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用于检测大肠杆菌不耐热肠毒素的神经节苷脂免疫吸附测定法的评估

Evaluation of a ganglioside immunosorbent assay for detection of Escherichia coli heat-labile enterotoxin.

作者信息

Bäck E, Svennerholm A M, Holmgren J, Möllby R

出版信息

J Clin Microbiol. 1979 Dec;10(6):791-5. doi: 10.1128/jcm.10.6.791-795.1979.

Abstract

The GM1 ganglioside enzyme-linked immunosorbent assay (GM1-ELISA), an immunological method for detection of Escherichia coli heat-labile enterotoxin (LT), was quantitatively and qualitatively compared with the conventional adrenal cell test for the identification of LT-producing strains. A micromodification model of the assay was developed. Enterotoxin preparations from 120 E. coli isolates from individuals with diarrhea, which had been previously shown to be enterotoxigenic by the adrenal cell test, and from 44 control strains of E. coli were compared in parallel by the two methods. Quantitatively the covariation of the enterotoxin titers was highly significant (RS = 0.98, P less than 0.001), the GM1-ELISA being somewhat more sensitive than the adrenal cell test. The methodological error was less than 5% in both tests. Qualitatively the overall agreement for positive and negative reactions for the two methods was 89%. The GM1-ELISA is practical for routine use in the diagnosis of enterotoxigenic E. coli, especially in laboratories without facilities for cell culture.

摘要

GM1神经节苷脂酶联免疫吸附测定法(GM1-ELISA)是一种检测大肠杆菌不耐热肠毒素(LT)的免疫学方法,本研究将其与传统的肾上腺细胞试验进行了定量和定性比较,以鉴定产LT菌株。建立了该测定法的微改良模型。采用这两种方法对先前经肾上腺细胞试验证明具有产肠毒素能力的120株腹泻患者分离的大肠杆菌肠毒素制剂,以及44株大肠杆菌对照菌株进行了平行比较。定量分析表明,两种方法测定的肠毒素效价具有高度显著的协变关系(RS = 0.98,P < 0.001),GM1-ELISA比肾上腺细胞试验稍敏感。两种试验的方法误差均小于5%。定性分析表明,两种方法对阳性和阴性反应的总体一致性为89%。GM1-ELISA可实际应用于产肠毒素大肠杆菌的常规诊断,尤其适用于没有细胞培养设施的实验室。

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