Evidence map›Paper›PMID 20357099›Full record

ArticleJournal of virology2010

Murine coronavirus delays expression of a subset of interferon-stimulated genes.

Kristine M Rose, Ruth Elliott, Luis Martínez-Sobrido, Adolfo García-Sastre, Susan R Weiss

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

36 citing papers in PubMed, 39 citations in OpenAlex.

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  12. Coronavirus endoribonuclease targets viral polyuridine sequences to evade activating host sensors.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
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  17. Extracellular matrix in the CNS induced by neuropathogenic viral infection.Neuropathology : official journal of the Japanese Society of Neuropathology · 2017
    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

5 authors at 3 institutions in 1 country.

Kristine M RoseDepartment of Microbiology, University of Pennsylvania, School of Medicine, 36th Street and Hamilton Walk, Philadelphia, PA 19104-6076, USA.
Ruth Elliott
Luis Martínez-Sobrido
Adolfo García-Sastre
Susan R Weiss
University of Pennsylvania · USIcahn School of Medicine at Mount Sinai · USOffice of Infectious Diseases · US

Funding

TRAINING IN VIROLOGYT32AI007324 · NIAID · WISTAR INSTITUTE · PI Paul Bates, Matthew D. Weitzman · 1989 to 2026
$6.8M
VIRULENCE FACTORS OF INFLUENZA VIRUS--THE NS1 PROTEINR01AI046954 · NIAID · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI GARCIA-SASTRE, ADOLFO · 2000 to 2010
$3.1M
Neurovirulence of murine coronavirus: roles of viral genesR01NS054695 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI WEISS, SUSAN R · 2006 to 2010
$1.7M
NIAID NIH HHS R01 AI046954NIAID NIH HHS R01-AI-46954NIAID NIH HHS T32 AI007324NIAID NIH HHS T32 AI-07324NINDS NIH HHS NS-54695NINDS NIH HHS R01 NS054695NINDS NIH HHS R01-NS-54695
6 · The paper itself

Abstract

The importance of the type I interferon (IFN-I) system in limiting coronavirus replication and dissemination has been unequivocally demonstrated by rapid lethality following infection of mice lacking the alpha/beta IFN (IFN-alpha/beta) receptor with mouse hepatitis virus (MHV), a murine coronavirus. Interestingly, MHV has a cell-type-dependent ability to resist the antiviral effects of IFN-alpha/beta. In primary bone-marrow-derived macrophages and mouse embryonic fibroblasts, MHV replication was significantly reduced by the IFN-alpha/beta-induced antiviral state, whereas IFN treatment of cell lines (L2 and 293T) has only minor effects on replication (K. M. Rose and S. R. Weiss, Viruses 1:689-712, 2009). Replication of other RNA viruses, including Theiler's murine encephalitis virus (TMEV), vesicular stomatitis virus (VSV), Sindbis virus, Newcastle disease virus (NDV), and Sendai virus (SeV), was significantly inhibited in L2 cells treated with IFN-alpha/beta, and MHV had the ability to rescue only SeV replication. We present evidence that MHV infection can delay interferon-stimulated gene (ISG) induction mediated by both SeV and IFN-beta but only when MHV infection precedes SeV or IFN-beta exposure. Curiously, we observed no block in the well-defined IFN-beta signaling pathway that leads to STAT1-STAT2 phosphorylation and translocation to the nucleus in cultures infected with MHV. This observation suggests that MHV must inhibit an alternative IFN-induced pathway that is essential for early induction of ISGs. The ability of MHV to delay SeV-mediated ISG production may partially involve limiting the ability of IFN regulatory factor 3 (IRF-3) to function as a transcription factor. Transcription from an IRF-3-responsive promoter was partially inhibited by MHV; however, IRF-3 was transported to the nucleus and bound DNA in MHV-infected cells superinfected with SeV.

Indexed as

Gene Expression RegulationActive Transport, Cell NucleusAnimalsCoronavirusCoronavirus InfectionsDNAInterferon-betaInterferon Regulatory Factor-3Interferon Type IMiceProtein TransportSendai virusTranscription, GeneticDNAInterferon-betaInterferon Regulatory Factor-3Interferon Type I

Identifiers

PMID20357099
PMCPMC2876584
OpenAlexW2043769768

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.