Brooks J L, Mirhabibollahi B, Kroll R G
Department of Microbiology, Agricultural and Food Research Council Institute of Food Research, Shinfield, Reading, United Kingdom.
Appl Environ Microbiol. 1990 Nov;56(11):3278-84. doi: 10.1128/aem.56.11.3278-3284.1990.
An amperometric electrochemical immunoassay specific for protein A-bearing Staphylococcus aureus was developed. The method was based on a sandwich immunosorbent assay and incorporated an enzyme amplification step, using a NAD-specific redox cycle generating NADH (C. H. Stanley, A. Johannsson, and C. H. Self, J. Immunol. Methods 83:89-95, 1985). Reduction of the mediator, ferricyanide, was dependent on the initial concentration of antigen. The final potential was measured by using a Pt disk electrode polarized at +0.8 V to the Ag/AgCl reference electrode. The assay was rapid (4 h) and generated protein A- and cell (S. aureus)-dependent signals. The system was highly sensitive and could detect 10 pg of protein A ml-1 and less than 100 CFU of S. aureus ml-1. Similar sensitivities were observed with S. aureus cultures inoculated into beef and milk, but the sensitivity was reduced slightly (ca. 10(3) g-1) with samples of Cheddar cheese.
开发了一种针对携带蛋白A的金黄色葡萄球菌的安培型电化学免疫分析法。该方法基于夹心免疫吸附测定法,并纳入了酶扩增步骤,使用产生NADH的NAD特异性氧化还原循环(C. H. Stanley、A. Johannsson和C. H. Self,《免疫学方法杂志》83:89 - 95,1985年)。媒介物铁氰化物的还原取决于抗原的初始浓度。通过使用相对于Ag/AgCl参比电极极化在 +0.8 V的铂盘电极测量最终电位。该测定法快速(4小时),并产生依赖于蛋白A和细胞(金黄色葡萄球菌)的信号。该系统高度灵敏,能够检测到10 pg/ml的蛋白A以及每毫升少于100 CFU的金黄色葡萄球菌。将金黄色葡萄球菌培养物接种到牛肉和牛奶中时观察到类似的灵敏度,但在切达干酪样品中灵敏度略有降低(约10³ CFU/g)。