Abstract
We present a taxonomic proposal for revision of the family Secoviridae, a taxon of plant viruses in the order Picornavirales. We propose the reorganization of the genus Sadwavirus to create three new subgenera and to update the classification of five existing species. The proposed subgenera are “Satsumavirus” (one species: Satsuma dwarf virus), “Stramovirus” (two species: Strawberry mottle virus and Black raspberry necrosis virus) and “Cholivirus” (two species: Chocolate lily virus A and Dioscorea mosaic associated virus).
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Introduction
The family Secoviridae was created in 2009 after amalgamation of the now-dissolved families Comoviridae and Sequiviridae and is the only family of plant viruses assigned to the order Picornavirales [13]. Members of the family, referred to as secovirids, share common properties with other members of the order: (1) a positive-strand RNA genome, which can be monopartite or bipartite, with each RNA linked at its 5’ end to a small viral protein termed “VPg”, (2) the production of large polyproteins that are cleaved by viral proteases, (3) a conserved “replication block” within the RNA1-encoded polyprotein that includes a type III helicase, the VPg, a cysteine protease related to the picornavirus 3C protease, and a type I RNA-dependent RNA polymerase, (4) a 25- to 30-nm icosahedral capsid with a pseudo T = 3 symmetry. The capsid is composed of 60 coat protein (CP) subunits, each consisting of three β-barrel domains that can be divided into a single large CP, or into two or three smaller CPs depending on the genus.
Currently, there are eight genera in the family Secoviridae: the genera Sadwavirus, Torradovirus, Cheravirus, Sequivirus and Waikavirus, which do not belong to a subfamily, and three genera (Comovirus, Fabavirus, Nepovirus) in the subfamily Comovirinae [16]. Within the family, phylogenetic relationships have been used to distinguish genera and subfamilies. In particular, the so-called “Pro-Pol” sequence, which is defined as the sequence between the conserved catalytic cysteine (or serine) of the 3C-like protease and the GDD motif of the RNA-dependent RNA polymerase, has been used to refine the taxonomy of the family Secoviridae and its relationship to other members of the order [7, 8, 13]. Additional criteria have also been used to distinguish genera in the family: (1) the number of genomic RNAs (one for sequiviruses and waikaviruses, two for all other genera), (2) the number of protein domains and/or processing sites within the polyproteins, (3) the number of CPs (one CP of 53-60 kDa for nepoviruses; two CPs of 35-40 kDa and 20-25 kDa for comoviruses, fabaviruses and sadwaviruses; and three CPs of 20-25 kDa for cheraviruses, torradoviruses, sequiviruses and waikaviruses), (4) the presence of additional open reading frames (ORFs), e.g., one additional ORF on the RNA2 of torradoviruses in addition to the large polyprotein, and (5) the presence of subgenomic RNAs. Not all criteria need to be met simultaneously.
The genus Sadwavirus was created in 2004 [7] and originally included the species Satsuma dwarf virus, Strawberry latent ringspot virus and Strawberry mottle virus in order to classify isolates of homonymous viruses (abbreviations: SDV, SLRSV and SMoV). At the time, few secovirid sequences were available and phylogenetic relationships could not be clearly established. SDV and SLRSV shared the common property of having two CPs, whereas the number of CPs of SMoV isolates had not been experimentally determined, owing to difficulties with purifying this virus [15]. In 2009, SLRSV and SMoV were demoted from the genus [13]. SLRSV does not branch together with SDV in the Pro-Pol phylogenetic tree. Rather it is related, albeit distantly, to cheraviruses [7] (see Fig. 1). SMoV is related to SDV in the Pro-Pol tree, but the number of protein domains in the RNA2 polyprotein was unclear, in particular the number of CPs.
New viruses with phylogenetic relationships to SDV have been described more recently (see Fig. 1). Black raspberry necrosis virus (BRNV) was found to be closely related to SMoV [5]. The number of protein domains in the RNA2 polyprotein of BRNV, which includes the CP(s), has also not been determined experimentally. The species Black raspberry necrosis virus was created in 2009 and was classified in the family Secoviridae but was not assigned to a genus [13]. In 2016 and 2017, two new viruses, chocolate lily virus A (CLVA) and dioscorea mosaic associated virus (DMaV) were classified in additional unassigned species in the family: Chocolate lily virus A and Dioscorea mosaic associated virus [1, 2, 6, 19].
Recent analysis of cleavage sites in the polyproteins of SMoV revealed that this virus encodes two proteases: the RNA1-encoded 3C-like protease, which is common to all viruses in the family, a characteristic also shared with other members of the order, and the RNA2-encoded glutamic protease, which corresponds to a novel type of viral protease [9, 11, 12]. The RNA1 protease cleaves the RNA1 polyprotein at five sites, defining six domains in the polyprotein (Fig. 2). The presence of two protein domains upstream of the nucleotide-binding protein (NTB, putative helicase) domain is a feature shared with nepoviruses [4, 17, 18]. Examination of the polyproteins of BRNV, CLVA, DMaV and SDV revealed the presence of putative cleavage sites at similar positions that would imply a similar organization of the RNA1 polyprotein [9, 10] (Fig. 2). The RNA2 polyprotein of a Canadian isolate of SMoV (isolate NsPer3) was cleaved at one site (between the MP and CP domains) by the RNA1-encoded protease [9]. It was also cleaved at two sites by the RNA2-encoded glutamic protease (Fig. 2) [11]. Sequence comparison of SMoV and BRNV implied a similar genomic organization for BRNV (Fig. 2) [11]. These results strongly suggest that SMoV and BRNV have unique characteristics that distinguish them from SDV: (1) they encode one large CP rather than two CPs; (2) the RNA2 polyprotein possesses additional protein domains downstream of the CP domain, including a novel glutamic protease domain. The presence of protein domains downstream of the CP is a new feature in the family Secoviridae. Signature sequences for the glutamic protease domain were not found in the RNA2 polyprotein of CLVA and DMaV [11]. Prediction of cleavage sites recognized by the RNA1-encoded 3C-like protease suggested the presence of a single large CP for CLVA and DMaV [9, 10], although this needs to be confirmed experimentally.
It was initially suggested that the identification of a novel protease domain in the RNA2 polyprotein of SMoV could justify the creation of a new genus to encompass BRNV and SMoV [11]. However, discussion within the ICTV Secoviridae Study Group (i.e., the authors of this manuscript) highlighted that phylogenetic relationships among BRNV, SMoV, SDV, CLVA and DMaV should also be recognized. Indeed, recent reexamination of phylogenetic relationships using the deduced amino acid sequence of the Pro-Pol region of type isolates for recognized species in the family confirmed that SDV, SMoV, BRNV, CLVA and DMaV group together as a single branch with a high degree of confidence (Fig. 1). In addition, phylogenetic trees based on the CP sequence (which is defined by the mapping of the cleavage sites as shown in Fig. 2) also suggested a common lineage for SDV, SMoV, BRNV, CLVA and DMaV, although the bootstrap analysis revealed a lower degree of confidence in the branching than with the Pro-Pol tree (Fig. 3). Thus, it was agreed that the corresponding five species should be classified in a common genus (Sadwavirus).
With the recent approval of additional taxonomic ranks including subgenera [14], we propose to create three subgenera in the genus Sadwavirus to classify these five viral species based upon the differences in the genomic organization of RNA2, including the presence (or absence) of the glutamic protease. The corresponding taxonomy proposal (2019.008P.N.v1.Sadwavirus_3subg) was conditionally approved by the ICTV executive committee and is awaiting ratification by the ICTV membership. Below is a summary of the taxonomic updates:
- (1)
Reorganization of the genus Sadwavirus to include three subgenera (proposed subgenera “Satsumavirus”, “Stramovirus” and “Cholivirus”) to classify five species (Satsuma dwarf virus, Strawberry mottle virus, Black raspberry necrosis virus, Chocolate lily virus A and Dioscorea mosaic associated virus), with Satsuma dwarf virus remaining the type species. Common characteristics of members of the genus Sadwavirus: group as a single lineage in both the Pro-Pol and CP trees, six protein domains in the RNA1 polyprotein. The name Sadwavirus is kept for the genus. Since Strawberry mottle virus was assigned to Sadwavirus between 2004 and 2009, this will prevent confusion.
- (2)
Creation of the subgenus “Satsumavirus”, with Satsuma dwarf virus as the only species. Characteristics of members of the subgenus: one viral protease (the RNA1-encoded cysteine protease), two CPs, group as a single sub-branch in the Pro-Pol and CP trees.
- (3)
Creation of the subgenus “Stramovirus”, encompassing Strawberry mottle virus and Black raspberry necrosis virus (proposed name derived from strawberry mottle virus, the best-characterized virus). Characteristics of members of the subgenus: two viral proteases (the RNA1-encoded 3C-like cysteine protease and the RNA2-encoded glutamic protease), a single large CP, group as a single sub-branch in the Pro-Pol and CP trees.
- (4)
Creation of the subgenus “Cholivirus”, encompassing Chocolate lily virus A and Dioscorea mosaic associated virus (proposed name derived from chocolate lily virus A, the first characterized member). Characteristics of members of the subgenus: one viral protease (the RNA1-encoded cysteine protease), probably a single large CP (based on putative cleavage sites), group as a single sub-branch in the Pro-Pol and CP trees.
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Sanfaçon, H., Dasgupta, I., Fuchs, M. et al. Proposed revision of the family Secoviridae taxonomy to create three subgenera, “Satsumavirus”, “Stramovirus” and “Cholivirus”, in the genus Sadwavirus. Arch Virol 165, 527–533 (2020). https://doi.org/10.1007/s00705-019-04468-7
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DOI: https://doi.org/10.1007/s00705-019-04468-7