首页> 美国卫生研究院文献>Journal of Veterinary Science >An enhanced immunochromatographic strip test using colloidal gold nanoparticle-labeled dual-type N proteins for detection of antibodies to PRRS virus
【2h】

An enhanced immunochromatographic strip test using colloidal gold nanoparticle-labeled dual-type N proteins for detection of antibodies to PRRS virus

机译:使用胶体金纳米颗粒标记的双型N蛋白的增强型免疫层析试纸条检测PRRS病毒抗体

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Porcine reproductive and respiratory syndrome (PRRS) is recognized as one of the most important infectious diseases causing serious economic loss in the swine industry worldwide. Due to its increasing genetic diversity, a rapid and accurate diagnosis is critical for PRRS control. The immunochromatographic strip test (ICST) is a rapid and convenient type of immunoassay. In this study, an on-site immunochromatographic assay-based diagnostic method was developed for detection of PRRS virus (PRRSV)-specific antibodies. The method utilized colloidal gold nanoparticle-labeled dual-type nucleocapsid proteins encoded by open reading frame 7. We evaluated 991 field samples from pig farms and 66 serum samples from experimentally PRRSV-inoculated pigs. Based on true PRRSV-specific antibody-positive or -negative sera determined by immunofluorescence assay and IgM enzyme-linked immunosorbent assay (ELISA), the specificity and sensitivity of the ICST were 97.5% and 91.1%, respectively, similar to those of a commercial ELISA (IDEXX PRRS X3 Ab). More importantly, the ICST was completed within 15 min and could detect the PRRSV-specific antibody at an earlier stage of infection (3–7 days) than that of ELISA (7+ days). The results demonstrate that the developed ICST has great potential as an on-farm diagnostic method, providing excellent diagnostic performance in a quick and convenient manner.
机译:猪繁殖与呼吸综合症(PRRS)被公认为是最重要的传染病之一,在全世界的养猪业中造成了严重的经济损失。由于其遗传多样性的增加,快速准确的诊断对于PRRS的控制至关重要。免疫色谱带检测(ICST)是一种快速便捷的免疫测定方法。在这项研究中,开发了一种基于现场免疫色谱分析的诊断方法来检测PRRS病毒(PRRSV)特异性抗体。该方法利用了由开放阅读框7编码的胶体金纳米颗粒标记的双型核衣壳蛋白。我们评估了991个猪场的田间样品和66个PRRSV接种猪的血清样品。根据免疫荧光法和IgM酶联免疫吸附法(ELISA)确定的真实PRRSV特异性抗体阳性或阴性血清,ICST的特异性和敏感性分别为97.5%和91.1%,与市售的相似。 ELISA(IDEXX PRRS X3 Ab)。更重要的是,ICST在15分钟内完成,并且可以在感染的早期阶段(3-7天)比ELISA阶段(7+天)检测到PRRSV特异性抗体。结果表明,所开发的ICST具有作为农场诊断方法的巨大潜力,可以快速方便地提供出色的诊断性能。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号