Antibiotic perturbation of the human gut phageome preserves its individuality and promotes blooms of virulent phages

Antibiotic use disrupts the gut microbiota, posing risks of long-term health issues and resistance. To study its impact on gut phages, we followed 22 healthy individuals 2 weeks before and up to 6 months after a 3-day course of 3<sup>rd</sup>-generation cephalosporins. Our results show that gut phages rarely encode antibiotic resistance genes and are mostly temperate, including many phage plasmids. Furthermore, phage populations remain individual-specific even after microbiome perturbation. Yet, we report a 20% decline in phage diversity the day after treatment, alongside blooms of a few, mostly virulent, phages. We suggest that some of these phages contribute to the recovery of bacterial diversity via "kill-the-winner" dynamics. This is supported by (temporarily) dominant phages targeting Parabacteroides distasonis, a bacterium that thrives post-treatment only in the absence of these phages. Our findings suggest gut phages are crucial to the microbiome response to antibiotics, aiding the restoration of balance and diversity.

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Publication Details

Journal
Cell Reports
Published
2025-07-21
DOI
https://doi.org/10.1016/j.celrep.2025.116020
Citations
3
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
5.15

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article

Antibiotic perturbation of the human gut phageome preserves its individuality and promotes blooms of virulent phages

Rémi Denise, Charles Burdet, Marie Touchon, Camille d’Humières et al.
3 citations
Cell Reports
Bacteriophages and microbial interactions
5.15
article

Antibiotic perturbation of the human gut phageome preserves its individuality and promotes blooms of virulent phages

Rémi Denise, Charles Burdet, Marie Touchon, Camille d’Humières, Quentin Lamy-Besnier, Eduardo P. C. Rocha, France Mentré, Bénédicte Condamine, Laurence Ma, Erick Denamur, Eugen Pfeifer, Florian Plaza Oñate, Sara Dion
article en
3 citations

Abstract

Antibiotic use disrupts the gut microbiota, posing risks of long-term health issues and resistance. To study its impact on gut phages, we followed 22 healthy individuals 2 weeks before and up to 6 months after a 3-day course of 3<sup>rd</sup>-generation cephalosporins. Our results show that gut phages rarely encode antibiotic resistance genes and are mostly temperate, including many phage plasmids. Furthermore, phage populations remain individual-specific even after microbiome perturbation. Yet, we report a 20% decline in phage diversity the day after treatment, alongside blooms of a few, mostly virulent, phages. We suggest that some of these phages contribute to the recovery of bacterial diversity via "kill-the-winner" dynamics. This is supported by (temporarily) dominant phages targeting Parabacteroides distasonis, a bacterium that thrives post-treatment only in the absence of these phages. Our findings suggest gut phages are crucial to the microbiome response to antibiotics, aiding the restoration of balance and diversity.

Cell ReportsVol. 44(8)
Délégation Paris 5 (FR), Centre National de la Recherche Scientifique (FR), Inserm (FR), Institut Pasteur (FR), Université Paris Cité (FR), AgroParisTech (FR), Université Paris-Saclay (FR), Microbiologie de l’alimentation au service de la santé (FR), Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR), Sorbonne Paris Cité (FR), Evolutionary Genomics (United States) (US)
Agence Nationale de la Recherche
Zero hunger
Openalex Percentile: Top 5%
Bacteriophages and microbial interactions
5.15
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