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阻断酶联免疫吸附试验检测 H6 流感抗体。

Detection of H6 influenza antibody by blocking enzyme-linked immunosorbent assay.

机构信息

School of Veterinary Medicine, National Taiwan University, Taipei, Taiwan.

出版信息

Vet Microbiol. 2010 May 19;142(3-4):205-10. doi: 10.1016/j.vetmic.2009.09.064. Epub 2009 Oct 20.

Abstract

Low pathogenic H6N1 avian influenza viruses (AIVs) have circulated in domestic chickens since 1972 in Taiwan. Detection of avian influenza (AI) antibody is a routine work for AI control in Taiwan. The currently available commercial enzyme-linked immunosorbent assays (ELISAs) are unable to differentiate antibody responses between different subtypes. To this end, a panel of monoclonal antibodies (mAbs) to A/chicken/Taiwan/2838V/00 (H6N1) was developed and implemented a blocking ELISA (bELISA) to detect the H6 antibody. These mAbs were confirmed specific to H6 AIVs. One monoclonal antibody was purified and labeled with horseradish peroxidase to set up a bELISA. The cut-off value was calculated to be 30% inhibition percentage from 138 H6-negative sera. The sensitivity and specificity of the bELISA were 100% and 97%, respectively. The bELISA detected seroconversion in H6-infected farms earlier than hemagglutination inhibition test. The results show that this bELISA could be used to detect H6 infection in the field.

摘要

低致病性 H6N1 禽流感病毒(AIV)自 1972 年以来一直在台湾的家鸡中传播。在台湾,检测禽流感(AI)抗体是 AI 控制的常规工作。目前可用的商业酶联免疫吸附测定(ELISA)无法区分不同亚型的抗体反应。为此,开发了一组针对 A/chicken/Taiwan/2838V/00(H6N1)的单克隆抗体(mAbs),并实施了阻断 ELISA(bELISA)来检测 H6 抗体。这些 mAbs 被确认为特异性针对 H6 AIV。一种单克隆抗体被纯化并标记辣根过氧化物酶,以建立 bELISA。从 138 份 H6 阴性血清中计算出 30%抑制率作为截断值。bELISA 的灵敏度和特异性分别为 100%和 97%。bELISA 比血凝抑制试验更早地检测到 H6 感染的农场中的血清转换。结果表明,该 bELISA 可用于现场检测 H6 感染。

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