IDEAS home Printed from https://ideas.repec.org/a/nat/nature/v528y2015i7582d10.1038_nature16192.html
   My bibliography  Save this article

Functional overlap of the Arabidopsis leaf and root microbiota

Author

Listed:
  • Yang Bai

    (Max Planck Institute for Plant Breeding Research)

  • Daniel B. Müller

    (Institute of Microbiology, ETH Zurich)

  • Girish Srinivas

    (Max Planck Institute for Plant Breeding Research)

  • Ruben Garrido-Oter

    (Max Planck Institute for Plant Breeding Research
    Heinrich Heine University Düsseldorf
    Cluster of Excellence on Plant Sciences (CEPLAS), Max Planck Institute for Plant Breeding Research)

  • Eva Potthoff

    (Institute of Microbiology, ETH Zurich)

  • Matthias Rott

    (Max Planck Institute for Plant Breeding Research)

  • Nina Dombrowski

    (Max Planck Institute for Plant Breeding Research)

  • Philipp C. Münch

    (Computational Biology of Infection Research, Helmholtz Center for Infection Research
    Max-von-Pettenkofer Institute, Ludwig Maximilian University, German Center for Infection Research (DZIF), partner site LMU Munich
    German Center for Infection Research (DZIF), partner site Hannover-Braunschweig)

  • Stijn Spaepen

    (Max Planck Institute for Plant Breeding Research)

  • Mitja Remus-Emsermann

    (Institute of Microbiology, ETH Zurich)

  • Bruno Hüttel

    (Max Planck Genome Center, Max Planck Institute for Plant Breeding Research)

  • Alice C. McHardy

    (Cluster of Excellence on Plant Sciences (CEPLAS), Max Planck Institute for Plant Breeding Research
    Computational Biology of Infection Research, Helmholtz Center for Infection Research)

  • Julia A. Vorholt

    (Institute of Microbiology, ETH Zurich)

  • Paul Schulze-Lefert

    (Max Planck Institute for Plant Breeding Research
    Cluster of Excellence on Plant Sciences (CEPLAS), Max Planck Institute for Plant Breeding Research)

Abstract

Roots and leaves of healthy plants host taxonomically structured bacterial assemblies, and members of these communities contribute to plant growth and health. We established Arabidopsis leaf- and root-derived microbiota culture collections representing the majority of bacterial species that are reproducibly detectable by culture-independent community sequencing. We found an extensive taxonomic overlap between the leaf and root microbiota. Genome drafts of 400 isolates revealed a large overlap of genome-encoded functional capabilities between leaf- and root-derived bacteria with few significant differences at the level of individual functional categories. Using defined bacterial communities and a gnotobiotic Arabidopsis plant system we show that the isolates form assemblies resembling natural microbiota on their cognate host organs, but are also capable of ectopic leaf or root colonization. While this raises the possibility of reciprocal relocation between root and leaf microbiota members, genome information and recolonization experiments also provide evidence for microbiota specialization to their respective niche.

Suggested Citation

  • Yang Bai & Daniel B. Müller & Girish Srinivas & Ruben Garrido-Oter & Eva Potthoff & Matthias Rott & Nina Dombrowski & Philipp C. Münch & Stijn Spaepen & Mitja Remus-Emsermann & Bruno Hüttel & Alice C., 2015. "Functional overlap of the Arabidopsis leaf and root microbiota," Nature, Nature, vol. 528(7582), pages 364-369, December.
  • Handle: RePEc:nat:nature:v:528:y:2015:i:7582:d:10.1038_nature16192
    DOI: 10.1038/nature16192
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/nature16192
    File Function: Abstract
    Download Restriction: Access to the full text of the articles in this series is restricted.

    File URL: https://libkey.io/10.1038/nature16192?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Lucas Hemmerle & Benjamin A. Maier & Miriam Bortfeld-Miller & Birgitta Ryback & Christoph G. Gäbelein & Martin Ackermann & Julia A. Vorholt, 2022. "Dynamic character displacement among a pair of bacterial phyllosphere commensals in situ," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    2. Nathan Vannier & Fantin Mesny & Felix Getzke & Guillaume Chesneau & Laura Dethier & Jana Ordon & Thorsten Thiergart & Stéphane Hacquard, 2023. "Genome-resolved metatranscriptomics reveals conserved root colonization determinants in a synthetic microbiota," Nature Communications, Nature, vol. 14(1), pages 1-17, December.
    3. Benjamin H. Good & Layton B. Rosenfeld, 2023. "Eco-evolutionary feedbacks in the human gut microbiome," Nature Communications, Nature, vol. 14(1), pages 1-9, December.
    4. Lige Ma & Yu Luo & Chen Chen & Huan Luo & Shuqi Wang & Yue Yuan & Wenhua Yang & Can Liu & Xulv Cao & Nannan Li, 2023. "Bacterial Strategies for Improving the Yield, Quality, and Adaptability of Oil Crops," Agriculture, MDPI, vol. 14(1), pages 1-29, December.
    5. Carmen Escudero-Martinez & Max Coulter & Rodrigo Alegria Terrazas & Alexandre Foito & Rumana Kapadia & Laura Pietrangelo & Mauro Maver & Rajiv Sharma & Alessio Aprile & Jenny Morris & Pete E. Hedley &, 2022. "Identifying plant genes shaping microbiota composition in the barley rhizosphere," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    6. Ke Tao & Ib T. Jensen & Sha Zhang & Eber Villa-Rodríguez & Zuzana Blahovska & Camilla Lind Salomonsen & Anna Martyn & Þuríður Nótt Björgvinsdóttir & Simon Kelly & Luc Janss & Marianne Glasius & Rasmus, 2024. "Nitrogen and Nod factor signaling determine Lotus japonicus root exudate composition and bacterial assembly," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
    7. John McEnany & Benjamin H. Good, 2024. "Predicting the first steps of evolution in randomly assembled communities," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
    8. Jing Liang & Jiafan Zhang & Zongmu Yao & Shouyang Luo & Lei Tian & Chunjie Tian & Yu Sun, 2022. "Preliminary Findings of Polypropylene Carbonate (PPC) Plastic Film Mulching Effects on the Soil Microbial Community," Agriculture, MDPI, vol. 12(3), pages 1-13, March.
    9. Mingxing Wang & An-Hui Ge & Xingzhu Ma & Xiaolin Wang & Qiujin Xie & Like Wang & Xianwei Song & Mengchen Jiang & Weibing Yang & Jeremy D. Murray & Yayu Wang & Huan Liu & Xiaofeng Cao & Ertao Wang, 2024. "Dynamic root microbiome sustains soybean productivity under unbalanced fertilization," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
    10. Barbara Emmenegger & Julien Massoni & Christine M. Pestalozzi & Miriam Bortfeld-Miller & Benjamin A. Maier & Julia A. Vorholt, 2023. "Identifying microbiota community patterns important for plant protection using synthetic communities and machine learning," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    11. Carin J. Ragland & Kevin Y. Shih & José R. Dinneny, 2024. "Choreographing root architecture and rhizosphere interactions through synthetic biology," Nature Communications, Nature, vol. 15(1), pages 1-11, December.
    12. Guy Amit & Amir Bashan, 2023. "Top-down identification of keystone taxa in the microbiome," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    13. Zhaohui Cao & Wenlong Zuo & Lanxiang Wang & Junyu Chen & Zepeng Qu & Fan Jin & Lei Dai, 2023. "Spatial profiling of microbial communities by sequential FISH with error-robust encoding," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    14. Xin Zhou & Jinting Wang & Fang Liu & Junmin Liang & Peng Zhao & Clement K. M. Tsui & Lei Cai, 2022. "Cross-kingdom synthetic microbiota supports tomato suppression of Fusarium wilt disease," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    15. Shikai La & Jiafan Li & Si Ma & Xingqun Liu & Lihong Gao & Yongqiang Tian, 2024. "Protective role of native root-associated bacterial consortium against root-knot nematode infection in susceptible plants," Nature Communications, Nature, vol. 15(1), pages 1-18, December.
    16. Frederickson Entila & Xiaowei Han & Akira Mine & Paul Schulze-Lefert & Kenichi Tsuda, 2024. "Commensal lifestyle regulated by a negative feedback loop between Arabidopsis ROS and the bacterial T2SS," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
    17. Chengjia Tan & Mohammad Talib Kalhoro & Yahya Faqir & Jiahua Ma & Matthew Duah Osei & Ghulam Khaliq, 2022. "Climate-Resilient Microbial Biotechnology: A Perspective on Sustainable Agriculture," Sustainability, MDPI, vol. 14(9), pages 1-29, May.
    18. Felix Getzke & Lei Wang & Guillaume Chesneau & Nils Böhringer & Fantin Mesny & Nienke Denissen & Hidde Wesseler & Priscilla Tijesuni Adisa & Michael Marner & Paul Schulze-Lefert & Till F. Schäberle & , 2024. "Physiochemical interaction between osmotic stress and a bacterial exometabolite promotes plant disease," Nature Communications, Nature, vol. 15(1), pages 1-16, December.
    19. Li Fan & Katja Fröhlich & Eric Melzer & Rory N. Pruitt & Isabell Albert & Lisha Zhang & Anna Joe & Chenlei Hua & Yanyue Song & Markus Albert & Sang-Tae Kim & Detlef Weigel & Cyril Zipfel & Eunyoung Ch, 2022. "Genotyping-by-sequencing-based identification of Arabidopsis pattern recognition receptor RLP32 recognizing proteobacterial translation initiation factor IF1," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    20. Lisa Thoenen & Marco Kreuzer & Christine Pestalozzi & Matilde Florean & Pierre Mateo & Tobias Züst & Anlun Wei & Caitlin Giroud & Liza Rouyer & Valentin Gfeller & Matheus D. Notter & Eva Knoch & Siegf, 2024. "The lactonase BxdA mediates metabolic specialisation of maize root bacteria to benzoxazinoids," Nature Communications, Nature, vol. 15(1), pages 1-17, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:nature:v:528:y:2015:i:7582:d:10.1038_nature16192. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.