GENOME ANNOUNCEMENT
Viruses within the family Narnaviridae are composed of a positive single-stranded RNA segment (2.3 to 3.6 kb) encoding a single protein, the RNA-dependent RNA polymerase (RDRP) (1–3). Narnavirus derives from “naked RNA,” reflecting the absence of a capsid or envelope, and narnaviruses do not form infectious viral particles. Two genera are recognized: Mitovirus, found in the mitochondrion of fungi and translated using the mitochondrial genetic code, and cytoplasmic Narnavirus, comprising the 20S/23S elements of Saccharomyces cerevisiae and one from the oomycete Phytophthora infestans (3–5). Here, we report the discovery and complete genome sequence (including termini) of Phytomonas serpens narnavirus 1 (PserNV1).
Total cellular RNA from P. serpens isolate 9T (6) was extracted using TRIzol reagent (Thermo Fisher), treated with DNase I (Thermo Fisher) at 37°C for 45 min, and purified with RNA Clean & Concentrator-25 (Zymo Research). Replicative viral double-stranded RNAs (dsRNAs) were visualized following treatment with S1 nuclease (Thermo Fisher), separation by agarose gel electrophoresis, and visualization by ethidium bromide staining (7). A prominent dsRNA band of about 4 kb was observed, eluted, and used as a template to generate a cDNA library, with fragment sizes ranging from 200 to 600 nucleotides (nt). A multiplexed TruSeq RNA library was sequenced (2 × 101 cycles, paired-end reads) on the HiSeq 2500 (Illumina). A total of 64,373 reads were obtained, of which 47,690 assembled into a single contig, which was confirmed by reverse transcriptase PCR and sequencing. The adaptor (5′-PO4-CCCGTCGTTTGCTGGCTCTTT-NH2) was added to the eluted RNA band with T4 RNA ligase (NEB), amplified using primers complementary to the adapter and virus, and sequenced to determine the termini.
The PserNV1 RNA genome is 3,782 nt in length, with a G+C composition comparable to that of the P. serpens nuclear genome (48.2 versus 46.6%, respectively) (6). As in other narnaviruses, short hairpins are evident at both the 5′ and 3′ termini. From the first AUG (nt 83), translation with the nuclear genetic code revealed a single open reading frame (ORF) encoding a 1,208-amino-acid protein exhibiting motifs seen in narnaviral RNA-dependent RNA polymerases (1). Phylogenetic comparisons with accepted members of the Narnaviridae placed it firmly within the monophyletic genus Narnavirus. As the overall RDRP amino acid sequence difference was >80%, this element warrants status as a new Narnavirus species.
Members of the genus Phytomonas affect >100 plant species, including economically important plants, such as coffee, coconut, cassava, and oil palms (8), which may bear relatives of PserNV1. Classification as a narnavirus suggests that PserNV1 differs from the virus-like particles described previously in other Phytomonas species. (9). Some data suggest that PserNV1 may be unstable during culture, as reverse transcriptase PCR tests of this strain acquired independently from another source did not reveal PserNV1 (the authenticity of this strain was confirmed by sequence of two nuclear genes, GAPDH and PTR1). In the future, studies of NV1-positive and -negative lines of Phytomonas may establish potential roles of this viral element in plant pathogenicity (1).
Nucleotide sequence accession number.
The full-length viral genomic sequence of PserNV1 from Phytomonas serpens 9T strain was deposited in GenBank under the accession no. KU882057.
b Biology Centre and Faculty of Sciences, Institute of Parasitology, University of South Bohemia, České Budějovice, Czech Republic
c Canadian Institute for Advanced Research, Toronto, Ontario, Canada
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Abstract
We describe here a new RNA virus (PserNV1) from the plant protist parasite Phytomonas serpens (family Trypanosomatidae, Kinetoplastida, supergroup Excavata). The properties of PserNV1 permit assignment to the genus Narnavirus (Narnaviridae), the first reported from a host other than fungi or oomycetes.
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Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer