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H5特异性单克隆抗体的制备以及用于检测多种物种中H5抗体的竞争性酶联免疫吸附测定法的开发。

Production of H5-specific monoclonal antibodies and the development of a competitive enzyme-linked immunosorbent assay for detection of H5 antibodies in multiple species.

作者信息

Dlugolenski Daniel, Hauck Rüdiger, Hogan Robert J, Michel Frank, Mundt Egbert

机构信息

Department of Population Health, College of Veterinary Medicine, University of Georgia, 953 College Station Road, Athens, GA 30602, USA.

出版信息

Avian Dis. 2010 Mar;54(1 Suppl):644-9. doi: 10.1637/8683-030909-ResNote.1.

Abstract

The hemagglutinin gene of an avian influenza virus (AIV) A/duck/NC/674964/07 (H5N2) was cloned and expressed in a baculovirus system (H5-Bac). In parallel, a recombinant hemagglutinin of A/Vietnam/1203/04 (H5N1) was expressed in mammalian cells, purified, and used for generation of H5-specific monoclonal antibodies (MAb). The purified H5-Bac was used to develop a competitive enzyme-linked immunosorbent assay (cELISA) to detect H5 antibodies in a species-independent approach using one of the established H5-specific MAbs as the competitor antibody. The cELISA performed with influenza antibody-free sera or with sera of animals infected with other than H5-encoding AIV showed no significant inhibition of H5-MAb binding, indicating high test specificity. In contrast, sera of poultry (chickens, turkeys, ducks) experimentally infected with H5-encoding AIV were able to significantly inhibit the binding of the MAb in a species-independent approach. Comparison of the results of the cELISA with results obtained by a hemagglutination inhibition assay showed a gradient of the sensitivity (turkeys > ducks > chicken). The described results show that H5-specific antibodies in sera can be detected in a species-independent approach by using a recombinant protein.

摘要

克隆了禽流感病毒(AIV)A/duck/NC/674964/07(H5N2)的血凝素基因,并在杆状病毒系统(H5-Bac)中进行表达。同时,在哺乳动物细胞中表达、纯化了A/越南/1203/04(H5N1)的重组血凝素,并用于制备H5特异性单克隆抗体(MAb)。纯化后的H5-Bac用于开发一种竞争酶联免疫吸附测定(cELISA),以一种独立于物种的方法检测H5抗体,使用一种已确立的H5特异性MAb作为竞争抗体。用无流感抗体的血清或感染非H5编码AIV的动物血清进行的cELISA显示,对H5-MAb结合没有明显抑制,表明检测特异性高。相比之下,经实验感染H5编码AIV的家禽(鸡、火鸡、鸭)血清能够以独立于物种的方法显著抑制MAb的结合。将cELISA结果与血凝抑制试验结果进行比较,显示出敏感性梯度(火鸡>鸭>鸡)。所述结果表明,使用重组蛋白可以以独立于物种的方法检测血清中的H5特异性抗体。

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