Structure and biological activities of beta toxin from Staphylococcus aureus.

Abstract

Beta toxin is a neutral sphingomyelinase secreted by certain strains of Staphylococcus aureus. This virulence factor lyses erythrocytes in order to evade the host immune system as well as scavenge nutrients. The structure of beta toxin was determined at 2.4-A resolution using crystals that were merohedrally twinned. This structure is similar to that of the sphingomyelinases of Listeria ivanovii and Bacillus cereus. Beta toxin belongs to the DNase I folding superfamily; in addition to sphingomyelinases, the proteins most structurally related to beta toxin include human endonuclease HAP1, Escherichia coli endonuclease III, bovine pancreatic DNase I, and the endonuclease domain of TRAS1 from Bombyx mori. Our biological assays demonstrated for the first time that beta toxin kills proliferating human lymphocytes. Structure-directed active site mutations show that biological activities, including hemolysis and lymphotoxicity, are due to the sphingomyelinase activity of the enzyme.

• Authors: Medora Huseby, Ke Shi, C Kent Brown, Jeff Digre, Fikre Mengistu, Keun Seok Seo, Gregory A Bohach, Patrick M Schlievert, Douglas H Ohlendorf, Cathleen A Earhart
• Journal: Journal of bacteriology (J Bacteriol) Vol. 189 Issue 23 Pg. 8719-26 (Dec 2007) ISSN: 1098-5530 [Electronic] United States
• PMID: 17873030 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)

Chemical References

• Bacterial Toxins
• Hemolysin Proteins
• Sphingomyelin Phosphodiesterase
• hlb protein, Staphylococcus aureus

Topics

• Amino Acid Sequence
• Bacterial Toxins (chemistry, genetics, metabolism, pharmacology)
• Binding Sites
• Cell Proliferation (drug effects, radiation effects)
• Cells, Cultured
• Dose-Response Relationship, Drug
• Hemolysin Proteins (chemistry, genetics, metabolism, pharmacology)
• Humans
• Lymphocytes (drug effects)
• Models, Molecular
• Molecular Sequence Data
• Protein Conformation
• Sphingomyelin Phosphodiesterase (chemistry, genetics, metabolism, pharmacology)
• Staphylococcus aureus (chemistry, genetics)