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Construction of a Noninfectious SARS-CoV-2 Replicon for Antiviral-Drug Testing and Gene Function Studies.
Nguyen, Hai Trong; Falzarano, Darryl; Gerdts, Volker; Liu, Qiang.
  • Nguyen HT; Vaccine and Infectious Disease Organization, University of Saskatchewangrid.25152.31, Saskatoon, Saskatchewan, Canada.
  • Falzarano D; Vaccine and Infectious Disease Organization, University of Saskatchewangrid.25152.31, Saskatoon, Saskatchewan, Canada.
  • Gerdts V; Department of Veterinary Microbiology, Western College of Veterinary Medicine, University of Saskatchewangrid.25152.31, Saskatoon, Saskatchewan, Canada.
  • Liu Q; Vaccine and Infectious Disease Organization, University of Saskatchewangrid.25152.31, Saskatoon, Saskatchewan, Canada.
J Virol ; 95(18): e0068721, 2021 08 25.
Article in English | MEDLINE | ID: covidwho-1373942
ABSTRACT
The emerging coronavirus disease 2019 (COVID-19) outbreak caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has rapidly spread worldwide, resulting in global public health emergencies and economic crises. In the present study, a noninfectious and biosafety level 2 (BSL2)-compatible SARS-CoV-2 replicon expressing a nano luciferase (nLuc) reporter was constructed in a bacterial artificial chromosomal (BAC) vector by reverse genetics. The nLuc reporter is highly sensitive, easily quantifiable, and high throughput adaptable. Upon transfecting the SARS-CoV-2 replicon BAC plasmid DNA into Vero E6 cells, we could detect high levels of nLuc reporter activity and viral RNA transcript, suggesting the replication of the replicon. The replicon replication was further demonstrated by the findings that deleting nonstructural protein 15 or mutating its catalytic sites significantly reduced replicon replication, whereas providing the nucleocapsid protein in trans enhanced replicon replication in a dose-dependent manner. Finally, we showed that remdesivir, a U.S. Food and Drug Administration-approved antiviral drug, significantly inhibited the replication of the replicon, providing proof of principle for the application of our replicon as a useful tool for developing antivirals. Taken together, this study established a sensitive and BSL2-compatible reporter system in a single BAC plasmid for investigating the functions of SARS-CoV-2 proteins in viral replication and evaluating antiviral compounds. This should contribute to the global effort to combat this deadly viral pathogen. IMPORTANCE The COVID-19 pandemic caused by SARS-CoV-2 is having a catastrophic impact on human lives. Combatting the pandemic requires effective vaccines and antiviral drugs. In the present study, we developed a SARS-CoV-2 replicon system with a sensitive and easily quantifiable reporter. Unlike studies involving infectious SARS-CoV-2 virus that must be performed in a biosafety level 3 (BSL3) facility, the replicon is noninfectious and thus can be safely used in BSL2 laboratories. The replicon will provide a valuable tool for testing antiviral drugs and studying SARS-CoV-2 biology.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Replicon / Virus Replication / Green Fluorescent Proteins / Drug Evaluation, Preclinical / SARS-CoV-2 / COVID-19 Drug Treatment Type of study: Diagnostic study / Experimental Studies / Prognostic study Topics: Traditional medicine / Vaccines Limits: Animals / Humans Language: English Journal: J Virol Year: 2021 Document Type: Article Affiliation country: JVI.00687-21

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Replicon / Virus Replication / Green Fluorescent Proteins / Drug Evaluation, Preclinical / SARS-CoV-2 / COVID-19 Drug Treatment Type of study: Diagnostic study / Experimental Studies / Prognostic study Topics: Traditional medicine / Vaccines Limits: Animals / Humans Language: English Journal: J Virol Year: 2021 Document Type: Article Affiliation country: JVI.00687-21