Evidence map›Paper›PMID 34215179›Full record

ArticleBMC microbiology2021

The infant gut resistome is associated with E. coli and early-life exposures.

Rebecca M Lebeaux, Modupe O Coker, Erika F Dade, Thomas J Palys, Hilary G Morrison, Benjamin D Ross, Emily R Baker, Margaret R Karagas, Juliette C Madan, Anne G Hoen

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 2 pooled it
4.9field-weighted citation impact, top 3% 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

45 citing papers in PubMed, 2 syntheses or guidelines pooled it, 68 citations in OpenAlex.

  1. Pooled it
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  12. Fluoroquinolone Resistance Patterns in Multidrug-ResistantAntibiotics (Basel, Switzerland) · 2026
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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

10 authors at 4 institutions in 1 country.

Rebecca M LebeauxDepartment of Epidemiology, Geisel School of Medicine at Dartmouth, Hanover, NH, USA. Rebecca.m.lebeaux.gr@dartmouth.edu.ORCID 0000-0002-3046-1225
Modupe O CokerDepartment of Epidemiology, Geisel School of Medicine at Dartmouth, Hanover, NH, USA.
Erika F DadeDepartment of Epidemiology, Geisel School of Medicine at Dartmouth, Hanover, NH, USA.
Thomas J PalysCenter for Molecular Epidemiology, Geisel School of Medicine at Dartmouth, Hanover, NH, USA.
Hilary G MorrisonMarine Biological Laboratory, Woods Hole, MA, USA.
Benjamin D RossDepartment of Microbiology & Immunology, Geisel School of Medicine at Dartmouth, Hanover, NH, USA.
Emily R BakerDepartment of Pediatrics, Children's Hospital at Dartmouth, Lebanon, NH, USA.
Margaret R KaragasDepartment of Epidemiology, Geisel School of Medicine at Dartmouth, Hanover, NH, USA.
Juliette C MadanDepartment of Epidemiology, Geisel School of Medicine at Dartmouth, Hanover, NH, USA.
Anne G HoenDepartment of Epidemiology, Geisel School of Medicine at Dartmouth, Hanover, NH, USA.
Dartmouth College · USChildren's Hospital at Dartmouth Hitchcock · USMarine Biological Laboratory · USRutgers, The State University of New Jersey · US

Funding

Relation Between In-utero Vitamin D and Immune Function in Early Childhood P20GM104416 · NIGMS · DARTMOUTH COLLEGE · PI CHRISTENSEN, BROCK CLARKE · 2013 to 2022
$23.7M
HOST-MICROBE INTERACTIONST32AI007519 · NIAID · DARTMOUTH COLLEGE · PI DEBORAH A HOGAN · 1997 to 2026
$5.9M
Project 3: Placental Biomarkers of Exposure and Outcome (Marsit)P01ES022832 · NIEHS · DARTMOUTH COLLEGE · PI KARAGAS, MARGARET RITA · 2013 to 2018
$4.7M
Multi-omic Functional Integration Using NetworksR01LM012723 · NLM · DARTMOUTH COLLEGE · PI HOEN, ANNE GATEWOOD · 2017 to 2020
$1.4M
Project 4: Determining How Arsenic Modulates Hedgehog Signaling During DevelopmenP20ES018175 · NIEHS · DARTMOUTH COLLEGE · PI KARAGAS, MARGARET RITA · 2010 to 2012
$892k
Bioinformatics strategies for early life microbiomicsK01LM011985 · NLM · DARTMOUTH COLLEGE · PI HOEN, ANNE GATEWOOD · 2014 to 2016
$345k
NIAID NIH HHS T32 AI007519NIEHS NIH HHS P01 ES022832NIEHS NIH HHS P20 ES018175NIGMS NIH HHS P20 GM104416NLM NIH HHS K01 LM011985NLM NIH HHS R01 LM012723
6 · The paper itself

Abstract

backgroundThe human gut microbiome harbors a collection of bacterial antimicrobial resistance genes (ARGs) known as the resistome. The factors associated with establishment of the resistome in early life are not well understood. We investigated the early-life exposures and taxonomic signatures associated with resistome development over the first year of life in a large, prospective cohort in the United States. Shotgun metagenomic sequencing was used to profile both microbial composition and ARGs in stool samples collected at 6 weeks and 1 year of age from infants enrolled in the New Hampshire Birth Cohort Study. Negative binomial regression and statistical modeling were used to examine infant factors such as sex, delivery mode, feeding method, gestational age, antibiotic exposure, and infant gut microbiome composition in relation to the diversity and relative abundance of ARGs.

resultsMetagenomic sequencing was performed on paired samples from 195 full term (at least 37 weeks' gestation) and 15 late preterm (33-36 weeks' gestation) infants. 6-week samples compared to 1-year samples had 4.37 times (95% CI: 3.54-5.39) the rate of harboring ARGs. The majority of ARGs that were at a greater relative abundance at 6 weeks (chi-squared p < 0.01) worked through the mechanism of antibiotic efflux. The overall relative abundance of the resistome was strongly correlated with Proteobacteria (Spearman correlation = 78.9%) and specifically Escherichia coli (62.2%) relative abundance in the gut microbiome. Among infant characteristics, delivery mode was most strongly associated with the diversity and relative abundance of ARGs. Infants born via cesarean delivery had a trend towards a higher risk of harboring unique ARGs [relative risk = 1.12 (95% CI: 0.97-1.29)] as well as having an increased risk for overall ARG relative abundance [relative risk = 1.43 (95% CI: 1.12-1.84)] at 1 year compared to infants born vaginally.

conclusionsOur findings suggest that the developing infant gut resistome may be alterable by early-life exposures. Establishing the extent to which infant characteristics and early-life exposures impact the resistome can ultimately lead to interventions that decrease the transmission of ARGs and thus the risk of antibiotic resistant infections.

Indexed as

BacteriaDelivery, ObstetricDrug Resistance, MicrobialEnvironmental ExposureEscherichia coliFecesFeeding MethodsFemaleGastrointestinal MicrobiomeHigh-Throughput Nucleotide SequencingHumansInfantMaleMetagenomicsAntibiotic resistanceCohort studiesEpidemiologyGastrointestinal microbiomeInfants

Identifiers

PMID34215179
PMCPMC8252198
OpenAlexW3111490008

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LicenceCC BY
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Registered trials

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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.