Author
Listed:
- Anne Grießhammer
(University of Tübingen
University of Tübingen
University Hospital Tübingen)
- Jacobo de la Cuesta-Zuluaga
(University of Tübingen
University of Tübingen
University Hospital Tübingen)
- Patrick Müller
(University of Tübingen
University of Tübingen
University Hospital Tübingen)
- Cordula Gekeler
(University of Tübingen
University of Tübingen
University Hospital Tübingen)
- Jan Homolak
(University of Tübingen
University of Tübingen
University Hospital Tübingen
University of Zagreb School of Medicine)
- Hsuan Chang
(Genome Biology)
- Katharina Schmitt
(University of Tübingen
University of Tübingen)
- Chiara Planker
(University of Tübingen
University of Tübingen)
- Verena Schmidtchen
(University of Tübingen
University of Tübingen)
- Suchira Gallage
(University Hospital Tübingen)
- Erwin Bohn
(University of Tübingen
University of Tübingen)
- Taylor H. Nguyen
(Stanford University)
- Jenny Hetzer
(University Hospital Tübingen)
- Mathias Heikenwälder
(University Hospital Tübingen
Division of Chronic Inflammation and Cancer)
- Kerwyn Casey Huang
(Stanford University
Stanford University School of Medicine
Chan Zuckerberg Biohub)
- Taiyeb Zahir
(University of Tübingen
University of Tübingen)
- Lisa Maier
(University of Tübingen
University of Tübingen
University Hospital Tübingen)
Abstract
Non-antibiotic drugs can alter the composition of the gut microbiome1, but they have largely unknown implications for human health2. Here we examined how non-antibiotics affect the ability of gut commensals to resist colonization by enteropathogens3. We also developed an in vitro assay to assess enteropathogen growth in drug-perturbed microbial communities. Pathogenic Gammaproteobacteria were more resistant to non-antibiotics than commensals and their post-treatment expansion was potentiated. For 28% of the 53 drugs tested, the growth of Salmonella enterica subsp. enterica serovar Typhimurium. (S. Tm) in synthetic and human stool-derived communities was increased, and similar effects were observed for other enteropathogens. Non-antibiotics promoted pathogen proliferation by inhibiting the growth of commensals, altering microbial interactions and enhancing the ability of S. Tm to exploit metabolic niches. Drugs that promoted pathogen expansion in vitro increased the intestinal S. Tm load in mice. For the antihistamine terfenadine, drug-induced disruption of colonization resistance accelerated disease onset and increased inflammation caused by S. Tm. Our findings identify non-antibiotics as previously overlooked risk factors that may contribute to the development of enteric infections.
Suggested Citation
Anne Grießhammer & Jacobo de la Cuesta-Zuluaga & Patrick Müller & Cordula Gekeler & Jan Homolak & Hsuan Chang & Katharina Schmitt & Chiara Planker & Verena Schmidtchen & Suchira Gallage & Erwin Bohn &, 2025.
"Non-antibiotics disrupt colonization resistance against enteropathogens,"
Nature, Nature, vol. 644(8076), pages 497-505, August.
Handle:
RePEc:nat:nature:v:644:y:2025:i:8076:d:10.1038_s41586-025-09217-2
DOI: 10.1038/s41586-025-09217-2
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