Department of Ophthalmology, Howe Laboratory, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, MA 02114, USA.
Sci Rep. 2013;3:1812. doi: 10.1038/srep01812.
The recent emergence of highly virulent human adenoviruses (HAdVs) with new tissue tropisms underscores the need to determine their ontogeny. Here we report complete high quality genome sequences and analyses for all the previously unsequenced HAdV serotypes (n = 20) within HAdV species D. Analysis of nucleotide sequence variability for these in conjunction with another 40 HAdV prototypes, comprising all seven HAdV species, confirmed the uniquely hypervariable regions within species. The mutation rate among HAdV-Ds was low when compared to other HAdV species. Homologous recombination was identified in at least two of five examined hypervariable regions for every virus, suggesting the evolution of HAdV-Ds has been highly dependent on homologous recombination. Patterns of alternating GC and AT rich motifs correlated well with hypervariable region recombination sites across the HAdV-D genomes, suggesting foci of DNA instability lead to formulaic patterns of homologous recombination and confer agility to adenovirus evolution.
最近出现了具有新组织嗜性的高毒力人腺病毒(HAdV),这突显出确定其起源的必要性。在这里,我们报告了所有以前未测序的 HAdV 血清型(n=20)在 HAdV 种 D 内的完整高质量基因组序列和分析。对这些与另外 40 种 HAdV 原型(包括所有七种 HAdV 种)的核苷酸序列变异性进行分析,证实了种内独特的高变区。与其他 HAdV 种相比,HAdV-D 的突变率较低。在至少两个受检的高变区中,每种病毒都发现了同源重组,表明 HAdV-D 的进化高度依赖于同源重组。GC 和 AT 丰富基序的交替模式与 HAdV-D 基因组中的高变区重组位点很好地相关,表明 DNA 不稳定性的焦点导致同源重组的定式模式,并赋予腺病毒进化的灵活性。