开发基于多克隆抗体的血清学方法,用于检测灯盏花淡色花叶病毒并将其应用于病毒认证计划。

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Molecular Biotechnology Pub Date : 2025-02-01 Epub Date: 2024-02-16 DOI:10.1007/s12033-024-01074-0
Nishant Srivastava, Rakesh Kumar, Reetika Kapoor, Ashwini Kumar, Susheel K Sharma, Nitika Gupta, Pooja Bhardwaj, Gopi Kishan, Rajendra P Pant, Virendra K Baranwal
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引用次数: 0

摘要

感染兰花的菖蒲轻度马赛克病毒(CalMMV)是一种重要的壶状病毒,已知会导致菖蒲和其他兰花植物出现轻度叶片马赛克和花朵褪色症状。本研究报告利用细菌表达的重组衣壳蛋白作为免疫原,生产出针对 CalMMV 的多克隆抗体,这将有助于对兰花种质进行常规索引和筛选。从受感染的兰花样本中分离出的 CalMMV 的衣壳蛋白(CP)基因(约 807 bp)被克隆到表达载体 pET-28a ( +) 中,产生了约 31 kDa 带组氨酸标签(His6BP)的融合蛋白。融合蛋白的表达通过 SDS-PAGE 和 Western 印迹法得到证实。纯化后可溶性的 His6BP-CalMMV-CP 被用于免疫新西兰白兔,以生产多克隆抗体(PAb)。在直接抗原包被酶联免疫吸附试验(DAC-ELISA)中,针对纯化的融合蛋白产生的多克隆抗体以 1:2000 的稀释度成功检测到了兰花样品中的 CAlMMV。本研究首次报道了基于组氨酸标签(His6BP)融合 CalMMV-CP 的抗体生产及其在兰花植物中病毒鉴定中的成功应用。这项研究的结果将有助于常规认证计划、兰花种质筛选和不含 CalMMV 的兰花种植材料的生产。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development of Polyclonal Antibodies-Based Serological Method for the Detection of Calanthe Mild Mosaic Virus and Application in Virus Certification Programme.

Development of Polyclonal Antibodies-Based Serological Method for the Detection of Calanthe Mild Mosaic Virus and Application in Virus Certification Programme.

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 (His6BP). The expression of fusion CP was confirmed through SDS-PAGE and Western blotting. The His6BP-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 (His6BP) 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.

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来源期刊
Molecular Biotechnology
Molecular Biotechnology 医学-生化与分子生物学
CiteScore
4.10
自引率
3.80%
发文量
165
审稿时长
6 months
期刊介绍: Molecular Biotechnology publishes original research papers on the application of molecular biology to both basic and applied research in the field of biotechnology. Particular areas of interest include the following: stability and expression of cloned gene products, cell transformation, gene cloning systems and the production of recombinant proteins, protein purification and analysis, transgenic species, developmental biology, mutation analysis, the applications of DNA fingerprinting, RNA interference, and PCR technology, microarray technology, proteomics, mass spectrometry, bioinformatics, plant molecular biology, microbial genetics, gene probes and the diagnosis of disease, pharmaceutical and health care products, therapeutic agents, vaccines, gene targeting, gene therapy, stem cell technology and tissue engineering, antisense technology, protein engineering and enzyme technology, monoclonal antibodies, glycobiology and glycomics, and agricultural biotechnology.
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