Department of Biomedical Sciences, University of Sassari, 07100 Sassari, Italy.
Department of Veterinary Medicine, University of Sassari, 07100 Sassari, Italy.
Int J Mol Sci. 2023 Sep 1;24(17):13573. doi: 10.3390/ijms241713573.
The XBB.1.16 SARS-CoV-2 variant, also known as , is a recent descendant lineage of the recombinant XBB (nicknamed ). Compared to its direct progenitor, XBB.1, XBB.1.16 carries additional spike mutations in key antigenic sites, potentially conferring an ability to evade the immune response compared to other circulating lineages. In this context, we conducted a comprehensive genome-based survey to gain a detailed understanding of the evolution and potential dangers of the XBB.1.16 variant, which became dominant in late June. Genetic data indicates that the XBB.1.16 variant exhibits an evolutionary background with limited diversification, unlike dangerous lineages known for rapid changes. The evolutionary rate of XBB.1.16, which amounts to 3.95 × 10 subs/site/year, is slightly slower than that of its direct progenitors, XBB and XBB.1.5, which have been circulating for several months. A Bayesian Skyline Plot reconstruction suggests that the peak of genetic variability was reached in early May 2023, and currently, it is in a plateau phase with a viral population size similar to the levels observed in early March. Structural analyses indicate that, overall, the XBB.1.16 variant does not possess structural characteristics markedly different from those of the parent lineages, and the theoretical affinity for ACE2 does not seem to change among the compared variants. In conclusion, the genetic and structural analyses of SARS-CoV-2 XBB.1.16 do not provide evidence of its exceptional danger or high expansion capability. Detected differences with previous lineages are probably due to genetic drift, which allows the virus constant adaptability to the host, but they are not necessarily connected to a greater danger. Nevertheless, continuous genome-based monitoring is essential for a better understanding of its descendants and other lineages.
新冠病毒 XBB.1.16 变异株,又称,是重组 XBB(绰号)的近期衍生谱系。与直接祖先 XBB.1 相比,XBB.1.16 在关键抗原位点携带额外的刺突突变,与其他循环谱系相比,可能具有逃避免疫反应的能力。在这种情况下,我们进行了全面的基于基因组的调查,以详细了解 XBB.1.16 变异株的进化和潜在危险,该变异株在 6 月底成为主要流行株。遗传数据表明,XBB.1.16 变异株表现出进化背景有限多样化的特征,与以快速变化为特征的危险谱系不同。XBB.1.16 的进化率为 3.95×10-3 取代/位点/年,略低于其直接祖先 XBB 和 XBB.1.5 的进化率,这两种变异株已经流行了几个月。贝叶斯天空线图重建表明,遗传变异性的峰值出现在 2023 年 5 月初,目前正处于平台期,病毒种群规模与 3 月初观察到的水平相似。结构分析表明,总体而言,XBB.1.16 变异株没有明显不同于母系的结构特征,与比较的变异株相比,对 ACE2 的理论亲和力似乎没有变化。总之,对 SARS-CoV-2 XBB.1.16 的遗传和结构分析并没有提供其异常危险或高扩张能力的证据。与以前的谱系相比,检测到的差异可能是由于遗传漂移,这使病毒能够不断适应宿主,但它们不一定与更大的危险有关。然而,连续的基于基因组的监测对于更好地了解其后代和其他谱系是必要的。