Xu Yin-Di, Guo Ai-Zhen, Liu Wei-Hong, Jia Ai-Qing, Chen Huan-Chun
State Key Laboratory of Agricultural Microbiology, Provincial Key Laboratory of Preventive Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, China.
Sheng Wu Gong Cheng Xue Bao. 2006 May;22(3):366-72.
Salmonella choleraesuis C500 strain was an attenuated vaccine strain to prevent piglet paratyphoid, attenuated by chemical method. Although the vaccine has good immunogenicity, it remains some residual virulence. In order to develop a safer vaccine strain and exploit C500 as a live vaccine vector for mucosal immunization, delta crp delta asd double deletion mutant was constructed. Firstly, the recombination suicide vector with 320 bp-deleted crp (cAMP receptor protein) gene and sacB (sucrose-sensitive gene) gene was constructed and conjugated with C500. The unmarked crp deleted strain without resistance was selected by two-step method and crp deletion on the genome was determined by PCR. Then the asd (beta-aspartic semialdehyde dehydrogenase) gene was further deleted in the delta crp strain by the same method. Foreign DAP (diaminopimelic acid) must be supplied for delta crp delta asd mutant to grow. The phenotype, growth properties and virulence in mice of delta crp mutant were further characterized. In conclusion, the delta crp delta asd double-deletion mutant was successfully constructed. The delta crp delta asd mutant can be used as a live vector to express foreign genes and to develop potential oral multivalent vaccines.
猪霍乱沙门氏菌C500株是一株通过化学方法致弱的预防仔猪副伤寒的疫苗株。尽管该疫苗具有良好的免疫原性,但仍存在一定的残余毒力。为了开发更安全的疫苗株并将C500用作黏膜免疫的活疫苗载体,构建了ΔcrpΔasd双缺失突变株。首先,构建了缺失320 bp的crp(cAMP受体蛋白)基因和sacB(蔗糖敏感基因)基因的重组自杀载体,并将其与C500接合。通过两步法筛选出无抗性的未标记crp缺失株,并通过PCR确定基因组上的crp缺失情况。然后,采用相同方法在Δcrp株中进一步缺失asd(β-天冬氨酸半醛脱氢酶)基因。ΔcrpΔasd突变体生长必须供应外源二氨基庚二酸。进一步对Δcrp突变体在小鼠中的表型、生长特性和毒力进行了表征。总之,成功构建了ΔcrpΔasd双缺失突变体。ΔcrpΔasd突变体可作为表达外源基因的活载体,用于开发潜在的口服多价疫苗。