Beuvery E C, Miedema F, van Delft R W, Haverkamp J, Leussink A B, te Pas B J, Teppema K S, Tiesjema R H
Infect Immun. 1983 Apr;40(1):369-80. doi: 10.1128/iai.40.1.369-380.1983.
A crude complex containing group C polysaccharide, outer membrane proteins, and lipopolysaccharide (LPS) was isolated from the cell-free culture liquid of Neisseria meningitidis serogroup C, serotype 2a. Group C polysaccharide and LPS were removed from this complex, resulting in an outer membrane complex and a purified complex, respectively. Analysis by electron microscopy showed the outer membrane origin of the crude complex and the outer membrane complex, whereas such a structure was absent in the purified complex. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis patterns of the three complexes were identical. Pyrolysis-mass spectrometry data correlated well with those obtained by the biochemical assays and suggested a low LPS content in the purified complex and a low polysaccharide content in the outer membrane complex. The purified complex was shown to be nonpyrogenic and could be prepared with the same yield as that of purified polysaccharide. The immunogenic activities of the complexes were studied in mice. The antibodies were measured by the enzyme-linked immunosorbent assay; and the bactericidal antibody assay. All complexes induced immunoglobulin G antibodies to group C polysaccharide as well as to the serotype antigen, although the removal of polysaccharide and LPS resulted in a reduction of the immunogenic activities of outer membrane complex and purified complex, respectively. A second dose of all complexes produced a clear booster effect of both antibody responses. The antibodies were bactericidal.
从脑膜炎奈瑟菌C群2a血清型的无细胞培养液中分离出一种含有C群多糖、外膜蛋白和脂多糖(LPS)的粗复合物。从该复合物中去除C群多糖和LPS,分别得到外膜复合物和纯化复合物。电子显微镜分析显示粗复合物和外膜复合物源自外膜,而纯化复合物中不存在这种结构。三种复合物的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳图谱相同。热解质谱数据与生化分析结果相关性良好,表明纯化复合物中LPS含量低,外膜复合物中多糖含量低。纯化复合物显示无致热原性,且制备产率与纯化多糖相同。在小鼠中研究了复合物的免疫原活性。通过酶联免疫吸附测定法和杀菌抗体测定法检测抗体。所有复合物均诱导产生针对C群多糖以及血清型抗原的免疫球蛋白G抗体,尽管去除多糖和LPS分别导致外膜复合物和纯化复合物的免疫原活性降低。所有复合物的第二剂均对两种抗体反应产生明显的增强作用。这些抗体具有杀菌作用。