Aquaculture Biotechnology Laboratory, Department of Integrative Biology, School of Biosciences and Technology, Vellore Institute of Technology University, Vellore-632014, Tamil Nadu, India.
Nano and Bioelectrochemistry Research Laboratory, Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology University, Vellore-632014, Tamil Nadu, India.
Sci Rep. 2017 Apr 10;7:46169. doi: 10.1038/srep46169.
White spot syndrome virus (WSSV) is a major devastating virus in aquaculture industry. A sensitive and selective diagnostic method for WSSV is a pressing need for the early detection and protection of the aquaculture farms. Herein, we first report, a simple electrochemical immunosensor based on methylene blue dye (MB) immobilized graphene oxide modified glassy carbon electrode (GCE/GO@MB) for selective, quick (35 ± 5 mins) and raw sample analysis of WSSV. The immunosensor was prepared by sequential modification of primary antibody, blocking agent (bovine serum album), antigen (as vp28 protein), secondary antibody coupled with horseradish peroxidase (Ab2-HRP) on the GCE/GO@MB. The modified electrode showed a well-defined redox peak at an equilibrium potential (E), -0.4 V vs Ag/AgCl and mediated HO reduction reaction without any false positive result and dissolved oxygen interferences in pH 7 phosphate buffer solution. Under an optimal condition, constructed calibration plot was linear in a range of 1.36 × 10 to 1.36 × 10 copies μL of vp28. It is about four orders higher sensitive than that of the values observed with polymerase chain reaction (PCR) and western blot based WSSV detection techniques. Direct electrochemical immunosensing of WSSV in raw tissue samples were successfully demonstrated as a real sample system.
白斑综合征病毒(WSSV)是水产养殖业的主要毁灭性病毒。针对 WSSV 的灵敏和选择性诊断方法是早期检测和保护水产养殖场的迫切需要。在此,我们首次报道了一种基于亚甲基蓝染料(MB)固定化氧化石墨烯修饰玻碳电极(GCE/GO@MB)的简单电化学免疫传感器,用于选择性、快速(35±5 分钟)和原始样品分析 WSSV。该免疫传感器通过在 GCE/GO@MB 上依次修饰一抗、封闭剂(牛血清白蛋白)、抗原(作为 vp28 蛋白)、与辣根过氧化物酶偶联的二抗(Ab2-HRP)来制备。修饰后的电极在平衡电位(E)处显示出明确的氧化还原峰,为-0.4 V 相对于 Ag/AgCl,并且在 pH 7 磷酸盐缓冲溶液中没有任何假阳性结果和溶解氧干扰的情况下介导 HO 还原反应。在最佳条件下,构建的校准曲线在 1.36×10 至 1.36×10 拷贝μL vp28 的范围内呈线性。它比聚合酶链反应(PCR)和基于 Western blot 的 WSSV 检测技术观察到的值高约四个数量级。成功地在原始组织样品中直接进行了 WSSV 的电化学免疫传感作为真实样品系统。