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欧洲一种与女贞黄花叶病相关的新型大麦病毒的鉴定与分子特征分析

Identification and Molecular Characterization of a Novel Hordeivirus Associated With Yellow Mosaic Disease of Privet () in Europe.

作者信息

Reynard Jean-Sébastien, Turco Silvia, Brodard Justine, Kellenberger Isabelle, Maclot François, Schumpp Olivier, Gugerli Paul, Pooggin Mikhail M

机构信息

Virology-Phytoplasmology Laboratory, Agroscope, Nyon, Switzerland.

Department of Environmental Sciences, Botany, University of Basel, Basel, Switzerland.

出版信息

Front Microbiol. 2021 Sep 27;12:723350. doi: 10.3389/fmicb.2021.723350. eCollection 2021.

Abstract

Wild plants serve as a large reservoir of known and yet-unknown viruses and as a source of viral pathogens of cultivated plants. Yellow mosaic disease of forest shrub (privet) was recurrently observed in Europe for more than 100 years. Using a universal virus identification approach based on deep sequencing and assembly of viral small interfering (si)RNAs we identified a causative agent of this disease in Switzerland and reconstructed its complete 3-segmented RNA genome. Notably, a short 3'-terminal common region (CR) attached to each segment via a ∼53-71 nucleotide poly(A) tract, as determined by RT-PCR sequencing, was initially identified as an orphan siRNA contig with conserved tRNA-like secondary structure. Phylogenomic analysis classified this virus as a novel member in the genus of family , which we named ligustrum mosaic virus (LigMV). Similar to other hordeiviruses, LigMV formed rod-shape virions (visualized by electron microscopy), was transmitted through seeds and could also be mechanically transmitted to herbaceous hosts and . Blot hybridization analysis identified genomic and subgenomic RNAs, sharing the 3'-CR and likely serving as monocistronic mRNAs for seven evolutionarily-conserved viral proteins including two subunits of viral RNA-dependent RNA polymerase, coat protein, triple gene block proteins mediating viral movement and cysteine-rich suppressor of RNA silencing. Analysis of size, polarity, and hotspot profiles of viral siRNAs suggested that they are produced by the plant antiviral Dicer-like (DCL) proteins DCL2 and DCL4 processing double-stranded intermediates of genomic RNA replication. Whole genome sequencing of French and Austrian isolates of LigMV revealed its genetic stability over a wide geographic range (>99% nucleotide identity to Swiss isolates and each other), suggesting its persistence and spread in Europe via seed dispersal.

摘要

野生植物是已知和未知病毒的巨大储存库,也是栽培植物病毒病原体的来源。森林灌木(女贞)的黄花叶病在欧洲反复出现已有100多年。我们采用基于深度测序和病毒小干扰(si)RNA组装的通用病毒鉴定方法,在瑞士鉴定出了这种疾病的病原体,并重建了其完整的三段RNA基因组。值得注意的是,通过逆转录聚合酶链反应测序确定,每个片段通过约53 - 71个核苷酸的聚腺苷酸(poly(A))序列连接到一个短的3'末端共同区域(CR),该区域最初被鉴定为具有保守tRNA样二级结构的孤儿siRNA重叠群。系统基因组分析将这种病毒归类为 科 属的一个新成员,我们将其命名为女贞花叶病毒(LigMV)。与其他大麦病毒相似,LigMV形成杆状病毒粒子(通过电子显微镜观察),通过种子传播,也可以机械传播到草本宿主 和 。印迹杂交分析鉴定出基因组RNA和亚基因组RNA,它们共享3'-CR,可能作为七种进化上保守的病毒蛋白的单顺反子mRNA,包括病毒RNA依赖性RNA聚合酶的两个亚基、外壳蛋白、介导病毒移动的三基因块蛋白以及富含半胱氨酸的RNA沉默抑制因子。对病毒siRNA的大小、极性和热点图谱分析表明,它们是由植物抗病毒Dicer样(DCL)蛋白DCL2和DCL4加工基因组RNA复制的双链中间体产生的。对法国和奥地利LigMV分离株的全基因组测序显示,其在广泛的地理范围内具有遗传稳定性(与瑞士分离株以及彼此之间的核苷酸同一性>99%),表明它通过种子传播在欧洲持续存在和扩散。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dca/8503643/f08b0f72f278/fmicb-12-723350-g001.jpg

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