Luk J M, Flock J I, Wadström T
Department of Medical Microbiology, Lund University, Sweden.
FEMS Microbiol Immunol. 1989 Dec;1(8-9):505-10. doi: 10.1111/j.1574-6968.1989.tb02442.x.
Antibody titres against fibronectin-binding protein (FnBP) of Staphylococcus aureus were determined in sera from rabbits immunized with staphylococcal whole cells or purified native fibronectin receptor. An ELISA technique for detection of antibody titres blocking the binding of soluble fibronectin to immobilized FnBP was developed. A recombinant staphylococcal FnBP fused to E. coli beta-galactosidase (gal-FnBp) was used as the immobilized antigen in this test. Serum samples from two different rabbits immunized with native fibronectin receptor gave significant blocking titres, whereas the blocking titres of antisera against staphylococcal whole cells were about 4- to 5-fold lower. Using the gal-FnBP fusion protein, the sensitivity for detection of fibronectin by ELISA was also determined. The detection limit is around 5 ng. The findings are discussed with a view to developing an anti-staphylococcal adherence vaccine and quantitating fibronectin in solution.
测定了用金黄色葡萄球菌全细胞或纯化的天然纤连蛋白受体免疫的兔血清中针对金黄色葡萄球菌纤连蛋白结合蛋白(FnBP)的抗体滴度。开发了一种用于检测阻断可溶性纤连蛋白与固定化FnBP结合的抗体滴度的ELISA技术。在该试验中,将与大肠杆菌β-半乳糖苷酶融合的重组金黄色葡萄球菌FnBP(gal-FnBp)用作固定化抗原。用天然纤连蛋白受体免疫的两只不同兔子的血清样本给出了显著的阻断滴度,而抗金黄色葡萄球菌全细胞抗血清的阻断滴度约低4至5倍。使用gal-FnBP融合蛋白,还测定了ELISA检测纤连蛋白的灵敏度。检测限约为5 ng。结合开发抗葡萄球菌黏附疫苗和定量溶液中纤连蛋白的目的对这些发现进行了讨论。