Groupe de Recherche en Écologie Buccale (GREB), Faculté de Médecine Dentaire, Université Laval, Quebec City, Quebec, Canada.
Centre de Recherche en Infectiologie Porcine (CRIP), Fonds de Recherche du Québec - Nature et Technologies (FRQNT), Quebec City, Quebec, Canada.
J Med Microbiol. 2013 Jul;62(Pt 7):1073-1080. doi: 10.1099/jmm.0.057877-0. Epub 2013 Apr 25.
Streptococcus suis is a major swine pathogen and an emerging zoonotic agent. The ability of pathogenic bacteria to bind the complement regulator factor H on their cell surface may allow them to avoid complement attack and phagocytosis. The aim of this study was to characterize a new cell surface protein possessing factor H-binding activity in S. suis serotype 2. The capacity of S. suis to bind the complement regulator factor H on its surface was demonstrated by ELISA. Using a factor I-cofactor assay, it was found that the functional activity of factor H bound to S. suis was kept. Since the product of gene SSU0186 in S. suis P1/7 shared similarity with a Streptococcus pneumoniae protein (named PspC) possessing factor H-binding activity, it was proposed as a putative factor H receptor in S. suis. SSU0186 has a 1686 bp open reading frame encoding a 561 amino acid protein containing the Gram-positive cell wall anchoring motif (LPXTG) at the carboxy-terminal, an amino-terminal signal sequence, an α-helix domain, a proline-rich region and a G5 domain. The SSU0186 gene was cloned in Escherichia coli and the purified recombinant factor H-binding protein showed a molecular mass of 95 kDa, as determined by SDS-PAGE. The protein possessed the functional property of binding factor H. Sera from S. suis-infected pigs reacted with the recombinant factor H receptor, suggesting that it is produced during the course of infections. In conclusion, we identified a novel S. suis cell surface protein that binds the complement factor H. This cell surface protein may help S. suis to resist complement attack and phagocytosis and contribute to pathogenesis.
猪链球菌是一种主要的猪病原体,也是一种新兴的人畜共患病原体。致病性细菌在其细胞表面结合补体调控因子 H 的能力可能使它们能够避免补体攻击和吞噬。本研究旨在鉴定血清型 2 猪链球菌中具有结合补体调控因子 H 活性的新细胞表面蛋白。通过 ELISA 证明了猪链球菌能够在其表面结合补体调控因子 H。通过因子 I 辅因子测定,发现结合至猪链球菌的因子 H 保持其功能活性。由于猪链球菌 P1/7 中的基因 SSU0186 的产物与具有结合因子 H 活性的肺炎链球菌蛋白(命名为 PspC)具有相似性,因此被提议为猪链球菌中的潜在因子 H 受体。SSU0186 具有 1686bp 的开放阅读框,编码 561 个氨基酸的蛋白质,在羧基末端包含革兰氏阳性细胞壁锚定基序(LPXTG)、氨基末端信号序列、α-螺旋结构域、富含脯氨酸的区域和 G5 结构域。SSU0186 基因在大肠杆菌中克隆,纯化的重组因子 H 结合蛋白通过 SDS-PAGE 测定分子量为 95kDa。该蛋白具有结合因子 H 的功能特性。来自猪链球菌感染猪的血清与重组因子 H 受体发生反应,表明它在感染过程中产生。总之,我们鉴定了一种新的猪链球菌细胞表面蛋白,它结合补体因子 H。这种细胞表面蛋白可能有助于猪链球菌抵抗补体攻击和吞噬作用,并有助于发病机制。