A high throughput Cre-lox activated viral membrane fusion assay identifies pharmacological inhibitors of HIV entry

Virology. 2016 Mar:490:6-16. doi: 10.1016/j.virol.2015.10.013. Epub 2016 Jan 21.

Abstract

Enveloped virus entry occurs when viral and cellular membranes fuse releasing particle contents into the target cell. Human immunodeficiency virus (HIV) entry occurs by cell-free virus or virus transferred between infected and uninfected cells through structures called virological synapses. We developed a high-throughput cell-based assay to identify small molecule inhibitors of cell-free or virological synapse-mediated entry. An HIV clone carrying Cre recombinase as a Gag-internal gene fusion releases active Cre into cells upon viral entry activating a recombinatorial gene switch changing dsRed to GFP-expression. A screen of a 1998 known-biological profile small molecule library identified pharmacological HIV entry inhibitors that block both cell-free and cell-to-cell infection. Many top hits were noted as HIV inhibitors in prior studies, but not previously recognized as entry antagonists. Modest therapeutic indices for simvastatin and nigericin were observed in confirmatory HIV infection assays. This robust assay is adaptable to study HIV and heterologous viral pseudotypes.

Keywords: Cre recombinase; Drug screening; Env; Gag; HIV-1; Viral membrane fusion; Virus entry.

Publication types

  • Evaluation Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Cell Line
  • Cell Membrane / drug effects
  • Cell Membrane / virology
  • Drug Evaluation, Preclinical / methods*
  • HIV Fusion Inhibitors / pharmacology*
  • HIV Infections / virology*
  • HIV-1 / drug effects*
  • HIV-1 / physiology
  • Humans
  • Virology / methods*
  • Virus Internalization / drug effects
  • Virus Replication / drug effects

Substances

  • HIV Fusion Inhibitors