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基于纳米颗粒的侧向流动生物传感器用于鱼类神经坏死病毒扩增产物的可视化检测。

Nanoparticle-based lateral flow biosensor for visual detection of fish nervous necrosis virus amplification products.

作者信息

Toubanaki Dimitra K, Margaroni Maritsa, Karagouni Evdokia

机构信息

Laboratory of Cellular Immunology, Department of Microbiology, Hellenic Pasteur Institute, 127 Vas. Sofias Ave., 11521 Athens, Greece.

出版信息

Mol Cell Probes. 2015 Jun;29(3):158-66. doi: 10.1016/j.mcp.2015.03.005. Epub 2015 Mar 20.

DOI:10.1016/j.mcp.2015.03.005
PMID:25797786
Abstract

Lateral flow paper biosensors are an attractive analytical platform for detection of human and veterinary disease pathogens because they are optimal for accurate, rapid and sensitive analysis in research laboratory setups, as well as field analysis. Since diseases of viral etiology have been wreaking havoc in aquaculture industry, as well as the environment, the present study aims at the development of a gold nanoparticle-based biosensor for fish nervous necrosis virus (Nodavirus) nucleic acids detection. Total viral RNA, isolated from fish samples was subjected to reverse transcription PCR amplification. The PCR products were mixed with a specific oligonucleotide probe and applied next to oligonucleotide conjugated Au NPs. A red test line was formed when nodavirus product was present. The visual detection of the RT-PCR product was completed within 20 min. Following optimization, the biosensor was able to visually detect 270 pg of nodavirus initial total RNA. The present study describes a simple, accurate, robust and low cost method for nodavirus detection in biological samples. Apart contribution on basic research, the proposed biosensor offers great potential for commercial kit development for use on the site of fish culture by fish farmers. This fact will have great impact on environmental safety and disease monitoring without time consuming and costly procedures.

摘要

侧向流动纸质生物传感器是用于检测人类和兽医疾病病原体的一种有吸引力的分析平台,因为它们对于研究实验室环境中的准确、快速和灵敏分析以及现场分析而言是最佳的。由于病毒性病因的疾病一直在给水产养殖业以及环境造成严重破坏,本研究旨在开发一种基于金纳米颗粒的生物传感器,用于检测鱼类神经坏死病毒(诺达病毒)核酸。从鱼类样本中分离出的总病毒RNA进行逆转录PCR扩增。将PCR产物与特定的寡核苷酸探针混合,然后应用于与寡核苷酸偶联的金纳米颗粒旁边。当存在诺达病毒产物时会形成一条红色检测线。RT-PCR产物的目视检测在20分钟内完成。经过优化后,该生物传感器能够目视检测到270 pg的诺达病毒初始总RNA。本研究描述了一种用于在生物样本中检测诺达病毒的简单、准确、稳健且低成本的方法。除了对基础研究有贡献外,所提出的生物传感器在开发供养鱼户在养鱼现场使用的商业试剂盒方面具有巨大潜力。这一事实将对环境安全和疾病监测产生重大影响且无需耗时且昂贵的程序。

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