Evidence map›Paper›PMID 31877196›Full record

ArticlePLoS pathogens2019

Resistance to ectromelia virus infection requires cGAS in bone marrow-derived cells which can be bypassed with cGAMP therapy.

Eric B Wong, Brian Montoya, Maria Ferez, Colby Stotesbury, Luis J Sigal

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

19 citing papers in PubMed, 19 citations in OpenAlex.

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  15. Cytosolic Sensors for Pathogenic Viral and Bacterial Nucleic Acids in Fish.International journal of molecular sciences · 2020
    Review
  16. Article
  17. Article
  18. Cytosolic DNA Sensors and CNS Responses to Viral Pathogens.Frontiers in cellular and infection microbiology · 2020
    Review
  19. Review
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 1 institution in 1 country.

Eric B WongThomas Jefferson University, Department of Microbiology and Immunology, Philadelphia, Pennsylvania, United States of America.ORCID 0000-0001-9018-2589
Brian MontoyaThomas Jefferson University, Department of Microbiology and Immunology, Philadelphia, Pennsylvania, United States of America.
Maria FerezThomas Jefferson University, Department of Microbiology and Immunology, Philadelphia, Pennsylvania, United States of America.ORCID 0000-0003-2255-7136
Colby StotesburyThomas Jefferson University, Department of Microbiology and Immunology, Philadelphia, Pennsylvania, United States of America.
Luis J SigalThomas Jefferson University, Department of Microbiology and Immunology, Philadelphia, Pennsylvania, United States of America.ORCID 0000-0001-6642-5472
Thomas Jefferson University · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Dietmar J Kappes · 1985 to 2026
$138.8M
X-Ray Crystallography and Macromolecular CharacterizationP30CA056036 · NCI · THOMAS JEFFERSON UNIVERSITY · PI Andrew Chapman · 1995 to 2026
$94.8M
Orthropoxvirus Pathogenesis and VaccinesR01AI065544 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI SIGAL, LUIS J · 2006 to 2016
$5.7M
Inflammatory monocytes in the draining lymph node of ECTV infected miceR01AI110457 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI SIGAL, LUIS J · 2015 to 2019
$2.3M
Natural Killer Cell Deficiencies in Aging MiceR01AG048602 · NIA · THOMAS JEFFERSON UNIVERSITY · PI SIGAL, LUIS J · 2014 to 2018
$1.8M
Training grant on Vaccines and Immunotherapies for Infectious Diseases and CancerT32AI134646 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI SCHNELL, MATTHIAS JOHANNES, SIGAL, LUIS J · 2018 to 2022
$1.1M
The role of skin-derived, migratory dendritic cells in ectromelia-infected miceF32AI129352 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI WONG, ERIC · 2017 to 2019
$144k
NCI NIH HHS P30 CA006927NCI NIH HHS P30 CA056036NIAID NIH HHS F32 AI129352NIAID NIH HHS R01 AI065544NIAID NIH HHS R01 AI110457NIAID NIH HHS T32 AI134646NIA NIH HHS R01 AG048602
6 · The paper itself

Abstract

Cells sensing infection produce Type I interferons (IFN-I) to stimulate Interferon Stimulated Genes (ISGs) that confer resistance to viruses. During lympho-hematogenous spread of the mouse pathogen ectromelia virus (ECTV), the adaptor STING and the transcription factor IRF7 are required for IFN-I and ISG induction and resistance to ECTV. However, it is unknown which cells sense ECTV and which pathogen recognition receptor (PRR) upstream of STING is required for IFN-I and ISG induction. We found that cyclic-GMP-AMP (cGAMP) synthase (cGAS), a DNA-sensing PRR, is required in bone marrow-derived (BMD) but not in other cells for IFN-I and ISG induction and for resistance to lethal mousepox. Also, local administration of cGAMP, the product of cGAS that activates STING, rescues cGAS but not IRF7 or IFN-I receptor deficient mice from mousepox. Thus, sensing of infection by BMD cells via cGAS and IRF7 is critical for resistance to a lethal viral disease in a natural host.

Indexed as

AnimalsBone MarrowEctromelia, InfectiousEctromelia virusHost-Pathogen InteractionsImmunity, InnateInterferon Type IMice, TransgenicNucleotides, CyclicNucleotidyltransferasesProtein Serine-Threonine Kinasescyclic guanosine monophosphate-adenosine monophosphateInterferon Type INucleotides, CyclicNucleotidyltransferasesProtein Serine-Threonine Kinases

Identifiers

PMID31877196
PMCPMC6974301
OpenAlexW2997715272

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.