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建立一种用于检测抗流感 A 病毒和新城疫病毒抗体反应的双荧光微球免疫分析(FMIA)。

Development of a duplex Fluorescent Microsphere Immunoassay (FMIA) for the detection of antibody responses to influenza A and newcastle disease viruses.

机构信息

Department of Animal Science, University of Manitoba, Winnipeg, Manitoba R3T 2 N2, Canada; National Centre for Foreign Animal Diseases, Winnipeg, Manitoba, Canada.

Department of Animal Science, University of Manitoba, Winnipeg, Manitoba R3T 2 N2, Canada; Atlantic Veterinary College, University of Prince Edward Island, Charlottetown, Prince Edward Island C1A 4P3, Canada.

出版信息

J Immunol Methods. 2014 Mar;405:167-77. doi: 10.1016/j.jim.2014.02.004. Epub 2014 Feb 17.

Abstract

Highly pathogenic avian influenza virus (HPAI) and virulent forms of avian paramyxovirus-1 (APMV-1) cause serious illnesses in domestic poultry, both of which are reportable to the World Organization of Animal Health (OIE). The clinical presentation of avian influenza (AI) and APMV-1 infections are difficult to differentiate, emphasizing the importance of rapid and sensitive serologic assays that are able to distinguish them. Currently, a variety of serological assays are used for the serologic diagnosis of both diseases, but these assays are not used in multiplex formats. In this study, development of a duplex fluorescent microsphere immunoassay (FMIA) based on Luminex xMAP Technology is described. The assay employs MagPlex magnetic microspheres that are covalently coated with recombinant avian influenza virus nucleoprotein and APMV-1 nucleocapsid antigens produced in a baculovirus insect cell expression system. The assay is able to detect AIV antibodies against all existing hemagglutinin (H1-H16) subtypes and simultaneously detect antibodies against APMV-1. In the process of this assay development different bead coupling conditions were compared. The assay has the capability of detecting serum antibodies from chickens and turkeys and optimization was accomplished by using 2462 chicken and 446 turkey field and experimental sera and had a comparable detection capability with currently used assays in the laboratory. Assay threshold values were calculated with Receiver Operating Characteristic Analysis (ROC) in non-parametric analysis due to a highly skewed data distribution; this analysis resulted in AIV nucleoprotein relative diagnostic sensitivity and specificity of 99.7%, and 97.3% respectively. The APMV-1 nucleocapsid relative diagnostic sensitivity and specificity were 95.4%, and 98.5% respectively.

摘要

高致病性禽流感病毒(HPAI)和强毒形式的禽副黏病毒-1(APMV-1)可导致家禽发生严重疾病,这两种病毒均需向世界动物卫生组织(OIE)报告。禽流感(AI)和 APMV-1 感染的临床症状难以区分,这强调了快速、灵敏的血清学检测方法的重要性,这种方法能够对它们进行区分。目前,有多种血清学检测方法可用于这两种疾病的血清学诊断,但这些检测方法不能以多重格式使用。在这项研究中,描述了基于 Luminex xMAP 技术的荧光微球免疫分析(FMIA)的开发。该检测方法采用 MagPlex 磁性微球,这些微球通过共价偶联包被了在杆状病毒昆虫细胞表达系统中产生的重组禽流感病毒核蛋白和 APMV-1 核衣壳抗原。该检测方法能够检测针对所有现有血凝素(H1-H16)亚型的 AIV 抗体,并且能够同时检测针对 APMV-1 的抗体。在该检测方法的开发过程中,比较了不同的微球偶联条件。该检测方法具有检测鸡和火鸡血清抗体的能力,通过使用 2462 份鸡和 446 份火鸡现场和实验血清进行优化,其检测能力与实验室中目前使用的检测方法相当。由于数据分布高度偏斜,使用非参数分析中的接收器工作特征分析(ROC)计算了检测阈值;该分析导致 AIV 核蛋白相对诊断灵敏度和特异性分别为 99.7%和 97.3%。APMV-1 核衣壳相对诊断灵敏度和特异性分别为 95.4%和 98.5%。

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