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Comparative mutational analyses of influenza A viruses
The error-prone RNA-dependent RNA polymerase (RdRP) and external selective pressures are the driving forces for RNA viral diversity. When confounded by selective pressures, it is difficult to assess if influenza A viruses (IAV) that have a wide host range possess comparable or distinct spontaneous m...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274636/ https://www.ncbi.nlm.nih.gov/pubmed/25404565 http://dx.doi.org/10.1261/rna.045369.114 |
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author | Cheung, Peter Pak-Hang Rogozin, Igor B. Choy, Ka-Tim Ng, Hoi Yee Peiris, Joseph Sriyal Malik Yen, Hui-Ling |
author_facet | Cheung, Peter Pak-Hang Rogozin, Igor B. Choy, Ka-Tim Ng, Hoi Yee Peiris, Joseph Sriyal Malik Yen, Hui-Ling |
author_sort | Cheung, Peter Pak-Hang |
collection | PubMed |
description | The error-prone RNA-dependent RNA polymerase (RdRP) and external selective pressures are the driving forces for RNA viral diversity. When confounded by selective pressures, it is difficult to assess if influenza A viruses (IAV) that have a wide host range possess comparable or distinct spontaneous mutational frequency in their RdRPs. We used in-depth bioinformatics analyses to assess the spontaneous mutational frequencies of two RdRPs derived from human seasonal (A/Wuhan/359/95; Wuhan) and H5N1 (A/Vietnam/1203/04; VN1203) viruses using the mini-genome system with a common firefly luciferase reporter serving as the template. High-fidelity reverse transcriptase was applied to generate high-quality mutational spectra which allowed us to assess and compare the mutational frequencies and mutable motifs along a target sequence of the two RdRPs of two different subtypes. We observed correlated mutational spectra (τ correlation P < 0.0001), comparable mutational frequencies (H3N2:5.8 ± 0.9; H5N1:6.0 ± 0.5), and discovered a highly mutable motif “(A)AAG” for both Wuhan and VN1203 RdRPs. Results were then confirmed with two recombinant A/Puerto Rico/8/34 (PR8) viruses that possess RdRP derived from Wuhan or VN1203 (RG-PR8×Wuhan(PB2, PB1, PA, NP) and RG-PR8×VN1203(PB2, PB1, PA, NP)). Applying novel bioinformatics analysis on influenza mutational spectra, we provide a platform for a comprehensive analysis of the spontaneous mutation spectra for an RNA virus. |
format | Online Article Text |
id | pubmed-4274636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-42746362016-01-01 Comparative mutational analyses of influenza A viruses Cheung, Peter Pak-Hang Rogozin, Igor B. Choy, Ka-Tim Ng, Hoi Yee Peiris, Joseph Sriyal Malik Yen, Hui-Ling RNA Articles The error-prone RNA-dependent RNA polymerase (RdRP) and external selective pressures are the driving forces for RNA viral diversity. When confounded by selective pressures, it is difficult to assess if influenza A viruses (IAV) that have a wide host range possess comparable or distinct spontaneous mutational frequency in their RdRPs. We used in-depth bioinformatics analyses to assess the spontaneous mutational frequencies of two RdRPs derived from human seasonal (A/Wuhan/359/95; Wuhan) and H5N1 (A/Vietnam/1203/04; VN1203) viruses using the mini-genome system with a common firefly luciferase reporter serving as the template. High-fidelity reverse transcriptase was applied to generate high-quality mutational spectra which allowed us to assess and compare the mutational frequencies and mutable motifs along a target sequence of the two RdRPs of two different subtypes. We observed correlated mutational spectra (τ correlation P < 0.0001), comparable mutational frequencies (H3N2:5.8 ± 0.9; H5N1:6.0 ± 0.5), and discovered a highly mutable motif “(A)AAG” for both Wuhan and VN1203 RdRPs. Results were then confirmed with two recombinant A/Puerto Rico/8/34 (PR8) viruses that possess RdRP derived from Wuhan or VN1203 (RG-PR8×Wuhan(PB2, PB1, PA, NP) and RG-PR8×VN1203(PB2, PB1, PA, NP)). Applying novel bioinformatics analysis on influenza mutational spectra, we provide a platform for a comprehensive analysis of the spontaneous mutation spectra for an RNA virus. Cold Spring Harbor Laboratory Press 2015-01 /pmc/articles/PMC4274636/ /pubmed/25404565 http://dx.doi.org/10.1261/rna.045369.114 Text en © 2014 Cheung et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Articles Cheung, Peter Pak-Hang Rogozin, Igor B. Choy, Ka-Tim Ng, Hoi Yee Peiris, Joseph Sriyal Malik Yen, Hui-Ling Comparative mutational analyses of influenza A viruses |
title | Comparative mutational analyses of influenza A viruses |
title_full | Comparative mutational analyses of influenza A viruses |
title_fullStr | Comparative mutational analyses of influenza A viruses |
title_full_unstemmed | Comparative mutational analyses of influenza A viruses |
title_short | Comparative mutational analyses of influenza A viruses |
title_sort | comparative mutational analyses of influenza a viruses |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274636/ https://www.ncbi.nlm.nih.gov/pubmed/25404565 http://dx.doi.org/10.1261/rna.045369.114 |
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