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多杀性巴氏杆菌aroA基因的分子分析及构建的aroA突变体的疫苗潜力

Molecular analysis of the aroA gene of Pasteurella multocida and vaccine potential of a constructed aroA mutant.

作者信息

Homchampa P, Strugnell R A, Adler B

机构信息

Department of Microbiology, Monash University, Clayton, Victoria, Australia.

出版信息

Mol Microbiol. 1992 Dec;6(23):3585-93. doi: 10.1111/j.1365-2958.1992.tb01794.x.

Abstract

The aroA gene from Pasteurella multocida was cloned by complementation of the Escherichia coli aroA mutant AB2829 with a DNA library constructed in pUC18. The nucleotide sequence of the P. multocida aroA gene indicated an open reading frame encoding a protein of 441 amino acids, which showed a high degree of homology with the amino acid sequences of various other bacterial AroA proteins. The cloned P. multocida aroA gene was inactivated by insertion of a kanamycin-resistance gene and reintroduced by allelic exchange into the chromosome of P. multocida using the suicide vector pJM703.1. The P. multocida aroA mutant was highly attenuated in a mouse model. Mice immunized intraperitoneally with two doses of live P. multocida aroA mutant were completely protected against a lethal parental strain challenge.

摘要

通过用构建于pUC18的DNA文库对大肠杆菌aroA突变体AB2829进行互补,克隆了多杀性巴氏杆菌的aroA基因。多杀性巴氏杆菌aroA基因的核苷酸序列显示有一个编码441个氨基酸的开放阅读框,该序列与其他各种细菌的AroA蛋白的氨基酸序列具有高度同源性。通过插入卡那霉素抗性基因使克隆的多杀性巴氏杆菌aroA基因失活,并使用自杀载体pJM703.1通过等位基因交换将其重新导入多杀性巴氏杆菌的染色体中。多杀性巴氏杆菌aroA突变体在小鼠模型中高度减毒。用两剂活的多杀性巴氏杆菌aroA突变体进行腹腔免疫的小鼠完全受到保护,免受致死性亲本菌株的攻击。

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