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Klebsiella oxytoca facilitates microbiome recovery via antibiotic degradation and restores colonization resistance in a diet-dependent manner

Author

Listed:
  • Éva d. H. Almási

    (Helmholtz Centre for Infection Research (HZI))

  • Lea Eisenhard

    (Helmholtz Centre for Infection Research (HZI))

  • Lisa Osbelt

    (Helmholtz Centre for Infection Research (HZI))

  • Till Robin Lesker

    (Helmholtz Centre for Infection Research (HZI))

  • Anna C. Vetter

    (Helmholtz Centre for Infection Research (HZI))

  • Nele Knischewski

    (Helmholtz Centre for Infection Research (HZI))

  • Agata Anna Bielecka

    (Helmholtz Centre for Infection Research (HZI))

  • Achim Gronow

    (Helmholtz Centre for Infection Research (HZI))

  • Uthayakumar Muthukumarasamy

    (Helmholtz Centre for Infection Research (HZI))

  • Marie Wende

    (Helmholtz Centre for Infection Research (HZI))

  • Caroline Tawk

    (Helmholtz Centre for Infection Research (HZI))

  • Meina Neumann-Schaal

    (Leibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures)

  • Mark Brönstrup

    (Helmholtz Centre for Infection Research (HZI))

  • Till Strowig

    (Helmholtz Centre for Infection Research (HZI)
    Center for Individualized Infection Medicine
    partner site Hannover-Braunschweig)

Abstract

Competition among bacteria for carbohydrates is pivotal for colonization resistance (CR). However, the impact of Western-style diets on CR remains unclear. Here we show how the competition between Klebsiella oxytoca and Klebsiella pneumoniae is modulated by consuming one of three Western-style diets characterized by high-starch, high-sucrose, or high-fat/high-sucrose content. In vivo competition experiments in ampicillin-treated mice reveal that K. oxytoca promotes K. pneumoniae decolonization on all dietary backgrounds. However, mice on the high-fat/high-sucrose diet show reduced pathogen clearance. Microbiome analysis reveals that the combination of Western-style diets and ampicillin treatment synergize in microbiome impairment, particularly noticeable in the presence of high dietary fat content. The diet-independent degradation of ampicillin in the gut lumen by K. oxytoca beta-lactamases facilitates rapid commensal outgrowth, which is required for subsequent pathogen clearance. Our findings provide insights into how diet modulates functional microbiome recovery and K. oxytoca-mediated pathogen elimination from the gut.

Suggested Citation

  • Éva d. H. Almási & Lea Eisenhard & Lisa Osbelt & Till Robin Lesker & Anna C. Vetter & Nele Knischewski & Agata Anna Bielecka & Achim Gronow & Uthayakumar Muthukumarasamy & Marie Wende & Caroline Tawk , 2025. "Klebsiella oxytoca facilitates microbiome recovery via antibiotic degradation and restores colonization resistance in a diet-dependent manner," Nature Communications, Nature, vol. 16(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-024-55800-y
    DOI: 10.1038/s41467-024-55800-y
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    References listed on IDEAS

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