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Microbiota mediated plasticity promotes thermal adaptation in the sea anemone Nematostella vectensis

At the current rate of climate change, it is unlikely that multicellular organisms will be able to adapt to changing environmental conditions through genetic recombination and natural selection alone. Thus, it is critical to understand alternative mechanisms that allow organisms to cope with rapid e...

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Autores principales: Baldassarre, Laura, Ying, Hua, Reitzel, Adam M., Franzenburg, Sören, Fraune, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249911/
https://www.ncbi.nlm.nih.gov/pubmed/35778405
http://dx.doi.org/10.1038/s41467-022-31350-z
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author Baldassarre, Laura
Ying, Hua
Reitzel, Adam M.
Franzenburg, Sören
Fraune, Sebastian
author_facet Baldassarre, Laura
Ying, Hua
Reitzel, Adam M.
Franzenburg, Sören
Fraune, Sebastian
author_sort Baldassarre, Laura
collection PubMed
description At the current rate of climate change, it is unlikely that multicellular organisms will be able to adapt to changing environmental conditions through genetic recombination and natural selection alone. Thus, it is critical to understand alternative mechanisms that allow organisms to cope with rapid environmental changes. Here, we use the sea anemone Nematostella vectensis, which has evolved the capability of surviving in a wide range of temperatures and salinities, as a model to investigate the microbiota as a source of rapid adaptation. We long-term acclimate polyps of Nematostella to low, medium, and high temperatures, to test the impact of microbiota-mediated plasticity on animal acclimation. Using the same animal clonal line, propagated from a single polyp, allows us to eliminate the effects of the host genotype. The higher thermal tolerance of animals acclimated to high temperature can be transferred to non-acclimated animals through microbiota transplantation. The offspring fitness is highest from F0 females acclimated to high temperature and specific members of the acclimated microbiota are transmitted to the next generation. These results indicate that microbiota plasticity can contribute to animal thermal acclimation and its transmission to the next generation may represent a rapid mechanism for thermal adaptation.
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spelling pubmed-92499112022-07-03 Microbiota mediated plasticity promotes thermal adaptation in the sea anemone Nematostella vectensis Baldassarre, Laura Ying, Hua Reitzel, Adam M. Franzenburg, Sören Fraune, Sebastian Nat Commun Article At the current rate of climate change, it is unlikely that multicellular organisms will be able to adapt to changing environmental conditions through genetic recombination and natural selection alone. Thus, it is critical to understand alternative mechanisms that allow organisms to cope with rapid environmental changes. Here, we use the sea anemone Nematostella vectensis, which has evolved the capability of surviving in a wide range of temperatures and salinities, as a model to investigate the microbiota as a source of rapid adaptation. We long-term acclimate polyps of Nematostella to low, medium, and high temperatures, to test the impact of microbiota-mediated plasticity on animal acclimation. Using the same animal clonal line, propagated from a single polyp, allows us to eliminate the effects of the host genotype. The higher thermal tolerance of animals acclimated to high temperature can be transferred to non-acclimated animals through microbiota transplantation. The offspring fitness is highest from F0 females acclimated to high temperature and specific members of the acclimated microbiota are transmitted to the next generation. These results indicate that microbiota plasticity can contribute to animal thermal acclimation and its transmission to the next generation may represent a rapid mechanism for thermal adaptation. Nature Publishing Group UK 2022-07-01 /pmc/articles/PMC9249911/ /pubmed/35778405 http://dx.doi.org/10.1038/s41467-022-31350-z Text en © The Author(s) 2022 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
Baldassarre, Laura
Ying, Hua
Reitzel, Adam M.
Franzenburg, Sören
Fraune, Sebastian
Microbiota mediated plasticity promotes thermal adaptation in the sea anemone Nematostella vectensis
title Microbiota mediated plasticity promotes thermal adaptation in the sea anemone Nematostella vectensis
title_full Microbiota mediated plasticity promotes thermal adaptation in the sea anemone Nematostella vectensis
title_fullStr Microbiota mediated plasticity promotes thermal adaptation in the sea anemone Nematostella vectensis
title_full_unstemmed Microbiota mediated plasticity promotes thermal adaptation in the sea anemone Nematostella vectensis
title_short Microbiota mediated plasticity promotes thermal adaptation in the sea anemone Nematostella vectensis
title_sort microbiota mediated plasticity promotes thermal adaptation in the sea anemone nematostella vectensis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249911/
https://www.ncbi.nlm.nih.gov/pubmed/35778405
http://dx.doi.org/10.1038/s41467-022-31350-z
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