Evidence map›Paper›PMID 27841267›Full record

ArticleNature communications2016

Akkermansia muciniphila mediates negative effects of IFNγ on glucose metabolism.

Renee L Greer, Xiaoxi Dong, Ana Carolina F Moraes, Ryszard A Zielke, Gabriel R Fernandes, Ekaterina Peremyslova, Stephany Vasquez-Perez, Alexi A Schoenborn, Everton P Gomes, Alexandre C Pereira and 9 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 170 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
170citing papers in PubMed, 3 pooled it
12.7field-weighted citation impact, top 1% 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

170 citing papers in PubMed, 3 syntheses or guidelines pooled it, 274 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
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  8. Article
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  11. Article
  12. Extracellular vesicles fromFrontiers in immunology · 2026
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  15. Gut microbes · 2025
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  16. Review
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  20. Article

110 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 6 institutions in 2 countries.

Renee L GreerCollege of Veterinary Medicine, Oregon State University, 105 Dryden Hall, 450 SW 30th Street, Corvallis, Oregon 97331, USA.
Xiaoxi DongCollege of Pharmacy, Oregon State University, 1601 SW Jefferson Way, Corvallis, Oregon 97331, USA.
Ana Carolina F MoraesDepartment of Epidemiology, School of Public Health, University of São Paulo, Av. Dr Arnaldo, 715, São Paulo, SP 01246-904, Brazil.
Ryszard A ZielkeCollege of Pharmacy, Oregon State University, 1601 SW Jefferson Way, Corvallis, Oregon 97331, USA.
Gabriel R FernandesOswaldo Cruz Foundation, René Rachou Research Center, Av. Augusto de Lima, 1715, Belo Horizonte, MG 30190-002, Brazil.ORCID 0000-0002-4897-8521
Ekaterina PeremyslovaCollege of Pharmacy, Oregon State University, 1601 SW Jefferson Way, Corvallis, Oregon 97331, USA.
Stephany Vasquez-PerezCollege of Veterinary Medicine, Oregon State University, 105 Dryden Hall, 450 SW 30th Street, Corvallis, Oregon 97331, USA.
Alexi A SchoenbornDivision of Pediatric Gastroenterology, University of North Carolina at Chapel Hill, 260 MacNider Building, CB# 7220, Chapel Hill, North Carolina 27599, USA.
Everton P GomesLaboratory of Genetics and Molecular Cardiology, Heart Institute (InCor), University of São Paulo Medical School, Av. Dr Eneas de Carvalho Aguiar, 44, São Paulo, SP 05403-000, Brazil.
Alexandre C PereiraLaboratory of Genetics and Molecular Cardiology, Heart Institute (InCor), University of São Paulo Medical School, Av. Dr Eneas de Carvalho Aguiar, 44, São Paulo, SP 05403-000, Brazil.
Sandra R G FerreiraDepartment of Epidemiology, School of Public Health, University of São Paulo, Av. Dr Arnaldo, 715, São Paulo, SP 01246-904, Brazil.
Michael YaoMucosal Immunity Section, Laboratory of Immune Defenses, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892, USA.
Ivan J FussMucosal Immunity Section, Laboratory of Immune Defenses, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892, USA.
Warren StroberMucosal Immunity Section, Laboratory of Immune Defenses, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892, USA.
Aleksandra E SikoraCollege of Pharmacy, Oregon State University, 1601 SW Jefferson Way, Corvallis, Oregon 97331, USA.
Gregory A TaylorGeriatric Research, Education and Clinical Center, VA Medical Center, Departments of Medicine, Molecular Genetics and Microbiology and Immunology, Division of Geriatrics and Center for the Study of Aging and Human Development, Duke Box 3003, Duke University Medical Center, Durham, North Carolina 27710, USA.
Ajay S GulatiDivision of Pediatric Gastroenterology, University of North Carolina at Chapel Hill, 260 MacNider Building, CB# 7220, Chapel Hill, North Carolina 27599, USA.
Andrey MorgunCollege of Pharmacy, Oregon State University, 1601 SW Jefferson Way, Corvallis, Oregon 97331, USA.
Natalia ShulzhenkoCollege of Veterinary Medicine, Oregon State University, 105 Dryden Hall, 450 SW 30th Street, Corvallis, Oregon 97331, USA.
Oregon State University · USUniversidade de São Paulo · BRNational Institute of Allergy and Infectious Diseases · USUniversity of North Carolina at Chapel Hill · USFundação Oswaldo Cruz · BRGeriatric Research Education and Clinical Center · US

Funding

Gut microbiota mediates the interplay between immunity and glucose metabolismR01DK103761 · NIDDK · OREGON STATE UNIVERSITY · PI SHULZHENKO, NATALIA · 2015 to 2019
$1.7M
Anti-IL-12p40 Treatment of CVID Enteropathy: Gene Expression/Microbiota AnalysisU01AI109695 · NIAID · OREGON STATE UNIVERSITY · PI MORGUN, ANDRIY · 2013 to 2015
$951k
Influences of the enteric microbiota on intestinal stem cell biologyR03DK104005 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI GULATI, AJAY S · 2015 to 2016
$152k
Regulation of Intestinal Inflammation by Irgm1I01BX002369 · VA · DURHAM VA MEDICAL CENTER · PI TAYLOR, GREGORY A · 2015 to 2018
–
BLRD VA I01 BX002369NIAID NIH HHS U01 AI109695NIDDK NIH HHS R01 DK103761NIDDK NIH HHS R03 DK104005
6 · The paper itself

Abstract

Cross-talk between the gut microbiota and the host immune system regulates host metabolism, and its dysregulation can cause metabolic disease. Here, we show that the gut microbe Akkermansia muciniphila can mediate negative effects of IFNγ on glucose tolerance. In IFNγ-deficient mice, A. muciniphila is significantly increased and restoration of IFNγ levels reduces A. muciniphila abundance. We further show that IFNγ-knockout mice whose microbiota does not contain A. muciniphila do not show improvement in glucose tolerance and adding back A. muciniphila promoted enhanced glucose tolerance. We go on to identify Irgm1 as an IFNγ-regulated gene in the mouse ileum that controls gut A. muciniphila levels. A. muciniphila is also linked to IFNγ-regulated gene expression in the intestine and glucose parameters in humans, suggesting that this trialogue between IFNγ, A. muciniphila and glucose tolerance might be an evolutionally conserved mechanism regulating metabolic health in mice and humans.

Indexed as

AnimalsCarbohydrate MetabolismGastrointestinal MicrobiomeGene ExpressionGlucoseGTP-Binding ProteinsHumansIleumInterferon-gammaMice, Inbred C57BLMice, KnockoutVerrucomicrobiaGlucoseGTP-Binding ProteinsIfi1 protein, mouseInterferon-gamma

Identifiers

PMID27841267
PMCPMC5114536
OpenAlexW2549293350

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.