首页> 美国卫生研究院文献>Clinical and Diagnostic Laboratory Immunology >Development of a Fluorescent Microsphere Immunoassay for Detection of Antibodies against Porcine Reproductive and Respiratory Syndrome Virus Using Oral Fluid Samples as an Alternative to Serum-Based Assays
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Development of a Fluorescent Microsphere Immunoassay for Detection of Antibodies against Porcine Reproductive and Respiratory Syndrome Virus Using Oral Fluid Samples as an Alternative to Serum-Based Assays

机译:荧光微球免疫测定技术的发展用于检测猪繁殖与呼吸综合征病毒的抗体使用口服液样品替代血清检测方法

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摘要

For effective disease surveillance, rapid and sensitive assays are needed to detect antibodies developed in response to porcine reproductive and respiratory syndrome virus (PRRSV) infection. In this study, we developed a multiplexed fluorescent microsphere immunoassay (FMIA) for detection of PRRSV-specific antibodies in oral fluid and serum samples. Recombinant nucleocapsid protein (N) and nonstructural protein 7 (nsp7) from both PRRSV genotypes (type I and type II) were used as antigens and covalently coupled to Luminex fluorescent microspheres. Based on an evaluation of 488 oral fluid samples with known serostatus, the oral fluid-based FMIAs achieved >92% sensitivity and 91% specificity. For serum samples (n = 1,639), the FMIAs reached >98% sensitivity and 95% specificity. The assay was further employed to investigate the kinetics of the antibody response in infected pigs. In oral fluid, the N protein was more sensitive for the detection of early infection (7 and 14 days postinfection), but nsp7 detected a higher level and longer duration of antibody response (28 days postinfection). In serum, the antibodies specific to nsp7 and N proteins were detected as early as 7 days postinfection, and the responses lasted more than 202 days. This study provides a framework from which a more robust assay could be developed to profile the immune response to multiple PRRSV antigens in a single test. The development of oral fluid-based diagnostic tests will change the way we survey diseases in swine herds and improve our ability to cheaply and efficiently track PRRSV infections in both populations and individual animals.
机译:为了进行有效的疾病监视,需要快速而灵敏的检测方法来检测针对猪繁殖与呼吸综合征病毒(PRRSV)感染而产生的抗体。在这项研究中,我们开发了一种用于检测口腔液和血清样品中PRRSV特异性抗体的多重荧光微球免疫测定(FMIA)。来自两种PRRSV基因型(I型和II型)的重组核衣壳蛋白(N)和非结构蛋白7(nsp7)被用作抗原并与Luminex荧光微球共价偶联。根据对488份具有已知血清状况的口腔液样品的评估,基于口腔液的FMIA达到了> 92%的敏感性和91%的特异性。对于血清样品(n = 1,639),FMIAs达到了> 98%的敏感性和95%的特异性。该测定法还用于研究感染猪中抗体应答的动力学。在口腔液中,N蛋白对于早期感染(感染后7天和14天)的检测更为敏感,但是nsp7检测到更高水平的抗体反应(感染后28天)更长且持续时间更长。在血清中,最早在感染后7天就检测到了对nsp7和N蛋白具有特异性的抗体,反应持续了超过202天。这项研究提供了一个框架,通过该框架可以开发出更强大的分析方法,以在一次测试中分析对多种PRRSV抗原的免疫反应。基于口服液的诊断测试的发展将改变我们调查猪群疾病的方式,并提高我们廉价,高效地跟踪种群和个体动物中PRRSV感染的能力。

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