Sultana Abeda, Banu Laila Anjuman, Hossain Mahmud, Azmin Nahid, Nila Nurun Nahar, Sinha Sharadindu Kanti, Hassan Zahid
Department of Anatomy, Dhaka Medical College, Dhaka 1000, Bangladesh.
Genetics and Molecular Biology Laboratory, Bangabandhu Sheikh Mujib Medical University, Dhaka 1000, Bangladesh.
Viruses. 2025 Jan 27;17(2):182. doi: 10.3390/v17020182.
The SARS-CoV-2-induced disease, COVID-19, remains a worldwide public health concern due to its high rate of transmission, even in vaccinated and previously infected people. In the endemic state, it continues to cause significant pathology. To elu- cidate the viral mutational changes and screen the emergence of new variants of concern, we conducted this study in Bangladesh. The viral RNA genomes extracted from 25 ran- domly collected samples of COVID-19-positive patients from March 2021 to February 2022 were sequenced using Illumina COVID Seq protocol and genomic data processing, as well as evaluations performed in DRAGEN COVID Lineage software. In this study, the percentage of Delta, Omicron, and Mauritius variants identified were 88%, 8%, and 4%, respectively. All of the 25 samples had 23,403 A>G (D614G, S gene), 3037 C>T (nsp3), and 14,408 C>T (nsp12) mutations, where 23,403 A>G was responsible for increased transmis- sion. Omicron had the highest number of unique mutations in the spike protein (i.e., sub- stitutions, deletions, and insertions), which may explain its higher transmissibility and immune-evading ability than Delta. A total of 779 mutations were identified, where 691 substitutions, 85 deletions, and 3 insertion mutations were observed. To sum up, our study will enrich the genomic database of SARS-CoV-2, aiding in treatment strategies along with understanding the virus's preferences in both mutation type and mutation site for predicting newly emerged viruses' survival strategies and thus for preparing to coun- teract them.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引发的疾病——冠状病毒病(COVID-19),因其高传播率,即便在接种过疫苗以及既往感染过的人群中也会传播,仍是全球公共卫生关注的焦点。在地方流行状态下,它仍会引发严重病变。为阐明病毒的突变变化并筛查新出现的值得关注的变异株,我们在孟加拉国开展了这项研究。使用Illumina COVID Seq方案对2021年3月至2022年2月期间随机收集的25份COVID-19阳性患者样本中提取的病毒RNA基因组进行测序,并进行基因组数据处理以及在DRAGEN COVID谱系软件中进行评估。在本研究中,所鉴定出的德尔塔、奥密克戎和毛里求斯变异株的比例分别为88%、8%和4%。所有25个样本均有23403 A>G(D614G,S基因)、3037 C>T(非结构蛋白3)和14408 C>T(非结构蛋白12)突变,其中23403 A>G导致传播性增强。奥密克戎在刺突蛋白中具有最多的独特突变(即替换、缺失和插入),这可能解释了其相较于德尔塔具有更高的传播性和免疫逃逸能力。总共鉴定出779个突变,其中观察到691个替换、85个缺失和3个插入突变。总之,我们的研究将丰富SARS-CoV-2的基因组数据库,有助于制定治疗策略,同时有助于了解病毒在突变类型和突变位点上的偏好,从而预测新出现病毒的生存策略并进而做好应对准备。