Lipopolysaccharide induces immune activation and SIV replication in rhesus macaques of Chinese origin

PLoS One. 2014 Jun 11;9(2):e98636. doi: 10.1371/journal.pone.0098636. eCollection 2014.

Abstract

Background: Chronic immune activation is a hallmark of progressive HIV infection and a key determinant of immunodeficiency in HIV-infected individuals. Bacterial lipopolysaccharide (LPS) in the circulation has been implicated as a key factor in HIV infection-related systemic immune activation. We thus investigate the impact of LPS on systemic immune activation in simian immunodeficiency virus (SIV)-infected rhesus macaques of Chinese origin.

Methods: The animals were inoculated intravenously with SIVmac239. The levels of plasma viral load and host inflammatory cytokines in PBMC were measured by real-time RT-PCR. CD4/CD8 ratio and systemic immune activation markers were examined by flow cytometric analysis of PBMCs. White blood cell and neutrophil counts and C Reactive Protein levels were determined using biochemistry analyzer. The plasma levels of LPS were determined by Tachypleus Amebocyte Lysate (TAL) test.

Results: The animals inoculated with SIVmac239 became infected as evidenced by the increased plasma levels of SIV RNA and decreased CD4/CD8 ratio. LPS administration of SIV-infected animals induced a transient increase of plasma SIV RNA and immune activation, which was indicated by the elevated expression of the inflammatory cytokines and CD4+HLA-DR+ T cells in PBMCs.

Conclusions: These data support the concept that LPS is a driving factor in systemic immune activation of HIV disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD4-CD8 Ratio
  • Cytokines / immunology
  • Female
  • Lipopolysaccharides / immunology*
  • Macaca mulatta / blood
  • Macaca mulatta / immunology
  • Macaca mulatta / virology*
  • Monkey Diseases / blood
  • Monkey Diseases / immunology*
  • Monkey Diseases / virology
  • Simian Immunodeficiency Virus / physiology*
  • Viral Load
  • Virus Replication*

Substances

  • Cytokines
  • Lipopolysaccharides