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Production and identification of monoclonal antibodies and development of a sandwich ELISA for detection of the H3-subtype avian influenza virus antigen

机译:用于检测H3亚型禽流感病毒抗原的单克隆抗体和夹层ELISA发育的生产和鉴定

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摘要

The H3 subtype of avian influenza virus (AIV) is widespread in avian species and is frequently isolated in surveillance projects; thus, we have developed a more effective diagnostic approach of a monoclonal antibody (mAb)-based sandwich ELISA for the H3 AIV detection. First, we have produced the essential reagent of mAb against AIV H3 strains with the development of an mAb-Mouse immunization with a purified H3-subtype AIV strain and cell fusion to generate hybridoma cells. These cells were screened with hemagglutination inhibition (HI) tests, and optimal cells were subcloned. We chose a hybridoma cell line that steadily secreted a specific H3-subtype AIV mAb, designated 9F12, that belongs to the IgG1 subclass and has a K-type light chain. 9F12 was shown to bind specifically to the H3-subtype AIV antigen by both immunofluorescence assay and Western blot analysis. Finally, a 9F12-based sandwich ELISA was successfully developed and used to specifically test for this antigen. The sandwich ELISA conditions were optimized, and the specificity and sensitivity were validated. The results for clinical sample detection were consistent with viral isolation. Consequently, the 9F12-based sandwich ELISA is a specific, sensitive, robust, rapid and versatile diagnostic tool for H3-subtype AIV and provides a promising strategy for effective influenza virus prevention and control.
机译:H3禽流感病毒(AIV)的H3亚型在禽类种类中普遍存在,经常在监测项目中孤立;因此,我们开发了一种更有效的单克隆抗体(MAB)的诊断方法 - 基于H3 AIV检测的夹层ELISA。首先,我们通过纯化的H3-亚型AIV菌株和细胞融合产生了MAB-小鼠免疫,产生了对AIV H3菌株的MAB的必需试剂。用血晶抑制(HI)试验筛选这些细胞,并且亚克隆最佳细胞。我们选择杂交瘤细胞系,其稳定地分泌特定的H3-亚型AIV MAb,其指定的9F12,其属于IgG1亚类并具有K型轻链。显示9F12通过免疫荧光测定和Western印迹分析,特异性地结合H3-亚型AIV抗原。最后,成功地开发了一种9F12的三明治ELISA并用于专门测试该抗原。夹层ELISA条件经过优化,验证了特异性和灵敏度。临床样品检测的结果与病毒分离一致。因此,基于9F12的夹心ELISA是H3-亚型AIV的特异性,敏感,鲁棒,快速且多功能诊断工具,并为有效的流感病毒预防和控制提供了有希望的策略。

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