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首页> 外文期刊>Trends in Ecology & Evolution >Monoclonal Antibody-Based Serological Detection of Rice Stripe Mosaic Virus Infection in Rice Plants or Leafhoppers
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Monoclonal Antibody-Based Serological Detection of Rice Stripe Mosaic Virus Infection in Rice Plants or Leafhoppers

机译:基于单克隆抗体的水稻条纹马赛克病毒感染的基于单克隆抗体的血清学检测

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Rice stripe mosaic virus (RSMV) is a rhabdovirus recently found in southern part of China and can cause severe reduction in rice production. To establish serological methods for RSMV epidemiological studies and to establish a control strategy for this virus, we first purified RSMV virions from infected rice plants and then used them as an immunogen to produce four RSMV-specific monoclonal antibodies (MAbs) (i.e.,1D4, 4A8, 8E4 and 11F11). With these MAbs, we have developed a highly specific and sensitive antigen-coated plate enzyme-linked immunosorbent assay (ACP-ELISA), a Dot-ELISA and a Tissue print-ELISA for rapid detections of RSMV infection in rice plants or in leafhoppers. Our results showed that RSMV can be readily detected in RSMV-infected rice plant tissue crude extracts diluted at 1:20,971,520 (w/v, g/mL) through ACP-ELISA or diluted at 1:327,680 (w/v, g/mL) through Dot-ELISA. Both ACP-ELISA and Dot-ELISA can also be used to detect RSMV infection in individual RSMV viruliferous leafhopper (Recilia dorsalis) homogenate diluted at 1:307,200 and 1:163,840 (individual leafhopper/mu L), respectively. Detection of RSMV infection in field-collected rice samples or in RSMV viruliferous leafhoppers indicated that the three serological methods can produce same results with that produced by RT-PCR (19 of the 33 rice samples and 5 of the 16 leafhoppers were RSMV-positive). We consider that the four MAbs produced in this study are very specific and sensitive, and the three new serological methods are very useful for detections of RSMV infection in rice plants or in leafhoppers and the establishment of the disease control strategies.
机译:水稻条纹马赛克病毒(RSMV)是近日发现在中国南部的rhabdovirus,可导致大米生产严重减少。为了建立RSMV流行病学研究的血清学方法,并建立该病毒的控制策略,我们首先从感染的水稻植物纯化RSMV病毒,然后用作免疫原以产生四种RSMV特异性单克隆抗体(MAB)(即,1D4, 4a8,8e4和11f11)。通过这些mAb,我们已经开发了一种高度特异性和敏感的抗原涂层板酶联免疫吸附试验(ACP-ELISA),DOT-ELISA和组织印刷ELISA,用于快速检测水稻植物或叶蝉的RSMV感染。我们的研究结果表明,通过ACP-ELISA以1:20,971,520(W / V,G / mL)稀释或以1:327,680(w / v,g / ml稀释(w / v,g,g / ml稀释),可以在RSMV感染的稻植物组织粗提取物中容易地检测到RSMV。 )通过DOT-ELISA。 ACP-ELISA和DOT-ELISA均可用于检测在1:307,200和1:163,840(个体叶蝉/μl)稀释的单个RSMV viulibhopper(Recilia Dorsalis)均匀素中的RSMV感染。检测现场收集的水稻样品中的RSMV感染或RSMV viuliberes叶蝉表明,三种血清学方法可以产生相同的结果,其通过RT-PCR产生的结果(33种水稻样品中的19种,16种叶蝉中的5个叶蝉的5种均为RSMV阳性) 。我们认为本研究中生产的四种MAB是非常具体和敏感的,并且三种新的血清学方法对于水稻植物或叶蝉中的RSMV感染和建立疾病控制策略非常有用。

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