4.4 Article

Spatiotemporal phylogenetic analysis and molecular characterization of coxsackievirus A4

Journal

INFECTION GENETICS AND EVOLUTION
Volume 11, Issue 6, Pages 1426-1435

Publisher

ELSEVIER
DOI: 10.1016/j.meegid.2011.05.010

Keywords

Coxsackievirus A4 (CV-A4); Human enterovirus A (HEV-A); Spatiotemporal phylogenetic analysis; Molecular epidemiology; Taiwan

Funding

  1. National Research Program for Genome Medicine [99-0324-01-F-12]
  2. Kaohsiung Medical University [KMU-M098034]

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Coxsackievirus A4 outbreaks occurred in Taiwan in 2004 and 2006. The spatiotemporal transmission of this error-prone RNA virus involves a continuous interaction between rapid sequence variation and natural selection. To elucidate the molecular characteristics of CV-A4 and the spatiotemporal dynamic changes in CV-A4 transmission, worldwide sequences of the 3' VP1 region (420 nt) obtained from GenBank were analyzed together with sequences isolated in Taiwan from 2002 to 2009. Sequences were characterized in terms of recombination, variability, and selection. Phylogenetic trees were constructed using neighbor-joining, maximum likelihood and Monte Carlo Markov Chain methods. Spatiotemporal dynamics of CV-A4 transmission were further estimated by a Bayesian statistical inference framework. No recombination was detected in the 420 nt region. The estimated evolution rate of CV-A4 was 8.65 x 10(-3) substitutions/site/year, and a purifying selection (d(N)/d(S) = 0.032) was noted over the 3' VP1 region. All trees had similar topology: two genotypes (Cl and GII), each including two subgenotypes (A and B), with the prototype and a Kenyan strain in separate branches. The results revealed that the virus first appeared in USA in 1950. Since 1998, it has evolved into the Kenya, GI-A (Asia) and GII-A (Asia and Europe) strains. Since 2004, GI-B and GII-B have evolved continuously and have remained prevalent. The co-existence of several positive selection lineages of GI-B in 2006 indicates that the subgenotype might have survived lineage extinction. This study revealed rapid lineage turnover of CV-A4 and the replacement of previously circulating strains by a new dominant variant. Therefore, continuous surveillance for further CV-A4 transmission is essential. (C) 2011 Elsevier B.V. All rights reserved.

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