Raeisi Hamideh, Safarnejad Mohammad Reza, Sadeghkhani Farideh
Foodborne and Waterborne Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Department of Plant Viruses, Iranian Research Institute of Plant Protection, Agricultural Research Education and Extension Organization of Iran, Tehran, Iran.
J Virol Methods. 2022 Feb;300:114412. doi: 10.1016/j.jviromet.2021.114412. Epub 2021 Dec 10.
Citrus tristeza virus (CTV) is the most economically important virus disease of citrus worldwide. To develop a specific serological assay for CTV, a Tomlinson phage display antibody library of single chain variable fragments (scFv) was screened with a recombinant CTV coat protein (CTV-CP) heterologously expressed in Escherichia coli. The phage clones were checked by ELISA to identify clones with high specificity for CTV-CP. Eight clones were strongly reactive with CTV-CP. Nucleotide sequencing of these clones revealed that all of them contained the same sequence. Thus, the phage-displayed scFv antibody was termed scFvF10. Evaluation of scFvF10 binding to CTV-CP by plate-trapped antigen ELISA (PTA-ELISA) and immunoblotting, showed that it was specific and allowed sensitive detection of CTV-CP. Homology-based molecular modeling and docking analysis confirmed that the interaction between CTV-CP and scFvF10, with a binding energy of -738 kj mol-1, occurred mainly by 12 intermolecular hydrogen bonds. Moreover, triple-antibody sandwich (TAS)-ELISA using scFvF10 as second antibody showed high sensitivity in the detection of CTV infected samples. The CTV detection limit of scFvF10 by PTA-ELISA and TAS-ELISA were 0.05 and 0.01 μg CP/mL, respectively. Our results with different diagnostic assays demonstrated that scFvF10 has the potential to be used as an efficient tool for CTV-infected plant diagnosis.
柑橘衰退病毒(CTV)是全球柑橘类作物中经济重要性最高的病毒病害。为开发针对CTV的特异性血清学检测方法,利用在大肠杆菌中异源表达的重组CTV外壳蛋白(CTV-CP)筛选了Tomlinson单链可变片段(scFv)噬菌体展示抗体库。通过酶联免疫吸附测定(ELISA)检查噬菌体克隆,以鉴定对CTV-CP具有高特异性的克隆。八个克隆与CTV-CP有强烈反应。对这些克隆进行核苷酸测序表明,它们均含有相同序列。因此,该噬菌体展示的scFv抗体被命名为scFvF10。通过平板包被抗原ELISA(PTA-ELISA)和免疫印迹评估scFvF10与CTV-CP的结合,结果表明其具有特异性,能够灵敏地检测CTV-CP。基于同源性的分子建模和对接分析证实,CTV-CP与scFvF10之间的相互作用主要通过12个分子间氢键发生,结合能为-738 kj mol-1。此外,以scFvF10作为二抗的三抗体夹心(TAS)-ELISA在检测CTV感染样品时显示出高灵敏度。通过PTA-ELISA和TAS-ELISA检测CTV时,scFvF10的检测限分别为0.05和0.01 μg CP/mL。我们使用不同诊断方法的结果表明,scFvF10有潜力作为一种高效工具用于诊断CTV感染的植物。