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Monosaccharides drive Salmonella gut colonization in a context-dependent or -independent manner

Author

Listed:
  • Christopher Schubert

    (ETH Zurich)

  • Bidong D. Nguyen

    (ETH Zurich)

  • Andreas Sichert

    (ETH Zurich)

  • Nicolas Näpflin

    (University of Zurich)

  • Anna Sintsova

    (ETH Zurich)

  • Lilith Feer

    (ETH Zurich)

  • Jana Näf

    (ETH Zurich)

  • Benjamin B. J. Daniel

    (ETH Zurich)

  • Yves Steiger

    (ETH Zurich)

  • Christian Mering

    (University of Zurich)

  • Uwe Sauer

    (ETH Zurich)

  • Wolf-Dietrich Hardt

    (ETH Zurich)

Abstract

The carbohydrates that fuel gut colonization by S. Typhimurium are not fully known. To investigate this, we designed a quality-controlled mutant pool to probe the metabolic capabilities of this enteric pathogen. Using neutral genetic barcodes, we tested 35 metabolic mutants across five different mouse models with varying microbiome complexities, allowing us to differentiate between context-dependent and context-independent nutrient sources. Results showed that S. Typhimurium uses D-mannose, D-fructose and likely D-glucose as context-independent carbohydrates across all five mouse models. The utilization of D-galactose, N-acetylglucosamine and hexuronates, on the other hand, was context-dependent. Furthermore, we showed that D-fructose is important in strain-to-strain competition between Salmonella serovars. Complementary experiments confirmed that D-glucose, D-fructose, and D-galactose are excellent niches for S. Typhimurium to exploit during colonization. Quantitative measurements revealed sufficient amounts of carbohydrates, such as D-glucose or D-galactose, in the murine cecum to drive S. Typhimurium colonization. Understanding these key substrates and their context-dependent or -independent use by enteric pathogens will inform the future design of probiotics and therapeutics to prevent diarrheal infections such as non-typhoidal salmonellosis.

Suggested Citation

  • Christopher Schubert & Bidong D. Nguyen & Andreas Sichert & Nicolas Näpflin & Anna Sintsova & Lilith Feer & Jana Näf & Benjamin B. J. Daniel & Yves Steiger & Christian Mering & Uwe Sauer & Wolf-Dietri, 2025. "Monosaccharides drive Salmonella gut colonization in a context-dependent or -independent manner," Nature Communications, Nature, vol. 16(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-56890-y
    DOI: 10.1038/s41467-025-56890-y
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    1. Franziska Faber & Lisa Tran & Mariana X. Byndloss & Christopher A. Lopez & Eric M. Velazquez & Tobias Kerrinnes & Sean-Paul Nuccio & Tamding Wangdi & Oliver Fiehn & Renée M. Tsolis & Andreas J. Bäumle, 2016. "Host-mediated sugar oxidation promotes post-antibiotic pathogen expansion," Nature, Nature, vol. 534(7609), pages 697-699, June.
    2. Katharine M. Ng & Jessica A. Ferreyra & Steven K. Higginbottom & Jonathan B. Lynch & Purna C. Kashyap & Smita Gopinath & Natasha Naidu & Biswa Choudhury & Bart C. Weimer & Denise M. Monack & Justin L., 2013. "Microbiota-liberated host sugars facilitate post-antibiotic expansion of enteric pathogens," Nature, Nature, vol. 502(7469), pages 96-99, October.
    3. Ian W. Campbell & Karthik Hullahalli & Jerrold R. Turner & Matthew K. Waldor, 2023. "Quantitative dose-response analysis untangles host bottlenecks to enteric infection," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
    4. Martin Ackermann & Bärbel Stecher & Nikki E. Freed & Pascal Songhet & Wolf-Dietrich Hardt & Michael Doebeli, 2008. "Self-destructive cooperation mediated by phenotypic noise," Nature, Nature, vol. 454(7207), pages 987-990, August.
    5. Médéric Diard & Victor Garcia & Lisa Maier & Mitja N. P. Remus-Emsermann & Roland R. Regoes & Martin Ackermann & Wolf-Dietrich Hardt, 2013. "Stabilization of cooperative virulence by the expression of an avirulent phenotype," Nature, Nature, vol. 494(7437), pages 353-356, February.
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