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链球菌和非链球菌口腔细菌的共同抗原:血链球菌、变形链球菌、唾液乳杆菌和黏性放线菌细胞外及细胞壁相关抗原的免疫化学研究

Common antigens of streptococcal and non-streptococcal oral bacteria: immunochemical studies of extracellular and cell-wall-associated antigens from Streptococcus sanguis, Streptococcus mutans, Lactobacillus salivarius, and Actinomyces viscosus.

作者信息

Schöller M, Klein J P, Frank R M

出版信息

Infect Immun. 1981 Jan;31(1):52-60. doi: 10.1128/iai.31.1.52-60.1981.

Abstract

Soluble extracellular antigens (ESA) were prepared from the culture supernatant of exponential growing cells of Streptococcus sanguis OMZ 9 by a combination of ammonium sulfate precipitation and chromatography on a Bio-Gel P6 column. Soluble cell wall antigens (WEA) were obtained from the bacterial pellet by extraction with 1 M phosphate buffer (pH 6). Antisera against whole cells of S. sanguis and S. mutans of different serotypes, 10% trichloroacetic extracts of bacterial cell walls, dextran, ESA, and WEA were prepared by injecting the different antigens several times in rabbits. ESA and WEA were prepared from a representative strain of Bratthall's seven serological groups, Lactobacillus salivarius, and Actinomyces viscosus. All sera showed various agglutinin titers against heat-killed cells, and titers were generally higher with homologous cells. The comparison of the different antigens using agar gel diffusion and immunoelectrophoresis showed the presence of extracellular common antigens in both ESA and WEA between the different strains. Absorption of anti-ESA sera with WEA, and anti-WEA sera with ESA, showed the existence of a specific antigen common to all bacteria in each fraction. Enzymatic treatment of the antigen before immunodiffusion demonstrated the protein nature of the two antigens present in ESA and WEA.

摘要

可溶性细胞外抗原(ESA)是通过硫酸铵沉淀和在Bio-Gel P6柱上进行层析相结合的方法,从血链球菌OMZ 9指数生长期细胞的培养上清液中制备的。可溶性细胞壁抗原(WEA)是通过用1 M磷酸盐缓冲液(pH 6)从细菌沉淀中提取获得的。通过在兔体内多次注射不同抗原,制备了针对不同血清型血链球菌和变形链球菌全细胞、细菌细胞壁的10%三氯乙酸提取物、葡聚糖、ESA和WEA的抗血清。ESA和WEA是从布拉特霍尔七个血清学组的代表性菌株、唾液乳杆菌和黏性放线菌中制备的。所有血清对热杀死的细胞均显示出不同的凝集素效价,且同源细胞的效价通常更高。使用琼脂凝胶扩散和免疫电泳对不同抗原进行比较,结果显示不同菌株的ESA和WEA中均存在细胞外共同抗原。用WEA吸收抗ESA血清,以及用ESA吸收抗WEA血清,结果显示每个组分中所有细菌都存在一种特异性抗原。在免疫扩散前对抗原进行酶处理,证明了ESA和WEA中存在的两种抗原的蛋白质性质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cedf/351751/0f7be70f3c7d/iai00165-0075-a.jpg

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