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Crop host signatures reflected by co-association patterns of keystone Bacteria in the rhizosphere microbiota

BACKGROUND: The native crop bacterial microbiota of the rhizosphere is envisioned to be engineered for sustainable agriculture. This requires the identification of keystone rhizosphere Bacteria and an understanding on how these govern crop-specific microbiome assembly from soils. We identified the m...

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Autores principales: Lewin, Simon, Francioli, Davide, Ulrich, Andreas, Kolb, Steffen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8513244/
https://www.ncbi.nlm.nih.gov/pubmed/34641981
http://dx.doi.org/10.1186/s40793-021-00387-w
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author Lewin, Simon
Francioli, Davide
Ulrich, Andreas
Kolb, Steffen
author_facet Lewin, Simon
Francioli, Davide
Ulrich, Andreas
Kolb, Steffen
author_sort Lewin, Simon
collection PubMed
description BACKGROUND: The native crop bacterial microbiota of the rhizosphere is envisioned to be engineered for sustainable agriculture. This requires the identification of keystone rhizosphere Bacteria and an understanding on how these govern crop-specific microbiome assembly from soils. We identified the metabolically active bacterial microbiota (SSU RNA) inhabiting two compartments of the rhizosphere of wheat (Triticum aestivum L.), barley (Hordeum vulgare L.), rye (Secale cereale), and oilseed rape (Brassica napus L.) at different growth stages. RESULTS: Based on metabarcoding analysis the bacterial microbiota was shaped by the two rhizosphere compartments, i.e. close and distant. Thereby implying a different spatial extent of bacterial microbiota acquirement by the cereals species versus oilseed rape. We derived core microbiota of each crop species. Massilia (barley and wheat) and unclassified Chloroflexi of group ‘KD4-96’ (oilseed rape) were identified as keystone Bacteria by combining LEfSe biomarker and network analyses. Subsequently, differential associations between networks of each crop species’ core microbiota revealed host plant-specific interconnections for specific genera, such as the unclassified Tepidisphaeraceae ‘WD2101 soil group’. CONCLUSIONS: Our results provide keystone rhizosphere Bacteria derived from for crop hosts and revealed that cohort subnetworks and differential associations elucidated host species effect that was not evident from differential abundance of single bacterial genera enriched or unique to a specific plant host. Thus, we underline the importance of co-occurrence patterns within the rhizosphere microbiota that emerge in crop-specific microbiomes, which will be essential to modify native crop microbiomes for future agriculture and to develop effective bio-fertilizers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40793-021-00387-w.
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spelling pubmed-85132442021-10-20 Crop host signatures reflected by co-association patterns of keystone Bacteria in the rhizosphere microbiota Lewin, Simon Francioli, Davide Ulrich, Andreas Kolb, Steffen Environ Microbiome Research Article BACKGROUND: The native crop bacterial microbiota of the rhizosphere is envisioned to be engineered for sustainable agriculture. This requires the identification of keystone rhizosphere Bacteria and an understanding on how these govern crop-specific microbiome assembly from soils. We identified the metabolically active bacterial microbiota (SSU RNA) inhabiting two compartments of the rhizosphere of wheat (Triticum aestivum L.), barley (Hordeum vulgare L.), rye (Secale cereale), and oilseed rape (Brassica napus L.) at different growth stages. RESULTS: Based on metabarcoding analysis the bacterial microbiota was shaped by the two rhizosphere compartments, i.e. close and distant. Thereby implying a different spatial extent of bacterial microbiota acquirement by the cereals species versus oilseed rape. We derived core microbiota of each crop species. Massilia (barley and wheat) and unclassified Chloroflexi of group ‘KD4-96’ (oilseed rape) were identified as keystone Bacteria by combining LEfSe biomarker and network analyses. Subsequently, differential associations between networks of each crop species’ core microbiota revealed host plant-specific interconnections for specific genera, such as the unclassified Tepidisphaeraceae ‘WD2101 soil group’. CONCLUSIONS: Our results provide keystone rhizosphere Bacteria derived from for crop hosts and revealed that cohort subnetworks and differential associations elucidated host species effect that was not evident from differential abundance of single bacterial genera enriched or unique to a specific plant host. Thus, we underline the importance of co-occurrence patterns within the rhizosphere microbiota that emerge in crop-specific microbiomes, which will be essential to modify native crop microbiomes for future agriculture and to develop effective bio-fertilizers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40793-021-00387-w. BioMed Central 2021-10-12 /pmc/articles/PMC8513244/ /pubmed/34641981 http://dx.doi.org/10.1186/s40793-021-00387-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Article
Lewin, Simon
Francioli, Davide
Ulrich, Andreas
Kolb, Steffen
Crop host signatures reflected by co-association patterns of keystone Bacteria in the rhizosphere microbiota
title Crop host signatures reflected by co-association patterns of keystone Bacteria in the rhizosphere microbiota
title_full Crop host signatures reflected by co-association patterns of keystone Bacteria in the rhizosphere microbiota
title_fullStr Crop host signatures reflected by co-association patterns of keystone Bacteria in the rhizosphere microbiota
title_full_unstemmed Crop host signatures reflected by co-association patterns of keystone Bacteria in the rhizosphere microbiota
title_short Crop host signatures reflected by co-association patterns of keystone Bacteria in the rhizosphere microbiota
title_sort crop host signatures reflected by co-association patterns of keystone bacteria in the rhizosphere microbiota
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8513244/
https://www.ncbi.nlm.nih.gov/pubmed/34641981
http://dx.doi.org/10.1186/s40793-021-00387-w
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