Dorji Tshering, Dorji Kunzang, Wangchuk Tandin, Pelki Tshering, Gyeltshen Sonam
Royal Centre for Disease Control, Ministry of Health, Royal Government of Bhutan, Thimphu, Bhutan.
Osong Public Health Res Perspect. 2023 Dec;14(6):494-507. doi: 10.24171/j.phrp.2023.0209. Epub 2023 Dec 14.
The coronavirus disease 2019 (COVID-19) pandemic, caused by a dynamic virus, has had a profound global impact. Despite declining global COVID-19 cases and mortality rates, the emergence of new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants remains a major concern. This study provides a comprehensive analysis of the genomic sequences of SARS-CoV-2 within the Bhutanese population during the pandemic. The primary aim was to elucidate the molecular epidemiology and evolutionary patterns of SARS-CoV-2 in Bhutan, with a particular focus on genetic variations and lineage dynamics.
Whole-genome sequences of SARS-CoV-2 collected from Bhutan between May 2020 and February 2023 (n=135) were retrieved from the Global Initiative on Sharing All Influenza Database.
The SARS-CoV-2 variants in Bhutan were predominantly classified within the Nextstrain clade 20A (31.1%), followed by clade 21L (20%) and clade 22D (15.6%). We identified 26 Pangolin lineages with variations in their spatial and temporal distribution. Bayesian time-scaled phylogenetic analysis estimated the time to the most recent common ancestor as February 15, 2020, with a substitution rate of 0.97×10-3 substitutions per site per year. Notably, the spike glycoprotein displayed the highest mutation frequency among major viral proteins, with 116 distinct mutations, including D614G. The Bhutanese isolates also featured mutations such as E484K, K417N, and S477N in the spike protein, which have implications for altered viral properties.
This is the first study to describe the genetic diversity of SARS-CoV-2 circulating in Bhutan during the pandemic, and this data can inform public health policies and strategies for preventing future outbreaks in Bhutan.
由一种动态变化的病毒引起的2019冠状病毒病(COVID-19)大流行对全球产生了深远影响。尽管全球COVID-19病例数和死亡率有所下降,但新型严重急性呼吸综合征冠状病毒2(SARS-CoV-2)变体的出现仍然是一个主要问题。本研究对大流行期间不丹人群中SARS-CoV-2的基因组序列进行了全面分析。主要目的是阐明不丹SARS-CoV-2的分子流行病学和进化模式,特别关注基因变异和谱系动态。
从全球共享所有流感数据倡议组织检索了2020年5月至2023年2月期间从不丹收集的SARS-CoV-2全基因组序列(n = 135)。
不丹的SARS-CoV-2变体主要归类于Nextstrain进化枝20A(31.1%),其次是进化枝21L(20%)和进化枝22D(15.6%)。我们确定了26个穿山甲谱系,它们在空间和时间分布上存在差异。贝叶斯时间尺度系统发育分析估计,最近共同祖先的时间为2020年2月15日,每个位点每年的替换率为0.97×10-3替换。值得注意的是,刺突糖蛋白在主要病毒蛋白中显示出最高的突变频率,有116个不同的突变,包括D614G。不丹分离株的刺突蛋白中还存在E484K、K417N和S477N等突变,这些突变对病毒特性的改变有影响。
这是第一项描述大流行期间在不丹传播的SARS-CoV-2基因多样性的研究,这些数据可为不丹预防未来疫情的公共卫生政策和策略提供参考。