Destructive effect of RNаse a on the SARS-CoV-2 virus (in vitro research)

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Abstract

BACKGROUND: For today, the most important and discussed issue in the professional medical community is the problem of prevention and treatment of a new coronaviral infection (COVID-19). The main reason for the non-decreasing increase in morbidity and mortality is the absence of an etiotropic drug. In our study, it is proposed to use a previously available drug for the treatment of tick-borne encephalitis, ribonuclease A, obtained from the pancreas of cattle.

AIM: The aim of investigation was to study the antiviral activity of RNаse A against SARS-CoV-2 in in vitro experiments.

MATERIALS AND METHODS: The experiment used samples of 50 patients with a confirmed (by PCR) primary diagnosis of a new coronoviral infection COVID-19. The preparation for the study was served by ribonuclease A (neoFroxx GmbH, Germany) at a concentration of 0.5; 1; 5 and 10 mg/ml, incubated at 4 and 37°C, the exposure was 20 minutes, 20 hours. A set of reagents OTT-PCR-RV-SARS-CoV-2 (Syntol, Russia) was used as test systems.

RESULTS: of the current study is the revealed antiviral activity of ribonuclease A at a minmal concentration of 0.5 mg/ml during incubation from 20 minutes to 20 hours, in the temperature range of 4–37°C.

CONCLUSIONS: The data obtained in the in vitro study confirmed the ability of ribonuclease A to destroy viral RNA, which suggests the possible use of the drug both for the treatment of patients and for the treatment of environmental objects.

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About the authors

Ilya A. Morozov

E.A. Vagner Perm State Medical University

Author for correspondence.
Email: Lonny8@yandex.ru
ORCID iD: 0000-0003-4233-3711

student, Faculty of Medicine

Russian Federation, Perm

Anatoly P. Godovalov

E.A. Vagner Perm State Medical University

Email: agodovalov@gmail.com

MD, PhD, Leading Research Associate at Central Scientific Laboratory, Associate Professor at Microbiology and Virology Department

Russian Federation, Perm

Denis A. Oborin

Perm Regional Center for the Prevention and Control of AIDS and Infectious Diseases

Email: DAOborin@yandex.ru

MD, bacteriologist

Russian Federation, Perm

References

  1. Romanov BK. Coronavirus disease COVID-2019. Safety and Risk of Pharmacotherapy. 2020;8(1):3–8. (In Russ.) doi: 10.30895/2312-7821-2020-8-1-3-8
  2. Nikiforov VV, Suranova TG, Chernobrovkina TYa, et al. New coronavirus infection (COVID-19): clinical and epidemiological aspects. The Russian Archives of Internal Medicine. 2020;10(2 (52)):87–93. (In Russ.) doi: 10.20514/2226-6704-2020-10-2-87-93
  3. Abaturov AE, Agafonova EA, Krivusha EL, Nikulina A.A. Pathogenesis of COVID-19. Zdorov'e rebenka. 2020;15(2):133–144. (In Russ.). doi: 10.22141/2224-0551.15.2.2020.200598
  4. Rosenberg HF. RNase A ribonucleases and host defense: an evolving story. J Leukoc Biol. 2008;83(5):1079–1087. doi: 10.1189/jlb.1107725
  5. Abaturov AYe. Ribonucleases А – the most ancient components of nonspecific protection of respiratory tract. Zdorov'e rebenka. 2011;(5(32)):136–142. (In Russ.)
  6. Ilinskaya ON, Shah Mahmud R. Ribonucleases as antiviral agents. Molecular Biology. 2014;48(5):615–623. doi: 10.1134/S0026893314040050
  7. Dyer KD, Rosenberg HF. The RNase a superfamily: generation of diversity and innate host defense. Mol Divers. 2006;10(4):585–597. doi: 10.1007/s11030-006-9028-2

Supplementary files

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2. Fig. 1. Kinetic growth curves of fluorescence signal per channel HEX, FAM, Cy5, ROX in sample No. 26: а — before incubation with RNase; b — after incubation with RNase at a concentration of 0.5 mg/ml for 20 minutes at 37 °C. Signal registration by green (FAM) and blue (Cy5) curves testifies to a successful isolation of RNA from the sample and successful the passage of the polymerase chain reaction with reverse transcription her in real time. Registration signals for red (HEX) and purple (ROX) curves witness indicates the presence of specific RNA of SARS-CoV-2 virus

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3. Fig. 2. Kinetic growth curves of fluorescence signal per channel HEX, FAM, Cy5, ROX in sample No. 26: а — before incubation with isotonic sodium chloride solution; b — after incubation with isotonic solution sodium chloride for 20 min at 37 °C. Signal registration by green (FAM) and blue (Cy5) curves testifies to a successful isolation of RNA from the sample and successful the passage of the polymerase chain reverse transcription reactions in real time. Registration signals for red (HEX) and purple (ROX) curves witness indicates the presence of specific RNA of SARS-CoV-2 virus

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Copyright (c) 2021 Morozov I.A., Godovalov A.P., Oborin D.A.

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