References: Solemoviridae


Abad-Zapatero, C., S. S. Abdel-Meguid, J. E. Johnson, A. G. Leslie, I. Rayment, M. G. Rossmann, D. Suck and T. Tsukihara (1980). Structure of southern bean mosaic virus at 2.8 A resolution. Nature 286: 33-9. [PubMed]

Alexander, M. M., J. P. Mohr, S. L. DeBlasio, J. D. Chavez, V. Ziegler-Graff, V. Brault, J. E. Bruce and M. C. Heck (2017). Insights in luteovirid structural biology guided by chemical cross-linking and high resolution mass spectrometry. Virus Res 241: 42-52. [PubMed]

Aus dem Siepen, M., J. O. Pohl, B. J. Koo, C. Wege and H. Jeske (2005). Poinsettia latent virus is not a cryptic virus, but a natural polerovirus-sobemovirus hybrid. Virology 336: 240-50. [PubMed]

Bahner, I., J. Lamb, M. A. Mayo and R. T. Hay (1990). Expression of the genome of potato leafroll virus: readthrough of the coat protein termination codon in vivo. J Gen Virol 71: 2251-6. [PubMed]

Barker, H.  (1989). Specificity of the effect of sap‐transmissible viruses in increasing the accumulation of luteoviruses in co‐infected plants. Ann Appl Biol 115: 71-78.

Bejerman, N., F. Giolitti, V. Trucco, S. de Breuil, R. G. Dietzgen and S. Lenardon (2016). Complete genome sequence of a new enamovirus from Argentina infecting alfalfa plants showing dwarfism symptoms. Arch Virol 161: 2029-32. [PubMed]

Boissinot, S., M. Erdinger, B. Monsion, V. Ziegler-Graff and V. Brault (2014). Both structural and non-structural forms of the readthrough protein of cucurbit aphid-borne yellows virus are essential for efficient systemic infection of plants. PLoS One 9: e93448. [PubMed]

Boissinot, S., E. Pichon, C. Sorin, C. Piccini, D. Scheidecker, V. Ziegler-Graff and V. Brault (2017). Systemic propagation of a fluorescent infectious clone of a polerovirus following inoculation by agrobacteria and aphids. Viruses 9: 166. [PubMed]

Brault, V., E. Herrbach and C. Reinbold (2007). Electron microscopy studies on luteovirid transmission by aphids. Micron (Oxford, England : 1993) 38: 302-12. [PubMed]

Brault, V., J. F. van den Heuvel, M. Verbeek, V. Ziegler-Graff, A. Reutenauer, E. Herrbach, J. C. Garaud, H. Guilley, K. Richards and G. Jonard (1995). Aphid transmission of beet western yellows luteovirus requires the minor capsid read-through protein P74. EMBO J 14: 650-9. [PubMed]

Byrne, M. J., J. F. C. Steele, E. L. Hesketh, M. Walden, R. F. Thompson, G. P. Lomonossoff and N. A. Ranson (2019). Combining transient expression and cryo-EM to obtain high-resolution structures of luteovirid particles. Structure 27: 1761-1770.e3. [PubMed]

Campbell, A. J., A. Erickson, E. Pellerin, N. Salem, X. Mo, B. W. Falk and I. Ferriol (2020). Phylogenetic classification of a group of self-replicating RNAs that are common in co-infections with poleroviruses. Virus Res 276: 197831. [PubMed]

Cao, M., S. Zhang, M. Li, Y. Liu, P. Dong, S. Li, M. Kuang, R. Li and Y. Zhou (2019). Discovery of four novel viruses associated with flower yellowing disease of green sichuan pepper (Zanthoxylum armatum) by virome analysis. Viruses 11: 696. [PubMed]

Csorba, T., L. Kontra and J. Burgyán (2015). Viral silencing suppressors: Tools forged to fine-tune host-pathogen coexistence. Virology 479-480: 85-103. [PubMed]

D’Arcy, C. J., L. Torrance and R. Martin (1989). Discrimination among luteoviruses and their strains by monoclonal antibodies and identification of common epitopes. Phytopathology 79: 869-872. 

Debat, H. J. and N. Bejerman (2019). Novel bird's-foot trefoil RNA viruses provide insights into a clade of legume-associated enamoviruses and rhabdoviruses. Arch Virol 164: 1419-1426. [PubMed]

DeBlasio, S. L., Y. Xu, R. S. Johnson, A. R. Rebelo, M. J. MacCoss, S. M. Gray and M. Heck (2018). The interaction dynamics of two potato leafroll virus movement proteins affects their localization to the outer membranes of mitochondria and plastids. Viruses 10: 585. [PubMed]

Demler, S. A., D. G. Rucker, G. A. de Zoeten, A. Ziegler, D. J. Robinson and A. F. Murant (1996). The satellite RNAs associated with the groundnut rosette disease complex and pea enation mosaic virus: sequence similarities and ability of each other's helper virus to support their replication. J Gen Virol 77 2847-55. [PubMed]

Demler, S. A., D. G. Rucker, L. Nooruddin and G. A. de Zoeten (1994). Replication of the satellite RNA of pea enation mosaic virus is controlled by RNA 2-encoded functions. J Gen Virol 75: 1399-406. [PubMed]

Doumayrou, J., M. Sheber, B. C. Bonning and W. A. Miller (2016). Role of pea enation mosaic virus coat protein in the host plant and aphid vector. Viruses 8: 312. [PubMed]

Esau, K. and L. L. Hoefert (1972). Ultrastructure of sugarbeet leaves infected with beet western yellows virus. J Ultrastruct Res 40: 556-71. [PubMed]

Fusaro, A. F., R. L. Correa, K. Nakasugi, C. Jackson, L. Kawchuk, M. F. Vaslin and P. M. Waterhouse (2012). The Enamovirus P0 protein is a silencing suppressor which inhibits local and systemic RNA silencing through AGO1 degradation. Virology 426: 178-87. [PubMed]

Ghosh, S., S. Kanakala, G. Lebedev, S. Kontsedalov, D. Silverman, T. Alon, N. Mor, N. Sela, N. Luria, A. Dombrovsky, M. Mawassi, S. Haviv, H. Czosnek and M. Ghanim (2019). Transmission of a new polerovirus infecting pepper by the whitefly Bemisia tabaci. J Virol 93: e00488-19. [PubMed]

Govind, K., K. Mäkinen and H. S. Savithri (2012). Sesbania mosaic virus (SeMV) infectious clone: possible mechanism of 3' and 5' end repair and role of polyprotein processing in viral replication. PLoS One 7: e31190. [PubMed]

Govind, K. and H. S. Savithri (2010). Primer-independent initiation of RNA synthesis by SeMV recombinant RNA-dependent RNA polymerase. Virology 401: 280-92. [PubMed]

Gray, S. and F. E. Gildow (2003). Luteovirus-aphid interactions. Annu Rev Phytopathol 41: 539-66. [PubMed]

Hacker, D. L. and K. Sivakumaran (1997). Mapping and expression of southern bean mosaic virus genomic and subgenomic RNAs. Virology 234: 317-27. [PubMed]

Hébrard, E., Y. Bessin, T. Michon, S. Longhi, V. N. Uversky, F. Delalande, A. Van Dorsselaer, P. Romero, J. Walter, N. Declerck and D. Fargette (2009). Intrinsic disorder in viral proteins genome-linked: experimental and predictive analyses. Virol J 6: doi: 10.1186/1743-422x-6-23. [PubMed]

Hébrard, E., N. Poulicard, C. Gérard, O. Traoré, H. C. Wu, L. Albar, D. Fargette, Y. Bessin and F. Vignols (2010). Direct interaction between the Rice yellow mottle virus (RYMV) VPg and the central domain of the rice eIF(iso)4G1 factor correlates with rice susceptibility and RYMV virulence. Mol Plant Microbe Interact 23: 1506-13. [PubMed]

Hipper, C., B. Monsion, D. Bortolamiol-Bécet, V. Ziegler-Graff and V. Brault (2014). Formation of virions is strictly required for turnip yellows virus long-distance movement in plants. J Gen Virol 95: 496-505. [PubMed]

Hogenhout, S. A., F. van der Wilk, M. Verbeek, R. W. Goldbach and J. F. van den Heuvel (2000). Identifying the determinants in the equatorial domain of Buchnera GroEL implicated in binding Potato leafroll virus. J Virol 74: 4541-8. [PubMed]

Hull, R.  (1977). The stabilization of the particles of turnip rosette virus and of other members of the southern bean mosaic virus group. Virology 79: 58-66. [PubMed]

Hwang, Y. T., M. Kalischuk, A. F. Fusaro, P. M. Waterhouse and L. Kawchuk (2013). Small RNA sequencing of Potato leafroll virus-infected plants reveals an additional subgenomic RNA encoding a sequence-specific RNA-binding protein. Virology 438: 61-9. [PubMed]

Jaag, H. M., L. Kawchuk, W. Rohde, R. Fischer, N. Emans and D. Prüfer (2003). An unusual internal ribosomal entry site of inverted symmetry directs expression of a potato leafroll polerovirus replication-associated protein. Proc Natl Acad Sci U S A 100: 8939-44. [PubMed]

Kaplan, I. B., L. Lee, D. R. Ripoll, P. Palukaitis, F. Gildow and S. M. Gray (2007). Point mutations in the potato leafroll virus major capsid protein alter virion stability and aphid transmission. J Gen Virol 88: 1821-1830. [PubMed]

Kraner, M. E., K. Link, M. Melzer, A. B. Ekici, S. Uebe, P. Tarazona, I. Feussner, J. Hofmann and U. Sonnewald (2017). Choline transporter-like1 (CHER1) is crucial for plasmodesmata maturation in Arabidopsis thaliana. Plant J 89: 394-406. [PubMed]

Lee, L., P. Palukaitis and S. M. Gray (2002). Host-dependent requirement for the Potato leafroll virus 17-kda protein in virus movement. Mol Plant Microbe Interact 15: 1086-94. [PubMed]

Li, X., C. Halpin and M. D. Ryan (2007). A novel cleavage site within the potato leafroll virus P1 polyprotein. J Gen Virol 88: 1620-1623. [PubMed]

Li, X., M. D. Ryan and J. W. Lamb (2000). Potato leafroll virus protein P1 contains a serine proteinase domain. J Gen Virol 81: 1857-64. [PubMed]

Ling, R., A. E. Pate, J. P. Carr and A. E. Firth (2013). An essential fifth coding ORF in the sobemoviruses. Virology 446: 397-408. [PubMed]

Linz, L. B., S. Liu, N. P. Chougule and B. C. Bonning (2015). In vitro evidence supports membrane alanyl aminopeptidase N as a receptor for a plant virus in the pea aphid vector. J Virol 89: 11203-12. [PubMed]

Mäkinen, K., K. Mäkeläinen, N. Arshava, T. Tamm, A. Merits, E. Truve, S. Zavriev and M. Saarma (2000). Characterization of VPg and the polyprotein processing of cocksfoot mottle virus (genus Sobemovirus). J Gen Virol 81: 2783-2789. [PubMed]

Mayo, M., E. Ryabov, G. Fraser and M. Taliansky (2000). Mechanical transmission of Potato leafroll virus. J Gen Virol 81: 2791-2795. [PubMed]

Mayo, M. A., D. J. Robinson, C. A. Jolly and L. Hyman (1989). Nucleotide sequence of potato leafroll luteovirus RNA. J Gen Virol 70 1037-51. [PubMed]

Menzel, W., E. Maiss and H. J. Vetten (2009). Nucleotide sequence of a satellite RNA associated with carrot motley dwarf in parsley and carrot. Virus Genes 38: 187-8. [PubMed]

Miller, W. A. and D. P. Giedroc (2010). Ribosomal frameshifting in decoding plant viral RNAs. In Recoding: expansion of decoding rules enriches gene expression Nucleic Acids and Molecular Biology, pp. 193-220. Edited by J. Atkins & R. Gesteland. New York, NY: Springer.

Miller, W. A., G. Koev and B. R. Mohan (1997). Are there risks associated with transgenic resistance to luteoviruses? Plant Dis 81: 700-710. [PubMed]

Moreno, A. B. and J. J. López-Moya (2020). When viruses play team sports: mixed infections in plants. Phytopathology 110: 29-48. [PubMed]

Mulot, M., B. Monsion, S. Boissinot, M. Rastegar, S. Meyer, N. Bochet and V. Brault (2018). Transmission of turnip yellows virus by Myzus persicae Is reduced by feeding aphids on double-stranded RNA targeting the ephrin receptor protein. Front Microbiol 9: 457. [PubMed]

Musser, R. O., S. M. Hum-Musser, S. E. Slaten-Bickford, G. W. Felton and R. C. Gergerich (2002). Evidence that ribonuclease activity present in beetle regurgitant is found to stimulate virus resistance in plants. J Chem Ecol 28: 1691-6. [PubMed]

Nair, S., P. Gayathri, M. R. Murthy and H. S. Savithri (2008). Stacking interactions of W271 and H275 of SeMV serine protease with W43 of natively unfolded VPg confer catalytic activity to protease. Virology 382: 83-90. [PubMed]

Nair, S. and H. S. Savithri (2010). Processing of SeMV polyproteins revisited. Virology 396: 106-17. [PubMed]

Nascimento, A. K. Q., J. A. A. Lima, A. L. L. Nascimento, E. A. Beserra, Jr. and D. E. Purcifull (2010). Biological, physical, and molecular properties of a papaya lethal yellowing virus Isolate. Plant Dis 94: 1206-1212. [PubMed]

Olspert, A., L. Arike, L. Peil and E. Truve (2011a). Sobemovirus RNA linked to VPg over a threonine residue. FEBS Lett 585: 2979-85. [PubMed]

Olspert, A., L. Peil, E. Hébrard, D. Fargette and E. Truve (2011b). Protein-RNA linkage and post-translational modifications of two sobemovirus VPgs. J Gen Virol 92: 445-52. [PubMed]

Opalka, N., C. Brugidou, C. Bonneau, M. Nicole, R. N. Beachy, M. Yeager and C. Fauquet (1998). Movement of rice yellow mottle virus between xylem cells through pit membranes. Proc Natl Acad Sci USA 95: 3323-8. [PubMed]

Opalka, N., M. Tihova, C. Brugidou, A. Kumar, R. N. Beachy, C. M. Fauquet and M. Yeager (2000). Structure of native and expanded sobemoviruses by electron cryo-microscopy and image reconstruction. J Mol Biol 303: 197-211. [PubMed]

Osman, T. A., R. H. Coutts and K. W. Buck (2006). In vitro synthesis of minus-strand RNA by an isolated cereal yellow dwarf virus RNA-dependent RNA polymerase requires VPg and a stem-loop structure at the 3' end of the virus RNA. J Virol 80: 10743-51. [PubMed]

Otsus, M., G. Uffert, M. Sõmera, H. Paves, A. Olspert, B. Islamov and E. Truve (2012). Cocksfoot mottle sobemovirus establishes infection through the phloem. Virus Res 166: 125-9. [PubMed]

Patton, M. F., A. Bak, J. M. Sayre, M. L. Heck and C. L. Casteel (2020). A polerovirus, Potato leafroll virus, alters plant-vector interactions using three viral proteins. Plant Cell Environ 43: 387-399. [PubMed]

Peter, K. A., F. Gildow, P. Palukaitis and S. M. Gray (2009). The C terminus of the polerovirus p5 readthrough domain limits virus infection to the phloem. J Virol 83: 5419-29. [PubMed]

Plevka, P., K. Tars, A. Zeltins, I. Balke, E. Truve and L. Liljas (2007). The three-dimensional structure of ryegrass mottle virus at 2.9 Å resolution. Virology 369: 364-74. [PubMed]

Prüfer, D., E. Tacke, J. Schmitz, B. Kull, A. Kaufmann and W. Rohde (1992). Ribosomal frameshifting in plants: a novel signal directs the -1 frameshift in the synthesis of the putative viral replicase of potato leafroll luteovirus. EMBO J 11: 1111-7. [PubMed]

Qu, C., L. Liljas, N. Opalka, C. Brugidou, M. Yeager, R. N. Beachy, C. M. Fauquet, J. E. Johnson and T. Lin (2000). 3D domain swapping modulates the stability of members of an icosahedral virus group. Structure 8: 1095-103. [PubMed]

Rashid, M. O., X. Y. Zhang, Y. Wang, D. W. Li, J. L. Yu and C. G. Han (2019). The three essential motifs in P0 for suppression of RNA silencing activity of potato leafroll virus are required for virus systemic infection. Viruses 11: 170. [PubMed]

Reinbold, C., S. Lacombe, V. Ziegler-Graff, D. Scheidecker, L. Wiss, M. Beuve, C. Caranta and V. Brault (2013). Closely related poleroviruses depend on distinct translation initiation factors to infect Arabidopsis thaliana. Mol Plant Microbe Interact 26: 257-65. [PubMed]

Rossmann, M. G., C. Abad-Zapatero, J. W. Erickson and H. S. Savithri (1983). RNA-protein interactions in some small plant viruses. J Biomol Struct Dyn 1: 565-79. [PubMed]

Roy Chowdhury, S. and H. S. Savithri (2011). Interaction of Sesbania mosaic virus movement protein with VPg and P10: implication to specificity of genome recognition. PLoS One 6: e15609. [PubMed]

Ryabov, E. V., G. Fraser, M. A. Mayo, H. Barker and M. Taliansky (2001). Umbravirus gene expression helps potato leafroll virus to invade mesophyll tissues and to be transmitted mechanically between plants. Virology 286: 363-72. [PubMed]

Satheshkumar, P. S., P. Gayathri, K. Prasad and H. S. Savithri (2005). "Natively unfolded" VPg is essential for Sesbania mosaic virus serine protease activity. J Biol Chem 280: 30291-300. [PubMed]

Shepardson, S., K. Esau and R. McCrum (1980). Ultrastructure of potato leaf phloem infected with potato leafroll virus. Virology 105: 379-92. [PubMed]

Shields, S. A., M. J. Brisco, T. M. Wilson and R. Hull (1989). Southern bean mosaic virus RNA remains associated with swollen virions during translation in wheat germ cell-free extracts. Virology 171: 602-6. [PubMed]

Silva, A. M. and M. G. Rossmann (1987). Refined structure of southern bean mosaic virus at 2.9 A resolution. J Mol Biol 197: 69-87. [PubMed]

Sivakumaran, K. and D. L. Hacker (1998). The 105-kDa polyprotein of southern bean mosaic virus is translated by scanning ribosomes. Virology 246: 34-44. [PubMed]

Skaf, J. S., M. H. Schultz, H. Hirata and G. A. de Zoeten (2000). Mutational evidence that the VPg is involved in the replication and not the movement of Pea enation mosaic virus-1. J Gen Virol 81: 1103-9. [PubMed]

Smirnova, E., A. E. Firth, W. A. Miller, D. Scheidecker, V. Brault, C. Reinbold, A. M. Rakotondrafara, B. Y. Chung and V. Ziegler-Graff (2015). Discovery of a small non-AUG-initiated ORF in poleroviruses and luteoviruses that is required for long-distance movement. PLoS Pathog 11: e1004868. [PubMed]

Sõmera, M., C. Sarmiento and E. Truve (2015). Overview on sobemoviruses and a proposal for the creation of the family Sobemoviridae. Viruses 7: 3076-115. [PubMed]

Sõmera, M. and E. Truve (2015). Rottboellia yellow mottle virus is a distinct species within the genus Sobemovirus. Arch Virol 160: 857-63. [PubMed]

Song, S. I. and W. A. Miller (2004). Cis and trans requirements for rolling circle replication of a satellite RNA. J Virol 78: 3072-82. [PubMed]

Symons, R. H. and J. W. Randles (1999). Encapsidated circular viroid-like satellite RNAs (virusoids) of plants. Curr Top Microbiol Immunol 239: 81-105. [PubMed]

Tacke, E., D. Prüfer, F. Salamini and W. Rohde (1990). Characterization of a potato leafroll luteovirus subgenomic RNA: differential expression by internal translation initiation and UAG suppression. J Gen Virol 71: 2265-72. [PubMed]

Tamborindeguy, C., M. S. Bereman, S. DeBlasio, D. Igwe, D. M. Smith, F. White, M. J. MacCoss, S. M. Gray and M. Cilia (2013). Genomic and proteomic analysis of Schizaphis graminum reveals cyclophilin proteins are involved in the transmission of cereal yellow dwarf virus. PLoS One 8: e71620. [PubMed]

Tamm, T., J. Suurväli, J. Lucchesi, A. Olspert and E. Truve (2009). Stem-loop structure of Cocksfoot mottle virus RNA is indispensable for programmed -1 ribosomal frameshifting. Virus Res 146: 73-80. [PubMed]

Tars, K., A. Zeltins and L. Liljas (2003). The three-dimensional structure of cocksfoot mottle virus at 2.7 A resolution. Virology 310: 287-97. [PubMed]

Trovão, N. S., G. Baele, B. Vrancken, F. Bielejec, M. A. Suchard, D. Fargette and P. Lemey (2015). Host ecology determines the dispersal patterns of a plant virus. Virus Evol 1: doi: 10.1093/ve/vev016. [PubMed]

Wintermantel, W. M.  (2005). Co-infection of beet mosaic virus with beet yellowing viruses leads to increased symptom expression on sugar beet. Plant Dis 89: 325-331. [PubMed]

Wolf, Y. I., D. Kazlauskas, J. Iranzo, A. Lucía-Sanz, J. H. Kuhn, M. Krupovic, V. V. Dolja and E. V. Koonin (2018). Origins and evolution of the global RNA virome. MBio 9: e02329-18. [PubMed]

Xu, Y., W. L. Da Silva, Y. Qian and S. M. Gray (2018a). An aromatic amino acid and associated helix in the C-terminus of the potato leafroll virus minor capsid protein regulate systemic infection and symptom expression. PLoS Pathog 14: e1007451. [PubMed]

Xu, Y., H. J. Ju, S. DeBlasio, E. J. Carino, R. Johnson, M. J. MacCoss, M. Heck, W. A. Miller and S. M. Gray (2018b). A stem-loop structure in potato leafroll virus open reading frame 5 (ORF5) is essential for readthrough translation of the coat protein ORF stop codon 700 bases upstream. J Virol 92: e01544-17. [PubMed]

Zhang, X. Y., T. Y. Zhao, Y. Y. Li, H. Y. Xiang, S. W. Dong, Z. Y. Zhang, Y. Wang, D. W. Li, J. L. Yu and C. G. Han (2018). The conserved proline18 in the polerovirus P3a is important for Brassica yellows virus systemic Infection. Front Microbiol 9: 613. [PubMed]

Zhou, C. J., X. Y. Zhang, S. Y. Liu, Y. Wang, D. W. Li, J. L. Yu and C. G. Han (2017). Synergistic infection of BrYV and PEMV 2 increases the accumulations of both BrYV and BrYV-derived siRNAs in Nicotiana benthamiana. Sci Rep 7: 45132. [PubMed]

Ziegler-Graff, V.  (2020). Molecular insights into host and vector manipulation by plant viruses. Viruses 12: 263. [PubMed]

Zink, M. and H. Grubmüller (2010). Primary changes of the mechanical properties of Southern Bean Mosaic Virus upon calcium removal. Biophys J 98: 687-95. [PubMed]