Evidence map›Paper›PMID 37716364›Full record

ArticleThe Lancet. Microbe2023

Gut microbiome perturbation, antibiotic resistance, and Escherichia coli strain dynamics associated with international travel: a metagenomic analysis.

Colin J Worby, Sushmita Sridhar, Sarah E Turbett, Margaret V Becker, Lucyna Kogut, Vanessa Sanchez, Ryan A Bronson, Sowmya R Rao, Elizabeth Oliver, Allison Taylor Walker and 9 more

Open access · goldAbstract read
In one paragraph

Article in The Lancet. Microbe, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

34 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
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  6. Domestic travel as a driver for the dissemination ofAntimicrobial agents and chemotherapy · 2026
    Article
  7. Review
  8. Article
  9. Bacteriophage Therapy AgainstAntibiotics (Basel, Switzerland) · 2026
    Review
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  15. Observational
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 11 institutions in 1 country.

Colin J WorbyInfectious Disease and Microbiome Program, The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Sushmita SridharDepartment of Medicine, Harvard Medical School, Boston, MA, USA; Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA.
Sarah E TurbettDepartment of Medicine, Harvard Medical School, Boston, MA, USA; Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA; Department of Pathology, Massachusetts General Hospital, Boston, MA, USA.
Margaret V BeckerDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA.
Lucyna KogutDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA.
Vanessa SanchezDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA.
Ryan A BronsonInfectious Disease and Microbiome Program, The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Sowmya R RaoDepartment of Global Health, Boston University School of Public Health, Boston, MA, USA.
Elizabeth OliverDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA.
Allison Taylor WalkerDivision of Global Migration and Quarantine, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Maroya Spalding WaltersDivision of Healthcare Quality Promotion, National Center for Emerging and Zoonotic Infectious Disease, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Paul KellyDivision of Infectious Diseases, Bronx Care Center, Bronx, NY, USA.
Daniel T LeungDivision of Infectious Diseases and Division of Microbiology and Immunology, University of Utah, Salt Lake City, UT, USA.
Mark C KnouseDepartment of Medicine, Lehigh Valley Health Network, Allentown, PA, USA.
Stefan H F HagmannDivision of Pediatric Infectious Diseases, Steven and Alexandra Cohen Children's Medical Center of New York/Northwell Health, New Hyde Park, NY, USA.
Jason B HarrisDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA; Division of Pediatric Global Health, Massachusetts General Hospital for Children, Boston, MA, USA.
Edward T RyanDepartment of Medicine, Harvard Medical School, Boston, MA, USA; Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA; Travellers' Advice and Immunization Center, Massachusetts General Hospital, Boston, MA, USA.
Ashlee M EarlInfectious Disease and Microbiome Program, The Broad Institute of MIT and Harvard, Cambridge, MA, USA. Electronic address: aearl@broadinstitute.org.
Regina C LaRocqueDepartment of Medicine, Harvard Medical School, Boston, MA, USA; Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA; Travellers' Advice and Immunization Center, Massachusetts General Hospital, Boston, MA, USA.
Massachusetts General Hospital · USBroad Institute · USHarvard University · USBoston Children's Hospital · USBoston University · USBronx Psychiatric Center · USCenters for Disease Control and Prevention · USCohen Children's Medical Center · USLehigh Valley Hospital-Pocono · USNational Center for Emerging and Zoonotic Infectious Diseases · USUniversity of Utah · US

Funding

Viral Genomics: evolution, spread, and host interactionsU19AI110818 · NIAID · BROAD INSTITUTE, INC. · PI EARL, ASHLEE MIRIAM · 2014 to 2024
$66.5M
ACL HHS U01CK000490NCEZID CDC HHS U01 CK000490NCEZID CDC HHS U01 CK000633NIAID NIH HHS U19 AI110818
6 · The paper itself

Abstract

backgroundCulture-based studies have shown that acquisition of extended-spectrum β-lactamase-producing Enterobacterales is common during international travel; however, little is known about the role of the gut microbiome before and during travel, nor about acquisition of other antimicrobial-resistant organisms. We aimed to identify (1) whether the gut microbiome provided colonisation resistance against antimicrobial-resistant organism acquisition, (2) the effect of travel and travel behaviours on the gut microbiome, and (3) the scale and global heterogeneity of antimicrobial-resistant organism acquisition.

methodsIn this metagenomic analysis, participants were recruited at three US travel clinics (Boston, MA; New York, NY; and Salt Lake City, UT) before international travel. Participants had to travel internationally between Dec 8, 2017, and April 30, 2019, and have DNA extractions for stool samples both before and after travel for inclusion. Participants were excluded if they had at least one low coverage sample (<1 million read pairs). Stool samples were collected at home before and after travel, sent to a clinical microbiology laboratory to be screened for three target antimicrobial-resistant organisms (extended-spectrum β-lactamase-producing Enterobacterales, carbapenem-resistant Enterobacterales, and mcr-mediated colistin-resistant Enterobacterales), and underwent DNA extraction and shotgun metagenomic sequencing. We profiled metagenomes for taxonomic composition, antibiotic-resistant gene content, and characterised the Escherichia coli population at the strain level. We analysed pre-travel samples to identify the gut microbiome risk factors associated with acquisition of the three targeted antimicrobial resistant organisms. Pre-travel and post-travel samples were compared to identify microbiome and resistome perturbation and E coli strain acquisition associated with travel.

findingsA total of 368 individuals travelled between the required dates, and 296 had DNA extractions available for both before and after travel. 29 travellers were excluded as they had at least one low coverage sample, leaving a final group of 267 participants. We observed a perturbation of the gut microbiota, characterised by a significant depletion of microbial diversity and enrichment of the Enterobacteriaceae family. Metagenomic strain tracking confirmed that 67% of travellers acquired new strains of E coli during travel that were phylogenetically distinct from their pre-travel strains. We observed widespread enrichment of antibiotic-resistant genes in the gut, with a median 15% (95% CI 10-20, p<1 × 10

interpretationThis work highlights a scale of E coli and antimicrobial-resistant organism acquisition by US travellers not apparent from previous culture-based studies, and suggests that strategies to control antimicrobial-resistant organisms addressing international traveller behaviour, rather than modulating the gut microbiome, could be worthwhile.

fundingUS Centers for Disease Control and Prevention and National Institute of Allergy and Infectious Diseases.

Indexed as

Escherichia coliGastrointestinal MicrobiomeAnti-Bacterial Agentsbeta-LactamasesDNADrug Resistance, MicrobialHumansMetagenomeTravelTravel-Related IllnessUnited StatesAnti-Bacterial Agentsbeta-LactamasesDNA

Identifiers

PMID37716364
PMCPMC10680401
OpenAlexW4386808172

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.