Evidence map›Paper›PMID 28786780›Full record

ArticleThe Journal of general virology2017

Analysis of tick-borne encephalitis virus-induced host responses in human cells of neuronal origin and interferon-mediated protection.

Martin Selinger, Gavin S Wilkie, Lily Tong, Quan Gu, Esther Schnettler, Libor Grubhoffer, Alain Kohl

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in The Journal of general virology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 9% 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, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Distribution ofInternational journal of environmental research and public health · 2021
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  12. The Causes and Long-Term Consequences of Viral Encephalitis.Frontiers in cellular neuroscience · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Martin SelingerInstitute of Parasitology, Biology Centre of the Academy of Sciences of the Czech Republic, Branišovská 31, 370 05 České Budějovice, Czech Republic.
Gavin S WilkieMRC-University of Glasgow Centre for Virus Research, Glasgow G61 1QH, Scotland, UK.
Lily TongMRC-University of Glasgow Centre for Virus Research, Glasgow G61 1QH, Scotland, UK.
Quan GuMRC-University of Glasgow Centre for Virus Research, Glasgow G61 1QH, Scotland, UK.
Esther SchnettlerMRC-University of Glasgow Centre for Virus Research, Glasgow G61 1QH, Scotland, UK.
Libor GrubhofferInstitute of Parasitology, Biology Centre of the Academy of Sciences of the Czech Republic, Branišovská 31, 370 05 České Budějovice, Czech Republic.
Alain KohlMRC-University of Glasgow Centre for Virus Research, Glasgow G61 1QH, Scotland, UK.
MRC University of Glasgow Centre for Virus Research · GBCzech Academy of Sciences, Biology Centre · CZUniversity of South Bohemia in České Budějovice · CZ

Funding

Medical Research Council G0801822Medical Research Council MC_UU_12014/12Medical Research Council MC_UU_12014/8
6 · The paper itself

Abstract

Tick-borne encephalitis virus (TBEV) is a member of the genus Flavivirus. It can cause serious infections in humans that may result in encephalitis/meningoencephalitis. Although several studies have described the involvement of specific genes in the host response to TBEV infection in the central nervous system (CNS), the overall network remains poorly characterized. Therefore, we investigated the response of DAOY cells (human medulloblastoma cells derived from cerebellar neurons) to TBEV (Neudoerfl strain, Western subtype) infection to characterize differentially expressed genes by transcriptome analysis. Our results revealed a wide panel of interferon-stimulated genes (ISGs) and pro-inflammatory cytokines, including type III but not type I (or II) interferons (IFNs), which are activated upon TBEV infection, as well as a number of non-coding RNAs, including long non-coding RNAs. To obtain a broader view of the pathways responsible for eliciting an antiviral state in DAOY cells we examined the effect of type I and III IFNs and found that only type I IFN pre-treatment inhibited TBEV production. The cellular response to TBEV showed only partial overlap with gene expression changes induced by IFN-β treatment - suggesting a virus-specific signature - and we identified a group of ISGs that were highly up-regulated following IFN-β treatment. Moreover, a high rate of down-regulation was observed for a wide panel of pro-inflammatory cytokines upon IFN-β treatment. These data can serve as the basis for further studies of host-TBEV interactions and the identification of ISGs and/or lncRNAs with potent antiviral effects in cases of TBEV infection in human neuronal cells.

Indexed as

CytokinesEncephalitis, Tick-BorneEncephalitis Viruses, Tick-BorneHost-Pathogen InteractionsHumansInterferonsNeuronsTranscriptional ActivationCytokinesInterferons

Identifiers

PMID28786780
PMCPMC5817271
OpenAlexW2743344876

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.