Show simple item record

Files in this item

Thumbnail

Item metadata

dc.contributor.authorBamford, Connor
dc.contributor.authorWignall-Fleming, Elizabeth
dc.contributor.authorSreenu, Vattipally B.
dc.contributor.authorRandall, Richard
dc.contributor.authorDuprex, Paul
dc.contributor.authorRima, Bertus
dc.date.accessioned2019-07-09T16:30:03Z
dc.date.available2019-07-09T16:30:03Z
dc.date.issued2019-07-05
dc.identifier.citationBamford , C , Wignall-Fleming , E , Sreenu , V B , Randall , R , Duprex , P & Rima , B 2019 , ' Unusual, stable replicating viruses generated from mumps virus cDNA clones ' , PLoS ONE , vol. 14 , no. 7 , e0219168 . https://doi.org/10.1371/journal.pone.0219168en
dc.identifier.issn1932-6203
dc.identifier.otherPURE: 259546739
dc.identifier.otherPURE UUID: 72ada6b5-bbbc-4aa7-afa6-c8311986a97f
dc.identifier.otherRIS: urn:86EA12BE1AAE13EB4B28250784333895
dc.identifier.otherORCID: /0000-0002-9304-6678/work/60427002
dc.identifier.otherORCID: /0000-0002-3626-8768/work/60631228
dc.identifier.otherScopus: 85069269790
dc.identifier.otherWOS: 000484936300044
dc.identifier.urihttp://hdl.handle.net/10023/18062
dc.descriptionThe authors have acknowledged funding from a Wellcome Trust grant 101788/Z/13/Z to RER and funding from the respective universities for studentships, Queen’s University Belfast to CGB, and University of St Andrews to EWF.en
dc.description.abstractIn 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.
dc.format.extent14
dc.language.isoeng
dc.relation.ispartofPLoS ONEen
dc.rightsCopyright: © 2019 Bamford et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en
dc.subjectQR Microbiologyen
dc.subjectDASen
dc.subject.lccQRen
dc.titleUnusual, stable replicating viruses generated from mumps virus cDNA clonesen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews.School of Biologyen
dc.contributor.institutionUniversity of St Andrews.Biomedical Sciences Research Complexen
dc.identifier.doihttps://doi.org/10.1371/journal.pone.0219168
dc.description.statusPeer revieweden


This item appears in the following Collection(s)

Show simple item record