Cargando…
A Multi-scale Analysis of Influenza A Virus Fitness Trade-offs due to Temperature-dependent Virus Persistence
Successful replication within an infected host and successful transmission between hosts are key to the continued spread of most pathogens. Competing selection pressures exerted at these different scales can lead to evolutionary trade-offs between the determinants of fitness within and between hosts...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3605121/ https://www.ncbi.nlm.nih.gov/pubmed/23555223 http://dx.doi.org/10.1371/journal.pcbi.1002989 |
_version_ | 1782263824585326592 |
---|---|
author | Handel, Andreas Brown, Justin Stallknecht, David Rohani, Pejman |
author_facet | Handel, Andreas Brown, Justin Stallknecht, David Rohani, Pejman |
author_sort | Handel, Andreas |
collection | PubMed |
description | Successful replication within an infected host and successful transmission between hosts are key to the continued spread of most pathogens. Competing selection pressures exerted at these different scales can lead to evolutionary trade-offs between the determinants of fitness within and between hosts. Here, we examine such a trade-off in the context of influenza A viruses and the differential pressures exerted by temperature-dependent virus persistence. For a panel of avian influenza A virus strains, we find evidence for a trade-off between the persistence at high versus low temperatures. Combining a within-host model of influenza infection dynamics with a between-host transmission model, we study how such a trade-off affects virus fitness on the host population level. We show that conclusions regarding overall fitness are affected by the type of link assumed between the within- and between-host levels and the main route of transmission (direct or environmental). The relative importance of virulence and immune response mediated virus clearance are also found to influence the fitness impacts of virus persistence at low versus high temperatures. Based on our results, we predict that if transmission occurs mainly directly and scales linearly with virus load, and virulence or immune responses are negligible, the evolutionary pressure for influenza viruses to evolve toward good persistence at high within-host temperatures dominates. For all other scenarios, influenza viruses with good environmental persistence at low temperatures seem to be favored. |
format | Online Article Text |
id | pubmed-3605121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36051212013-04-03 A Multi-scale Analysis of Influenza A Virus Fitness Trade-offs due to Temperature-dependent Virus Persistence Handel, Andreas Brown, Justin Stallknecht, David Rohani, Pejman PLoS Comput Biol Research Article Successful replication within an infected host and successful transmission between hosts are key to the continued spread of most pathogens. Competing selection pressures exerted at these different scales can lead to evolutionary trade-offs between the determinants of fitness within and between hosts. Here, we examine such a trade-off in the context of influenza A viruses and the differential pressures exerted by temperature-dependent virus persistence. For a panel of avian influenza A virus strains, we find evidence for a trade-off between the persistence at high versus low temperatures. Combining a within-host model of influenza infection dynamics with a between-host transmission model, we study how such a trade-off affects virus fitness on the host population level. We show that conclusions regarding overall fitness are affected by the type of link assumed between the within- and between-host levels and the main route of transmission (direct or environmental). The relative importance of virulence and immune response mediated virus clearance are also found to influence the fitness impacts of virus persistence at low versus high temperatures. Based on our results, we predict that if transmission occurs mainly directly and scales linearly with virus load, and virulence or immune responses are negligible, the evolutionary pressure for influenza viruses to evolve toward good persistence at high within-host temperatures dominates. For all other scenarios, influenza viruses with good environmental persistence at low temperatures seem to be favored. Public Library of Science 2013-03-21 /pmc/articles/PMC3605121/ /pubmed/23555223 http://dx.doi.org/10.1371/journal.pcbi.1002989 Text en © 2013 Handel et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Handel, Andreas Brown, Justin Stallknecht, David Rohani, Pejman A Multi-scale Analysis of Influenza A Virus Fitness Trade-offs due to Temperature-dependent Virus Persistence |
title | A Multi-scale Analysis of Influenza A Virus Fitness Trade-offs due to Temperature-dependent Virus Persistence |
title_full | A Multi-scale Analysis of Influenza A Virus Fitness Trade-offs due to Temperature-dependent Virus Persistence |
title_fullStr | A Multi-scale Analysis of Influenza A Virus Fitness Trade-offs due to Temperature-dependent Virus Persistence |
title_full_unstemmed | A Multi-scale Analysis of Influenza A Virus Fitness Trade-offs due to Temperature-dependent Virus Persistence |
title_short | A Multi-scale Analysis of Influenza A Virus Fitness Trade-offs due to Temperature-dependent Virus Persistence |
title_sort | multi-scale analysis of influenza a virus fitness trade-offs due to temperature-dependent virus persistence |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3605121/ https://www.ncbi.nlm.nih.gov/pubmed/23555223 http://dx.doi.org/10.1371/journal.pcbi.1002989 |
work_keys_str_mv | AT handelandreas amultiscaleanalysisofinfluenzaavirusfitnesstradeoffsduetotemperaturedependentviruspersistence AT brownjustin amultiscaleanalysisofinfluenzaavirusfitnesstradeoffsduetotemperaturedependentviruspersistence AT stallknechtdavid amultiscaleanalysisofinfluenzaavirusfitnesstradeoffsduetotemperaturedependentviruspersistence AT rohanipejman amultiscaleanalysisofinfluenzaavirusfitnesstradeoffsduetotemperaturedependentviruspersistence AT handelandreas multiscaleanalysisofinfluenzaavirusfitnesstradeoffsduetotemperaturedependentviruspersistence AT brownjustin multiscaleanalysisofinfluenzaavirusfitnesstradeoffsduetotemperaturedependentviruspersistence AT stallknechtdavid multiscaleanalysisofinfluenzaavirusfitnesstradeoffsduetotemperaturedependentviruspersistence AT rohanipejman multiscaleanalysisofinfluenzaavirusfitnesstradeoffsduetotemperaturedependentviruspersistence |