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白纹羽病菌中衣壳双链RNA真菌病毒间RNA沉默的差异诱导

Differential Inductions of RNA Silencing among Encapsidated Double-Stranded RNA Mycoviruses in the White Root Rot Fungus Rosellinia necatrix.

作者信息

Yaegashi Hajime, Shimizu Takeo, Ito Tsutae, Kanematsu Satoko

机构信息

Apple Research Division, Institute of Fruit Tree Science, National Agriculture and Food Research Organization (NARO), Morioka, JapanUniversity of Maryland

Apple Research Division, Institute of Fruit Tree Science, National Agriculture and Food Research Organization (NARO), Morioka, JapanUniversity of Maryland.

出版信息

J Virol. 2016 May 27;90(12):5677-92. doi: 10.1128/JVI.02951-15. Print 2016 Jun 15.

Abstract

UNLABELLED

RNA silencing acts as a defense mechanism against virus infection in a wide variety of organisms. Here, we investigated inductions of RNA silencing against encapsidated double-stranded RNA (dsRNA) fungal viruses (mycoviruses), including a partitivirus (RnPV1), a quadrivirus (RnQV1), a victorivirus (RnVV1), a mycoreovirus (RnMyRV3), and a megabirnavirus (RnMBV1) in the phytopathogenic fungus Rosellinia necatrix Expression profiling of RNA silencing-related genes revealed that a dicer-like gene, an Argonaute-like gene, and two RNA-dependent RNA polymerase genes were upregulated by RnMyRV3 or RnMBV1 infection but not by other virus infections or by constitutive expression of dsRNA in R. necatrix Massive analysis of viral small RNAs (vsRNAs) from the five mycoviruses showed that 19- to 22-nucleotide (nt) vsRNAs were predominant; however, their ability to form duplexes with 3' overhangs and the 5' nucleotide preferences of vsRNAs differed among the five mycoviruses. The abundances of 19- to 22-nt vsRNAs from RnPV1, RnQV1, RnVV1, RnMyRV3, and RnMBV1 were 6.8%, 1.2%, 0.3%, 13.0%, and 24.9%, respectively. Importantly, the vsRNA abundances and accumulation levels of viral RNA were not always correlated, and the origins of the vsRNAs were distinguishable among the five mycoviruses. These data corroborated diverse interactions between encapsidated dsRNA mycoviruses and RNA silencing. Moreover, a green fluorescent protein (GFP)-based sensor assay in R. necatrix revealed that RnMBV1 infection induced silencing of the target sensor gene (GFP gene and the partial RnMBV1 sequence), suggesting that vsRNAs from RnMBV1 activated the RNA-induced silencing complex. Overall, this study provides insights into RNA silencing against encapsidated dsRNA mycoviruses.

IMPORTANCE

Encapsidated dsRNA fungal viruses (mycoviruses) are believed to replicate inside their virions; therefore, there is a question of whether they induce RNA silencing. Here, we investigated inductions of RNA silencing against encapsidated dsRNA mycoviruses (a partitivirus, a quadrivirus, a victorivirus, a mycoreovirus, and a megabirnavirus) in Rosellinia necatrix We revealed upregulation of RNA silencing-related genes in R. necatrix infected with a mycoreovirus or a megabirnavirus but not with other viruses, which was consistent with the relatively high abundances of vsRNAs from the two mycoviruses. We also showed common and different molecular features and origins of the vsRNAs from the five mycoviruses. Furthermore, we demonstrated the activation of RNA-induced silencing complex by mycoviruses in R. necatrix Taken together, our data provide insights into an RNA silencing pathway against encapsidated dsRNA mycoviruses which is differentially induced among encapsidated dsRNA mycoviruses; that is, diverse replication strategies exist among encapsidated dsRNA mycoviruses.

摘要

未标记

RNA沉默作为一种防御机制,在多种生物体中抵御病毒感染。在此,我们研究了针对衣壳化双链RNA(dsRNA)真菌病毒(真菌病毒)的RNA沉默诱导情况,这些病毒包括分病毒(RnPV1)、四病毒(RnQV1)、维克托病毒(RnVV1)、真菌呼肠孤病毒(RnMyRV3)和巨双RNA病毒(RnMBV1),在植物病原真菌白纹羽病菌中进行研究。RNA沉默相关基因的表达谱分析表明,一个类Dicer基因、一个类AGO基因和两个RNA依赖的RNA聚合酶基因在RnMyRV3或RnMBV1感染后上调,但在其他病毒感染或白纹羽病菌中dsRNA的组成型表达后未上调。对这五种真菌病毒的病毒小RNA(vsRNA)进行大规模分析表明,19至22个核苷酸(nt)的vsRNA占主导;然而,它们形成具有3'突出端双链体的能力以及vsRNA的5'核苷酸偏好性在这五种真菌病毒中有所不同。来自RnPV1、RnQV1、RnVV1、RnMyRV3和RnMBV1的19至22 nt vsRNA的丰度分别为6.8%、1.2%、0.3%、13.0%和24.9%。重要的是,vsRNA丰度与病毒RNA的积累水平并不总是相关,并且vsRNA的来源在这五种真菌病毒中是可区分的。这些数据证实了衣壳化dsRNA真菌病毒与RNA沉默之间的多种相互作用。此外,在白纹羽病菌中基于绿色荧光蛋白(GFP)的传感器分析表明,RnMBV1感染诱导了靶标传感器基因(GFP基因和部分RnMBV1序列)的沉默,这表明来自RnMBV1的vsRNA激活了RNA诱导沉默复合体。总体而言,本研究为针对衣壳化dsRNA真菌病毒的RNA沉默提供了见解。

重要性

衣壳化dsRNA真菌病毒(真菌病毒)被认为在其病毒粒子内复制;因此,存在它们是否诱导RNA沉默的问题。在此,我们研究了在白纹羽病菌中针对衣壳化dsRNA真菌病毒(一种分病毒、一种四病毒、一种维克托病毒、一种真菌呼肠孤病毒和一种巨双RNA病毒)的RNA沉默诱导情况。我们发现感染真菌呼肠孤病毒或巨双RNA病毒的白纹羽病菌中RNA沉默相关基因上调,但感染其他病毒的未上调,这与来自这两种真菌病毒的vsRNA相对较高的丰度一致。我们还展示了来自这五种真菌病毒的vsRNA的共同和不同分子特征及来源。此外,我们证明了真菌病毒在白纹羽病菌中激活了RNA诱导沉默复合体。综上所述,我们的数据为针对衣壳化dsRNA真菌病毒的RNA沉默途径提供了见解,该途径在衣壳化dsRNA真菌病毒中差异诱导;也就是说,衣壳化dsRNA真菌病毒存在多种复制策略。

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