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Taxonomic and functional shifts in the beech rhizosphere microbiome across a natural soil toposequence

It has been rarely questioned as to whether the enrichment of specific bacterial taxa found in the rhizosphere of a given plant species changes with different soil types under field conditions and under similar climatic conditions. Understanding tree microbiome interactions is essential because, in...

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Autores principales: Colin, Y., Nicolitch, O., Van Nostrand, J. D., Zhou, J. Z., Turpault, M.-P., Uroz, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574896/
https://www.ncbi.nlm.nih.gov/pubmed/28851878
http://dx.doi.org/10.1038/s41598-017-07639-1
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author Colin, Y.
Nicolitch, O.
Van Nostrand, J. D.
Zhou, J. Z.
Turpault, M.-P.
Uroz, S.
author_facet Colin, Y.
Nicolitch, O.
Van Nostrand, J. D.
Zhou, J. Z.
Turpault, M.-P.
Uroz, S.
author_sort Colin, Y.
collection PubMed
description It has been rarely questioned as to whether the enrichment of specific bacterial taxa found in the rhizosphere of a given plant species changes with different soil types under field conditions and under similar climatic conditions. Understanding tree microbiome interactions is essential because, in contrast to annual plants, tree species require decades to grow and strongly depend on the nutritive resources of the soil. In this context, we tested using a natural toposequence the hypothesis that beech trees select specific taxa and functions in their rhizosphere based on the soil conditions and their nutritive requirements. Our 16S rRNA gene pyrosequencing analyses revealed that the soil type determines the taxa colonizing the beech rhizosphere. A rhizosphere effect was observed in each soil type, but a stronger effect was observed in the nutrient-poor soils. Although the communities varied significantly across the toposequence, we identified a core beech rhizosphere microbiome. Functionally, GeoChip analyses showed a functional redundancy across the toposequence, with genes related to nutrient cycling and to the bacterial immune system being significantly enriched in the rhizosphere. Altogether, the data suggest that, regardless of the soil conditions, trees enrich variable bacterial communities to maintain the functions necessary for their nutrition.
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spelling pubmed-55748962017-09-01 Taxonomic and functional shifts in the beech rhizosphere microbiome across a natural soil toposequence Colin, Y. Nicolitch, O. Van Nostrand, J. D. Zhou, J. Z. Turpault, M.-P. Uroz, S. Sci Rep Article It has been rarely questioned as to whether the enrichment of specific bacterial taxa found in the rhizosphere of a given plant species changes with different soil types under field conditions and under similar climatic conditions. Understanding tree microbiome interactions is essential because, in contrast to annual plants, tree species require decades to grow and strongly depend on the nutritive resources of the soil. In this context, we tested using a natural toposequence the hypothesis that beech trees select specific taxa and functions in their rhizosphere based on the soil conditions and their nutritive requirements. Our 16S rRNA gene pyrosequencing analyses revealed that the soil type determines the taxa colonizing the beech rhizosphere. A rhizosphere effect was observed in each soil type, but a stronger effect was observed in the nutrient-poor soils. Although the communities varied significantly across the toposequence, we identified a core beech rhizosphere microbiome. Functionally, GeoChip analyses showed a functional redundancy across the toposequence, with genes related to nutrient cycling and to the bacterial immune system being significantly enriched in the rhizosphere. Altogether, the data suggest that, regardless of the soil conditions, trees enrich variable bacterial communities to maintain the functions necessary for their nutrition. Nature Publishing Group UK 2017-08-29 /pmc/articles/PMC5574896/ /pubmed/28851878 http://dx.doi.org/10.1038/s41598-017-07639-1 Text en © The Author(s) 2017 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
Colin, Y.
Nicolitch, O.
Van Nostrand, J. D.
Zhou, J. Z.
Turpault, M.-P.
Uroz, S.
Taxonomic and functional shifts in the beech rhizosphere microbiome across a natural soil toposequence
title Taxonomic and functional shifts in the beech rhizosphere microbiome across a natural soil toposequence
title_full Taxonomic and functional shifts in the beech rhizosphere microbiome across a natural soil toposequence
title_fullStr Taxonomic and functional shifts in the beech rhizosphere microbiome across a natural soil toposequence
title_full_unstemmed Taxonomic and functional shifts in the beech rhizosphere microbiome across a natural soil toposequence
title_short Taxonomic and functional shifts in the beech rhizosphere microbiome across a natural soil toposequence
title_sort taxonomic and functional shifts in the beech rhizosphere microbiome across a natural soil toposequence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574896/
https://www.ncbi.nlm.nih.gov/pubmed/28851878
http://dx.doi.org/10.1038/s41598-017-07639-1
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