Staphylococcal enterotoxin microbial superantigens
- PMID: 1916093
- DOI: 10.1096/fasebj.5.12.1916093
Staphylococcal enterotoxin microbial superantigens
Abstract
Staphylococcal enterotoxins are a family of structurally related proteins that are produced by Staphylococcus aureus. In addition to their role in the pathogenicity of food poisoning, these microbial superantigens have profound effects on the immune system, which makes them useful tools for understanding its mechanism of action. These molecules (24-30 kDa) are highly hydrophilic and exhibit low alpha helix and high beta pleated sheet content, suggesting a flexible, accessible structure. Staphylococcal enterotoxins are among the most potent activators of T lymphocytes known. The receptors for staphylococcal enterotoxins on antigen-presenting cells are major histocompatibility complex (MHC) class II molecules. Further, the alpha-helical regions of the class II molecule are essential for function and appear to interact directly with the NH2-terminal region of staphylococcal enterotoxins such as SEA. Recent studies have shown that a complex of staphylococcal enterotoxin and MHC class II molecules is required for binding to the V beta region of the T cell antigen receptor. Staphylococcal enterotoxin mitogenic activity is dependent on induction of interleukin 2, which may be intimately involved in the mechanism of toxicity. The mouse minor lymphocyte stimulating (M1s) "endogenous" self-superantigen has been shown to be a retroviral gene product, so this too is apparently a microbial superantigen. An understanding of the mechanisms of action of these microbial superantigens has implications for normal and pathological immune functions.
Similar articles
-
Staphylococcal enterotoxin superantigens.Proc Soc Exp Biol Med. 1991 Dec;198(3):765-71. doi: 10.3181/00379727-198-43321a. Proc Soc Exp Biol Med. 1991. PMID: 1946470 Review.
-
Crystal structure of microbial superantigen staphylococcal enterotoxin B at 1.5 A resolution: implications for superantigen recognition by MHC class II molecules and T-cell receptors.J Mol Biol. 1998 Mar 20;277(1):61-79. doi: 10.1006/jmbi.1997.1577. J Mol Biol. 1998. PMID: 9514739
-
The crystal structure of staphylococcal enterotoxin H: implications for binding properties to MHC class II and TcR molecules.J Mol Biol. 2000 Sep 22;302(3):527-37. doi: 10.1006/jmbi.2000.4093. J Mol Biol. 2000. PMID: 10986116
-
Immunopharmacology of the superantigen staphylococcal enterotoxin A in T-cell receptor V beta 3 transgenic mice.Immunology. 1993 Aug;79(4):520-7. Immunology. 1993. PMID: 7691731 Free PMC article.
-
Superantigens: interaction of staphylococcal enterotoxins with MHC class II molecules.Trans Am Clin Climatol Assoc. 1990;101:195-204; discussion 204-6. Trans Am Clin Climatol Assoc. 1990. PMID: 2577245 Free PMC article. Review.
Cited by
-
Accelerated induction of experimental allergic encephalomyelitis in PL/J mice by a non-V beta 8-specific superantigen.Proc Natl Acad Sci U S A. 1995 Jun 20;92(13):6082-6. doi: 10.1073/pnas.92.13.6082. Proc Natl Acad Sci U S A. 1995. PMID: 7541140 Free PMC article.
-
Enterotoxigenic potential of coagulase-negative staphylococci.Int J Food Microbiol. 2013 Apr 15;163(1):34-40. doi: 10.1016/j.ijfoodmicro.2013.02.005. Epub 2013 Feb 16. Int J Food Microbiol. 2013. PMID: 23500613 Free PMC article. Review.
-
A novel approach for cancer immunotherapy: tumor cells with anchored superantigen SEA generate effective antitumor immunity.J Clin Immunol. 2004 May;24(3):294-301. doi: 10.1023/B:JOCI.0000025451.41948.94. J Clin Immunol. 2004. PMID: 15114060
-
In vitro biological activities of transmembrane superantigen staphylococcal enterotoxin A fusion protein.Cancer Immunol Immunother. 2004 Feb;53(2):118-24. doi: 10.1007/s00262-003-0437-0. Epub 2003 Oct 22. Cancer Immunol Immunother. 2004. PMID: 14574492 Free PMC article.
-
Enteric bacterial toxins: mechanisms of action and linkage to intestinal secretion.Microbiol Rev. 1996 Mar;60(1):167-215. doi: 10.1128/mr.60.1.167-215.1996. Microbiol Rev. 1996. PMID: 8852900 Free PMC article. Review. No abstract available.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials