The inflammatory cytokine response to Chlamydia trachomatis infection is endotoxin mediated
- PMID: 7542638
- PMCID: PMC173426
- DOI: 10.1128/iai.63.8.3125-3130.1995
The inflammatory cytokine response to Chlamydia trachomatis infection is endotoxin mediated
Abstract
Chlamydia trachomatis is a major etiologic agent of sexually transmitted diseases. Although C. trachomatis is a gram-negative pathogen, chlamydial infections are not generally thought of as endotoxin-mediated diseases. A molecular characterization of the acute immune response to chlamydia, especially with regard to the role of its lipopolysaccharide (LPS), remains to be undertaken. We extracted 15 mg of LPS from 5 x 10(12) C. trachomatis elementary bodies (EB) for analysis of structure and biological activity. When methylated lipid A was subjected to high-pressure liquid chromatography followed by mass spectrometry, the majority of the lipid A was found to be pentaacyl. The endotoxin activities of whole C. trachomatis EB and purified LPS were characterized in comparison with whole Salmonella minnesota R595 and with S. minnesota R595 LPS and lipooligosaccharide from Neisseria gonorrhoeae. Both C. trachomatis LPS and whole EB induced the release of tumor necrosis factor alpha from whole blood ex vivo, and C. trachomatis LPS was capable of inducing the translocation of nuclear factor kappa B in a Chinese hamster ovary fibroblast cell line transfected with the LPS receptor CD14. In both assays, however, C. trachomatis was approximately 100-fold less potent than S. minnesota and N. gonorrhoeae. The observation that C. trachomatis is a weak inducer of the inflammatory cytokine response correlates with the clinical observation that, unlike N. gonorrhoeae infection, genital tract infection with C. trachomatis is often asymptomatic. The ability of specific LPS antagonists to completely inhibit the tumor necrosis factor alpha-inducing activity of whole C. trachomatis EB suggests that the inflammatory cytokine response to chlamydia infection may be mediated primarily through LPS. This implies that the role of other surface protein antigens, at least in terms of eliciting the proinflammatory cytokine response, is likely to be minor.
Similar articles
-
The proinflammatory cytokine response to Chlamydia trachomatis elementary bodies in human macrophages is partly mediated by a lipoprotein, the macrophage infectivity potentiator, through TLR2/TLR1/TLR6 and CD14.J Immunol. 2008 Jan 15;180(2):1158-68. doi: 10.4049/jimmunol.180.2.1158. J Immunol. 2008. PMID: 18178856
-
Endotoxic activity and chemical structure of lipopolysaccharides from Chlamydia trachomatis serotypes E and L2 and Chlamydophila psittaci 6BC.Eur J Biochem. 2003 Feb;270(3):440-50. doi: 10.1046/j.1432-1033.2003.03392.x. Eur J Biochem. 2003. PMID: 12542694
-
Chlamydia trachomatis Lipopolysaccharide Evades the Canonical and Noncanonical Inflammatory Pathways To Subvert Innate Immunity.mBio. 2019 Apr 23;10(2):e00595-19. doi: 10.1128/mBio.00595-19. mBio. 2019. PMID: 31015326 Free PMC article.
-
The role of CD14 and lipopolysaccharide-binding protein (LBP) in the activation of different cell types by endotoxin.Med Microbiol Immunol. 1994 Dec;183(6):279-97. doi: 10.1007/BF00196679. Med Microbiol Immunol. 1994. PMID: 7541105 Review. No abstract available.
-
Chlamydia trachomatis infection of the male genital tract: an update.J Reprod Immunol. 2013 Nov;100(1):37-53. doi: 10.1016/j.jri.2013.05.002. Epub 2013 Jul 16. J Reprod Immunol. 2013. PMID: 23870458 Review.
Cited by
-
Differential regulation of CD4 lymphocyte recruitment between the upper and lower regions of the genital tract during Chlamydia trachomatis infection.Infect Immun. 2000 Mar;68(3):1519-28. doi: 10.1128/IAI.68.3.1519-1528.2000. Infect Immun. 2000. PMID: 10678969 Free PMC article.
-
Heterogeneity of Lipopolysaccharide as Source of Variability in Bioassays and LPS-Binding Proteins as Remedy.Int J Mol Sci. 2023 May 7;24(9):8395. doi: 10.3390/ijms24098395. Int J Mol Sci. 2023. PMID: 37176105 Free PMC article. Review.
-
TargeTron Inactivation of Chlamydia trachomatis gseA Results in a Lipopolysaccharide 3-Deoxy-d-Manno-Oct-2-Ulosonic Acid-Deficient Strain That Is Cytotoxic for Cells.Infect Immun. 2023 Jul 18;91(7):e0009623. doi: 10.1128/iai.00096-23. Epub 2023 May 31. Infect Immun. 2023. PMID: 37255490 Free PMC article.
-
Toll-like receptor 2-dependent activity of native major outer membrane protein proteosomes of Chlamydia trachomatis.Infect Immun. 2013 Jan;81(1):303-10. doi: 10.1128/IAI.01062-12. Epub 2012 Nov 6. Infect Immun. 2013. PMID: 23132491 Free PMC article.
-
Host cell death during infection with Chlamydia: a double-edged sword.FEMS Microbiol Rev. 2021 Jan 8;45(1):fuaa043. doi: 10.1093/femsre/fuaa043. FEMS Microbiol Rev. 2021. PMID: 32897321 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Research Materials