水族病毒检测与分析单克隆抗体的研制与应用

Xiao-chan Gao, Zhong-yuan Chen, Jia Liu, Qi-ya Zhang
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摘要

单克隆抗体(mab)在水样病毒检测中发挥着重要作用。制备了3株针对草鱼呼肠孤病毒(GCRV)的单克隆抗体。同型分析显示,这3个单抗均属于IgG2b亚类。Western blot检测显示,这三种单抗均与GCRV 69 kDa蛋白(推测的VP5)发生反应。除了GCRV的69 kDa蛋白外,mAb 4B6还能识别54 kDa蛋白。采用Western blot和间接免疫荧光法(IFA)检测水样病毒。它们均能与GCRV发生反应,mAb 4A3也能与大比目鱼呼肠孤病毒(SMReV)和大口黑鲈Microptererus salmonides呼肠孤病毒(MsReV)发生反应。病毒抗原仅在感染细胞的细胞质中观察到。最后,在感染后的不同时间,使用荧光素标记的4A3 mAb,在光镜和荧光显微镜下观察合胞体的形成。感染后36小时光镜下观察到合胞体,感染后12小时荧光显微镜下观察到合胞体。在接种的细胞培养物中,基于免疫荧光的检测比观察病毒诱导的细胞病变效应(CPE)检测更早发现病毒。这些单克隆抗体的敏感性和特异性可用于水样病毒的诊断和监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development and application of monoclonal antibodies for detection and analysis of aquareoviruses
ABSTRACT Monoclonal antibodies (mAbs) play an important role in detection of aquareoviruses. Three mAbs against grass carp reovirus (GCRV) were prepared. Isotyping revealed that all three mAbs were of subclass IgG2b. Western blot assay showed that all three mAbs reacted with GCRV 69 kDa protein (the putative VP5). In addition to the 69 kDa protein of GCRV, mAb 4B6 also recognize a 54 kDa protein. All three mAbs were used for detecting aquareovirus by Western blot assay and indirect immunofluorescence assay (IFA). All of them reacted with GCRV, and mAb 4A3 could also react with turbot Scophthalmus maximus reovirus (SMReV) and largemouth bass Microptererus salmonides reovirus (MsReV). Viral antigens were only observed in the cytoplasm of infected cells. Finally, syncytia formation was observed with light microscopy and fluorescence microscopy using fluorescein labelled 4A3 mAb at various times post-infection. Syncytia were observed at 36 hr post-infection (hpi) by light microscopy and at 12 hpi by fluorescence microscopy. The immunofluorescence based assay allowed earlier detection of virus than observation of virus-induced cytopathic effect (CPE) assay in inoculated cell cultures. The sensitivity and specificity of these mAbs may be useful for diagnosis and monitoring of aquareoviruses.
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