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Fitness Inference from Short-Read Data: Within-Host Evolution of a Reassortant H5N1 Influenza Virus

We present a method to infer the role of selection acting during the within-host evolution of the influenza virus from short-read genome sequence data. Linkage disequilibrium between loci is accounted for by treating short-read sequences as noisy multilocus emissions from an underlying model of hapl...

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Autor principal: Illingworth, Christopher J.R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4651230/
https://www.ncbi.nlm.nih.gov/pubmed/26243288
http://dx.doi.org/10.1093/molbev/msv171
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author Illingworth, Christopher J.R.
author_facet Illingworth, Christopher J.R.
author_sort Illingworth, Christopher J.R.
collection PubMed
description We present a method to infer the role of selection acting during the within-host evolution of the influenza virus from short-read genome sequence data. Linkage disequilibrium between loci is accounted for by treating short-read sequences as noisy multilocus emissions from an underlying model of haplotype evolution. A hierarchical model-selection procedure is used to infer the underlying fitness landscape of the virus insofar as that landscape is explored by the viral population. In a first application of our method, we analyze data from an evolutionary experiment describing the growth of a reassortant H5N1 virus in ferrets. Across two sets of replica experiments we infer multiple alleles to be under selection, including variants associated with receptor binding specificity, glycosylation, and with the increased transmissibility of the virus. We identify epistasis as an important component of the within-host fitness landscape, and show that adaptation can proceed through multiple genetic pathways.
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spelling pubmed-46512302015-11-25 Fitness Inference from Short-Read Data: Within-Host Evolution of a Reassortant H5N1 Influenza Virus Illingworth, Christopher J.R. Mol Biol Evol Methods We present a method to infer the role of selection acting during the within-host evolution of the influenza virus from short-read genome sequence data. Linkage disequilibrium between loci is accounted for by treating short-read sequences as noisy multilocus emissions from an underlying model of haplotype evolution. A hierarchical model-selection procedure is used to infer the underlying fitness landscape of the virus insofar as that landscape is explored by the viral population. In a first application of our method, we analyze data from an evolutionary experiment describing the growth of a reassortant H5N1 virus in ferrets. Across two sets of replica experiments we infer multiple alleles to be under selection, including variants associated with receptor binding specificity, glycosylation, and with the increased transmissibility of the virus. We identify epistasis as an important component of the within-host fitness landscape, and show that adaptation can proceed through multiple genetic pathways. Oxford University Press 2015-11 2015-08-04 /pmc/articles/PMC4651230/ /pubmed/26243288 http://dx.doi.org/10.1093/molbev/msv171 Text en © The Author 2015. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods
Illingworth, Christopher J.R.
Fitness Inference from Short-Read Data: Within-Host Evolution of a Reassortant H5N1 Influenza Virus
title Fitness Inference from Short-Read Data: Within-Host Evolution of a Reassortant H5N1 Influenza Virus
title_full Fitness Inference from Short-Read Data: Within-Host Evolution of a Reassortant H5N1 Influenza Virus
title_fullStr Fitness Inference from Short-Read Data: Within-Host Evolution of a Reassortant H5N1 Influenza Virus
title_full_unstemmed Fitness Inference from Short-Read Data: Within-Host Evolution of a Reassortant H5N1 Influenza Virus
title_short Fitness Inference from Short-Read Data: Within-Host Evolution of a Reassortant H5N1 Influenza Virus
title_sort fitness inference from short-read data: within-host evolution of a reassortant h5n1 influenza virus
topic Methods
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4651230/
https://www.ncbi.nlm.nih.gov/pubmed/26243288
http://dx.doi.org/10.1093/molbev/msv171
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