Translocation of bacterial DNA from Gram-positive microorganisms is associated with a species-specific inflammatory response in serum and ascitic fluid of patients with cirrhosis

Clin Exp Immunol. 2007 Nov;150(2):230-7. doi: 10.1111/j.1365-2249.2007.03494.x. Epub 2007 Sep 5.

Abstract

Translocation of bacterial-DNA in patients with cirrhosis and ascites triggers an innate immune response. Identification of characteristics to which this response is sensitive is relevant from a clinical standpoint. The aim of this study has been to determine if the proinflammatory immune response established in vivo in cirrhotic patients with ascites as a consequence of bacterial-DNA translocation is related to the identified bacterial species and their frequency of cytosine-guanosine content in serum and ascitic fluid. Patients with advanced cirrhosis and ascites were included in the study and distributed into groups I and II according to the absence or presence of bacterial-DNA translocation, respectively. Serum and ascitic fluid levels of proinflammatory cytokines after normalization of bacterial-DNA concentration and the activated form of nuclear factor-kappa B in ascitic fluid pellets were measured by enzyme-linked immunosorbent assay techniques. Translocation of bacterial-DNA with higher cytosine-guanosine content induced the highest cytokine response, which was higher than that in patients without bacterial-DNA translocation. The activated form of nuclear factor-kappa B in ascitic fluid pellets of patients with bacterial-DNA translocation was greater in patients with higher bacterial-DNA cytosine-guanosine content, whereas the amount of total nuclear factor-kappa B remained unaltered. Bacterial-DNA translocation induces a marked immune reaction in vivo in patients with advanced cirrhosis and ascites which is related, among other factors, to the bacterial-DNA cytosine-guanosine content. Therefore, the host's immune response to bacterial-DNA translocation constitutes a species-specific phenomenon.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Ascitic Fluid / immunology
  • Ascitic Fluid / microbiology*
  • Bacterial Translocation*
  • DNA, Bacterial / analysis
  • Female
  • Gram-Positive Bacteria / genetics
  • Gram-Positive Bacteria / physiology*
  • Humans
  • Inflammation / immunology
  • Inflammation / microbiology
  • Liver Cirrhosis / immunology
  • Liver Cirrhosis / microbiology*
  • Male
  • Middle Aged
  • NF-kappa B / metabolism
  • Neutrophils / immunology
  • Prospective Studies
  • Signal Transduction
  • Species Specificity
  • Th1 Cells / immunology

Substances

  • DNA, Bacterial
  • NF-kappa B