifts in the molecular regulation of fertility and longevity associated with insect sociality.
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spelling pubmed-76820462020-11-23 Immune challenge reduces gut microbial diversity and triggers fertility-dependent gene expression changes in a social insect Negroni, Matteo Antoine Segers, Francisca H. I. D. Vogelweith, Fanny Foitzik, Susanne BMC Genomics Research Article BACKGROUND: The gut microbiome can influence life history traits associated with host fitness such as fecundity and longevity. In most organisms, these two life history traits are traded-off, while they are positively linked in social insects. In ants, highly fecund queens can live for decades, while their non-reproducing workers exhibit much shorter lifespans. Yet, when fertility is induced in workers by death or removal of the queen, worker lifespan can increase. It is unclear how this positive link between fecundity and longevity is achieved and what role the gut microbiome and the immune system play in this. To gain insights into the molecular regulation of lifespan in social insects, we investigated fat body gene expression and gut microbiome composition in workers of the ant Temnothorax rugatulus in response to an experimental induction of fertility and an immune challenge. RESULTS: Fertile workers upregulated several molecular repair mechanisms, which could explain their extended lifespan. The immune challenge altered the expression of several thousand genes in the fat body, including many immune genes, and, interestingly, this transcriptomic response depended on worker fertility. For example, only fertile, immune-challenged workers upregulated genes involved in the synthesis of alpha-ketoglutarate, an immune system regulator, which extends the lifespan in Caenorhabditis elegans by down-regulating the TOR pathway and reducing oxidant production. Additionally, we observed a dramatic loss in bacterial diversity in the guts of the ants within a day of the immune challenge. Yet, bacterial density did not change, so that the gut microbiomes of many immune challenged workers consisted of only a single or a few bacterial strains. Moreover, the expression of immune genes was linked to the gut microbiome composition, suggesting that the ant host can regulate the microbiome in its gut. CONCLUSIONS: Immune system flare-ups can have negative consequence on gut microbiome diversity, pointing to a previously underrated cost of immunity. Moreover, our results provide important insights into shifts in the molecular regulation of fertility and longevity associated with insect sociality. BioMed Central 2020-11-23 /pmc/articles/PMC7682046/ /pubmed/33225893 http://dx.doi.org/10.1186/s12864-020-07191-9 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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
Negroni, Matteo Antoine
Segers, Francisca H. I. D.
Vogelweith, Fanny
Foitzik, Susanne
Immune challenge reduces gut microbial diversity and triggers fertility-dependent gene expression changes in a social insect
title Immune challenge reduces gut microbial diversity and triggers fertility-dependent gene expression changes in a social insect
title_full Immune challenge reduces gut microbial diversity and triggers fertility-dependent gene expression changes in a social insect
title_fullStr Immune challenge reduces gut microbial diversity and triggers fertility-dependent gene expression changes in a social insect
title_full_unstemmed Immune challenge reduces gut microbial diversity and triggers fertility-dependent gene expression changes in a social insect
title_short Immune challenge reduces gut microbial diversity and triggers fertility-dependent gene expression changes in a social insect
title_sort immune challenge reduces gut microbial diversity and triggers fertility-dependent gene expression changes in a social insect
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682046/
https://www.ncbi.nlm.nih.gov/pubmed/33225893
http://dx.doi.org/10.1186/s12864-020-07191-9
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