Population Variability Generated during Rescue Process and Passaging of Recombinant Mumps Viruses
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Updated: Oct 8, 2025

Isolation of Fidelity Variants of RNA Viruses and Characterization of Virus Mutation Frequency
Published on: June 16, 2011
Anamarija Slović1, Tanja Košutić-Gulija1, Dubravko Forčić1
1Centre for Research and Knowledge Transfer in Biotechnology, University of Zagreb, 10000 Zagreb, Croatia.
Abstract:
Recombinant mumps viruses (MuVs) based on established vaccine strains represent attractive vector candidates as they have known track records for high efficacy and the viral genome does not integrate in the host cells. We developed a rescue system based on the consensus sequence of the L-Zagreb vaccine and generated seven different recombinant MuVs by (a) insertion of one or two additional transcription units (ATUs), (b) lengthening of a noncoding region to the extent that the longest noncoding region in MuV genome is created, or (c) replacement of original L-Zagreb sequences with sequences rich in CG and AT dinucleotides. All viruses were successfully rescued and faithfully matched sequences of input plasmids. In primary rescued stocks, low percentages of heterogeneous positions were found (maximum 0.12%) and substitutions were predominantly obtained in minor variants, with maximally four substitutions seen in consensus. ATUs did not accumulate more mutations than the natural MuV genes. Six substitutions characteristic for recombinant viruses generated in our system were defined, as they repetitively occurred during rescue processes. In subsequent passaging of primary rescue stocks in Vero cells, different inconsistencies within quasispecies structures were observed. In order to assure that unwanted mutations did not emerge and accumulate, sub-consensus variability should be closely monitored. As we show for Pro408Leu mutation in L gene and a stop codon in one of ATUs, positively selected variants can rise to frequencies over 85% in only few passages.
Insights
Researchers created new recombinant mumps viruses (MuVs) using a vaccine strain. Careful monitoring of genetic variations is crucial during the rescue and passage of these novel MuV vectors.
Area of Science:
- Virology
- Molecular Biology
- Vaccine Development
Background:
- Recombinant mumps viruses (MuVs) are promising vectors due to high efficacy and non-integrating genomes.
- Established vaccine strains offer a reliable foundation for vector development.
Purpose of the Study:
- To develop a robust rescue system for generating diverse recombinant MuVs.
- To characterize the genetic stability and variability of novel recombinant MuVs.
Main Methods:
- Generation of seven recombinant MuVs using a modified L-Zagreb vaccine strain.
- Inclusion of additional transcription units (ATUs) or modified non-coding regions.
- Sequence analysis to assess genetic fidelity and identify characteristic mutations.
Main Results:
- Successful rescue of all seven recombinant MuVs, matching input plasmid sequences.
- Low initial heterogeneity (max 0.12%) with minor variants dominating.
- Identification of six characteristic substitutions recurring during rescue.
- Emergence of positively selected variants (e.g., Pro408Leu mutation) reaching >85% frequency in few passages.
Conclusions:
- The developed rescue system effectively generates recombinant MuVs with high genetic fidelity.
- Sub-consensus variability monitoring is essential to control the emergence of unwanted mutations during passaging.
- Positively selected variants can rapidly dominate the viral quasispecies, necessitating careful characterization.

