Evidence map›Paper›PMID 30550976›Full record

ArticleVirology2019

Cell-type specificity and functional redundancy of RIG-I-like receptors in innate immune sensing of Coxsackievirus B3 and encephalomyocarditis virus.

Esther Francisco, Mehul Suthar, Michael Gale, Amy B Rosenfeld, Vincent R Racaniello

Open access · greenAbstract read
In one paragraph

Article in Virology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
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

5 authors at 3 institutions in 1 country.

Esther FranciscoDepartment of Microbiology & Immunology, Vagelos College of Physicians & Surgeons of Columbia University, 701 W. 168th St., New York, NY 10032, USA.
Mehul SutharDepartment of Pediatrics, Division of Infectious Disease, Emory Vaccine Center, Yerkes National Primate Research Center, Emory University School of Medicine, Atlanta, GA 30322, USA.
Michael GaleDepartment of Immunology, School of Medicine, University of Washington, Seattle, WA, USA.
Amy B RosenfeldDepartment of Microbiology & Immunology, Vagelos College of Physicians & Surgeons of Columbia University, 701 W. 168th St., New York, NY 10032, USA.
Vincent R RacanielloDepartment of Microbiology & Immunology, Vagelos College of Physicians & Surgeons of Columbia University, 701 W. 168th St., New York, NY 10032, USA. Electronic address: vrr1@cumc.columbia.edu.
Columbia University · USEmory University · USUniversity of Washington · US

Funding

West Nile Virus and host control of innate defensesU19AI083019 · NIAID · UNIVERSITY OF WASHINGTON · PI DIAMOND, MICHAEL S · 2009 to 2018
$22.5M
Rhinovirus Pathogenesis and Host RangeR01AI050754 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI RACANIELLO, VINCENT R · 2002 to 2011
$3.4M
Mechanisms of hepatic innate immune activation by HCVR01AI127463 · NIAID · UNIVERSITY OF WASHINGTON · PI GALE, MICHAEL, ROSEN, HUGO RAMON · 2017 to 2021
$2.8M
The Host Response to Hepatitis C VirusR01AI118916 · NIAID · UNIVERSITY OF WASHINGTON · PI GALE, MICHAEL · 2016 to 2020
$2.5M
Mechanism of Zika virus induced corticogenesis defectsR21AI139775 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI RACANIELLO, VINCENT R · 2018 to 2019
$440k
NIAID NIH HHS R01 AI050754NIAID NIH HHS R01 AI118916NIAID NIH HHS R01 AI127463NIAID NIH HHS R21 AI139775NIAID NIH HHS U19 AI083019
6 · The paper itself

Abstract

The contributions of RIG-I and MDA5 receptors to sensing viruses of the Picornaviridae family were investigated. The picornaviruses encephalomyocarditis virus (EMCV) and Coxsackievirus B3 (CVB3) are detected by both MDA5 and RIG-I in bone marrow derived macrophages. In macrophages from wild type mice, type I IFN is produced early after infection; IFNβ synthesis is reduced in the absence of each sensor, while IFNα production is reduced in the absence of MDA5. EMCV and CVB3 do not replicate in murine macrophages, and their detection is different in murine embryonic fibroblasts (MEFs), in which the viruses replicate to high titers. In MEFs RIG-I was essential for the expression of type I IFNs but contributes to increased yields of CVB3, while MDA5 inhibited CVB3 replication but in an IFN independent manner. These observations demonstrate functional redundancy within the innate immune response to picornaviruses.

Indexed as

Immunity, InnateAnimalsDEAD Box Protein 58Encephalomyocarditis virusEnterovirus B, HumanFibroblastsHost-Pathogen InteractionsInterferon-Induced Helicase, IFIH1Interferon Type IMacrophagesMiceMice, 129 StrainMice, Inbred ICRMice, KnockoutSignal TransductionVirus ReplicationDdx58 protein, mouseDEAD Box Protein 58Ifih1 protein, mouseInterferon-Induced Helicase, IFIH1Interferon Type IInnate immunityInterferonMacrophageMDA5PicornavirusRIG-I

Identifiers

PMID30550976
PMCPMC6401217
OpenAlexW2904155138

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.