Complement activation and complement-dependent inflammation by Neisseria meningitidis are independent of lipopolysaccharide

Infect Immun. 2004 Jun;72(6):3344-9. doi: 10.1128/IAI.72.6.3344-3349.2004.

Abstract

Fulminant meningococcal sepsis has been termed the prototypical lipopolysaccharide (LPS)-mediated gram-negative septic shock. Systemic inflammation by activated complement and cytokines is important in the pathogenesis of this disease. We investigated the involvement of meningococcal LPS in complement activation, complement-dependent inflammatory effects, and cytokine or chemokine production. Whole blood anticoagulated with lepirudin was stimulated with wild-type Neisseria meningitidis H44/76 (LPS+), LPS-deficient N. meningitidis H44/76lpxA (LPS-), or purified meningococcal LPS (NmLPS) at concentrations that were relevant to meningococcal sepsis. Complement activation products, chemokines, and cytokines were measured by enzyme-linked immunosorbent assays, and granulocyte CR3 (CD11b/CD18) upregulation and oxidative burst were measured by flow cytometry. The LPS+ and LPS- N. meningitidis strains both activated complement effectively and to comparable extents. Purified NmLPS, used at a concentration matched to the amount present in whole bacteria, did not induce any complement activation. Both CR3 upregulation and oxidative burst were also induced, independent of LPS. Interleukin-1beta (IL-1beta), tumor necrosis factor alpha, and macrophage inflammatory protein 1alpha production was predominantly dependent on LPS, in contrast to IL-8 production, which was also markedly induced by the LPS- meningococci. In this whole blood model of meningococcal sepsis, complement activation and the immediate complement-dependent inflammatory effects of CR3 upregulation and oxidative burst occurred independent of LPS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Complement Activation*
  • Complement System Proteins / pharmacology
  • Cytokines / biosynthesis
  • Granulocytes / metabolism
  • Humans
  • Inflammation / physiopathology*
  • Lipopolysaccharides / pharmacology*
  • Macrophage-1 Antigen / metabolism
  • Meningococcal Infections / physiopathology*
  • Models, Biological
  • Neisseria meningitidis / pathogenicity*
  • Respiratory Burst
  • Sepsis / physiopathology
  • Up-Regulation

Substances

  • Cytokines
  • Lipopolysaccharides
  • Macrophage-1 Antigen
  • Complement System Proteins