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Development and optimized pairing of mouse monoclonal antibodies for detecting hemagglutinin in novel H7 subtype influenza viruses

机译:小鼠单克隆抗体检测血凝素血凝素的开发和优化配对,H7亚型流感病毒

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The H7 subtype avian influenza threatens public health with respect to poultry and humans. Thus, a specific and sensitive diagnostic test is essential for the management of H7 subtype influenza infections. In this study, five mouse monoclonal antibodies (mAbs) against hemagglutinin (HA) of influenza A/Anhui/1/2013 (H7N9) were produced and characterized by the Western blot, immunofluorescence, and hemagglutination inhibition assays. All five specific mAbs reacted with the HA protein of H7N9 but not with that of H1N1, H3N2, or H5N1. With the combination arrays of capture and detection antibodies, the matched pair mAbs (1C4-coated and 2D7-labeled) were selected and employed in a double-antibody sandwich ELISA (DAS-ELISA). Detection limits of the sandwich ELISA were 0.45 ng mL ?1 for the HA protein derived from A/Anhui/1/2013 (H7N9); or 1 and 2 HA units/50 μL for A/Anhui/1/2013 (H7N9) and A/GD/17SF003/2016 (H7N9), respectively. These anti-HA mAbs against subtype H7 and the novel DAS-ELISA provide a valuable approach for specific detection of the H7 subtype influenza virus and quantification of its HA protein, especially for the novel epidemic H7N9.
机译:H7亚型禽流感威胁与家禽和人类威胁着公共卫生。因此,特定和敏感的诊断测试对于H7亚型流感感染的管理是必不可少的。在本研究中,通过蛋白质印迹,免疫荧光和血血压抑制测定来产生并表征患流感A / ANHUI / 1/2013(H7N9)的五种小鼠单克隆抗体(MAB)。所有五种特异性mAb与H7N9的HA蛋白质反应,但不具有H1N1,H3N2或H5N1的HA蛋白。利用捕获和检测抗体的组合阵列,选择匹配的对mAb(涂覆的1C4涂层和2D7标记)并在双抗体夹心ELISA(Das-ELISA)中使用。夹心ELISA的检测限为0.45ng mlα1,用于衍生自A / Anhui / 1/2013(H7N9)的HA蛋白;对于A / Anhui / 1/2013(H7N9)和A / GD / 17SF003 / 2016(H7N9)的1和2 HA单元/50μL分别为1和2 HA单元/50μL。这些抗HA MAb对亚型H7和新型DAS-ELISA提供了一种有价值的方法,用于特异性检测H7亚型流感病毒和其HA蛋白的定量,特别是对于新的流行病H7N9。

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