Jerzak Greta, Bernard Kristen A, Kramer Laura D, Ebel Gregory D
The Arbovirus Laboratories, Wadsworth Center, New York State Department of Health, 5668 State Farm Road, Slingerlands, NY 12159, USA.
Department of Biomedical Sciences, School of Public Health, The University at Albany, State University of New York, Albany, NY 12144-3456, USA.
J Gen Virol. 2005 Aug;86(Pt 8):2175-2183. doi: 10.1099/vir.0.81015-0.
Intrahost genetic diversity was analysed in naturally infected mosquitoes and birds to determine whether West Nile virus (WNV) exists in nature as a quasispecies and to quantify selective pressures within and between hosts. WNV was sampled from ten infected birds and ten infected mosquito pools collected on Long Island, NY, USA, during the peak of the 2003 WNV transmission season. A 1938 nt fragment comprising the 3' 1159 nt of the WNV envelope (E) coding region and the 5' 779 nt of the non-structural protein 1 (NS1) coding region was amplified and cloned and 20 clones per specimen were sequenced. Results from this analysis demonstrate that WNV infections are derived from a genetically diverse population of genomes in nature. The mean nucleotide diversity was 0.016 % within individual specimens and the mean percentage of clones that differed from the consensus sequence was 19.5 %. WNV sequences in mosquitoes were significantly more genetically diverse than WNV in birds. No host-dependent bias for particular types of mutations was observed and estimates of genetic diversity did not differ significantly between E and NS1 coding sequences. Non-consensus clones obtained from two avian specimens had highly similar genetic signatures, providing preliminary evidence that WNV genetic diversity may be maintained throughout the enzootic transmission cycle, rather than arising independently during each infection. Evidence of purifying selection was obtained from both intra- and interhost WNV populations. Combined, these data support the observation that WNV populations may be structured as a quasispecies and document strong purifying natural selection in WNV populations.
对自然感染的蚊子和鸟类进行宿主体内遗传多样性分析,以确定西尼罗河病毒(WNV)在自然界中是否以准种形式存在,并量化宿主内部和宿主之间的选择压力。WNV样本采自2003年WNV传播季节高峰期美国纽约长岛的10只感染鸟类和10个感染蚊子池。扩增并克隆了一个1938 nt的片段,该片段包含WNV包膜(E)编码区3'端的1159 nt和非结构蛋白1(NS1)编码区5'端的779 nt,并对每个样本的20个克隆进行测序。该分析结果表明,WNV感染源自自然界中基因多样的基因组群体。单个样本内的平均核苷酸多样性为0.016%,与共有序列不同的克隆的平均百分比为19.5%。蚊子中的WNV序列在遗传上比鸟类中的WNV序列更加多样。未观察到特定类型突变的宿主依赖性偏差,并且E和NS1编码序列之间的遗传多样性估计没有显著差异。从两个鸟类样本中获得的非共有克隆具有高度相似的遗传特征,这提供了初步证据,表明WNV遗传多样性可能在整个动物间传播周期中得以维持,而不是在每次感染期间独立产生。从宿主体内和宿主间的WNV群体中均获得了纯化选择的证据。综合来看,这些数据支持了WNV群体可能以准种形式构成的观察结果,并证明了WNV群体中存在强大的纯化自然选择。