Evidence map›Paper›PMID 26933888›Full record

ArticlePLoS pathogens2016

Defensins Potentiate a Neutralizing Antibody Response to Enteric Viral Infection.

Anshu P Gounder, Nicolle D Myers, Piper M Treuting, Beth A Bromme, Sarah S Wilson, Mayim E Wiens, Wuyuan Lu, André J Ouellette, Katherine R Spindler, William C Parks and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
6.4field-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

32 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
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  9. Defensin-driven viral evolution.PLoS pathogens · 2020
    Article
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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

11 authors at 5 institutions in 1 country.

Anshu P GounderDepartment of Microbiology, University of Washington, Seattle, Washington, United States of America.
Nicolle D MyersDepartment of Microbiology, University of Washington, Seattle, Washington, United States of America.
Piper M TreutingDepartment of Comparative Medicine, University of Washington, Seattle, Washington, United States of America.
Beth A BrommeDepartment of Microbiology, University of Washington, Seattle, Washington, United States of America.
Sarah S WilsonDepartment of Microbiology, University of Washington, Seattle, Washington, United States of America.
Mayim E WiensDepartment of Microbiology, University of Washington, Seattle, Washington, United States of America.
Wuyuan LuInstitute of Human Virology and Department of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
André J OuelletteDepartment of Pathology and Laboratory Medicine, Keck School of Medicine of the University of Southern California, USC Norris Cancer Center, Los Angeles, California, United States of America.
Katherine R SpindlerDepartment of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan, United States of America.
William C ParksDepartment of Medicine, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.
Jason G SmithDepartment of Microbiology, University of Washington, Seattle, Washington, United States of America.
University of Washington · USCedars-Sinai Medical Center · USUniversity of Maryland, Baltimore · USUniversity of Michigan–Ann Arbor · USUniversity of Southern California · US

Funding

TRAINING IN MOLECULAR AND CELLULAR BIOLOGYT32GM007270 · NIGMS · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 1985 to 2020
$21.0M
Anti-viral Mechanisms of DefensinsR01AI104920 · NIAID · UNIVERSITY OF WASHINGTON · PI MCKENNA, ROBERT, SMITH, JASON G · 2014 to 2023
$6.1M
Viral Pathogenesis Training ProgramT32AI083203 · NIAID · UNIVERSITY OF WASHINGTON · PI BLOOM, JESSE D, LAGUNOFF, MICHAEL · 2009 to 2023
$2.7M
Mechanisms of blood-brain barrier disruption by an encephalitic virusR01AI091721 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SPINDLER, KATHERINE R. · 2011 to 2015
$2.5M
MOLECULAR BIOLOGY &PATHOGENESIS OF ADENOVIRUSR01AI023762 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SPINDLER, KATHERINE R. · 1987 to 2007
$2.2M
Innate enteric immunity during induced Paneth cell deficiencyR21AI105057 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI OUELLETTE, ANDRE J. · 2013 to 2014
$440k
Molecular biology and pathogenesis of mouse adenovirusR56AI023762 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SPINDLER, KATHERINE R. · 2010 to 2010
$387k
Defensins in Innate Immunity to VirusesR56AI097311 · NIAID · UNIVERSITY OF WASHINGTON · PI SMITH, JASON G · 2012 to 2012
$299k
Role of Defensins in Innate Immunity to VirusesK22AI081870 · NIAID · UNIVERSITY OF WASHINGTON · PI SMITH, JASON G · 2010 to 2011
$267k
NIAID NIH HHS K22 AI081870NIAID NIH HHS R01 AI023762NIAID NIH HHS R01 AI091721NIAID NIH HHS R01 AI104920NIAID NIH HHS R01/R56 AI023762NIAID NIH HHS R21 AI105057NIAID NIH HHS R56 AI023762NIAID NIH HHS R56 AI097311NIAID NIH HHS T32 AI083203NIGMS NIH HHS T32 GM007270
6 · The paper itself

Abstract

α-defensins are abundant antimicrobial peptides with broad, potent antibacterial, antifungal, and antiviral activities in vitro. Although their contribution to host defense against bacteria in vivo has been demonstrated, comparable studies of their antiviral activity in vivo are lacking. Using a mouse model deficient in activated α-defensins in the small intestine, we show that Paneth cell α-defensins protect mice from oral infection by a pathogenic virus, mouse adenovirus 1 (MAdV-1). Survival differences between mouse genotypes are lost upon parenteral MAdV-1 infection, strongly implicating a role for intestinal defenses in attenuating pathogenesis. Although differences in α-defensin expression impact the composition of the ileal commensal bacterial population, depletion studies using broad-spectrum antibiotics revealed no effect of the microbiota on α-defensin-dependent viral pathogenesis. Moreover, despite the sensitivity of MAdV-1 infection to α-defensin neutralization in cell culture, we observed no barrier effect due to Paneth cell α-defensin activation on the kinetics and magnitude of MAdV-1 dissemination to the brain. Rather, a protective neutralizing antibody response was delayed in the absence of α-defensins. This effect was specific to oral viral infection, because antibody responses to parenteral or mucosal ovalbumin exposure were not affected by α-defensin deficiency. Thus, α-defensins play an important role as adjuvants in antiviral immunity in vivo that is distinct from their direct antiviral activity observed in cell culture.

Indexed as

AdenoviridaeAdenoviridae Infectionsalpha-DefensinsAnimalsAntibodies, NeutralizingAnti-Infective AgentsDefensinsFemaleHumansIleumIntestinesIntestine, SmallMaleMiceMice, Inbred C57BLPaneth Cellsalpha-DefensinsAntibodies, NeutralizingAnti-Infective AgentsDefensins

Identifiers

PMID26933888
PMCPMC4774934
OpenAlexW2292787994

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.