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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...

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Autores principales: Cheung, Peter Pak-Hang, Rogozin, Igor B., Choy, Ka-Tim, Ng, Hoi Yee, Peiris, Joseph Sriyal Malik, Yen, Hui-Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2015
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.
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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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