Evidence map›Paper›PMID 27234299›Full record

ArticleThe EMBO journal2016

HSV-1 ICP27 targets the TBK1-activated STING signalsome to inhibit virus-induced type I IFN expression.

Maria H Christensen, Søren B Jensen, Juho J Miettinen, Stefanie Luecke, Thaneas Prabakaran, Line S Reinert, Thomas Mettenleiter, Zhijian J Chen, David M Knipe, Rozanne M Sandri-Goldin and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 169 papers.

0numbers the graph read from it
0cells of the map it votes in
169citing papers in PubMed
10.4field-weighted citation impact, top 1% 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

169 citing papers in PubMed, 226 citations in OpenAlex.

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109 more citing papers are in PubMed but not listed here.

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

17 authors at 9 institutions in 4 countries.

Maria H ChristensenDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark Aarhus Research Center for Innate Immunology, University of Aarhus, Aarhus, Denmark.
Søren B JensenDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark Aarhus Research Center for Innate Immunology, University of Aarhus, Aarhus, Denmark.
Juho J MiettinenUniversity of Helsinki, Helsinki, Finland.
Stefanie LueckeDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark Aarhus Research Center for Innate Immunology, University of Aarhus, Aarhus, Denmark.
Thaneas PrabakaranDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark Aarhus Research Center for Innate Immunology, University of Aarhus, Aarhus, Denmark.
Line S ReinertDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark Aarhus Research Center for Innate Immunology, University of Aarhus, Aarhus, Denmark.
Thomas MettenleiterFriedrich-Loeffler-Institut, Insel Riems, Germany.
Zhijian J ChenDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX, USA.
David M KnipeDepartment of Microbiology and Immunobiology, Harvard Medical School, Boston, MA, USA.
Rozanne M Sandri-GoldinDepartment of Microbiology & Molecular Genetics, University of California, Irvine, CA, USA.
Lynn W EnquistPrinceton University, Princeton, NJ, USA.
Rune HartmannDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark Aarhus Research Center for Innate Immunology, University of Aarhus, Aarhus, Denmark Department of Molecular Biology and Genetics, Aarhus Research Center for Innate Immunity, Aarhus University, Aarhus, Denmark.ORCID 0000-0003-1159-066X
Trine H MogensenDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark Aarhus Research Center for Innate Immunology, University of Aarhus, Aarhus, Denmark Aarhus University Hospital Skejby, Aarhus, Denmark.
Stephen A RiceDepartment of Microbiology, University of Minnesota Medical School, Minneapolis, MN, USA.
Tuula A NymanUniversity of Helsinki, Helsinki, Finland.
Sampsa MatikainenFinnish Institute of Occupational Health, Helsinki, Finland.
Søren R PaludanDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark Aarhus Research Center for Innate Immunology, University of Aarhus, Aarhus, Denmark srp@biomed.au.dk.ORCID 0000-0001-9180-4060
Aarhus University · DKUniversity of Helsinki · FIFinnish Institute of Occupational Health · FIFriedrich-Loeffler-Institut · DEHarvard University · USHoward Hughes Medical Institute · USPrinceton University · USUniversity of California, Irvine · USUniversity of Minnesota Medical Center · US

Funding

Nuclear Sensing of Herpesviral DNAR01AI106934 · NIAID · HARVARD MEDICAL SCHOOL · PI KNIPE, DAVID M. · 2014 to 2021
$3.8M
Neuronal Spread of Herpesvirus InfectionR01NS060699 · NINDS · PRINCETON UNIVERSITY · PI ENQUIST, LYNN W. · 2008 to 2017
$3.6M
MOLECULAR CHARACTERIZATION OF HERPES SIMPLEX VIRUS ICP27R01AI042737 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI RICE, STEPHEN A · 1998 to 2014
$3.2M
NIAID NIH HHS R01 AI042737NIAID NIH HHS R01 AI106934NINDS NIH HHS R01 NS060699
6 · The paper itself

Abstract

Herpes simplex virus (HSV) 1 stimulates type I IFN expression through the cGAS-STING-TBK1 signaling axis. Macrophages have recently been proposed to be an essential source of IFN during viral infection. However, it is not known how HSV-1 inhibits IFN expression in this cell type. Here, we show that HSV-1 inhibits type I IFN induction through the cGAS-STING-TBK1 pathway in human macrophages, in a manner dependent on the conserved herpesvirus protein ICP27. This viral protein was expressed de novo in macrophages with early nuclear localization followed by later translocation to the cytoplasm where ICP27 prevented activation of IRF3. ICP27 interacted with TBK1 and STING in a manner that was dependent on TBK1 activity and the RGG motif in ICP27. Thus, HSV-1 inhibits expression of type I IFN in human macrophages through ICP27-dependent targeting of the TBK1-activated STING signalsome.

Indexed as

Immune EvasionCells, CulturedHerpesvirus 1, HumanHost-Pathogen InteractionsHumansImmediate-Early ProteinsInterferon Type IMacrophagesMembrane ProteinsProtein Interaction MappingProtein Serine-Threonine KinasesSTING ProteinICP27 protein, human herpesvirus 1Immediate-Early ProteinsInterferon Type IMembrane ProteinsProtein Serine-Threonine KinasesSTING1 protein, humanSTING ProteinTBK1 protein, humanherpes simplex virusimmune evasioninnate immunitytype I IFN

Identifiers

PMID27234299
PMCPMC4931188
OpenAlexW2398563931

What OpenQuestion holds

Textmetadata
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.