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Microbial interactions lead to rapid micro-scale successions on model marine particles

Author

Listed:
  • Manoshi S. Datta

    (Computational and Systems Biology Graduate Program, Massachusetts Institute of Technology)

  • Elzbieta Sliwerska

    (Environmental and Geomatic Engineering, Institute of Environmental Engineering, ETH Zürich)

  • Jeff Gore

    (Computational and Systems Biology Graduate Program, Massachusetts Institute of Technology
    Physics of Living Systems, Massachusetts Institute of Technology)

  • Martin F. Polz

    (Massachusetts Institute of Technology)

  • Otto X. Cordero

    (Computational and Systems Biology Graduate Program, Massachusetts Institute of Technology
    Massachusetts Institute of Technology
    Institute of Biogeochemistry and Pollutant Dynamics, ETH Zürich)

Abstract

In the ocean, organic particles harbour diverse bacterial communities, which collectively digest and recycle essential nutrients. Traits like motility and exo-enzyme production allow individual taxa to colonize and exploit particle resources, but it remains unclear how community dynamics emerge from these individual traits. Here we track the taxon and trait dynamics of bacteria attached to model marine particles and demonstrate that particle-attached communities undergo rapid, reproducible successions driven by ecological interactions. Motile, particle-degrading taxa are selected for during early successional stages. However, this selective pressure is later relaxed when secondary consumers invade, which are unable to use the particle resource but, instead, rely on carbon from primary degraders. This creates a trophic chain that shifts community metabolism away from the particle substrate. These results suggest that primary successions may shape particle-attached bacterial communities in the ocean and that rapid community-wide metabolic shifts could limit rates of marine particle degradation.

Suggested Citation

  • Manoshi S. Datta & Elzbieta Sliwerska & Jeff Gore & Martin F. Polz & Otto X. Cordero, 2016. "Microbial interactions lead to rapid micro-scale successions on model marine particles," Nature Communications, Nature, vol. 7(1), pages 1-7, September.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms11965
    DOI: 10.1038/ncomms11965
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    Citations

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    Cited by:

    1. Xiaoyu Shan & Rachel E. Szabo & Otto X. Cordero, 2023. "Mutation-induced infections of phage-plasmids," Nature Communications, Nature, vol. 14(1), pages 1-10, December.
    2. Kapil Amarnath & Avaneesh V. Narla & Sammy Pontrelli & Jiajia Dong & Jack Reddan & Brian R. Taylor & Tolga Caglar & Julia Schwartzman & Uwe Sauer & Otto X. Cordero & Terence Hwa, 2023. "Stress-induced metabolic exchanges between complementary bacterial types underly a dynamic mechanism of inter-species stress resistance," Nature Communications, Nature, vol. 14(1), pages 1-20, December.
    3. Trang T. H. Nguyen & Emily J. Zakem & Ali Ebrahimi & Julia Schwartzman & Tolga Caglar & Kapil Amarnath & Uria Alcolombri & François J. Peaudecerf & Terence Hwa & Roman Stocker & Otto X. Cordero & Naom, 2022. "Microbes contribute to setting the ocean carbon flux by altering the fate of sinking particulates," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    4. Yichao Wu & Chengxia Fu & Caroline L. Peacock & Søren J. Sørensen & Marc A. Redmile-Gordon & Ke-Qing Xiao & Chunhui Gao & Jun Liu & Qiaoyun Huang & Zixue Li & Peiyi Song & Yongguan Zhu & Jizhong Zhou , 2023. "Cooperative microbial interactions drive spatial segregation in porous environments," Nature Communications, Nature, vol. 14(1), pages 1-14, December.

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