Detection of SARS‑CoV‑2 S Gene Mutations Using PCR during Seasons of Increased Incidence of Coronavirus Infection in the Chuvash Republic

Author:

Prishchepa N. P.1ORCID,Dobrovol’skaya N. Yu.1ORCID,Nikiforova V. I.1ORCID,Tarasova T. S.1ORCID,Preobrazhenskaya E. V.1ORCID

Affiliation:

1. Federal Center for Traumatology, Orthopedics, and Endoprosthetics of the Ministry of Health of the Russian Federation

Abstract

Mutations in the SARS‑CoV‑2 genome make it possible to effectively escape defense mechanisms of the host, which explains the spread of infection among vaccinated or previously affected by the virus individuals.The aim of the study was to investigate the dynamics of mutations in the SARS‑CoV‑2 virus genome during the rise of the seasonal incidence in the Chuvash Republic.Materials and methods. Under conditions of the clinical diagnostic laboratory of the Federal Center for Traumatology, Orthopedics and Endoprosthetics of the Ministry of Health of Russia (Cheboksary), samples, containing SARS‑CoV‑2 RNA, taken in January-February and July-October, 2022 were tested using reverse transcription PCR. The “MBS-Test SARS‑CoV‑2 RNA” (Technical Specifications 21.20.23-068-26329720-2021, Russia) and “AmpliTest SARS‑CoV‑2 VOC v.3” (Series V017, Certificate of Registration No. 2022/16307, Russia) were utilized in compliance with the manufacturer’s instructions.Results and discussion. Variations in the sets of SARS‑CoV‑2 S gene mutations have been revealed in the studied samples obtained during different periods of the spread of SARS‑CoV‑2 coronavirus. Timely detection of various mutations in the virus genome at the beginning of the epidemiological season and the alleged rise in the incidence of coronavirus infection is valuable information for forecasting the rate of virus transmission. It can also be used to create vaccines (taking into account changes in the virus genome) and to choose the adequate tactics for treating coronavirus infection.

Publisher

Russian Research Anti-Plague Institute Microbe

Subject

Infectious Diseases,Microbiology (medical),Immunology,Microbiology,Epidemiology

Reference15 articles.

1. Statement on the second meeting of the International Health Regulations (2005) Emergency Committee regarding the outbreak of novel coronavirus (2019-nCoV). 30 January 2020. WHO. (Cited 31 May 2023). [Internet]. Available from: https://www.who.int/news-room/detail/30-01-2020-statement-on-the-second-meetingofthe-international-health-regulations-(2005)-emergency-committeeregarding-the-outbreak-of-novel-coronavirus-(2019-ncov).

2. Lupala C.S., Ye Y., Chen H., Su X.D., Liu H. Mutations on RBD of SARS CoV 2 Omicron variant result in stronger binding to human ACE2 receptor. Biochem. Biophys. Res. Commun. 2022; 590:34–41. DOI: 10.1016/j.bbrc.2021.12.079.

3. Hirabara S.M., Serdan T.D.A., Gorjao R., Masi L.N., Pithon-Curi T.C., Covas D.T., Curi R., Durigon E.L. SARS COV 2 variants: differences and potential of immune evasion. Front. Cell. Infect. Microbiol. 2022; 11:781429. DOI: 10.3389/fcimb.2021.781429.

4. Motozono C., Toyoda M., Zahradnik J., Saito A., Nasser H., Tan T.S., Ngare I., Kimura I., Uriu K., Kosugi Y., Yue Y., Shimizu R., Ito J., Torii S., Yonekawa A., Shimono N., Nagasaki Y., Minami R., Toya T., Sekiya N., Fukuhara T., Matsuura Y., Schreiber G.; Genotype to Phenotype Japan (G2P-Japan) Consortium; Ikeda T., Nakagawa S., Ueno T., Sato K. SARS CoV 2 spike L452R variant evades cellular immunity and increases infectivity. Cell Host Microbe. 2021; 29(7):1124–1136.e11. DOI: 10.1016/j.chom.2021.06.006.

5. Wang Q., Guo Y., Iketani S., Nair M.S., Li Z., Mohri H., Wang M., Yu J., Bowen A.D., Chang J.Y., Shah J.G., Nguyen N., Chen Z., Meyers K., Yin M.T., Sobieszczyk M.E., Sheng Z., Huang Y., Liu L., Ho D.D. Antibody evasion by SARS CoV 2 Omicron subvariants BA.2.12.1, BA.4 and BA.5. Nature. 2022; 608(7923):603–8. DOI: 10.1038/s41586-022-05053-w.

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3