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Infection and Immunity, March 2003, p. 1361-1369, Vol. 71, No. 3
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.3.1361-1369.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Two Novel Superantigens Found in Both Group A and Group C Streptococcus

Thomas Proft, Phillip D. Webb, Vanessa Handley, and John D. Fraser*

Department of Molecular Medicine and Pathology, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand

Received 16 July 2002/ Returned for modification 16 October 2002/ Accepted 21 November 2002

Two novel streptococcal superantigen genes (speLSe and speMSe) were identified from the Streptococcus equi genome database at the Sanger Center. Genotyping of 8 S. equi isolates and 40 Streptococcus pyogenes isolates resulted in the detection of the orthologous genes speL and speM in a restricted number of S. pyogenes isolates (15 and 5%, respectively). Surprisingly, the novel superantigen genes could not be found in any of the analyzed S. equi isolates. The results suggest that both genes are located on a mobile element that enables gene transfer between individual isolates and between streptococci from different Lancefield groups. S. equi pyrogenic exotoxin L (SPE-LSe)/streptococcal pyrogenic exotoxin L (SPE-L) and SPE-MSe/SPE-M are most closely related to SMEZ, SPE-C, SPE-G, and SPE-J, but build a separate branch within this group. Recombinant SPE-L (rSPE-L) and rSPE-M were highly mitogenic for human peripheral blood lymphocytes, with half-maximum responses at 1 and 10 pg/ml, respectively. The results from competitive binding experiments suggest that both proteins bind major histocompatibility complex class II at the ß-chain, but not at the {alpha}-chain. The most common targets for both toxins were human Vß1.1 expressing T cells. Seroconversion against SPE-L and SPE-M was observed in healthy blood donors, suggesting that the toxins are expressed in vivo. Interestingly, the speL gene is highly associated with S. pyogenes M89, a serotype that is linked to acute rheumatic fever in New Zealand.


* Corresponding author. Mailing address: Department of Molecular Medicine and Pathology, Faculty of Medical and Health Sciences, University of Auckland, Private Bag 92019, Auckland, New Zealand. Phone: 64-9-373-7599, ext. 6036. Fax: 64-9-373-7492. E-mail: jd.fraser{at}auckland.ac.nz.

Editor: V. J. DiRita


Infection and Immunity, March 2003, p. 1361-1369, Vol. 71, No. 3
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.3.1361-1369.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.




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