van der Ley P, van der Biezen J, Poolman J T
National Institute of Public Health and Environmental Protection, Antonie van Leeuwenhoeklaan 9, Bilthoven, The Netherlands.
Vaccine. 1995 Mar;13(4):401-7. doi: 10.1016/0264-410x(95)98264-b.
Starting with Neisseria meningitidis strain H44/76, a set of strains was constructed for use in production of a multivalent outer membrane vesicle vaccine. The aim was to remove unwanted outer membrane components and at the same time to improve the range of protection. This was accomplished through transformation with plasmid constructs made in Escherichia coli and their homologous recombination into the meningococcal chromosome. Deletion of the cps locus resulted in loss of expression of the group B capsular polysaccharide as well as the lacto-N-neotetraose structure in lipopolysaccharide. Deletion of the porB gene abolished expression of the class 3 outer membrane protein. Additional copies of the porA gene, encoding the immunodominant class 1 outer membrane protein, were inserted into one of the opa genes and into the rmpM gene encoding the class 4 outer membrane protein. This construction was done with three sets of porA alleles, resulting in three trivalent strains, each of which expressed a different combination of class 1 epitopes.
从脑膜炎奈瑟菌H44/76菌株开始,构建了一组用于生产多价外膜囊泡疫苗的菌株。目的是去除不需要的外膜成分,同时扩大保护范围。这是通过用在大肠杆菌中构建的质粒构建体进行转化,并使其同源重组到脑膜炎球菌染色体中来实现的。cps位点的缺失导致B群荚膜多糖以及脂多糖中乳糖-N-新四糖结构的表达缺失。porB基因的缺失消除了3类外膜蛋白的表达。编码免疫显性1类外膜蛋白的porA基因的额外拷贝被插入到一个opa基因和编码4类外膜蛋白的rmpM基因中。这种构建使用了三组porA等位基因,产生了三个三价菌株,每个菌株表达不同组合的1类表位。