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单核细胞增生李斯特菌和伊氏李斯特菌鞭毛蛋白的物理及抗原异质性。

Physical and antigenic heterogeneity in the flagellins of Listeria monocytogenes and L. ivanovii.

作者信息

Peel M, Donachie W, Shaw A

机构信息

Moredun Research Institute, Edinburgh, UK.

出版信息

J Gen Microbiol. 1988 Sep;134(9):2593-8. doi: 10.1099/00221287-134-9-2593.

Abstract

Listeria monocytogenes serotypes 4a, 4b and 7, and L. ivanovii, all grown at 20 degrees C, were negatively stained and examined by electron microscopy. Crude extracts of the cell surface of L. monocytogenes serotypes 1/2b, 3b, 3c, 4a, 4b, 4d and 7 and of L. ivanovii (all grown at 20 degrees C) were examined by SDS-PAGE and Western blotting using (i) affinity-purified polyclonal monospecific antibody, and (ii) monoclonal antibody, each raised against 29 kDa flagellin of serotype 4b. No flagella were seen on serotype 7 by electron microscopy and no flagellin was detected in crude cell surface extracts of serotype 7 either in silver-stained gels or in Western blots. The monospecific polyclonal antibody detected flagellins of approximate molecular mass 29 kDa in each of the seven flagellate strains including L. ivanovii. The monoclonal antibody detected 29 kDa flagellin in serotypes 1/2b, 3b, 4a, 4b and 4d, but not the flagellins of serotype 3c or L. ivanovii, which had a slightly lower molecular mass. Following prolonged electrophoresis of crude flagellar extracts the 29 kDa complex was resolved into three closely migrating bands. In a heterologous system using serotype 1/2b crude flagellar extract, all three bands were detected using the polyclonal antibody whereas only two bands were detected by the monoclonal antibody. It is concluded that polyclonal anti-flagellin antibodies are not useful tools with which to distinguish serotypes of L. monocytogenes sensu lato in immunoblotting, but that differences can be determined using a monoclonal antibody directed against particular components of the flagellar complex. These differences did not fully correspond to those anticipated from results of agglutination tests.

摘要

将单核细胞增生李斯特菌血清型4a、4b和7以及伊凡诺夫李斯特菌在20℃下培养,进行负染色并通过电子显微镜检查。对单核细胞增生李斯特菌血清型1/2b、3b、3c、4a、4b、4d和7以及伊凡诺夫李斯特菌(均在20℃下培养)的细胞表面粗提物进行SDS-PAGE和蛋白质印迹分析,使用(i)亲和纯化的多克隆单特异性抗体,以及(ii)单克隆抗体,每种抗体均针对血清型4b的29 kDa鞭毛蛋白产生。通过电子显微镜在血清型7上未观察到鞭毛,并且在血清型7的粗细胞表面提取物中,无论是在银染凝胶还是在蛋白质印迹中均未检测到鞭毛蛋白。单特异性多克隆抗体在包括伊凡诺夫李斯特菌在内的七个有鞭毛菌株中的每一个中均检测到了分子量约为29 kDa的鞭毛蛋白。单克隆抗体在血清型1/2b、3b、4a、4b和4d中检测到了29 kDa鞭毛蛋白,但未检测到血清型3c或分子量略低的伊凡诺夫李斯特菌的鞭毛蛋白。在粗鞭毛提取物长时间电泳后,29 kDa复合物被解析为三条紧密迁移的条带。在使用血清型1/2b粗鞭毛提取物的异源系统中,使用多克隆抗体检测到了所有三条条带,而单克隆抗体仅检测到了两条条带。得出的结论是,多克隆抗鞭毛蛋白抗体不是在免疫印迹中区分广义单核细胞增生李斯特菌血清型的有用工具,但使用针对鞭毛复合物特定成分的单克隆抗体可以确定差异。这些差异与凝集试验结果预期的差异并不完全一致。

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