Mycobacterium tuberculosis enhances human immunodeficiency virus-1 replication by transcriptional activation at the long terminal repeat

J Clin Invest. 1995 May;95(5):2324-31. doi: 10.1172/JCI117924.

Abstract

Tuberculosis has emerged as an epidemic fueled by the large number of individuals infected with the human immunodeficiency virus, especially those who are injecting drug users. We found a striking increase from 4- to 208-fold in p24 levels in bronchoalveolar lavage fluid from involved sites of Mycobacterium tuberculosis infection vs uninvolved sites in three HIV+ patients. We used an in vitro cell culture model to determine if tuberculosis could activate replication of HIV-1. Mononuclear phagocyte cell lines U937 and THP-1 infected with HIV-1JR-CSF, in vitro and stimulated with live M. tuberculosis H37Ra, had a threefold increase in p24 in culture supernatants. Using the HIV-1 long terminal repeat with a chloramphenicol acetyltransferase (CAT) reporter construct, live M. tuberculosis increased transcription 20-fold in THP-1 cells, and cell wall components stimulated CAT expression to a lesser extent. The nuclear factor-kappa B enhancer element was responsible for the majority of the increased CAT activity although two upstream nuclear factor-IL6 sites may also contribute to enhanced transcription. Antibodies to TNF-alpha and IL-1 inhibited the increase in CAT activity of the HIV-1 long terminal repeat by M. tuberculosis from 21-fold to 8-fold. Stimulation of HIV-1 replication by M. tuberculosis may exacerbate dysfunction of the host immune response in dually infected individuals.

Publication types

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

MeSH terms

  • AIDS-Related Opportunistic Infections / virology
  • Adult
  • Antibodies / pharmacology
  • Base Sequence
  • CCAAT-Enhancer-Binding Proteins
  • Cell Line
  • Cell Nucleus / metabolism
  • Chloramphenicol O-Acetyltransferase / analysis
  • Chloramphenicol O-Acetyltransferase / biosynthesis
  • DNA-Binding Proteins / metabolism
  • HIV Core Protein p24 / analysis
  • HIV Core Protein p24 / biosynthesis
  • HIV Long Terminal Repeat*
  • HIV Seropositivity / virology
  • HIV-1 / genetics
  • HIV-1 / physiology*
  • Humans
  • Interleukin-1 / physiology
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Mycobacterium tuberculosis / physiology*
  • NF-kappa B / metabolism
  • Nuclear Proteins / metabolism
  • Oligodeoxyribonucleotides
  • Transcription Factors / metabolism
  • Transcription, Genetic
  • Transcriptional Activation*
  • Transfection
  • Tuberculosis / virology
  • Tumor Necrosis Factor-alpha / physiology
  • Virus Replication*

Substances

  • Antibodies
  • CCAAT-Enhancer-Binding Proteins
  • DNA-Binding Proteins
  • HIV Core Protein p24
  • Interleukin-1
  • NF-kappa B
  • Nuclear Proteins
  • Oligodeoxyribonucleotides
  • Transcription Factors
  • Tumor Necrosis Factor-alpha
  • Chloramphenicol O-Acetyltransferase