The effects of infection of thermal injury by Pseudomonas aeruginosa PAO1 on the murine cytokine response.

Abstract

Pseudomonas aeruginosa infection, one of the major complications of burn wounds, may lead to sepsis and death. Using the Multi-Probe Template/RNase protection assay, we have compared the expression of different cytokine genes within the skin and livers of thermally injured mice infected with P. aeruginosa PAO1. Thermal injury alone enhanced or up-regulated certain cytokines, including macrophage colony-stimulating factor (M-CSF), interleukin 1 (IL-1)RI, IL-1 beta, macrophage inflammatory protein (MIP)-1 beta and MIP-2; while PAO1 challenge alone up-regulated tumour necrosis factor alpha (TNF-alpha) and transforming growth factor beta (TGF-beta) expression. The combination of thermal injury plus PAO1 infection enhanced the expression of several pro-inflammatory and haematopoietic cytokines [stem cell factor (SCF), leukocyte inhibitory factor (LIF), IL-6 and TNF-alpha]; induced the expression of granulocyte-macrophage colony-stimulating factor (GM-CSF) and G-CSF by 5 h and the expression of additional cytokines, including TGF-beta, TNF-beta, lymphotoxin beta (LT-beta), interferon gamma (IFN-gamma), and IFN-beta by 40 h post-burn/infection. While the most intense cytokine expression occurred in the skin, the majority of cytokines tested were also expressed in the liver by 40 h post-burn/infection. These results suggest that in P. aeruginosa infection of burn wounds: (1) up-regulation of the expression of different cytokines, locally and within the livers of burned mice, is an indication of P. aeruginosa -induced sepsis; and (2) IL-6 and G-CSF play an important role in the host response mechanism.

• Authors: K P Rumbaugh, J A Colmer, J A Griswold, A N Hamood
• Journal: Cytokine (Cytokine) Vol. 16 Issue 4 Pg. 160-8 (Nov 21 2001) ISSN: 1043-4666 [Print] England
• PMID: 11792126 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright 2001 Academic Press.

Chemical References

• Cytokines
• Interleukin-6
• Interleukins
• Transforming Growth Factor beta
• Tumor Necrosis Factor-alpha
• Granulocyte Colony-Stimulating Factor
• Macrophage Colony-Stimulating Factor

Topics

• Animals
• Burns (complications, genetics, immunology)
• Cytokines (genetics)
• Female
• Gene Expression Profiling
• Granulocyte Colony-Stimulating Factor (genetics)
• Interleukin-6 (genetics)
• Interleukins (genetics)
• Liver (immunology)
• Macrophage Colony-Stimulating Factor (genetics)
• Mice
• Mice, Inbred C57BL
• Pseudomonas Infections (etiology, genetics, immunology)
• Sepsis (etiology, genetics, immunology)
• Skin (immunology)
• Transforming Growth Factor beta (genetics)
• Tumor Necrosis Factor-alpha (genetics)
• Up-Regulation