Evidence map›Paper›PMID 38468305›Full record

ArticleMicrobiome2024

Perturbation and resilience of the gut microbiome up to 3 months after β-lactams exposure in healthy volunteers suggest an important role of microbial β-lactamases.

Camille d'Humières, Margot Delavy, Laurie Alla, Farid Ichou, Emilie Gauliard, Amine Ghozlane, Florence Levenez, Nathalie Galleron, Benoit Quinquis, Nicolas Pons and 25 more

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Microbiome, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 2 syntheses or guidelines pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. The hallmarks of host-microbiome decoupling.Frontiers in microbiology · 2026
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

35 authors at 14 institutions in 3 countries.

Camille d'Humières *Université Paris Cité, IAME, INSERM, Paris, F-75018, France.
Margot Delavy *Institut Pasteur, Université Paris Cité, INRAE, USC2019, Unité Biologie Et Pathogénicité Fongiques, Paris, F-75015, France.
Laurie Alla *Université Paris-Saclay, INRAE, MetaGenoPolis, Jouy-en-Josas, F-78350, France.
Farid IchouICANomics, Foundation of Innovation in Cardiometabolism and Nutrition (IHU ICAN), Paris, F-75013, France.
Emilie GauliardSorbonne Université, INSERM U938, Centre de Recherche Saint-Antoine, Paris, F-75012, France.
Amine GhozlaneInstitut Pasteur, Université Paris Cité, Bioinformatics and Biostatistics Hub, Paris, F-75015, France.
Florence LevenezUniversité Paris-Saclay, INRAE, MetaGenoPolis, Jouy-en-Josas, F-78350, France.
Nathalie GalleronUniversité Paris-Saclay, INRAE, MetaGenoPolis, Jouy-en-Josas, F-78350, France.
Benoit QuinquisUniversité Paris-Saclay, INRAE, MetaGenoPolis, Jouy-en-Josas, F-78350, France.
Nicolas PonsUniversité Paris-Saclay, INRAE, MetaGenoPolis, Jouy-en-Josas, F-78350, France.
Jimmy MullaertUniversité Paris Cité, IAME, INSERM, Paris, F-75018, France.
Antoine Bridier-NahmiasUniversité Paris Cité, IAME, INSERM, Paris, F-75018, France.
Bénédicte CondamineUniversité Paris Cité, IAME, INSERM, Paris, F-75018, France.
Marie TouchonInstitut Pasteur, Université Paris Cité, CNRS UMR3525, Microbial Evolutionary Genomics, Paris, 75015, France.
Dominique RainteauSorbonne Université, INSERM U938, Centre de Recherche Saint-Antoine, Paris, F-75012, France.
Antonin LamazièreSorbonne Université, INSERM U938, Centre de Recherche Saint-Antoine, Paris, F-75012, France.
Philippe LesnikINSERM UMR-S 1166, Institute of Cardiometabolism and Nutrition, Sorbonne Université, Hôpital Pitié-Salpêtrière, Paris, F-75013, France.
Maharajah PonnaiahICANomics, Foundation of Innovation in Cardiometabolism and Nutrition (IHU ICAN), Paris, F-75013, France.
Marie LhommeICANomics, Foundation of Innovation in Cardiometabolism and Nutrition (IHU ICAN), Paris, F-75013, France.
Natacha SertourInstitut Pasteur, Université Paris Cité, INRAE, USC2019, Unité Biologie Et Pathogénicité Fongiques, Paris, F-75015, France.
Savannah DeventeDipartimento di Biotecnologie Mediche, Università di Siena, Siena, I-53100, Italy.
Jean-Denis DocquierDipartimento di Biotecnologie Mediche, Università di Siena, Siena, I-53100, Italy.
Marie-Elisabeth BougnouxInstitut Pasteur, Université Paris Cité, INRAE, USC2019, Unité Biologie Et Pathogénicité Fongiques, Paris, F-75015, France.
Olivier TenaillonUniversité Paris Cité, IAME, INSERM, Paris, F-75018, France.
Mélanie MagnanUniversité Paris Cité, IAME, INSERM, Paris, F-75018, France.
Etienne RuppéUniversité Paris Cité, IAME, INSERM, Paris, F-75018, France.
Nathalie GrallUniversité Paris Cité, IAME, INSERM, Paris, F-75018, France.
Xavier DuvalUniversité Paris Cité, IAME, INSERM, Paris, F-75018, France.
Dusko EhrlichUniversité Paris-Saclay, INRAE, MetaGenoPolis, Jouy-en-Josas, F-78350, France.
France MentréUniversité Paris Cité, IAME, INSERM, Paris, F-75018, France.
Erick DenamurUniversité Paris Cité, IAME, INSERM, Paris, F-75018, France.
Eduardo P C RochaInstitut Pasteur, Université Paris Cité, CNRS UMR3525, Microbial Evolutionary Genomics, Paris, 75015, France.
Emmanuelle Le ChatelierUniversité Paris-Saclay, INRAE, MetaGenoPolis, Jouy-en-Josas, F-78350, France.
Charles BurdetUniversité Paris Cité, IAME, INSERM, Paris, F-75018, France. charles.burdet@inserm.fr.
PrediRes study group
Université Paris Cité · FRUniversité Paris-Saclay · FRFondation pour l’innovation en Cadiométabolisme et Nutrition · FRInserm · FRInstitut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement · FRInstitut Pasteur · FRAssistance Publique – Hôpitaux de Paris · FRHôpital Bichat-Claude-Bernard · FRSorbonne Paris Cité · FRSorbonne Université · FRUniversity of Siena · ITCentre de Recherche Saint-Antoine · FRCentre National de la Recherche Scientifique · FRHôpital Necker-Enfants Malades · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAntibiotics notoriously perturb the gut microbiota. We treated healthy volunteers either with cefotaxime or ceftriaxone for 3 days, and collected in each subject 12 faecal samples up to day 90. Using untargeted and targeted phenotypic and genotypic approaches, we studied the changes in the bacterial, phage and fungal components of the microbiota as well as the metabolome and the β-lactamase activity of the stools. This allowed assessing their degrees of perturbation and resilience.

resultsWhile only two subjects had detectable concentrations of antibiotics in their faeces, suggesting important antibiotic degradation in the gut, the intravenous treatment perturbed very significantly the bacterial and phage microbiota, as well as the composition of the metabolome. In contrast, treatment impact was relatively low on the fungal microbiota. At the end of the surveillance period, we found evidence of resilience across the gut system since most components returned to a state like the initial one, even if the structure of the bacterial microbiota changed and the dynamics of the different components over time were rarely correlated. The observed richness of the antibiotic resistance genes repertoire was significantly reduced up to day 30, while a significant increase in the relative abundance of β-lactamase encoding genes was observed up to day 10, consistent with a concomitant increase in the β-lactamase activity of the microbiota. The level of β-lactamase activity at baseline was positively associated with the resilience of the metabolome content of the stools.

conclusionsIn healthy adults, antibiotics perturb many components of the microbiota, which return close to the baseline state within 30 days. These data suggest an important role of endogenous β-lactamase-producing anaerobes in protecting the functions of the microbiota by de-activating the antibiotics reaching the colon. Video Abstract.

Indexed as

Gastrointestinal MicrobiomeResilience, PsychologicalAdultAnti-Bacterial AgentsBacteriabeta-Lactamasesbeta-LactamsFecesHealthy VolunteersHumansAnti-Bacterial Agentsbeta-Lactamasesbeta-LactamsAntibioticsHuman gut microbiotaMetabolomicsMetagenomicsResilienceβ-lactamase

Identifiers

PMID38468305
PMCPMC10929231
OpenAlexW4392713439

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.