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Published on: June 24, 2019
Unusual, stable replicating viruses generated from mumps virus cDNA clones
Connor Bamford1,2, Elizabeth Wignall-Fleming1,3, Vattipally B Sreenu1
1Centre for Virus Research, Glasgow University, Glasgow, Scotland, United Kingdom.
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.
Insights
Researchers created novel recombinant mumps viruses (rMuV) with clustered, synonymous mutations. These mutations were stable during cell passage, suggesting unique genetic properties of these engineered mumps viruses.
Area of Science:
- Virology
- Molecular Biology
- Genetics
Background:
- Reverse genetics allows for the creation of modified viruses.
- Mumps virus (MuV) is a paramyxovirus with a segmented RNA genome.
- Understanding viral mutation patterns is crucial for studying viral evolution and pathogenesis.
Purpose of the Study:
- To investigate the generation and stability of recombinant mumps viruses (rMuV) with clustered mutations.
- To characterize the nature and frequency of mutations in specific viral genomic regions.
- To explore the stability of these mutations during serial passage in different cell types.
Main Methods:
- Isolation and characterization of recombinant mumps viruses (rMuV) using reverse genetics.
- Next-generation sequencing to identify and quantify mutations in the viral genome.
- Serial passage of rMuV in Vero cells and human B-lymphocyte cell lines (B-LCL).
- Analysis of mutation stability and frequency during passage.
Main Results:
- Two rMuV strains were generated, one with 11 mutations in the V/P region and another with 32 mutations in the N gene.
- The majority of observed mutations (48/51) were synonymous, a pattern not seen in natural MuV isolates.
- Mutations were stable across multiple passages in both Vero and B-LCL cells, with no reversion to the consensus sequence.
- Defective interfering RNAs accumulated during passage in Vero cells but not in B-LCL cells.
- The EGFP gene, when present, showed variation levels similar to viral genes, irrespective of functional constraints.
Conclusions:
- Reverse genetics can produce rMuV with unique, clustered, and stable synonymous mutations.
- The mechanism generating these specific mutation patterns and their stability is currently unknown.
- The stability of these mutations suggests potential implications for viral genetic engineering and research.
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