Chernyaeva Ekaterina N, Ayginin Andrey A, Bulusheva Irina A, Vinogradov Kirill S, Stetsenko Ivan F, Romanova Svetlana V, Tsypkina Anastasia V, Matsvay Alina D, Savochkina Yulia A, Shipulin German A
Federal State Budgetary Institution, Centre for Strategic Planning and Management of Biomedical Health Risks, Federal Medical Biological Agency, 119121 Moscow, Russia.
Pathogens. 2022 Dec 2;11(12):1461. doi: 10.3390/pathogens11121461.
Analysis of genomic variability of pathogens associated with heightened public health concerns is an opportunity to track transmission routes of the disease and helps to develop more effective vaccines and specific diagnostic tests. We present the findings of a detailed genomic analysis of the genomic variability of the SARS-CoV-2 Omicron variant that spread in Russia between 8 December 2021 and 30 January 2022. We performed phylogenetic analysis of Omicron viral isolates collected in Moscow ( = 589) and downloaded from GISAID ( = 397), and identified that the BA.1 lineage was predominant in Russia during this period. The BA.2 lineage was also identified early in December 2021. We identified three cases of BA.1/BA.2 coinfections and one case of Delta/Omicron coinfection. A comparative genomic analysis of SARS-CoV-2 viral variants that spread in other countries allowed us to identify possible cases of transmission. We also found that some mutations that are quite rare in the Global Omicron dataset have a higher incidence rate, and identified genetic markers that could be associated with ways of Omicron transmission in Russia. We give the genomic variability of single nucleotide variations across the genome and give a characteristic of haplotype variability of Omicron strains in both Russia and around the world, and we also identify them.
分析与公共卫生高度相关的病原体的基因组变异性,有助于追踪疾病的传播途径,并有助于开发更有效的疫苗和特定的诊断测试。我们展示了对2021年12月8日至2022年1月30日在俄罗斯传播的新冠病毒奥密克戎变种的基因组变异性进行详细基因组分析的结果。我们对在莫斯科收集的(n = 589)和从全球共享流感数据倡议组织(GISAID)下载的(n = 397)奥密克戎病毒分离株进行了系统发育分析,确定在此期间BA.1谱系在俄罗斯占主导地位。BA.2谱系也于2021年12月初被发现。我们发现了3例BA.1/BA.2合并感染病例和1例德尔塔/奥密克戎合并感染病例。对在其他国家传播的新冠病毒变种进行的比较基因组分析,使我们能够确定可能的传播病例。我们还发现,一些在全球奥密克戎数据集中相当罕见的突变具有较高的发生率,并确定了可能与奥密克戎在俄罗斯的传播方式相关的遗传标记。我们给出了全基因组单核苷酸变异的基因组变异性,并给出了俄罗斯和世界各地奥密克戎毒株单倍型变异的特征,同时我们也对它们进行了识别。