Stiffler-Rosenberg G, Fey H
J Clin Microbiol. 1978 Nov;8(5):473-9. doi: 10.1128/jcm.8.5.473-479.1978.
The enzyme-linked immunosorbent assay (ELISA) introduced for the detection of staphylococcal enterotoxins by Saunders et al., Simon and Terplan, and ourselves has proved to be a simple, reliable, and sensitive test. A new modification is described that uses polystyrene balls (diameter, 6 mm) coated individually with antibody against one of the toxins A, B, or C. In a single tube, 20 ml of the food extract was incubated with the three balls differently stained, which were then each tested for the uptake of enterotoxin by a competitive ELISA. A concentration of 0.1 ng or less of enterotoxin per ml can be measured, making tedious concentration procedures of the extracts superfluous. Culture supernatants and extracts from foods artificially or naturally contaminated with toxin were successfully examined. Cross-reactions did not occur, and nonspecific interfering substances did not create serious problems.
桑德斯等人、西蒙和特尔普朗以及我们自己引入的用于检测葡萄球菌肠毒素的酶联免疫吸附测定(ELISA)已被证明是一种简单、可靠且灵敏的检测方法。本文描述了一种新的改进方法,该方法使用分别包被有针对毒素A、B或C之一的抗体的聚苯乙烯球(直径6毫米)。在单个试管中,将20毫升食物提取物与三个颜色不同的球一起孵育,然后通过竞争性ELISA对每个球进行肠毒素摄取检测。每毫升可检测到浓度为0.1纳克或更低的肠毒素,使得提取物繁琐的浓缩程序变得多余。成功检测了人工或天然被毒素污染的食物的培养上清液和提取物。未发生交叉反应,非特异性干扰物质也未造成严重问题。