Department of Biology, Srinakharinwirot University, Sukhumvit 23, Bangkok 10110, Thailand.
J Virol Methods. 2011 Apr;173(1):85-91. doi: 10.1016/j.jviromet.2011.01.011. Epub 2011 Jan 21.
A strip test for the dual detection of white spot syndrome virus (WSSV) and yellow head virus (YHV) was developed using monoclonal antibodies (MAbs) specific to the WSSV major envelope protein VP28 (W1 and W30) and the YHV nucleocapsid protein p20 (Y19 and Y21). The MAbs W30 and Y19 were conjugated with colloidal gold and sprayed onto a glass fiber pad that was placed adjacent to a sample chamber. The MAbs W1 and Y21 and the goat anti-mouse immunoglobulin G (GAM) antibody were sprayed onto a nitrocellulose membrane in strips at positions designated W, Y and C, respectively. These test strips were placed in plastic cases and stored desiccated in a plastic bag. The test strips were assessed for their ability to detect WSSV and YHV simultaneously using pleopods sampled from shrimp. A pleopod homogenate in application buffer 100μl was applied to the sample chamber to flow through the nitrocellulose membrane strip, and antibody-protein complexes could be observed within 15min. In sample from shrimp infected with WSSV and/or YHV, viral protein bound to the colloidal gold-conjugated MAbs. These complexes were captured by the MAbs at the W and/or Y test lines, resulting in the appearance of reddish-purple coloured bands. Any unbound colloidal gold-conjugated MAbs migrated pass the W and Y lines would be captured by the GAM antibody, forming a band at position C. When samples not containing WSSV and YHV proteins or containing viral proteins at below the detection limit of the test, only the band at position C was observed. The sensitivity of the test was comparable to dot blot tests using single MAbs, and ∼500-fold less sensitive than a 1-step PCR test for WSSV and 1000-fold less sensitive than an RT-PCR test for YHV. Despite this lower sensitivity, the dual strip test has advantages in speed and simplicity in not requiring sophisticated equipment or specialized skills. The ability to co-detect WSSV and YHV provides simultaneously cost savings.
一种用于同时检测白斑综合征病毒 (WSSV) 和黄头病毒 (YHV) 的条带检测法已经开发出来,该方法使用针对 WSSV 主要包膜蛋白 VP28(W1 和 W30)和 YHV 核衣壳蛋白 p20(Y19 和 Y21)的单克隆抗体 (MAb)。MAb W30 和 Y19 与胶体金偶联,并喷涂在与样品室相邻的玻璃纤维垫上。MAb W1 和 Y21 以及山羊抗小鼠免疫球蛋白 G (GAM) 抗体分别以条带形式喷涂在硝酸纤维素膜上的 W、Y 和 C 位置。这些测试条带被放置在塑料盒中,并在塑料袋中干燥储存。使用从虾中采集的对虾足来评估这些测试条带同时检测 WSSV 和 YHV 的能力。将 100μl 应用缓冲液中的对虾足匀浆施加到样品室中,使其流过硝酸纤维素膜条带,在 15 分钟内可以观察到抗体-蛋白复合物。在感染 WSSV 和/或 YHV 的虾样本中,病毒蛋白与胶体金偶联的 MAb 结合。这些复合物被 W 和/或 Y 测试线上的 MAb 捕获,导致出现红紫色带。任何未结合的胶体金偶联 MAb 迁移超过 W 和 Y 线的,将被 GAM 抗体捕获,在 C 位置形成一条带。当样品中不含有 WSSV 和 YHV 蛋白或含有低于测试检测限的病毒蛋白时,仅观察到 C 位置的带。该测试的灵敏度与使用单克隆抗体的斑点印迹测试相当,比一步法 PCR 测试 WSSV 的灵敏度低约 500 倍,比 RT-PCR 测试 YHV 的灵敏度低约 1000 倍。尽管灵敏度较低,但双条带测试在速度和简单性方面具有优势,不需要复杂的设备或专门的技能。同时检测 WSSV 和 YHV 的能力提供了同时节省成本的优势。