Evidence map›Paper›PMID 26907325›Full record

ArticleViruses2016

In Vitro and in Vivo Evaluation of Mutations in the NS Region of Lineage 2 West Nile Virus Associated with Neuroinvasiveness in a Mammalian Model.

Katalin Szentpáli-Gavallér, Stephanie M Lim, László Dencső, Krisztián Bányai, Penelope Koraka, Albert D M E Osterhaus, Byron E E Martina, Tamás Bakonyi, Ádám Bálint

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
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

9 authors at 4 institutions in 3 countries.

Katalin Szentpáli-GavallérVeterinary Diagnostic Directorate, National Food Chain Safety Office, H-1143, Budapest, Hungary. szgkati@gmail.com.
Stephanie M LimViroscience Laboratory, Erasmus Medical Centre, 3015CN, Rotterdam, The Netherlands. s.lim@erasmusmc.nl.
László DencsőVeterinary Diagnostic Directorate, National Food Chain Safety Office, H-1143, Budapest, Hungary. balintad@nebih.gov.hu.
Krisztián BányaiInstitute for Veterinary Medical Research, Centre for Agricultural Research, Hungarian Academy of Sciences, H-1143, Budapest, Hungary. bkrota@hotmail.com.
Penelope KorakaViroscience Laboratory, Erasmus Medical Centre, 3015CN, Rotterdam, The Netherlands. p.koraka@erasmusmc.nl.
Albert D M E OsterhausViroscience Laboratory, Erasmus Medical Centre, 3015CN, Rotterdam, The Netherlands. a.osterhaus@erasmusmc.nl.
Byron E E MartinaViroscience Laboratory, Erasmus Medical Centre, 3015CN, Rotterdam, The Netherlands. b.martina@erasmusmc.nl.
Tamás BakonyiDepartment of Microbiology and Infectious Diseases, Faculty of Veterinary Science, Szent István University, H-1143, Budapest, Hungary. Bakonyi.Tamas@aotk.szie.hu.
Ádám BálintVeterinary Diagnostic Directorate, National Food Chain Safety Office, H-1143, Budapest, Hungary. dencsol@nebih.gov.hu.
Erasmus University Rotterdam · NLNational Food Chain Safety Office · HUHungarian Academy of Sciences · HUUniversity of Veterinary Medicine Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

West Nile virus (WNV) strains may differ significantly in neuroinvasiveness in vertebrate hosts. In contrast to genetic lineage 1 WNVs, molecular determinants of pathogenic lineage 2 strains have not been experimentally confirmed so far. A full-length infectious clone of a neurovirulent WNV lineage 2 strain (578/10; Central Europe) was generated and amino acid substitutions that have been shown to attenuate lineage 1 WNVs were introduced into the nonstructural proteins (NS1 (P250L), NS2A (A30P), NS3 (P249H) NS4B (P38G, C102S, E249G)). The mouse neuroinvasive phenotype of each mutant virus was examined following intraperitoneal inoculation of C57BL/6 mice. Only the NS1-P250L mutation was associated with a significant attenuation of virulence in mice compared to the wild-type. Multiplication kinetics in cell culture revealed significantly lower infectious virus titres for the NS1 mutant compared to the wild-type, as well as significantly lower amounts of positive and negative stranded RNA.

Indexed as

MutationAnimalsBrainDisease Models, AnimalFemaleHumansMiceMice, Inbred C57BLViral Nonstructural ProteinsVirulenceWest Nile FeverWest Nile virusViral Nonstructural Proteinsinfectious clonelineage 2virulence markersWest Nile virus

Identifiers

PMID26907325
PMCPMC4776204
OpenAlexW2277877248

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.