Inhibition of Rabies Virus by 1,2,3,4,6-Penta- O-galloyl-β-d-Glucose Involves mTOR-Dependent Autophagy

Viruses. 2018 Apr 17;10(4):201. doi: 10.3390/v10040201.

Abstract

The compound 1,2,3,4,6-penta-O-galloyl-β-d-glucose (PGG), a gallotannin present in various plants such as Rhus chinensis Mill and Paeonia suffruticosa, has a broad spectrum of antiviral effects. The present study investigated its potency against infection of mice with rabies virus (RABV). Results demonstrated that PGG strongly inhibited virus titers (50-fold), viral mRNA expression (up to 90%), and protein synthesis in vitro. Importantly, we found that PGG not only suppressed viral adsorption and entry, but also directly inactivated RABV through suppression of autophagy by mediating activation of the mTOR-dependent autophagy signaling pathway. In vivo, PGG (10 mg/kg) alleviated the clinical symptoms and reduced the mortality of infected mice by 27.3%. Collectively, our results indicate that PGG has potent anti-RABV effect, and merits further investigation as an anti-RABV drug.

Keywords: CVS-11; IPS; PGG; RABV; antiviral.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents / administration & dosage
  • Antiviral Agents / metabolism*
  • Autophagy / drug effects
  • Disease Models, Animal
  • Female
  • Hydrolyzable Tannins / administration & dosage
  • Hydrolyzable Tannins / metabolism*
  • Mice
  • Rabies / drug therapy
  • Rabies / pathology
  • Rabies / virology
  • Rabies virus / drug effects*
  • Rabies virus / growth & development*
  • Survival Analysis
  • Sweetening Agents
  • TOR Serine-Threonine Kinases / metabolism
  • Virus Replication / drug effects*

Substances

  • Antiviral Agents
  • Hydrolyzable Tannins
  • Sweetening Agents
  • pentagalloylglucose
  • mTOR protein, mouse
  • TOR Serine-Threonine Kinases