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Rapid, Seamless Generation of Recombinant Poxviruses using Host Range and Visual Selection
Published on: May 24, 2020
Recombination patterns in aphthoviruses mirror those found in other picornaviruses
Livio Heath1, Eric van der Walt, Arvind Varsani
1Department of Molecular and Cell Biology, Faculty of Science, University of Cape Town, Rondebosch 7701, South Africa.
Abstract:
Foot-and-mouth disease virus (FMDV) is thought to evolve largely through genetic drift driven by the inherently error-prone nature of its RNA polymerase. There is, however, increasing evidence that recombination is an important mechanism in the evolution of these and other related picornoviruses. Here, we use an extensive set of recombination detection methods to identify 86 unique potential recombination events among 125 publicly available FMDV complete genome sequences. The large number of events detected between members of different serotypes suggests that horizontal flow of sequences among the serotypes is relatively common and does not incur severe fitness costs. Interestingly, the distribution of recombination breakpoints was found to be largely nonrandom. Whereas there are clear breakpoint cold spots within the structural genes, two statistically significant hot spots precisely separate these from the nonstructural genes. Very similar breakpoint distributions were found for other picornovirus species in the genera Enterovirus and Teschovirus. Our results suggest that genome regions encoding the structural proteins of both FMDV and other picornaviruses are functionally interchangeable modules, supporting recent proposals that the structural and nonstructural coding regions of the picornaviruses are evolving largely independently of one another.
Insights
Recombination significantly impacts Foot-and-mouth disease virus (FMDV) evolution, with frequent sequence exchange between serotypes. Breakpoint distributions suggest structural and nonstructural genes evolve independently.
Area of Science:
- Virology
- Molecular Biology
- Evolutionary Biology
Background:
- Foot-and-mouth disease virus (FMDV) evolution is traditionally attributed to RNA polymerase errors (genetic drift).
- Emerging evidence highlights the role of genetic recombination in picornavirus evolution.
- Understanding recombination's role is crucial for FMDV and related virus evolution.
Purpose of the Study:
- To investigate the extent and patterns of genetic recombination in FMDV.
- To determine if recombination occurs between different FMDV serotypes.
- To analyze the distribution of recombination breakpoints within the FMDV genome.
Main Methods:
- Utilized an extensive suite of recombination detection methods.
- Analyzed 125 publicly available complete FMDV genome sequences.
- Compared breakpoint distributions with other picornaviruses (Enterovirus, Teschovirus).
Main Results:
- Identified 86 unique potential recombination events in FMDV genomes.
- Detected significant recombination between different FMDV serotypes, indicating frequent horizontal gene flow.
- Found a nonrandom distribution of breakpoints, with hot spots separating structural and nonstructural genes.
Conclusions:
- Recombination is a major driver of FMDV evolution, alongside genetic drift.
- Structural and nonstructural genes of FMDV and other picornaviruses may function as interchangeable modules.
- Independent evolution of structural and nonstructural coding regions is supported by breakpoint patterns.
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