Shah D B, Kauffman P E, Boutin B K, Johnson C H
J Clin Microbiol. 1982 Sep;16(3):504-8. doi: 10.1128/jcm.16.3.504-508.1982.
A solid-phase sandwich assay that was able to differentiate heat-labile-enterotoxin-producing colonies of Escherichia coli and choleratoxin-producing colonies of Vibrio cholerae from nontoxigenic colonies is described. Flexible polyvinyl chloride plastic film coated with antibody molecules was allowed to react with partially lysed bacterial colonies in a standard petri dish. The immobilized antigen on the plastic film was then labeled with radioiodinated antibody. Autoradiography identified antigen-containing colonies. As little as 5 to 25 pg of pure toxin contained in a 3- to 4-mm-diameter circle was reliably detected by this method. The synthesis of heat-labile enterotoxin and choleratoxin by cells growing on selective media such as eosin methylene blue agar, MacConkey agar, Endo agar, and thiosulfate-citrate-bile salts-sucrose agar was demonstrated. The method appears to be suitable for large-scale surveys.
本文描述了一种固相夹心测定法,该方法能够从非产毒菌落中区分出产生不耐热肠毒素的大肠杆菌菌落和产生霍乱毒素的霍乱弧菌菌落。将涂有抗体分子的柔性聚氯乙烯塑料薄膜与标准培养皿中部分裂解的细菌菌落进行反应。然后用放射性碘标记的抗体对塑料薄膜上固定的抗原进行标记。放射自显影法可鉴定出含抗原的菌落。用此方法可可靠地检测出直径3至4毫米的圆圈中低至5至25皮克的纯毒素。已证明在伊红美蓝琼脂、麦康凯琼脂、远藤琼脂和硫代硫酸盐-柠檬酸盐-胆盐-蔗糖琼脂等选择性培养基上生长的细胞能合成不耐热肠毒素和霍乱毒素。该方法似乎适用于大规模调查。