Petros B L, Procell P M, Campbell G H, Collins F H
Bull World Health Organ. 1989;67(5):525-33.
A nitrocellulose (NC) membrane was evaluated as a solid-phase support for the detection of malaria-infected mosquitos using monoclonal antibodies (MAb) with a laboratory model based on Plasmodium inui and Anopheles dirus. MAbs produced against sporozoites of the N34 strain of P. inui, and selected by immunofluorescence assay and the circumsporozoite precipitin test, were used. A one-site indirect NC-ELISA that used unlabelled MAb and enzyme-labelled anti-mouse IgG was developed. Its sensitivity was about 200 sporozoites and it reliably detected one infected mosquito in a pool of 20. This indirect NC-ELISA has the advantage that it does not require direct conjugation of the MAb to an enzyme or biotin. In the direct one-site NC-ELISA, which is also reported, the relatively simple biotinylation procedure was an alternative to the enzyme- or radiolabelled MAbs. The NC-ELISAs were simple and rapid. Furthermore, the indirect NC-ELISA can be used to detect sporozoite antigen localized in various body sectors of mosquitos.
使用基于约氏疟原虫和大劣按蚊的实验室模型,评估了硝酸纤维素(NC)膜作为使用单克隆抗体(MAb)检测感染疟疾蚊子的固相支持物。使用针对约氏疟原虫N34株子孢子产生的、通过免疫荧光测定和环子孢子沉淀试验筛选出的单克隆抗体。开发了一种使用未标记单克隆抗体和酶标记抗小鼠IgG的一步间接NC-ELISA。其灵敏度约为200个子孢子,并且能可靠地检测出20只蚊子混合样本中的一只感染蚊子。这种间接NC-ELISA的优点是不需要将单克隆抗体直接与酶或生物素偶联。在同样报道的直接一步NC-ELISA中,相对简单的生物素化程序是酶标记或放射性标记单克隆抗体的替代方法。NC-ELISA方法简单、快速。此外,间接NC-ELISA可用于检测定位于蚊子身体各个部位的子孢子抗原。