Analysis of nucleotide-binding oligomerization domain proteins in a murine model of pneumococcal meningitis

BMC Infect Dis. 2014 Dec 2:14:648. doi: 10.1186/s12879-014-0648-3.

Abstract

Background: The innate immune system recognizes pathogens via its pattern recognition receptors. The objective of this study was to investigate the role of the nucleotide-binding oligomerization domain (NOD) proteins, a family of the novel bacterial pattern recognition receptors, in host responses to the gram-positive bacteria Streptococcus pneumoniae.

Methods: Sprague-Dawley rats were infected via intracisternal injections of viable S. pneumoniae, and rats in the control group were injected with sterile saline. After infection, real-time PCR was performed to determine the presence of mRNAs encoding NOD1 and NOD2. Quantitative analyses of the NOD1, NOD2 and NF-kB proteins were also performed western blotting following challenge infections with viable S. pneumoniae. The TNF-α and IL-6 levels in brain homogenates were evaluated using enzyme-linked immunosorbent assays (ELISAs).

Results: The results revealed up-regulations of the mRNA and protein levels of NOD2 within the CNS of rats with S. pneumoniae meningitis. Moreover, the activation of NF-κB in the brain tissues following infection with live S. pneumoniae was also significantly increased, which indicates that NOD2 mediated NF-κB activation in experimental pneumococcal meningitis. Similarly, TNF-α and IL-6 levels were increased in the brain following in vivo S. pneumoniae administration.

Conclusions: These results suggest that NOD2 is involved in the host response to the gram-positive bacteria S. pneumoniae in the CNS and that NOD2 might play an important role in the initiation and/or progression of CNS inflammation associated with pneumococcal meningitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / metabolism
  • Brain / microbiology
  • Disease Models, Animal
  • Enzyme-Linked Immunosorbent Assay
  • Interleukin-6 / metabolism
  • Meningitis, Pneumococcal / metabolism
  • Meningitis, Pneumococcal / microbiology*
  • NF-kappa B / metabolism
  • Nod Signaling Adaptor Proteins / genetics
  • Nod Signaling Adaptor Proteins / metabolism*
  • Nod2 Signaling Adaptor Protein / genetics
  • Nod2 Signaling Adaptor Protein / metabolism
  • RNA, Messenger / analysis
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • Real-Time Polymerase Chain Reaction
  • Streptococcus pneumoniae / pathogenicity
  • Tumor Necrosis Factor-alpha / metabolism
  • Up-Regulation

Substances

  • Interleukin-6
  • NF-kappa B
  • NOD2 protein, rat
  • Nod Signaling Adaptor Proteins
  • Nod2 Signaling Adaptor Protein
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha