Molecular Virology Lab, ICAR-National Research Centre for Banana, Thogamalai Road, Thayanur Post, Tiruchirappalli, 620102, Tamil Nadu, India.
Molecular Virology Lab, ICAR-National Research Centre for Banana, Thogamalai Road, Thayanur Post, Tiruchirappalli, 620102, Tamil Nadu, India.
J Virol Methods. 2020 Oct;284:113929. doi: 10.1016/j.jviromet.2020.113929. Epub 2020 Jul 11.
Banana bract mosaic virus (BBrMV) is a serious pathogen threatening the cultivation of banana and plantain worldwide. This study reports the development of a practical, rapid, sensitive, specific and user-friendly lateral flow immunoassay (LFIA) test for the on-site detection of BBrMV. The BBrMV coat protein (CP) was expressed in Escherichia coli and purified and used to immunize rabbits to produce a polyclonal antiserum (anti-BBrMVCP). The test was based on a double-antibody sandwich format. Protein-A affinity column-purified anti-BBrMVCP Immunoglobulins (IgG) (16 μg/mL), conjugated to ∼30 nm gold nanoparticles, was applied onto the conjugate pad. The anti-BBrMVCP IgG and goat anti-rabbit IgG were printed on the surface of a nitrocellulose filter membrane as the test line and control line, respectively. A positive result could be confirmed visually by the presence of a pink band that developed on the LFIA strip within 5-10 min. The detection limit of the test was 10 ng of the expressed recombinant BBrMV CP (rBBrMVCP), and a 1:20 dilution of the BBrMV-infected crude extract. This LFIA test was validated using 114 banana leaf samples randomly collected from the field and the results indicated a very high diagnostic sensitivity (99.04 %) and specificity (100 %) for the test. A Cohen's kappa coefficient of 0.861 obtained also indicated a very good agreement between the LFIA developed in this study and ELISA. This assay could be adopted by farmers, tissue culture industries and quarantine departments for surveys and surveillance. This is the first report on the development of a LFIA-based test for BBrMV detection.
香蕉束顶病毒(BBrMV)是一种严重威胁香蕉和大蕉全球种植的病原体。本研究报告了一种实用、快速、灵敏、特异、易于使用的侧向流动免疫分析(LFIA)检测方法的开发,用于现场检测 BBrMV。BBrMV 外壳蛋白(CP)在大肠杆菌中表达并纯化,用于免疫兔子以产生多克隆抗血清(抗-BBrMVCP)。该测试基于双抗体夹心格式。蛋白 A 亲和柱纯化的抗-BBrMVCP 免疫球蛋白(IgG)(16μg/mL)与约 30nm 金纳米颗粒偶联,应用于偶联垫上。抗-BBrMVCP IgG 和山羊抗兔 IgG 分别作为测试线和控制线打印在硝酸纤维素滤膜的表面。阳性结果可在 5-10 分钟内通过 LFIA 条带出现粉红色条带来目视确认。该测试的检测限为 10ng 表达的重组 BBrMV CP(rBBrMVCP)和 1:20 稀释的 BBrMV 感染粗提物。该 LFIA 测试使用从田间随机收集的 114 个香蕉叶片样本进行验证,结果表明该测试对 BBrMV 的诊断灵敏度(99.04%)和特异性(100%)非常高。获得的 Cohen's kappa 系数为 0.861,也表明本研究中开发的 LFIA 和 ELISA 之间具有非常好的一致性。该检测方法可被农民、组织培养行业和检疫部门用于调查和监测。这是第一个关于开发基于 LFIA 的 BBrMV 检测方法的报告。