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Foot-and-Mouth Disease Virus Evolution: Exploring Pathways Towards Virus Extinction

Foot-and-mouth disease virus (FMDV) is genetically and phenotypically variable. As a typical RNA virus, FMDV follows a quasispecies dynamics, with the many biological implications of such a dynamics. Mutant spectra provide a reservoir of FMDV variants, and minority subpopulations may become dominant...

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Autores principales: Domingo, E., Pariente, N., Airaksinen, A., González-Lopez, C., Sierra, S., Herrera, M., Grande-Pérez, A., Lowenstein, P. R., Manrubia, S. C., Lázaro, E., Escarmís, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7121672/
https://www.ncbi.nlm.nih.gov/pubmed/15648178
http://dx.doi.org/10.1007/3-540-27109-0_7
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author Domingo, E.
Pariente, N.
Airaksinen, A.
González-Lopez, C.
Sierra, S.
Herrera, M.
Grande-Pérez, A.
Lowenstein, P. R.
Manrubia, S. C.
Lázaro, E.
Escarmís, C.
author_facet Domingo, E.
Pariente, N.
Airaksinen, A.
González-Lopez, C.
Sierra, S.
Herrera, M.
Grande-Pérez, A.
Lowenstein, P. R.
Manrubia, S. C.
Lázaro, E.
Escarmís, C.
author_sort Domingo, E.
collection PubMed
description Foot-and-mouth disease virus (FMDV) is genetically and phenotypically variable. As a typical RNA virus, FMDV follows a quasispecies dynamics, with the many biological implications of such a dynamics. Mutant spectra provide a reservoir of FMDV variants, and minority subpopulations may become dominant in response to environmental demands or as a result of statistical fluctuations in population size. Accumulation of mutations in the FMDV genome occurs upon subjecting viral populations to repeated bottleneck events and upon viral replication in the presence of mutagenic base or nucleoside analogs. During serial bottleneck passages, FMDV survive during extended rounds of replication maintaining low average relative fitness, despite linear accumulation of mutations in the consensus genomic sequence. The critical event is the occurrence of a low frequency of compensatory mutations. In contrast, upon replication in the presence of mutagens, the complexity of mutant spectra increases, apparently no compensatory mutations can express their fitness-enhancing potential, and the virus can cross an error threshold for maintenance of genetic information, resulting in virus extinction. Low relative fitness and low viral load favor FMDV extinction in cell culture. The comparison of the molecular basis of resistance to extinction upon bottleneck passage and extinction by enhanced mutagenesis is providing new insights in the understanding of quasispecies dynamics. Such a comparison is contributing to the development of new antiviral strategies based on the transition of viral replication into error catastrophe.
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spelling pubmed-71216722020-04-06 Foot-and-Mouth Disease Virus Evolution: Exploring Pathways Towards Virus Extinction Domingo, E. Pariente, N. Airaksinen, A. González-Lopez, C. Sierra, S. Herrera, M. Grande-Pérez, A. Lowenstein, P. R. Manrubia, S. C. Lázaro, E. Escarmís, C. Foot-and-Mouth Disease Virus Article Foot-and-mouth disease virus (FMDV) is genetically and phenotypically variable. As a typical RNA virus, FMDV follows a quasispecies dynamics, with the many biological implications of such a dynamics. Mutant spectra provide a reservoir of FMDV variants, and minority subpopulations may become dominant in response to environmental demands or as a result of statistical fluctuations in population size. Accumulation of mutations in the FMDV genome occurs upon subjecting viral populations to repeated bottleneck events and upon viral replication in the presence of mutagenic base or nucleoside analogs. During serial bottleneck passages, FMDV survive during extended rounds of replication maintaining low average relative fitness, despite linear accumulation of mutations in the consensus genomic sequence. The critical event is the occurrence of a low frequency of compensatory mutations. In contrast, upon replication in the presence of mutagens, the complexity of mutant spectra increases, apparently no compensatory mutations can express their fitness-enhancing potential, and the virus can cross an error threshold for maintenance of genetic information, resulting in virus extinction. Low relative fitness and low viral load favor FMDV extinction in cell culture. The comparison of the molecular basis of resistance to extinction upon bottleneck passage and extinction by enhanced mutagenesis is providing new insights in the understanding of quasispecies dynamics. Such a comparison is contributing to the development of new antiviral strategies based on the transition of viral replication into error catastrophe. 2005 /pmc/articles/PMC7121672/ /pubmed/15648178 http://dx.doi.org/10.1007/3-540-27109-0_7 Text en © Springer-Verlag 2005 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Domingo, E.
Pariente, N.
Airaksinen, A.
González-Lopez, C.
Sierra, S.
Herrera, M.
Grande-Pérez, A.
Lowenstein, P. R.
Manrubia, S. C.
Lázaro, E.
Escarmís, C.
Foot-and-Mouth Disease Virus Evolution: Exploring Pathways Towards Virus Extinction
title Foot-and-Mouth Disease Virus Evolution: Exploring Pathways Towards Virus Extinction
title_full Foot-and-Mouth Disease Virus Evolution: Exploring Pathways Towards Virus Extinction
title_fullStr Foot-and-Mouth Disease Virus Evolution: Exploring Pathways Towards Virus Extinction
title_full_unstemmed Foot-and-Mouth Disease Virus Evolution: Exploring Pathways Towards Virus Extinction
title_short Foot-and-Mouth Disease Virus Evolution: Exploring Pathways Towards Virus Extinction
title_sort foot-and-mouth disease virus evolution: exploring pathways towards virus extinction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7121672/
https://www.ncbi.nlm.nih.gov/pubmed/15648178
http://dx.doi.org/10.1007/3-540-27109-0_7
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