Molecular Epidemiology ofngaand NAD Glycohydrolase/ADP‐Ribosyltransferase Activity amongStreptococcus pyogenesCausing Streptococcal Toxic Shock Syndrome
Author(s) -
Dennis L. Stevens,
Daniel B. Salmi,
Eric R. McIndoo,
Amy E. Bryant
Publication year - 2000
Publication title -
the journal of infectious diseases
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/315850
Subject(s) - streptococcus pyogenes , toxic shock syndrome , microbiology and biotechnology , streptococcus , superantigen , medicine , streptococcal infections , nad+ kinase , biology , virology , immunology , staphylococcus aureus , genetics , bacteria , enzyme , immune system , biochemistry , t cell
Severe invasive group A streptococcal (GAS) infections emerged in the late 1980s, yet no single virulence factor has been common to all isolates from infected patients. A strong association was recently found between isolates of such cases (regardless of M type) and the production of NAD glycohydrolase (NADase). Of interest, all M-1 strains isolated after 1988 were positive for NADase, whereas virtually all M-1 GAS were previously negative for NADase. Genetic analysis demonstrated that GAS isolates were >96% identical in nga and >99% identical in their upstream regulatory sequences. Furthermore, because NADase-negative strains did not produce immunoreactive NADase, we concluded that additional regulatory element(s) control NADase production. NADase purified from GAS altered neutrophil-directed migration and chemiluminescence responses and had potent ADP-ribosyltransferase activity. In summary, the temporal relationship of NADase expression, alone or with other streptococcal virulence factors, may contribute to the pathogenesis of invasive GAS infections.
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