Svennerholm A M, Wiklund G
J Clin Microbiol. 1983 Apr;17(4):596-600. doi: 10.1128/jcm.17.4.596-600.1983.
A modified, quicker and simpler GM1-enzyme-linked immunosorbent assay procedure for detection of Escherichia coli heat-labile enterotoxin (LT) has been developed with the intent that it should be useful in less well-equipped laboratories. The method, which makes use of stable reagents including commercially available horseradish peroxidase immunoglobulin conjugate, can detect LT in overnight cultures within 1 working day (8 h), and the tests can be read with the naked eye. This GM1-horseradish peroxidase-enzyme-linked immunosorbent assay shows excellent quantitative and qualitative correlation with the conventional GM1-enzyme-linked immunosorbent assay. When 100 human E. coli strains were analyzed blindly and in parallel by the two methods, LT production was identified in 50 out of 50 LT-positive strains and in 0 out of 50 LT-negative strains by either method.
已开发出一种改良的、更快且更简单的GM1酶联免疫吸附测定法,用于检测大肠杆菌热不稳定肠毒素(LT),目的是使其在设备不太完善的实验室中有用。该方法利用包括市售辣根过氧化物酶免疫球蛋白缀合物在内的稳定试剂,可在1个工作日(8小时)内检测过夜培养物中的LT,且检测结果可用肉眼读取。这种GM1-辣根过氧化物酶-酶联免疫吸附测定法与传统的GM1-酶联免疫吸附测定法在定量和定性方面具有极好的相关性。当用这两种方法对100株人源大肠杆菌菌株进行盲法平行分析时,两种方法在50株LT阳性菌株中均鉴定出50株产生LT,在50株LT阴性菌株中均未鉴定出LT产生。