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利用二维凝胶电泳对瑞士立克次氏体蛋白抗原性的研究。

A study of the antigenicity of Rickettsia helvetica proteins using two-dimensional gel electrophoresis.

作者信息

Hajem Nedaa, Weintraub Andrej, Nimtz Manfred, Römling Ute, Påhlson Carl

机构信息

School of Sustainable Development of Society and Technology, Mälardalens University, Eskilstuna, Sweden.

出版信息

APMIS. 2009 Apr;117(4):253-62. doi: 10.1111/j.1600-0463.2009.02435.x.

Abstract

Rickettsia helvetica is an obligate intracellular Gram-negative microorganism found in Ixodes ricinus ticks. When R. helvetica was first discovered in 1979, little was known about its physiology and it fell into oblivion until it recently was suspected of being pathogenic to humans. However, all efforts to isolate R. helvetica from patients have been unsuccessful, although serological responses against R. helvetica can be demonstrated. The aim of our study was to investigate the protein profile of R. helvetica and study the antigenicity of its proteins using two-dimensional (2D) immunoblot in order to characterize the immunological response against R. helvetica infection. Our results show that in addition to the known PS120 and OmpB antigenic R. helvetica proteins, three other antigens exist: a 60 kDa GroEL protein, a 10 kDa GroES protein and a hitherto unknown 35 kDa hypothetical protein that has similarities with ORF-RC0799 of Rickettsia conorii. Furthermore, the lipopolysaccharide showed strong antigenicity. In this study, we present the first proteome map and the first 2D immunoblot profile of R. helvetica and finally we present the 35 kDa R. helvetica as an additional antigen to the previously known rickettsial antigens.

摘要

瑞士立克次氏体是一种专性细胞内革兰氏阴性微生物,存在于蓖麻硬蜱中。1979年首次发现瑞士立克次氏体时,对其生理学知之甚少,它一度被遗忘,直到最近被怀疑对人类致病。然而,尽管可以证明针对瑞士立克次氏体的血清学反应,但从患者身上分离出瑞士立克次氏体的所有努力均未成功。我们研究的目的是研究瑞士立克次氏体的蛋白质谱,并使用二维(2D)免疫印迹法研究其蛋白质的抗原性,以便表征针对瑞士立克次氏体感染的免疫反应。我们的结果表明,除了已知的具有抗原性的瑞士立克次氏体PS120和OmpB蛋白外,还存在其他三种抗原:一种60 kDa的GroEL蛋白、一种10 kDa的GroES蛋白和一种迄今未知的35 kDa假设蛋白,该蛋白与康氏立克次氏体的ORF-RC0799有相似性。此外,脂多糖显示出很强的抗原性。在本研究中,我们展示了瑞士立克次氏体的首张蛋白质组图谱和首张2D免疫印迹图谱,最后我们将35 kDa的瑞士立克次氏体蛋白作为一种新的抗原呈现出来,补充到先前已知的立克次氏体抗原中。

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