Boyle David B, Amos-Ritchie Rachel, Broz Ivano, Walker Peter J, Melville Lorna, Flanagan David, Davis Steven, Hunt Neville, Weir Richard
CSIRO Biosecurity, Australian Animal Health Laboratory, Geelong, Victoria, Australia
CSIRO Biosecurity, Australian Animal Health Laboratory, Geelong, Victoria, Australia.
J Virol. 2014 Dec;88(24):13981-9. doi: 10.1128/JVI.02055-14. Epub 2014 Sep 24.
Bluetongue virus serotype 1 (BTV 1) was first isolated in Australia from cattle blood collected in 1979 at Beatrice Hill Farm (BHF), Northern Territory (NT). From long-term surveillance programs (1977 to 2011), 2,487 isolations of 10 BTV serotypes were made. The most frequently isolated serotype was BTV 1 (41%, 1,019) followed by BTV 16 (17.5%, 436) and BTV 20 (14%, 348). In 3 years, no BTVs were isolated, and in 12 years, no BTV 1 was isolated. Seventeen BTV 1 isolates were sequenced and analyzed in comparison with 10 Australian prototype serotypes. BTV 1 showed an episodic pattern of evolutionary change characterized by four distinct periods. Each period consisted primarily of slow genetic drift which was punctuated from time to time by genetic shifts generated by segment reassortment and the introduction of new genome segments. Evidence was found for coevolution of BTV genome segments. Evolutionary dynamics and selection pressure estimates showed strong temporal and clock-like molecular evolutionary dynamics of six Australian BTV genome segments. Bayesian coalescent estimates of mean substitution rates clustered in the range of 3.5 × 10(-4) to 5.3 × 10(-4) substitutions per site per year. All BTV genome segments evolved under strong purifying (negative) selection, with only three sites identified as under pervasive diversifying (positive) selection. The obligate replication in alternate hosts (insect vector and vertebrate hosts) imposed strong evolutionary constraints. The dominant mechanism generating genetic diversity of BTV 1 at BHF was through the introduction of new viruses and reassortment of genome segments with existing viruses.
Bluetongue virus (BTV) is the causative agent of bluetongue disease in ruminants. It is a disease of concern globally and is transmitted by biting midges (Culicoides species). Analysis of the evolutionary and selection pressures on BTV 1 at a single surveillance site in northern Australia showed strong temporal and clock-like dynamics. Obligate replication in alternate hosts of insect and vertebrate imposed strong evolutionary constraints, with all BTV genome segments evolving under strong purifying (negative) selection. Generation of genetic diversity of BTV 1 in northern Australia is through genome segment reassortment and the introduction of new serotypes.
蓝舌病毒血清型1(BTV 1)于1979年首次在澳大利亚从北领地(NT)比阿特丽斯山农场(BHF)采集的牛血中分离出来。从长期监测项目(1977年至2011年)中,共分离出10种BTV血清型的2487株病毒。最常分离出的血清型是BTV 1(41%,1019株),其次是BTV 16(17.5%,436株)和BTV 20(14%,348株)。有3年未分离到BTV,有12年未分离到BTV 1。对17株BTV 1分离株进行了测序,并与10种澳大利亚原型血清型进行了比较分析。BTV 1呈现出一种阶段性的进化变化模式,其特征为四个不同时期。每个时期主要由缓慢的基因漂变组成,偶尔会因片段重配和新基因组片段的引入所产生的基因转移而中断。发现了BTV基因组片段共同进化的证据。进化动力学和选择压力估计显示,澳大利亚6种BTV基因组片段具有强烈的时间性和类似时钟的分子进化动力学。贝叶斯合并估计的平均替换率聚集在每年每个位点3.5×10⁻⁴至5.3×10⁻⁴个替换的范围内。所有BTV基因组片段都在强烈的纯化(负)选择下进化,只有三个位点被确定为处于普遍的多样化(正)选择之下。在交替宿主(昆虫媒介和脊椎动物宿主)中的专性复制施加了强大的进化限制。在BHF产生BTV 1遗传多样性的主要机制是通过引入新病毒以及与现有病毒的基因组片段重配。
蓝舌病毒(BTV)是反刍动物蓝舌病的病原体。它是一种全球关注的疾病,通过叮咬蠓(库蠓属物种)传播。对澳大利亚北部一个单一监测点的BTV 1的进化和选择压力分析显示出强烈的时间性和类似时钟的动力学。在昆虫和脊椎动物交替宿主中的专性复制施加了强大的进化限制,所有BTV基因组片段都在强烈的纯化(负)选择下进化。澳大利亚北部BTV 1遗传多样性的产生是通过基因组片段重配和新血清型的引入。