Aubert D, Toubas D, Foudrinier F, Villena I, Gomez J E, Marx C, Lepan H, Lemaire P, Jacquier P, Bonhomme A, Pinon J M
Laboratoire de Parasitologie-Mycologie, UPRES EA2070, Equipe IV INSERM U314, IFR 53, Hôpital Maison-Blanche, Reims, France.
Anal Biochem. 1997 Apr 5;247(1):25-9. doi: 10.1006/abio.1997.2030.
Methods used to detect DNA after transfer to nitro-cellulose or nylon membranes are all based on slow incubation with agitation. We describe an application of the ELIFA technique (enzyme-linked immunofiltration assay) for rapid detection of DNA immobilized on a membrane by active filtration of the reagents across the membrane. The different steps (saturation, hybridization to a nonisotopically labeled probe, washing, and immunoenzymatic revelation) are automated and controlled by a microcomputer that determines the direction of flow and flow rates of the solutions through the membrane. We applied this method to the detection of Toxoplasma gondii DNA in 108 samples of amniotic fluid during antenatal tests for toxoplasmosis and compared the results with those obtained by the conventional method. In addition to a major time saving (2 h against almost 15 h), automation improves reproducibility and avoids manipulation of the membranes between the different steps, while keeping the same sensitivity and specificity as the standard method.
将DNA转移至硝酸纤维素或尼龙膜上后用于检测的方法均基于在搅拌下缓慢孵育。我们描述了一种ELIFA技术(酶联免疫过滤测定)的应用,通过试剂在膜上的主动过滤来快速检测固定在膜上的DNA。不同步骤(封闭、与非同位素标记探针杂交、洗涤和免疫酶显色)由微型计算机自动控制,该微型计算机确定溶液通过膜的流动方向和流速。我们将该方法应用于产前弓形虫病检测中108份羊水样本中弓形虫DNA的检测,并将结果与传统方法所得结果进行比较。除了大幅节省时间(2小时对比近15小时)外,自动化还提高了重现性,避免了不同步骤之间对膜的操作,同时保持与标准方法相同的灵敏度和特异性。