The study of mutations and phylogenetics of the SARS-CoV-2 spike gene in population from Tehran province

Document Type : Original Articles

Authors

1 Razi vaccine and Sera institute

2 Department of Virology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran

3 Applied Biotechnology Research Center, Baqiyatallah University of Medical Science, Tehran, Iran

4 Department of Electrical and Computer Engineering, Faculty of Engineering, University of Waterloo, Waterloo, ON N2L Canada

5 Department of Microbiology, Faculty of Sciences, Islamic Azad University, Karaj Branch, Karaj, Iran

6 Razi vaccine and sera research institute

10.32592/ARI.2025.80.1.185

Abstract

In December 2019, an outbreak of pneumonia of unknown etiology was reported in Wuhan, China. The virus, known as SARS-CoV-2, is contagious and infects the lower respiratory tract. Since various coherent research needs to be conducted in Iran to detect mutations in the SARS-CoV-2 S gene, the present study was conducted to determine the sequence, mutation pattern, and phylogenetic evaluation of this gene. For this purpose, 120 positive samples were included to evaluate the complete S gene sequence by Reverse transcriptase-PCR. After sequencing, the gene assembly, blasting, mutation analysis, and phylogenetic analyzes were performed using MEGA-X. A total of 161 mutations were observed in the S gene sequences of Iran. The results of the phylogenetic tree showed that all the S gene sequences of Iranian samples were divergent from the Wuhan strain and had the most similarity to it and also alpha variants. 161 nonsynonymous variations were found along the complete coding S gene with a high frequency of A262T, D614G, and P863H, which were embedded in HVR1, HVR2, and HVR3, respectively. Most of Highly variable fragments have been identified in loop secondary structure of protein.
In the current study, the predominant variants (mostly alpha variants) and mutations were in parallel with the evolution of the virus and its fitness. We provided a wide picture of the genetic mutation of first three waves of SARS-CoV-2 in Iran which could be used to make big decisions and take effective decisions in the next pandemics to develop vaccines and kits and effective therapeutics.

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  1. Kesheh MM, Hosseini P, Soltani S, Zandi M. An overview on the seven pathogenic human coronaviruses. Reviews in Medical Virology. 2021:e2282.
  2. Novel Coronavirus (2019-nCoV) - World Health Organization 20 January 2020 [Available from: www.who.int › docs › 20200121-sitrep-1-2019-ncov.
  3. Ren L-L, Wang Y-M, Wu Z-Q, Xiang Z-C, Guo L, Xu T, et al. Identification of a novel coronavirus causing severe pneumonia in human: a descriptive study. Chinese medical journal. 2020;133(9):1015.
  4. Yang Y, Du L. SARS-CoV-2 spike protein: a key target for eliciting persistent neutralizing antibodies. Signal Transduction and Targeted Therapy. 2021;6(1):95.
  5. Masre SF, Jufri NF, Ibrahim FW, Abdul Raub SH. Classical and alternative receptors for SARS-CoV-2 therapeutic strategy. Reviews in medical virology. 2021;31(5):1-9.
  6. Hu B, Guo H, Zhou P, Shi Z-L. Characteristics of SARS-CoV-2 and COVID-19. Nature Reviews Microbiology. 2021;19(3):141-54.
  7. Jelinek HF, Mousa M, Alefishat E, Osman W, Spence I, Bu D, et al. Evolution, Ecology, and Zoonotic Transmission of Betacoronaviruses: A Review. Frontiers in Veterinary Science. 2021;8.
  8. Harvey WT, Carabelli AM, Jackson B, Gupta RK, Thomson EC, Harrison EM, et al. SARS-CoV-2 variants, spike mutations and immune escape. Nature Reviews Microbiology. 2021;19(7):409-24.
  9. Volz E, Hill V, McCrone JT, Price A, Jorgensen D, O’Toole Á, et al. Evaluating the Effects of SARS-CoV-2 Spike Mutation D614G on Transmissibility and Pathogenicity. Cell. 2021;184(1):64-75.e11.
  10. Hall TA. BioEdit : a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser. 1999;41:95-8.
  11. Kumar S, Stecher G, Li M, Knyaz C, Tamura K. MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms. Mol Biol Evol. 2018;35(6):1547-9.
  12. Tracking SARS-CoV-2 variants: World Health Organization (WHO); 2021.
  13. Yurkovetskiy L, Wang X, Pascal KE, Tomkins-Tinch C, Nyalile TP, Wang Y, et al. Structural and Functional Analysis of the D614G SARS-CoV-2 Spike Protein Variant. Cell. 2020;183(3):739-51.e8.
  14. Hou YJ, Chiba S, Halfmann P, Ehre C, Kuroda M, Dinnon KH, 3rd, et al. SARS-CoV-2 D614G variant exhibits efficient replication ex vivo and transmission in vivo. Science (New York, NY). 2020;370(6523):1464-8.
  15. Winstone H, Lista Maria J, Reid Alisha C, Bouton C, Pickering S, Galao Rui P, et al. The Polybasic Cleavage Site in SARS-CoV-2 Spike Modulates Viral Sensitivity to Type I. Interferon and IFITM2. Journal of Virology. 95(9):e02422-20.
  16. Eslami S, Glassy MC, Ghafouri-Fard S. A comprehensive overview of identified mutations in SARS CoV-2 spike glycoprotein among Iranian patients. Gene. 2022; 813:146113-.
  17. Aliabadi N, Jamaliduost M, Pouladfar G, Marandi NH, Ziyaeyan M. Characterization and phylogenetic analysis of Iranian SARS-CoV-2 genomes: A phylogenomic study. Health Sci Rep. 2023; 6(1):e1052.
  18. Yavarian J, Nejati A, Salimi V, Shafiei Jandaghi NZ, Sadeghi K, Abedi A, Sharifi Zarchi A, Gouya MM, Mokhtari-Azad T. Whole genome sequencing of SARS-CoV2 strains circulating in Iran during five waves of pandemic. PLoS One. 2022;17(5):e0267847.
  19. Sofonea MT, Roquebert B, Foulongne V, Verdurme L, Trombert-Paolantoni S, Roussel M, et al. From Delta to Omicron: analysing the SARS-CoV-2 epidemic in France using variant-specific screening tests (September 1 to December 18, 2021). medRxiv. 2022:12.