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. 2013 Oct 25;529(2):288-95.
doi: 10.1016/j.gene.2013.07.028. Epub 2013 Aug 6.

Identification, genotyping, and molecular evolution analysis of duck circovirus

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Identification, genotyping, and molecular evolution analysis of duck circovirus

Zhilong Zhang et al. Gene. .

Abstract

Duck circovirus (DuCV) is a contagious immunosuppressive virus affecting many duck species, which is responsible for multiple outbreaks in poultry industries worldwide. In this study, the first DuCV isolate GH01 was identified in Sichuan by PCR, which shared a high level of nucleotide identity (81.8-99.4%) with sequences of other DuCV isolates available in GenBank. Comparative phylogenetic and pairwise sequence comparison analyses indicated that DuCV could be divided into two genotypes (DuCV-1 and DuCV-2) and six subtypes (1a, 1b, 1c, 2a, 2b and 2c) based on the complete genome sequence. The results revealed that both DuCV-1 and DuCV-2 had evolved from the same ancestor but undergone divergent evolution. Interestingly, phylogenetic analyses indicated that three isolates were classified into a cluster DuCV-2a using complete DuCV genome sequence and cap gene, except rep gene. Recombination analyses revealed that DuCV-2a arose from recombination between DuCV-1a and DuCV-2b isolates within the rep genes, and the recombination events mainly occur both in non-structural protein coding region and structural protein coding region. In addition, the mechanisms of recombination supporting the genetic variability in DuCV isolates were investigated. Likewise, selective pressure indicated that purifying selection had been a major driving force in maintaining diversity among the DuCV isolates. Because eradicating the virus from commercial ducks is impossible, it is necessary to take effective control measures and implement them throughout the world.

Keywords: DuCV; Duck circovirus; Evolution; Genotype; ML; MP; NJ; PASC; PCR; PRE; Phylogenetic; Recombination; Selective pressure; dN; dS; duck circovirus; maximum parsimony; maximum-likelihood; neighbor-joining; non-synonymous substitutions; nt; nucleotide; pairwise sequence comparison; polymerase chain reaction; potential recombination event; synonymous substitutions.

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