Evidence map›Paper›PMID 32711559›Full record

ArticleGenome medicine2020

A single early-in-life antibiotic course increases susceptibility to DSS-induced colitis.

Ceren Ozkul, Victoria E Ruiz, Thomas Battaglia, Joseph Xu, Claire Roubaud-Baudron, Ken Cadwell, Guillermo I Perez-Perez, Martin J Blaser

Open access · goldAbstract read
In one paragraph

Article in Genome medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

38 citing papers in PubMed, 47 citations in OpenAlex.

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  13. Alleviating Effect ofMicroorganisms · 2025
    Article
  14. Antibiotic-perturbed microbiota and the role of probiotics.Nature reviews. Gastroenterology & hepatology · 2025
    Review
  15. Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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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

8 authors at 5 institutions in 3 countries.

Ceren OzkulDepartment of Pharmaceutical Microbiology, Faculty of Pharmacy, Hacettepe University, Sihhiye, Ankara, Turkey.
Victoria E RuizDepartments of Medicine and Microbiology, New York University School of Medicine (NYUSM), New York, NY, 10016, USA.
Thomas BattagliaDepartments of Medicine and Microbiology, New York University School of Medicine (NYUSM), New York, NY, 10016, USA.
Joseph XuDepartments of Medicine and Microbiology, New York University School of Medicine (NYUSM), New York, NY, 10016, USA.
Claire Roubaud-BaudronDepartments of Medicine and Microbiology, New York University School of Medicine (NYUSM), New York, NY, 10016, USA.
Ken CadwellKimmel Center for Biology and Medicine at the Skirball Institute, New York University School of Medicine, New York, NY, 10016, USA.
Guillermo I Perez-PerezDepartments of Medicine and Microbiology, New York University School of Medicine (NYUSM), New York, NY, 10016, USA.
Martin J BlaserDepartments of Medicine and Microbiology, New York University School of Medicine (NYUSM), New York, NY, 10016, USA. Martin.Blaser@cabm.rutgers.edu.
New York University · USNYU Langone Health · USRutgers, The State University of New Jersey · USSt. Francis College · USUniversité de Bordeaux · FR

Funding

NIH HHS U01 A122285
6 · The paper itself

Abstract

backgroundThere is increasing evidence that the intestinal microbiota plays a crucial role in the maturation of the immune system and the prevention of diseases during childhood. Early-life short-course antibiotic use may affect the progression of subsequent disease conditions by changing both host microbiota and immunologic development. Epidemiologic studies provide evidence that early-life antibiotic exposures predispose to inflammatory bowel disease (IBD).

methodsBy using a murine model of dextran sodium sulfate (DSS)-induced colitis, we evaluated the effect on disease outcomes of early-life pulsed antibiotic treatment (PAT) using tylosin, a macrolide and amoxicillin, a beta-lactam. We evaluated microbiota effects at the 16S rRNA gene level, and intestinal T cells by flow cytometry. Antibiotic-perturbed or control microbiota were transferred to pups that then were challenged with DSS.

resultsA single PAT course early-in-life exacerbated later DSS-induced colitis by both perturbing the microbial community and altering mucosal immune cell composition. By conventionalizing germ-free mice with either antibiotic-perturbed or control microbiota obtained 40 days after the challenge ended, we showed the transferrable and direct effect of the still-perturbed microbiota on colitis severity in the DSS model.

conclusionsThe findings in this experimental model provide evidence that early-life microbiota perturbation may increase risk of colitis later in life.

Indexed as

Disease SusceptibilityAge FactorsAnimalsAnti-Bacterial AgentsBiodiversityColitisDextran SulfateDisease Models, AnimalDysbiosisGastrointestinal MicrobiomeIntestinal MucosaMicePermeabilityT-Lymphocytes, Helper-InducerAnti-Bacterial AgentsDextran SulfateChildhood antibiotic useDSS-induced colitisGastrointestinal microbiotaMacrolidePulsed antibiotic treatment

Identifiers

PMID32711559
PMCPMC7382806
OpenAlexW3045021857

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.