Literature DB >> 15648178

Foot-and-mouth disease virus evolution: exploring pathways towards virus extinction.

E Domingo1, N Pariente, A Airaksinen, C Gonzaĺez-Lopez, S Sierra, M Herrera, A Grande-Pérez, P R Lowenstein, S C Manrubia, E Lázaro, C Escarmís.   

Abstract

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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Year:  2005        PMID: 15648178      PMCID: PMC7121672          DOI: 10.1007/3-540-27109-0_7

Source DB:  PubMed          Journal:  Curr Top Microbiol Immunol        ISSN: 0070-217X            Impact factor:   4.291


  74 in total

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Review 2.  Ribavirin--current status of a broad spectrum antiviral agent.

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Authors:  T R Doel
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Journal:  Nature       Date:  1989-02-23       Impact factor: 49.962

6.  Efficient virus extinction by combinations of a mutagen and antiviral inhibitors.

Authors:  N Pariente; S Sierra; P R Lowenstein; E Domingo
Journal:  J Virol       Date:  2001-10       Impact factor: 5.103

7.  The hypercycle. A principle of natural self-organization. Part A: Emergence of the hypercycle.

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Authors:  L Chao
Journal:  Nature       Date:  1990-11-29       Impact factor: 49.962

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Authors:  S Crotty; C E Cameron; R Andino
Journal:  Proc Natl Acad Sci U S A       Date:  2001-05-22       Impact factor: 11.205

Review 10.  Quasispecies, error catastrophe, and the antiviral activity of ribavirin.

Authors:  Jason D Graci; Craig E Cameron
Journal:  Virology       Date:  2002-07-05       Impact factor: 3.616

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  20 in total

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5.  Phylogenetic analyses of the polyprotein coding sequences of serotype O foot-and-mouth disease viruses in East Africa: evidence for interserotypic recombination.

Authors:  Sheila N Balinda; Hans R Siegismund; Vincent B Muwanika; Abraham K Sangula; Charles Masembe; Chrisostom Ayebazibwe; Preben Normann; Graham J Belsham
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Review 6.  Quasispecies theory and the behavior of RNA viruses.

Authors:  Adam S Lauring; Raul Andino
Journal:  PLoS Pathog       Date:  2010-07-22       Impact factor: 6.823

7.  A multi-step process of viral adaptation to a mutagenic nucleoside analogue by modulation of transition types leads to extinction-escape.

Authors:  Rubén Agudo; Cristina Ferrer-Orta; Armando Arias; Ignacio de la Higuera; Celia Perales; Rosa Pérez-Luque; Nuria Verdaguer; Esteban Domingo
Journal:  PLoS Pathog       Date:  2010-08-26       Impact factor: 6.823

Review 8.  Epidemiological situation of transboundary animal diseases in North African countries-proposition of a regional control strategy.

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9.  The molecular epidemiology of foot-and-mouth disease virus serotypes A and O from 1998 to 2004 in Turkey.

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Journal:  BMC Vet Res       Date:  2006-12-04       Impact factor: 2.741

10.  Antigenicity and Immunogenicity Analysis of the E. coli Expressed FMDV Structural Proteins; VP1, VP0, VP3 of the South African Territories Type 2 Virus.

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Journal:  Viruses       Date:  2021-05-27       Impact factor: 5.048

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