On the way from SARS-CoV-sensitive mice to murine COVID-19 model

The coronavirus disease 2019 (COVID-19) is a master killer which appeared suddenly and which has already claimed more than 200,000 human lives. In this situation, laboratories are in urgent need for a COVID-19 murine model to search for effective antiviral compounds. Here we propose a novel strategy...

Full description

Bibliographic Details
Main Authors: Vladislav O. Soldatov, Marina V. Kubekina, Yulia Yu. Silaeva, Alexandra V. Bruter, Alexey V. Deykin
Format: Article
Language:English
Published: Belgorod National Research University 2020-05-01
Series:Research Results in Pharmacology
Online Access:https://rrpharmacology.pensoft.net/article/53633/download/pdf/
_version_ 1797429121802829824
author Vladislav O. Soldatov
Marina V. Kubekina
Yulia Yu. Silaeva
Alexandra V. Bruter
Alexey V. Deykin
author_facet Vladislav O. Soldatov
Marina V. Kubekina
Yulia Yu. Silaeva
Alexandra V. Bruter
Alexey V. Deykin
author_sort Vladislav O. Soldatov
collection DOAJ
description The coronavirus disease 2019 (COVID-19) is a master killer which appeared suddenly and which has already claimed more than 200,000 human lives. In this situation, laboratories are in urgent need for a COVID-19 murine model to search for effective antiviral compounds. Here we propose a novel strategy for the development of mice that can be inoculated by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the COVID-19 causative agent. In humans, two proteins – ACE2 and TMPRSS2 – are involved in SARS-CoV-2 cells entry and, thus, we decided to introduce their genes into a murine genome. These genes will be placed with LoxP sites under the murine Tmprss2 promoter. Such an approach can provide a representative model with the opportunity to control the viral sensitivity of an animal population and tissue specificity of hACE2 and hTMPRSS2 expression. Graphical abstract The new COVID-19 model should be based on inducible co-expression of the human ACE2 and TMPRSS2 genes. Activation of ACE2 and TMPRSS2 genes will occur only in the virological laboratory, after crossbreeding with Cre-mice. Before activation, mice will be resistant to SARS-CoV-2 for their biological safety during the pandemic.
first_indexed 2024-03-09T09:08:39Z
format Article
id doaj.art-0369c47572364b588c9ebb49491c8975
institution Directory Open Access Journal
issn 2658-381X
language English
last_indexed 2024-03-09T09:08:39Z
publishDate 2020-05-01
publisher Belgorod National Research University
record_format Article
series Research Results in Pharmacology
spelling doaj.art-0369c47572364b588c9ebb49491c89752023-12-02T09:28:42ZengBelgorod National Research UniversityResearch Results in Pharmacology2658-381X2020-05-01621710.3897/rrpharmacology.6.5363353633On the way from SARS-CoV-sensitive mice to murine COVID-19 modelVladislav O. Soldatov0Marina V. Kubekina1Yulia Yu. Silaeva2Alexandra V. Bruter3Alexey V. Deykin4Belgorod State UniversityInstitute of Gene Biology of the Russian Academy of SciencesInstitute of Gene Biology of the Russian Academy of SciencesInstitute of Gene Biology of the Russian Academy of SciencesInstitute of General Pathology and Pathophysiology of the Russian Academy of Medical SciencesThe coronavirus disease 2019 (COVID-19) is a master killer which appeared suddenly and which has already claimed more than 200,000 human lives. In this situation, laboratories are in urgent need for a COVID-19 murine model to search for effective antiviral compounds. Here we propose a novel strategy for the development of mice that can be inoculated by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the COVID-19 causative agent. In humans, two proteins – ACE2 and TMPRSS2 – are involved in SARS-CoV-2 cells entry and, thus, we decided to introduce their genes into a murine genome. These genes will be placed with LoxP sites under the murine Tmprss2 promoter. Such an approach can provide a representative model with the opportunity to control the viral sensitivity of an animal population and tissue specificity of hACE2 and hTMPRSS2 expression. Graphical abstract The new COVID-19 model should be based on inducible co-expression of the human ACE2 and TMPRSS2 genes. Activation of ACE2 and TMPRSS2 genes will occur only in the virological laboratory, after crossbreeding with Cre-mice. Before activation, mice will be resistant to SARS-CoV-2 for their biological safety during the pandemic.https://rrpharmacology.pensoft.net/article/53633/download/pdf/
spellingShingle Vladislav O. Soldatov
Marina V. Kubekina
Yulia Yu. Silaeva
Alexandra V. Bruter
Alexey V. Deykin
On the way from SARS-CoV-sensitive mice to murine COVID-19 model
Research Results in Pharmacology
title On the way from SARS-CoV-sensitive mice to murine COVID-19 model
title_full On the way from SARS-CoV-sensitive mice to murine COVID-19 model
title_fullStr On the way from SARS-CoV-sensitive mice to murine COVID-19 model
title_full_unstemmed On the way from SARS-CoV-sensitive mice to murine COVID-19 model
title_short On the way from SARS-CoV-sensitive mice to murine COVID-19 model
title_sort on the way from sars cov sensitive mice to murine covid 19 model
url https://rrpharmacology.pensoft.net/article/53633/download/pdf/
work_keys_str_mv AT vladislavosoldatov onthewayfromsarscovsensitivemicetomurinecovid19model
AT marinavkubekina onthewayfromsarscovsensitivemicetomurinecovid19model
AT yuliayusilaeva onthewayfromsarscovsensitivemicetomurinecovid19model
AT alexandravbruter onthewayfromsarscovsensitivemicetomurinecovid19model
AT alexeyvdeykin onthewayfromsarscovsensitivemicetomurinecovid19model