van Winkelhoff A J, Appelmelk B J, Kippuw N, de Graaff J
Department of Oral Microbiology, Academic Centre for Dentistry Amsterdam (ACTA), The Netherlands.
Oral Microbiol Immunol. 1993 Oct;8(5):259-65. doi: 10.1111/j.1399-302x.1993.tb00571.x.
We investigated antigens in spreading and non-spreading Porphyromonas gingivalis strains. On the basis of differences in virulence in the mouse model, 8 strains were selected for antiserum production in rabbits. Hyperimmune sera were tested by double immunoprecipitation and immunoelectrophoresis. Besides a common antigen, differences in antigenic composition were observed in the thermolabile antigens between all strains tested. Two different heat-stable antigens were found after heating at 120 degrees C. One such antigen was detected after sonication of the pellet fraction of autoclaved P. gingivalis cells. This antigen cross-reacted with 6 of the 8 immune sera. This somatic antigen was almost neutrally charged and sensitive to sodium periodate treatment, suggestive of lipopolysaccharide. A second heat-stable antigen was detected in the supernatant of autoclaved strains of W83, W50, HG184 and A7A1-28. These non-somatic antigens were strain-specific, i.e., no cross-reactivity was found with heterologous hyperimmune sera. An exception was strain W50, which had a non-somatic heat-stable antigen which was recognized by W83 antiserum. These antigens were resistant to DNAse, RNAse and proteinase-K treatment but were degraded by sodium periodate. In immunoelectrophoresis, these antigens appeared to be negatively charged. These properties are characteristics of a K-antigen, which likely represent a thermostable carbohydrate capsule. The presence of K-antigen correlates very well with the serum resistance, the low chemiluminescence, the resistance to phagocytosis and the need for opsonization with specific antibodies for complement-mediated killing of virulent P. gingivalis strains.(ABSTRACT TRUNCATED AT 250 WORDS)
我们研究了具核梭杆菌传播菌株和非传播菌株中的抗原。基于小鼠模型中毒力的差异,选择了8株菌株用于在兔体内制备抗血清。通过双向免疫沉淀和免疫电泳检测了超免疫血清。除了一种共同抗原外,在所测试的所有菌株的热不稳定抗原中观察到了抗原组成的差异。在120℃加热后发现了两种不同的热稳定抗原。其中一种抗原是在高压灭菌的具核梭杆菌细胞沉淀部分超声处理后检测到的。这种抗原与8种免疫血清中的6种发生交叉反应。这种菌体抗原几乎呈中性电荷,对高碘酸钠处理敏感,提示为脂多糖。在W83、W50、HG184和A7A1-28高压灭菌菌株的上清液中检测到了第二种热稳定抗原。这些非菌体抗原具有菌株特异性,即与异源超免疫血清未发现交叉反应。例外的是菌株W50,其具有一种非菌体热稳定抗原,能被W83抗血清识别。这些抗原对DNA酶、RNA酶和蛋白酶K处理具有抗性,但能被高碘酸钠降解。在免疫电泳中,这些抗原似乎带负电荷。这些特性是K抗原的特征,K抗原可能代表一种热稳定的碳水化合物荚膜。K抗原的存在与血清抗性、低化学发光、抗吞噬作用以及补体介导的杀伤有毒力的具核梭杆菌菌株时需要用特异性抗体进行调理作用密切相关。(摘要截断于250字)