Identification and characterization of potent small molecule inhibitor of hemorrhagic fever New World arenaviruses

Antiviral Res. 2006 Feb;69(2):86-97. doi: 10.1016/j.antiviral.2005.10.008. Epub 2005 Nov 28.

Abstract

Category A arenaviruses as defined by the National Institute of Allergy and Infectious Diseases (NIAID) are human pathogens that could be weaponized by bioterrorists. Many of these deadly viruses require biosafety level-4 (BSL-4) containment for all laboratory work, which limits traditional laboratory high-throughput screening (HTS) for identification of small molecule inhibitors. For those reasons, a related BSL-2 New World arenavirus, Tacaribe virus, 67-78% identical to Junín virus at the amino acid level, was used in a HTS campaign where approximately 400,000 small molecule compounds were screened in a Tacaribe virus-induced cytopathic effect (CPE) assay. Compounds identified in this screen showed antiviral activity and specificity against not only Tacaribe virus, but also the Category A New World arenaviruses (Junín, Machupo, and Guanarito). Drug resistant variants were isolated, suggesting that these compounds act through inhibition of a viral protein, the viral glycoprotein (GP2), and not through cellular toxicity mechanisms. A lead compound, ST-294, has been chosen for drug development. This potent and selective compound, with good bioavailability, demonstrated protective anti-viral efficacy in a Tacaribe mouse challenge model. This series of compounds represent a new class of inhibitors that may warrant further development for potential inclusion in a strategic stockpile.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antiviral Agents / chemistry*
  • Antiviral Agents / pharmacology
  • Arenaviridae Infections / drug therapy
  • Arenaviridae Infections / virology
  • Arenaviruses, New World / drug effects*
  • Chlorocebus aethiops
  • Cytopathogenic Effect, Viral
  • Hemorrhagic Fevers, Viral / drug therapy
  • Hemorrhagic Fevers, Viral / virology
  • Humans
  • Lead / chemistry*
  • Lead / pharmacology
  • Mice
  • Mice, Inbred BALB C
  • Molecular Sequence Data
  • Rats
  • Rats, Sprague-Dawley
  • Sulfonamides / chemistry
  • Sulfonamides / pharmacology
  • Urea / analogs & derivatives
  • Urea / chemistry
  • Urea / pharmacology
  • Vero Cells
  • Viral Proteins / antagonists & inhibitors*
  • Viral Proteins / metabolism

Substances

  • Antiviral Agents
  • ST 294
  • ST 336
  • Sulfonamides
  • Viral Proteins
  • Lead
  • Urea