Institutes of Biomedical Engineering, National Yang Ming University, Taipei, Taiwan, ROC.
Intervirology. 2012;55(3):225-30. doi: 10.1159/000327786. Epub 2011 Aug 3.
In view of the rising prevalence of dengue virus and mixing of host and vector populations, complete full-length sequence determination of dengue strains isolated from different epidemic areas is important for the study of virus evolution, pathogenicity, vaccine efficiency and diagnosis. Based on the genomic analysis of 51 complete dengue virus sequences, all of which cocirculated in Thailand between 1974 and 2001, we report here the occurrence of homologous recombination in the NS5 nonstructural gene region of dengue virus type 2 (DENV-2) strains. In order to analyze those 51 virus sequences at one time, we chose to use a highly sensitive recombination detection program called RDP. When RDP detects a possible recombination event, further bootscanning and phylogenetic tree analyses are applied to these candidate sequences to identify this recombination event. We found that within the DENV-2 subfamily, the strain ThNH63/93 is the evolutionary product of a recombination event between ThNH62/93 and ThD2_0284_90 strains. The strain ThNH62/93 was identified as the major parent, while the strain ThD2_0284_90 was the minor parent. The recombination site was determined to localize between positions 7967 (± 36 nt) and 8283 (± 36 nt) with a significance level of p < 0.001. Our results showed, for the first time, that an intraserotype recombination event occurred between DENV-2 strains in the nonstructural gene region; by contrast, an interserotype recombination between different serotypes of dengue strains was not identified. This study thus supports the theory that homologous recombination plays a key role in dengue virus evolution.
鉴于登革热病毒的流行率不断上升,以及宿主和媒介种群的混合,对来自不同疫区的登革热病毒株进行完整的全长序列测定,对于研究病毒进化、致病性、疫苗效率和诊断都非常重要。本研究基于对 1974 年至 2001 年间在泰国同时流行的 51 株登革病毒全基因组序列的分析,报告了登革病毒 2 型(DENV-2)株在 NS5 非结构基因区发生同源重组的情况。为了同时分析这 51 个病毒序列,我们选择使用一种高灵敏度的重组检测程序 RDP。当 RDP 检测到可能的重组事件时,进一步对候选序列进行 bootscanning 和系统进化树分析,以确定该重组事件。结果发现,在 DENV-2 亚组内,ThNH63/93 株是 ThNH62/93 株和 ThD2_0284_90 株之间重组事件的进化产物。ThNH62/93 株被鉴定为主要亲本,而 ThD2_0284_90 株为次要亲本。重组发生的位置确定在 7967(±36nt)和 8283(±36nt)之间,其显著性水平 p < 0.001。我们的结果首次表明,在非结构基因区 DENV-2 株之间发生了一种同型重组事件;相比之下,不同血清型登革热病毒株之间没有发生异型重组。本研究支持了同源重组在登革病毒进化中起关键作用的理论。