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Convergent shifts in host-associated microbial communities across environmentally elicited phenotypes
Morphological plasticity is a genotype-by-environment interaction that enables organisms to increase fitness across varying environments. Symbioses with diverse microbiota may aid in acclimating to this variation, but whether the associated bacteria community is phenotype specific remains understudi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838112/ https://www.ncbi.nlm.nih.gov/pubmed/29507332 http://dx.doi.org/10.1038/s41467-018-03383-w |
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author | Carrier, Tyler J. Reitzel, Adam M. |
author_facet | Carrier, Tyler J. Reitzel, Adam M. |
author_sort | Carrier, Tyler J. |
collection | PubMed |
description | Morphological plasticity is a genotype-by-environment interaction that enables organisms to increase fitness across varying environments. Symbioses with diverse microbiota may aid in acclimating to this variation, but whether the associated bacteria community is phenotype specific remains understudied. Here we induce morphological plasticity in three species of sea urchin larvae and measure changes in the associated bacterial community. While each host species has unique bacterial communities, the expression of plasticity results in the convergence on a phenotype-specific microbiome that is, in part, driven by differential association with α- and γ-proteobacteria. Furthermore, these results suggest that phenotype-specific signatures are the product of the environment and are correlated with ingestive and digestive structures. By manipulating diet quantity over time, we also show that differentially associating with microbiota along a phenotypic continuum is bidirectional. Taken together, our data support the idea of a phenotype-specific microbial community and that phenotypic plasticity extends beyond a genotype-by-environment interaction. |
format | Online Article Text |
id | pubmed-5838112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58381122018-03-08 Convergent shifts in host-associated microbial communities across environmentally elicited phenotypes Carrier, Tyler J. Reitzel, Adam M. Nat Commun Article Morphological plasticity is a genotype-by-environment interaction that enables organisms to increase fitness across varying environments. Symbioses with diverse microbiota may aid in acclimating to this variation, but whether the associated bacteria community is phenotype specific remains understudied. Here we induce morphological plasticity in three species of sea urchin larvae and measure changes in the associated bacterial community. While each host species has unique bacterial communities, the expression of plasticity results in the convergence on a phenotype-specific microbiome that is, in part, driven by differential association with α- and γ-proteobacteria. Furthermore, these results suggest that phenotype-specific signatures are the product of the environment and are correlated with ingestive and digestive structures. By manipulating diet quantity over time, we also show that differentially associating with microbiota along a phenotypic continuum is bidirectional. Taken together, our data support the idea of a phenotype-specific microbial community and that phenotypic plasticity extends beyond a genotype-by-environment interaction. Nature Publishing Group UK 2018-03-05 /pmc/articles/PMC5838112/ /pubmed/29507332 http://dx.doi.org/10.1038/s41467-018-03383-w Text en © The Author(s) 2018 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/. |
spellingShingle | Article Carrier, Tyler J. Reitzel, Adam M. Convergent shifts in host-associated microbial communities across environmentally elicited phenotypes |
title | Convergent shifts in host-associated microbial communities across environmentally elicited phenotypes |
title_full | Convergent shifts in host-associated microbial communities across environmentally elicited phenotypes |
title_fullStr | Convergent shifts in host-associated microbial communities across environmentally elicited phenotypes |
title_full_unstemmed | Convergent shifts in host-associated microbial communities across environmentally elicited phenotypes |
title_short | Convergent shifts in host-associated microbial communities across environmentally elicited phenotypes |
title_sort | convergent shifts in host-associated microbial communities across environmentally elicited phenotypes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838112/ https://www.ncbi.nlm.nih.gov/pubmed/29507332 http://dx.doi.org/10.1038/s41467-018-03383-w |
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