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The Omicron Variant of SARS-CoV-2 Virus: the Ability to Cause Disease in Persons with Immunity against COVID-19

https://doi.org/10.35825/2587-5728-2022-6-1-44-55

EDN: jfxeeb

Abstract

During the COVID-19 pandemic the experts noted the emergence and periodic change of the dominant variants of the coronavirus (SARS-CoV-2) that caused the disease. The line B.1.1529, the omicron variant according to the WHO classification, became dominant in the fifth wave of the COVID-19 pandemic. The aim of the work is to analyze the properties of B.1.1529 (omicron) viruses that ensure its ability to cause disease in vaccinated or previously recovered from COVID-19. The fifth wave is characterized by the parallel distribution of the delta and omicron variants, with the domination of the latter. The omicron variant arose as a result of multiple passages of SARS-CoV-2 through the organisms of immunocompromised patients. If the delta variant is the most virulent for humans, the omicron variant is certainly the most infectious - the value of the basic reproductive number (R0) for it is ≈ 10.0, for the delta variant ≈ 6, 0. A person infected with the omicron variant is capable of transmitting the SARS-CoV-2 virus within a day. This is caused by a combination of N501Y and Q498R mutations in the omicron variant, which increase the affinity of the receptor-binding domain of the S1 subunit of the viral S protein for the ACE-2 receptor in the human lung. Mutations H655Y and N679K are located near the furin cleavage site, which in turn promotes accelerated cleavage of the S-protein and increases the level of infectiousness of the pathogen. The omicron variant is significantly superior to the delta variant in terms of ability to overcome the immunity caused by vaccination. The spread of the disease was not stopped by the fact that the number of people who completed the full course of vaccination at the beginning of the fifth wave in Russia reached 64%.Therefore, the achieved level of vaccination cannot be considered sufficient to stop the spread of this variant of the virus. It is shown in the article, that this indicator should be at least 80% to prevent the spread of the disease, and only if vaccination is carried out in a short time. However, it is possible that the mutational potential of the SARS-CoV-2 virus has not yet been exhausted, and the pandemic on the omicron variant will not end.

About the Authors

T. E. Sizikova
Federal State Budgetary Establishment «48 Central Scientific Research Institute» of the Ministry of the Defense of the Russian Federation
Russian Federation

Researcher, Candidate of Biologic Sciences

141306 Sergiev Posad, Oktyabrskaya st., 11



O. V. Chuhralya
Federal State Budgetary Establishment «48 Central Scientific Research Institute» of the Ministry of the Defense of the Russian Federation
Russian Federation

Assistant of chief of department

141306 Sergiev Posad, Oktyabrskaya st., 11



V. N. Lebedev
Federal State Budgetary Establishment «48 Central Scientific Research Institute» of the Ministry of the Defense of the Russian Federation
Russian Federation

Leading researcher, Doctor of Biologic Sciences, Professor

141306 Sergiev Posad, Oktyabrskaya st., 11



S. V. Borisevich
Federal State Budgetary Establishment «48 Central Scientific Research Institute» of the Ministry of the Defense of the Russian Federation
Russian Federation

Head of Federal State Budgetary Establishment «48 Central Scientific Research Institute» of the Ministry of the Defense of the Russian Federation, Corresponding member of Russian Academy of Sciences, Doctor of Biologic Sciences, Professor.

141306 Sergiev Posad, Oktyabrskaya st., 11



References

1. Singanayagam A., Hakki S., Dunning J. et al. Community transmission and viral load kinetics of the SARS-CoV-2 delta (B.1.617.2) variant in vaccinated and unvaccinated individuals in the UK: a prospective, longitudinal, cohort study // Lancet Infect. Dis. 2022. V. 22. № 2. P. 183–195. https://doi.org/10.1016/S1473-3099(21)00648-4

2. Li Q., Guan X., Wu P., et al. Early transmission dynamics in Wuhan, China, of novel coronavirusinfected pneumonia // N. Engl. J. Med. 2020. V. 382. № 13. P. 1199–1207. https://doi.org/10.1056/NEJMoa2001316

3. Riou J., Althaus C.L. Pattern of early human-tohuman transmission of Wuhan 2019 novel coronavirus (2019-nCoV), December 2019 to January 2020 // Euro Surveill. 2020. V. 25. № 4. P. 2000058. https://doi.org/10.2807/1560-7917.ES.2020.25.4.2000058

4. Wu J.T., Leung K., Bushman M. et al. Estimating clinical severity of COVID-19 from the transmission dynamics in Wuhan, China // Nat. Med. 2020. V. 26. № 4. P. 506–510. https://doi.org/10.1038/s41591-020-0822-7

5. Sanche S., Lin Y.T., Xu C. et al. High contagiousness and rapid spread of severe acute respiratory syndrome Coronavirus 2 // Emerg. Infect. Dis. 2020. V. 26. № 7. P. 1470–1477. https://doi.org/10.3201/eid2607.200282

6. Torjesen I. Covid-19: Omicron may be more transmissible than other variants and partly resistant to existing vaccines, scientists fear // BMJ. 2021. V. 375. P. 2943. https://doi.org/10.1136/bmj.n2943

7. Grant M.C., Geoghegan L., Arbyn M. et al. The prevalence of symptoms in 24,410 adults infected by the novel coronavirus (SARS-CoV-2; COVID-19): a systematic review and meta-analysis of 148 studies from 9 countries // PLoS One. 2020. V. 15. № 6. P. e0234765. https://doi.org/10.1371/journal.pone.0234765

8. Fu L., Wang B., Yuan T. et al. Clinical characteristics of coronavirus disease 2019 (COVID-19) in China: A systematic review and meta-analysis // J. Infect. 2020. V. 80. № 6. P. 656–665. https://doi.org/10.1016/j.jinf.2020.03.041

9. Oran D.P., Topol E.J. Prevalence of asymptomatic SARS-CoV-2 Infection: a narrative review // Ann. Intern. Med. 2020. V. 173. № 5. P. 362–367. https://doi.org/10.7326/M20-3012

10. Walls A.C., Park Y.J., Tortorici M.A. et al. Structure, function, and antigenicity of the SARS-CoV-2 spike glycoprotein // Cell. 2020. V. 181. № 2. P. 281–292. e6. https://doi.org/10.1016/j.cell.2020.02.058

11. Sun Y., Lin W., Dong W., Xu J. Origin and evolutionary analysis of the SARS-CoV-2 Omicron variant // J. Biosafety Biosecurity. 2022. V. 4. № 1. P. 33–37. https://doi.org/10.1016/j.jobb.2021.12.001

12. Yeh T.Y., Contreras G.P. Full vaccination suppresses SARS-CoV-2 delta variant mutation frequency // medRxiv. 2021. https://doi.org/10.1101/2021.08.08.21261768

13. Cele S., Jackson L., Khoury D.S. et al. Omicron extensively but incompletely escapes Pfizer BNT162b2 neutralization // Nature. 2022. V. 602. P. 654–656. https://doi.org/10.1038/s41586-021-04387-1

14. Supotnitskiy M.V. COVID-19: the difficult exam of humanity. Moscow: «Russian panorama», 2021. (in Russian).

15. Shahhosseini N., Babuadze G.G., Wong G., Kobinger G.P. Mutation Signatures and In Silico Docking of Novel SARS-CoV-2 Variants of Concern. Microorganisms // 2021. V. 9. № 5. P. 926. https://doi.org/10.3390/microorganisms9050926

16. Gazit S., Shlezinger R., Perez G. et al. Comparing SARS-CoV-2 natural immunity to vaccine-induced immunity: reinfections versus breakthrough infections // medRxiv. 2021. https://doi.org/10.1101/2021.08.24.21262415

17. Khaitov R.M. Immunology: structure and functions of the immune system: textbook. Moscow: GEOTAR-Media, 2013 (in Russian).

18. Onishchenko G.G., Sizikova T.E., Lebedev V.N., Borisevich S.V. Analysis of promising approaches to COVID-19 vaccine development // BIOpreparations. Prevention, Diagnosis, Treatment // 2020. V. 20. № 4. P. 216–227 (In Russ.). https://doi.org/10.30895/2221-996X-2020-20-4-216-227 (in Russian).

19. Iyer A.S., Jones F.K., Nodoushani A. et al. Persistence and decay of human antibody responses to the receptor binding domain of SARS-CoV-2 spike protein in COVID-19 patients // Sci. Immunol. 2020. V. 5. № 52. P. eabe0367. https://doi.org/10.1126/sciimmunol.abe0367

20. Wei C., Shan K.J., Wang W. et al. Evidence for a mouse origin of the SARS-CoV-2 Omicron variant // J. Genet. Genomics. 2021. V. 48. № 12. P. 1111–1121. https://doi.org/10.1016/j.jgg.2021.12.003


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For citations:


Sizikova T.E., Chuhralya O.V., Lebedev V.N., Borisevich S.V. The Omicron Variant of SARS-CoV-2 Virus: the Ability to Cause Disease in Persons with Immunity against COVID-19. Journal of NBC Protection Corps. 2022;6(1):44-55. (In Russ.) https://doi.org/10.35825/2587-5728-2022-6-1-44-55. EDN: jfxeeb

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ISSN 2587-5728 (Print)
ISSN 3034-2791 (Online)