Baseline sensitivity of HSV-1 and HSV-2 clinical isolates and defined acyclovir-resistant strains to the helicase-primase inhibitor pritelivir

Antiviral Res. 2013 Nov;100(2):297-9. doi: 10.1016/j.antiviral.2013.08.024. Epub 2013 Sep 8.

Abstract

Fifty-nine US isolates of HSV-1 and HSV-2 obtained between 1998 and 2004 were tested for sensitivity to the helicase-primase inhibitor, pritelivir (AIC316, BAY 57-1293) by plaque-reduction assay. All isolates, which were collected prior to any clinical use of primase-helicase inhibitors, were sensitive and showed mean EC50 values of 0.026 and 0.029μM for HSV-1 and HSV-2, respectively. Furthermore, several laboratory-selected acyclovir-resistant HSV mutants were also sensitive to pritelivir. These data provide a baseline for HSV sensitivity to pritelivir in general population before it is introduced and broadly used to treat HSV infection. The data also validate pritelivir as an appropriate therapy for nucleoside-resistant HSV infections.

Keywords: AIC316; BAY 57-1293; HSV; Helicase–primase; Pritelivir.

MeSH terms

  • Acyclovir / pharmacology
  • Antiviral Agents / pharmacology*
  • DNA Helicases / antagonists & inhibitors*
  • Herpesvirus 1, Human / drug effects*
  • Herpesvirus 1, Human / isolation & purification
  • Herpesvirus 2, Human / drug effects*
  • Herpesvirus 2, Human / isolation & purification
  • Humans
  • Microbial Sensitivity Tests
  • Pyridines / pharmacology*
  • Sulfonamides
  • Thiazoles / pharmacology*
  • United States
  • Viral Plaque Assay

Substances

  • Antiviral Agents
  • Pyridines
  • Sulfonamides
  • Thiazoles
  • pritelivir
  • DNA Helicases
  • Acyclovir