The Pseudomonas secretory product pyocyanin inhibits catalase activity in human lung epithelial cells

Am J Physiol Lung Cell Mol Physiol. 2003 Nov;285(5):L1077-86. doi: 10.1152/ajplung.00198.2003. Epub 2003 Jul 18.


Pyocyanin, produced by Pseudomonas aeruginosa, has many deleterious effects on human cells that relate to its ability to generate reactive oxygen species (ROS), such as superoxide and hydrogen peroxide. Human cells possess several mechanisms to protect themselves from ROS, including manganese superoxide dismutase (MnSOD), copper zinc superoxide dismutase (CuZnSOD), and catalase. Given the link between pyocyanin-mediated epithelial cell injury and oxidative stress, we assessed pyocyanin's effect on MnSOD, CuZnSOD, and catalase levels in the A549 human alveolar epithelial cell line and in normal human bronchial epithelial cells. In both cell types, CuZnSOD and MnSOD were unaltered, but over 24 h pyocyanin significantly decreased cellular catalase activity and protein content. Pyocyanin also decreased catalase mRNA. Overexpression of MnSOD in A549 cells prevented pyocyanin-mediated loss of catalase protein, but catalase activity still declined. Furthermore, pyocyanin decreased catalase activity, but not protein, in A549 cells overexpressing human catalase. These data suggest a direct effect of pyocyanin on catalase activity. Addition of pyocyanin to catalase in a cell-free system also decreased catalase activity. Mammalian catalase binds four NADPH molecules, helping maintain enzyme activity. Spin-trapping data suggest that pyocyanin directly oxidizes this NADPH, producing superoxide. We conclude that pyocyanin may decrease cellular catalase activity via both transcriptional regulation and direct inactivation of the enzyme. Decreased cellular catalase activity and failure to augment MnSOD could contribute to pyocyanin-dependent cytotoxicity.

Publication types

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

MeSH terms

  • Binding Sites
  • Bronchi / enzymology
  • Catalase / antagonists & inhibitors*
  • Catalase / genetics
  • Cell Line
  • Enzyme Inhibitors / pharmacology*
  • Humans
  • Isoenzymes / antagonists & inhibitors
  • Isoenzymes / genetics
  • Lung / enzymology*
  • NADP / metabolism
  • Oxidation-Reduction
  • Pseudomonas aeruginosa
  • Pulmonary Alveoli / enzymology
  • Pyocyanine / pharmacology*
  • Reactive Oxygen Species
  • Respiratory Mucosa / enzymology*
  • Transcription, Genetic / drug effects


  • Enzyme Inhibitors
  • Isoenzymes
  • Reactive Oxygen Species
  • NADP
  • Pyocyanine
  • Catalase