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Dynamic character displacement among a pair of bacterial phyllosphere commensals in situ

Author

Listed:
  • Lucas Hemmerle

    (ETH Zurich)

  • Benjamin A. Maier

    (ETH Zurich)

  • Miriam Bortfeld-Miller

    (ETH Zurich)

  • Birgitta Ryback

    (ETH Zurich)

  • Christoph G. Gäbelein

    (ETH Zurich)

  • Martin Ackermann

    (ETH Zurich
    Department of Environmental Microbiology, Eawag)

  • Julia A. Vorholt

    (ETH Zurich)

Abstract

Differences between species promote stable coexistence in a resource-limited environment. These differences can result from interspecies competition leading to character shifts, a process referred to as character displacement. While character displacement is often interpreted as a consequence of genetically fixed trait differences between species, it can also be mediated by phenotypic plasticity in response to the presence of another species. Here, we test whether phenotypic plasticity leads to a shift in proteome allocation during co-occurrence of two bacterial species from the abundant, leaf-colonizing families Sphingomonadaceae and Rhizobiaceae in their natural habitat. Upon mono-colonizing of the phyllosphere, both species exhibit specific and shared protein functions indicating a niche overlap. During co-colonization, quantitative differences in the protein repertoire of both bacterial populations occur as a result of bacterial coexistence in planta. Specifically, the Sphingomonas strain produces enzymes for the metabolization of xylan, while the Rhizobium strain reprograms its metabolism to beta-oxidation of fatty acids fueled via the glyoxylate cycle and adapts its biotin acquisition. We demonstrate the conditional relevance of cross-species facilitation by mutagenesis leading to loss of fitness in competition in planta. Our results show that dynamic character displacement and niche facilitation mediated by phenotypic plasticity can contribute to species coexistence.

Suggested Citation

  • 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.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-30469-3
    DOI: 10.1038/s41467-022-30469-3
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    References listed on IDEAS

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    1. 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.
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    3. Alan R. Pacheco & Mauricio Moel & Daniel Segrè, 2019. "Costless metabolic secretions as drivers of interspecies interactions in microbial ecosystems," Nature Communications, Nature, vol. 10(1), pages 1-12, December.
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    Cited by:

    1. Cong Zhang & Di-Fei Zhou & Meng-Ying Wang & Ya-Zhen Song & Chong Zhang & Ming-Ming Zhang & Jing Sun & Lu Yao & Xu-Hua Mo & Zeng-Xin Ma & Xiao-Jie Yuan & Yi Shao & Hao-Ran Wang & Si-Han Dong & Kai Bao , 2024. "Phosphoribosylpyrophosphate synthetase as a metabolic valve advances Methylobacterium/Methylorubrum phyllosphere colonization and plant growth," Nature Communications, Nature, vol. 15(1), pages 1-16, December.

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