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Phylodynamics with Migration: A Computational Framework to Quantify Population Structure from Genomic Data
When viruses spread, outbreaks can be spawned in previously unaffected regions. Depending on the time and mode of introduction, each regional outbreak can have its own epidemic dynamics. The migration and phylodynamic processes are often intertwined and need to be taken into account when analyzing t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948704/ https://www.ncbi.nlm.nih.gov/pubmed/27189573 http://dx.doi.org/10.1093/molbev/msw064 |
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author | Kühnert, Denise Stadler, Tanja Vaughan, Timothy G. Drummond, Alexei J. |
author_facet | Kühnert, Denise Stadler, Tanja Vaughan, Timothy G. Drummond, Alexei J. |
author_sort | Kühnert, Denise |
collection | PubMed |
description | When viruses spread, outbreaks can be spawned in previously unaffected regions. Depending on the time and mode of introduction, each regional outbreak can have its own epidemic dynamics. The migration and phylodynamic processes are often intertwined and need to be taken into account when analyzing temporally and spatially structured virus data. In this article, we present a fully probabilistic approach for the joint reconstruction of phylodynamic history in structured populations (such as geographic structure) based on a multitype birth–death process. This approach can be used to quantify the spread of a pathogen in a structured population. Changes in epidemic dynamics through time within subpopulations are incorporated through piecewise constant changes in transmission parameters. We analyze a global human influenza H3N2 virus data set from a geographically structured host population to demonstrate how seasonal dynamics can be inferred simultaneously with the phylogeny and migration process. Our results suggest that the main migration path among the northern, tropical, and southern region represented in the sample analyzed here is the one leading from the tropics to the northern region. Furthermore, the time-dependent transmission dynamics between and within two HIV risk groups, heterosexuals and injecting drug users, in the Latvian HIV epidemic are investigated. Our analyses confirm that the Latvian HIV epidemic peaking around 2001 was mainly driven by the injecting drug user risk group. |
format | Online Article Text |
id | pubmed-4948704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49487042016-07-20 Phylodynamics with Migration: A Computational Framework to Quantify Population Structure from Genomic Data Kühnert, Denise Stadler, Tanja Vaughan, Timothy G. Drummond, Alexei J. Mol Biol Evol Methods When viruses spread, outbreaks can be spawned in previously unaffected regions. Depending on the time and mode of introduction, each regional outbreak can have its own epidemic dynamics. The migration and phylodynamic processes are often intertwined and need to be taken into account when analyzing temporally and spatially structured virus data. In this article, we present a fully probabilistic approach for the joint reconstruction of phylodynamic history in structured populations (such as geographic structure) based on a multitype birth–death process. This approach can be used to quantify the spread of a pathogen in a structured population. Changes in epidemic dynamics through time within subpopulations are incorporated through piecewise constant changes in transmission parameters. We analyze a global human influenza H3N2 virus data set from a geographically structured host population to demonstrate how seasonal dynamics can be inferred simultaneously with the phylogeny and migration process. Our results suggest that the main migration path among the northern, tropical, and southern region represented in the sample analyzed here is the one leading from the tropics to the northern region. Furthermore, the time-dependent transmission dynamics between and within two HIV risk groups, heterosexuals and injecting drug users, in the Latvian HIV epidemic are investigated. Our analyses confirm that the Latvian HIV epidemic peaking around 2001 was mainly driven by the injecting drug user risk group. Oxford University Press 2016-08 2016-04-09 /pmc/articles/PMC4948704/ /pubmed/27189573 http://dx.doi.org/10.1093/molbev/msw064 Text en © The Author 2016. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Methods Kühnert, Denise Stadler, Tanja Vaughan, Timothy G. Drummond, Alexei J. Phylodynamics with Migration: A Computational Framework to Quantify Population Structure from Genomic Data |
title | Phylodynamics with Migration: A Computational Framework to Quantify Population Structure from Genomic Data |
title_full | Phylodynamics with Migration: A Computational Framework to Quantify Population Structure from Genomic Data |
title_fullStr | Phylodynamics with Migration: A Computational Framework to Quantify Population Structure from Genomic Data |
title_full_unstemmed | Phylodynamics with Migration: A Computational Framework to Quantify Population Structure from Genomic Data |
title_short | Phylodynamics with Migration: A Computational Framework to Quantify Population Structure from Genomic Data |
title_sort | phylodynamics with migration: a computational framework to quantify population structure from genomic data |
topic | Methods |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948704/ https://www.ncbi.nlm.nih.gov/pubmed/27189573 http://dx.doi.org/10.1093/molbev/msw064 |
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