Identification and sequence determination of a new chrysovirus infecting the phytopathogenic fungus Dothistroma septosporum

A new double-stranded (ds) RNA mycovirus has been identified in isolate Ds752-1 of the phytopathogenic fungus Dothistroma septosporum, the causal agent of Dothistroma needle blight, also known as red band needle blight or pine needle blight. Dothistroma septosporum chrysovirus 1 (DsCV-1) is a new member of the genus Alphachrysovirus in the family Chrysoviridae. The DsCV-1 genome comprises four dsRNA elements designated 1, 2, 3, and 4 from largest to smallest. dsRNA1 encodes an RNA-dependent RNA polymerase (RdRP) that is most similar to the RdRP of Erysiphe necator associated chrysovirus 3. dsRNA2 potentially encodes two hypothetical proteins, one of which is small and has no homology to known proteins, and one of which is large with significant sequence similarity to the alphachryso-P3 of other alphachrysoviruses. dsRNA3 and dsRNA4 encode a coat protein (CP) and a putative cysteine protease, respectively. This is the first report of a mycovirus infecting the fungus D. septosporum, and DsCV-1 is one of three Chrysoviridae family members found to possess genomic dsRNAs potentially encoding more than one protein. Supplementary Information The online version contains supplementary material available at 10.1007/s00705-023-05768-9.

Fungal viruses, or mycoviruses, are widespread across the major taxa of fungi [1]. The diversity of known mycoviruses has increased rapidly over the last few years, mainly due to the development and widespread use of state-of-theart next-generation sequencing techniques. Currently, the International Committee on Taxonomy of Viruses officially recognizes over 25 taxa, 10 of which are families or genera accommodating mycoviruses with double-stranded (ds) RNA genomes (Amalga-, Chryso-, Curvula-, Megabirna-, Partiti-, Polymyco-, Quadri-, Spinareo-, and Totiviridae and Botybirnavirus). Additionally, there are still many taxonomically unclassified dsRNA mycoviruses [1,2]. dsRNA mycoviruses do not have an extracellular phase in their replication cycle and are not vectored but instead rely on horizontal transmission through anastomosis and/or vertical transmission through spores [2]. Despite some of them being asymptomatic in their hosts, the development of mycoviruses as biological control agents is of great interest, since they may reduce [3] or increase [4] the virulence of their fungal hosts.
In Britain, Dothistroma needle blight, also known as red band needle blight or pine needle blight, is caused by the fungus Dothistroma septosporum. D. septosporum has been found on a range of conifer species, but pines are its most common hosts. Defoliation can continue annually and gradually weaken the tree, significantly reducing timber yields and resulting in tree death [5]. No mycovirus infections have been reported previously in D. septosporum. In this study, we report a new member of the genus Alphachrysovirus in the family Chrysoviridae, designated "Dothistroma septosporum chrysovirus 1" (DsCV-1).
D. septosporum isolate Ds752.1, which harbors DsCV-1, was isolated in 2012 in West Argyll, Scotland, from Corsican pine and was identified morphologically and by molecular analysis as mating type 1. dsRNA elements were extracted from fresh mycelium and treated with DNase I and S1 nuclease prior to separation by agarose gel electrophoresis, together with DNA size standards (HyperLadder I; Bioline), as indicated in Fig. 1a. Purified dsRNA was used as a template for random polymerase chain reaction (PCR) amplification, genome walking, and RNA-ligase-mediated rapid amplification of cDNA ends (RLM RACE) [6]. All products were cloned and sequenced as described previously [4].
The genome organization of DsCV-1 is shown in Fig. 1b, and the sequences have been deposited in public databases (project accession number PRJEB57200). The dsRNA elements comprising the genome were numbered 1 to 4 from largest to smallest. dsRNA1 is 3584 bp in length (GC content, 44.61%), contains a single open reading frame (ORF) encoding a 1095-amino-acid (aa) protein (126.45 kDa) with eight conserved motifs that are typically present in RNA-dependent RNA polymerases (RdRPs) of eukaryotic dsRNA viruses [7], and shows a high degree of sequence similarity to alphachrysovirus RdRPs. dsRNA2 is 3280 bp in length (GC content, 45.25%) and has two ORFs, which potentially encode 141-and 852-aa proteins, 15.80 kDa and 95.83 kDa in size, respectively. BLAST searches showed, for the latter, a high degree of sequence similarity to hypothetical alphachryso-P3 proteins of unknown function, while for the former, designated alphachryso-P3S (S for small), no similarity to any database-accessed protein sequences was found. As for other alphachrysoviruses, the hypothetical alphachryso-P3 protein contains a ''phytoreovirus S7 domain'', found in viral core proteins with nucleic acid binding activity [2,8], and its N-terminal region shares a degree of sequence similarity with comparable N-terminal regions of alphachrysovirus RdRPs. dsRNA3 is 3069 bp in length (GC content, 46.97%), containing an ORF that encodes a 938-aa protein (104.21 kDa) with a high degree of sequence similarity to alphachrysovirus capsid protein (CP) genes. dsRNA4 is 2817 bp in length (GC content, 47.80%) and contains an ORF that encodes an 846-aa protein (93.49 kDa) with motifs typical of cysteine proteases and a high degree of sequence similarity to putative proteases of alphachrysoviruses.
Phylogenetic analysis based on the complete or almost complete aa sequence of the RdRP genes of DsCV-1 and selected members of the family Chrysoviridae was performed using the programme MEGA 11 [11]. A multiple alignment of RdRP aa sequences was produced using MUSCLE as implemented in MEGA 11, all positions with less than 30% site coverage were eliminated, and the LG+G+I+F substitution model was used. A maximumlikelihood (ML) phylogenetic tree was constructed in MEGA 11 with 100 bootstrap replicates. The ML phylogenetic tree revealed that the putative RdRP encoded by DsCV-1 most strongly resembled those of viruses within the genus Alphachrysovirus, family Chrysoviridae (Fig. 2). Based on the established chrysovirus species demarcation criteria, including the novel host D. septosporum, the unusually long 5'-UTR of dsRNA2, and the <70% aa sequence identity in the RdRP to representatives of already recognised species, DsCV-1 should be considered a member of a new species, for which we propose the name "Alphachrysovirus dothistromae". The potential pathogenic effects of DsCV-1 in D. septosporum were not evaluated in the present work.
In conclusion, DsCV-1 is a new member of the genus Alphachrysovirus in the family Chrysoviridae and is one of the three chrysoviruses reported whose alphachryso-P3-encoding dsRNA potentially produces an additional protein of unknown function. This is the first identification of a mycovirus infecting D. septosporum.
Acknowledgements This work is dedicated to the memory of Bob Stubbs, former Director of the Scottish Forestry Trust, who was instrumental in orchestrating our funding and whose encouragement is gratefully appreciated.
Author contributions IK-L and RHAC conceived and designed the study. KVT provided the biological material. UAS, JOD, CF, and IK-L performed the experiments. RHAC and IK-L analysed the data and wrote the manuscript. All authors read and approved the final manuscript.
Funding This work was supported by the Scottish Forestry Trust (proof of concept and scoping studies award SS/16/09/02 and general assistance award P17-272).

Data availability
The sequences generated and analysed during the current study are available in the European Nucleotide Archive, project accession number PRJEB57200.

Conflict of interest
The authors have no relevant financial or non-financial interests to disclose.
Ethical approval This study does not involve human participants or animals; no ethical approval was required.
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