Division of General Internal Medicine, Tohoku University Hospital.
Department of Education and Support for Regional Medicine, Tohoku University Hospital.
Tohoku J Exp Med. 2022 Aug 4;258(1):23-27. doi: 10.1620/tjem.2022.J049. Epub 2022 Jun 16.
Virus genome mutation profiles with insertion, deletion, and point mutations have recently been revealed to differ remarkably between viruses. In RNA viruses like human coronaviruses or influenza viruses, genome samples collected over two to three decades usually show point mutations in 10-20% of the bases, while the rate of insertion and/or deletion mutations (indels) largely depends on the virus. This study evaluates the mutation profiles of DNA viruses by comparing a recently sampled genome of human adenovirus species C type 2 (isolate SG06/HAdvC2/2016) with a genome of the same species sampled in the 1970s. It was found insertions of 23 bases at seven sites and deletions of 22 bases at nine sites. The longest indels were 6-base insertions in E2B and L4. All indels in the coding regions were in-frame mutations with base lengths in multiples of three. In the non-coding regions, the lengths of the indels ranged from 1-4 consecutive bases. Long indels with more than 10 consecutive bases, which comprise nearly half of indels in the SARS-CoV-2 genome, were absent. In other sites, the point mutation rate was approximately 0.3%, which was significantly lower than in RNA viruses. In summary, the estimated point mutation rate in human adenovirus species C type 2 (HAdvC-2) was over 10 times lower than in RNA viruses. Unlike the relatively long indels in the SARS-CoV-2 genome, the indels in HAdvC-2 were short, with 6 or fewer consecutive bases.
病毒基因组中的突变谱,包括插入、缺失和点突变,最近被发现与不同病毒之间存在显著差异。在像人类冠状病毒或流感病毒这样的 RNA 病毒中,在过去 20 到 30 年收集的基因组样本中,通常有 10-20%的碱基发生点突变,而插入和/或缺失突变(indels)的发生率在很大程度上取决于病毒。本研究通过比较最近采样的人类腺病毒 C 型 2 种(分离株 SG06/HAdvC2/2016)的基因组与 20 世纪 70 年代采样的同一物种的基因组,评估了 DNA 病毒的突变谱。结果发现,在 7 个位点有 23 个碱基的插入,在 9 个位点有 22 个碱基的缺失。最长的插入是 E2B 和 L4 中的 6 个碱基插入。所有编码区的 indels 都是框内突变,碱基长度为 3 的倍数。在非编码区,indels 的长度从 1-4 个连续碱基不等。长插入缺失超过 10 个连续碱基,占 SARS-CoV-2 基因组中几乎一半的插入缺失,不存在。在其他位点,点突变率约为 0.3%,明显低于 RNA 病毒。综上所述,人类腺病毒 C 型 2 (HAdvC-2)的估计点突变率比 RNA 病毒低 10 倍以上。与 SARS-CoV-2 基因组中相对较长的 indels 不同,HAdvC-2 的 indels 较短,只有 6 个或更少的连续碱基。