Evidence map›Paper›PMID 19625458›Full record

ArticleThe Journal of general virology2009

Mumps virus Enders strain is sensitive to interferon (IFN) despite encoding a functional IFN antagonist.

D F Young, M C Galiano, K Lemon, Y-H Chen, J Andrejeva, W P Duprex, B K Rima, R E Randall

Abstract read
In one paragraph

Article in The Journal of general virology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Recombinant mumps virus as a cancer therapeutic agent.Molecular therapy oncolytics · 2016
    Article
  6. Article
  7. Oncolytic virotherapy for ovarian cancer.Oncolytic virotherapy · 2012
    Article
  8. Article
  9. 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

8 authors.

D F YoungCentre for Biomolecular Sciences, University of St Andrews, St Andrews, Fife KY16 9ST, UK.
M C GalianoCentre for Biomolecular Sciences, University of St Andrews, St Andrews, Fife KY16 9ST, UK.
K LemonCentre for Infection and Immunity, School of Medicine, Dentistry and Biomedical Sciences, The Queen's University of Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK.
Y-H ChenCentre for Biomolecular Sciences, University of St Andrews, St Andrews, Fife KY16 9ST, UK.
J AndrejevaCentre for Biomolecular Sciences, University of St Andrews, St Andrews, Fife KY16 9ST, UK.
W P DuprexCentre for Infection and Immunity, School of Medicine, Dentistry and Biomedical Sciences, The Queen's University of Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK.
B K RimaCentre for Infection and Immunity, School of Medicine, Dentistry and Biomedical Sciences, The Queen's University of Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK.
R E RandallCentre for Biomolecular Sciences, University of St Andrews, St Andrews, Fife KY16 9ST, UK.

Funding

Biotechnology and Biological Sciences Research CouncilWellcome Trust
6 · The paper itself

Abstract

Although the Enders strain of mumps virus (MuV) encodes a functional V protein that acts as an interferon (IFN) antagonist, in multi-cycle growth assays MuV Enders grew poorly in naïve ('IFN-competent' Hep2) cells but grew to high titres in 'IFN-compromised' Hep2 cells. Even so, the growth rate of MuV Enders was significantly slower in 'IFN-compromised' Hep2 cells when compared with its replication rate in Vero cells and with the replication rate of parainfluenza virus type 5 (a closely related paramyxovirus) in both naïve and 'IFN-compromised' Hep2 cells. This suggests that a consequence of slower growth is that the IFN system of naïve Hep2 cells can respond quickly enough to control the growth of MuV Enders. This is supported by the finding that rapidly growing variants of MuV Enders that were selected on 'IFN-compromised' Hep2 cells (i.e. in the absence of any selection pressure exerted by the IFN response) also grew to high titres on naïve Hep2 cells. Sequencing of the complete genome of one of these variants identified a single point mutation that resulted in a substitution of a conserved asparagine by histidine at position 498 of the haemagglutinin-neuraminidase protein, although this mutation was not present in all rapidly growing variants. These results support the concept that there is a race between the ability of a cell to detect and respond to virus infection and the ability of a virus to block the IFN response. Importantly, this emphasizes that factors other than viral IFN antagonists influence the sensitivity of viruses to IFN.

Indexed as

Virus ReplicationAmino Acid SubstitutionAnimalsCell LineChlorocebus aethiopsDNA Mutational AnalysisHN ProteinHumansInterferonsMumps virusMutation, MissenseViral Plaque AssayHN ProteinInterferons

Identifiers

PMID19625458
PMCPMC2885035

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Registered trials

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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.