Application of real-time PCR for determination of antiviral drug susceptibility of herpes simplex virus

Antimicrob Agents Chemother. 2002 Sep;46(9):2943-7. doi: 10.1128/AAC.46.9.2943-2947.2002.

Abstract

A quantitative real-time PCR (TaqMan) assay was developed for determination of antiviral drug susceptibility of herpes simplex virus (HSV). After short-time culture of the virus, the antiviral drug susceptibility of HSV isolates for acyclovir (ACV) was determined by measuring the reduction of the HSV type 1 (HSV-1) DNA levels in culture supernatants using real-time PCR. The 50% inhibitory concentration was reported as the concentration of antiviral drug that reduced the number of HSV-1 DNA copies by 50%. A total of 15 well-characterized ACV-sensitive or -resistant strains and clinical isolates were used for assay evaluation. The new assay with real-time PCR readout permitted rapid (3 days), objective, and reproducible determination of HSV-1 drug susceptibilities with no need for stringent control of initial multiplicity of infection. Furthermore, the real-time PCR assay results showed good correlation (r = 0.86) with those for the plaque reduction assay. In conclusion, the real-time PCR assay described here is a suitable quantitative method for determination of antiviral susceptibility of HSV-1, amenable for use in the routine diagnostic virology laboratory.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents / pharmacology*
  • Chlorocebus aethiops
  • Computer Systems
  • DNA Replication / drug effects
  • DNA, Viral / analysis
  • DNA, Viral / biosynthesis
  • Herpesvirus 1, Human / drug effects
  • Kinetics
  • Reproducibility of Results
  • Reverse Transcriptase Polymerase Chain Reaction / methods*
  • Simplexvirus / drug effects*
  • Vero Cells
  • Viral Plaque Assay

Substances

  • Antiviral Agents
  • DNA, Viral