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基于基因组的重组严重急性呼吸综合征冠状病毒2(SARS-CoV-2)XBB与其亲本谱系之间的比较。

Genome-based comparison between the recombinant SARS-CoV-2 XBB and its parental lineages.

作者信息

Scarpa Fabio, Sanna Daria, Azzena Ilenia, Casu Marco, Cossu Piero, Fiori Pier Luigi, Benvenuto Domenico, Imperia Elena, Giovanetti Marta, Ceccarelli Giancarlo, Cauda Roberto, Cassone Antonio, Pascarella Stefano, Ciccozzi Massimo

机构信息

Department of Biomedical Sciences, University of Sassari, Sassari, Italy.

Department of Veterinary Medicine, University of Sassari, Sassari, Italy.

出版信息

J Med Virol. 2023 Mar;95(3):e28625. doi: 10.1002/jmv.28625.

DOI:10.1002/jmv.28625
PMID:36852665
Abstract

Recombination is the main contributor to RNA virus evolution, and SARS-CoV-2 during the pandemic produced several recombinants. The most recent SARS-CoV-2 recombinant is the lineage labeled XBB, also known as Gryphon, which arose from BJ.1 and BM.1.1.1. Here we performed a genome-based survey aimed to compare the new recombinant with its parental lineages that never became dominant. Genetic analyses indicated that the recombinant XBB and its first descendant XBB.1 show an evolutionary condition typical of an evolutionary blind background with no further epidemiologically relevant descendant. Genetic variability and expansion capabilities are slightly higher than parental lineages. Bayesian Skyline Plot indicates that XBB reached its plateau around October 6, 2022 and after an initial rapid growth the viral population size did not further expand, and around November 10, 2022 its levels of genetic variability decreased. Simultaneously with the reduction of the XBB population size, an increase of the genetic variability of its first sub-lineage XBB.1 occurred, that in turn reached the plateau around November 9, 2022 showing a kind of vicariance with its direct progenitors. Structure analysis indicates that the affinity for ACE2 surface in XBB/XBB.1 RBDs is weaker than for BA.2 RBD. In conclusion, at present XBB and XBB.1 do not show evidence about a particular danger or high expansion capability. Genome-based monitoring must continue uninterrupted to individuate if further mutations can make XBB more dangerous or generate new subvariants with different expansion capability.

摘要

重组是RNA病毒进化的主要因素,在疫情期间,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)产生了几种重组毒株。最新的SARS-CoV-2重组毒株是标记为XBB的谱系,也称为狮鹫毒株,它由BJ.1和BM.1.1.1进化而来。在此,我们进行了一项基于基因组的调查,旨在将这种新的重组毒株与其从未占据主导地位的亲本谱系进行比较。遗传分析表明,重组毒株XBB及其首个后代XBB.1呈现出一种典型的进化盲背景下的进化状态,没有进一步出现具有流行病学相关性的后代。其遗传变异性和传播能力略高于亲本谱系。贝叶斯天际线图表明,XBB在2022年10月6日左右达到平台期,在最初的快速增长之后,病毒种群规模没有进一步扩大,并且在2022年11月10日左右其遗传变异性水平下降。在XBB种群规模减少的同时,其首个亚谱系XBB.1的遗传变异性增加,该亚谱系继而在2022年11月9日左右达到平台期,与其直接祖先呈现出一种替代分布。结构分析表明,XBB/XBB.1的受体结合结构域(RBD)对血管紧张素转换酶2(ACE2)表面的亲和力低于BA.2的RBD。总之,目前XBB和XBB.1没有显示出特别危险或高传播能力的迹象。必须持续不间断地进行基于基因组的监测,以确定是否有进一步的突变会使XBB更危险或产生具有不同传播能力的新亚变体。

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