Evidence map›Paper›PMID 26377648›Full record

ArticleMicrobiome2015

Type 2 immunity-dependent reduction of segmented filamentous bacteria in mice infected with the helminthic parasite Nippostrongylus brasiliensis.

W Florian Fricke, Yang Song, An-Jiang Wang, Allen Smith, Viktoriya Grinchuk, Emmanuel Mongodin, Chenlin Pei, Bing Ma, Nonghua Lu, Joseph F Urban and 2 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Microbiome, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
5.8field-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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 96 citations in OpenAlex.

  1. Pooled it
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  11. Tuft cells in the intestine, immunity and beyond.Nature reviews. Gastroenterology & hepatology · 2024
    Review
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  18. Cross talk between Paneth and tuft cells drives dysbiosis and inflammation in the gut mucosa.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  19. Tuft cells mediate commensal remodeling of the small intestinal antimicrobial landscape.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 3 countries.

W Florian FrickeDepartment of Microbiology and Immunology, Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD, USA. w.florian.fricke@uni-hohenheim.de.
Yang SongDepartment of Microbiology and Immunology, Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD, USA.
An-Jiang WangDepartment of Radiation Oncology, University of Maryland School of Medicine, Baltimore, MD, USA.
Allen SmithU.S. Department of Agriculture, Agriculture Research Service, Beltsville Human Nutrition Research Center, Diet, Genomics, and Immunology Laboratory, Beltsville, MD, USA.
Viktoriya GrinchukDepartment of Radiation Oncology, University of Maryland School of Medicine, Baltimore, MD, USA.
Emmanuel MongodinDepartment of Microbiology and Immunology, Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD, USA
Chenlin PeiDepartment of Radiation Oncology, University of Maryland School of Medicine, Baltimore, MD, USA.
Bing MaDepartment of Microbiology and Immunology, Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD, USA.
Nonghua LuDepartment of Gastroenterology and Hepatology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Joseph F UrbanU.S. Department of Agriculture, Agriculture Research Service, Beltsville Human Nutrition Research Center, Diet, Genomics, and Immunology Laboratory, Beltsville, MD, USA.
Terez Shea-DonohueDepartment of Radiation Oncology, University of Maryland School of Medicine, Baltimore, MD, USA.
Aiping ZhaoDepartment of Radiation Oncology, University of Maryland School of Medicine, Baltimore, MD, USA. azhao@mbrc.umaryland.edu.
University of Maryland, Baltimore · USHuman Genome Sciences (United States) · USUnited States Department of Agriculture · USNanchang University · CNUniversity of Hohenheim · DE

Funding

GI Nematodes and Gut Functional Responses to InflammationR01AI049316 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI SHEA-DONOHUE, TEREZ · 2002 to 2012
$3.6M
PPAR Mediated Gene Expression in HIV PatientsR01DK049316 · NIDDK · STATE UNIVERSITY NEW YORK STONY BROOK · PI GELATO, MARIE C · 1994 to 2007
$3.5M
Novel Cytokine Regulation of Gut Function and InflammationR01DK083418 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI SHEA-DONOHUE, TEREZ · 2009 to 2013
$1.5M
NIAID NIH HHS R01-AI/DK49316NIDDK NIH HHS R01 DK049316NIDDK NIH HHS R01 DK083418NIDDK NIH HHS R01-DK083418
6 · The paper itself

Abstract

backgroundDynamic interactions between the host and gastrointestinal microbiota play an important role for local and systemic immune homeostasis. Helminthic parasites modulate the host immune response, resulting in protection against autoimmune disease but also increased susceptibility to pathogen infection. The underlying mechanisms remain largely unknown.

resultsWe showed that the type 2 immune response to enteric Nippostrongylus brasiliensis infection in mice was associated with altered intestinal mucin and AMP expression and shifts in microbiota composition. Most strikingly, infection reduced concentrations of intestinal segmented filamentous bacteria (SFB), known inducers of T helper 17 cells, and IL-17-associated gene expression. Infected mice deficient in IL-13 or STAT6 did not reduce SFB or IL-17, and exogenous IL-25 replicated the effects of parasite infection in wild type mice.

conclusionsOur data show that parasite infection acts through host type 2 immunity to reduce intestinal SFB and expression of IL-17, providing an example of a microbiota-dependent immune modulation by parasites.

Indexed as

ImmunityNippostrongylusAnimalsAntimicrobial Cationic PeptidesBacteriaBiomarkersGene ExpressionImmunomodulationInterleukin-13Interleukin-17Intestinal MucosaIntestinesMiceMucinsSTAT6 Transcription FactorStrongylida InfectionsAntimicrobial Cationic PeptidesBiomarkersInterleukin-13Interleukin-17MucinsSTAT6 Transcription Factor

Identifiers

PMID26377648
PMCPMC4574229
OpenAlexW1911175303

What OpenQuestion holds

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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.