Probenecid Inhibits Respiratory Syncytial Virus (RSV) Replication

Viruses. 2022 Apr 27;14(5):912. doi: 10.3390/v14050912.

Abstract

RNA viruses like SARS-CoV-2, influenza virus, and respiratory syncytial virus (RSV) are dependent on host genes for replication. We investigated if probenecid, an FDA-approved and safe urate-lowering drug that inhibits organic anion transporters (OATs) has prophylactic or therapeutic efficacy to inhibit RSV replication in three epithelial cell lines used in RSV studies, i.e., Vero E6 cells, HEp-2 cells, and in primary normal human bronchoepithelial (NHBE) cells, and in BALB/c mice. The studies showed that nanomolar concentrations of all probenecid regimens prevent RSV strain A and B replication in vitro and RSV strain A in vivo, representing a potential prophylactic and chemotherapeutic for RSV.

Keywords: antiviral; prophylactic; respiratory syncytial virus (RSV); therapeutic.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • COVID-19*
  • Mice
  • Probenecid / pharmacology
  • Probenecid / therapeutic use
  • Respiratory Syncytial Virus Infections* / drug therapy
  • Respiratory Syncytial Virus Infections* / metabolism
  • Respiratory Syncytial Virus Infections* / prevention & control
  • Respiratory Syncytial Virus, Human* / genetics
  • SARS-CoV-2
  • Virus Replication

Substances

  • Probenecid

Grants and funding

This research received no external funding. The APC was funded by the Georgia Research Alliance.