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Stress-induced metabolic exchanges between complementary bacterial types underly a dynamic mechanism of inter-species stress resistance

Author

Listed:
  • Kapil Amarnath

    (U.C. San Diego)

  • Avaneesh V. Narla

    (U.C. San Diego)

  • Sammy Pontrelli

    (ETH Zürich)

  • Jiajia Dong

    (U.C. San Diego
    Bucknell University)

  • Jack Reddan

    (U.C. San Diego)

  • Brian R. Taylor

    (U.C. San Diego)

  • Tolga Caglar

    (U.C. San Diego)

  • Julia Schwartzman

    (MIT)

  • Uwe Sauer

    (ETH Zürich)

  • Otto X. Cordero

    (MIT)

  • Terence Hwa

    (U.C. San Diego
    U.C. San Diego)

Abstract

Metabolic cross-feeding plays vital roles in promoting ecological diversity. While some microbes depend on exchanges of essential nutrients for growth, the forces driving the extensive cross-feeding needed to support the coexistence of free-living microbes are poorly understood. Here we characterize bacterial physiology under self-acidification and establish that extensive excretion of key metabolites following growth arrest provides a collaborative, inter-species mechanism of stress resistance. This collaboration occurs not only between species isolated from the same community, but also between unrelated species with complementary (glycolytic vs. gluconeogenic) modes of metabolism. Cultures of such communities progress through distinct phases of growth-dilution cycles, comprising of exponential growth, acidification-triggered growth arrest, collaborative deacidification, and growth recovery, with each phase involving different combinations of physiological states of individual species. Our findings challenge the steady-state view of ecosystems commonly portrayed in ecological models, offering an alternative dynamical view based on growth advantages of complementary species in different phases.

Suggested Citation

  • 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.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-38913-8
    DOI: 10.1038/s41467-023-38913-8
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    References listed on IDEAS

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    1. 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.
    2. Martin T. Croft & Andrew D. Lawrence & Evelyne Raux-Deery & Martin J. Warren & Alison G. Smith, 2005. "Algae acquire vitamin B12 through a symbiotic relationship with bacteria," Nature, Nature, vol. 438(7064), pages 90-93, November.
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    1. Junbo Tang & Wenlong Zuo & Lizhen Guo & Zhihao Han & Chengfeng Yang & Benfeng Han & Lei Dai & Xue Zhang & Xin Zhou, 2024. "Synergistic pectin deconstruction is a prerequisite for mutualistic interactions between honeybee gut bacteria," Nature Communications, Nature, vol. 15(1), pages 1-16, December.

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