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首页> 外文期刊>Infection and immunity >Fine structure of A and M antigens from Brucella biovars.
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Fine structure of A and M antigens from Brucella biovars.

机译:来自布鲁氏菌生物变种的A和M抗原的精细结构。

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Brucella A and M epitopes were found on single O-polysaccharide chains of all biotype strains of this species. Lipopolysaccharides from the type and reference strains of five of the six Brucella species, B. abortus, B. melitensis, B. suis, B. canis, and B. neotomae, were extracted and purified. Analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, in conjunction with silver staining and immunoblotting developed by monoclonal antibodies, showed bands characteristic of A, M, or mixed A and M antigens. The A antigen previously described as an exclusively alpha 1,2-linked homopolymer of 4,6-dideoxy-4-formamido-D-mannopyranose was shown by 1H and 13C nuclear magnetic resonance spectroscopy to possess a fine structure consistent with the low-frequency occurrence of alpha 1, 3-linked 4,6-dideoxy-4-formamido-D-mannopyranose residues. This feature was previously attributed only to the M antigen, which is also a homopolymer of the same sugar. B. melitensis biotype 3 and B. suis biotype 4 lipopolysaccharides showed characteristics of mixed A and M antigens. Immunoabsorption of these O polysaccharides on a column of immobilized A-antigen-specific monoclonal antibody enriched polymer chains with A-antigen characteristics but did not eliminate M epitopes. Composite A- and M-antigen characteristics resulted from O polysaccharides in which the frequency of alpha 1,3 linkages, and hence, M-antigen characteristics, varied. All biotypes assigned as A+ M- expressed one or two alpha 1,3-linked residues per polysaccharide O chain. M antigens (M+ A-) also possessed a unique M epitope as well as a tetrasaccharide determinant common to A-antigen structures. B. canis and B. abortus 45/20, both rough strains, expressed low-molecular-weight A antigen.
机译:在该物种所有生物型菌株的单个O-多糖链上发现布鲁氏菌A和M表位。提取并纯化了六种布鲁氏菌属中的五种的类型和参考菌株的脂多糖,即流产芽孢杆菌,肉芽孢杆菌,猪芽孢杆菌,犬芽孢杆菌和新芽孢杆菌。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析,结合单克隆抗体开发的银染和免疫印迹法,显示出A,M或A和M混合抗原的条带。 1H和13C核磁共振波谱显示先前描述为4,6-二脱氧-4-甲酰胺基-D-甘露吡喃糖的仅由1,2连接的均聚物的A抗原具有与低频一致的精细结构α1,3-连接的4,6-二脱氧-4-甲酰胺基-D-甘露吡喃糖残基的出现。该特征以前仅归因于M抗原,M抗原也是同一糖的均聚物。 B. melitensis生物型3和B. suis生物型4脂多糖表现出混合的A和M抗原的特征。这些O多糖在具有A抗原特性但未消除M表位的固定化A抗原特异性单克隆抗体富集的聚合物链上进行免疫吸收。复合的A和M抗原特性来自O多糖,其中α1,3键的频率以及M抗原特性发生了变化。分配为A + M-的所有生物型每个多糖O链均表达一个或两个与α1,3连接的残基。 M抗原(M + A-)也具有独特的M表位以及A抗原结构共有的四糖决定簇。均为粗糙菌株的犬双歧杆菌和流产双歧杆菌45/20均表达低分子量A抗原。

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