首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Microfluidic chip analysis of outer membrane proteins responsible for serological cross-reaction between three Gram-negative bacteria: Proteus morganii O34, Escherichia coli O111 and Salmonella Adelaide O35
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Microfluidic chip analysis of outer membrane proteins responsible for serological cross-reaction between three Gram-negative bacteria: Proteus morganii O34, Escherichia coli O111 and Salmonella Adelaide O35

机译:外膜蛋白的微流控芯片分析负责三种革兰氏阴性细菌之间的血清学交叉反应:变形杆菌O34,大肠杆菌O111和沙门氏菌O35

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摘要

Bacterial strains have complex and individual antigenic structure, which provides basis for their serological identification. However, serological cross-reaction may occur when antibodies against a certain strain recognize other strains too. The molecular basis of this phenomenon is the expression of similar or identical antigenic epitopes on the surface of different bacterial cells. Such cross-reactions might harden the serological diagnosis of pathogenic bacteria. But it can be also advantageous, when antigens of non-pathogenic strains can be used in the serological examinations. Serological cross-reaction between three taxonomically different strains - Proteus morganii O34 (8662/64), Escherichia coli O111 and Salmonella Adelaide O35 - have been described. It has been proven that it is based partially on the similar lipopolysaccharide structures of these pathogens. In this study the involvement of the outer membrane proteins of these strains in the serological cross-reaction is presented. Microfluidic chip technology was applied for the detection of common proteins, which provided fast and quantitative data about the proteins that might be responsible for serological cross-reaction. Two outer membrane proteins with apparent molecular mass of 36 and 41 kDa, respectively, could be detected in the profile of each strain, while individual dominating protein peaks have also appeared in the protein profiles. The presence of common protein antigens was proven by Western blotting. (C) 2007 Elsevier B.V. All rights reserved.
机译:细菌菌株具有复杂的个体抗原结构,为它们的血清学鉴定提供了基础。但是,当针对某个菌株的抗体也识别其他菌株时,可能会发生血清学交叉反应。这种现象的分子基础是在不同细菌细胞表面上表达相似或相同的抗原表位。这种交叉反应可能会加强病原菌的血清学诊断。但是,当非病原性菌株的抗原可以用于血清学检查时,这也可能是有利的。已经描述了三种分类学不同的菌株-变形杆菌O34(8662/64),大肠杆菌O111和沙门氏菌阿德莱德O35之间的血清学交叉反应。已经证明其部分基于这些病原体的相似脂多糖结构。在这项研究中,提出了这些菌株的外膜蛋白参与血清学交叉反应。微流控芯片技术已用于检测常见蛋白质,该蛋白质提供了可能与血清学交叉反应有关的蛋白质的快速定量数据。在每个菌株的谱图中可以检测到两种外膜蛋白,其表观分子量分别为36和41 kDa,而在蛋白谱中也出现了单独的主要蛋白峰。蛋白质印迹法证实了常见蛋白质抗原的存在。 (C)2007 Elsevier B.V.保留所有权利。

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