Tin oxide nanowires suppress herpes simplex virus-1 entry and cell-to-cell membrane fusion

PLoS One. 2012;7(10):e48147. doi: 10.1371/journal.pone.0048147. Epub 2012 Oct 24.

Abstract

The advent of nanotechnology has ushered in the use of modified nanoparticles as potential antiviral agents against diseases such as herpes simplex virus 1 and 2 (HSV-1) (HSV-2), human immunodeficiency virus (HIV), monkeypox virus, and hepatitis B virus. Here we describe the application of tin oxide (SnO(2)) nanowires as an effective treatment against HSV-1 infection. SnO(2) nanowires work as a carrier of negatively charged structures that compete with HSV-1 attachment to cell bound heparan sulfate (HS), therefore inhibiting entry and subsequent cell-to-cell spread. This promising new approach can be developed into a novel form of broad-spectrum antiviral therapy especially since HS has been shown to serve as a cellular co-receptor for a number of other viruses as well, including the respiratory syncytial virus, adeno-associated virus type 2, and human papilloma virus.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology
  • Cell Line
  • Heparitin Sulfate / chemistry
  • Herpes Simplex / prevention & control*
  • Herpesvirus 1, Human / drug effects
  • Herpesvirus 1, Human / pathogenicity*
  • Herpesvirus 2, Human / drug effects
  • Herpesvirus 2, Human / pathogenicity
  • Humans
  • Membrane Fusion / drug effects*
  • Nanowires / chemistry*
  • Nanowires / therapeutic use*
  • Tin Compounds / chemistry
  • Tin Compounds / pharmacology*

Substances

  • Antiviral Agents
  • Tin Compounds
  • Heparitin Sulfate
  • stannic oxide