Abstract

BackgroundWhen 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.ResultsThe 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.ConclusionsInterference 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.

Highlights

  • When beneficial mutations present in different genomes spread simultaneously in an asexual population, their fixation can be delayed due to competition among them

  • Previous results In our previous work [31] a population of bacteriophage Qβ was evolved during 70 transfers under two parallel transmission regimes that differed in the presence of the mutagenic nucleoside analogue AZC

  • 6 polymorphic mutations (U1520C in the coat protein gene, and A2982G, C3413G+U, U3582C, G3945A, and U3989C in the replicase gene) were detected in population Qβ-AZC (t70). In contrast to this result, population Qβ-control (t70) showed no polymorphisms in its consensus sequence, and only one substitution was represented at a frequency of 0.2 when the mutant spectrum was analyzed through sequencing of 10 biological clones

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Summary

Introduction

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. For a beneficial mutation to fix in a population it is necessary that it survives genetic drift and that under the influence of selection displaces the rest of genomes. The fixation of beneficial mutations can be delayed by the coexistence of several lines carrying different mutations and because at high error rate beneficial mutations arise in deleterious backgrounds, hampering the action of selection [14,15,16]

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