Activation of plasminogen activator inhibitor implicates protease InhA in the acute-phase response to Bacillus anthracis infection

J Med Microbiol. 2009 Jun;58(Pt 6):737-744. doi: 10.1099/jmm.0.007427-0.

Abstract

Anthrax is a zoonotic disease caused by Bacillus anthracis. The infection is associated with inflammation and sepsis, but little is known about the acute-phase response during disease and the nature of the bacterial factors causing it. In this study, we examined the levels of the acute-phase proteins (APPs) in comparative experiments using mice challenged with spores and a purified B. anthracis protease InhA as a possible factor mediating the response. A strong increase in the plasma levels of APPs such as haptoglobin and serum amyloid A was observed during infection. Protein and mRNA levels of plasminogen activator inhibitor (PAI)-1 in the liver were also increased concurrently with bacterial dissemination at 72 h post-infection. Similar effects were observed at 6 h post injection with InhA. Induction of hepatic transforming growth factor-beta1, a PAI-1 inducer, was also found in the liver of InhA-injected mice. PAI-1 elevation by InhA resulted in an increased level of urokinase-type plasminogen activator complex with PAI-1 and a decreased level of D-dimers indicating inhibition of blood fibrinolysis. These results reveal an acute liver response to anthrax infection and provide a plausible pathophysiological link between the host inflammatory response and the pro-thrombotic haemostatic imbalance in the course of disease through PAI-1 induction in the liver.

Publication types

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

MeSH terms

  • Acute-Phase Proteins / metabolism*
  • Animals
  • Anthrax / immunology
  • Anthrax / microbiology
  • Anthrax / physiopathology*
  • Bacillus anthracis / enzymology*
  • Bacillus anthracis / pathogenicity*
  • Bacillus anthracis / physiology
  • Bacterial Proteins / metabolism
  • Female
  • Haptoglobins / metabolism
  • Humans
  • Inflammation / immunology
  • Inflammation / microbiology
  • Liver / metabolism
  • Metalloproteases / metabolism*
  • Mice
  • Mice, Inbred DBA
  • Plasminogen Activator Inhibitor 1 / metabolism*
  • Spores, Bacterial / pathogenicity
  • Thrombosis / immunology
  • Thrombosis / microbiology
  • Up-Regulation*

Substances

  • Acute-Phase Proteins
  • Bacterial Proteins
  • Haptoglobins
  • Plasminogen Activator Inhibitor 1
  • Metalloproteases