Evidence map›Paper›PMID 32785284›Full record

ArticlePloS one2020

Epidemiology and associated microbiota changes in deployed military personnel at high risk of traveler's diarrhea.

William A Walters, Faviola Reyes, Giselle M Soto, Nathanael D Reynolds, Jamie A Fraser, Ricardo Aviles, David R Tribble, Adam P Irvin, Nancy Kelley-Loughnane, Ramiro L Gutierrez and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
4.3field-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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. WORKbiota: A Systematic Review about the Effects of Occupational Exposure on Microbiota and Workers' Health.International journal of environmental research and public health · 2022
    Pooled it
  2. EnteroaggregativeEcoSal Plus · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. NutriClayJournal of food protection · 2025
    Article
  7. Article
  8. Article
  9. Extracellular components in enteroaggregativeFrontiers in cellular and infection microbiology · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. 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

14 authors at 7 institutions in 3 countries.

William A WaltersMax Planck Institute for Developmental Biology, Tuebingen, Germany.
Faviola ReyesAsociacion Benefica PRISMA, San Miguel, Peru.
Giselle M SotoU.S. Naval Medical Research Unit No. 6 (NAMRU-6),Callao, Lima, Peru.
Nathanael D ReynoldsInfectious Diseases Directorate, U.S. Naval Medical Research Center, Silver Spring, MD, United States of America.
Jamie A FraserInfectious Disease Clinical Research Program, Department of Preventive Medicine and Biostatistics, Uniformed Services University of the Health Sciences, Bethesda, MD, United States of America.
Ricardo AvilesAsociacion Benefica PRISMA, San Miguel, Peru.
David R TribbleInfectious Disease Clinical Research Program, Department of Preventive Medicine and Biostatistics, Uniformed Services University of the Health Sciences, Bethesda, MD, United States of America.
Adam P Irvin711th Human Performance Wing, Air Force Research Laboratory, Wright-Patterson AFB, OH, United States of America.
Nancy Kelley-Loughnane711th Human Performance Wing, Air Force Research Laboratory, Wright-Patterson AFB, OH, United States of America.
Ramiro L GutierrezInfectious Diseases Directorate, U.S. Naval Medical Research Center, Silver Spring, MD, United States of America.
Mark S RiddleInfectious Disease Clinical Research Program, Department of Preventive Medicine and Biostatistics, Uniformed Services University of the Health Sciences, Bethesda, MD, United States of America.
Ruth E LeyMax Planck Institute for Developmental Biology, Tuebingen, Germany.
Michael S Goodson711th Human Performance Wing, Air Force Research Laboratory, Wright-Patterson AFB, OH, United States of America.ORCID 0000-0002-5004-551X
Mark P SimonsInfectious Diseases Directorate, U.S. Naval Medical Research Center, Silver Spring, MD, United States of America.
Naval Medical Research Command · USUnited States Air Force Research Laboratory · USMax Planck Institute for Developmental Biology · DEPrisma · PEUniformed Services University of the Health Sciences · USHenry M. Jackson Foundation · USUnited States Naval Medical Research Unit SOUTH · PE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Travelers' diarrhea (TD) is the most prevalent illness encountered by deployed military personnel and has a major impact on military operations, from reduced job performance to lost duty days. Frequently, the etiology of TD is unknown and, with underreporting of cases, it is difficult to accurately assess its impact. An increasing number of ailments include an altered or aberrant gut microbiome. To better understand the relationships between long-term deployments and TD, we studied military personnel during two nine-month deployment cycles in 2015-2016 to Honduras. To collect data on the prevalence of diarrhea and impact on duty, a total of 1173 personnel completed questionnaires at the end of their deployment. 56.7% reported reduced performance and 21.1% reported lost duty days. We conducted a passive surveillance study of all cases of diarrhea reporting to the medical unit with 152 total cases and a similar pattern of etiology. Enteroaggregative E. coli (EAEC, 52/152), enterotoxigenic E. coli (ETEC, 50/152), and enteropathogenic E. coli (EPEC, 35/152) were the most prevalent pathogens detected. An active longitudinal surveillance of 67 subjects also identified diarrheagenic E. coli as the primary etiology (7/16 EPEC, 7/16 EAEC, and 6/16 ETEC). Eleven subjects were recruited into a nested longitudinal substudy to examine gut microbiome changes associated with deployment. A 16S rRNA amplicon survey of fecal samples showed differentially abundant baseline taxa for subjects who contracted TD versus those who did not, as well as detection of taxa positively associated with self-reported gastrointestinal distress. Disrupted microbiota was also qualitatively observable for weeks preceding and following the incidents of TD. These findings illustrate the complex etiology of diarrhea amongst military personnel in deployed settings and its impacts on job performance. Potential factors of resistance or susceptibility can provide a foundation for future clinical trials to evaluate prevention and treatment strategies.

Indexed as

AdultDiarrheaDysenteryEnteropathogenic Escherichia coliEscherichia coli InfectionsFecesFemaleGastrointestinal MicrobiomeHondurasHumansMaleMilitary PersonnelRisk FactorsRNA, Ribosomal, 16STravelTravel-Related IllnessRNA, Ribosomal, 16S

Identifiers

PMID32785284
PMCPMC7423091
OpenAlexW3048591595

What OpenQuestion holds

Textmetadata
LicenceCC0
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.