» Articles » PMID: 27189438

Generation of a High Resolution Map of SRNAs from Fusarium Graminearum and Analysis of Responses to Viral Infection

Overview
Journal Sci Rep
Specialty Science
Date 2016 May 19
PMID 27189438
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Previously, we characterized F. graminearum hypovirus 1 (FgHV1) and F. graminearum hypovirus 2 (FgHV2), which are the only two hypoviruses in F. graminearum that are closely related to Cryphonectria hypovirus 1 (CHV1) and Cryphonectria hypovirus 2 (CHV2) in the Hypoviridae family. In this study, we preliminarily elucidated the RNA silencing mechanism of the F. graminearum/hypovirus system from a small RNA (sRNA) perspective by using HiSeq deep sequencing. The length distributions of F. graminearum sRNA were altered by hypoviral infection. Potential microRNA-like (milRNA) candidates were differentially expressed between the hypovirus-free and hypovirus-infected library types. Extensive virus-derived small interfering RNAs (vsiRNAs) were also principally defined. The 1,831,081 and 3,254,758 total reads generated from the FgHV1 and FgHV2 genomes in F. graminearum yielded the first high-resolution sRNA maps of fungal viruses. In addition, extensive bioinformatics searches identified a large number of transcripts that are potentially targeted by vsiRNAs, several of which were effectively down-regulated. In particular, the RNA silencing-related genes FgDicer1 and FgRdRp5 were predicted targets of FgHV1- and FgHV2-derived siRNAs, possibly revealing a novel anti-RNA silencing strategy employed by mycoviruses.

Citing Articles

Mycologists and Virologists Align: Proposing for Global Mycovirus Studies.

Khalifa M, Ayllon M, Rodriguez Coy L, Plummer K, Gendall A, Chooi K Viruses. 2024; 16(9).

PMID: 39339959 PMC: 11437445. DOI: 10.3390/v16091483.


Adaptive regulation of miRNAs/milRNAs in tissue-specific interaction between apple and .

Gao C, Zhao B, Zhang J, Du X, Wang J, Guo Y Hortic Res. 2024; 11(5):uhae094.

PMID: 38799130 PMC: 11116833. DOI: 10.1093/hr/uhae094.


Interference of Small RNAs in through FgGMTV1 Infection.

Wang S, Ruan S, Zhang M, Nie J, Nzabanita C, Guo L J Fungi (Basel). 2022; 8(12).

PMID: 36547570 PMC: 9781238. DOI: 10.3390/jof8121237.


Similar Characteristics of siRNAs of Plant Viruses Which Replicate in Plant and Fungal Hosts.

Pang T, Peng J, Bian R, Liu Y, Zhang D, Andika I Biology (Basel). 2022; 11(11).

PMID: 36421386 PMC: 9687825. DOI: 10.3390/biology11111672.


Fungal Virus, FgHV1-Encoded p20 Suppresses RNA Silencing through Single-Strand Small RNA Binding.

Wang S, Zhang J, Nzabanita C, Zhang M, Nie J, Guo L J Fungi (Basel). 2022; 8(11).

PMID: 36354938 PMC: 9693516. DOI: 10.3390/jof8111171.


References
1.
Eusebio-Cope A, Sun L, Tanaka T, Chiba S, Kasahara S, Suzuki N . The chestnut blight fungus for studies on virus/host and virus/virus interactions: from a natural to a model host. Virology. 2014; 477:164-175. DOI: 10.1016/j.virol.2014.09.024. View

2.
Zhang D, Spiering M, Nuss D . Characterizing the roles of Cryphonectria parasitica RNA-dependent RNA polymerase-like genes in antiviral defense, viral recombination and transposon transcript accumulation. PLoS One. 2014; 9(9):e108653. PMC: 4182546. DOI: 10.1371/journal.pone.0108653. View

3.
Chen Y, Gao Q, Huang M, Liu Y, Liu Z, Liu X . Characterization of RNA silencing components in the plant pathogenic fungus Fusarium graminearum. Sci Rep. 2015; 5:12500. PMC: 4515635. DOI: 10.1038/srep12500. View

4.
Catalanotto C, Azzalin G, Macino G, Cogoni C . Involvement of small RNAs and role of the qde genes in the gene silencing pathway in Neurospora. Genes Dev. 2002; 16(7):790-5. PMC: 186333. DOI: 10.1101/gad.222402. View

5.
Zamore P . Ancient pathways programmed by small RNAs. Science. 2002; 296(5571):1265-9. DOI: 10.1126/science.1072457. View