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OspA,一种鲑鱼立克次氏体(Piscirickettsia salmonis)的脂蛋白抗原,该病原体是一种专性细胞内寄生菌。

OspA, a lipoprotein antigen of the obligate intracellular bacterial pathogen Piscirickettsia salmonis.

作者信息

Kuzyk M A, Burian J, Thornton J C, Kay W W

机构信息

Canadian Bacterial Diseases Network, Department of Biochemistry and Microbiology, University of Victoria, British Columbia.

出版信息

J Mol Microbiol Biotechnol. 2001 Jan;3(1):83-93.

Abstract

No effective recombinant vaccines are currently available for any rickettsial diseases. In this regard the first non-ribosomal DNA sequences from the obligate intracellular pathogen Piscirickettsia salmonis are presented. Genomic DNA isolated from Percoll density gradient purified P. salmonis, was used to construct an expression library in lambda ZAP II. In the absence of preexisting DNA sequence, rabbit polyclonal antiserum raised against P. salmonis, with a bias toward P. salmonis surface antigens, was used to identify immunoreactive clones. Catabolite repression of the lac promoter was required to obtain a stable clone of a 4,983 bp insert in Escherichia coli due to insert toxicity exerted by the accompanying radA open reading frame (ORF). DNA sequence analysis of the insert revealed 1 partial and 4 intact predicted ORF's. A 486 bp ORF, ospA, encoded a 17 kDa antigenic outer surface protein (OspA) with 62% amino acid sequence homology to the genus common 17 kDa outer membrane lipoprotein of Rickettsia prowazekii, previously thought confined to members of the genus Rickettsia. Palmitate incorporation demonstrated that OspA is posttranslationally lipidated in E. coli, albeit poorly expressed as a lipoprotein even after replacement of the signal sequence with the signal sequence from lpp (Braun lipoprotein) or the rickettsial 17 kDa homologue. To enhance expression, ospA was optimized for codon usage in E. coli by PCR synthesis. Expression of ospA was ultimately improved (approximately 13% of total protein) with a truncated variant lacking a signal sequence. High level expression (approximately 42% tot. prot.) was attained as an N-terminal fusion protein with the fusion product recovered as inclusion bodies in E. coli BL21. Expression of OspA in P. salmonis was confirmed by immunoblot analysis using polyclonal antibodies generated against a synthetic peptide of OspA (110-129) and a strong antibody response against OspA was detected in convalescent sera from coho salmon (Oncorhynchus kisutch).

摘要

目前尚无针对任何立克次氏体病的有效重组疫苗。在这方面,本文首次报道了专性胞内病原体鲑鱼立克次氏体的非核糖体DNA序列。从经Percoll密度梯度纯化的鲑鱼立克次氏体中分离的基因组DNA,被用于构建λZAP II表达文库。由于缺乏预先存在的DNA序列,因此使用针对鲑鱼立克次氏体产生的兔多克隆抗血清(偏向于鲑鱼立克次氏体表面抗原)来鉴定免疫反应性克隆。由于伴随的radA开放阅读框(ORF)施加的插入毒性,需要对lac启动子进行分解代谢物阻遏,以在大肠杆菌中获得一个4983 bp插入片段的稳定克隆。对插入片段的DNA序列分析揭示了1个部分和4个完整的预测ORF。一个486 bp的ORF,ospA,编码一种17 kDa的抗原性外表面蛋白(OspA),与普氏立克次氏体属常见的17 kDa外膜脂蛋白具有62%的氨基酸序列同源性,此前认为该蛋白仅限于立克次氏体属成员。棕榈酸掺入实验表明,OspA在大肠杆菌中进行了翻译后脂化,尽管即使在用lpp( Braun脂蛋白)或立克次氏体17 kDa同源物的信号序列替换信号序列后,其作为脂蛋白的表达仍很差。为了提高表达,通过PCR合成对ospA在大肠杆菌中的密码子使用进行了优化。最终,缺失信号序列的截短变体使ospA的表达得到改善(约占总蛋白的13%)。作为N端融合蛋白,在大肠杆菌BL21中以包涵体形式回收融合产物,实现了高水平表达(约占总蛋白的42%)。使用针对OspA合成肽(110 - 129)产生的多克隆抗体通过免疫印迹分析证实了OspA在鲑鱼立克次氏体中的表达,并在银大麻哈鱼(Oncorhynchus kisutch)的恢复期血清中检测到了针对OspA的强烈抗体反应。

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