Differential gene expression in gram-negative and gram-positive sepsis

Am J Respir Crit Care Med. 2004 May 15;169(10):1135-43. doi: 10.1164/rccm.200211-1278OC. Epub 2004 Mar 4.

Abstract

Sepsis is the most common cause of death in patients in the intensive care unit. Genome-wide gene expression analysis can provide insights into the molecular alterations of sepsis. Total mRNA was extracted from the livers of 6 uninfected control mice and 60 septic mice after infusion of either live Escherichia coli or Staphylococcus aureus. Using a murine complementary DNA microarray system, changes in gene expression were monitored at six time points (uninfected, 2, 8, 24, 48, and 72 hours). Overall, 4.8% of 6,144 assessed genes were differentially regulated with a greater than twofold change across all time points. Most of the genes with altered expression were commonly present in gram-negative and gram-positive sepsis, but the expression levels of 17 genes were different between both types of sepsis at particular time points after infection. The microarray results support the hypothesis that both gram-positive and gram-negative sepsis share a final common pathway involved in the pathogenesis of sepsis, but certain genes are differentially expressed under distinct regulation. These results may provide insights into the pathogenesis of sepsis and may also help identify some altered genes that can serve as new targets for diagnostic tools and therapeutic strategies.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Apoptosis / genetics
  • Bacteremia / genetics*
  • Blotting, Northern
  • Disease Models, Animal
  • Escherichia coli / genetics
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation, Bacterial*
  • Genes, Bacterial*
  • Gram-Negative Bacterial Infections / genetics*
  • Gram-Positive Bacterial Infections / genetics*
  • Mice
  • Mice, Inbred BALB C
  • Oligonucleotide Array Sequence Analysis
  • Probability
  • RNA, Messenger / analysis
  • Sensitivity and Specificity
  • Staphylococcus aureus / genetics

Substances

  • RNA, Messenger