Evidence map›Paper›PMID 19463721›Full record

ArticleVirus research2009

The interplay between infectious pancreatic necrosis virus (IPNV) and the IFN system: IFN signaling is inhibited by IPNV infection.

Astrid Skjesol, Toril Aamo, Marit Nøst Hegseth, Børre Robertsen, Jorunn B Jørgensen

Abstract read
In one paragraph

Article in Virus research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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, 1 synthesis or guideline pooled it, 75 citations in OpenAlex.

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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 1 institution in 1 country.

Astrid SkjesolDepartment of Marine Biotechnology, Norwegian College of Fishery Sciences, University of Tromsø, Breivika, N- 9037 Tromsø, Norway.
Toril Aamo
Marit Nøst Hegseth
Børre Robertsen
Jorunn B Jørgensen
UiT The Arctic University of Norway · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infectious pancreatic necrosis virus (IPNV) is a major pathogen in the aquaculture industry worldwide. Factors contributing to IPNV pathogenicity are yet poorly understood. Indications of IPNV being able to evade or counteract innate host defense come from its lack of ability to induce strong type I interferon (IFN) responses in cell culture. We show here that addition of salmon rIFN-alpha1 to cells prior to IPNV infection halts the viral protein synthesis and prevents processing of pVP2 into mature VP2. Furthermore, compared to pre-treatment with IFN-alpha1 the antiviral state in cells infected with IPNV prior to IFN-treatment, was antagonized by IPNV, as detected by higher viral titers, faster viral protein synthesis and also by reduced Mx expression. The longer headstart the virus gets, the more prominent is the weakening of IFN signaling. IPNV VP4 and VP5 inhibit IFN-induced expression from the Mx promoter, indicating that these proteins contribute to the antagonistic effect.

Indexed as

Signal TransductionAnimalsAntiviral AgentsBirnaviridae InfectionsCell LineFish DiseasesGene Expression RegulationGTP-Binding ProteinsHost-Pathogen InteractionsInfectious pancreatic necrosis virusInterferon-alphaMyxovirus Resistance ProteinsSalmonSerine EndopeptidasesViral Nonstructural ProteinsViral Structural ProteinsAntiviral AgentsGTP-Binding ProteinsInterferon-alphaMyxovirus Resistance ProteinsSerine EndopeptidasesViral Nonstructural ProteinsViral Structural ProteinsVP2 protein, infectious pancreatic necrosis virusVP4 protease, birnavirusVP5 protein, infectious bursal disease virus

Identifiers

PMID19463721
PMCPMC7114382
OpenAlexW2072339788

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.