Leung K P, Fukushima H, Nesbitt W E, Clark W B
Periodontal Disease Research Center and Department of Oral Biology, College of Dentistry, University of Florida, Gainesville 32610, USA.
Oral Microbiol Immunol. 1996 Feb;11(1):42-50. doi: 10.1111/j.1399-302x.1996.tb00335.x.
Our earlier studies demonstrated that clinical strains of Prevotella intermedia, isolated from human periodontal pockets, possess various types of fimbria (surface appendages) as determined ultrastructurally. These bacteria have the ability to agglutinate selected mammalian erythrocytes. Hemagglutinating activity exhibited by these cells may be attributable to these surface structures. Strain 17, which possess fimbriae of 8 nm in diameter and readily agglutinates human, monkey, sheep, rabbit, and mouse erythrocytes was selected to determine whether these fimbriae possessed the hemagglutinating activity. Fimbriae were mechanically sheared, concentrated by ammonium sulfate precipitation, solubilized in 10 mM Tris-HCl buffer containing 0.5% deoxycholate and partly purified by ultracentrifugation in a 10-50% linear sucrose gradient. Isolated fimbriae banded at a density of 1.20-1.15 g/ml, appeared fairly uniform ultrastructurally, and possessed hemagglutinating activity. The hemagglutinating activity of P. intermedia whole cells and isolated fimbriae was reduced by treatment with proteases and eliminated by treatment with heat at 80 degrees C for 10 min. The optimal pH for the hemagglutination was 7.0. In the process of hemagglutination, P. intermedia whole cells and isolated fimbriae bound to rabbit erythrocytes as observed by: (a) decrease in the hemagglutinating activity of bacterial whole cells and isolated fimbriae after incubation with rabbit erythrocytes, (b) increase in hemagglutinating activity of the red cells used for absorption, and (c) the presence of P. intermedia whole cells and fimbriae on red cells after absorption as revealed by immunoelectron microscopy. Both the immune immunoglobulin G of the rabbit polyclonal anti-fimbriae antibody and the immune immunoglobulin G and its Fab fragments of the murine monoclonal anti-fimbriae antibody were effective inhibitors of hemagglutination mediated by isolated fimbriae. Immunogold labeling showed that the monoclonal antibody bound specifically to P. intermedia fimbriae. These results collectively suggest that the hemagglutination exhibited by P. intermedia may be attributable to the fimbriae or the fimbrial-associated components.
我们早期的研究表明,从人类牙周袋中分离出的中间普氏菌临床菌株,经超微结构测定具有多种类型的菌毛(表面附属物)。这些细菌有凝集特定哺乳动物红细胞的能力。这些细胞表现出的血凝活性可能归因于这些表面结构。选择具有直径8nm菌毛且能轻易凝集人、猴、羊、兔和小鼠红细胞的17号菌株,以确定这些菌毛是否具有血凝活性。菌毛经机械剪切,通过硫酸铵沉淀浓缩,溶解于含0.5%脱氧胆酸盐的10mM Tris-HCl缓冲液中,并在10-50%线性蔗糖梯度中通过超速离心进行部分纯化。分离出的菌毛在密度为1.20-1.15g/ml处形成条带,超微结构上看起来相当均匀,并具有血凝活性。中间普氏菌全细胞和分离出的菌毛的血凝活性经蛋白酶处理后降低,在80℃加热10分钟后消除。血凝的最佳pH值为7.0。在血凝过程中,观察到中间普氏菌全细胞和分离出的菌毛与兔红细胞结合,表现为:(a)细菌全细胞和分离出的菌毛与兔红细胞孵育后血凝活性降低;(b)用于吸收的红细胞血凝活性增加;(c)免疫电子显微镜显示吸收后红细胞上存在中间普氏菌全细胞和菌毛。兔多克隆抗菌毛抗体的免疫免疫球蛋白G以及鼠单克隆抗菌毛抗体的免疫免疫球蛋白G及其Fab片段都是分离出的菌毛介导的血凝的有效抑制剂。免疫金标记显示单克隆抗体与中间普氏菌菌毛特异性结合。这些结果共同表明,中间普氏菌表现出的血凝可能归因于菌毛或与菌毛相关的成分。