Rettcher Stefanie, Jungk Felicitas, Kühn Christoph, Krause Hans-Joachim, Nölke Greta, Commandeur Ulrich, Fischer Rainer, Schillberg Stefan, Schröper Florian
Fraunhofer Institute for Molecular Biology and Applied Ecology IME, Aachen, Germany.
Peter Grünberg Institute PGI-8, Research Center Jülich, Jülich, Germany.
Appl Environ Microbiol. 2015 May 1;81(9):3039-48. doi: 10.1128/AEM.03667-14. Epub 2015 Feb 20.
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.
植物病原体给农业产业造成了重大经济损失,因为检测延迟会延误采取措施来防止病原体传播。因此,需要灵敏且可靠的程序来快速检测植物病原体,以减少产量损失,并减少使用昂贵且对环境有害的化学物质。在此,我们描述了一种基于免疫过滤、后续磁检测以及对磁性标记病毒颗粒进行定量分析的简单便携式系统,用于快速检测受感染植物中的病毒病原体。葡萄扇叶病毒(GFLV)被选为模型病原体。将识别GFLV衣壳蛋白的单克隆抗体固定在免疫过滤柱上,并将相同的抗体与磁性纳米颗粒相连。采用双抗体夹心配置,通过磁性标记免疫过滤对GFLV进行定量分析。一种磁频混合技术,即使用双频磁激发场在共振检测线圈中诱导一个和频信号,该信号与免疫过滤柱内的病毒浓度相对应,用于高灵敏度定量分析。我们能够在不到30分钟的时间内测量出浓度范围在6纳克/毫升至20微克/毫升之间的GFLV。这种磁性免疫分析方法也可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,检测限为2至60纳克/毫升。