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María Laura García, Elena Dal Bó, John V. da Graça, Selma Gago-Zachert, John Hammond, Pedro Moreno, Tomohide Natsuaki, Vicente Pallás, Jose A. Navarro, Carina A. Reyes, Gabriel Robles Luna, Takahide Sasaya, Ioannis E. Tzanetakis, Anna María Vaira and Martin Verbeek
A summary of this ICTV Report chapter has been published as an ICTV Virus Taxonomy Profile article in the Journal of General Virology, and should be cited when referencing this online chapter as follows:
García, M.L., Dal Bó, E., da Graça, J.V., Gago-Zachert, S., Hammond, J., Moreno, P., Natsuaki, T., Pallás, V., Navarro, J.A., Reyes, C.A., Luna, G.R., Sasaya, T., Tzanetakis, I.E., Vaira, A.M., Verbeek, M., and ICTV Report Consortium, 2017, ICTV Virus Taxonomy Profile: Ophioviridae, Journal of General Virology, 98: 1161–1162.
The Aspiviridae (formerly Ophioviridae) is a family of filamentous plant viruses, with single-stranded negative-sense, and possibly ambi-sense, RNA genomes of 11.3–12.5 kb divided into 3–4 segments. Virions are naked filamentous nucleocapsids, non-enveloped, in the shape of kinked circles of at least two different contour lengths. Since only one genus is currently recognized, the family description corresponds to that of the genus Ophiovirus; the type species is Citrus psorosis ophiovirus. The family includes seven species, of which four are known to be soil-transmitted. Natural hosts of aspiviruses include trees, shrubs, vegetables and bulbous or corm-forming ornamentals, both monocots and dicots.
Table 1.Aspiviridae. Characteristics of the family Aspiviridae.
citrus psorosis virus P-121 (RNA1 AY654892; RNA2: AY654893; RNA3: AY654894), species Citrus psorosis ophiovirus, genus Ophiovirus
Non-enveloped, naked filamentous nucleocapsids about 3 nm in diameter, forming kinked circles of at least two different contour lengths (700 nm and about 2000 nm). Pseudo-linear duplex structures are about 9–10 nm in diameter
11.3–12.5 kb of negative-sense, segmented RNA (3 or 4 segments)
From mRNAs, which are complementary to the vRNAs
Citrus, blueberry, pittosporum, lettuce, sowthistle, tulip, ranunculus, anemone, lachenalia and freesia
Realm Riboviria, phylum Negarnaviricota, subphylum Haploviricotina, class Milneviricetes and order Serpentovirales; one genus, Ophiovirus, including 7 species
The particles are naked filamentous nucleocapsids about 3 nm in diameter (Figure 1.Aspiviridae), forming kinked (probably internally coiled) circles of at least two different contour lengths, the shortest being about 700 nm. The circles (open form) can collapse to form pseudo-linear duplex structures of 9–10 nm in diameter (collapsed form) (Milne et al., 1996).
The relative molecular masses and sedimentation coefficients of virions are unknown. The particles are unstable in CsCl but the buoyant density in cesium sulfate has been determined to be 1.22 g cm−3 for both ranunculus white mottle virus [RWMV, Rn3 isolate], and Mirafiori lettuce big-vein virus [MLBVV, I-47 isolate] (Roggero et al., 2000, Vaira et al., 1997). The particles are unstable between pH 6 and 8. Viruses lose infectivity in crude sap held at 50 °C for 10 min (40–45 °C for tulip mild mottle mosaic virus, TMMMV) (Morikawa et al., 1995). Virus structures are resistant to limited treatment with organic solvents and nonionic or zwitterionic detergents.
Aspiviruses have a single-stranded negative-sense, and possibly ambi-sense RNA genome (11.3–12.5 kb in total) divided into 3 or 4 segments. The virions encapsidate both the viral and viral complementary RNAs (vRNA and vcRNA), but a larger amount of vRNA (negative-sense) is detected in purified virion preparations (Roggero et al., 2000, Garcia et al., 1991, Naum-Ongania et al., 2003, Sánchez de la Torre et al., 1998, van der Wilk et al., 2002). As virions appear circularized, the presence of panhandle structures has been suggested; however, significant sequence complementarity was not found between the 5′- and the 3′-terminal sequences of genomic RNAs of citrus psorosis virus (CPsV), MLBVV or blueberry mosaic associated virus (BlMaV) (Naum-Ongania et al., 2003, van der Wilk et al., 2002, Thekke-Veetil et al., 2014). At the 5′- and 3′-ends of MLBVV genomic RNAs, there are orthomyxovirus-like palindromic sequences that could fold into a symmetrically hooked conformation. These structures could not be predicted for other sequenced members.
RNA1 is 7.5–8.2 kb, RNA2 is 1.6–1.9 kb and RNA3 is 1.4–1.5 kb. A fourth genomic RNA of about 1.4 kb has been reported for MLBVV and lettuce ring necrosis virus (LRNV). In the case of CPsV, RWMV, freesia sneak virus (FreSV) and BlMaV RNA4 was not found; no information is available for TMMMV (Vaira et al., 1997, Morikawa et al., 1995, Naum-Ongania et al., 2003, Sánchez de la Torre et al., 1998, Thekke-Veetil et al., 2014, Sánchez de la Torre et al., 2002, Torok and Vetten 2002, Torok and Vetten 2003, Vaira et al., 2003, Vaira et al., 2009, Vaira et al., 1996).
Virions consist of a single type of coat protein (CP) subunit of 43–50 kDa, varying in mass according to species and isolate (Roggero et al., 2000, Vaira et al., 1997, Morikawa et al., 1995, Sánchez de la Torre et al., 1998, van der Wilk et al., 2002, Torok and Vetten 2003, Derrick et al., 1988, Garcia et al., 1994, Jeong et al., 2014, Navas‐Castillo et al., 1993).
The genome of aspiviruses consists of three or four individually encapsidated vRNA segments (Figure 2. Aspiviridae) although vcRNAs are also encapsidated (Vaira et al., 1997, Naum-Ongania et al., 2003, Sánchez de la Torre et al., 1998, van der Wilk et al., 2002, Thekke-Veetil et al., 2014, Sánchez de la Torre et al., 2002, Vaira et al., 2003, Martin et al., 2005). The vcRNA1, the longest RNA segment (7.5–8.2 kb), contains two ORFs. The ORF located at its 5′-end encodes a protein with a predicted molecular mass of 22–25 kDa. The 24K ortholog of CPsV localizes at the nucleus and was reported to be involved in miRNA misprocessing in citrus (Reyes et al., 2016), and to possess RNA silencing suppressor activity (Robles Luna et al., 2017). Separated by an intergenic region of about a hundred nucleotides, a second ORF in the same strand encodes a protein (261–280 kDa) that contains the core polymerase module with the characteristic five conserved motifs (A–E) of the RNA-dependent RNA polymerases (RdRP). The SDD sequence, a signature for segmented negative-stranded RNA viruses (Orthomyxoviridae, Arenaviridae and Bunyaviridae) occurs in motif C of the RdRP (Naum-Ongania et al., 2003). Since no other segmented RNA viruses have two ORFs coded in the vcRNA of the larger segment (RNA1), this genomic organization is a particular feature of members of the Aspiviridae family.
The vcRNA2 (1.6–1.9 kb) of CPsV, LRNV, FreSV and BlMaV contains a single ORF, whereas for MLBVV a second ORF in vRNA2 encoding a putative protein of 37–38 kDa of unknown function has been reported. This would make MLBVV the sole ophiovirus with ambisense RNA2 (van der Wilk et al., 2002). The vcRNA2 encodes the cell-to-cell movement protein (MP) of 50-58 kDa, which has been characterized for CPsV (54K) and MLBVV (55K) (Hiraguri et al., 2013, Robles Luna et al., 2013). The MP is also involved in RNA silencing suppression activity (Robles Luna et al., 2017). The vcRNA3 codes for the CP (Roggero et al., 2000, Sánchez de la Torre et al., 1998, Vaira et al., 2011); the CP molecules of MLBVV and CPsV can interact among themselves, and localize in the cytoplasm of N. benthamiana epithelial cells, when expressed ectopically (Peña et al., 2012). RWMV CP accumulates in the cytoplasm of parenchyma cells (Roggero et al., 2000). The CPs of MLBVV and CPsV interact with the virus-specific MP in the cytoplasm suggesting a potential role of the CP in ophiovirus movement (Robles Luna et al., 2013).
RNA4 (ca. 1.4 kb) has been identified only from MLBVV and LRNV (Roggero et al., 2000, Torok and Vetten 2003). Whereas the vcRNA4 of LRNV potentially encodes only one protein (ca. 38 kDa) of unknown function, that of MLBVV contains two ORFs overlapping by 38 nt, potentially encoding a 37 and 10.6 kDa proteins. The second ORF lacks an initiation codon and is proposed to be expressed by a +1 translational frameshift (van der Wilk et al., 2002).
Nuclear localization signals (NLS) have been reported for the CPsV, MLBVV, BlMaV and RWMV polymerases, for the MPs of CPsV and MLBVV, and for the 23K protein of BlMaV (Naum-Ongania et al., 2003, van der Wilk et al., 2002, Thekke-Veetil et al., 2014, Sánchez de la Torre et al., 2002).
For CPsV and BlMaV, the 5′-ends of the vcRNA1, vcRNA2 and vcRNA3 are identical, GATAC(T)7, but the 3′-ends are all different. For MLBVV, the respective 5′- and 3′-ends are conserved among the four viral RNA segments. In addition, the vRNA terminal ends are able to anneal and fold into structures resembling the ‘corkscrew’ conformation of the RNA termini of the Orthomyxoviridae (van der Wilk et al., 2002).
For BlMaV, there are indications of natural reassortments between RNA2 and RNA3 (Thekke-Veetil et al., 2015). Natural reassortments between RNA1 and RNA3 of CPsV have been suggested (Martin et al., 2006), and genome compatibility, between the bottom (RNA1) and top (RNA2 and RNA3) components of two CPsV isolates, has been observed in the experimental host Chenopodium quinoa (Garcia et al., 1993).
The CP is the only significant antigenic element. In Western blots, the CPs of RWMV, TMMMV, MLBVV and LRNV, but not CPsV, appear to be serologically related to varying degrees (Roggero et al., 2000).
Ophioviruses can be mechanically transmitted to a limited range of test plants, the most used being Nicotiana benthamiana and N. occidentalis P1, inducing local lesions and systemic mottle, and Chenopodium quinoa producing local lesions. The natural hosts of CPsV, RWMV, MLBVV and LRNV are dicotyledonous plants of widely differing taxonomy. In contrast, TMMMV and FreSV infect monocots. CPsV is commonly transmitted by vegetative propagation of the host. Although natural dispersion of psorosis disease has been observed in Texas and Argentina (Danós 1990, Timmer and Garnsey 1980) no natural vector has been identified, since limited vector-transmission experiments have been performed (Beñatena and Portillo 1984, Palle et al., 2004). No vector is known for either RWMV or BlMaV. The zoospores of Olpidium spp. transmit MLBVV, TMMMV, LRNV and FreSV (Lot et al., 2002, Meekes and Verbeek 2011, Navarro et al., 2004, Sasaya and Koganezawa 2006, Vaira et al., 2006). MLBVV has been shown to be present in the weed Sonchus oleraceus which can act as a natural reservoir for lettuce infection by means of the fungus vector (Navarro et al., 2005).
CPsV has a wide geographical distribution in Citrus spp. and citrus relatives in the Americas, in the Mediterranean basin, New Zealand and South Africa (Quemin et al., 2011, Roistacher 1993, Sippel et al., 2015).
RWMV has been reported in two species of the family Ranunculaceae from Northern Italy (ranunculus and anemone hybrids) (Vaira et al., 1997, Vaira et al., 2003), in lettuce in France and Germany (Torok and Vetten 2010) and recently in the evergreen shrub Pittosporum tobira in Southern Italy (Morelli et al., 2015).
FreSV has been reported in Europe, South Africa, North America, South Korea and New Zealand (Vaira et al., 2009, Jeong et al., 2014, Vaira et al., 2006, Pearson et al., 2009, Vaira et al., 2007, Verbeek et al., 2004) in freesia (Freesia refracta hyb., Iridaceae) and in lachenalia (Lachenalia hyb., Hyacinthaceae).
TMMMV has been reported in tulips (Tulipa hyb., Liliaceae) in Japan (Morikawa et al., 1995). MLBVV is the causal agent of big-vein symptoms (zones cleared of chlorophyll, parallel to the veins) in lettuce; this widespread and damaging disease probably occurs worldwide.
LRNV is closely associated with lettuce ring necrosis disease in The Netherlands and Belgium (Torok and Vetten 2002). BlMaV has been reported in blueberry (Vaccinium spp., Ericaceae) in several regions of North America as well as several other parts of the globe including South America, Europe, New Zealand, South Africa and Japan (Isogai et al., 2016, Martin et al., 2012).
Aspiviridae: from Latin aspis, “viper, snake”, referring to the morphology of virions.
Ophiovirus: from the Greek ophis, “snake”, referring to the snaky appearance of the virion (Garcia et al., 1994).
Ophiovirus-specific primers, based on a highly conserved sequence of RNA1, have been tested in RT-PCR with all ophiovirus species. In all cases, a 136 bp fragment was amplified (Vaira et al., 2003). Phylogenetic analysis of the coat protein from one isolate for each species (Figure 3.Aspiviridae) supported the positions of each species and indicated a closer relationship between MLBVV and TMMMV, as already suggested by coat protein serological tests. BlMaV and CPsV cluster in a distinct clade and seem more distantly related to the other ophioviruses by molecular characteristics. These differences, if reinforced, might also lead to the re-assignment of the existing species into two separate genera in the family. Analysis of the conserved RdRP motifs show again a distinct clade of CPsV and BlMaV, as well as higher identities between the orthologous CP and MP, with respect to the rest of the ophioviruses (Thekke-Veetil et al., 2015).
The higher taxonomy of the Aspiviridae family is: realm Riboviria, phylum Negarnaviricota, subphylum Haploviricotina, class Milneviricetes and order Serpentovirales (Figure 4). Ophiovirus virion morphology resembles that of polyploviricotene viruses in the genus Tenuivirus, family Phenuiviridae, and the internal nucleocapsid component resembles that of members of the family Tospoviridae. Unlike tenuiviruses, ophioviruses do not infect plants in the Gramineae, and unlike members of the family Tospoviridae, there is no evidence of enveloped virions. Moreover, ophioviruses do not have the conserved identical nucleotides at the genomic RNA termini that are typical of these two families. MLBVV appears to have a terminal “corkscrew”-like conformation similar to that in viruses in the Orthomyxoviridae. RdRP aa sequences show ophioviruses to be similar to members of the haploviricotine families Paramyxoviridae, Pneumoviridae, Rhabdoviridae, Bornaviridae and Filoviridae (Figure 5.Aspiviridae). The RdRP also contains the SDD amino acid sequence in motif C, a signature for segmented negative-stranded RNA viruses (family Orthomyxoviridae and order Bunyavirales). However, phylogenetic reconstructions using sequences of the core module of RdRPs of representative negative-stranded RNA viruses reinforce the phylogenetic relatedness of the aspiviruses and suggest their separation as a monophyletic group (Figure 5.Aspiviridae).
Figure 4.Aspiviridae. Higher taxonomic structure of the phylum Negarnaviricota. For simplicity, only the genus Ophiovirus is indicated.
Figure 5.Aspiviridae. Phylogenetic analysis of members of the family Aspiviridae and other negative-stranded RNA viruses based on the amino acid sequences of their conserved RdRP core modules. (Top) unrooted and (Bottom) midpoint rooted trees were generated by the neighbor-joining method and bootstrap values (indicated for each branch node when >50%) were estimated using 100 replicates. Families are coloured according to subphyum as follows: Haploviricotina - blue (Aspiviridae - light blue), Polyploviricotina - green. This phylogenetic tree and corresponding sequence alignment are available to download from the Resources page.
There are two reports regarding aspivirus-like isolates. In one study, RdRP sequences corresponding to 3 negative-stranded RNA viruses (Rhizoctonia solani negative-stranded RNA viruses 1 to 3, RsNSRV-1, -2, and -3 ) were found in the transcriptome of Rhizoctonia solani (Marzano et al., 2016) . The predicted amino acid sequences of RsNSRV-1, -2, and -3 were similar to those of the RdRP encoded by the RNA1 of LRNV and other members of the family Aspiviridae. The second report describes the detection of an RdRP sequence (Fusarium poae negative-stranded RNA virus (FpNSV) 1) in metagenomic data from Fusarium poae with 23% identity to the RdRP of MLBVV (Osaki et al., 2016). Further characterization, including particle morphology, will be required in order to define if these (putative) aspivirus-like viruses belong to the family Aspiviridae; if so they are unlikely to belong to the genus Ophiovirus.
Rhizoctonia solani negative-stranded RNA virus-1
Rhizoctonia solani negative-stranded RNA virus-2
Rhizoctonia solani negative-stranded RNA virus-3
Fusarium poae negative-stranded RNA virus-1
Since only one genus (Ophiovirus) is currently recognized in the family Aspiviridae, the family description above corresponds to the genus description. For clarity, the additional information that can be found on the genus page is also presented below.
The different criteria considered for species demarcation in the genus are:
Alignments between citrus psorosis virus, freesia sneak virus, Mirafiori lettuce big-vein virus, lettuce ring necrosis virus, blueberry mosaic associated virus and ranunculus white mottle virus (partial sequence) CP amino acid sequences show 31–52% identity, whereas isolates of the same species show over 92% identity. Since CPs of Mirafiori lettuce big-vein virus and tulip mild mottle mosaic virus (partial cds) share about 80% amino acid sequence identity, this may warrant the establishment of the following molecular criterion for ophiovirus species demarcation: CP amino acid sequence identity <85%.
Since only one genus is currently recognized, the genus description corresponds to the family description.
See discussion under family description.
Elena Dal Bó Facultad de Ciencias Agrarias y Forestales Universidad de La Plata La Plata Argentina E-mail: email@example.com
María Laura García* Aspiviridae Study Group ChairInstituto de Biotecnología y Biología Molecular Universidad de La Plata La Plata Argentina E-mail: firstname.lastname@example.org
John V. da Graça Texas A&M University-Kingsville Citrus Center Weslaco USA E-mail: email@example.com
Selma Gago-Zachert Department of Molecular Signal Processing Leibniz Institute of Plant Biochemistry Halle (Saale) Germany E-mail: firstname.lastname@example.org
John Hammond U.S. Department of Agriculture Agricultural Research Service Beltsville Maryland USA E-mail: John.Hammond@ars.usda.gov
Pedro Moreno Centro de Protección Vegetal y Biotecnología Instituto Valenciano de Investigaciones Agrarias Moncada Valencia Spain E-mail: email@example.com
Tomohide Natsuaki Faculty of Agriculture Utsunomiya University Utsunomiya Japan E-mail: firstname.lastname@example.org
José A. Navarro Instituto de Biología Molecular y Celular de plantas (IBMCP) Universidad Politécnica de Valencia-Consejo Superior de Investigaciones Científicas Valencia Spain E-mail: email@example.com
Vicente Pallás Instituto de Biología Molecular y Celular de plantas (IBMCP) Universidad Politécnica de Valencia-Consejo Superior de Investigaciones Científicas Valencia Spain E-mail: firstname.lastname@example.org
Carina A. ReyesInstituto de Biotecnología y Biología Molecular Universidad de La Plata La Plata Argentina E-mail: email@example.com
Gabriel Robles Luna Instituto de Biotecnología y Biología Molecular Universidad de La Plata La Plata Argentina E-mail: firstname.lastname@example.org
Takahide Sasaya Department of Planning and Coordination National Agriculture and Food Research Organization Tsukuba Japan E-mail: email@example.com
Ioannis E. Tzanetakis Department of Plant Pathology Division of Agriculture University of Arkansas USA E-mail: firstname.lastname@example.org
Anna María Vaira Institute for Sustainable Plant Protection (IPSP) CNR Torino Italy E-mail: email@example.com
Martin Verbeek Wageningen Plant Research Wageningen University and Research Wageningen The Netherlands E-mail: firstname.lastname@example.org
* to whom correspondence should be addressed
The chapter in the Ninth ICTV Report, which served as the template for this chapter, was contributed by Vaira, A.M., Gago-Zachert, S., Garcia, M.L., Guerri, J., Hammond, J., Milne, R.G., Moreno, P., Morikawa, T., Natsuaki, T., Navarro, J.A., Pallas, V., Torok, V., Verbeek, M. and Vetten, H.J.
Alignment file (FASTA format)
Tree file (newick format)
Moreno, P., Guerri, J. & García, M. L. (2015). The psorosis disease of citrus: a pale light at the end of the tunnel. Journal of Citrus Pathology 2.
Vaira, A. M. & Milne, R. G. (2008). Ophiovirus. In Encyclopedia of Virology (Third edition) Edited by B. W. J. Mahy & M. H. Van Regenmortel. Oxford: Academic Press.
Beñatena, H. N. & Portillo, M. M. (1984). Natural spread of psorosis in sweet orange seedlings. In Proceedings of the 9th Conference of the International Organization of Citrus Virologists, pp. 159-164. Edited by S. M. Garnsey, L. W. Timmer & J. A. Doods. Concordia, Entre Rios, Argentina: IOCV.
Danós, E. (1990). La psorosis de los cítricos: la epidemia en curso en Argentina y el desafio de su control. Revista de Investigaciones Agropecuarias 22, 265-277
Derrick, K. S., Brlansky, R. H., Lee, R. F., Timmer, L. W., Garnsey, S. M. & Nguyen, T. K. (1988). Two components associated with the citrus ringspot virus. In Proceedings of the 10th Conference of the International Organization of Citrus Virologists, pp. 340-342. Edited by L. W. Timmer, S. M. Garnsey & L. Navarro. Riverside, California, USA.
Garcia, M. L., Dal Bo, E., Grau, O. & Milne, R. G. (1994). The closely related citrus ringspot and citrus psorosis viruses have particles of novel filamentous morphology. J Gen Virol 75, 3585-3590. [PubMed]
Garcia, M. L., Derrick, K. S. & Grau, O. (1993). Citrus psorosis associated virus and citrus ringspot virus belong to a new virus group. In Proceedings of 12th Conference of the International Organization of Citrus Virologists, pp. 430-431. Edited by P. Moreno, J. V. da Graça & L. W. Timmer. New Delhi, India: IOCV.
Garcia, M. L., Grau, O. & Sarachu, A. N. (1991). Citrus psorosis is probably caused by a bipartite ssRNA virus. Res Virol 142, 303-311. [PubMed]
Hiraguri, A., Ueki, S., Kondo, H., Nomiyama, K., Shimizu, T., Ichiki-Uehara, T., Omura, T., Sasaki, N., Nyunoya, H. & Sasaya, T. (2013). Identification of a movement protein of Mirafiori lettuce big-vein ophiovirus. Journal of General Virology 94, 1145-1150. [PubMed]
Isogai, M., Matsuhashi, Y., Suzuki, K., Yashima, S., Watanabe, M. & Yoshikawa, N. (2016). Occurrence of blueberry mosaic associated virus in highbush blueberry trees with blueberry mosaic disease in Japan. Journal of General Plant Pathology 82, 177-179
Jeong, M. I., Choi, Y. J., Joa, J. H., Choi, K. S. & Chung, B. N. (2014). First Report of Freesia sneak virus in Commercial Freesia hybrida Cultivars in Korea. Plant Disease 98, 162
Lot, H., Campbell, R. N., Souche, S., Milne, R. G. & Roggero, P. (2002). Transmission by Olpidium brassicae of Mirafiori lettuce virus and Lettuce big-vein virus, and Their Roles in Lettuce Big-Vein Etiology. Phytopathology 92, 288-293. [PubMed]
Martin, R. R., Polashock, J. J. & Tzanetakis, I. E. (2012). New and emerging viruses of blueberry and cranberry. Viruses 4, 2831-2852. [PubMed]
Martin, S., Garcia, M. L., Troisi, A., Rubio, L., Legarreta, G., Grau, O., Alioto, D., Moreno, P. & Guerri, J. (2006). Genetic variation of populations of Citrus psorosis virus. Journal of General Virology 87, 3097-3102. [PubMed]
Martin, S., Lopez, C., Garcia, M. L., Naum-Ongania, G., Grau, O., Flores, R., Moreno, P. & Guerri, J. (2005). The complete nucleotide sequence of a Spanish isolate of Citrus psorosis virus: comparative analysis with other ophioviruses. Archives of Virology 150, 167-176. [PubMed]
Marzano, S. Y., Nelson, B. D., Ajayi-Oyetunde, O., Bradley, C. A., Hughes, T. J., Hartman, G. L., Eastburn, D. M. & Domier, L. L. (2016). Identification of Diverse Mycoviruses through Metatranscriptomics Characterization of the Viromes of Five Major Fungal Plant Pathogens. Journal of Virology 90, 6846-6863. [PubMed]
Meekes, E. T. M. & Verbeek, M. (2011). New insights in Freesia leaf necrosis disease. Acta Horticulturae 901, 231-236
Milne, R. G., Djelouah, K., Garcia, L. M., Dal Bo, E. & Grau, O. (1996). Structure of citrus- psorosis-associated virus particles: Implications for diagnosis and taxonomy. In 13th Conference of the International Organization of Citrus Virologists, pp. 189-197. Edited by J. V. Da Graça, P. Moreno & R. K. Yokomi. Fuzhou, Fujian, China: IOCV.
Morelli, M., De Stradis, A., Minafra, A., Saldarelli, P. & Martelli, G. P. (2015). Mixed infection by Eggplant mottled dwarf virus and an ophiovirus species in Japanese pittosporum. Journal of Plant Pathology 97, 548
Morikawa, T., Nomura, Y., Yamamoto, T. & Natsuaki, T. (1995). Partial characterization of virus-like particles associated with tulip mild mottle mosaic. . Annals of the Phytopathological Society of Japan 61, 578-581
Naum-Ongania, G., Gago-Zachert, S., Peña, E., Grau, O. & Garcia, M. L. (2003). Citrus psorosis virus RNA 1 is of negative polarity and potentially encodes in its complementary strand a 24K protein of unknown function and 280K putative RNA dependent RNA polymerase. Virus Research 96, 49-61. [PubMed]
Navarro, J. A., Botella, F., Marhuenda, A., Sastre, P., Sánchez-Pina, M. A. & Pallas, V. (2005). Identification and partial characterisation of Lettuce big-vein associated virus and Mirafiori lettuce big-vein virus in common weeds found amongst Spanish lettuce crops and their role in lettuce big-vein disease transmission. European journal of plant pathology 113, 25-34
Navarro, J. A., Botella, F., Maruhenda, A., Sastre, P., Sánchez-Pina, M. A. & Pallas, V. (2004). Comparative Infection Progress Analysis of Lettuce big-vein virus and Mirafiori lettuce virus in Lettuce Crops by Developed Molecular Diagnosis Techniques. Phytopathology 94, 470-477. [PubMed]
Navas‐Castillo, J., Moreno, P., Cambra, M. & Derrick, K. (1993). Partial purification of a virus associated with a Spanish isolate of citrus ringspot. Plant Pathology 42, 339-346
Osaki, H., Sasaki, A., Nomiyama, K. & Tomioka, K. (2016). Multiple virus infection in a single strain of Fusarium poae shown by deep sequencing. Virus Genes 52, 835-847. [PubMed]
Palle, S. R., Miao, H., Seyran, M., Louzada, E. S., Da Graça, J. V. & Skaria, M. (2004). Evidence for Natural Transmission of Citrus psorosis virus by an Olpidium-Like Fungus. In Proceedings of the 16th Conference of the International Organization of Citrus Virologists, p. 423.
Pearson, M. N., Cohen, D., Cowell, S. J., Jones, D., Blouin, A., Lebas, B. S. M., Shiller, J. B. & Clover, G. R. G. (2009). A survey of viruses of flower bulbs in New Zealand. Australasian Plant Pathology 38, 305-309
Peña, E. J., Robles Luna, G., Zanek, M. C., Borniego, M. B., Reyes, C. A., Heinlein, M. & Garcia, M. L. (2012). Citrus psorosis and Mirafiori lettuce big-vein ophiovirus coat proteins localize to the cytoplasm and self interact in vivo. Virus Research 170, 34-43. [PubMed]
Quemin, M., Lebas, B., Veerakone, S., Harper, S., Clover, G. & Dawson, T. (2011). First Molecular Evidence of Citrus psorosis virus and Citrus viroid III from Citrus spp. in New Zealand. Plant Disease 95, 775
Reyes, C. A., Ocolotobiche, E. E., Marmisolle, F. E., Robles Luna, G., Borniego, M. B., Bazzini, A. A., Asurmendi, S. & Garcia, M. L. (2016). Citrus psorosis virus 24K protein interacts with citrus miRNA precursors, affects their processing and subsequent miRNA accumulation and target expression. Molecular Plant Pathology On-Line 17, 317-329. [PubMed]
Robles Luna, G., Peña, E. J., Borniego, M. B., Heinlein, M. & Garcia, M. L. (2013). Ophioviruses CPsV and MiLBVV movement protein is encoded in RNA 2 and interacts with the coat protein. Virology 441, 152-161. [PubMed]
Robles Luna, G., Reyes, C. A., Peña, E. J., Ocolotobiche, E., Baeza, C., Borniego, M. B., Kormelink, R. & Garcia, M. L. (2017). Identification and characterization of two RNA silencing suppressors encoded by ophioviruses. Virus Research 235, 96-105
Roggero, P., Ciuffo, M., Vaira, A. M., Accotto, G. P., Masenga, V. & Milne, R. G. (2000). An Ophiovirus isolated from lettuce with big-vein symptoms. Archives of Virology 145, 2629-2642. [PubMed]
Roistacher, C. N. (1993). Psorosis - a review. In Proceedings of the 12th Conference of the International Organization of Citrus Virologists, pp. 139-162. Riverside, California, USA.
Sánchez de la Torre, E., Riva, O., Zandomeni, R., Grau, O. & García, M. L. (1998). The top component of citrus psorosis virus contains two ssRNAs, the smaller encodes the coat protein In Molecular Plant Pathology On-Line.
Sánchez de la Torre, M. E., Lopez, C., Grau, O. & Garcia, M. L. (2002). RNA 2 of Citrus psorosis virus is of negative polarity and has a single open reading frame in its complementary strand. Journal of General Virology 83, 1777-1781. [PubMed]
Sasaya, T. & Koganezawa, H. (2006). Molecular analysis and virus transmission tests place Olpidium virulentus, a vector of Mirafiori lettuce big-vein virus and tobacco stunt virus, as a distinct species rather than a strain of Olpidium brassicae. Journal of General Plant Pathology 72, 20-25
Sippel, A. D., Bijzet, Z., Froneman, I. J., Combrink, N. K., Maritz, J. G., Hannweg, K. F., Severn-Ellis, A. A. & Manicom, B. Q. (2015). Citrus Breeding in South Africa: the Latest Developments in the Programme Run by the ARC-Institute for Tropical and Subtropical Crops. Acta Horticulturae 1065, 397-403
Thekke-Veetil, T., Ho, T., Keller, K. E., Martin, R. R. & Tzanetakis, I. E. (2014). A new ophiovirus is associated with blueberry mosaic disease. Virus Research 189, 92-96. [PubMed]
Thekke-Veetil, T., Polashock, J. J., Marn, M. V., Plesko, I. M., Schilder, A. C., Keller, K. E., Martin, R. R. & Tzanetakis, I. E. (2015). Population structure of blueberry mosaic associated virus: Evidence of reassortment in geographically distinct isolates. Virus Research 201, 79-84. [PubMed]
Timmer, L. W. & Garnsey, S. M. (1980). Natural spread of citrus ringspot virus in Texas and its association with psorosis-like diseases in Florida and Texas. In Proceedings of the 8th Conference of the International Organization of Citrus Virologists, pp. 167-193. Edited by E. C. Calavan, S. M. Garnsey & L. W. Timmer. Mildura, Victoria, Australia: IOCV.
Torok, V. A. & Vetten, H. J. (2002). Characterisation of an ophiovirus associated with lettuce ring necrosis. In Joint Conf Int Working Groups on Legume and Vegetable Viruses, p. 4. Bonn, Germany.
Torok, V. A. & Vetten, H. J. (2003). Identification and molecular characterisation of a new ophiovirus associated with lettuce ring necrosis disease. In Proceedings of Arbeitskreis Viruskrankheiten der Pflanzen. Heidelberg, Germany.
Torok, V. A. & Vetten, H. J. (2010). Ophiovirus associated with lettuce ring necrosis. In European Society for Virology Meeting, p. 282. Cernobbio, Italy.
Vaira, A., Hansen, M., Murphy, C., Reinsel, M. & Hammond, J. (2009). First Report of Freesia sneak virus in Freesia sp. in Virginia. Plant Disease 93, 965
Vaira, A., Kleynhans, R. & Hammond, J. (2007). First report of Freesia sneak virus infecting Lachenalia cultivars in South Africa. Plant Disease 91, 770
Vaira, A. M., Accotto, G. P., Costantini, A. & Milne, R. G. (2003). The partial sequence of RNA 1 of the ophiovirus Ranunculus white mottle virus indicates its relationship to rhabdoviruses and provides candidate primers for an ophiovirus-specific RT-PCR test. Arch Virol 148, 1037-1050. [PubMed]
Vaira, A. M., Garcia, M. L., Vetten, H. J., Navarro, J. A., Guerri, J., Hammond, J., Verbeek, M., Moreno, P., Natsuaki, T., Gago-Zachert, S., Morikawa, T., Torok, V. & Pallas, V. (2011). Ophioviridae. In Virus Taxonomy IX Report of the International Committee on Taxonomy of Viruses, pp. 743-748. Edited by A. M. Q. King, M. J. Adams, E. B. Carstens & E. J. Lefkowitz. Oxford, UK: Elsevier.
Vaira, A. M., Lisa, V., Accotto, G. P., Borghi, V., Masenga, V., Luisoni, E. & Milne, R. G. (1996). A new virus isolated from Ranunculus hyb. with particles resembling supercoiled filamentous nucleocapsids. Acta Horticulturae 432, 36-43
Vaira, A. M., Lisa, V., Costantini, A., Masenga, V., Rapetti, S. & Milne, R. G. (2006). Ophioviruses infecting ornamentals and a probable new species associated with a severe disease in Freesia. Acta Horticulturae 722, 191-200
Vaira, A. M., Milne, R. G., Accotto, G. P., Luisoni, E., Masenga, V. & Lisa, V. (1997). Partial characterization of a new virus from ranunculus with a divided RNA genome and circular supercoiled thread-like particles. Archives of Virology 142, 2131-2146. [PubMed]
van der Wilk, F., Dullemans, A. M., Verbeek, M. & van den Heuvel, J. F. (2002). Nucleotide sequence and genomic organization of an ophiovirus associated with lettuce big-vein disease. J Gen Virol 83, 2869-2877. [PubMed]
Verbeek, M., Lindner, J., Bowen, I., Dullemans, A. & van der Vlugt, R. (2004). Ophiovirus isolated from freesia with freesia leaf necrosis disease. In 11th ISVDOP. Taichung, Taiwan.
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