Literature DB >> 12621031

SIC, a secreted protein of Streptococcus pyogenes that inactivates antibacterial peptides.

Inga-Maria Frick1, Per Akesson, Magnus Rasmussen, Artur Schmidtchen, Lars Björck.   

Abstract

Some isolates of the significant human pathogen Streptococcus pyogenes, including virulent strains of the M1 serotype, secrete protein SIC. This molecule, secreted in large quantities, interferes with complement function. As a result of natural selection, SIC shows a high degree of variation. Here we provide a plausible explanation for this variation and the fact that strains of the M1 serotype are the most frequent cause of severe invasive S. pyogenes infections. Thus, protein SIC was found to inactivate human neutrophil alpha-defensin and LL-37, two major antibacterial peptides involved in bacterial clearance. This inactivation protected S. pyogenes against the antibacterial effect of the peptides. Moreover, SIC isolated from S. pyogenes of the M1 serotype was more powerful in this respect than SIC variants from strains of M serotypes 12 and 55, serotypes rarely connected with invasive infections.

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Year:  2003        PMID: 12621031     DOI: 10.1074/jbc.M301995200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  58 in total

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Review 8.  Bacterial resistance mechanisms against host defense peptides.

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9.  Protective mechanisms of respiratory tract Streptococci against Streptococcus pyogenes biofilm formation and epithelial cell infection.

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Review 10.  Host defense peptides as effector molecules of the innate immune response: a sledgehammer for drug resistance?

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