Abstract

The staphylococcal enterotoxin-like toxins (SETs) are a family of proteins encoded within the Staphylococcus aureus genome that were identified by their similarity to the well described bacterial superantigens. The first crystal structure of a member of the SET family, SET3, has been determined to 1.9 A (R = 0.205, R(free) = 0.240) and reveals a fold characteristic of the superantigen family but with significant differences. The SET proteins are secreted at varying levels by staphylococcal isolates, and seroconversion studies of normal individuals indicate that they are strongly antigenic to humans. Recombinant SETs do not exhibit any of the properties expected of superantigens such as major histocompatibility complex class II binding or broad T-cell activation, suggesting they have an entirely different function. The fact that the whole gene family is clustered within the pathogenicity island SaIn2 of the S. aureus genome suggests that they are involved in host/pathogen interactions.

Highlights

  • The bacterial superantigen (SAg)1 family is a large protein family exclusive to three pathogenic species: Staphylococcus aureus, Streptococcus pyogenes, and Streptococcus equi

  • The fact that the whole gene family is clustered within the pathogenicity island SaIn2 of the S. aureus genome suggests that they are involved in host/ pathogen interactions

  • SET3 and toxic shock syndrome toxin (TSST) form an out-group from the remainder of the SAg-like proteins such that if these two structures are omitted from the alignment, 113 residues share equivalent C␣ positions and 16 residues are conserved in the sequence

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Summary

Introduction

The bacterial superantigen (SAg)1 family is a large protein family exclusive to three pathogenic species: Staphylococcus aureus, Streptococcus pyogenes, and Streptococcus equi. The staphylococcal enterotoxin-like toxins (SETs) are a family of proteins encoded within the Staphylococcus aureus genome that were identified by their similarity to the well described bacterial superantigens.

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