Spatial analysis of the root system coupled to microbial community inoculation shed light on rhizosphere bacterial community assembly

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Although studied for more than a century, the spatial distribution of microorganisms in a root system still remains partly understood. In a repeated greenhouse experiment using the model plant Brachypodium distachyon, we investigated the composition and distribution of rhizosphere bacteria and their response to inoculation with artificially selected microbial communities, using two different sampling scales: root sections from distinct individual roots (apical, middle, and rear sections) and the remaining entire system recovered after homogenization. Using 16S rRNA gene sequencing, we identified that root section identity was the most influential factor on the microbiota composition (R2 = 44.4%), followed by batch (R2 = 34.4%), and plant identity (R2 = 15.2%). Apical sections were characterized by increased abundances for Firmicutes members, while the rear sections featured more Verrucomicrobia. Root section sampling showed better sensitivity at detecting significant effects of the inoculation on the microbiota composition (e.g., local influence of inoculation on rear sections), in contrast, the homogenized sampling showed improved reproducibility (e.g., smaller sample dispersion). The comparison of the two sampling strategies highlighted a clear tradeoff between reproducibility and sensitivity, encouraging to complement traditional approaches with fine-scale sampling to improve our capacity to understand biological effects that could be otherwise missed.

OriginalsprogEngelsk
TidsskriftBiology and Fertility of Soils
Vol/bind57
Udgave nummer7
Sider (fra-til)973-989
Antal sider17
ISSN0178-2762
DOI
StatusUdgivet - 2021

Bibliografisk note

Funding Information:
We thank the Lundbeck Foundation (grant number R223-2016-179) for funding this study. S.W. was supported by the China Scholarship Council. S.J. was supported by the University of Bourgogne Franche-Comté via the FABER program (grant number 2017-9201AAO049S01302) and via the ISITE-BFC International Junior Fellowship award (AAP3: RA19028.AEC.IS). We express our gratitude to the members of the 4PMI platform lead by Christophe Salon and Céline Bernard for their expertise and help during plant phenotyping (For Plant and Microbe Interaction, INRA Center Dijon, France, https://www6.dijon.inrae.fr/plateforme4pmi_eng/Technical-description/High-Throughput-phenotyping ). Respectively, we thank Damien Gironde, Frédéric Saignole, Noureddine El-Mjiyad and Karine Palavioux for helping during plant growth monitoring; Franck Zenk and Julien Martinet for image capture; and Mickael Lamboeuf for image processing; Sébastien Anselme, Richard Sibout, and Thomas Girin from the Brachypodium resources center at the Institut Jean Pierre-Bourgin, (INRAVersailles, France) for seeds provision; Beatriz Decencière, Amandine Hansart, and Florent Massol of the CEREEP—Ecotron IDF/UMS CNRS/ENS 3194 for soil provision.

Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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