Evidence map›Paper›PMID 24211608›Full record

ReviewVirus research2014

Induction and control of the type I interferon pathway by Bluetongue virus.

Damien Vitour, Virginie Doceul, Suzana Ruscanu, Emilie Chauveau, Isabelle Schwartz-Cornil, Stéphan Zientara

Open access · greenAbstract readReview
In one paragraph

Review in Virus research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 36 citations in OpenAlex.

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  19. Activation of TLR3/interferon signaling pathway by bluetongue virus results in HIV inhibition in macrophages.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
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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

6 authors at 3 institutions in 1 country.

Damien VitourUMR1161 ANSES-INRA-ENVA, 23 Avenue du Général de Gaulle, 94704 Maisons-Alfort, France. Electronic address: dvitour@vet-alfort.fr.
Virginie DoceulUMR1161 ANSES-INRA-ENVA, 23 Avenue du Général de Gaulle, 94704 Maisons-Alfort, France. Electronic address: vdoceul@vet-alfort.fr.
Suzana RuscanuVirologie et Immunologie Moléculaires, UR892 INRA, Jouy-en-Josas, France. Electronic address: suzana.ruscanu@jouy.inra.fr.
Emilie ChauveauUMR1161 ANSES-INRA-ENVA, 23 Avenue du Général de Gaulle, 94704 Maisons-Alfort, France. Electronic address: echauveau@vet-alfort.fr.
Isabelle Schwartz-CornilVirologie et Immunologie Moléculaires, UR892 INRA, Jouy-en-Josas, France. Electronic address: isabelle.schwartz@jouy.inra.fr.
Stéphan ZientaraUMR1161 ANSES-INRA-ENVA, 23 Avenue du Général de Gaulle, 94704 Maisons-Alfort, France. Electronic address: szientara@vet-alfort.fr.
École Nationale Vétérinaire d'Alfort · FRVirologie et Immunologie Moléculaires · FRInstitut de Virologie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The innate immune response is the first line of defence against viruses, involving the production of type I IFN (IFN-α/β) and other pro-inflammatory cytokines that control the infection. It also shapes the adaptive immune response generated by both T and B cells. Production of type I IFN occurs both in vivo and in vitro in response to Bluetongue virus (BTV), an arthropod-borne virus. However, the mechanisms responsible for the production of IFN-β in response to BTV remained unknown until recently and are still not completely understood. In this review, we describe the recent advances in the identification of cellular sensors and signalling pathways involved in this process. The RNA helicases retinoic acid-inducible gene-I (RIG-I) and melanoma differentiation-associated gene 5 (MDA5) were shown to be involved in the expression of IFN-β as well as in the control of BTV infection in non-haematopoietic cells. In contrast, induction of IFN-α/β synthesis in sheep primary plasmacytoid dendritic cells (pDCs) required the MyD88 adaptor independently of the Toll-like receptor 7 (TLR7), as well as the kinases dsRNA-activated protein kinase (PKR) and stress-activated protein kinase (SAPK)/Jun N-terminal protein kinase (JNK). As type I IFN is essential for the establishment of an antiviral cellular response, most of viruses have elaborated counteracting mechanisms to hinder its action. This review also addresses the ability of BTV to interfere with IFN-β synthesis and the recent findings describing the non-structural viral protein NS3 as a powerful antagonist of the host cellular response.

Indexed as

Immune EvasionAnimalsBluetongue virusInterferon Type IReceptors, ImmunologicSheepSignal TransductionInterferon Type IReceptors, ImmunologicBTVImmune evasionInterferon synthesis

Identifiers

PMID24211608
PMCPMC7114367
OpenAlexW2076074285

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.