Why the study?
Both the molecular mechanism and initial products of genetic recombination in RNA viruses are relatively poorly understood.
Genome function and fitness, rather than RNA identity or structure, primarily determine the identity of recombinant progeny in enteroviruses.
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Recombination proceeds independently of sequence identity or RNA structure; leaves open the role of functional selection in vivo.
Genetic recombination in RNA viruses is an important evolutionary mechanism. It contributes to population diversity, host/tissue adaptation and compromises vaccine efficacy. Both the molecular mechanism and initial products of recombination are relatively poorly understood. We used an established poliovirus-based in vitro recombination assay to investigate the roles of sequence identity and RNA structure, both implicated or inferred from analysis of circulating recombinant viruses, in the process. In addition, we used next generation sequencing to investigate the early products of recombination after cellular co-infection with different poliovirus serotypes. In independent studies we find no evidence for a role for RNA identity or structure in determining recombination junctions location. Instead, genome function and fitness are of greater importance in determining the identity of recombinant progeny. These studies provide further insights into this important evolutionary mechanism and emphasise the critical nature of the selection process on a mixed virus population.
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Alnaji et al. (2020) studied this question.
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