Stevenson Andrew, Roberts Mark
Molecular Bacteriology Group, Faculty of Veterinary Medicine, Institute of Comparative Medicine, University of Glasgow, Bearsden Road, Glasgow G61 1QH, UK.
Vaccine. 2004 Oct 22;22(31-32):4300-5. doi: 10.1016/j.vaccine.2004.04.020.
Mice were immunised intranasally with live Bordetella bronchiseptica aroA strains possessing plasmids encoding fragment C (FrgC) of tetanus toxin. FrgC was expressed either from a constitutive tac promoter (strain GVB120) or the Bvg-dependent fhaB promoter (strain GVB1543). Serum anti-FrgC antibody titres were detected in all mice immunised with GVB1543 and GVB120 but the average titres were higher and the responses to FrgC were more consistent in GVB1543 immunised animals. This was reflected in the protective immunity conferred by the different strains: 100% of GVB1543 immunised mice were protected against tetanus toxin challenge whereas only 60% of animals immunised with GVB120 survived tetanus challenge. Viability of the B. bronchiseptica vector strain was shown to be critical to its efficacy as a vector for FrgC.
用携带编码破伤风毒素C片段(FrgC)质粒的支气管败血波氏杆菌aroA活菌株经鼻内免疫小鼠。FrgC由组成型tac启动子(菌株GVB120)或Bvg依赖性fhaB启动子(菌株GVB1543)表达。在用GVB1543和GVB120免疫的所有小鼠中均检测到血清抗FrgC抗体滴度,但平均滴度较高,且在用GVB1543免疫的动物中对FrgC的反应更一致。这反映在不同菌株赋予的保护性免疫中:100%用GVB1543免疫的小鼠受到保护,免受破伤风毒素攻击,而用GVB120免疫的动物中只有60%在破伤风攻击中存活。支气管败血波氏杆菌载体菌株的生存能力对其作为FrgC载体的功效至关重要。