Аннотация
Prompt determination of the etiological agent is important in an outbreak of pathogens with pandemic potential particularly dangerous infectious diseases. Molecular genetic methods allow for arriving at an accurate diagnosis, employing timely preventive measures and controlling the spread of the disease causing agent. In this study, whole-genome sequencing of three SARS-CoV-2 strains was performed using the Sanger method, which provides high accuracy in determining nucleotide sequences and avoids errors associated with multiple DNA amplification. Complete nucleotide sequences of samples KAZ/Britain/2021, KAZ/B1.1/2021 and KAZ/Delta020/2021 were obtained with sizes of 29.751 bp, 29.815 bp and 29.840 bp, respectively. According to the COVID-19 Genome Annotator, 127 mutations were detected in the studied samples compared to the reference strain. The strain KAZ/Britain/2021 contained 3 deletions, 7 synonymous mutations and 27 non-synonymous mutations, the second strain KAZ/B1.1/2021 contained 1 deletion, 5 synonymous mutations and 31 non-synonymous mutations and the third strain KAZ/Delta020/2021 contained 1 deletion, 5 synonymous mutations and 37 non-synonymous mutations, respectively. Variations C241T, F106F, P314L and D614G found in the 5' UTR, ORF1ab and S region were common to all three studied samples, respectively. According to PROVEAN data, the loss-of-function mutations identified in strains KAZ/Britain/2021, KAZ/B1.1/2021 and KAZ/Delta020/2021 include 5 mutations (P218L, T716I, W149L, R52I and Y73C), 2 mutations (S813I and Q992H) and 8 mutations (P77L, L452R, I82T, P45L, V82A, F120L, F120L and R203M), respectively. Phylogenetic analysis showed that the strains studied (KAZ/Britain/2021, KAZ/B1.1/2021 and KAZ/Delta020/2021) belong to different SARS-CoV-2 lineages, which are closely related to samples from Germany (OU141323.1 and OU365922.1), Mexico (OK432605.1) and again, Germany (OV375251.1 and OU375174.1), respectively. The nucleotide sequences of the studied SARS-CoV-2 virus strains were registered in the Genbank database with the accession numbers: ON692539.1, OP684305, and OQ561548.1.