Division of Infectious Diseases and Vaccinology, School of Public Health, University of California, Berkeley, Berkeley, California, USA.
J Virol. 2012 Aug;86(16):8546-58. doi: 10.1128/JVI.00736-12. Epub 2012 May 30.
Analogous to observations in RNA viruses such as human immunodeficiency virus, genetic variation associated with intrahost dengue virus (DENV) populations has been postulated to influence viral fitness and disease pathogenesis. Previous attempts to investigate intrahost genetic variation in DENV characterized only a few viral genes or a limited number of full-length genomes. We developed a whole-genome amplification approach coupled with deep sequencing to capture intrahost diversity across the entire coding region of DENV-2. Using this approach, we sequenced DENV-2 genomes from the serum of 22 Nicaraguan individuals with secondary DENV infection and captured ∼75% of the DENV genome in each sample (range, 40 to 98%). We identified and quantified variants using a highly sensitive and specific method and determined that the extent of diversity was considerably lower than previous estimates. Significant differences in intrahost diversity were detected between genes and also between antigenically distinct domains of the Envelope gene. Interestingly, a strong association was discerned between the extent of intrahost diversity in a few genes and viral clade identity. Additionally, the abundance of viral variants within a host, as well as the impact of viral mutations on amino acid encoding and predicted protein function, determined whether intrahost variants were observed at the interhost level in circulating Nicaraguan DENV-2 populations, strongly suggestive of purifying selection across transmission events. Our data illustrate the value of high-coverage genome-wide analysis of intrahost diversity for high-resolution mapping of the relationship between intrahost diversity and clinical, epidemiological, and virological parameters of viral infection.
类似于人类免疫缺陷病毒(HIV)等 RNA 病毒的观察结果,与宿主内登革热病毒(DENV)种群相关的遗传变异被认为会影响病毒适应性和疾病发病机制。以前尝试研究 DENV 中的宿主内遗传变异仅表征了少数几个病毒基因或有限数量的全长基因组。我们开发了一种全基因组扩增方法,结合深度测序,以捕获 DENV-2 整个编码区域内的宿主内多样性。使用这种方法,我们对 22 名尼加拉瓜继发 DENV 感染个体的血清中的 DENV-2 基因组进行了测序,并在每个样本中捕获了约 75%的 DENV 基因组(范围为 40 到 98%)。我们使用一种高度敏感和特异的方法鉴定和量化了变体,并确定多样性的程度明显低于以前的估计。在基因之间以及包膜基因的抗原不同结构域之间都检测到了宿主内多样性的显著差异。有趣的是,在少数几个基因中,宿主内多样性的程度与病毒分支身份之间存在很强的关联。此外,宿主内病毒变异的丰度以及病毒突变对氨基酸编码和预测蛋白功能的影响,决定了宿主内变异是否在尼加拉瓜 DENV-2 循环流行群体中在宿主间水平上被观察到,这强烈提示了跨传播事件的纯化选择。我们的数据说明了对宿主内多样性进行高覆盖率全基因组分析的价值,用于高分辨率映射宿主内多样性与病毒感染的临床、流行病学和病毒学参数之间的关系。