Departments of Biology and of Biochemistry and Molecular Biology; Center for Infectious Disease Dynamics; and Huck Institutes of the Life Sciences, Pennsylvania State University, University Park, Pennsylvania, USA; email:
Annu Rev Virol. 2024 Sep;11(1):67-87. doi: 10.1146/annurev-virology-100422-010336. Epub 2024 Aug 30.
The arrival of novel sequencing technologies throughout the past two decades has led to a paradigm shift in our understanding of herpesvirus genomic diversity. Previously, herpesviruses were seen as a family of DNA viruses with low genomic diversity. However, a growing body of evidence now suggests that herpesviruses exist as dynamic populations that possess standing variation and evolve at much faster rates than previously assumed. In this review, we explore how strategies such as deep sequencing, long-read sequencing, and haplotype reconstruction are allowing scientists to dissect the genomic composition of herpesvirus populations. We also discuss the challenges that need to be addressed before a detailed picture of herpesvirus diversity can emerge.
过去二十年来,新型测序技术的出现使我们对疱疹病毒基因组多样性的认识发生了重大转变。以前,疱疹病毒被认为是一组具有低基因组多样性的 DNA 病毒。然而,越来越多的证据表明,疱疹病毒实际上是一个具有遗传多样性的动态群体,其具有固定的变异,并以比以前认为的更快的速度进化。在这篇综述中,我们探讨了深度测序、长读测序和单倍型重建等策略如何使科学家能够剖析疱疹病毒群体的基因组组成。我们还讨论了在全面了解疱疹病毒多样性之前需要解决的挑战。