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针对里约热内卢夸尔图病毒主要衣壳蛋白 P9-1 开发纳米抗体,用于诊断夹心 ELISA 和免疫检测。

Development of Nanobodies against Mal de Río Cuarto virus major viroplasm protein P9-1 for diagnostic sandwich ELISA and immunodetection.

机构信息

Instituto de Agrobiotecnología y Biología Molecular (IABIMO), CICVyA INTA, UEDD INTA/CONICET, Buenos Aires, Argentina.

INCUINTA, Instituto de Virología e Innovaciones Tecnológicas (IVIT), CICVyA INTA, UEDD INTA/CONICET, Buenos Aires, Argentina.

出版信息

Sci Rep. 2021 Oct 8;11(1):20013. doi: 10.1038/s41598-021-99275-z.

Abstract

Mal de Río Cuarto virus (MRCV) is a member of the genus Fijivirus of the family Reoviridae that causes a devastating disease in maize and is persistently and propagatively transmitted by planthopper vectors. Virus replication and assembly occur within viroplasms formed by viral and host proteins. This work describes the isolation and characterization of llama-derived Nanobodies (Nbs) recognizing the major viral viroplasm component, P9-1. Specific Nbs were selected against recombinant P9-1, with affinities in the nanomolar range as measured by surface plasmon resonance. Three selected Nbs were fused to alkaline phosphatase and eGFP to develop a sandwich ELISA test which showed a high diagnostic sensitivity (99.12%, 95% CI 95.21-99.98) and specificity (100%, 95% CI 96.31-100) and a detection limit of 0.236 ng/ml. Interestingly, these Nanobodies recognized different P9-1 conformations and were successfully employed to detect P9-1 in pull-down assays of infected maize extracts. Finally, we demonstrated that fusions of the Nbs to eGFP and RFP allowed the immunodetection of virus present in phloem cells of leaf thin sections. The Nbs developed in this work will aid the study of MRCV epidemiology, assist maize breeding programs, and be valuable tools to boost fundamental research on viroplasm structure and maturation.

摘要

里奥夸尔托病毒(MRCV)是呼肠孤病毒科斐济病毒属的一种成员,可导致玉米严重疾病,并通过粉虱介体持续传播。病毒复制和组装发生在由病毒和宿主蛋白形成的类病毒体中。本工作描述了分离和鉴定识别主要病毒类病毒体成分 P9-1 的骆驼源纳米抗体(Nbs)。通过表面等离子体共振测量,针对重组 P9-1 特异性选择具有纳摩尔亲和力的特定 Nbs。选择的三个 Nbs 与碱性磷酸酶和 eGFP 融合,开发了夹心 ELISA 测试,该测试显示出高诊断灵敏度(99.12%,95%CI 95.21-99.98)和特异性(100%,95%CI 96.31-100),检测限为 0.236 ng/ml。有趣的是,这些纳米抗体识别不同的 P9-1 构象,并成功用于检测感染玉米提取物的下拉实验中的 P9-1。最后,我们证明了 Nbs 与 eGFP 和 RFP 的融合允许在叶片薄片的韧皮部细胞中检测到存在的病毒。本工作中开发的 Nbs 将有助于 MRCV 流行病学研究,辅助玉米育种计划,并成为研究类病毒体结构和成熟的基础研究的有价值工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d2/8501053/26261991fdf7/41598_2021_99275_Fig1_HTML.jpg

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