Homchampa P, Strugnell R A, Adler B
Department of Microbiology, Monash University, Clayton, Melbourne, Vic., Australia.
Vet Microbiol. 1994 Sep;42(1):35-44. doi: 10.1016/0378-1135(94)90075-2.
The aroA gene, encoding 5-enolpyruvylshikimate 3-phosphate synthase, from Pasteurella haemolytica biotype A, serotype 1 was cloned by complementation of the aroA mutation in Escherichia coli strain AB2829 after electroporation with a DNA library constructed in pUC18. The cloned P. haemolytica aroA gene was inactivated by insertion of a kanamycin resistance gene and reintroduced by allelic exchange into the chromosome of the parental P. haemolytica using PbluescriptII SK+. The P. haemolytica aroA mutant was highly attenuated in a mouse septicaemic model. Mice immunized intraperitoneally with two doses of live P. haemolytica aroA mutant were protected against a lethal parental strain challenge.
通过用构建于pUC18的DNA文库对大肠杆菌菌株AB2829进行电穿孔后互补aroA突变,克隆了来自溶血巴斯德菌生物型A、血清型1的编码5-烯醇丙酮酸莽草酸-3-磷酸合酶的aroA基因。通过插入卡那霉素抗性基因使克隆的溶血巴斯德菌aroA基因失活,并使用PbluescriptII SK+通过等位基因交换将其重新导入亲本溶血巴斯德菌的染色体中。溶血巴斯德菌aroA突变体在小鼠败血症模型中高度减毒。用两剂活的溶血巴斯德菌aroA突变体腹腔免疫的小鼠受到保护,免受致死性亲本菌株的攻击。