Nielsen K, Yu W L, Lin M, Davis S A Nadin, Elmgren C, Mackenzie R, Tanha J, Li S, Dubuc G, Brown E G, Keleta L, Pasick J
Canadian Food Inspection Agency, Ottawa Laboratories (Fallowfield), 3851 Fallowfield Road, Ottawa, Ontario, Canada.
J Immunoassay Immunochem. 2007;28(4):307-18. doi: 10.1080/15321810701603443.
A rapid and effective lateral flow assay (LFA) for detection of avian influenza virus (AIV) was developed. For antigen capture, the assay used monoclonal antibody specific for a conserved nuclear protein (NP) epitope, immobilized on a cellulose acetate matrix, in conjunction with a second NP monoclonal antibody chemically linked to either coloured latex beads or colloidal gold particles contained in a sample pad for detection. Virus sample added to the sample pad flowed into the trapping antibody to form a visible band as well as a second, control band further along the acetate strip. The control band consisted of recombinant protein A/G, also immobilized on the matrix. A second LFA for detection of chicken antibody to AIV was developed where NP antigen was immobilized on the matrix with recombinant protein A/G immobilized as a control band. Latex beads or colloidal gold particles to which monoclonal anti-chicken antibody was attached, were used as the indicator system.
开发了一种用于检测禽流感病毒(AIV)的快速有效的侧向流动分析(LFA)方法。为了捕获抗原,该分析使用了针对保守核蛋白(NP)表位的单克隆抗体,其固定在醋酸纤维素基质上,并与化学连接到彩色乳胶珠或样品垫中包含的胶体金颗粒上的第二种NP单克隆抗体结合用于检测。添加到样品垫中的病毒样品流入捕获抗体中,在醋酸纤维素条上形成可见条带以及更远的第二条对照条带。对照条带由同样固定在基质上的重组蛋白A/G组成。开发了第二种用于检测鸡抗AIV抗体的LFA,其中NP抗原固定在基质上,重组蛋白A/G固定作为对照条带。附着有抗鸡单克隆抗体的乳胶珠或胶体金颗粒用作指示系统。