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首页> 外文期刊>Veterinary Microbiology >Identification and immunological characterization of conserved Mycoplasma hyopneumoniae lipoproteins Mhp378 and Mhp651
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Identification and immunological characterization of conserved Mycoplasma hyopneumoniae lipoproteins Mhp378 and Mhp651

机译:保守的猪肺炎支原体脂蛋白Mhp378和Mhp651的鉴定和免疫学表征

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摘要

Mycoplasma hyopneumoniae, the etiological agent of swine enzootic pneumonia, is an important pathogen in the swine industry worldwide. Investigations on pathogenicity mechanisms as well as current serological detection methods and the development of new recombinant subunit vaccines are hampered by the lack of known and well characterized, species-specific M. hyopneumoniae antigens. As a first step to solve these problems membrane and membrane-associated proteins were enriched from M. hyopneumoniae cells by Triton X-114 fractionation and further analyzed by 2D gel electrophoresis and Western blot analyses using convalescent sera. Two previously unknown immunogenic proteins were identified by quadrupole time-of-flight mass spectrometry and database analyses as the conserved putative lipoproteins, Mhp378 and Mhp651. Both proteins were expressed as recombinant GST fusion proteins and reacted with sera from convalescent pigs. Coated as solid-phase antigen, Mhp651 showed a distinct cross-reaction only with Mycoplasma flocculare specific rabbit hyperimmune serum, whereas Mhp378 was only recognized by the positive control serum directed against M. hyopneumoniae, thereby indicating its species specificity.
机译:猪支原体肺炎的病原体猪肺炎支原体是全世界养猪业的重要病原体。缺乏已知的和特征明确的,物种特异性的猪肺炎支原体抗原阻碍了对致病机理的研究以及当前的血清学检测方法和新的重组亚基疫苗的开发。解决这些问题的第一步是通过Triton X-114分离从猪肺炎支原体细胞中富集膜和膜相关蛋白,并通过2D凝胶电泳和使用恢复期血清的Western印迹分析进行进一步分析。通过四极杆飞行时间质谱和数据库分析鉴定了两个先前未知的免疫原性蛋白,即保守的推定脂蛋白Mhp378和Mhp651。两种蛋白均表达为重组GST融合蛋白,并与恢复期猪的血清反应。作为固相抗原包被,Mhp651仅与絮状支原体特异性兔超免疫血清显示出明显的交叉反应,而Mhp378仅被针对猪肺炎支原体的阳性对照血清识别,从而表明其物种特异性。

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