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PMID: 8349810 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A novel superantigen isolated from pathogenic strains of Streptococcus pyogenes with aminoterminal homology to staphylococcal enterotoxins B and C.

The Journal of clinical investigation ·Vol. 92 ·No. 2 ·1993-08-00 ·Pages 710-9

Mollick JA, Miller GG, Musser JM, Cook RG, Grossman D, Rich RR

Abstract

Streptococcus pyogenes (group A Streptococcus) has re-emerged in recent years as a cause of severe human disease. Because extracellular products are involved in streptococcal pathogenesis, we explored the possibility that a disease isolate expresses an uncharacterized superantigen. We screened culture supernatants for superantigen activity with a major histocompatibility complex class II-dependent T cell proliferation assay. Initial fractionation with red dye A chromatography indicated production of a class II-dependent T cell mitogen by a toxic shock-like syndrome (TSLS) strain. The amino terminus of the purified streptococcal superantigen was more homologous to the amino termini of staphylococcal enterotoxins B, C1, and C3 (SEB, SEC1, and SEC3), than to those of pyrogenic exotoxins A, B, C or other streptococcal toxins. The molecule, designated SSA, had the same pattern of class II isotype usage as SEB in T cell proliferation assays. However, it differed in its pattern of human T cell activation, as measured by quantitative polymerase chain reaction with V beta-specific primers. SSA activated human T cells that express V beta 1, 3, 15 with a minor increase of V beta 5.2-bearing cells, whereas SEB activated V beta 3, 12, 15, and 17-bearing T cells. Immunoblot analysis of 75 disease isolates from several localities detected SSA production only in group A streptococci, and found that SSA is apparently confined to only three clonal lineages as defined by multilocus enzyme electrophoresis typing. Isolates of one of these lineages, (electrophoretic type 2) are strongly associated with TSLS. The data identify SSA as a novel streptococcal superantigen that appears to be more related structurally to staphylococcal enterotoxins than to streptococcal exotoxins. Because abundant SSA production is apparently confined to only three streptococcal clonal lineages, the data also suggest that the SSA gene has only recently been acquired by S. pyogenes.

MeSH Terms
Amino Acid Sequence Antibodies Antigens, Bacterial/biosynthesis,chemistry,immunology Chromatography, Affinity Electrophoresis, Polyacrylamide Gel Enterotoxins/chemistry,immunology HLA-D Antigens/immunology Humans Molecular Sequence Data Peptides/chemical synthesis,immunology Polymerase Chain Reaction/methods Sequence Homology, Amino Acid Staphylococcus aureus/chemistry Streptococcus pyogenes/immunology,isolation & purification,pathogenicity
Chemicals
Antibodies Antigens, Bacterial Enterotoxins HLA-D Antigens Peptides enterotoxin A, Staphylococcal enterotoxin C, staphylococcal
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Mollick J A
Department of Microbiology and Immunology, Baylor College of Medicine, Houston, Texas 77030.
Miller G G
Musser J M
Cook R G
Grossman D
Rich R R
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Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
0021-9738
Published
1993-08-00
Pages
710-9
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC294905
Subset
IM
Grants
NIAID NIH HHS · AI-15394 · United States
NIAID NIH HHS · AI-30036 · United States
NIDDK NIH HHS · DK41312 · United States
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