Quantitative analysis of human immunodeficiency virus type-1 DNA in asymptomatic carriers using the polymerase chain reaction

Biochem Biophys Res Commun. 1990 Feb 28;167(1):1-8. doi: 10.1016/0006-291x(90)91721-4.

Abstract

A method for detecting human immunodeficiency virus type 1 (HIV-1) provirus DNA in lymphocytes with improved sensitivity and reproducibility was developed using the polymerase chain reaction (PCR). Amplified HIV-1 DNA was hybridized with a 32P-labeled probe and quantitated with a beta-scanner after electrophoresis. A linear relationship was obtained between the common logarithms of the counts detected and the number of HIV-1 DNA copies applied to the PCR. Detectability was from 3 copies/10(5) lymphocytes, and linearity was maintained from 10 to 10(3) copies. HIV-1 DNA was detected in all 9 asymptomatic carriers tested (18 to 2,857 copies/10(5) CD4+ T lymphocytes). The viral burden was inversely related to the CD4+ lymphocyte count, suggesting that quantitation of provirus levels may serve as a predictor of progress in early HIV infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autoradiography
  • DNA, Viral / analysis*
  • Electrophoresis, Polyacrylamide Gel
  • Female
  • HIV Seropositivity / genetics*
  • HIV-1 / genetics*
  • Humans
  • Lymphocytes / microbiology
  • Male
  • Polymerase Chain Reaction

Substances

  • DNA, Viral