Genomics and Bioinformatics Unit, Department of Infectious Diseases, National Institute of Health Doutor Ricardo Jorge (INSA), Lisbon, Portugal.
Technology and Innovation Unit, Department of Human Genetics, National Institute of Health Doutor Ricardo Jorge (INSA), Lisbon, Portugal.
Nat Med. 2022 Aug;28(8):1569-1572. doi: 10.1038/s41591-022-01907-y. Epub 2022 Jun 24.
The largest monkeypox virus (MPXV) outbreak described so far in non-endemic countries was identified in May 2022 (refs. ). In this study, shotgun metagenomics allowed the rapid reconstruction and phylogenomic characterization of the first MPXV outbreak genome sequences, showing that this MPXV belongs to clade 3 and that the outbreak most likely has a single origin. Although 2022 MPXV (lineage B.1) clustered with 2018-2019 cases linked to an endemic country, it segregates in a divergent phylogenetic branch, likely reflecting continuous accelerated evolution. An in-depth mutational analysis suggests the action of host APOBEC3 in viral evolution as well as signs of potential MPXV human adaptation in ongoing microevolution. Our findings also indicate that genome sequencing may provide resolution to track the spread and transmission of this presumably slow-evolving double-stranded DNA virus.
迄今为止,在非流行国家中描述的最大规模猴痘病毒(MPXV)疫情于 2022 年 5 月被发现(参考文献)。在这项研究中,鸟枪法宏基因组学使得快速重建和全基因组特征分析首个 MPXV 爆发基因组序列成为可能,表明该 MPXV 属于 3 分支,此次疫情很可能只有一个单一来源。虽然 2022 年的 MPXV(B.1 谱系)与与流行国家相关的 2018-2019 年病例聚类,但它在一个分化的系统发育分支中分离出来,可能反映了持续的加速进化。深入的突变分析表明 APOBEC3 在病毒进化中的作用,以及潜在的 MPXV 人类适应在持续的微观进化中的迹象。我们的研究结果还表明,基因组测序可能提供解决办法,以追踪这种推测的缓慢进化的双链 DNA 病毒的传播和传播。