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Development and application of a monoclonal antibody-based blocking ELISA for detection of antibodies to Tembusu virus in multiple poultry species

机译:基于单克隆抗体的阻断ELISA的开发和应用,用于检测多个家禽种类的Tembusu病毒抗体

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Tembusu virus (TMUV) is a member of the genus Flavivirus. Outbreak of this virus infection in duck flocks was first observed in China in April 2010, causing severe egg drop and neurological signs in laying ducks. Recently reported duck infections in southeastern Asia highlighted the need for well-validated diagnostic methods of TMUV surveillance to understand its epidemiological characteristics and maintenance in nature. Several enzyme-linked immunosorbent assays (ELISAs) for the detection of TMUV infection have been reported, but none have been applied to high-throughput diagnostics. In this study, a monoclonal antibody (MAb) against TMUV was generated and characterized. MAb 9E4 was shown to bind specifically to a disulfide bond-dependent epitope on the domain I/II of TMUV E protein, and a blocking ELISA was established based on this MAb. The cut-off percentage inhibition value for negative sera was set at 30%. By comparison with the virus neutralization test, the specificity and sensitivity of the blocking ELISA were 96.37% and 100%, respectively, and the kappa value was 0.966, based on 416 serum samples collected from both experimentally and clinically infected ducks, geese and chickens. A good correlation (r2?=?07998, P??0.001) was observed between the blocking ELISA and plaque reduction neutralization test (PRNT) titers. Using archived duck serum samples collected between 2009 and 2015, the seroprevalence in duck flocks raised in Northern China was estimated by blocking ELISA. Our MAb-based blocking ELISA provides a reliable and rapid diagnostic tool for serological monitoring of TMUV infection and evaluation of immune status following TMUV vaccination in multiple poultry species.
机译:Tembusu病毒(TMUV)是黄病毒属的成员。在2010年4月首次在中国观察到这种病毒感染的这种病毒感染,导致严重的蛋下降和铺设鸭子的神经系统。最近报道了东南亚的鸭感染强调了需要验证的TMUV监控诊断方法,以了解其本质上的流行病学特征和维护。已经报道了几种用于检测TMUV感染的酶联免疫吸附测定(ELISAS),但没有应用于高通量诊断。在该研究中,产生抗TMUV的单克隆抗体(MAB)并表征。显示MAB 9E4特异性地结合在TMUV E蛋白的结构域I / II上的二硫键依赖性表位,并且基于该MAb建立阻断ELISA。阴性血清的截止百分比抑制值设定为30%。通过与病毒中和试验的比较,阻断ELISA的特异性和敏感性分别为96.37%,达到100%,kappa值为0.966,基于从实验和临床感染的鸭子,鹅和鸡的416个血清样本。在阻断ELISA和斑块还原中和测试(PRNT)滴度之间观察到良好的相关性(R2?= 07998,p≤0.001)。在2009年至2015年间收集的存档鸭血清样本,通过阻塞ELISA估计,中国北部养殖的鸭绒植物中的Seroprevalience。我们基于MAB的阻断ELISA提供了一种可靠且快速的诊断工具,可用于TMUV感染的血清学监测,并在多种家禽种类中接种TMUV疫苗接种后的免疫状态评估。

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