Evidence map›Paper›PMID 36910129›Full record

ArticleGastro hep advances2022

The G Protein-Coupled Receptor, VPAC1, Mediates Vasoactive Intestinal Peptide-Dependent Functional Homeostasis of the Gut Microbiota.

Aaron C Ericsson, Manpreet Bains, Zachary McAdams, Justin Daniels, Susheel B Busi, James A Waschek, Glenn P Dorsam

Open access · goldAbstract read
In one paragraph

Article in Gastro hep advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

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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

7 authors at 4 institutions in 2 countries.

Aaron C EricssonDepartment of Veterinary Pathobiology, University of Missouri Metagenomics Center, College of Veterinary Medicine, University of Missouri, Columbia, Missouri.
Manpreet BainsDepartment of Microbiological Sciences, College of Agriculture, Food Systems and Natural Resources, North Dakota State University, Fargo, North Dakota.
Zachary McAdamsDepartment of Veterinary Pathobiology, University of Missouri Metagenomics Center, College of Veterinary Medicine, University of Missouri, Columbia, Missouri.
Justin DanielsDepartment of Microbiological Sciences, College of Agriculture, Food Systems and Natural Resources, North Dakota State University, Fargo, North Dakota.
Susheel B BusiDepartment of Systems Ecology, Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
James A WaschekDepartment of Psychiatry and Biobehavioral Sciences, Intellectual and Developmental Disabilities Research Center, Semel Institute for Neuroscience and Human Behavior/Neuropsychiatric Institute, University of California, Los Angeles, Los Angeles, California.
Glenn P DorsamDepartment of Microbiological Sciences, College of Agriculture, Food Systems and Natural Resources, North Dakota State University, Fargo, North Dakota.
North Dakota State University · USUniversity of Missouri · USUniversity of California, Los Angeles · USUniversity of Luxembourg · LU

Funding

TARGETING AND DELIVERYP20RR015566 · NCRR · NORTH DAKOTA STATE UNIVERSITY · PI SIBI, MUKUND P. · 2001 to 2011
$19.0M
Eosinophil trafficking in fungal allergic asthmaR15AI101968 · NIAID · NORTH DAKOTA STATE UNIVERSITY · PI DORSAM, GLENN PAUL · 2013 to 2013
$435k
NCRR NIH HHS P20 RR015566NIAID NIH HHS R15 AI101968
6 · The paper itself

Abstract

BACKGROUND AND

aimsVasoactive intestinal peptide (VIP) is a neuropeptide involved in the regulation of feeding behavior and circadian rhythms, metabolism, and immunity. Previous studies revealed the homeostatic effects of VIP signaling on the gut microbiota. VIP-deficient mice demonstrate a gut microbiota dysbiosis characterized by reduced

methodsTo investigate the role of the 2 cognate G protein-coupled receptors for VIP (VPAC1 and VPAC2) in VIP-mediated homeostasis of the microbiota, fecal samples from VPAC1- and VPAC2-deficient, heterozygous, and wild-type littermate mice were assessed via targeted amplicon sequencing. Their microbiota profiles were additionally compared with microbiota from VIP-deficient, heterozygous, and wild-type littermates, where genotype-dependent changes in the composition and predicted function of each cohort were compared.

resultsWhile wild-type mice in each line differed in

conclusionWe conclude that VIP signaling through VPAC1 is critical for the maintenance of normal function of the gut microbiota.

Indexed as

FirmicutesGut DysbiosisMicrobiomeMicrobiotaNeuropeptide

Identifiers

PMID36910129
PMCPMC9997614
OpenAlexW3216194780

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.