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紫云英矮缩病毒全长感染性克隆的构建与片段重组

Construction and Segmental Reconstitution of Full-Length Infectious Clones of Milk Vetch Dwarf Virus.

作者信息

Lal Aamir, Qureshi Muhammad Amir, Son Man-Cheol, Lee Sukchan, Kil Eui-Joon

机构信息

Department of Integrative Biotechnology, Sungkyunkwan University, Suwon 16419, Republic of Korea.

Department of Plant Medicals, Gyeongkuk National University, Andong 36729, Republic of Korea.

出版信息

Viruses. 2025 Sep 5;17(9):1213. doi: 10.3390/v17091213.

Abstract

The construction of infectious clones (ICs) is essential for studying viral replication, pathogenesis, and host interactions. Milk vetch dwarf virus (MDV), a nanovirus with a multipartite, single-stranded DNA genome, presents unique challenges for IC development due to its segmented genome organization. To enable functional analysis of its genome, we constructed full-length tandem-dimer-based ICs for all eight MDV genomic segments. Each segment was cloned into a binary vector and co-delivered into , , , and plants via -mediated inoculation. Systemic infection was successfully reconstituted in all host plants, with PCR-based detection confirming the presence of all viral segments in the infected leaves of nearly all tested plants. Segmental accumulation in infected plants was quantified using qPCR, revealing non-equimolar distribution across hosts. This study establishes the first complete IC system for MDV, enabling reproducible infection, replication analysis, and quantitative segment profiling. It provides a foundational tool for future molecular investigations into MDV replication, host interactions, and viral movement, advancing our understanding of nanovirus biology and transmission dynamics.

摘要

构建感染性克隆(ICs)对于研究病毒复制、发病机制和宿主相互作用至关重要。紫云英矮缩病毒(MDV)是一种具有多分体单链DNA基因组的纳米病毒,由于其基因组的分段组织,在IC开发方面面临独特挑战。为了对其基因组进行功能分析,我们针对MDV的所有八个基因组片段构建了基于全长串联二聚体的ICs。每个片段都被克隆到一个二元载体中,并通过农杆菌介导的接种共同导入本氏烟草、番茄、拟南芥和菜豆植物中。在所有宿主植物中均成功重建了系统感染,基于PCR的检测证实几乎所有测试植物的感染叶片中都存在所有病毒片段。使用qPCR对感染植物中的片段积累进行定量,结果显示不同宿主间的分布并非等摩尔。本研究建立了首个完整的MDV IC系统,可实现可重复的感染、复制分析和定量片段分析。它为未来对MDV复制、宿主相互作用和病毒移动的分子研究提供了基础工具,推动了我们对纳米病毒生物学和传播动态的理解。

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