The Functional Implications of Broad Spectrum Bioactive Compounds Targeting RNA-Dependent RNA Polymerase (RdRp) in the Context of the COVID-19 Pandemic

Viruses. 2023 Nov 25;15(12):2316. doi: 10.3390/v15122316.

Abstract

Background: As long as COVID-19 endures, viral surface proteins will keep changing and new viral strains will emerge, rendering prior vaccines and treatments decreasingly effective. To provide durable targets for preventive and therapeutic agents, there is increasing interest in slowly mutating viral proteins, including non-surface proteins like RdRp.

Methods: A scoping review of studies was conducted describing RdRp in the context of COVID-19 through MEDLINE/PubMed and EMBASE. An iterative approach was used with input from content experts and three independent reviewers, focused on studies related to either RdRp activity inhibition or RdRp mechanisms against SARS-CoV-2.

Results: Of the 205 records screened, 43 studies were included in the review. Twenty-five evaluated RdRp activity inhibition, and eighteen described RdRp mechanisms of existing drugs or compounds against SARS-CoV-2. In silico experiments suggested that RdRp inhibitors developed for other RNA viruses may be effective in disrupting SARS-CoV-2 replication, indicating a possible reduction of disease progression from current and future variants. In vitro, in vivo, and human clinical trial studies were largely consistent with these findings.

Conclusions: Future risk mitigation and treatment strategies against forthcoming SARS-CoV-2 variants should consider targeting RdRp proteins instead of surface proteins.

Keywords: NSP12 protein; RNA synthesis inhibitors; SARS-CoV-2; antiviral agents; coronavirus RNA-dependent RNA; drug repurposing; polymerase; scoping review.

Publication types

  • Review

MeSH terms

  • Antiviral Agents* / metabolism
  • Antiviral Agents* / pharmacology
  • Antiviral Agents* / therapeutic use
  • COVID-19 Drug Treatment / methods
  • COVID-19* / genetics
  • COVID-19* / metabolism
  • Humans
  • Membrane Proteins
  • Molecular Docking Simulation
  • Pandemics
  • RNA-Dependent RNA Polymerase* / drug effects
  • RNA-Dependent RNA Polymerase* / genetics
  • SARS-CoV-2 / metabolism

Substances

  • Antiviral Agents
  • Membrane Proteins
  • RNA-Dependent RNA Polymerase

Supplementary concepts

  • SARS-CoV-2 variants

Grants and funding

This research received no external funding.