Yang Shieh Yueh, Wu Jen Leih, Tso Chun Hsi, Ngou Fang Huar, Chou Hsin Yiu, Nan Fan Hua, Horng Herng Er, Lu Ming Wei
Institute of Electro-optical Science and Technology, National Taiwan Normal University, Taipei, Taiwan.
J Vet Diagn Invest. 2012 Sep;24(5):911-7. doi: 10.1177/1040638712455796. Epub 2012 Aug 1.
Rapid, sensitive, and automatic detection platforms are among the major approaches of controlling viral diseases in aquaculture. An efficient detection platform permits the monitoring of pathogen spread and helps to enhance the economic benefits of commercial aquaculture. Nervous necrosis virus (NNV), the cause of viral encephalopathy and retinopathy, is among the most devastating aquaculture viruses that infect marine fish species worldwide. In the present study, a highly sensitive magnetoreduction assay was developed for detecting target biomolecules with a primary focus on NNV antigens. A standard curve of the different NNV concentrations that were isolated from infected Malabar grouper (Epinephelus malabaricus) was established before experiments were conducted. The test solution was prepared by homogeneous dispersion of magnetic nanoparticles coated with rabbit anti-NNV antibody. The magnetic nanoparticles in the solution were oscillated by magnetic interaction with multiple externally applied, alternating current magnetic fields. The assay's limit of detection was approximately 2 × 10(1) TCID(50)/ml for NNV. Moreover, the immunomagnetic reduction readings for other aquatic viruses (i.e., 1 × 10(7) TCID(50)/ml for Infectious pancreatic necrosis virus and 1 × 10(6.5) TCID(50)/ml for grouper iridovirus) were below the background noise in the NNV solution, demonstrating the specificity of the new detection platform.
快速、灵敏且自动化的检测平台是控制水产养殖中病毒性疾病的主要方法之一。高效的检测平台能够监测病原体的传播,并有助于提高商业水产养殖的经济效益。神经坏死病毒(NNV)是病毒性脑病和视网膜病的病原体,是感染全球海洋鱼类的最具毁灭性的水产养殖病毒之一。在本研究中,开发了一种高度灵敏的磁还原检测法,主要用于检测目标生物分子,重点是NNV抗原。在进行实验之前,建立了从感染的马拉巴石斑鱼(Epinephelus malabaricus)中分离出的不同NNV浓度的标准曲线。测试溶液是通过将涂有兔抗NNV抗体的磁性纳米颗粒均匀分散而制备的。溶液中的磁性纳米颗粒通过与多个外部施加的交变磁场的磁相互作用而振荡。该检测法对NNV的检测限约为2×10(1) TCID(50)/ml。此外,其他水生病毒(即传染性胰腺坏死病毒为1×10(7) TCID(50)/ml,石斑鱼虹彩病毒为1×10(6.5) TCID(50)/ml)在NNV溶液中的免疫磁还原读数低于背景噪声,证明了新检测平台的特异性。