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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