Artigo Acesso aberto Revisado por pares

The Classical Lancefield Antigen of Group A Streptococcus Is a Virulence Determinant with Implications for Vaccine Design

2014; Cell Press; Volume: 15; Issue: 6 Linguagem: Inglês

10.1016/j.chom.2014.05.009

ISSN

1934-6069

Autores

Nina M. van Sorge, Jason N. Cole, Kirsten Kuipers, Anna Henningham, Ramy K. Aziz, Ana Kasirer‐Friede, Leo Lin, Evelien T.M. Berends, Mark R. Davies, Gordon Dougan, Fan Zhang, Samira Dahesh, Laura Shaw, Jennifer Gin, Madeleine W. Cunningham, Joseph A. Merriman, Julia Hütter, Bernd Lepenies, Suzan H. M. Rooijakkers, Richard Malley, Mark J. Walker, Sanford J. Shattil, Patrick M. Schlievert, Biswa Choudhury, Victor Nizet,

Tópico(s)

Neonatal and Maternal Infections

Resumo

Group A Streptococcus (GAS) is a leading cause of infection-related mortality in humans. All GAS serotypes express the Lancefield group A carbohydrate (GAC), comprising a polyrhamnose backbone with an immunodominant N-acetylglucosamine (GlcNAc) side chain, which is the basis of rapid diagnostic tests. No biological function has been attributed to this conserved antigen. Here we identify and characterize the GAC biosynthesis genes, gacA through gacL. An isogenic mutant of the glycosyltransferase gacI, which is defective for GlcNAc side-chain addition, is attenuated for virulence in two infection models, in association with increased sensitivity to neutrophil killing, platelet-derived antimicrobials in serum, and the cathelicidin antimicrobial peptide LL-37. Antibodies to GAC lacking the GlcNAc side chain and containing only polyrhamnose promoted opsonophagocytic killing of multiple GAS serotypes and protected against systemic GAS challenge after passive immunization. Thus, the Lancefield antigen plays a functional role in GAS pathogenesis, and a deeper understanding of this unique polysaccharide has implications for vaccine development.

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