Steroid hormone synthesis by a vaccinia enzyme: a new type of virus virulence factor

EMBO J. 1992 May;11(5):1973-80. doi: 10.1002/j.1460-2075.1992.tb05251.x.

Abstract

Vaccinia virus open reading frame (ORF) SalF7L has 31% amino acid identity to human 3 beta-hydroxysteroid dehydrogenase/delta 5-delta 4 isomerase (3 beta-HSD). Here we show that SalF7L encodes an active 3 beta-HSD, by the conversion of pregnenolone to the steroid hormone progesterone. The gene is transcribed early during infection into a 1.4 kb mRNA from an initiation site 12 bp upstream of the ORF. An antiserum raised against bacterially expressed SalF7L immunoprecipitated a 38 kDa polypeptide from infected cells, but not from mock infected cells or from cells infected with a mutant virus from which the SalF7L ORF had been removed. Deletion of the gene had no effect on virus replication in CV-1 cells in culture, yet the deletion mutant was attenuated when intranasally inoculated into mice. This steroid hormone synthesizing enzyme is a novel type of virus virulence factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3-Hydroxysteroid Dehydrogenases / genetics*
  • 3-Hydroxysteroid Dehydrogenases / metabolism
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Blotting, Northern
  • Blotting, Southern
  • Cells, Cultured
  • DNA, Viral / genetics
  • Genes, Viral
  • Hormones / biosynthesis*
  • Humans
  • Mice
  • Mice, Inbred BALB C
  • Molecular Sequence Data
  • Open Reading Frames
  • Precipitin Tests
  • RNA, Messenger / genetics
  • Steroids / biosynthesis*
  • Transcription, Genetic
  • Vaccinia virus / enzymology*
  • Vaccinia virus / genetics
  • Vaccinia virus / pathogenicity
  • Virulence / genetics

Substances

  • DNA, Viral
  • Hormones
  • RNA, Messenger
  • Steroids
  • 3-Hydroxysteroid Dehydrogenases