Frick Inga-Maria, Akesson Per, Rasmussen Magnus, Schmidtchen Artur, Björck Lars
Department of Cell and Molecular Biology, Lund University, S-221 85 Lund, Sweden.
J Biol Chem. 2003 May 9;278(19):16561-6. doi: 10.1074/jbc.M301995200. Epub 2003 Mar 5.
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.
重要的人类病原体化脓性链球菌的一些分离株,包括M1血清型的强毒株,会分泌蛋白SIC。这种大量分泌的分子会干扰补体功能。由于自然选择,SIC表现出高度的变异性。在此,我们对这种变异性以及M1血清型菌株是严重侵袭性化脓性链球菌感染最常见病因这一事实给出了一个合理的解释。因此,发现蛋白SIC可使人类中性粒细胞α-防御素和LL-37失活,这两种是参与细菌清除的主要抗菌肽。这种失活保护化脓性链球菌免受这些肽的抗菌作用。此外,从M1血清型化脓性链球菌中分离出的SIC在这方面比来自M12和M55血清型菌株的SIC变体更强,而M12和M55血清型很少与侵袭性感染相关。