Bacterial vaginosis-associated microflora isolated from the female genital tract activates HIV-1 expression

J Acquir Immune Defic Syndr. 1999 Jul 1;21(3):194-202. doi: 10.1097/00126334-199907010-00003.

Abstract

Alteration of cervicovaginal microbial flora can lead to vaginosis, which is associated with an increased risk of HIV-1 transmission. We recently characterized a soluble HIV-inducing factor (HIF) from the cervicovaginal lavage (CVL) samples of women. The goals of this study were to determine the effect of cervicovaginal microflora on HIV-1 expression and to elucidate the relationship between HIF activity and microflora. Physiologically relevant microorganisms, Mycoplasma, diphtheroid-like bacteria, Gardnerella vaginalis, Streptococcus agalactiae, and Streptococcus constellatus, cultured from the CVL of a representative woman with a clinical condition of bacterial vaginosis and possessing HIF activity, induced HIV-1 expression. The magnitude of virus induction varied widely with the greatest stimulation induced by diphtheroid-like bacteria and Mycoplasma. The transcriptional induction by Mycoplasma was mediated by activation of the KB enhancer, an activation mechanism shared with HIF. Also as with HIF, Mycoplasma induced AP-1 dependent transcription. Polymerase chain reaction (PCR)-based speciation showed that the isolate was M. hominis. Our data indicate that bacterial vaginosis-associated microflora can enhance HIV-1 transcription and replication and identify M. hominis as a potential source for HIF activity. The virus-enhancing activities associated with the microflora and HIF may increase genital tract viral load, potentially contributing to HIV transmission.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Chemical Fractionation
  • Enhancer Elements, Genetic
  • Female
  • Gene Expression Regulation, Viral*
  • Genitalia, Female / microbiology*
  • HIV Long Terminal Repeat*
  • HIV-1 / genetics*
  • Humans
  • Jurkat Cells
  • Mycoplasma / metabolism
  • Mycoplasma / physiology
  • NF-kappa B / metabolism
  • Solubility
  • Transcription Factor AP-1 / metabolism
  • Transcription, Genetic
  • Vaginosis, Bacterial / microbiology

Substances

  • NF-kappa B
  • Transcription Factor AP-1