Evidence map›Paper›PMID 34245762›Full record

ArticleGastroenterology2021

Multi-Omics Analyses Show Disease, Diet, and Transcriptome Interactions With the Virome.

Kathie A Mihindukulasuriya, Ruben A T Mars, Abigail J Johnson, Tonya Ward, Sambhawa Priya, Heather R Lekatz, Krishna R Kalari, Lindsay Droit, Tenghao Zheng, Ran Blekhman and 5 more

Open access · greenAbstract read
In one paragraph

Article in Gastroenterology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
4.0field-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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 70 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Dietary Effects on the Gut Phageome.International journal of molecular sciences · 2024
    Review
  15. Review
  16. Article
  17. The Human Microbiome-A Physiologic Perspective.Comprehensive Physiology · 2024
    Review
  18. Article
  19. Review
  20. Review
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

15 authors at 6 institutions in 3 countries.

Kathie A MihindukulasuriyaDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, Missouri.
Ruben A T MarsDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Abigail J JohnsonDivision of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis, Minnesota.
Tonya WardBioTechnology Institute, College of Biological Sciences, University of Minnesota, Minneapolis, Minnesota.
Sambhawa PriyaDepartment of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, Minnesota.
Heather R LekatzDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Krishna R KalariDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.
Lindsay DroitDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, Missouri.
Tenghao ZhengSchool of Biological Sciences, Monash University, Clayton, Victoria, Australia.
Ran BlekhmanDepartment of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, Minnesota.
Mauro D'AmatoGastrointestinal Genetics Laboratory, CIC bioGUNE, Basque Research and Technology Alliance, Derio, Spain; Ikerbasque, Basque Foundation for Science, Bilbao, Spain.
Gianrico FarrugiaDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Dan KnightsDivision of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis, Minnesota; Department of Computer Science and Engineering, University of Minnesota, Minneapolis, Minnesota. Electronic address: dknights@umn.edu.
Scott A HandleyDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, Missouri. Electronic address: shandley@wustl.edu.
Purna C KashyapDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota; Department of Medicine and Physiology, Mayo Clinic, Rochester, Minnesota. Electronic address: kashyap.purna@mayo.edu.
University of Minnesota · USMayo Clinic · USWashington University in St. Louis · USIkerbasque · ESMayo Clinic in Florida · USMonash University · AU

Funding

PILOT AND FEASIBILTY PROGRAMP30DK084567 · NIDDK · MAYO CLINIC ROCHESTER · PI GREGORY J. GORES · 2009 to 2026
$22.2M
Computational and Experimental Resources for Virome Analysis in Inflammatory Bowel Disease (CERVAID)RC2DK116713 · NIDDK · WASHINGTON UNIVERSITY · PI WANG, DAVID · 2019 to 2023
$8.9M
Mechanisms of alteration of GI physiology by gut microbesR01DK114007 · NIDDK · MAYO CLINIC ROCHESTER · PI Purna C Kashyap · 2017 to 2026
$4.7M
Population Genomics of Host-Microbiome InteractionsR35GM128716 · NIGMS · UNIVERSITY OF MINNESOTA · PI Ran Blekhman · 2018 to 2026
$3.5M
NIDDK NIH HHS P30 DK084567NIDDK NIH HHS R01 DK114007NIDDK NIH HHS RC2 DK116713NIGMS NIH HHS R35 GM128716
6 · The paper itself

Abstract

BACKGROUND &

aimsThe gut virome includes eukaryotic viruses and bacteriophages that can shape the gut bacterial community and elicit host responses. The virome can be implicated in diseases, such as irritable bowel syndrome (IBS), where gut bacteria play an important role in pathogenesis. We provide a comprehensive and longitudinal characterization of the virome, including DNA and RNA viruses and paired multi-omics data in a cohort of healthy subjects and patients with IBS.

methodsWe selected 2 consecutive stool samples per subject from a longitudinal study cohort and performed metagenomic sequencing on DNA and RNA viruses after enriching for viral-like particles. Viral sequence abundance was evaluated over time, as well as in the context of diet, bacterial composition and function, metabolite levels, colonic gene expression, host genetics, and IBS subsets.

resultsWe found that the gut virome was temporally stable and correlated with the colonic transcriptome. We identified IBS-subset-specific changes in phage populations; Microviridae, Myoviridae, and Podoviridae species were elevated in diarrhea-predominant IBS, and other Microviridae and Myoviridae species were elevated in constipation-predominant IBS compared to healthy controls. We identified correlations between subsets of the virome and bacterial composition (unclassifiable "dark matter" and phages) and diet (eukaryotic viruses).

conclusionsWe found that the gut virome is stable over time but varies among subsets of patients with IBS. It can be affected by diet and potentially influences host function via interactions with gut bacteria and/or altering host gene expression.

Indexed as

DietTranscriptomeViromeAdultBacteriophagesCase-Control StudiesFemaleGastrointestinal MicrobiomeGene Expression ProfilingGene Expression RegulationHost-Pathogen InteractionsHumansIntestinesIrritable Bowel SyndromeLongitudinal StudiesMaleBacteriaBacteriophageEukaryotic VirusesIrritable Bowel SyndromeMicrobiome

Identifiers

PMID34245762
PMCPMC8463486
OpenAlexW3180860571

What OpenQuestion holds

Textmetadata
LicenceTDM
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.