Enterotoxin type B

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Enterotoxin type B
Identifiers
Organism Staphylococcus aureus
Symbol entB
UniProt P01552
Staphylococcal/Streptococcal toxin, N-terminal domain
PDB 1eu4 EBI.jpg
Crystal structure of the superantigen Spe-H (zinc bound) from Streptococcus pyogenes
Identifiers
Symbol Staphylococcal/Streptococcal toxin, N-terminal domain
Pfam PF01123
InterPro IPR006173
PROSITE PDOC00250
SCOP 1se3
SUPERFAMILY 1se3
Staphylococcal/Streptococcal toxin, beta-grasp domain
Identifiers
Symbol Stap_Strp_tox_C
Pfam PF02876
InterPro IPR006123
PROSITE PDOC00250
SCOP 1se3
SUPERFAMILY 1se3

In the field of molecular biology, enterotoxin type B, also known as Staphylococcal enterotoxin B (SEB), is an enterotoxin produced by the gram-positive bacteria Staphylococcus aureus. It is a common cause of food poisoning, with severe diarrhea, nausea and intestinal cramping often starting within a few hours of ingestion.[1] Being quite stable,[2] the toxin may remain active even after the contaminating bacteria are killed. It can withstand boiling at 100 °C for a few minutes.[1] Gastroenteritis occurs because SEB is a superantigen, causing the immune system to release a large amount of cytokines that lead to significant inflammation.

Additionally, this protein is the causative agent of toxic shock syndrome.

Function

The function of this protein is to facilitate the infection of the host organism. It is a virulence factor designed to induce pathogenesis.[3] One of the major virulence exotoxins is the toxic shock syndrome toxin (TSST), which is secreted by the organism upon successful invasion. It causes a major inflammatory response in the host via superantigenic properties, and is the causative agent of toxic shock syndrome. It functions as a superantigen through activation of a significant fraction of T-cells (up to 20%) by cross-linking MHC class II molecules with T-cell receptors. TSST is a multisystem illness with several symptoms such as high fever, hypotension, dizziness, rash and peeling skin.[3]

Structure

All of these toxins share a similar two-domain fold (N and C-terminal domains) with a long alpha-helix in the middle of the molecule, a characteristic beta-barrel known as the "oligosaccharide/oligonucleotide fold" at the N-terminal domain and a beta-grasp motif at the C-terminal domain. Each superantigen possesses slightly different binding mode(s) when it interacts with MHC class II molecules or the T-cell receptor.[4]

N-terminal domain

The N-terminal domain is also referred to as OB-fold, or in other words the oligonuclucleotide binding fold. This region contains a low-affinity major histocompatibility complex class II (MHC II) site which causes an inflammatory response.[5]

The N-terminal domain contains regions involved in Major Histocompatibility Complex class II association. It is a five stranded beta barrel that forms an OB fold.[6][7][8]

C-terminal domain

The beta-grasp domain has some structural similarities to the beta-grasp motif present in immunoglobulin-binding domains, ubiquitin, 2Fe-2 S ferredoxin and translation initiation factor 3 as identified by the SCOP database.

References

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This article incorporates text from the public domain Pfam and InterPro IPR006123 This article incorporates text from the public domain Pfam and InterPro IPR006173