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Simple and Portable Magnetic Immunoassay for Rapid Detection and Sensitive Quantification of Plant Viruses

机译:简单,便携式的磁性免疫测定法,用于植物病毒的快速检测和灵敏定量

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Plant pathogens cause major economic losses in the agricultural industry because late detection delays the implementation of measures that can prevent their dissemination. Sensitive and robust procedures for the rapid detection of plant pathogens are therefore required to reduce yield losses and the use of expensive, environmentally damaging chemicals. Here we describe a simple and portable system for the rapid detection of viral pathogens in infected plants based on immunofiltration, subsequent magnetic detection, and the quantification of magnetically labeled virus particles. Grapevine fanleaf virus (GFLV) was chosen as a model pathogen. Monoclonal antibodies recognizing the GFLV capsid protein were immobilized onto immunofiltration columns, and the same antibodies were linked to magnetic nanoparticles. GFLV was quantified by immunofiltration with magnetic labeling in a double-antibody sandwich configuration. A magnetic frequency mixing technique, in which a two-frequency magnetic excitation field was used to induce a sum frequency signal in the resonant detection coil, corresponding to the virus concentration within the immunofiltration column, was used for high-sensitivity quantification. We were able to measure GFLV concentrations in the range of 6 ng/ml to 20 μg/ml in less than 30 min. The magnetic immunoassay could also be adapted to detect other plant viruses, including Potato virus X and Tobacco mosaic virus, with detection limits of 2 to 60 ng/ml.
机译:植物病原体在农业中造成重大的经济损失,因为延迟发现会延缓实施可以阻止其传播的措施。因此,需要用于快速检测植物病原体的灵敏且稳健的程序,以减少产量损失和使用昂贵的,对环境有害的化学物质。在这里,我们描述了一种基于免疫过滤,随后的磁检测和磁标记病毒颗粒定量的快速检测感染植物中病毒病原体的简单便携式系统。选择葡萄扇叶病毒(GFLV)作为模型病原体。将识别GFLV衣壳蛋白的单克隆抗体固定在免疫过滤柱上,并将相同的抗体连接到磁性纳米颗粒上。通过双抗体夹心结构的磁性标记免疫过滤对GFLV进行定量。磁混频技术用于高灵敏度定量分析,在该技术中,使用了一个双频磁激励场在共振检测线圈中感应出一个总频率信号,该信号对应于免疫过滤柱中的病毒浓度。我们能够在不到30分钟的时间内测量GFLV浓度在6 ng / ml至20μg/ ml的范围内。磁免疫测定法还可适用于检测其他植物病毒,包括马铃薯X病毒和烟草花叶病毒,检出限为2至60 ng / ml。

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