Evidence map›Paper›PMID 31276568›Full record

ArticlePloS one2019

Unusual, stable replicating viruses generated from mumps virus cDNA clones.

Connor Bamford, Elizabeth Wignall-Fleming, Vattipally B Sreenu, Richard Randall, Paul Duprex, Bertus Rima

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 5 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

6 authors at 4 institutions in 2 countries.

Connor BamfordCentre for Virus Research, Glasgow University, Glasgow, Scotland, United Kingdom.
Elizabeth Wignall-FlemingCentre for Virus Research, Glasgow University, Glasgow, Scotland, United Kingdom.
Vattipally B SreenuCentre for Virus Research, Glasgow University, Glasgow, Scotland, United Kingdom.
Richard RandallSchool of Biology, St Andrews University, St Andrews, Scotland, United Kingdom.
Paul DuprexCenter for Vaccine Research, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Bertus RimaCentre for Experimental Medicine, Queen's University Belfast, Belfast Northern Ireland, United Kingdom.ORCID 0000-0002-1427-4120
Queen's University Belfast · GBUniversity of St Andrews · GBMRC University of Glasgow Centre for Virus Research · GBUniversity of Pittsburgh · US

Funding

Medical Research Council MC_UU_12014/12Wellcome TrustWellcome Trust 101788/Z/13/Z
6 · The paper itself

Abstract

In reverse genetic experiments we have isolated recombinant mumps viruses (rMuV) that carry large numbers of mutations clustered in small parts of their genome, which are not caused by biased hyper-mutation. In two separate experiments we obtained such recombinant viruses: one virus had 11 mutations in the V/P region of the genome; the other, which also contained an extra transcription unit encoding green fluorescent protein (EGFP), had 32 mutations in the N gene. These specific sets of mutations have not been observed in naturally occurring MuV isolates. Unusually, the vast majority of the mutations (48/51) were synonymous. On passage in Vero cells and human B-LCL cells, a B lymphocyte-like cell line, these mutations appear stable as no reversion occurred to the original consensus sequence, although mutations in other parts of the genome occurred and changed in frequency during passage. Defective interfering RNAs accumulate in passage in Vero cells but not in B-LCL cells. Interestingly, in all passaged samples the level of variation in the EGFP gene is the same as in the viral genes, though it is unlikely that this gene is under any functionality constraint. What mechanism gave rise to these viruses with clustered mutations and their stability remains an open question, which is likely of interest to a wider field than mumps reverse genetics.

Indexed as

MutationAnimalsCell Line, TumorChlorocebus aethiopsDNA, ComplementaryGreen Fluorescent ProteinsHumansMumps virusReverse GeneticsSerial PassageVero CellsViral ProteinsVirus ReplicationDNA, ComplementaryGreen Fluorescent ProteinsViral Proteins

Identifiers

PMID31276568
PMCPMC6611571
OpenAlexW2955124103

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.