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Population Variability Generated during Rescue Process and Passaging of Recombinant Mumps Viruses
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 vacc...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8707793/ https://www.ncbi.nlm.nih.gov/pubmed/34960819 http://dx.doi.org/10.3390/v13122550 |
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author | Slović, Anamarija Košutić-Gulija, Tanja Forčić, Dubravko Šantak, Maja Jagušić, Maja Jurković, Mirna Pali, Dorotea Ivančić-Jelečki, Jelena |
author_facet | Slović, Anamarija Košutić-Gulija, Tanja Forčić, Dubravko Šantak, Maja Jagušić, Maja Jurković, Mirna Pali, Dorotea Ivančić-Jelečki, Jelena |
author_sort | Slović, Anamarija |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8707793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87077932021-12-25 Population Variability Generated during Rescue Process and Passaging of Recombinant Mumps Viruses Slović, Anamarija Košutić-Gulija, Tanja Forčić, Dubravko Šantak, Maja Jagušić, Maja Jurković, Mirna Pali, Dorotea Ivančić-Jelečki, Jelena Viruses Article 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. MDPI 2021-12-20 /pmc/articles/PMC8707793/ /pubmed/34960819 http://dx.doi.org/10.3390/v13122550 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Slović, Anamarija Košutić-Gulija, Tanja Forčić, Dubravko Šantak, Maja Jagušić, Maja Jurković, Mirna Pali, Dorotea Ivančić-Jelečki, Jelena Population Variability Generated during Rescue Process and Passaging of Recombinant Mumps Viruses |
title | Population Variability Generated during Rescue Process and Passaging of Recombinant Mumps Viruses |
title_full | Population Variability Generated during Rescue Process and Passaging of Recombinant Mumps Viruses |
title_fullStr | Population Variability Generated during Rescue Process and Passaging of Recombinant Mumps Viruses |
title_full_unstemmed | Population Variability Generated during Rescue Process and Passaging of Recombinant Mumps Viruses |
title_short | Population Variability Generated during Rescue Process and Passaging of Recombinant Mumps Viruses |
title_sort | population variability generated during rescue process and passaging of recombinant mumps viruses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8707793/ https://www.ncbi.nlm.nih.gov/pubmed/34960819 http://dx.doi.org/10.3390/v13122550 |
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