Handl C, Rönnberg B, Nilsson B, Olsson E, Jonsson H, Flock J I
Center for Biotechnology, F82 Huddinge University Hospital, Sweden.
J Clin Microbiol. 1988 Aug;26(8):1555-60. doi: 10.1128/jcm.26.8.1555-1560.1988.
The gene for Escherichia coli heat-stable enterotoxin type II (STII) was fused to the genes for protein A from Staphylococcus aureus and beta-galactosidase in two different expression systems. Antibodies raised in rabbits against the protein A-STII fusion protein recognized the beta-galactosidase-STII fusion protein. The latter fusion protein was used as the immobilized antigen in an enzyme-linked immunosorbent assay (ELISA) for detection of STII. The correlation between the results of the ELISA and the intestinal loop test in piglets was 95%, suggesting that the ELISA can be used to reliably detect STII.
在两种不同的表达系统中,将大肠杆菌II型热稳定肠毒素(STII)基因与金黄色葡萄球菌蛋白A基因及β-半乳糖苷酶基因融合。用兔制备的针对蛋白A-STII融合蛋白的抗体可识别β-半乳糖苷酶-STII融合蛋白。后一种融合蛋白被用作酶联免疫吸附测定(ELISA)中的固定抗原,用于检测STII。ELISA结果与仔猪肠袢试验结果之间的相关性为95%,表明该ELISA可用于可靠地检测STII。