Characteristics of full-genome sequence of four imported Omicron variants of SARS-CoV-2 in Changsha City
HUANG Zheng1, XU Ming-zhong1, OU Xin-hua1, XIANG Xing-yu2, ZHAN Zhi-fei2, YAO Dong1
1. Changsha Municipal Center for Disease Control and Prevention, Changsha, Hunan 410004, China; 2. Hunan Provincial Center for Disease Control and Prevention, Changsha, Hunan 410000, China
Abstract:Objective To analyze the characteristics and genetic variation based on full-genome of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) from imported cases in Changsha City. Methods The high-throughput sequencing technology was used to perform whole genome sequencing of SARS-CoV-2 isolated in December 2021. Nucleotide sequences were compared, and phylogenetic analysis was conducted. Results Genome sequences of four SARS-CoV-2 strains were obtained in this research. The full length of genome sequences was 29,685 bp. Based on nucleotide sequences, homology comparison showed that four SARS-CoV-2 strains shared 99.6% and 99.9% similarity with Wuhan-Hu-1 reference strain (EPI_ISL_402125) and Omicron strain (EPI_ISL_8890653), respectively. Phylogenetic analysis revealed that the strains belonged to BA.1.1 branch which SARS-CoV-2 Omicron variants presented. The amino acid sequences revealed that four SARS-CoV-2 strains contained the mutation sites that had been reported in Omicron variants. We also found some novel substitution sites in ORF1ab amino acid sequences, including G5494S, K4346R, T5035I and E6945D, and R346K novel substitution in receptor-binding domain of S sequences. Conclusion The imported Omicron variants of SARS-CoV-2 in Changsha City contained all representative mutation sites that had been reported to increase the viral transmission and pathogenicity. We should continue to strengthen prophylactic measures against SARS-CoV-2.
[1] WHO.Coronavirus disease (COVID-2019) situation reports[EB/OL].(2022-03-02)[2022-03-04].https://www.who.int/emergencies/diseases/novel-coronavirus-2019/situation-reports/. [2] Huang C, Wang Y, Li X, et al.Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China[J].Lancet, 2020, 395(10223):497-506. [3] Wang L, Cheng G.Sequence analysis of the emerging SARS-CoV-2 variant Omicron in South Africa[J].J Med Virol, 2022, 94(4):1728-1733. [4] Sharma V,Rai H,Gautam DNS,et al. Emerging evidence on Omicron (B.1.1.529) SARS-CoV-2 variant[J].J Med Virol, 2022,94(5):1876-1885. [5] Vanmechelen B, Logist AS, Tony WB, et al.Identification of the first SARS-CoV-2 lineage B.1.1.529 virus detected in Europe[J].Microbiol Resour Ann, 2022, 11(2):e0116121. [6] Khandia R,Singhal S,Alqahtani T,et al. Emergence of SARS-CoV-2 Omicron (B.1.1.529) variant, salient features, high global health concerns and strategies to counter it amid ongoing COVID-19 pandemic[J]. Environ Res, 2022, 209:112816. [7] Saxena SK, Kumar S, Ansari S, et al.Characterization of the novel SARS-CoV-2 Omicron (B.1.1.529) variant of concern and its global perspective[J].J Med Virol, 2022, 94(4):1738-1744. [8] Hoffmann M,Krüger N,Schulz S,et al. The Omicron variant is highly resistant against antibody-mediated neutralization: implications for control of the COVID-19 pandemic[J].Cell, 2022, 185(3):447-456. [9] Jia HL, Wang H, Cao L, et al.Genetic analysis of a SARS-CoV-2 Omicron variant from a Chinese traveller returning from overseas[J].Emerg Microbes Infect, 2022, 11(1):306-309. [10] Lupala CS,Ye YJ,Chen H,et al. Mutations on RBD of SARS-CoV-2 Omicron variant result in stronger binding to human ACE2 receptor[J].Biochem Biophys RES Commun, 2022, 590:34-41. [11] Rath SL,Padhi AK,Mandal N. Scanning the RBD-ACE2 molecular interactions in Omicron variant[J]. Biochem Biophys RES Commun, 2022, 592:18-23. [12] Starr TN, Greaney AJ, Hilton SK, et al.Deep mutational scanning of SARS-CoV-2 receptor binding domain reveals constraints on folding and ACE2 binding[J].Cell, 2020, 182(5):1295-1310. [13] Greaney AJ,Loes AN,Crawford KHD,et al. Comprehensive mapping of mutations in the SARS-CoV-2 receptor-binding domain that affect recognition by polyclonal human plasma antibodies[J].Cell Host Microbe, 2021, 29(3):463-476. [14] Wibmer CK, Ayres F, Hermanus T, et al.SARS-CoV-2 501Y.V2 escapes neutralization by South African COVID-19 donor plasma[J]. Nat Med, 2021, 27(4):622-625. [15] Koley T,Kumar M,Goswami A,et al. Structural modeling of Omicron spike protein and its complex with human ACE-2 receptor: molecular basis for high transmissibility of the virus[J].Biochem Biophys RES Commun, 2022, 592:51-53. [16] Greaney AJ, Starr TN, Gilchuk P, et al.Complete mapping of mutations to the SARS-CoV-2 spike receptor-binding domain that escape antibody recognition[J].Cell Host Microbe, 2021, 29(1):44-57. [17] Su YCF, Anderson DE, Young BE, et al.Discovery and genomic characterization of a 382-nucleotide deletion in ORF7b and ORF8 during the early evolution of SARS-CoV-2[J].mBio, 2020, 11(4):e01610-e01620.