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反刍动物考德里氏体免疫原性21 kDa蛋白编码基因的分子克隆

Molecular cloning of a gene encoding the immunogenic 21 kDa protein of Cowdria ruminantium.

作者信息

Mahan S M, McGuire T C, Semu S M, Bowie M V, Jongejan F, Rurangirwa F R, Barbet A F

机构信息

Department of Infectious Diseases, College of Veterinary Medicine, University of Florida, Gainesville 32611-0880.

出版信息

Microbiology (Reading). 1994 Aug;140 ( Pt 8):2135-42. doi: 10.1099/13500872-140-8-2135.

Abstract

Major immunogenic polypeptides (21, 32, 40, 46, 58, 85 and 160 kDa) of Cowdria ruminantium were identified by immunoprecipitation and immunoblotting. A pUC13 library of C. ruminantium genomic DNA was screened with hyperimmune sheep serum to identify Escherichia coli colonies which expressed genes encoding these immunogenic proteins. A recombinant E. coli colony, F5.2, was identified containing plasmid insert DNA of 2773 bp. The cloned DNA insert contained two long open reading frames (ORFs) of 627 bp (complete) and 831 bp (incomplete), both potentially encoding proteins containing an N-terminal signal peptide. Deletion experiments suggested that the hyperimmune sheep serum recognized a protein that was encoded by the 627 bp ORF. The 627 bp ORF was amplified by polymerase chain reaction (PCR), subcloned and expressed to a high level in E. coli. A sheep antiserum made to the expressed recombinant fusion protein recognized a 21 kDa protein of all strains of C. ruminantium tested, confirming that the 627 bp ORF encodes a native 21 kDa protein in C. ruminantium. Similarly, the recombinant protein was recognized by all sera tested from heartwater-infected animals. The antigenic conservation of the 21 kDa protein and its immunogenic nature are reasons for further testing of this recombinant protein in subunit diagnostic tests.

摘要

通过免疫沉淀和免疫印迹法鉴定了反刍兽考德里氏体的主要免疫原性多肽(21、32、40、46、58、85和160 kDa)。用超免疫绵羊血清筛选反刍兽考德里氏体基因组DNA的pUC13文库,以鉴定表达编码这些免疫原性蛋白基因的大肠杆菌菌落。鉴定出一个重组大肠杆菌菌落F5.2,其含有2773 bp的质粒插入DNA。克隆的DNA插入片段包含两个长开放阅读框(ORF),分别为627 bp(完整)和831 bp(不完整),两者都可能编码含有N端信号肽的蛋白质。缺失实验表明,超免疫绵羊血清识别的一种蛋白质是由627 bp的ORF编码的。通过聚合酶链反应(PCR)扩增627 bp的ORF,亚克隆并在大肠杆菌中高水平表达。用表达的重组融合蛋白制备的绵羊抗血清识别了所有测试的反刍兽考德里氏体菌株的一种21 kDa蛋白质,证实627 bp的ORF在反刍兽考德里氏体中编码一种天然的21 kDa蛋白质。同样,该重组蛋白被所有来自感染心水病动物的血清识别。21 kDa蛋白的抗原保守性及其免疫原性是在亚单位诊断试验中进一步测试该重组蛋白的原因。

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