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鉴定并分析引起西瓜叶枯病的链格孢多角体病毒的基因组特征

Identification and genomic characterization of a novel polymycovirus from Alternaria alternata causing watermelon leaf blight.

机构信息

College of Plant Protection, China Agricultural University, No. 2 Yuanmingyuan West Road, Haidian District, Beijing, 100193, People's Republic of China.

Institute of Plant Protection, Shandong Academy of Agricultural Sciences/Shandong Key Laboratory of Plant Virology, Jinan, 250100, People's Republic of China.

出版信息

Arch Virol. 2022 Jan;167(1):223-227. doi: 10.1007/s00705-021-05272-y. Epub 2021 Oct 12.

Abstract

A double-stranded RNA (dsRNA) mycovirus from the phytopathogenic fungus Alternaria alternata, which causes watermelon leaf blight, was characterized. The genome of this virus has eight dsRNA segments, ranging from 1039 bp to 2398 bp. DsRNAs 1-6 each contain a single large open reading frame (ORF), while dsRNAs 7 and 8 each dsRNA contain two ORFs. The RNA-dependent RNA polymerase (RdRp) encoded by dsRNA1 and the viral methyltransferase encoded by dsRNA3 share 97.6% and 98.9% amino acid sequence identity, respectively, with the corresponding proteins of Plasmopara viticola lesion associated polymycovirus 1. The dsRNA5-encoded proline-alanine-serine-rich protein shows 48.1% sequence identity to that of Beauveria bassiana polymycovirus 3. The proteins encoded on dsRNAs 2, 4, and 8 have 99.7%, 98.2%, and 65.1% sequence identity, respectively, to the corresponding proteins of a mycovirus identified in Alternaria sp. FA0703 (AltR1). The proteins encoded by dsRNAs 6 and 7 do not match any known proteins of mycoviruses. Phylogenetic analysis of the RdRp domain showed that the virus clustered with members of the family Polymycoviridae. Based on these characteristics, the mycovirus was identified as a polymycovirus and designated as "Alternaria alternata polymycovirus 1" (AaPmV1). This is the first report of a polymycovirus associated with A. alternata.

摘要

一种双链 RNA (dsRNA) 真菌病毒,来自引起西瓜叶枯病的植物病原菌链格孢菌,其特征如下。该病毒的基因组有 8 个 dsRNA 片段,长度从 1039 个碱基对到 2398 个碱基对不等。dsRNA1-6 每个都包含一个单一的大开放阅读框(ORF),而 dsRNA7 和 8 每个 dsRNA 都包含两个 ORF。dsRNA1 编码的 RNA 依赖性 RNA 聚合酶(RdRp)和 dsRNA3 编码的病毒甲基转移酶,分别与 Plasmopara viticola 损伤相关多聚病毒 1 的相应蛋白具有 97.6%和 98.9%的氨基酸序列同一性。dsRNA5 编码的脯氨酸-丙氨酸-丝氨酸丰富蛋白与 Beauveria bassiana 多聚病毒 3 的相应蛋白具有 48.1%的序列同一性。dsRNA2、4 和 8 编码的蛋白分别与在 Alternaria sp. FA0703 中鉴定的多病毒的相应蛋白具有 99.7%、98.2%和 65.1%的序列同一性。dsRNA6 和 7 编码的蛋白与任何已知的真菌病毒蛋白都不匹配。RdRp 结构域的系统发育分析表明,该病毒与多聚病毒科的成员聚类在一起。基于这些特征,该真菌病毒被鉴定为多聚病毒,并命名为“Alternaria alternata 多聚病毒 1”(AaPmV1)。这是首次报道与链格孢菌相关的多聚病毒。

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