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悬钩子黄网病毒整合到红树莓基因组中的证据。

Evidence of Rubus Yellow Net Virus Integration into the Red Raspberry Genome.

作者信息

Diaz-Lara Alfredo, Mosier Nola J, Stevens Kristian, Keller Karen E, Martin Robert R

出版信息

Cytogenet Genome Res. 2020;160(6):329-334. doi: 10.1159/000509845. Epub 2020 Jul 18.

Abstract

Rubus yellow net virus (RYNV) infects Rubus spp., causing a severe decline when present in mixed infections with other viruses. RYNV belongs to the family Caulimoviridae, also known as plant pararetroviruses, which can exist as episomal or integrated elements (endogenous). Most of integrated pararetroviruses are noninfectious; however, a few cases have been reported where they excised from the plant genome and formed infectious particles. Graft transmission onto indicator plants R. occidentalis "Munger" has been the standard test method for RYNV detection in certification programs. Previously, it was noticed that some RYNV PCR-positive plants did not induce symptoms on "Munger", suggesting an integration event. In this study, bio-indexing and different molecular techniques were employed to differentiate between integrated and episomal RYNV sequences. Reverse transcription-PCR using RYNV-specific oligonucleotides after DNase treatment generated positive results for the virus in graft transmissible isolates (episomal) only. To confirm these results, rolling circle amplification on DNA preparations from the same samples resulted in amplicons identified as RYNV only from plants with graft transmissible RYNV. High-throughput sequencing was used to identify the RYNV-like sequences present in the host DNA. These results indicate the integration of RYNV into the red raspberry genome and highlight the necessity to recognize this phenomenon (integration) in future Rubus quarantine and certification programs.

摘要

悬钩子黄网病毒(RYNV)感染悬钩子属植物,当与其他病毒混合感染时会导致严重衰退。RYNV属于花椰菜花叶病毒科,也被称为植物副逆转录病毒,它可以以附加体或整合元件(内源性)的形式存在。大多数整合的副逆转录病毒是无感染性的;然而,已有少数案例报道它们从植物基因组中切除并形成感染性颗粒。将病毒嫁接传播到指示植物西方悬钩子“芒格”上一直是认证项目中检测RYNV的标准测试方法。此前,人们注意到一些RYNV PCR检测呈阳性的植物在“芒格”上并未引发症状,这表明发生了整合事件。在本研究中,采用生物索引和不同的分子技术来区分整合型和游离型RYNV序列。仅在经过DNA酶处理后使用RYNV特异性寡核苷酸进行逆转录PCR,对嫁接可传播分离株(游离型)中的病毒产生了阳性结果。为了证实这些结果,对来自相同样本的DNA制剂进行滚环扩增,结果仅从具有嫁接可传播RYNV的植物中获得了被鉴定为RYNV的扩增子。高通量测序用于鉴定宿主DNA中存在的类似RYNV的序列。这些结果表明RYNV已整合到红树莓基因组中,并强调了在未来悬钩子属植物检疫和认证项目中认识到这种现象(整合)的必要性。

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