The role of bacterial DNA in septic arthritis.

  • Authors:
    • G M Deng
    • A Tarkowski
  • View Affiliations

  • Published online on: July 1, 2000     https://doi.org/10.3892/ijmm.6.1.29
  • Pages: 29-62
Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

Unmethylated CpG motifs are frequently found in bacterial DNA and have recently been shown to exert immunostimulatory effects on leukocytes. Bacteria produce severe septic arthritis; bacterial DNA may be involved in this process. We injected intraarticularly bacterial DNA and oligonucleotides containing unmethylated CpG motifs into knee joints of mice. Arthritis was seen by histopathology within 2 h and lasted for at least 14 days, and was characterized by an influx of monocytic, Mac-1+ cells and by a lack of T lymphocytes. Macrophages and their products such as tumor necrosis factor (TNF) alpha are essential for development of arthritis triggered by bacterial DNA containing CpG motifs. In contrast, neurophils, NK cells, and T/B cells were not instrumental in this condition. This review demonstrates that bacterial DNA containing unmethylated CpG motifs induces arthritis and indicates an important pathogenic role for bacterial DNA in septic arthritis.

Related Articles

Journal Cover

Jul 2000
Volume 6 Issue 1

Print ISSN: 1107-3756
Online ISSN:1791-244X

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
Deng G and Deng G: The role of bacterial DNA in septic arthritis.. Int J Mol Med 6: 29-62, 2000
APA
Deng, G., & Deng, G. (2000). The role of bacterial DNA in septic arthritis.. International Journal of Molecular Medicine, 6, 29-62. https://doi.org/10.3892/ijmm.6.1.29
MLA
Deng, G., Tarkowski, A."The role of bacterial DNA in septic arthritis.". International Journal of Molecular Medicine 6.1 (2000): 29-62.
Chicago
Deng, G., Tarkowski, A."The role of bacterial DNA in septic arthritis.". International Journal of Molecular Medicine 6, no. 1 (2000): 29-62. https://doi.org/10.3892/ijmm.6.1.29