Lakio Laura, Paju Susanna, Alfthan Georg, Tiirola Terttu, Asikainen Sirkka, Pussinen Pirkko J
Institute of Dentistry, University of Helsinki, and Department of Oral and Maxillofacial Diseases, Helsinki University Central Hospital, Finland.
Infect Immun. 2003 Sep;71(9):5005-11. doi: 10.1128/IAI.71.9.5005-5011.2003.
Actinobacillus actinomycetemcomitans is a gram-negative, facultatively anaerobic bacterium which is associated especially with aggressive forms of periodontitis. Contradictory results on the localization of the A. actinomycetemcomitans serotype-specific antigen have been reported. The aim of the present study was to characterize the A. actinomycetemcomitans serotype d-specific antigen. The antigen was isolated by affinity chromatography. The affinity column was prepared from immunoglobulin G isolated from rabbit antiserum raised against A. actinomycetemcomitans serotype d. The isolated antigen was analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, Western blotting, and silver staining, all of which revealed a ladder-like structure typical for the O antigen of lipopolysaccharide (LPS). In a displacement enzyme-linked immunosorbent assay (ELISA), the isolated antigen displaced in a concentration-dependent manner the binding of the polyclonal rabbit antiserum raised against A. actinomycetemcomitans serotype d to the competing whole-cell serotype d antigen. The isolated antigen contained LPS, and an equal concentration of LPS isolated from A. actinomycetemcomitans serotype d gave a similar displacement curve in the ELISA. In order to test the immunogenic properties of the isolated antigen, it was used to immunize a rabbit. The antiserum raised against the isolated antigen displayed specificity in Western blotting and ELISA similar to that of antibody raised against LPS isolated from A. actinomycetemcomitans serotype d. In conclusion, our results show that the A. actinomycetemcomitans serotype d-specific antigen contains the O-antigenic structure of LPS.
伴放线放线杆菌是一种革兰氏阴性兼性厌氧菌,尤其与侵袭性牙周炎相关。关于伴放线放线杆菌血清型特异性抗原的定位,已有相互矛盾的研究结果报道。本研究的目的是对伴放线放线杆菌血清型d特异性抗原进行特性分析。通过亲和层析法分离该抗原。亲和柱由从针对伴放线放线杆菌血清型d的兔抗血清中分离出的免疫球蛋白G制备而成。对分离出的抗原进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳、蛋白质印迹法和银染分析,所有这些分析均显示出脂多糖(LPS)O抗原典型的梯状结构。在置换酶联免疫吸附测定(ELISA)中,分离出的抗原以浓度依赖的方式置换了针对伴放线放线杆菌血清型d的兔多克隆抗血清与竞争性全细胞血清型d抗原的结合。分离出的抗原含有LPS,并且从伴放线放线杆菌血清型d中分离出的等浓度LPS在ELISA中给出了相似的置换曲线。为了测试分离出的抗原的免疫原性,用其免疫一只兔子。针对分离出的抗原产生的抗血清在蛋白质印迹法和ELISA中显示出与针对从伴放线放线杆菌血清型d中分离出的LPS产生的抗体相似的特异性。总之,我们的结果表明,伴放线放线杆菌血清型d特异性抗原含有LPS的O抗原结构。