Mamo W, Jonsson P, Flock J I, Lindberg M, Müller H P, Wadström T, Nelson L
Swedish University of Agricultural Sciences, Department of Veterinary Microbiology, Uppsala.
Vaccine. 1994 Aug;12(11):988-92. doi: 10.1016/0264-410x(94)90333-6.
Mice were immunized with fusion proteins encompassing the fibronectin-binding domain of a staphylococcal fibronectin-binding protein (FnBP-A). A specific antibody response against the fibronectin-binding part of the fusion proteins was detected in the serum of all vaccinated animals. The protective potential of these vaccinations was evaluated in a mouse mastitis model, using Staphylococcus aureus, strain SA113, for challenge. The mice vaccinated with FnBP fusion proteins showed a decreased number of bacteria recovered from the mammary glands and significantly reduced cases of severe mastitis. Histopathological examination of tissue from challenged glands of vaccinated mice revealed either no pathological reactions or disseminated inflammatory reactions with focal necrosis whereas four of six examined tissues from challenged glands of non-vaccinated animals showed total necrosis. A combination of FnBP fusion protein with staphylococcal alpha-toxoid did not increase the efficacy of the vaccination and animals vaccinated with alpha-toxoid alone were as sensitive to challenge as those from the non-vaccinated control group. Thus vaccination of mice with recombinant FnBP resulted in significant protection against challenge with S. aureus.
用包含葡萄球菌纤连蛋白结合蛋白(FnBP - A)纤连蛋白结合结构域的融合蛋白对小鼠进行免疫。在所有接种疫苗的动物血清中均检测到针对融合蛋白纤连蛋白结合部分的特异性抗体反应。在小鼠乳腺炎模型中,使用金黄色葡萄球菌SA113菌株进行攻击,评估这些疫苗接种的保护潜力。接种FnBP融合蛋白的小鼠乳腺中回收的细菌数量减少,严重乳腺炎病例显著减少。对接种疫苗小鼠受攻击腺体的组织进行组织病理学检查发现,要么没有病理反应,要么有局灶性坏死的弥漫性炎症反应,而未接种疫苗动物受攻击腺体的六个检查组织中有四个显示完全坏死。FnBP融合蛋白与葡萄球菌类毒素的组合并未提高疫苗接种的效果,单独接种类毒素的动物对攻击的敏感性与未接种疫苗的对照组动物相同。因此,用重组FnBP对小鼠进行疫苗接种可显著保护其免受金黄色葡萄球菌的攻击。