Roggentin T, Kleineidam R G, Majewski D M, Tirpitz D, Roggentin P, Schauer R
Biochemisches Institut der Universität, Kiel, Germany.
J Immunol Methods. 1993 Jan 4;157(1-2):125-33. doi: 10.1016/0022-1759(93)90078-l.
A rapid and methodologically unusual diagnostic test was developed for the specific detection of Clostridium perfringens, C. septicum and C. sordellii, which cause clostridial myonecrosis. Sialidases (EC 3.2.1.18) secreted by these bacterial species were bound to polyclonal antibodies raised against the respective enzyme and immobilized onto microtiter plates. The activity of bound sialidase was determined with the fluorogenic substrate 4-methylumbelliferyl-alpha-D-N-acetylneuraminic acid. The assay permits the detection of a minimum sialidase activity of about 0.1-1 mU/ml of sample solution within 2 h. The sensitivity of the test was reduced by about three-fold for sialidase activities in samples containing 50% serum. Only a few, low cross-reactivities, which never exceeded 10% of the homologous reaction, were observed with 12 sialidases from other bacterial sources. Clinical isolates of the three clostridial species were analysed by this assay and gave positive signals in the homologous test. The assay for the detection of C. perfringens was applied to nine samples from patients suspected to be suffering from clostridial myonecrosis. There was a high correlation between the results of the immunoassay and the bacteriological analysis of infection.
开发了一种快速且方法独特的诊断测试,用于特异性检测导致梭菌性肌坏死的产气荚膜梭菌、败血梭菌和索氏梭菌。这些细菌分泌的唾液酸酶(EC 3.2.1.18)与针对相应酶产生的多克隆抗体结合,并固定在微量滴定板上。用荧光底物4-甲基伞形酮基-α-D-N-乙酰神经氨酸测定结合唾液酸酶的活性。该检测方法可在2小时内检测出样品溶液中最低约0.1-1 mU/ml的唾液酸酶活性。对于含有50%血清的样品中的唾液酸酶活性,该测试的灵敏度降低了约三倍。用来自其他细菌来源的12种唾液酸酶进行检测时,仅观察到少数低交叉反应性,且从未超过同源反应的10%。用该检测方法对三种梭菌的临床分离株进行分析,在同源测试中均给出阳性信号。将检测产气荚膜梭菌的检测方法应用于9例疑似患有梭菌性肌坏死患者的样本。免疫测定结果与感染的细菌学分析结果之间存在高度相关性。