Biomedical Research Center (CINBIO), University of Vigo, 36310 Vigo, Spain.
Department of Biochemistry, Genetics and Immunology, University of Vigo, 36310 Vigo, Spain.
Genes (Basel). 2023 Feb 4;14(2):407. doi: 10.3390/genes14020407.
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) produced diverse molecular variants during its recent expansion in humans that caused different transmissibility and severity of the associated disease as well as resistance to monoclonal antibodies and polyclonal sera, among other treatments. In order to understand the causes and consequences of the observed SARS-CoV-2 molecular diversity, a variety of recent studies investigated the molecular evolution of this virus during its expansion in humans. In general, this virus evolves with a moderate rate of evolution, in the order of 10-10 substitutions per site and per year, which presents continuous fluctuations over time. Despite its origin being frequently associated with recombination events between related coronaviruses, little evidence of recombination was detected, and it was mostly located in the spike coding region. Molecular adaptation is heterogeneous among SARS-CoV-2 genes. Although most of the genes evolved under purifying selection, several genes showed genetic signatures of diversifying selection, including a number of positively selected sites that affect proteins relevant for the virus replication. Here, we review current knowledge about the molecular evolution of SARS-CoV-2 in humans, including the emergence and establishment of variants of concern. We also clarify relationships between the nomenclatures of SARS-CoV-2 lineages. We conclude that the molecular evolution of this virus should be monitored over time for predicting relevant phenotypic consequences and designing future efficient treatments.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)在近期人类传播过程中产生了多种分子变异体,导致相关疾病的传染性和严重程度不同,以及对单克隆抗体和多克隆血清等治疗方法的耐药性。为了了解观察到的 SARS-CoV-2 分子多样性的原因和后果,最近的多项研究调查了该病毒在人类传播过程中的分子进化。一般来说,这种病毒的进化速度适中,每个位点和每年约有 10-10 个替换,这在时间上呈现出持续的波动。尽管它的起源经常与相关冠状病毒之间的重组事件有关,但很少有证据表明存在重组,而且重组大多发生在刺突编码区。SARS-CoV-2 基因之间的分子适应是异质的。尽管大多数基因在净化选择下进化,但有几个基因显示出多样化选择的遗传特征,包括一些影响病毒复制的相关蛋白质的正选择位点。在这里,我们综述了 SARS-CoV-2 在人类中的分子进化的最新知识,包括关注变体的出现和建立。我们还澄清了 SARS-CoV-2 谱系命名法之间的关系。我们的结论是,应该随着时间的推移监测这种病毒的分子进化,以预测相关的表型后果并设计未来有效的治疗方法。