Silva Thaís de Souza, Salvato Richard Steiner, Gregianini Tatiana Schäffer, Gomes Ighor Arantes, Pereira Elisa Cavalcante, de Oliveira Eneida, de Menezes André Luiz, Barcellos Regina Bones, Godinho Fernanda Marques, Riediger Irina, Debur Maria do Carmo, de Oliveira Cristina Mendes, Ribeiro-Rodrigues Rodrigo, Miyajima Fabio, Dias Fernando Stehling, Abbud Adriano, do Monte-Neto Rubens, Calzavara-Silva Carlos Eduardo, Siqueira Marilda Mendonça, Wallau Gabriel Luz, Resende Paola Cristina, Fernandes Gabriel da Rocha, Alves Pedro
Instituto René Rachou, Fundação Oswaldo Cruz, Belo Horizonte, Brazil.
Laboratório Central de Saúde Pública do Estado do Rio Grande do Sul, Porto Alegre, Brazil.
Front Med (Lausanne). 2022 Sep 28;9:1008600. doi: 10.3389/fmed.2022.1008600. eCollection 2022.
Recombination events have been described in the Coronaviridae family. Since the beginning of the SARS-CoV-2 pandemic, a variable degree of selection pressure has acted upon the virus, generating new strains with increased fitness in terms of viral transmission and antibody scape. Most of the SC2 variants of concern (VOC) detected so far carry a combination of key amino acid changes and indels. Recombination may also reshuffle existing genetic profiles of distinct strains, potentially giving origin to recombinant strains with altered phenotypes. However, co-infection and recombination events are challenging to detect and require in-depth curation of assembled genomes and sequencing reds. Here, we present the molecular characterization of a new SARS-CoV-2 recombinant between BA.1.1 and BA.2.23 Omicron lineages identified in Brazil. We characterized four mutations that had not been previously described in any of the recombinants already identified worldwide and described the likely breaking points. Moreover, through phylogenetic analysis, we showed that the newly named XAG lineage groups in a highly supported monophyletic clade confirmed its common evolutionary history from parental Omicron lineages and other recombinants already described. These observations were only possible thanks to the joint effort of bioinformatics tools auxiliary in genomic surveillance and the manual curation of experienced personnel, demonstrating the importance of genetic, and bioinformatic knowledge in genomics.
冠状病毒科中已描述了重组事件。自新冠病毒大流行开始以来,病毒受到了不同程度的选择压力,产生了在病毒传播和抗体逃逸方面适应性增强的新毒株。迄今为止检测到的大多数新冠病毒变异株(VOC)都携带关键氨基酸变化和插入缺失的组合。重组也可能会重新排列不同毒株现有的基因图谱,有可能产生表型改变的重组毒株。然而,共感染和重组事件难以检测,需要对组装好的基因组和测序结果进行深入整理。在此,我们展示了在巴西鉴定出的一种新型新冠病毒重组体的分子特征,该重组体存在于BA.1.1和BA.2.23奥密克戎谱系之间。我们鉴定了四个此前在全球已鉴定出的任何重组体中均未描述过的突变,并描述了可能的断点。此外,通过系统发育分析,我们表明新命名的XAG谱系聚集在一个得到高度支持的单系分支中,证实了其与亲本奥密克戎谱系及其他已描述的重组体有着共同的进化历史。这些发现得益于基因组监测中生物信息学工具的辅助以及经验丰富人员的人工整理,证明了遗传学和生物信息学知识在基因组学中的重要性。