Evidence map›Paper›PMID 27280500›Full record

ArticleAnnals of surgery2017

Amelioration of Clostridium difficile Infection in Mice by Dietary Supplementation With Indole-3-carbinol.

Walker Julliard, Travis J De Wolfe, John H Fechner, Nasia Safdar, Rashmi Agni, Joshua D Mezrich

Abstract read
In one paragraph

Article in Annals of surgery, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 47 citations in OpenAlex.

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  10. Targeting AhR as a Novel Therapeutic Modality against Inflammatory Diseases.International journal of molecular sciences · 2021
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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

6 authors at 2 institutions in 1 country.

Walker Julliard*Division of Transplant Surgery, Department of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, WI †Department of Food Sciences, University of Wisconsin, Madison, WI ‡William S. Middleton Memorial Veterans Hospital and the Division of Infectious Diseases, University of Wisconsin School of Medicine and Public Health, Madison, WI §Department of Pathology and Laboratory Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI.
Travis J De Wolfe
John H Fechner
Nasia Safdar
Rashmi Agni
Joshua D Mezrich
University of Wisconsin–Madison · USWilliam S. Middleton Memorial Veterans Hospital · US

Funding

UW Surgical Oncology Research Training Program (UW-SORT)T32CA090217 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Muhammed Murtaza, Heather B Neuman · 2001 to 2026
$8.3M
A Novel mechanism for Environmentally Induced Airway DiseaseR01ES023842 · NIEHS · UNIVERSITY OF WISCONSIN-MADISON · PI MEZRICH, JOSHUA D · 2015 to 2019
$1.7M
Pollution Aggravates Autoimmunity Through the Aryl Hydrocarbon ReceptorR21ES025304 · NIEHS · UNIVERSITY OF WISCONSIN-MADISON · PI MEZRICH, JOSHUA D · 2015 to 2016
$421k
NCI NIH HHS T32 CA090217NIEHS NIH HHS R01 ES023842NIEHS NIH HHS R21 ES025304
6 · The paper itself

Abstract

objectiveTo determine the therapeutic effects of dietary supplementation on Clostridium difficile infection (CDI).

backgroundWith limited treatment options, the rise of C. difficile-associated disease has spurred on the search for novel therapies. Recent data define a role for the aryl hydrocarbon receptor (AHR) and diet-derived AHR ligands in mucosal immunity. We investigated the efficacy of indole-3-carbinol (I3C), a dietary supplement, and AHR precursor ligand in a murine model of CDI.

methodsC57BL/6 (B6), AHR, and AHR mice were placed on either grain-based or semipurified diets with or without I3C before and during CDI. Mice were followed clinically for a minimum of 6 days or euthanized between days 0 and 4 of inoculation for analysis of the inflammatory response and microbiota.

resultsB6 mice fed an AHR ligand-deficient, semipurified diet have significantly increased disease severity (P<0.001) and mortality (P < 0.001) compared with mice fed on diet containing I3C. The addition of I3C to the diet of AHR null mice had less of an impact than in AHR heterozygous littermates, although some protection was seen. Mice on semipurified I3C-diet had increased cecal Tregs, ILC3s, and γδ T cells and an increased neutrophilic response without increased inflammation or bacterial translocation compared with controls.

conclusionsI3C is a powerful treatment to reduce impact of CDI in mice. The findings indicate I3C may be acting through both AHR-dependent and -independent mechanisms in this model. Dietary supplementation with I3C is a potential new therapy for prevention and amelioration of C. difficile disease.

Indexed as

Clostridioides difficileDietary SupplementsAnimalsAnti-Bacterial AgentsBacterial TranslocationClostridium InfectionsDisease Models, AnimalImmunity, MucosalIndolesMaleMice, Inbred C57BLNeutrophil ActivationReceptors, Aryl HydrocarbonSeverity of Illness IndexTreatment OutcomeAnti-Bacterial Agentsindole-3-carbinolIndolesReceptors, Aryl Hydrocarbon

Identifiers

PMID27280500
PMCPMC5743052
OpenAlexW2419079388

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.