Sección Genética Evolutiva, Departamento de Biología Animal, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
Sección Virología. Instituto de Biología e Instituto de Química Biológica. Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
Transbound Emerg Dis. 2021 Nov;68(6):3075-3082. doi: 10.1111/tbed.14002. Epub 2021 Mar 5.
The analysis of genetic diversity in SARS-CoV-2 is the focus of several studies, providing insights into how the virus emerged and evolves. Most common changes in SARS-CoV-2 are single or point nucleotide substitutions; meanwhile, insertions and deletions (indels) have been identified as a less frequent source of viral genetic variability. Here, we report the emergence of a 12-nucleotide deletion in ORF7a, resulting in a 4-amino acid in-frame deletion. The Δ12 variant was identified in viruses from patients of a single outbreak and represents the first report of this deletion in South American isolates. Phylogenetic analysis revealed that Δ12 strains belong to the lineage B.1.1 and clustered separated from the remaining Uruguayan strains. The ∆12 variant was detected in 14 patients of this outbreak by NGS sequencing and/or two rapid and economic methodologies: Sanger amplicon sequencing and capillary electrophoresis. The presence of strong molecular markers as the deletion described here are useful for tracking outbreaks and reveal a significant aspect of the SARS-CoV-2 evolution on the robustness of the virus to keep its functionality regardless loss of genetic material.
对 SARS-CoV-2 的遗传多样性进行分析是多项研究的重点,为了解病毒的出现和进化提供了线索。SARS-CoV-2 中最常见的变化是单个或点核苷酸替换;同时,插入和缺失(indels)已被确定为病毒遗传变异的较少发生来源。在这里,我们报告了 ORF7a 中 12 个核苷酸的缺失,导致 4 个氨基酸的框内缺失。在单一暴发患者的病毒中发现了 Δ12 变体,这是在南美分离株中首次报告这种缺失。系统进化分析表明,Δ12 株属于 B.1.1 谱系,并与其余乌拉圭株分离聚类。通过 NGS 测序和/或两种快速且经济的方法:Sanger 扩增子测序和毛细管电泳,在该暴发的 14 名患者中检测到了 Δ12 变体。如本文所述,存在强分子标记,如缺失,可用于跟踪暴发,并揭示了 SARS-CoV-2 进化的一个重要方面,即病毒保持其功能的稳健性,而不受遗传物质损失的影响。