Complete sequence of a double-stranded RNA from the phytopathogenic fungus Erysiphe cichoracearum that might represent a novel endornavirus

2016 ◽  
Vol 161 (8) ◽  
pp. 2343-2346 ◽  
Author(s):  
Zhenguo Du ◽  
Wenzhong Lin ◽  
Ping Qiu ◽  
Xiaojuan Liu ◽  
Lingfang Guo ◽  
...  
2018 ◽  
Vol 6 (8) ◽  
Author(s):  
Hao He ◽  
Xiaoguang Chen ◽  
Pengfei Li ◽  
Dewen Qiu ◽  
Lihua Guo

ABSTRACT We describe here a double-stranded RNA mycovirus, termed Fusarium graminearum alternavirus 1 (FgAV1/AH11), from the isolate AH11 of the phytopathogenic fungus F. graminearum . Phylogenetic analysis showed that FgAV1/AH11 belongs to a newly proposed family, Alternaviridae . This is the first report of a mycovirus in the family Alternaviridae that infects F. graminearum .


2012 ◽  
Vol 86 (12) ◽  
pp. 6605-6619 ◽  
Author(s):  
M. Wu ◽  
F. Jin ◽  
J. Zhang ◽  
L. Yang ◽  
D. Jiang ◽  
...  

2021 ◽  
Author(s):  
Samira Mokhtari ◽  
Akhtar Ali

Abstract A double-stranded RNA (dsRNA) mycovirus was isolated from airborne spores of Fusarium bullatum and was named Fusarium bullatum alternavirus 1 (FbAV1). Sequencing analysis and the rapid amplification of cDNA ends (RACE) of 5’ and 3’-end confirmed three segments: dsRNA1 (3546 nt), dsRNA2 (2511 nt) and dsRNA3 (2484 nt). BLASTN search of sequences showed that FbAV1 has 92-96% identity with Fusarium incarnatum Alternavirus 1 (FiAV1). Phylogenetic analysis of the RdRp amino acid sequences suggested that the dsRNA mycovirus in this study clustered with the newly proposed family “Alternaviridae”. This is the first report of FbAV1 mycovirus from airborne spores of a fungus F. bullatum.


2016 ◽  
Vol 90 (12) ◽  
pp. 5677-5692 ◽  
Author(s):  
Hajime Yaegashi ◽  
Takeo Shimizu ◽  
Tsutae Ito ◽  
Satoko Kanematsu

ABSTRACTRNA 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 fungusRosellinia 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 inR. 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 inR. necatrixrevealed 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.IMPORTANCEEncapsidated 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) inRosellinia necatrix. We revealed upregulation of RNA silencing-related genes inR. necatrixinfected 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 inR. 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.


2021 ◽  
Author(s):  
Chenghui Hu ◽  
Siwei Li ◽  
Chunyan Wu ◽  
Yiran Mi ◽  
Qingnian Cai ◽  
...  

Abstract The full genome of a double-stranded RNA (dsRNA) mycovirus, which was isolated from Alternaria solani strain DT-10 causing potato foliar disease and designated as Alternaria solani chrysovirus 1 (AsCV1), consisted of four dsRNA segments (dsRNA 1–4) with the length of 3600 bp, 3128 bp, 2996 bp, and 2714 bp, respectively. RNA-dependent RNA polymerase (RdRp, 1084 amino acids (aa)), putative capsid protein (905 aa), Alphachryso-P3 (835 aa), and Alphachryso-P4 (729 aa) were encoded by dsRNA1, dsRNA2, dsRNA3, and dsRNA4, respectively, which had the highest identities of 41.77%-72.38% to the counterparts of Helminthosporium victoriae virus 145S (HvV145S) in the genus Alphachrysovirus of the family Chrysoviridae. Moreover, the 5′-untranslated regions (UTRs) with several unique inserts (3–37 bp) and deletions (5–64 bp) of AsCV1 dsRNA 1–4 shared 51.65%-68.01% identities to those of HvV145S. Phylogenetic analysis of RdRp suggested that AsCV1 clustered the most closely with HvV145S. Based on the characteristics of distinct host, low identities of encoded proteins, special traits in 5′-UTRs of dsRNA 1–4, and phylogenetic analysis of RdRp, AsCV1 was confirmed to be a new species in the genus Alphachrysovirus. To our best knowledge, this is the first alphachrysovirus identified from phytopathogenic A. solani.


2009 ◽  
Vol 90 (6) ◽  
pp. 1423-1432 ◽  
Author(s):  
A. C. Potgieter ◽  
N. A. Page ◽  
J. Liebenberg ◽  
I. M. Wright ◽  
O. Landt ◽  
...  

This paper reports significant improvements in the efficacy of sequence-independent amplification and quality of sequencing of viruses with segmented double-stranded RNA (dsRNA) genomes. We demonstrate that most remaining bottlenecks in dsRNA virus genome characterization have now been eliminated. Both the amplification and sequencing technologies used require no previous sequence knowledge of the viral dsRNA, there is no longer a need to separate genome segments or amplicons and the sequence-determined bias observed in cloning has been overcome. Combining very efficient genome amplification with pyrophosphate-based 454 (GS20/FLX) sequencing enabled sequencing of complete segmented dsRNA genomes and accelerated the sequence analysis of the amplified viral genomes. We report the complete consensus sequence of seven viruses from four different dsRNA virus groups, which include the first complete sequence of the genome of equine encephalosis virus (EEV), the first complete sequence of an African horsesickness virus (AHSV) genome determined directly from a blood sample and a complete human rotavirus genome determined from faeces. We also present the first comparison between the complete consensus sequence of a virulent and an attenuated strain of AHSV1. Ultra-deep sequencing (>400-fold coverage) of the AHSV1 reference and attenuated strains revealed different ratios of reassortants in the reference strain and allowed quasispecies detection in the plaque-purified attenuated strain of AHSV1. This approach amounts to a paradigm shift in dsRNA virus research, since it is sensitive and specific enough for comprehensive investigations of the evolution and genetic diversity in dsRNA virus populations.


2018 ◽  
Vol 163 (12) ◽  
pp. 3467-3470
Author(s):  
Xiaoqin Peng ◽  
Shexiang Gan ◽  
Xiaoting Zhang ◽  
Yingying Zhai ◽  
Lina Cai ◽  
...  

Author(s):  
Lifeng Zhai ◽  
Mengmeng Yang ◽  
Meixing Zhang ◽  
Ni Hong ◽  
Guoping Wang

A double-stranded RNA (dsRNA) virus was isolated and characterized from a strain EW220 of the phytopathogenic fungus Botryosphaeria dothidea. The full-length cDNAs of dsRNAs were 6,434 bp and 5,986 bp in size, respectively. The largest dsRNA of BdBRV1 encodes a cap-pol fusion protein that contains part coat protein gene and a RNA-dependent RNA polymerase (RdRp) domain, and the second dsRNA encodes a hypothetical protein. The dsRNA virus was named Botryosphaeria dothidea botybirnavirus 1 (BdBRV1). BdBRV1 contains spherical virions that are 37 nm in diameter consisting of two segments. The structural proteins of BdBRV1 virus particles were 110 kDa, 90 kDa, and 80 kDa, which encoded by dsRNA1 and 2-ORFs. The analysis of genome sequences revealed that the sequences of BdBRV1 shared 99% identity with Bipolaris maydis botybirnavirus 1(BmBRV1). Phylogenetic reconstruction indicated that BdBRV1 and BmBRV1 are phylogenetically related to the genus Botybirnavirus. Importantly, BdBRV1 influences the growth of B. dothidea and confers hypovirulence to the fungal host. BdBRV1 and BmBRV1 were two strains of the same virus. To our knowledge, this is the first report of a botybirnavirus in B. dothidea and our result might be the first funding in the different fungi infected by the same virus.


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