肺炎衣原体表面的分子生物学。

G Christiansen, L Ostergaard, S Birkelund
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引用次数: 0

摘要

肺炎衣原体是一种挑剔的微生物,具有典型的双相生命周期,可引起多种人类呼吸道感染。关于肺炎球菌的分子生物学知识有限,只有少数基因被测序。衣原体表面结构与沙眼衣原体不同。为了研究肺炎原胞菌的表面,我们制备了针对肺炎原胞菌VR-1310的单克隆抗体(mab),并选择了14种能与肺炎原胞菌表面反应的单克隆抗体。在免疫电镜下,所有单克隆抗体均与整个肺炎c - VR-1310基本体的表面和纯化的肌基提取的外膜复合物发生反应。然而,在免疫印迹中,只有2个单克隆抗体与肺炎衣原体蛋白反应,并且仅与未在sds样品缓冲液中热处理的抗原反应。这表明肺炎球菌表面的构象表位占主导地位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular biology of the Chlamydia pneumoniae surface.

Chlamydia pneumoniaeis a fastidious microorganism with a characteristic biphasic lifecycle causing a variety of human respiratory tract infections. There is limited knowledge about the molecular biology of C. pneumoniae, and only a few genes have been sequenced. The structure of the chlamydial surface differs from that of Chlamydia trachomatis. In order to study the surface of C. pneumoniae we generated monoclonal antibodies (MAbs) against C. pneumoniae strain VR-1310 and selected 14 MAbs that reacted with the surface of C. pneumoniae. All MAbs reacted in immunoelectron microscopy with the surface of both whole C. pneumoniae VR-1310 elementary bodies and with purified sarcosyl extracted outer membrane complexes. However, only 2 of the MAbs reacted in immunoblotting with C. pneumoniae proteins and only with antigen that had not been heat treated in SDS-sample buffer. This indicates the dominance of conformational epitopes at the C. pneumoniae surface.

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