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Spread Throughout the Plant: Systemic Transport of Viruses

  • Shoko UekiEmail author
  • Vitaly Citovsky
Chapter
Part of the Plant Cell Monographs book series (CELLMONO, volume 7)

Abstract

Viral long distant transport is an essential step for systemic infection. Because the process involves different types of highly differentiated vascular-associated cells, the virus systemic movement is regulated differentially at each tissue interface. In this chapter, we review current knowledge about viral systemic transport process in non-Arabidopsis hosts. We especially focus on viral and host factors participating in viral systemic transport. We also briefly overview the effect of RNA silencing, the host innate immunity, on viral systemic movement.

Keywords

Tobacco Mosaic Virus Cucumber Mosaic Virus Maize Streak Virus Rice Yellow Mottle Virus Tomato Golden Mosaic Virus 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. Andersen K, Johansen IE (1998) A single conserved amino acid in the coat protein gene of pea seed-borne mosaic potyvirus modulates the ability of the virus to move systemically in Chenopodium quinoa. Virology 241:304–311 PubMedGoogle Scholar
  2. Andrianifahanana M, Louvins K, Dute R, Sikora EJ, Murphy JF (1997) Pathway for phloem-dependent movment of pepper mottle potyvirus in the stem of Capsicum annuum. Phytopathology 87:892–898 PubMedGoogle Scholar
  3. Angell SM, Davies C, Baulcombe DC (1996) Cell-to-cell movement of potato virus X is associated with a change in the size exclusion limit of plasmodesmata in trichome cells of Nicotiana clevelandii. Virology 216:197–201 PubMedGoogle Scholar
  4. Arroyo R, Soto MJ, Martinez-Zapater JM, Ponz F (1996) Impaired cell-to-cell movement of potato virus Y in pepper plants carrying the ya(pr21) resistance gene. Mol Plant-Microbe Interact 9:314–318 Google Scholar
  5. Bahner I, Lamb J, Mayo MA, Hay RT (1990) Expression of the genome of potato leafroll virus: readthrough of the coat protein termination codon in vivo. J Gen Virol 71:2251–2256 PubMedGoogle Scholar
  6. Barker H, Harrison BD (1986) Restricted distribution of potato leafroll virus antigen in resistant potato genotypes and its effect on transmission of the virus by aphids. Ann Appl Biol 109:595–604 Google Scholar
  7. Barker H (1987) Invasion of non-phloem tissue in Nicotiana clevelandii by leafoll luteovirus is enhance in plants also infected with potato virus Y. J Gen Virol 68:1223–1227 Google Scholar
  8. 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 Google Scholar
  9. Baulcombe DC (2001) RNA silencing. Diced defence. Nature 409:295–596 PubMedGoogle Scholar
  10. Baulcombe DC (2002) Viral suppression of systemic silencing. Trends Microbiol 10:306–308 PubMedGoogle Scholar
  11. Baulcombe DC (2004) RNA silencing in plants. Nature 431:356–363 PubMedGoogle Scholar
  12. Bayne EH, Rakitina DV, Morozov SY, Baulcombe DC (2005) Cell-to-cell movement of Potato Potexvirus X is dependent on suppression of RNA silencing. Plant J 44:471–482 PubMedGoogle Scholar
  13. Beck DL, Guilford PJ, Voot DM, Andersen MT, Forster RLS (1991) Triple gene block proteins of white clover mosaic potexvirus are required for transport. Virology 183:695–702 PubMedGoogle Scholar
  14. Beffa R, Meins Jr F (1996) Pathogenesis-related functions of plant beta-1,3-glucanases investigated by antisense transformation – a review. Gene 179:97–103 PubMedGoogle Scholar
  15. Beffa RS, Hofer R-M, Thomas M, Meins Jr F (1996) Decreased susceptibility to virus disease of β-1,3-glucanase-deficient plants generated by antisense transformation. Plant Cell 8:1001–1011 PubMedGoogle Scholar
  16. Bisaro DM (2006) Silencing suppression by geminivirus proteins. Virology 344:158–168 PubMedGoogle Scholar
  17. Blackman LM, Boevink P, Santa Cruz S, Palukaitis P, Oparka KJ (1998) The movement protein of cucumber mosaic virus traffics into sieve elements in minor veins of Nicotiana clevelandii. Plant Cell 10:525–537 PubMedGoogle Scholar
  18. Boevink P, Oparka KJ (2005) Virus–host interactions during movement processes. Plant Physiol 138:1815–1821 PubMedGoogle Scholar
  19. Botha CEJ, Cross RHM, van Bel AJE, Peter CI (2000) Phloem loading in the sucrose-export-defective (SXD1) mutant maize is limited by callose deposition at plasmodesmata in bundle sheath–vascular parenchyma interface. Protoplasma 214:65–72 Google Scholar
  20. Boulton M, Steinkellner H, Donson J, Markham PG, King DI, Davies JW (1989) Mutational analysis of the virus-sense genes of maize streak virus. J Gen Virol 70:2309–2323 PubMedGoogle Scholar
  21. Boulton MI, Pallaghy CK, Chatani M, MacFarlane S, Davies JW (1993) Replication of maize streak virus mutants in maize protoplasts: evidence for a movement protein. Virology 192:85–93 PubMedGoogle Scholar
  22. Brault V, van den Heuvel JF, Verbeek M, Ziegler-Graff V, Reutenauer A, Herrbach E, Garaud JC, Guilley H, Richards K, Jonard G (1995) Aphid transmission of beet western yellows luteovirus requires the minor capsid read-through protein P74. EMBO J 14:650–659 PubMedGoogle Scholar
  23. Briddon RW (2003) Cotton leaf curl disease, a multicomponent begomovirus complex. Mol Plant Pathol 4:427–434 PubMedGoogle Scholar
  24. Brough CL, Hayes RJ, Morgan AJ, Coutts RHA, Buck KW (1988) Effects of mutagenesis in vitro on the ability of cloned tomato golden mosaic virus DNA to infect Nicotiana benthamiana. J Gen Virol 69:503–514 Google Scholar
  25. Bucher GL, Tarina C, Heinlein M, Di Serio F, Meins Jr F, Iglesias VA (2001) Local expression of enzymatically active class I beta-1,3-glucanase enhances symptoms of TMV infection in tobacco. Plant J 28:361–369 PubMedGoogle Scholar
  26. Carrington JC, Freed DD, Sanders TC (1989) Autocatalytic processing of the potyvirus helper component proteinase in Escherichia coli and in vitro. J Virol 63:4459–4463 PubMedGoogle Scholar
  27. Chay CA, Gunasinge UB, Dinesh-Kumar SP, Miller WA, Gray SM (1996) Aphid transmission and systemic plant infection determinants of barley yellow dwarf luteovirus-PAV are contained in the coat protein readthrough domain and - 17kDa protein, respectively. Virology 219:57–65 PubMedGoogle Scholar
  28. Chen J, Watanabe Y, Sako N, Ohshima K, Okada Y (1996) Mapping of host range restriction of the rakkyo strain of tobacco mosaic virus in Nicotiana tabacum cv. bright yellow. Virology 226:198–204 PubMedGoogle Scholar
  29. Chen MH, Sheng J, Hind G, Handa A, Citovsky V (2000) Interaction between the tobacco mosaic virus movement protein and host cell pectin methylesterases is required for viral cell-to-cell movement. EMBO J 19:913–920 PubMedGoogle Scholar
  30. Chen MH, Citovsky V (2003) Systemic movement of a tobamovirus requires host cell pectin methylesterase. Plant J 35:386–392 PubMedGoogle Scholar
  31. Cheng NH, Su CL, Carter SA, Nelson RS (2000) Vascular invasion routes and systemic accumulation patterns of tobacco mosaic virus in Nicotiana benthamiana. Plant J 23:349–362 PubMedGoogle Scholar
  32. Choi SK, Yoon JY, Ryu KH, Choi JK, Palukaitis P, Park WM (2002) Systemic movement of a movement-deficient strain of Cucumber mosaic virus in zucchini squash is facilitated by a cucurbit-infecting potyvirus. J Gen Virol 83:3173–3178 PubMedGoogle Scholar
  33. Citovsky V, Ghoshroy S, Tsui F, Klessig DF (1998) Non-toxic concentrations of cadmium inhibit tobamoviral systemic movement by a salicylic acid-independent mechanism. Plant J 16:13–20 PubMedGoogle Scholar
  34. 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 PubMedGoogle Scholar
  35. Culver JN, Dawson WO, Plonk K, Stubbs G (1995) Site-directed mutagenesis confirms the involvement of carboxylate groups in the disassembly of tobacco mosaic virus. Virology 206:724–730 PubMedGoogle Scholar
  36. Dalmay T, Rubino L, Burgyan J, Russo M (1992) Replication and movement of a coat protein mutant of cymbidium ringspot tombusvirus. Mol Plant-Microbe Interact 5:379–383 PubMedGoogle Scholar
  37. Dawson WO, Bubrick P, Grantham GL (1988) Modifications of the tobacco mosaic virus coat protein gene affecting replication, movement and symptomatology. Phytopathology 78:783–789 Google Scholar
  38. De Jong W, Chu A, Ahlquist P (1995) Coding changes in the 3a cell-to-cell movement gene can extend the host range of brome mosaic virus systemic infection. Virology 214:464–474 PubMedGoogle Scholar
  39. Delmer DP, Volokita M, Solomon M, Fritz U, Delphendahl W, Herth W (1993) A monoclonal antibody recognizes a 65 kDahigher plant membrane polypeptide which undergoes cation-dependent association with callose deposition in vivo. Protoplasma 176:33–42 Google Scholar
  40. Derrick PM, Barker H (1992) The restricted distribution of potato leafroll luteovirus antigen in potato plants with transgenic resistance resembles that in clones with one type of host gene-mediated resistance. Ann Appl Biol 120:451–457 Google Scholar
  41. Derrick PM, Barker H (1997) Short and long distance spread of potato leafroll luteovirus: effects of host genes and transgenes conferring resistance to virus accumulation in potato. J Gen Virol 78:243–251 PubMedGoogle Scholar
  42. Desvoyes B, Scholthof HB (2002) Host-dependent recombination of a Tomato bushy stunt virus coat protein mutant yields truncated capsid subunits that form virus-like complexes which benefit systemic spread. Virology 304:434–442 PubMedGoogle Scholar
  43. Ding B, Haudenshield JS, Hull RJ, Wolf S, Beachy RN, Lucas WJ (1992) Secondary plasmodesmata are specific sites of localization of the tobacco mosaic virus movement protein in transgenic tobacco plants. Plant Cell 4:915–928 PubMedGoogle Scholar
  44. Ding XS, Shintaku MH, Arnold SA, Nelson RS (1995) Accumulation of mild and severe strains of tobacco mosaic virus in minor veins of tobacco. Mol Plant-Microbe Interact 8:32–40 Google Scholar
  45. Ding XS, Shintaku MH, Carter SA, Nelson RS (1996) Invasion of minor veins of tobacco leaves inoculated with tobacco mosaic virus mutants defective in phloem-dependent movement. Proc Natl Acad Sci USA 93:11155–11160 PubMedGoogle Scholar
  46. Ding XS, Liu J, Cheng NH, Folimonov A, Hou YM, Bao Y, Katagi C, Carter SA, Nelson RS (2004) The Tobacco mosaic virus - 126kDa protein associated with virus replication and movement suppresses RNA silencing. Mol Plant-Microbe Interact 17:583–592 PubMedGoogle Scholar
  47. Dolja VV, Haldeman R, Robertson NL, Dougherty WG, Carrington JC (1994) Distinct functions of capsid protein in assembly and movement of tobacco etch potyvirus in plants. EMBO J 13:1482–1491 PubMedGoogle Scholar
  48. Dolja VV, Haldeman-Cahill R, Montgomery AE, Vandenbosch KA, Carrington JC (1995) Capsid protein determinants involved in cell-to-cell and long distance movement of tobacco etch potyvirus. Virology 206:1007–1016 PubMedGoogle Scholar
  49. Dorokhov YL, Makinen K, Frolova OY, Merits A, Saarinen J, Kalkkinen N, Atabekov JG, Saarma M (1999) A novel function for a ubiquitous plant enzyme pectin methylesterase: the host-cell receptor for the tobacco mosaic virus movement protein. FEBS Lett 461:223–228 PubMedGoogle Scholar
  50. Dunoyer P, Thomas CL, Harrison S, Revers F, Maule AJ (2004) A cysteine-rich plant protein potentiates Potyvirus movement through an interaction with the virus genome-linked protein VPg. J Virol 78:2301–2309 PubMedGoogle Scholar
  51. Dunoyer P, Voinnet O (2005) The complex interplay between plant viruses and host RNA-silencing pathways. Curr Opin Plant Biol 8:415–423 PubMedGoogle Scholar
  52. Esau K, Cronshaw J (1967) Tubular components in cells of healthy and tobacco mosaic virus-infected Nicotiana. Virology 33:26–35 PubMedGoogle Scholar
  53. Esau K, Hoefert LL (1972) Ultrastructure of sugarbeet leaves infected with beet western yellows virus. J Ultrastruct Res 40:556–571 PubMedGoogle Scholar
  54. Esau K, Hoefert LL (1972) Development of infection with beet western yellows virus in the sugarbeet. Virology 48:724–738 PubMedGoogle Scholar
  55. Filichkin SA, Lister RM, McGrath PF, Young MJ (1994) In vivo expression and mutational analysis of the barley yellow dwarf virus readthrough gene. Virology 205:290–299 PubMedGoogle Scholar
  56. 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 PubMedGoogle Scholar
  57. Gaffney T, Friedrich L, Vernooij B, Negrotto D, Nye G, Uknes S, Ward E, Kessmann H, Ryals J (1993) Requirement of salicylic acid for the induction of systemic acquired resistance. Science 261:754–756 PubMedGoogle Scholar
  58. Gao Z, Eyers S, Thomas CL, Ellis N, Maule AJ (2004) Identification of markers tightly linked to sbm recessive genes for resistance to Pea seed-borne mosaic virus. Theor Appl Genet 109:488–494 PubMedGoogle Scholar
  59. Gao Z, Johansen E, Eyers S, Thomas CL, Ellis THN, Maule AJ (2004) The potyvirus recessive resistance gene, sbm1, identifies a novel role for translation initiation factor eIF4E in cell-to-cell trafficking. Plant J 40:376–385 PubMedGoogle Scholar
  60. Gardiner WE, Sunter G, Brand L, Elmer JS, Rogers SG, Bisaro DM (1988) Genetic analysis of tomato golden mosaic virus: the coat protein is not required for systemic spread or symptom development. EMBO J 7:899–904 PubMedGoogle Scholar
  61. Germundsson A, Valkonen JP (2006) P1- and VPg-transgenic plants show similar resistance to Potato virus A and may compromise long distance movement of the virus in plant sections expressing RNA silencing-based resistance. Virus Res 116:208–213 PubMedGoogle Scholar
  62. Ghoshroy S, Freedman K, Lartey R, Citovsky V (1998) Inhibition of plant viral systemic infection by non-toxic concentrations of cadmium. Plant J 13:591–602 PubMedGoogle Scholar
  63. Gibbs AJ (1976) Viruses and plasmodesmata. In: Gunning BES, Robards AW (eds) Intercellular communication in plants: studies on plasmodesmata. Springer, Berlin Heidelberg New York, pp 149–164 Google Scholar
  64. Gill CC, Chong J (1975) Development of the infection in oat leaves inoculated with barley yellow dwarf virus. Virology 66:440–453 PubMedGoogle Scholar
  65. Goodrick BJ, Kuhn CW, Hussey RS (1991) Restricted systemic movement of cowpea chlorotic mottle virus in soybean with nonnecrotic resistance. Phytopathology 81:1426–1431 Google Scholar
  66. Guerini MN, Murphy JF (1999) Resistance of Capsicum annuum ‘Avelar’ to pepper mottle potyvirus and alleviation of this resistance by co-infection with cucumber mosaic cucumovirus are associated with virus movement. J Gen Virol 80:2785–2792 PubMedGoogle Scholar
  67. Haupt S, Duncan GH, Holzberg S, Oparka KJ (2001) Evidence for symplastic phloem unloading in sink leaves of barley. Plant Physiol 125:209–218 PubMedGoogle Scholar
  68. Hofius D, Herbers K, Melzer M, Omid A, Tacke E, Wolf S, Sonnewald U (2001) Evidence for expression level-dependent modulation of carbohydrate status and viral resistance by the potato leafroll virus movement protein in transgenic tobacco plants. Plant J 28:529–543 PubMedGoogle Scholar
  69. Holt CA, Beachy RN (1991) In vivo complementation of infectious transcripts from mutant tobacco mosaic virus cDNAs in transgenic plants. Virology 181:109–117 PubMedGoogle Scholar
  70. Huppert E, Szilassy D, Salánki K, Divéki Z, Balázs E (2002) Heterologous movement protein strongly modifies the infection phenotype of cucumber mosaic virus. J Virol 76:3554–3557 PubMedGoogle Scholar
  71. Iglesias VA, Meins Jr F (2000) Movement of plant viruses is delayed in a β-1,3-glucanase-deficient mutant showing a reduced plasmodesmatal size exclusion limit and enhanced callose deposition. Plant J 21:157–166 PubMedGoogle Scholar
  72. Itaya A, Ma F, Qi Y, Matsuda Y, Zhu Y, Liang G, Ding B (2002) Plasmodesma-mediated selective protein traffic between “symplasmically isolated” cells probed by a viral movement protein. Plant Cell 14:2071–2083 PubMedGoogle Scholar
  73. Jeffrey JL, Pooma W, Petty IT (1996) Genetic requirements for local and systemic movement of tomato golden mosaic virus in infected plants. Virology 223:208–218 PubMedGoogle Scholar
  74. Jensen SG (1969) Occurrence of virus particles in the phloem tissue of BYDV-infected barley. Virology 38:83–91 PubMedGoogle Scholar
  75. Kalinina NO, Rakitina DA, Yelina NE, Zamyatnin Jr AA, Stroganova TA, Klinov DV, Prokhorov VV, Ustinova SV, Chernov BK, Schiemann J, Solovyev AG, Morozov SY (2001) RNA-binding properties of the - 63kDa protein encoded by the triple gene block of poa semilatent hordeivirus. J Gen Virol 82:2569–2578 PubMedGoogle Scholar
  76. Kaplan IB, Gal-On A, Palukaitis P (1997) Characterization of cucumber mosaic virus. III. Localization of sequences in the movement protein controlling systemic infection in cucurbits. Virology 230:343–349 PubMedGoogle Scholar
  77. Kasschau KD, Cronin S, Carrington JC (1997) Genome amplification and long-distance movement functions associated with the central domain of tobacco etch potyvirus helper component-proteinase. Virology 228:251–262 PubMedGoogle Scholar
  78. Kasschau KD, Carrington JC (2001) Long-distance movement and replication maintenance functions correlate with silencing suppression activity of potyviral HC-Pro. Virology 285:71–81 PubMedGoogle Scholar
  79. Kauss H (1985) Callose biosynthesis as a Ca2+-regulated process and possible relations to the induction of other metabolic changes. J Cell Sci Suppl 2:89–103 PubMedGoogle Scholar
  80. Kauss H (1996) Callose synthesis. In: Smallwood M, Knox JP, Bowles DJ (eds) Membranes: specialized functions in plants. BIOS Scientific, Oxford, pp 77–92 Google Scholar
  81. Kempers R, Prior DAM, van Bel AJE, Oparka KJ (1993) Plasmodesmata between sieve elements and companion cells in extracellular phloem of Cucurbita maxima stems permit intercellular passage of fluorescent - 3kDa probes. Plant J 4:567–575 Google Scholar
  82. Kempers R, van Bel AJE (1997) Symplasmic connections between sieve element and companion cell in the stem phloem of Vicia faba L have a molecular exclusion limit of at least 10 kD. Planta 201:195–201 Google Scholar
  83. Kim SH, Ryabov EV, Brown JW, Taliansky M (2004) Involvement of the nucleolus in plant virus systemic infection. Biochem Soc Trans 32:557–560 PubMedGoogle Scholar
  84. Klein PG, Klein RR, Rodriguez-Cerezo E, Hunt AG, Shaw JG (1994) Mutational analysis of the tobacco vein mottling virus genome. Virology 204:759–769 PubMedGoogle Scholar
  85. Kreuze JF, Savenkov EI, Cuellar W, Li X, Valkonen JP (2005) Viral class 1 RNase III involved in suppression of RNA silencing. J Virol 79:7227–7238 PubMedGoogle Scholar
  86. Lee LY, Palukaitis P, Gray SM (2002) Host-dependent requirement for the Potato leafroll virus - 17kDa protein in virus movement. Mol Plant-Microbe Interact 15:1086–1094 PubMedGoogle Scholar
  87. Leisner SM, Howell SH (1993) Long-distance movement of viruses in plants. Trends Microbiol 1:314–317 PubMedGoogle Scholar
  88. Leisner SM, Turgeon R (1993) Movement of virus and photoassimilate in the phloem – a comparative analysis. BioEssays 15:741–748 PubMedGoogle Scholar
  89. Leisner SM, Turgeon R, Howell SH (1993) Effects of host plant development and genetic determinants on the long-distance movement of cauliflower mosaic virus in Arabidopsis. Plant Cell 5:191–202 PubMedGoogle Scholar
  90. Leonard S, Plante D, Wittmann S, Daigneault N, Fortin MG, Laliberte JF (2000) Complex formation between potyvirus VPg and translation eukaryotic initiation factor 4E correlates with virus infectivity. J Virol 74:7730–7737 PubMedGoogle Scholar
  91. Leonard S, Viel C, Beauchemin C, Daigneault N, Fortin MG, Laliberte JF (2004) Interaction of VPg-Pro of Turnip mosaic virus with the translation initiation factor 4E and the poly(A)-binding protein in planta. J Gen Virol 85:1055–1063 PubMedGoogle Scholar
  92. Leubner-Mezger G, Meins Jr F (1999) Functions and regulation of plant beta-1,3-glucanases (PR-2). In: Datta SK, Muthkrishnan S (eds) Pathogenesis-related proteins in plants. CRC, Boca Raton, FL, pp 49–76 Google Scholar
  93. Levy A, Czosnek H (2003) The DNA-B of the non-phloem-limited bean dwarf mosaic virus (BDMV) is able to move the phloem-limited Abutilon mosaic virus (AbMV) out of the phloem, but DNA-B of AbMV is unable to confine BDMV to the phloem. Plant Mol Biol 53:789–803 PubMedGoogle Scholar
  94. Li Q, Ryu KH, Palukaitis P (2001) Cucumber mosaic virus-plant interactions: identification of 3a protein sequences affecting infectivity, cell-to-cell movement, and long-distance movement. Mol Plant-Microbe Interact 14:378–385 PubMedGoogle Scholar
  95. Li Y, Wu MY, Song HH, Hu X, Qiu BS (2005) Identification of a tobacco protein interacting with tomato mosaic virus coat protein and facilitating long-distance movement of virus. Arch Virol 150:1993–2008 PubMedGoogle Scholar
  96. Liu H, Boulton MI, Lucy AP, Davies JW (2001) A single amino acid change in the coat protein of Maize streak virus abolishes systemic infection and encapsidation, but not interaction with viral DNA or movement protein. Mol Plant Pathol 2:223–228 PubMedGoogle Scholar
  97. Liu L, Davies JW, Stanley J (1998) Mutational analysis of bean yellow dwarf virus, a geminivirus of the genus Mastrevirus that is adapted to dicotyledonous plants. J Gen Virol 79:2265–2274 PubMedGoogle Scholar
  98. Liu L, Pinner MS, Davies JW, Stanley J (1999) Adaptation of the geminivirus bean yellow dwarf virus to dicotyledonous hosts involves both virion-sense and complementary-sense genes. J Gen Virol 80:501–506 PubMedGoogle Scholar
  99. Lopez-Moya JJ, Pirone TP (1998) Charge changes near the N-terminus of the coat protein of two potyviruses affect virus movement. J Gen Virol 79:161–165 PubMedGoogle Scholar
  100. Lough TJ, Emerson SJ, Lucas WJ, Forster RL (2001) Trans-complementation of long-distance movement of White clover mosaic virus triple gene block (TGB) mutants: phloem-associated movement of TGBp1. Virology 288:18–28 PubMedGoogle Scholar
  101. Marathe R, Anandalakshmi R, Smith TH, Pruss GJ, Vance VB (2000) RNA viruses as inducers, suppressors and targets of post-transcriptional gene silencing. Plant Mol Biol 43:295–306 PubMedGoogle Scholar
  102. Martin RR, Keese PK, Young MJ, Waterhouse PM, Geriach WL (1990) Evolution and molecular biology of luteovirus. Annu Rev Phytopathol 28:341–363 Google Scholar
  103. Mayo MA, Ziegler-Graff V (1996) Molecular biology of luteoviruses. Adv Virus Res 46:413–460 PubMedCrossRefGoogle Scholar
  104. McLean GP, Hamilton RI, Ronchon DM (1993) Symptomatology and movement of cucumber necrosis virus mutant lacking the coat protein protruding domain. Virology 193:932–939 PubMedGoogle Scholar
  105. Michelson I, Zeidan M, Zamski E, Zamir D, Czosneck H (1997) Localization of tomato yellow leaf curl virus (TYLCV) in susceptible and tolerant nearly isogenic tomato lines. Acta Hortic 477:407–414 Google Scholar
  106. Michon T, Estevez Y, Walter J, German-Retana S, Le Gall O (2006) The potyviral virus genome-linked protein VPg forms a ternary complex with the eukaryotic initiation factors eIF4E and eIF4G and reduces eIF4E affinity for a mRNA cap analogue. FEBS J 273:1312–1322 PubMedGoogle Scholar
  107. Moissiard G, Voinnet O (2004) Viral suppression of RNA silencing in plants. Mol Plant Pathol 5:71–82 PubMedGoogle Scholar
  108. Moreno IM, Thompson JR, Garcia-Arenal F (2004) Analysis of the systemic colonization of cucumber plants by Cucumber green mottle mosaic virus. J Gen Virol 85:749–759 PubMedGoogle Scholar
  109. Morra MR, Petty IT (2000) Tissue specificity of geminivirus infection is genetically determined. Plant Cell 12:2259–2270 PubMedGoogle Scholar
  110. Mourrain P, Béclin C, Elmayan T, Feuerbach F, Godon C, Morel JB, Jouette D, Lacombe AM, Nikic S, Picault N, Rémoué K, Sanial M, Vo TA, Vaucheret H (2000) Arabidopsis SGS2 and SGS3 genes are required for posttranscriptional gene silencing and natural virus resistance. Cell 101:533–542 PubMedGoogle Scholar
  111. Mutterer JD, Stussi-Garaud C, Michler P, Richards KE, Jonard G, Ziegler-Graff V (1999) Role of the beet western yellows virus readthrough protein in virus movement in Nicotiana clevelandii. J Gen Virol 80:2771–2778 PubMedGoogle Scholar
  112. Nelson RS, Li G, Hodgson RA, Beachy RN, Shintaku MH (1993) Impeded phloem-dependent accumulation of the masked strain of tobacco mosaic virus. Mol Plant-Microbe Interact 6:45–54 Google Scholar
  113. Nicaise V, German-Retana S, Sanjuán R, Dubrana MP, Mazier M, Maisonneuve B, Candresse T, Caranta C, LeGall O (2003) The eukaryotic translation initiation factor 4E controls lettuce susceptibility to the Potyvirus Lettuce mosaic virus. Plant Physiol 132:1272–1282 PubMedGoogle Scholar
  114. Noris E, Vaira AM, Caciagli P, Masenga V, Gronenborn B, Accotto GP (1998) Amino acids in the capsid protein of tomato yellow leaf curl virus that are crucial for systemic infection, particle formation, and insect transmission. J Virol 72:10050–10057 PubMedGoogle Scholar
  115. Northcote DH, Davey R, Lay J (1989) Use of antisera to localize callose, xylan and arabinogalactan in the cell-plate, primary and secondary cell walls of plant cells. Planta 178:353–366 Google Scholar
  116. Opalka N, Brugidou C, Bonneau C, Nicole M, Beachy RN, Yeager M, Fauquet C (1998) Movement of rice yellow mottle virus between xylem cells through pit membranes. Proc Natl Acad Sci USA 95:3323–3328 PubMedGoogle Scholar
  117. Oparka KJ, Santa Cruz S (2000) The great escape: phloem transport and unloading of macromoleculaes. Annu Rev Plant Physiol Plant Mol Biol 51:323–347 PubMedGoogle Scholar
  118. Osbourn JK, Sarkar S, Wilson TM (1990) Complementation of coat protein-defective TMV mutants in transgenic tobacco plants expressing TMV coat protein. Virology 179:921–925 PubMedGoogle Scholar
  119. Pooma W, Gillette WK, Jeffrey JL, Petty IT (1996) Host and viral factors determine the dispensability of coat protein for bipartite geminivirus systemic movement. Virology 218:264–268 PubMedGoogle Scholar
  120. Qin Y, Petty IT (2001) Genetic analysis of bipartite geminivirus tissue tropism. Virology 291:311–323 PubMedGoogle Scholar
  121. Qu F, Morris TJ (2005) Suppressors of RNA silencing encoded by plant viruses and their role in viral infections. FEBS Lett 579:5958–5964 PubMedGoogle Scholar
  122. Räjamaki ML, Valkonen JP (1999) The 6K2 protein and the VPg of potato virus A are determinants of systemic infection in Nicandra physaloides. Mol Plant-Microbe Interact 12:1074–1081 PubMedGoogle Scholar
  123. Räjamaki ML, Valkonen JP (2002) Viral genome-linked protein (VPg) controls accumulation and phloem-loading of a potyvirus in inoculated potato leaves. Mol Plant-Microbe Interact 15:138–149 PubMedGoogle Scholar
  124. Räjamaki ML, Valkonen JP (2003) Localization of a potyvirus and the viral genome-linked protein in wild potato leaves at an early stage of systemic infection. Mol Plant-Microbe Interact 16:25–34 PubMedGoogle Scholar
  125. Rao AL, Grantham GL (1996) Molecular studies on bromovirus capsid protein. II. Functional analysis of the amino-terminal arginine-rich motif and its role in encapsidation, movement, and pathology. Virology 226:294–305 PubMedGoogle Scholar
  126. Revers F, Le Gall O, Candresse T, Maule AJ (1999) New advances in understanding the molecular biology of plant/potyvirus interactions. Mol Plant-Microbe Interact 12:367–376 Google Scholar
  127. Robaglia C, Caranta C (2006) Translation initiation factors: a weak link in plant RNA virus infection. Trends Plant Sci 11:40–45 PubMedGoogle Scholar
  128. Roberts AG, Santa Cruz S, Roberts IM, Prior DAM, Turgeon R, Oparka KJ (1997) Phloem unloading in sink leaves of Nicotiana benthamiana: comparison of a fluorescent solute with a fluorescent virus. Plant Cell 9:1381–1396 PubMedGoogle Scholar
  129. Robinson DJ, Murant AF (1999) Umbravirus. In: Granoff A, Webster RG (eds) Encyclopedia of virology. Academic Press, New York, pp 1855–1859 Google Scholar
  130. Rogers HJ, Bate N, Combe J, Sullivan J, Sweetman J, Swan C, Lonsdale DM, Twell D (2001) Functional analysis of cis-regulatory elements within the promoter of the tobacco late pollen gene g10. Plant Mol Biol 45:577–585 PubMedGoogle Scholar
  131. Rojas MR, Jiang H, Salati R, Xoconostle-Cázares B, Sudarshana MR, Lucas WJ, Gilbertson RL (2001) Functional analysis of proteins involved in movement of the monopartite begomovirus, Tomato yellow leaf curl virus. Virology 291:110–125 PubMedGoogle Scholar
  132. Ruffel S, Dussault MH, Palloix A, Moury B, Bendahmane A, Robaglia C, Caranta C (2002) A natural recessive resistance gene against potato virus Y in pepper corresponds to the eukaryotic initiation factor 4E (eIF4E). Plant J 32:1067–1075 PubMedGoogle Scholar
  133. Ryabov EV, Robinson DJ, Taliansky ME (1999) A plant virus-encoded protein facilitates long-distance movement of heterologous viral RNA. Proc Natl Acad Sci USA 96:1212–1217 PubMedGoogle Scholar
  134. Ryabov EV, Fraser G, Mayo MA, Barker H, Taliansky M (2001) Umbravirus gene expression helps potato leafroll virus to invade mesophyll tissues and to be transmitted mechanically between plants. Virology 286:363–372 PubMedGoogle Scholar
  135. Ryabov EV, Robinson DJ, Taliansky M (2001) Umbravirus-encoded proteins both stabilize heterologous viral RNA and mediate its systemic movement in some plant species. Virology 288:391–400 PubMedGoogle Scholar
  136. Saito T, Yamanaka K, Okada Y (1990) Long distance movement and viral assembly of tobacco mosaic virus mutants. Virology 176:329–336 PubMedGoogle Scholar
  137. Santa Cruz S, Roberts AG, Prior DAM, Chapman S, Oparka KJ (1998) Cell-to-cell and phloem-mediated transport of potato virus X: the role of virions. Plant Cell 10:495–510 Google Scholar
  138. Santa Cruz S (1999) Phloem transport of viruses and macromolecules – what goes in must come out. Trends Microbiol 7:237–241 PubMedGoogle Scholar
  139. Sanz AI, Serra MT, Garcia-Luque I (2000) Altered local and systemic spread of movement deficient virus in transgenic tobacco plants expressing the cucumber mosaic virus 3a protein. Arch Virol 145:2387–2401 PubMedGoogle Scholar
  140. Savenkov EI, Valkonen JP (2001) Potyviral helper-component proteinase expressed in transgenic plants enhances titers of Potato leaf roll virus but does not alleviate its phloem limitation. Virology 283:285–293 PubMedGoogle Scholar
  141. Schaad MC, Carrington JC (1996) Suppression of long-distance movement of tobacco etch virus in a nonsusceptible host. J Virol 70:2556–2561 PubMedGoogle Scholar
  142. Schaad MC, Lellis AD, Carrington JC (1997) VPg of tobacco etch potyvirus is a host genotype-specific determinant for long-distance movement. J Virol 71:8624–8631 PubMedGoogle Scholar
  143. Schaad MC, Anderberg RJ, Carrington JC (2000) Strain-specific interaction of the tobacco etch virus NIa protein with the translation initiation factor eIF4E in the yeast two-hybrid system. Virology 273:300–306 PubMedGoogle Scholar
  144. Schaffer RL, Miller CG, Petty IT (1995) Virus and host-specific adaptations in the BL1 and BR1 genes of bipartite geminiviruses. Virology 214:330–338 PubMedGoogle Scholar
  145. Schindler U, Beckmann H, Cashmore AR (1993) HAT3.1, a novel Arabidopsis homeodomain protein containing a conserved cysteine-rich region. Plant J 4:137–150 PubMedGoogle Scholar
  146. Schmitz J, Stussi-Garaud C, Tacke E, Prufer D, Rohde W, Rohfritsch O (1997) In situ localization of the putative movement protein (pr17) from potato leafroll luteovirus (PLRV) in infected and transgenic potato plants. Virology 235:311–322 PubMedGoogle Scholar
  147. Schneider WL, Greene AE, Allison RF (1997) The carboxy-terminal two-thirds of the cowpea chlorotic mottle bromovirus capsid protein is incapable of virion formation yet supports systemic movement. J Virol 71:4862–4865 PubMedGoogle Scholar
  148. Scholthof HB, Morris TJ, Jackson AO (1993) The capsid protein gene of tomato bushy stunt virus is dispensable for systemic movement and can be replaced for localized expression of foreign genes. Mol Plant-Microbe Interact 6:309–322 Google Scholar
  149. Scholthof HB, Scholthof K-BG, Kikkert M, Jackson AO (1995) Tomato bushy stunt virus spread is regulated by two nested genes that function in cell-to-cell movement and host-dependent systemic invasion. Virology 213:425–438 PubMedGoogle Scholar
  150. Scholthof HB (2005) Plant virus transport: motions of functional equivalence. Trends Plant Sci 10:376–382 PubMedGoogle Scholar
  151. 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 PubMedGoogle Scholar
  152. Shepardson S, McCrum R (1980) Extracytoplasmic tubules in leafroll-infected and leafroll-free potato leaf tissue. J Ultrastruct Res 72:47–51 PubMedGoogle Scholar
  153. Shintaku MH, Carter SA, Bao Y, Nelson RS (1996) Mapping nucleotides in the - 126kDa protein gene that control the differential symptoms induced by two strains of tobacco mosaic virus. Virology 221:218–225 PubMedGoogle Scholar
  154. Siegal A, Zaitlin M, Sehgal OP (1962) The isolation of defective tobacco mosaic virus strains. Proc Natl Acad Sci USA 48:1845–1851 Google Scholar
  155. Simon-Buela L, Garcia-Arenal F (1999) Virus particles of cucumber green mottle mosaic tobamovirus move systemically in the phloem of infected cucumber plants. Mol Plant-Microbe Interact 12:112–118 PubMedGoogle Scholar
  156. Sit TL, Haikal PR, Callaway AS, Lommel SA (2001) A single amino acid mutation in the carnation ringspot virus capsid protein allows virion formation but prevents systemic infection. J Virol 75:9538–9542 PubMedGoogle Scholar
  157. Smith HG, Barker H (1999) The Luteoviridae. Oxford University Press, New York Google Scholar
  158. Soards AJ, Murphy AM, Palukaitis P, Carr JP (2002) Virulence and differential local and systemic spread of Cucumber mosaic virus in tobacco are affected by the CMV 2b protein. Mol Plant-Microbe Interact 15:647–653 PubMedGoogle Scholar
  159. Solovyev AG, Savenkov EI, Grdzelishvili VZ, Kalinina NO, Morozov SY, Schiemann J, Atabekov JG (1999) Movement of hordeivirus hybrids with exchanges in the triple gene block. Virology 253:278–287 PubMedGoogle Scholar
  160. Soosaar JL, Burch-Smith TM, Dinesh-Kumar SP (2005) Mechanisms of plant resistance to viruses. Nat Rev Microbiol 3:789–798 PubMedGoogle Scholar
  161. Soto MJ, Chen LF, Seo YS, Gilbertson RL (2005) Identification of regions of the Beet mild curly top virus (family Geminiviridae) capsid protein involved in systemic infection, virion formation and leafhopper transmission. Virology 341:257–270 PubMedGoogle Scholar
  162. Spitsin S, Steplewski K, Fleysh N, Belanger H, Mikheeva T, Shivprasad S, Dawson W, Koprowski H, Yusibov V (1999) Expression of alfalfa mosaic virus coat protein in tobacco mosaic virus (TMV) deficient in the production of its native coat protein supports long-distance movement of a chimeric TMV. Proc Natl Acad Sci USA 96:2549–2553 PubMedGoogle Scholar
  163. Stone BA, Clarke AE (1992) Chemistry and biology of 1->3-β-glucans. La Trobe University Press, Victoria, Australia Google Scholar
  164. Susi P, Pehu E, Lehto K (1999) Replication in the phloem is not necessary for efficient vascular transport of tobacco mosaic tobamovirus. FEBS Lett 447:121–123 PubMedGoogle Scholar
  165. Takamatsu N, Ishiakwa M, Meshi T, Okada Y (1987) Expression of bacterial chloramphenicol acetyltransferase gene in tobacco plants infected by TMV-RNA. EMBO J 6:307–311 PubMedGoogle Scholar
  166. Takeshita M, Suzuki M, Kuwata S, Takanami Y (1998) Involvement of cucumber mosaic cucumovirus RNA2 and RNA3 in viral systemic spread in radish plant. Arch Virol 143:1109–1117 PubMedGoogle Scholar
  167. Taliansky M, Roberts IM, Kalinina N, Ryabov EV, Raj SK, Robinson DJ, Oparka KJ (2003) An umbraviral protein, involved in long-distance RNA movement, binds viral RNA and forms unique, protective ribonucleoprotein complexes. J Virol 77:3031–3040 PubMedGoogle Scholar
  168. Taliansky ME, Garcia-Arenal F (1995) Role of cucumovirus capsid protein in long-distance movement within the infected plant. J Virol 69:916–922 PubMedGoogle Scholar
  169. Taliansky ME, Robinson DJ (2003) Molecular biology of umbraviruses: phantom warriors. J Gen Virol 84:1951–1960 PubMedGoogle Scholar
  170. Thompson JR, Garcia-Arenal FG (1998) The bundle sheath-phloem interface of Cucumis sativus is a boundary to systemic infection by tomato aspermy virus. Mol Plant-Microbe Interact 11:109–114 Google Scholar
  171. Tomenius K, Clapham D, Meshi T (1987) Localization by immunogold cytochemistry of the virus coded 30 K protein in plasmodesmata of leaves infected with tobacco mosaic virus. Virology 160:363–371 PubMedGoogle Scholar
  172. Turgeon R (1989) The sink-source transition in leaves. Annu Rev Plant Physiol Plant Mol Biol 40:119–138 Google Scholar
  173. Ueki S, Citovsky V (2001) Inhibition of post transcriptional gene silencing by non-toxic concentrations of cadmium. Plant J 28:283–291 PubMedGoogle Scholar
  174. Ueki S, Citovsky V (2002) Cadmium ion-induced glycine-rich protein inhibits systemic movement of a tobamovirus. Nat Cell Biol 4:478–485 PubMedGoogle Scholar
  175. Ueki S, Citovsky V (2005) Identification of an interactor of cadmium ion-induced glycine-rich protein involved in regulation of callose levels in plant vasculature. Proc Natl Acad Sci USA 102:12089–12094 PubMedGoogle Scholar
  176. Ueki S, Citovsky V (2006) Arrest in viral transport as the basis for plant resistance to infection. In: Loebenstein G, Carr JP (eds) Natural resistance mechanisms of plants to viruses. Springer, Berlin Heidelberg New York, pp 280–315 Google Scholar
  177. Urcuqui-Inchima S, Haenni AL, Bernardi F (2001) Potyvirus proteins: wealth of functions. Virus Res 74:157–175 PubMedGoogle Scholar
  178. Vaewhongs AA, Lommel SA (1995) Virion formation is required for the long-distance movement of red clover necrotic mosaic virus in movement protein transgenic plants. Virology 212:607–613 PubMedGoogle Scholar
  179. van Bel AJE (2003) The phloem, a miracle of ingenuity. Plant Cell Environ 26:125–149 Google Scholar
  180. van Bel AJE, Ehlers K, Knoblauch M (2003) Sieve elements caught in the act. Trends Plant Sci 7:126–132 Google Scholar
  181. van der Boogaart T, Lomonossoff GP, Davies JW (1998) Can we explain RNA-mediated virus resistance by homology-dependent gene silencing? Mol Plant-Microbe Interact 11:717–723 Google Scholar
  182. van der Kuyl AC, Neeleman L, Bol JF (1991) Complementation and recombination between alfalfa mosaic virus RNA3 mutants in tobacco plants. Virology 183:731–738 PubMedGoogle Scholar
  183. Verchot J, Driskel BA, Zhu Y, Hunger RM, Littlefield LJ (2001) Evidence that soilborne wheat mosaic virus moves long distance through the xylem in wheat. Protoplasma 218:57–66 PubMedGoogle Scholar
  184. Voinnet O, Pinto YM, Baulcombe DC (1999) Suppression of gene silencing: a general strategy used by diverse DNA and RNA viruses of plants. Proc Natl Acad Sci USA 96:14147–14152 PubMedGoogle Scholar
  185. Voinnet O (2001) RNA silencing as a plant immune system against viruses. Trends Genet 17:449–459 PubMedGoogle Scholar
  186. von Arnim A, Frischmuch T, Stanley J (1993) Detection and possible functions of African cassava mosaic virus DNA B gene products. Virology 192:264–272 Google Scholar
  187. Waigmann E, Lucas WJ, Citovsky V, Zambryski PC (1994) Direct functional assay for tobacco mosaic virus cell-to-cell movement protein and identification of a domain involved in increasing plasmodesmal permeability. Proc Natl Acad Sci USA 91:1433–1437 PubMedGoogle Scholar
  188. Waigmann E, Ueki S, Trutnyeva K, Citovsky V (2004) The ins and outs of non-destructive cell-to-cell and systemic movement of plant viruses. Crit Rev Plant Sci 23:195–250 Google Scholar
  189. Wang HL, Wang Y, Giesman-Cookmeyer D, Lommel SA, Lucas WJ (1998) Mutations in viral movement protein alter systemic infection and identify an intercellular barrier to entry into the phloem long-distance transport system. Virology 245:75–89 PubMedGoogle Scholar
  190. Wang JY, Chay C, Gildow FE, Gray SM (1995) Readthrough protein associated with virions of barley yellow dwarf luteovirus and its potential role in regulating the efficiency of aphid transmission. Virology 206:954–962 PubMedGoogle Scholar
  191. Wang MB, Metzlaff M (2005) RNA silencing and antiviral defense in plants. Curr Opin Plant Biol 8:216–222 PubMedGoogle Scholar
  192. Wintermantel WM, Banerjee N, Oliver JC, Paolillo DJ, Zaitlin M (1997) Cucumber mosaic virus is restricted from entering minor veins in transgenic tobacco exhibiting replicase-mediated resistance. Virology 231:248–257 PubMedGoogle Scholar
  193. Wisler GC, Li RH, Liu HY, Lowry DS, Duffus JE (1998) Tomato chlorosis virus: a new whitefly-transmitted, phloem-limited, bipartite closterovirus of tomato. Phytopathology 88:402–409 PubMedGoogle Scholar
  194. Wittmann S, Chatel H, Fortin MG, Laliberte JF (1997) Interaction of the viral protein genome linked of turnip mosaic potyvirus with the translational eukaryotic initiation factor (iso) 4E of Arabidopsis thaliana using the yeast two-hybrid system. Virology 234:84–92 PubMedGoogle Scholar
  195. Xie Z, Fan B, Chen C, Chen Z (2001) An important role of an inducible RNA-dependent RNA polymerase in plant antiviral defense. Proc Natl Acad Sci USA 98:6516–6521 PubMedGoogle Scholar
  196. Xiong Z, Kim KH, Giesman-Cookmeyer D, Lommel SA (1993) The roles of the red clover necrotic mosaic virus capsid and cell-to-cell movement proteins in systemic infection. Virology 192:27–32 PubMedGoogle Scholar
  197. Ziegler-Graff V, Brault V, Mutterer JD, Simonis M-T, Herrbach E, Guilley H, Richards KE, Jonard G (1996) The coat protein of beet western yellow luteovirus is essential for systemic infection but the viral gene products p29 and p19 are dispensable for systemic infection and aphid transmission. Mol Plant-Microbe Interact 9:501–510 Google Scholar

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© Springer-Verlag Berlin Heidelberg 2007

Authors and Affiliations

  1. 1.Department of Biochemistry and Cell BiologyState University of New York at Stony BrookStony BrookUSA

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