Volume 151, Issue 1 pp. 65-70

M protein mediated adhesion of M type 24 Streptococcus pyogenes stimulates release of interleukin-6 by HEp-2 tissue culture cells

Harry S Courtney

Corresponding Author

Harry S Courtney

Veterans Affairs Medical Center, University of Tennessee, Memphis, TN, USA

Department of Medicine, University of Tennessee, Memphis, TN, USA

Corresponding author. Veterans Affairs Medical Center, University of Tennessee, Research Service (151), 1030 Jefferson Avenue, Memphis, TN, USA. Fax: +1 (901) 577-7273; e-mail: [email protected]Search for more papers by this author
Itzhak Ofek

Itzhak Ofek

Department of Human Microbiology, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel

Search for more papers by this author
David L Hasty

David L Hasty

Veterans Affairs Medical Center, University of Tennessee, Memphis, TN, USA

Department of Anatomy and Neurobiology, University of Tennessee, Memphis, TN, USA

Search for more papers by this author
First published: 17 January 2006
Citations: 17

Abstract

We investigated the contributions of lipoteichoic acid and M protein to reversible and irreversible adhesion of group A streptococci and the effects of such adhesion on release of interleukin-6. Streptococci in which lipoteichoic acid was masked by the hyaluronate capsule were readily washed from HEp-2 cells, indicating no attachment. Unencapsulated, M-negative streptococci in which lipoteichoic acid was exposed were removed more slowly, indicating loose attachment. Only unencapsulated streptococci that expressed both lipoteichoic acid and M protein remained stably adherent to HEp-2 cells throughout multiple washes. Streptococci expressing both M protein and lipoteichoic acid induced release of interleukin-6 from HEp-2 cells, whereas an isogenic, M-negative mutant failed to induce release of interleukin-6. These data suggest that lipoteichoic acid mediates reversible adhesion and that M protein is required for irreversible adhesion and for inducing release of interleukin-6 from HEp-2 cells.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.