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Soil origin and plant genotype structure distinct microbiome compartments in the model legume Medicago truncatula

BACKGROUND: Understanding the genetic and environmental factors that structure plant microbiomes is necessary for leveraging these interactions to address critical needs in agriculture, conservation, and sustainability. Legumes, which form root nodule symbioses with nitrogen-fixing rhizobia, have se...

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Autores principales: Brown, Shawn P., Grillo, Michael A., Podowski, Justin C., Heath, Katy D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523075/
https://www.ncbi.nlm.nih.gov/pubmed/32988416
http://dx.doi.org/10.1186/s40168-020-00915-9
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author Brown, Shawn P.
Grillo, Michael A.
Podowski, Justin C.
Heath, Katy D.
author_facet Brown, Shawn P.
Grillo, Michael A.
Podowski, Justin C.
Heath, Katy D.
author_sort Brown, Shawn P.
collection PubMed
description BACKGROUND: Understanding the genetic and environmental factors that structure plant microbiomes is necessary for leveraging these interactions to address critical needs in agriculture, conservation, and sustainability. Legumes, which form root nodule symbioses with nitrogen-fixing rhizobia, have served as model plants for understanding the genetics and evolution of beneficial plant-microbe interactions for decades, and thus have added value as models of plant-microbiome interactions. Here we use a common garden experiment with 16S rRNA gene amplicon and shotgun metagenomic sequencing to study the drivers of microbiome diversity and composition in three genotypes of the model legume Medicago truncatula grown in two native soil communities. RESULTS: Bacterial diversity decreased between external (rhizosphere) and internal plant compartments (root endosphere, nodule endosphere, and leaf endosphere). Community composition was shaped by strong compartment × soil origin and compartment × plant genotype interactions, driven by significant soil origin effects in the rhizosphere and significant plant genotype effects in the root endosphere. Nevertheless, all compartments were dominated by Ensifer, the genus of rhizobia that forms root nodule symbiosis with M. truncatula, and additional shotgun metagenomic sequencing suggests that the nodulating Ensifer were not genetically distinguishable from those elsewhere in the plant. We also identify a handful of OTUs that are common in nodule tissues, which are likely colonized from the root endosphere. CONCLUSIONS: Our results demonstrate strong host filtering effects, with rhizospheres driven by soil origin and internal plant compartments driven by host genetics, and identify several key nodule-inhabiting taxa that coexist with rhizobia in the native range. Our results set the stage for future functional genetic experiments aimed at expanding our pairwise understanding of legume-rhizobium symbiosis toward a more mechanistic understanding of plant microbiomes.
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spelling pubmed-75230752020-09-30 Soil origin and plant genotype structure distinct microbiome compartments in the model legume Medicago truncatula Brown, Shawn P. Grillo, Michael A. Podowski, Justin C. Heath, Katy D. Microbiome Research BACKGROUND: Understanding the genetic and environmental factors that structure plant microbiomes is necessary for leveraging these interactions to address critical needs in agriculture, conservation, and sustainability. Legumes, which form root nodule symbioses with nitrogen-fixing rhizobia, have served as model plants for understanding the genetics and evolution of beneficial plant-microbe interactions for decades, and thus have added value as models of plant-microbiome interactions. Here we use a common garden experiment with 16S rRNA gene amplicon and shotgun metagenomic sequencing to study the drivers of microbiome diversity and composition in three genotypes of the model legume Medicago truncatula grown in two native soil communities. RESULTS: Bacterial diversity decreased between external (rhizosphere) and internal plant compartments (root endosphere, nodule endosphere, and leaf endosphere). Community composition was shaped by strong compartment × soil origin and compartment × plant genotype interactions, driven by significant soil origin effects in the rhizosphere and significant plant genotype effects in the root endosphere. Nevertheless, all compartments were dominated by Ensifer, the genus of rhizobia that forms root nodule symbiosis with M. truncatula, and additional shotgun metagenomic sequencing suggests that the nodulating Ensifer were not genetically distinguishable from those elsewhere in the plant. We also identify a handful of OTUs that are common in nodule tissues, which are likely colonized from the root endosphere. CONCLUSIONS: Our results demonstrate strong host filtering effects, with rhizospheres driven by soil origin and internal plant compartments driven by host genetics, and identify several key nodule-inhabiting taxa that coexist with rhizobia in the native range. Our results set the stage for future functional genetic experiments aimed at expanding our pairwise understanding of legume-rhizobium symbiosis toward a more mechanistic understanding of plant microbiomes. BioMed Central 2020-09-28 /pmc/articles/PMC7523075/ /pubmed/32988416 http://dx.doi.org/10.1186/s40168-020-00915-9 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
Brown, Shawn P.
Grillo, Michael A.
Podowski, Justin C.
Heath, Katy D.
Soil origin and plant genotype structure distinct microbiome compartments in the model legume Medicago truncatula
title Soil origin and plant genotype structure distinct microbiome compartments in the model legume Medicago truncatula
title_full Soil origin and plant genotype structure distinct microbiome compartments in the model legume Medicago truncatula
title_fullStr Soil origin and plant genotype structure distinct microbiome compartments in the model legume Medicago truncatula
title_full_unstemmed Soil origin and plant genotype structure distinct microbiome compartments in the model legume Medicago truncatula
title_short Soil origin and plant genotype structure distinct microbiome compartments in the model legume Medicago truncatula
title_sort soil origin and plant genotype structure distinct microbiome compartments in the model legume medicago truncatula
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523075/
https://www.ncbi.nlm.nih.gov/pubmed/32988416
http://dx.doi.org/10.1186/s40168-020-00915-9
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