Geographic and Temporal Distribution and Molecular Characterization of Two Highly Pathogenic Clones of Streptococcus pyogenes Expressing Allelic Variants of Pyrogenic Exotoxin A (Scarlet Fever Toxin)

The molecular population genetics and pathogenic potential of North American and European invasive strains of Streptococcus pyogenes were assessed. Isolates from recent invasive infections and from infections in the 1920s and 1930s were characterized for multilocus enzyme genotype and allelic variat...

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Published inThe Journal of infectious diseases Vol. 167; no. 2; pp. 337 - 346
Main Authors Musser, James M., Kapur, Vivek, Kanjilal, Sagarika, Shah, Uma, Musher, Daniel M., Barg, Neil L., Johnston, Kenneth H., Schlievert, Patrick M., Henrichsen, Jorgen, Gerlach, Dieter, Rakita, Robert M., Tanna, Asha, Cookson, Barry D., Huang, Jay C.
Format Journal Article
LanguageEnglish
Published Chicago, IL The University of Chicago Press 01.02.1993
University of Chicago Press
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Summary:The molecular population genetics and pathogenic potential of North American and European invasive strains of Streptococcus pyogenes were assessed. Isolates from recent invasive infections and from infections in the 1920s and 1930s were characterized for multilocus enzyme genotype and allelic variation in the gene (speA) that encodes streptococcal pyrogenic exotoxin (SPE) A (scarlet fever toxin). A subset of strains was studied for allelic variation in genes that encode SPE B and streptokinase. All contemporary strains assigned to electrophoretic types (ETs) 1 and 2 that synthesize SPE A have the speA2 and speA3 allelic variants, respectively, and their relative virulence in two mouse models is similar to that of strains of the same ET and M protein types recovered earlier. In contrast, ET 1 and 2 isolates from disease episodes in the 1920s and 1930s contain the speA1 allele. The data suggest there may be temporal and geographic variation in the occurrence of clone-virulence factor allele combinations, an observation that may in part explain fluctuations in disease frequency, severity, and character.
Bibliography:Reprints, correspondence, or complete list of organisms studied: Dr. James M. Musser, Department of Pathology, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030.
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ISSN:0022-1899
1537-6613
DOI:10.1093/infdis/167.2.337