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Genetic Instability of Influenza pH1N1 Viruses
Here, we report full-length genome sequences of influenza pH1N1 viruses obtained prior to and after propagation in MDCK cells. Paired comparisons of the genomes showed that each strain acquired 1.0 to 18.8 mutations per genome per replication cycle, which corresponds to 0.5 to 5.8 mutations per viru...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4183864/ https://www.ncbi.nlm.nih.gov/pubmed/25278520 http://dx.doi.org/10.1128/genomeA.00841-14 |
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author | Jalovaara, Petri Bychkov, Dmitrii Ahtiainen, Laura Kallio-Kokko, Hannimari Valkonen, Miia Kantele, Anu Mattila, Pirkko Almusa, Henrikki Kallioniemi, Olli Kainov, Denis |
author_facet | Jalovaara, Petri Bychkov, Dmitrii Ahtiainen, Laura Kallio-Kokko, Hannimari Valkonen, Miia Kantele, Anu Mattila, Pirkko Almusa, Henrikki Kallioniemi, Olli Kainov, Denis |
author_sort | Jalovaara, Petri |
collection | PubMed |
description | Here, we report full-length genome sequences of influenza pH1N1 viruses obtained prior to and after propagation in MDCK cells. Paired comparisons of the genomes showed that each strain acquired 1.0 to 18.8 mutations per genome per replication cycle, which corresponds to 0.5 to 5.8 mutations per virus proteome per replication cycle. Our analysis indicates that pH1N1 viruses accumulated adaptive mutations among others in response to propagation in cell culture. These results could be important for vaccine and drug-sensitivity surveillance studies, as well as for vaccine and antiviral drug development programs where cell cultures are used for influenza propagation. |
format | Online Article Text |
id | pubmed-4183864 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-41838642014-10-06 Genetic Instability of Influenza pH1N1 Viruses Jalovaara, Petri Bychkov, Dmitrii Ahtiainen, Laura Kallio-Kokko, Hannimari Valkonen, Miia Kantele, Anu Mattila, Pirkko Almusa, Henrikki Kallioniemi, Olli Kainov, Denis Genome Announc Viruses Here, we report full-length genome sequences of influenza pH1N1 viruses obtained prior to and after propagation in MDCK cells. Paired comparisons of the genomes showed that each strain acquired 1.0 to 18.8 mutations per genome per replication cycle, which corresponds to 0.5 to 5.8 mutations per virus proteome per replication cycle. Our analysis indicates that pH1N1 viruses accumulated adaptive mutations among others in response to propagation in cell culture. These results could be important for vaccine and drug-sensitivity surveillance studies, as well as for vaccine and antiviral drug development programs where cell cultures are used for influenza propagation. American Society for Microbiology 2014-10-02 /pmc/articles/PMC4183864/ /pubmed/25278520 http://dx.doi.org/10.1128/genomeA.00841-14 Text en Copyright © 2014 Jalovaara et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 3.0 Unported license (http://creativecommons.org/licenses/by/3.0/) . |
spellingShingle | Viruses Jalovaara, Petri Bychkov, Dmitrii Ahtiainen, Laura Kallio-Kokko, Hannimari Valkonen, Miia Kantele, Anu Mattila, Pirkko Almusa, Henrikki Kallioniemi, Olli Kainov, Denis Genetic Instability of Influenza pH1N1 Viruses |
title | Genetic Instability of Influenza pH1N1 Viruses |
title_full | Genetic Instability of Influenza pH1N1 Viruses |
title_fullStr | Genetic Instability of Influenza pH1N1 Viruses |
title_full_unstemmed | Genetic Instability of Influenza pH1N1 Viruses |
title_short | Genetic Instability of Influenza pH1N1 Viruses |
title_sort | genetic instability of influenza ph1n1 viruses |
topic | Viruses |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4183864/ https://www.ncbi.nlm.nih.gov/pubmed/25278520 http://dx.doi.org/10.1128/genomeA.00841-14 |
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