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...

Descripción completa

Detalles Bibliográficos
Autores principales: Handel, Andreas, Brown, Justin, Stallknecht, David, Rohani, Pejman
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