Ginkgolic acid inhibits orthopneumo- and metapneumo- virus infectivity

Maria I Luck1,2, Erick J Subillaga1,2, Ronen Borenstein3

  • 1Aaron Diamond AIDS Research Center, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, 10032, USA.

Scientific Reports
|April 8, 2024
PubMed

Insights

Ginkgolic acid (GA) effectively inhibits human respiratory syncytial virus (hRSV) and human metapneumovirus (hMPV) by blocking viral entry. This natural compound shows potential for treating acute respiratory infections caused by these Pneumoviridae family viruses.

Area of Science:

  • Virology
  • Pharmacology
  • Natural Products

Background:

  • Human respiratory syncytial virus (hRSV) and human metapneumovirus (hMPV) are significant respiratory pathogens.
  • Infections pose severe risks to vulnerable populations, including infants, the elderly, and immunocompromised individuals.
  • Limited treatment options and recent vaccine introduction highlight the need for novel therapeutic strategies.

Purpose of the Study:

  • To investigate the antiviral potential of Ginkgolic acid (GA), a compound from Ginkgo biloba extract.
  • To determine GA's efficacy against hRSV and hMPV.
  • To elucidate the mechanism of action of GA on viral replication.

Main Methods:

  • In vitro cell culture experiments were performed to assess viral infectivity and spread.
  • Dose-dependent inhibition assays were conducted using GA.
  • Viral life cycle stages, including entry, transcription, replication, and assembly, were analyzed to identify the mechanism of action.

Main Results:

  • Ginkgolic acid demonstrated dose-dependent inhibition of hRSV and hMPV infectivity and spread in cell cultures.
  • GA specifically targets the viral entry step, inhibiting early-stage infection.
  • No significant effect was observed on post-entry events such as viral gene transcription, genome replication, assembly, or particle release.

Conclusions:

  • Ginkgolic acid is an effective antiviral agent against members of the Pneumoviridae family, including hRSV and hMPV.
  • GA's mechanism involves inhibiting the crucial viral entry process.
  • GA holds promise as a potential therapeutic agent for treating acute infections caused by these respiratory viruses.