Cargando…

Domestication-driven changes in plant traits associated with changes in the assembly of the rhizosphere microbiota in tetraploid wheat

Despite the large morphological and physiological changes that plants have undergone through domestication, little is known about their impact on their microbiome. Here we characterized rhizospheric bacterial and fungal communities as well as the abundance of N-cycling microbial guilds across thirty...

Descripción completa

Detalles Bibliográficos
Autores principales: Spor, Aymé, Roucou, Agathe, Mounier, Arnaud, Bru, David, Breuil, Marie-Christine, Fort, Florian, Vile, Denis, Roumet, Pierre, Philippot, Laurent, Violle, Cyrille
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376052/
https://www.ncbi.nlm.nih.gov/pubmed/32699344
http://dx.doi.org/10.1038/s41598-020-69175-9
_version_ 1783561967727804416
author Spor, Aymé
Roucou, Agathe
Mounier, Arnaud
Bru, David
Breuil, Marie-Christine
Fort, Florian
Vile, Denis
Roumet, Pierre
Philippot, Laurent
Violle, Cyrille
author_facet Spor, Aymé
Roucou, Agathe
Mounier, Arnaud
Bru, David
Breuil, Marie-Christine
Fort, Florian
Vile, Denis
Roumet, Pierre
Philippot, Laurent
Violle, Cyrille
author_sort Spor, Aymé
collection PubMed
description Despite the large morphological and physiological changes that plants have undergone through domestication, little is known about their impact on their microbiome. Here we characterized rhizospheric bacterial and fungal communities as well as the abundance of N-cycling microbial guilds across thirty-nine accessions of tetraploid wheat, Triticum turgidum, from four domestication groups ranging from the wild subspecies to the semi dwarf elite cultivars. We identified several microbial phylotypes displaying significant variation in their relative abundance depending on the wheat domestication group with a stronger impact of domestication on fungi. The relative abundance of potential fungal plant pathogens belonging to the Sordariomycetes class decreased in domesticated compared to wild emmer while the opposite was found for members of the Glomeromycetes, which are obligate plant symbionts. The depletion of nitrifiers and of arbuscular mycorrhizal fungi in elite wheat cultivars compared to primitive domesticated forms suggests that the Green Revolution has decreased the coupling between plant and rhizosphere microbes that are potentially important for plant nutrient availability. Both plant diameter and fine root percentage exhibited the highest number of associations with microbial taxa, highlighting their putative role in shaping the rhizosphere microbiota during domestication. Aside from domestication, significant variation of bacterial and fungal community composition was found among accessions within each domestication group. In particular, the relative abundances of Ophiostomataceae and of Rhizobiales were strongly dependent on the host accession, with heritability estimates of ~ 27% and ~ 25%, indicating that there might be room for genetic improvement via introgression of ancestral plant rhizosphere-beneficial microbe associations.
format Online
Article
Text
id pubmed-7376052
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-73760522020-07-24 Domestication-driven changes in plant traits associated with changes in the assembly of the rhizosphere microbiota in tetraploid wheat Spor, Aymé Roucou, Agathe Mounier, Arnaud Bru, David Breuil, Marie-Christine Fort, Florian Vile, Denis Roumet, Pierre Philippot, Laurent Violle, Cyrille Sci Rep Article Despite the large morphological and physiological changes that plants have undergone through domestication, little is known about their impact on their microbiome. Here we characterized rhizospheric bacterial and fungal communities as well as the abundance of N-cycling microbial guilds across thirty-nine accessions of tetraploid wheat, Triticum turgidum, from four domestication groups ranging from the wild subspecies to the semi dwarf elite cultivars. We identified several microbial phylotypes displaying significant variation in their relative abundance depending on the wheat domestication group with a stronger impact of domestication on fungi. The relative abundance of potential fungal plant pathogens belonging to the Sordariomycetes class decreased in domesticated compared to wild emmer while the opposite was found for members of the Glomeromycetes, which are obligate plant symbionts. The depletion of nitrifiers and of arbuscular mycorrhizal fungi in elite wheat cultivars compared to primitive domesticated forms suggests that the Green Revolution has decreased the coupling between plant and rhizosphere microbes that are potentially important for plant nutrient availability. Both plant diameter and fine root percentage exhibited the highest number of associations with microbial taxa, highlighting their putative role in shaping the rhizosphere microbiota during domestication. Aside from domestication, significant variation of bacterial and fungal community composition was found among accessions within each domestication group. In particular, the relative abundances of Ophiostomataceae and of Rhizobiales were strongly dependent on the host accession, with heritability estimates of ~ 27% and ~ 25%, indicating that there might be room for genetic improvement via introgression of ancestral plant rhizosphere-beneficial microbe associations. Nature Publishing Group UK 2020-07-22 /pmc/articles/PMC7376052/ /pubmed/32699344 http://dx.doi.org/10.1038/s41598-020-69175-9 Text en © The Author(s) 2020 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
Spor, Aymé
Roucou, Agathe
Mounier, Arnaud
Bru, David
Breuil, Marie-Christine
Fort, Florian
Vile, Denis
Roumet, Pierre
Philippot, Laurent
Violle, Cyrille
Domestication-driven changes in plant traits associated with changes in the assembly of the rhizosphere microbiota in tetraploid wheat
title Domestication-driven changes in plant traits associated with changes in the assembly of the rhizosphere microbiota in tetraploid wheat
title_full Domestication-driven changes in plant traits associated with changes in the assembly of the rhizosphere microbiota in tetraploid wheat
title_fullStr Domestication-driven changes in plant traits associated with changes in the assembly of the rhizosphere microbiota in tetraploid wheat
title_full_unstemmed Domestication-driven changes in plant traits associated with changes in the assembly of the rhizosphere microbiota in tetraploid wheat
title_short Domestication-driven changes in plant traits associated with changes in the assembly of the rhizosphere microbiota in tetraploid wheat
title_sort domestication-driven changes in plant traits associated with changes in the assembly of the rhizosphere microbiota in tetraploid wheat
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376052/
https://www.ncbi.nlm.nih.gov/pubmed/32699344
http://dx.doi.org/10.1038/s41598-020-69175-9
work_keys_str_mv AT sporayme domesticationdrivenchangesinplanttraitsassociatedwithchangesintheassemblyoftherhizospheremicrobiotaintetraploidwheat
AT roucouagathe domesticationdrivenchangesinplanttraitsassociatedwithchangesintheassemblyoftherhizospheremicrobiotaintetraploidwheat
AT mounierarnaud domesticationdrivenchangesinplanttraitsassociatedwithchangesintheassemblyoftherhizospheremicrobiotaintetraploidwheat
AT brudavid domesticationdrivenchangesinplanttraitsassociatedwithchangesintheassemblyoftherhizospheremicrobiotaintetraploidwheat
AT breuilmariechristine domesticationdrivenchangesinplanttraitsassociatedwithchangesintheassemblyoftherhizospheremicrobiotaintetraploidwheat
AT fortflorian domesticationdrivenchangesinplanttraitsassociatedwithchangesintheassemblyoftherhizospheremicrobiotaintetraploidwheat
AT viledenis domesticationdrivenchangesinplanttraitsassociatedwithchangesintheassemblyoftherhizospheremicrobiotaintetraploidwheat
AT roumetpierre domesticationdrivenchangesinplanttraitsassociatedwithchangesintheassemblyoftherhizospheremicrobiotaintetraploidwheat
AT philippotlaurent domesticationdrivenchangesinplanttraitsassociatedwithchangesintheassemblyoftherhizospheremicrobiotaintetraploidwheat
AT viollecyrille domesticationdrivenchangesinplanttraitsassociatedwithchangesintheassemblyoftherhizospheremicrobiotaintetraploidwheat