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Updated: Jun 11, 2026

Isolation of Fidelity Variants of RNA Viruses and Characterization of Virus Mutation Frequency
Published on: June 16, 2011
Repeated genomic transfers from echovirus 30 to echovirus 6 lineages indicate co-divergence between co-circulating
J-L Bailly1, A Mirand, C Henquell
1Clermont Université, Université d'Auvergne, EA 3843, BP 10448, F-63000 Clermont-Ferrand, France. j-luc.bailly@u-clermont1.fr
Abstract:
Human echovirus types 6 (E-6) and 30 (E-30) cause seasonal epidemics of aseptic meningitis. These two enteroviruses are frequently observed in co-circulation, an epidemiological pattern that is prerequisite for the occurrence of dual infections, which can lead to recombination between co-infecting virus strains. Viral sequences were determined at loci 1D (VP1 capsid protein) and 3CD (non structural proteins) in 49 E-6 strains recovered in a single geographical region in France from 1999 to 2007, during the epidemiological survey of enterovirus infections. They were compared with previously recorded sequences of E-30 strains to investigate their evolutionary histories and possible recombination patterns. Phylogenetic analyses identified two distinct E-6 populations and different subpopulations. Assuming a relaxed molecular clock model and a Bayesian skyline demographic model in coalescent analyses with the BEAST program, the substitution rate in E-6 was estimated at 8.597×10(-3) and 6.252×10(-3) substitution/site/year for loci 1D and 3CD respectively. Consistent estimates of divergence times (t(MRCA)) were obtained for loci 1D and 3CD indicating that two distinct E-6 populations originated in 1997 and 1999. Incongruent phylogenetic patterns inferred for the two loci were indicative of recombination events between the two populations. Phylogenies including the E-30 3CD sequences showed close genetic relationships between E-6 and discrete E-30 subpopulations. Recombination breakpoints were located with statistical significance in E-6 and E-30 genomes. Estimates of t(MRCA) of phylogenetic recombinant clades indicated directional genetic transfers from E-30 to E-6 populations and their co-divergence over the time period studied.
Insights
Human echovirus types 6 and 30 (E-6 and E-30) cause aseptic meningitis. Genetic analysis revealed recombination between these viruses, with evidence of directional gene transfer from E-30 to E-6 populations.
Area of Science:
- Virology
- Molecular Evolution
- Epidemiology
Background:
- Human echovirus types 6 (E-6) and 30 (E-30) are significant causes of aseptic meningitis.
- Co-circulation of these enteroviruses creates opportunities for dual infections and genetic recombination.
Purpose of the Study:
- To investigate the evolutionary history and recombination patterns of E-6 strains.
- To compare E-6 evolution with co-circulating E-30 strains.
- To identify potential genetic exchange between E-6 and E-30.
Main Methods:
- Phylogenetic analysis of viral sequences at the 1D (VP1) and 3CD (non-structural proteins) loci.
- Coalescent analyses using a relaxed molecular clock and Bayesian skyline demographic model (BEAST program).
- Identification and statistical localization of recombination breakpoints.
Main Results:
- Phylogenetic analyses revealed two distinct E-6 populations originating in 1997 and 1999.
- Incongruent phylogenetic patterns between loci 1D and 3CD indicated recombination events within E-6.
- Close genetic relationships and statistically significant recombination breakpoints were found between E-6 and E-30 subpopulations.
- Estimates of divergence times suggested directional genetic transfers from E-30 to E-6.
Conclusions:
- Recombination is a significant evolutionary force shaping the genetic landscape of E-6 and E-30.
- Evidence supports directional gene flow from E-30 to E-6, contributing to their co-divergence.
- Understanding these viral interactions is crucial for tracking and controlling enterovirus epidemics.
Related Concept Videos
Viral Recombination
Convergent Evolution
Retroviruses
Horizontal Gene Transfer
Viral Mutations
Types of Genetic Transfer Between Organisms

