Renner Daniel W, Szpara Moriah L
Department of Biochemistry and Molecular Biology, Center for Infectious Disease Dynamics, and the Huck Institutes of the Life Sciences, Pennsylvania State University, University Park, Pennsylvania, USA.
Department of Biochemistry and Molecular Biology, Center for Infectious Disease Dynamics, and the Huck Institutes of the Life Sciences, Pennsylvania State University, University Park, Pennsylvania, USA
J Virol. 2017 Dec 14;92(1). doi: 10.1128/JVI.00908-17. Print 2018 Jan 1.
Until fairly recently, genome-wide evolutionary dynamics and within-host diversity were more commonly examined in the context of small viruses than in the context of large double-stranded DNA viruses such as herpesviruses. The high mutation rates and more compact genomes of RNA viruses have inspired the investigation of population dynamics for these species, and recent data now suggest that herpesviruses might also be considered candidates for population modeling. High-throughput sequencing (HTS) and bioinformatics have expanded our understanding of herpesviruses through genome-wide comparisons of sequence diversity, recombination, allele frequency, and selective pressures. Here we discuss recent data on the mechanisms that generate herpesvirus genomic diversity and underlie the evolution of these virus families. We focus on human herpesviruses, with key insights drawn from veterinary herpesviruses and other large DNA virus families. We consider the impacts of cell culture on herpesvirus genomes and how to accurately describe the viral populations under study. The need for a strong foundation of high-quality genomes is also discussed, since it underlies all secondary genomic analyses such as RNA sequencing (RNA-Seq), chromatin immunoprecipitation, and ribosome profiling. Areas where we foresee future progress, such as the linking of viral genetic differences to phenotypic or clinical outcomes, are highlighted as well.
直到最近,全基因组进化动态和宿主内多样性在小病毒的背景下比在疱疹病毒等大型双链DNA病毒的背景下得到了更普遍的研究。RNA病毒的高突变率和更紧凑的基因组激发了对这些物种群体动态的研究,最近的数据表明,疱疹病毒也可能被视为群体建模的候选对象。高通量测序(HTS)和生物信息学通过对序列多样性、重组、等位基因频率和选择压力进行全基因组比较,扩展了我们对疱疹病毒的理解。在这里,我们讨论了有关产生疱疹病毒基因组多样性并构成这些病毒家族进化基础的机制的最新数据。我们重点关注人类疱疹病毒,并从兽医疱疹病毒和其他大型DNA病毒家族中汲取关键见解。我们考虑细胞培养对疱疹病毒基因组的影响以及如何准确描述所研究的病毒群体。还讨论了高质量基因组坚实基础的必要性,因为它是所有二级基因组分析(如RNA测序(RNA-Seq)、染色质免疫沉淀和核糖体谱分析)的基础。我们还强调了预计未来会取得进展的领域,例如将病毒遗传差异与表型或临床结果联系起来。