Evolution at increased error rate leads to the coexistence of multiple adaptive pathways in an RNA virus

<p>Abstract</p> <p>Background</p> <p>When beneficial mutations present in different genomes spread simultaneously in an asexual population, their fixation can be delayed due to competition among them. This interference among mutations is mainly determined by the rate of...

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Main Authors: Cabanillas Laura, Arribas María, Lázaro Ester
Format: Article
Language:English
Published: BMC 2013-01-01
Series:BMC Evolutionary Biology
Subjects:
Online Access:http://www.biomedcentral.com/1471-2148/13/11
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spelling doaj-7c7f85fa0c504f53ac2b34496d6797992021-09-02T05:40:59ZengBMCBMC Evolutionary Biology1471-21482013-01-011311110.1186/1471-2148-13-11Evolution at increased error rate leads to the coexistence of multiple adaptive pathways in an RNA virusCabanillas LauraArribas MaríaLázaro Ester<p>Abstract</p> <p>Background</p> <p>When beneficial mutations present in different genomes spread simultaneously in an asexual population, their fixation can be delayed due to competition among them. This interference among mutations is mainly determined by the rate of beneficial mutations, which in turn depends on the population size, the total error rate, and the degree of adaptation of the population. RNA viruses, with their large population sizes and high error rates, are good candidates to present a great extent of interference. To test this hypothesis, in the current study we have investigated whether competition among beneficial mutations was responsible for the prolonged presence of polymorphisms in the mutant spectrum of an RNA virus, the bacteriophage Qβ, evolved during a large number of generations in the presence of the mutagenic nucleoside analogue 5-azacytidine.</p> <p>Results</p> <p>The analysis of the mutant spectra of bacteriophage Qβ populations evolved at artificially increased error rate shows a large number of polymorphic mutations, some of them with demonstrated selective value. Polymorphisms distributed into several evolutionary lines that can compete among them, making it difficult the emergence of a defined consensus sequence. The presence of accompanying deleterious mutations, the high degree of recurrence of the polymorphic mutations, and the occurrence of epistatic interactions generate a highly complex interference dynamics.</p> <p>Conclusions</p> <p>Interference among beneficial mutations in bacteriophage Qβ evolved at increased error rate permits the coexistence of multiple adaptive pathways that can provide selective advantages by different molecular mechanisms. In this way, interference can be seen as a positive factor that allows the exploration of the different local maxima that exist in rugged fitness landscapes.</p> http://www.biomedcentral.com/1471-2148/13/11RNA virusesInterferenceBeneficial mutationsMutagenesis5-azacytidineEpistasisPolymorphisms
collection DOAJ
language English
format Article
sources DOAJ
author Cabanillas Laura
Arribas María
Lázaro Ester
spellingShingle Cabanillas Laura
Arribas María
Lázaro Ester
Evolution at increased error rate leads to the coexistence of multiple adaptive pathways in an RNA virus
BMC Evolutionary Biology
RNA viruses
Interference
Beneficial mutations
Mutagenesis
5-azacytidine
Epistasis
Polymorphisms
author_facet Cabanillas Laura
Arribas María
Lázaro Ester
author_sort Cabanillas Laura
title Evolution at increased error rate leads to the coexistence of multiple adaptive pathways in an RNA virus
title_short Evolution at increased error rate leads to the coexistence of multiple adaptive pathways in an RNA virus
title_full Evolution at increased error rate leads to the coexistence of multiple adaptive pathways in an RNA virus
title_fullStr Evolution at increased error rate leads to the coexistence of multiple adaptive pathways in an RNA virus
title_full_unstemmed Evolution at increased error rate leads to the coexistence of multiple adaptive pathways in an RNA virus
title_sort evolution at increased error rate leads to the coexistence of multiple adaptive pathways in an rna virus
publisher BMC
series BMC Evolutionary Biology
issn 1471-2148
publishDate 2013-01-01
description <p>Abstract</p> <p>Background</p> <p>When beneficial mutations present in different genomes spread simultaneously in an asexual population, their fixation can be delayed due to competition among them. This interference among mutations is mainly determined by the rate of beneficial mutations, which in turn depends on the population size, the total error rate, and the degree of adaptation of the population. RNA viruses, with their large population sizes and high error rates, are good candidates to present a great extent of interference. To test this hypothesis, in the current study we have investigated whether competition among beneficial mutations was responsible for the prolonged presence of polymorphisms in the mutant spectrum of an RNA virus, the bacteriophage Qβ, evolved during a large number of generations in the presence of the mutagenic nucleoside analogue 5-azacytidine.</p> <p>Results</p> <p>The analysis of the mutant spectra of bacteriophage Qβ populations evolved at artificially increased error rate shows a large number of polymorphic mutations, some of them with demonstrated selective value. Polymorphisms distributed into several evolutionary lines that can compete among them, making it difficult the emergence of a defined consensus sequence. The presence of accompanying deleterious mutations, the high degree of recurrence of the polymorphic mutations, and the occurrence of epistatic interactions generate a highly complex interference dynamics.</p> <p>Conclusions</p> <p>Interference among beneficial mutations in bacteriophage Qβ evolved at increased error rate permits the coexistence of multiple adaptive pathways that can provide selective advantages by different molecular mechanisms. In this way, interference can be seen as a positive factor that allows the exploration of the different local maxima that exist in rugged fitness landscapes.</p>
topic RNA viruses
Interference
Beneficial mutations
Mutagenesis
5-azacytidine
Epistasis
Polymorphisms
url http://www.biomedcentral.com/1471-2148/13/11
work_keys_str_mv AT cabanillaslaura evolutionatincreasederrorrateleadstothecoexistenceofmultipleadaptivepathwaysinanrnavirus
AT arribasmaria evolutionatincreasederrorrateleadstothecoexistenceofmultipleadaptivepathwaysinanrnavirus
AT lazaroester evolutionatincreasederrorrateleadstothecoexistenceofmultipleadaptivepathwaysinanrnavirus
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