Dynamics of the antiviral activity of N-methanocarbathymidine against herpes simplex virus type 1 in cell culture

Mahmoud Huleihel, Marina Talishanisky, Harry Ford, Victor E. Marquez, James A. Kelley, David G. Johns, Riad Agbaria

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

N-Methanocarbathymidine [(N)-MCT], a thymidine analogue, exhibits potent activity in cell culture against herpes simplex virus1 (HSV-1). (N)-MCT showed higher antiviral activity than ganciclovir (GCV). Continuous treatment of Vero cells with (N)-MCT immediately or 10 h post-infection (p.i.) fully prevented the development of viral infection. However, when infected cells were treated with (N)-MCT at 12 h p.i., there was only a partial inhibition (ca. 50%). Additionally, continuous treatment of infected cells with (N)-MCT for about 48 h was sufficient to achieve full prevention of viral infection without further treatment. These findings suggest the complete loss of herpes simplex thymidine kinase (HSV-tk) activity occurs after 48 h of treatment with (N)-MCT. This study helps to understand the mechanism and dynamics of antiHSV activity of (N)-MCT, which is necessary for its future development as an antiviral drug.

Original languageEnglish
Pages (from-to)427-432
Number of pages6
JournalInternational Journal of Antimicrobial Agents
Volume25
Issue number5
DOIs
StatePublished - 1 Jan 2005

Keywords

  • Antiviral activity
  • Ganciclovir
  • Herpes simplex thymidine kinase
  • Herpes simplex virus
  • N- Methanocarbathymidine
  • Phosphorylation

ASJC Scopus subject areas

  • Microbiology (medical)
  • Infectious Diseases
  • Pharmacology (medical)

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