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Enhanced surface colonisation and competition during bacterial adaptation to a fungus

Author

Listed:
  • Anne Richter

    (Technical University of Denmark
    Friedrich Schiller University Jena)

  • Felix Blei

    (Friedrich Schiller University Jena
    Friedrich-Schiller-Universität)

  • Guohai Hu

    (Technical University of Denmark
    BGI-Shenzhen
    BGI-Shenzhen
    BGI-Shenzhen)

  • Jan W. Schwitalla

    (Friedrich Schiller University Jena)

  • Carlos N. Lozano-Andrade

    (Technical University of Denmark)

  • Jiyu Xie

    (Leiden University)

  • Scott A. Jarmusch

    (Technical University of Denmark)

  • Mario Wibowo

    (Technical University of Denmark
    Technology and Research)

  • Bodil Kjeldgaard

    (Technical University of Denmark)

  • Surabhi Surabhi

    (Friedrich Schiller University Jena)

  • Xinming Xu

    (Leiden University)

  • Theresa Jautzus

    (Friedrich Schiller University Jena)

  • Christopher B. W. Phippen

    (Technical University of Denmark)

  • Olaf Tyc

    (Netherlands Institute of Ecology
    Goethe University Hospital)

  • Mark Arentshorst

    (Leiden University)

  • Yue Wang

    (BGI-Shenzhen
    BGI-Shenzhen)

  • Paolina Garbeva

    (Netherlands Institute of Ecology)

  • Thomas Ostenfeld Larsen

    (Technical University of Denmark)

  • Arthur F. J. Ram

    (Leiden University)

  • Cees A. M. Hondel

    (Leiden University)

  • Gergely Maróti

    (Eötvös Loránd Research Network (ELKH))

  • Ákos T. Kovács

    (Technical University of Denmark
    Friedrich Schiller University Jena
    Leiden University)

Abstract

Bacterial-fungal interactions influence microbial community performance of most ecosystems and elicit specific microbial behaviours, including stimulating specialised metabolite production. Here, we use a co-culture experimental evolution approach to investigate bacterial adaptation to the presence of a fungus, using a simple model of bacterial-fungal interactions encompassing the bacterium Bacillus subtilis and the fungus Aspergillus niger. We find in one evolving population that B. subtilis was selected for enhanced production of the lipopeptide surfactin and accelerated surface spreading ability, leading to inhibition of fungal expansion and acidification of the environment. These phenotypes were explained by specific mutations in the DegS-DegU two-component system. In the presence of surfactin, fungal hyphae exhibited bulging cells with delocalised secretory vesicles possibly provoking an RlmA-dependent cell wall stress. Thus, our results indicate that the presence of the fungus selects for increased surfactin production, which inhibits fungal growth and facilitates the competitive success of the bacterium.

Suggested Citation

  • Anne Richter & Felix Blei & Guohai Hu & Jan W. Schwitalla & Carlos N. Lozano-Andrade & Jiyu Xie & Scott A. Jarmusch & Mario Wibowo & Bodil Kjeldgaard & Surabhi Surabhi & Xinming Xu & Theresa Jautzus &, 2024. "Enhanced surface colonisation and competition during bacterial adaptation to a fungus," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-48812-1
    DOI: 10.1038/s41467-024-48812-1
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    References listed on IDEAS

    as
    1. Yuanchen Zhang & Erik K. Kastman & Jeffrey S. Guasto & Benjamin E. Wolfe, 2018. "Fungal networks shape dynamics of bacterial dispersal and community assembly in cheese rind microbiomes," Nature Communications, Nature, vol. 9(1), pages 1-12, December.
    2. Marivic Martin & Anna Dragoš & Theresa Hölscher & Gergely Maróti & Balázs Bálint & Martin Westermann & Ákos T. Kovács, 2017. "De novo evolved interference competition promotes the spread of biofilm defectors," Nature Communications, Nature, vol. 8(1), pages 1-12, August.
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