Srivastava Nishant, Kumar Rakesh, Kapoor Reetika, Kumar Ashwini, Sharma Susheel K, Gupta Nitika, Bhardwaj Pooja, Kishan Gopi, Pant Rajendra P, Baranwal Virendra K
Advanced Centre for Plant Virology, Division of Plant Pathology, ICAR-Indian Agricultural Research Institute, New Delhi, 110012, India.
ICAR-Indian Institute of Seed Science, Kushmaur, Mau, Uttar Pradesh, India.
Mol Biotechnol. 2025 Feb;67(2):628-637. doi: 10.1007/s12033-024-01074-0. Epub 2024 Feb 16.
Calanthe mild mosaic virus (CalMMV) infecting orchids is an important potyvirus which is known to cause mild leaf mosaic and flower colour-breaking symptoms in Calanthe and other orchid plants. The present study reports the production of polyclonal antibodies against CalMMV using bacterially expressed recombinant coat protein as immunogen, which in turn would be useful in routine indexing and screening of orchid germplasm. The coat protein (CP) gene (~ 807 bp) of CalMMV isolated from infected orchid sample was cloned in expression vector, pET-28a ( +) that yielded ~ 31 kDa fusion protein with Histidine tag (HisBP). The expression of fusion CP was confirmed through SDS-PAGE and Western blotting. The HisBP-CalMMV-CP obtained in soluble state after purification was used to immunize New Zealand white rabbit for the production of polyclonal antibodies (PAb). The PAb produced against the purified fusion protein successfully detected CAlMMV in the orchid samples at a dilution of 1:2000 in direct antigen-coated enzyme-linked immunosorbent assay (DAC-ELISA). This study presents the first report of Histidine tag (HisBP) fusion CalMMV-CP-based antibody production and its successful application in the identification of the virus in orchid plants. Outcome of this study will be helpful in routine certification programmes, screening of orchid germplasm and production of CalMMV-free planting materials of orchids.
感染兰花的美花兰温和花叶病毒(CalMMV)是一种重要的马铃薯Y病毒,已知会在美花兰和其他兰花植物中引起轻微的叶片花叶症状和花色破坏症状。本研究报道了以细菌表达的重组外壳蛋白作为免疫原制备抗CalMMV的多克隆抗体,这反过来将有助于兰花种质的常规检测和筛选。从感染的兰花样本中分离出的CalMMV外壳蛋白(CP)基因(约807 bp)克隆到表达载体pET-28a(+)中,产生了带有组氨酸标签(HisBP)的约31 kDa融合蛋白。通过SDS-PAGE和Western印迹证实了融合CP的表达。纯化后以可溶状态获得的HisBP-CalMMV-CP用于免疫新西兰白兔以产生多克隆抗体(PAb)。在直接抗原包被酶联免疫吸附测定(DAC-ELISA)中,针对纯化融合蛋白产生的PAb在1:2000稀释度下成功检测到兰花样本中的CAlMMV。本研究首次报道了基于组氨酸标签(HisBP)融合CalMMV-CP的抗体生产及其在兰花植物病毒鉴定中的成功应用。本研究结果将有助于常规认证计划、兰花种质筛选以及生产无CalMMV的兰花种植材料。