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Quasispecies Spatial Models for RNA Viruses with Different Replication Modes and Infection Strategies

Empirical observations and theoretical studies suggest that viruses may use different replication strategies to amplify their genomes, which impact the dynamics of mutation accumulation in viral populations and therefore, their fitness and virulence. Similarly, during natural infections, viruses rep...

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Autores principales: Sardanyés, Josep, Elena, Santiago F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176287/
https://www.ncbi.nlm.nih.gov/pubmed/21949777
http://dx.doi.org/10.1371/journal.pone.0024884
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author Sardanyés, Josep
Elena, Santiago F.
author_facet Sardanyés, Josep
Elena, Santiago F.
author_sort Sardanyés, Josep
collection PubMed
description Empirical observations and theoretical studies suggest that viruses may use different replication strategies to amplify their genomes, which impact the dynamics of mutation accumulation in viral populations and therefore, their fitness and virulence. Similarly, during natural infections, viruses replicate and infect cells that are rarely in suspension but spatially organized. Surprisingly, most quasispecies models of virus replication have ignored these two phenomena. In order to study these two viral characteristics, we have developed stochastic cellular automata models that simulate two different modes of replication (geometric vs stamping machine) for quasispecies replicating and spreading on a two-dimensional space. Furthermore, we explored these two replication models considering epistatic fitness landscapes (antagonistic vs synergistic) and different scenarios for cell-to-cell spread, one with free superinfection and another with superinfection inhibition. We found that the master sequences for populations replicating geometrically and with antagonistic fitness effects vanished at low critical mutation rates. By contrast, the highest critical mutation rate was observed for populations replicating geometrically but with a synergistic fitness landscape. Our simulations also showed that for stamping machine replication and antagonistic epistasis, a combination that appears to be common among plant viruses, populations further increased their robustness by inhibiting superinfection. We have also shown that the mode of replication strongly influenced the linkage between viral loci, which rapidly reached linkage equilibrium at increasing mutations for geometric replication. We also found that the strategy that minimized the time required to spread over the whole space was the stamping machine with antagonistic epistasis among mutations. Finally, our simulations revealed that the multiplicity of infection fluctuated but generically increased along time.
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spelling pubmed-31762872011-09-26 Quasispecies Spatial Models for RNA Viruses with Different Replication Modes and Infection Strategies Sardanyés, Josep Elena, Santiago F. PLoS One Research Article Empirical observations and theoretical studies suggest that viruses may use different replication strategies to amplify their genomes, which impact the dynamics of mutation accumulation in viral populations and therefore, their fitness and virulence. Similarly, during natural infections, viruses replicate and infect cells that are rarely in suspension but spatially organized. Surprisingly, most quasispecies models of virus replication have ignored these two phenomena. In order to study these two viral characteristics, we have developed stochastic cellular automata models that simulate two different modes of replication (geometric vs stamping machine) for quasispecies replicating and spreading on a two-dimensional space. Furthermore, we explored these two replication models considering epistatic fitness landscapes (antagonistic vs synergistic) and different scenarios for cell-to-cell spread, one with free superinfection and another with superinfection inhibition. We found that the master sequences for populations replicating geometrically and with antagonistic fitness effects vanished at low critical mutation rates. By contrast, the highest critical mutation rate was observed for populations replicating geometrically but with a synergistic fitness landscape. Our simulations also showed that for stamping machine replication and antagonistic epistasis, a combination that appears to be common among plant viruses, populations further increased their robustness by inhibiting superinfection. We have also shown that the mode of replication strongly influenced the linkage between viral loci, which rapidly reached linkage equilibrium at increasing mutations for geometric replication. We also found that the strategy that minimized the time required to spread over the whole space was the stamping machine with antagonistic epistasis among mutations. Finally, our simulations revealed that the multiplicity of infection fluctuated but generically increased along time. Public Library of Science 2011-09-19 /pmc/articles/PMC3176287/ /pubmed/21949777 http://dx.doi.org/10.1371/journal.pone.0024884 Text en Sardanyes, Elena. 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
Sardanyés, Josep
Elena, Santiago F.
Quasispecies Spatial Models for RNA Viruses with Different Replication Modes and Infection Strategies
title Quasispecies Spatial Models for RNA Viruses with Different Replication Modes and Infection Strategies
title_full Quasispecies Spatial Models for RNA Viruses with Different Replication Modes and Infection Strategies
title_fullStr Quasispecies Spatial Models for RNA Viruses with Different Replication Modes and Infection Strategies
title_full_unstemmed Quasispecies Spatial Models for RNA Viruses with Different Replication Modes and Infection Strategies
title_short Quasispecies Spatial Models for RNA Viruses with Different Replication Modes and Infection Strategies
title_sort quasispecies spatial models for rna viruses with different replication modes and infection strategies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176287/
https://www.ncbi.nlm.nih.gov/pubmed/21949777
http://dx.doi.org/10.1371/journal.pone.0024884
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