Abstract
Logically, most plant viruses being vector-transmitted, the majority of viral transport mechanisms associated to the transmission step have been approached through the study of virus-vector relationships. However, in the case of non-vector vertical transmission through the seeds, some viruses have evolved specific patterns to colonize either the gametes or the embryo, thereby connecting viral transport within the plant to that in between plants. Moreover, though it may appear counter intuitive and has been largely overlooked, some specific virus accumulation within cells or organs, as well as specific control of multiple infections of single cells, can also directly affect the success and efficiency of vector transmission, again connecting viral transport mechanisms inside and outside the host plants. This work summarizes the data available on viral transport outside the plant in various vectors, and also highlights a few available examples and proposes hypotheses for illustrating the concept that some viral trafficking within plants is specifically intended to prepare ulterior acquisition by the vectors.
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References
Akad F, Dotan N, Czosnek H (2004) Trapping of Tomato yellow leaf curl virus (TYLCV) and other plant viruses with a GroEL homologue from the whitefly Bemisia tabaci. Arch Virol 149:1481–1497
Armour SL, Melcher U, Pirone TP, Lyttle DJ, Essenberg RC (1983) Helper component for aphid transmission encoded by region II of cauliflower mosaic virus DNA. Virology 129:25–30.
Blanc S (2004) Insect transmission of viruses. In: Gillespie SH, Smith GL, Osbourn A (eds) Microbe-vector interactions in vector-borne diseases. Cambridge University Press, Cambridge, pp 42–61
Blanc S, Ammar ED, Garcia-Lampasona S, Dolja VV, Llave C, Baker J, Pirone TP (1998) Mutations in the potyvirus helper component protein: effects on interactions with virions and aphid stylets. J Gen Virol 79:3119–22
Blanc S, Cerutti M, Chaabihi H, Louis C, Devauchelle G, Hull R (1993a) Gene II product of an aphid-nontransmissible isolate of cauliflower mosaic virus expressed in a baculovirus system possesses aphid transmission factor activity. Virology 192:651–654
Blanc S, Cerutti M, Usmany M, Vlak JM, Hull R (1993b) Biological activity of cauliflower mosaic virus aphid transmission factor expressed in a heterologous system. Virology 192:643–650
Blanc S, Lopez-Moya JJ, Wang R, Garcia-Lampasona S, Thornbury D W, Pirone TP (1997) A specific interaction between coat protein and helper component correlates with aphid transmission of a potyvirus. Virology 231:141–147
Blanc S, Schmidt I, Vantard M, Scholthof HB, Khul G, Esperandieu P, Cerutti M, Louis C (1996) The aphid transmission factor of cauliflower mosaic virus forms a stable complex with microtubules in both insect and plant cells. Proc Natl Acad Sci USA 93:15158–15163
Bocharov G, Ford N J, Edwards J, Breinig T, Wain-Hobson S, Meyerhans A (2005) A genetic-algorithm approach to simulating human immunodeficiency virus evolution reveals the strong impact of multiply infected cells and recombination. J Gen Virol 86:3109–3118
Boevink P, Oparka KJ (2005) Virus-host interactions during movement processes. Plant Physiol 138:1815–1821
Bosque-Perez NA (2000) Eight decades of maize streak virus research. Virus Res 71:107–121
Brault V, Perigon S, Reinbold C, Erdinger M, Scheidecker D, Herrbach E, Richards K, Ziegler-Graff V (2005) The polerovirus minor capsid protein determines vector specificity and intestinal tropism in the aphid. J Virol 79:9685–9693
Brigneti G, Voinnet O, Li WX, Ji LH, Ding SW, Baulcombe DC (1998) Viral pathogenicity determinants are suppressors of transgene silencing in Nicotiana benthamiana. EMBO J 17:6739–6746
Broadbent L (1965) The epidemiology of tomato mosaic virus, IX. Seed transmission of TMV. Ann Appl Biol 56:177–205
Champagne J, Benhamou N, Leclerc D (2004) Localization of the N-terminal domain of cauliflower mosaic virus coat protein precursor. Virology 324:257–262
Cronin S, Verchot J, Haldeman-Cahill R, Schaad MC, Carrington JC (1995) Long-distance movement factor: a transport function of the potyvirus helper component proteinase. Plant Cell 7:549–559
de Assis Filho FM, Stavisky J, Reitz SR, Deom CM, Sherwood JL (2005) Midgut infection by Tomato spotted wilt virus and vector incompetence of Frankliniella tritici. J Appl Entomol 129:548–550
Dietrich C, Maiss E (2003) Fluorescent labelling reveals spatial separation of potyvirus populations in mixed infected Nicotiana benthamiana plants. J Gen Virol 84:2871–2876
Doolittle SP, Walker MN (1928) Aphid transmission of cucumber mosaic. Phytopathology 18:143
Drucker M, Froissart R, Hebrard E, Uzest M, Ravallec M, Esperandieu P, Mani J C, Pugniere M, Roquet F, Fereres A, Blanc S (2002) Intracellular distribution of viral gene products regulates a complex mechanism of cauliflower mosaic virus acquisition by its aphid vector. Proc Natl Acad Sci USA 99:2422–2427
Edwards MC (1995) Mapping of the seed transmission determinants of barley stripe mosaic virus. Mol Plant Microbe Interact 8:906–915
Espinoza AM, Medina V, Hull R, Markham PG (1991) Cauliflower mosaic virus gene II product forms distinct inclusion bodies in infected plant cells. Virology 185:337–344
Filichkin SA, Brumfield S, Filichkin TP, Young MJ (1997) In vitro interactions of the aphid endosymbiotic SymL chaperonin with barley yellow dwarf virus. J Virol 71:569–577
Fontes EP, Santos AA, Luz DF, Waclawovsky AJ, Chory J (2004) The geminivirus nuclear shuttle protein is a virulence factor that suppresses transmembrane receptor kinase activity. Genes Dev 18:2545–2556
Foster TM, Lough TJ, Emerson SJ, Lee RH, Bowman JL, Forster RL, Lucas WJ (2002) A surveillance system regulates selective entry of RNA into the shoot apex. Plant Cell 14:1497–1508
Froissart R, Michalakis Y, Blanc S (2002) Helper component-transcomplementation in the vector transmission of plant viruses. Phytopathology 92:576–579
Froissart R, Roze D, Uzest M, Galibert L, Blanc S, Michalakis Y (2005) Recombination every day: Abundant recombination in a virus during a single multi-cellular host infection. PLOS Biology 3:389–395
Froissart R, Wilke CO, Montville R, Remold SK, Chao L, Turner PE (2004) Co-infection weakens selection against epistatic mutations in RNA viruses. Genetics 168:9–19
Gardner RC, Howarth AJ, Hahn P, Brown-Luedi M, Shepherd RJ, Messing J (1981) The complete nucleotide sequence of an infectious clone of cauliflower mosaic virus by M13mp7 shotgun sequencing. Nucleic Acids Res 9:2871–2888
Gergerich RC (2001) Elucidation of transmission mechanisms: Mechanism of virus transmission by leaf-feeding beetles. In: Harris K, Smith OP, Duffus JE (eds) Virus-Insect-Plant interactions. Academic Press, San Diego, pp 133–140
Gergerich RC, Scott HA (1991) Determinants in the specificity of virus transmission by leaf-feeding beetles. In: Harris KF (eds) Advances in disease vector research. Springer, Berlin Heidelberg New York, pp 1–13
Ghanim M, Czosnek H (2000) Tomato yellow leaf curl geminivirus (TYLCV-Is) is transmitted among whiteflies (Bemisia tabaci) in a sex-related manner. J Virol 74:4738–4745
Ghanim M, Morin S, Zeidan M, Czosnek H (1998) Evidence for transovarial transmission of tomato yellow leaf curl virus by its vector, the whitefly Bemisia tabac. Virology 240:295–303
Gildow F (1993) Evidence for receptor-mediated endocytosis regulating luteovirus acquisition by aphids. Phytopathology 83:270–277
Goldman V, Czosnek H (2002) Whiteflies (Bemisia tabaci) issued from eggs bombarded with infectious DNA clones of Tomato yellow leaf curl virus from Israel (TYLCV) are able to infect tomato plants. Arch Virol 147:787–801
Govier DA, Kassanis B (1974) A virus induced component of plant sap needed when aphids acquire potato virus Y from purified preparations. Virology 61:420–426
Gray S, Gildow FE (2003) Luteovirus-aphid interactions. Annu Rev Phytopathol 41:539–566
Gray SM, Banerjee N (1999) Mechanisms of arthropod transmission of plant and animal viruses. Microbiol Mol Biol Rev 63:128–148
Haas M, Geldreich A, Bureau M, Dupuis L, Leh V, Vetter G, Kobayashi K, Hohn T, Ryabova L, Yot P, Keller M (2005) The open reading frame VI product of Cauliflower mosaic virus is a nucleocytoplasmic protein: its N terminus mediates its nuclear export and formation of electron-dense viroplasms. Plant Cell 17:927–943
Harris KF (1977) An ingestion-egestion hypothesis of non circulative virus transmission. In: Harris KF, Maramorosch K (eds) Aphids as virus vectors. Academic Press, New York, pp 166–208
Harris KF, Smith OP, Duffus JE (2001) Virus-insect-plant interactions. Academic Press, San Diego, pp 376
Hibino H, Cabauatan PQ (1987) Infectivity neutralization of rice tungro-associated viruses acquired by vector leafhoppers. Phytopathology 77:473–476
Hogenhout SA, Redinbaugh MG, Ammar ED (2003) Plant and animal rhabdovirus host range: a bug's view. Trends Microbiol 11:264–271
Hohn T, Fütterer J (1997) The proteins and functions of plant pararetroviruses: knowns and unknowns. Crit Rev Plant Sci 16:133–167
Howarth AJ, Gardner RC, Messing J, Shepherd RJ (1981) Nucleotide sequence of naturally occurring deletion mutants of cauliflower mosaic virus. Virology 112:678–685
Hull R (2001) Matthews' plant virology, 4th ed. Academic Press, San Diego
Hull R, Plaskitt A (1970) Electron microscopy on the behavior of two strains of alfalfa mosaic virus in mixed infections. Virology 42:773–776
Hunt RE, Nault LR, Gingery LE (1988) Evidence for infectivity of maize chlorotic dwarf virus and for an helper component in its leafhopper transmission. Phytopathology 78:499–504
Jridi C, Martin JF, Marie-Jeanne V, Labonne G, Blanc S (2006) Distinct viral populations differentiate and evolve independently in a single perennial host plant. J Virol 80:2349–2357
Jung A, Maier R, Vartanian JP, Bocharov G, Jung V, Fischer U, Meese E, Wain-Hobson S, Meyerhans A (2002) Multiply infected spleen cells in HIV patients. Nature 418:144
Kakani K, Reade R, Rochon D (2004) Evidence that vector transmission of a plant virus requires conformational change in virus particles. J Mol Biol 338:507–517
Kakani K, Robbins M, Rochon D (2003) Evidence that binding of cucumber necrosis virus to vector zoospores involves recognition of oligosaccharides. J Virol 77:3922–3928
Kakani K, Sgro JY, Rochon D (2001) Identification of specific cucumber necrosis virus coat protein amino acids affecting fungus transmission and zoospore attachment. J Virol 75:5576–5583
Karsies A, Merkle T, Szurek B, Bonas U, Hohn T, Leclerc D (2002) Regulated nuclear targeting of cauliflower mosaic virus. J Gen Virol 83:1783–1790
Kassanis B, Govier DA (1971a) The role of the helper virus in aphid transmission of potato aucuba mosaic virus and potato virus C. J Gen Virol 13:221–228
Kassanis B, Govier DA (1971b) New evidence on the mechanism of transmission of potato C and potato aucuba mosaic viruses. J Gen Virol 10:99–101
Kassanis B, Russell GE, White RF (1978) Seed and pollen transmission of beet cryptic virus in sugar beet plants. Phytopathology 91:76–79
Kim I, Kobayashi K, Cho E, Zambryski PC (2005) Subdomains for transport via plasmodesmata corresponding to the apical-basal axis are established during Arabidopsis embryogenesis. Proc Natl Acad Sci USA 102:11945–11950
Kunik T, Palanichelvam K, Czosnek H, Citovsky V, Gafni Y (1998) Nuclear import of the capsid protein of tomato yellow leaf curl virus (TYLCV) in plant and insect cells. Plant J 13:393–399
Kuno G, Chang GJ (2005) Biological transmission of arboviruses: reexamination of and new insights into components, mechanisms, and unique traits as well as their evolutionary trends. Clin Microbiol Rev 18:608–637
Leclerc D, Burri L, Kajava AV, Mougeot JL, Hess D, Lustig A, Kleemann G, Hohn T (1998) The open reading frame III product of cauliflower mosaic virus forms a tetramer through a N-terminal coiled-coil. J Biol Chem 273:29015–29021
Leh V, Jacquot E, Geldreich A, Haas M, Blanc S, Keller M, Yot P (2001) Interaction between cauliflower mosaic virus ORFIII product and the coat protein is required for transmission of the virus by aphids. J Virol 75:100–106
Leh V, Jacquot E, Geldreich A, Hermann T, Leclerc D, Cerrutti M, Yot P, Keller M, Blanc S (1999) Aphid transmission of cauliflower mosaic virus requires the viral PIII protein. EMBO J 18:7077–7085
Lett JM, Granier M, Hippolyte I, Grondin M, Royer M, Blanc S, Reynaud B, Peterschmitt M (2002) Spatial and temporal distribution of geminiviruses in leafhoppers of the genus Cicadulina monitored by conventional and quantitative polymerase chain reaction. Phytopathology 92:65–74
Liu S, He X, Park G, Josefsson C, Perry KL (2002) A conserved capsid protein surface domain of Cucumber mosaic virus is essential for efficient aphid vector transmission. J Virol 76:9756–9762
Lung MCY, Pirone TP (1973) Studies on the reason for differential transmissibility of cauliflower mosaic virus isolates by aphids. Phytopathology 63:910–914
Lung MCY, Pirone TP (1974) Acquisition factor required for aphid transmission of purified cauliflower mosaic virus. Virology 60:260–264
MacFarlane S (2003) Molecular determinants of the transmission of plant viruses by nematodes. Mol Plant Pathol 4:211–215
Martin B, Collar JL, Tjallingii WF, Fereres A (1997) Intracellular ingestion and salivation by aphids may cause the acquisition and inoculation of non-persistently transmitted plant viruses. J Gen Virol 78:2701–2705
Maule AJ, Wang D (1996) Seed transmission of plant viruses: a lesson in biological complexity. Trends Microbiol 4:153–158
Mellor PS (2000) Replication of arboviruses in Insect Vectors. J Comp Pathol 123:231–247
Mink GI (1993) Pollen- and seed-transmitted viruses and viroids. Annu Rev Phytopathol 31:375–402
Moreno A, Hebrard E, Uzest M, Blanc S, Fereres A (2005a) A single amino acid position in the helper component of cauliflower mosaic virus can change the spectrum of transmitting vector species. J Virol 79:13587–13593
Moreno A, Palacios I, Blanc S, Fereres A (2005b) Intracellular salivation is the mechanism involved in the inoculation of Cauliflower mosaic virus by its major vectors brevicoryne brassicae and Myzus persicae. Ann Entomol Soc Am 98:763–769
Morilla G, Krenz B, Jeske H, Bejarano ER, Wege C (2004) Tete a tete of tomato yellow leaf curl virus and tomato yellow leaf curl sardinia virus in single nuclei. J Virol 78:10715–10723
Morin S, Ghanim M, Sobol I, Czosnek H (2000) The GroEL protein of whitefly Bemisia tabaci interacts with the coat protein of transmissible and non-transmissible begomoviruses in the yeast two-hybrid system. Virology 276:404–416
Morin S, Ghanim M, Zeidan M, Czosnek H, Verbeek M, Van den Heuvel JFJM (1999) A GroEL homologue from endosymbiotic bacteria of the whitefly Bemisia tabaci is implicated in the circulative transmission of Tomato yellow leaf curl virus. Virology 256:75–84
Nault LR (1997) Arthropod transmission of plant viruses: a new synthesis. Ann Entomol Soc Am 90:521–541
Nault LR, Ammar ED (1989) Leafhopper and planthopper transmission of plant viruses. Ann Rev Entomol 34:503–529
Ng JC, Josefsson C, Clark AJ, Franz AW, Perry KL (2005) Virion stability and aphid vector transmissibility of Cucumber mosaic virus mutants. Virology 332:397–405
Ng JC, Liu S, Perry KL (2000) Cucumber mosaic virus mutants with altered physical properties and defective in aphid vector transmission. Virology 276:395–403
Ng JC, Tian T, Falk BW (2004) Quantitative parameters determining whitefly (Bemisia tabaci) transmission of Lettuce infectious yellows virus and an engineered defective RNA. J Gen Virol 85:2697–2707
Oparka KJ, Prior DA, Santa Cruz S, Padgett HS, Beachy R N (1997) Gating of epidermal plasmodesmata is restricted to the leading edge of expanding infection sites of tobacco mosaic virus (TMV). Plant J 12:781–789
Peng YH, Kadoury D, Gal-On A, Huet H, Wang Y, Raccah B (1998) Mutations in the HC-Pro gene of zucchini yellow mosaic potyvirus: effects on aphid transmission and binding to purified virions. J Gen Virol 79(4):897–904
Perry KL, Zhang L, Palukaitis P (1998) Amino acid changes in the coat protein of cucumber mosaic virus differentially affect transmission by the aphids Myzus persicae and Aphis gossypii. Virology 242:204–210
Perry KL, Zhang L, Shintaku MH, Palukaitis P (1994) Mapping determinants in cucumber mosaic virus for transmission by Aphis gossypii. Virology 205:591–595
Pfeiffer ML, Gildow FE, Gray SM (1997) Two distinct mechanisms regulate luteovirus transmission efficiency and specificity at the aphid salivary gland. J General Virol 78:495–503
Pirone TP, Blanc S (1996) Helper-dependent vector transmission of plant viruses. Annu Rev Phytopathol 34:227–247
Pirone TP, Megahed ES (1966) Aphid transmissibility of some purified viruses and viral RNAs. Virology 30:631–637
Pirone TP, Perry KL (2002) Aphids-Non-Persistent Transmission. In: Plumb RT (ed) Advances in Botanical Research. Academic Press, New York, pp 1–19
Plisson C, Drucker M, Blanc S, German-Retana S, Le Gall O, Thomas D, Bron P (2003) Structural characterization of HC-Pro, a plant virus multifunctional protein. J Biol Chem 278:23753–23761
Plisson C, Uzest M, Drucker M, Froissart R, Dumas C, Conway J, Thomas D, Blanc S, Bron P (2005) Structure of the mature P3-virus particle complex of cauliflower mosaic virus revealed by cryo-electron microscopy. J Mol Biol 346:267–277
Powell G (2005) Intracellular salivation is the aphid activity associated with inoculation of non-persistently transmitted viruses. J Gen Virol 86:469–472
Power AG (2000) Insect transmission of plant viruses: a constraint on virus variability. Curr Opin Plant Biol 3:336–340
Raccah B, Huet H, Blanc S (2001) Potyviruses. In: Harris K, Duffus JE, Smith OP (eds) Virus-Insect-Plant interactions. Academic Press, San Diego, pp 181–206
Ratcliff FG, MacFarlane SA, Baulcombe DC (1999) Gene silencing without DNA. rna-mediated cross-protection between viruses. Plant Cell 11:1207–1216
Redinbaugh MG, Hogenhout SA (2005) Plant rhabdoviruses. Curr Top Microbiol Immunol 292:143–163
Reichel C, Beachy RN (2000) Degradation of tobacco mosaic virus movement protein by the 26S proteasome. J Virol 74:3330–3337
Reinbold C, Herrbach E, Brault V (2003) Posterior midgut and hindgut are both sites of acquisition of Cucurbit aphid-borne yellows virus in Myzus persicae and Aphis gossypii. J Gen Virol 84:3473–3484
Riedel D, Lesemann DE, Maiss E (1998) Ultrastructural localization of nonstructural and coat proteins of 19 potyviruses using antisera to bacterially expressed proteins of plum pox potyvirus. Arch Virol 143:2133–2158
Roberts IM, Wang D, Findlay K, Maule AJ (1998) Ultrastructural and temporal observations of the potyvirus cylindrical inclusions (Cls) show that the Cl protein acts transiently in aiding virus movement. Virology 245:173–181
Roberts IM, Wang D, Thomas CL, Maule AJ (2003) Pea seed-borne mosaic virus seed transmission exploits novel symplastic pathways to infect the pea embryo and is, in part, dependent upon chance. Protoplasma 222:31–43
Rochon D, Kakani K, Robbins M, Reade R (2004) Molecular aspects of plant virus transmission by olpidium and plasmodiophorid vectors. Annu Rev Phytopathol 42:211–241
Roossinck MJ (1997) Mechanisms of plant virus evolution. Annu Rev Phytopathol 35:191–209
Ruiz-Ferrer V, Boskovic J, Alfonso C, Rivas G, Llorca O, Lopez-Abella D, Lopez-Moya JJ (2005) Structural analysis of tobacco etch potyvirus HC-pro oligomers involved in aphid transmission. J Virol 79:3758–3765
Saenz P, Salvador B, Simon-Mateo C, Kasschau KD, Carrington JC, Garcia JA (2002) Host-specific involvement of the HC protein in the long-distance movement of potyviruses. J Virol 76:1922–1931
Sanderfoot AA, Lazarowitz SG (1996) Getting it together in plant virus movement: cooperative interactions between bipartite geminivirus movement proteins. Trends Cell Biol 6:353–358
Schwach F, Vaistij FE, Jones L, Baulcombe DC (2005) An RNA-dependent RNA polymerase prevents meristem invasion by potato virus X and is required for the activity but not the production of a systemic silencing signal. Plant Physiol 138:1842–1852
Seddas P, Boissinot S, Strub JM, Van Dorsselaer A, Van Regenmortel MH, Pattus F (2004) Rack-1, GAPDH3, and actin: proteins of Myzus persicae potentially involved in the transcytosis of beet western yellows virus particles in the aphid. Virology 325:399–412
Stenger DC, Hein GL, Gildow FE, Horken KM, French R (2005) Plant virus HC-Pro is a determinant of eriophyid mite transmission. J Virol 79:9054–9061
Storey HH (1933) Investigations of the mechanims of transmission of plant viruses by insect vectors. Proc R Soc Lond Ser B 113:463–485
Szecsi J, Ding XS, Lim CO, Bendahmane M, Cho MJ, Nelson R S, Beachy RN (1999) Development of Tobacco mosaic virusinfection sites in Nicotiana benthamiana. Mol Plant Microbe Interact 12:143–152
Tegeder M, Offler CE, Frommer WB, Patrick JW (2000) Amino acid transporters are localized to transfer cells of developing pea seeds. Plant Physiol 122:319–326
Tegeder M, Wang XD, Frommer WB, Offler CE, Patrick JW (1999) Sucrose transport into developing seeds of Pisum sativum L. Plant J 18:151–161
Thornbury DW, Hellman GM, Rhoads RE, Pirone TP (1985) Purification and characterization of potyvirus helper component. Virology 144:260–267
Trutnyeva K, Bachmaier R, Waigmann E (2005) Mimicking carboxyterminal phosphorylation differentially effects subcellular distribution and cell-to-cell movement of Tobacco mosaic virus movement protein. Virology 332:563–577
Ullman DE, Whitfield AE, German TL (2005) Thrips and tospoviruses come of age: mapping determinants of insect transmission. Proc Natl Acad Sci USA 102:4931–4932
Unseld S, Höhnle M, Ringel M, Frischmuth T (2001) Subecellular targetting of the coat protein of African cassava mosaic geminivirus. Virology 286:373–383
Van den Heuvel J, Verbeek M, van der Wilk F (1994) Endosymbiotic bacteria associated with circulative transmission of Potato Leafroll Virus by Myzus persicae. J Virol 75:2559–2565
van den Heuvel JF, Bruyere A, Hogenhout SA, Ziegler-Graff V, Brault V, Verbeek M, van der Wilk F, Richards K (1997) The N-terminal region of the luteovirus readthrough domain determines virus binding to Buchnera GroEL and is essential for virus persistence in the aphid. J Virol 71:7258–7265
Van den Heuvel JFJM, Saskia A, Hogenhout SA, van der Wilk F (1999) Recognition and receptors in virus transmission by arthropods. Trends Microbiol 7:71–76
Vignuzzi M, Stone JK, Arnold JJ, Cameron CE, Andino R (2006) Quasispecies diversity determines pathogenesis through cooperative interactions in a viral population. Nature 439:344–348
Waigmann E, Chen MH, Bachmaier R, Ghoshroy S, Citovsky V (2000) Regulation of plasmodesmal transport by phosphorylation of tobacco mosaic virus cell-to-cell movement protein. EMBO J 19:4875–4884
Wang D, MacFarlane SA, Maule AJ (1997) Viral determinants of pea early browning virus seed transmission in pea. Virology 234:112–117
Wang D, Maule AJ (1992) Early embryo invasion as a determinant in pea of the seed transmission of pea seed-borne mosaic virus. J Gen Virol 73(7):1615–1620
Wang RY, Ammuar ED, Thornbury DW, Lopez-Moya JJ, Pirone TP (1996) Loss of potyvirus transmissibility and helper-component activity correlate with non-retention of virions in aphid stylets. J Gen Virol 77:861–867
Weber KA, Hampton RO (1980) Transmission of two purified carlaviruses by the pea aphid. Phypathology 70:631–633
Whittaker GR, Helenius A (1998) Nuclear import and export of viruses and virus genomes. Virology 246:1–23
Whittaker GR, Kann M, Helenius A (2000) Viral entry into the nucleus. Annu Rev Cell Dev Biol 16:627–651
Woolston CJ, Czaplewski LG, Markham PG, Goad AS, Hull R, Davies JW (1987) Location and sequence of a region of Cauliflower Mosaic virus gene II responsible for Aphid transmissibility. Virology 160:246–251
Yelina NE, Savenkov EI, Solovyev AG, Morozov SY, Valkonen JP (2002) Long-distance movement, virulence, and RNA silencing suppression controlled by a single protein in hordei- and potyviruses: complementary functions between virus families. J Virol 76:12981–12991
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Blanc, S. (2007). Virus Transmission—Getting Out and In. In: Waigmann, E., Heinlein, M. (eds) Viral Transport in Plants. Plant Cell Monographs, vol 7. Springer, Berlin, Heidelberg. https://doi.org/10.1007/7089_2006_099
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