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瞬时表达抗 HrpE scFv 抗体可降低非宿主植物对细菌性植物病原菌柑橘溃疡病菌的过敏性反应。

Transient expression of anti-HrpE scFv antibody reduces the hypersensitive response in non-host plant against bacterial phytopathogen Xanthomonas citri subsp. citri.

机构信息

Foodborne and Waterborne Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Shahid Arabi Ave., Yemen St., Velenjak, Tehran, Iran.

Department of Plant Viruses, Agricultural Research Education and Extension Organization of Iran, Iranian Research Institute of Plant Protection, Tehran, Iran.

出版信息

Sci Rep. 2024 Mar 26;14(1):7121. doi: 10.1038/s41598-024-57355-w.

Abstract

Citrus canker is a bacterial disease caused by Xanthomonas citri subsp. citri (Xcc) that affects the citrus industry worldwide. Hrp pili subunits (HrpE), an essential component of Type III secretion system (T3SS) bacteria, play a crucial role in the pathogenesis of Xcc by transporting effector proteins into the host cell and causing canker symptoms. Therefore, development of antibodies that block HrpE can suppress disease progression. In this study, a specific scFv detecting HrpE was developed using phage display technique and characterized using sequencing, ELISA, Western blotting, and molecular docking. In addition, a plant expression vector of pCAMBIA-scFvH6 was constructed and agroinfiltrated into Nicotiana tabacum cv. Samson leaves. The hypersensitive response (HR) in the leaves of transformed and non-transformed plants was evaluated by inoculating leaves with Xcc. After three rounds of biopanning of the phage library, a specific human scFv antibody, named scFvH6, was identified that showed high binding activity against HrpE in ELISA and Western blotting. Molecular docking results showed that five intermolecular hydrogen bonds are involved in HrpE-scFvH6 interaction, confirming the specificity and high binding activity of scFvH6. Successful transient expression of pCAMBIA-scFvH6 in tobacco leaves was verified using immunoassay tests. The binding activity of plant-produced scFvH6 to detect HrpE in Western blotting and ELISA was similar to that of bacterial-produced scFvH6 antibody. Interestingly, tobacco plants expressing scFvH6 showed a remarkable reduction in HR induced by Xcc compared with control plants, so that incidence of necrotic lesions was significantly higher in non-transformed controls (≥ 1.5 lesions/cm) than in the plants producing scFvH6 (≤ 0.5 lesions/cm) after infiltration with Xcc inoculum. Our results revealed that the expression of scFvH6 in tobacco leaves can confer resistance to Xcc, indicating that this approach could be considered to provide resistance to citrus bacterial canker disease.

摘要

溃疡病是一种由柑橘溃疡病菌(Xanthomonas citri subsp. citri,Xcc)引起的细菌性疾病,它影响着全球的柑橘产业。Hrp 菌毛亚基(HrpE)是细菌 III 型分泌系统(T3SS)的一个重要组成部分,通过将效应蛋白输送到宿主细胞中并引起溃疡症状,在 Xcc 的发病机制中起着关键作用。因此,开发能够阻断 HrpE 的抗体可以抑制疾病的进展。在这项研究中,使用噬菌体展示技术开发了一种针对 HrpE 的特异性 scFv,并通过测序、ELISA、Western blot 和分子对接对其进行了表征。此外,还构建了 pCAMBIA-scFvH6 的植物表达载体,并将其农杆菌浸润到烟草 cv. Samson 的叶片中。通过用 Xcc 接种叶片来评估转化和非转化植物叶片中的过敏反应(HR)。经过三轮噬菌体文库的生物淘选,鉴定出一种特异性的人 scFv 抗体,命名为 scFvH6,它在 ELISA 和 Western blot 中显示出对 HrpE 的高结合活性。分子对接结果表明,HrpE-scFvH6 相互作用涉及五个分子间氢键,证实了 scFvH6 的特异性和高结合活性。使用免疫检测试验验证了 pCAMBIA-scFvH6 在烟草叶片中的瞬时表达。植物产生的 scFvH6 在 Western blot 和 ELISA 中检测 HrpE 的结合活性与细菌产生的 scFvH6 抗体相似。有趣的是,与对照植物相比,表达 scFvH6 的烟草植物在 Xcc 诱导的 HR 中表现出显著减少,因此在浸润 Xcc 接种物后,非转化对照植物(≥1.5 个坏死病变/cm)的坏死病变发生率明显高于产生 scFvH6 的植物(≤0.5 个坏死病变/cm)。我们的结果表明,scFvH6 在烟草叶片中的表达可以赋予对 Xcc 的抗性,表明这种方法可以考虑用于提供对柑橘细菌性溃疡病的抗性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f17d/10965896/9fa05522efaf/41598_2024_57355_Fig1_HTML.jpg

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