Intercellular Spread of Potato Leafroll Luteovirus: Effects of Co-Infection and Plant Resistance

  • B. D. Harrison
  • H. Barker
  • P. M. Derrick
Part of the NATO ASI Series book series (volume 41)

Abstract

Potato leafroll luteovirus (PLRV) moves inefficiently from cell to cell and, in intact plants, is virtually confined to phloem tissue. Its spread to non-phloem tissue is enhanced by co-infection with some sap-transmissible viruses whereas others have no effect. The effective sap-transmissible viruses seem not to increase plasmodesmatal permeability to small peptides. Viruses which can aid intercellular movement of PLRV may themselves pass through virus-modified plasmodesmata as virus nucleic acid whereas some other viruses probably pass from cell to cell, as virus nucleoprotein particles, through virus-induced tubules which lead to plasmodesmata.

Keywords

Phloem Tissue Alfalfa Mosaic Virus Potato Leafroll Virus Beet Western Yellow Virus Intercellular Movement 
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. Anon (1988) Interaction of potato viruses. Annual Report of the International Potato Center, Lima, Peru, 1987–1988, p 80Google Scholar
  2. Arai K, Doi Y, Yora K, Asuyama H (1969) Electron microscopy of the potato leafroll virus in leaves of three kinds of host plants and the partial purification of the virus. Ann Phytopathol Soc Jpn 35:10–15CrossRefGoogle Scholar
  3. Atebekov JG, Taliansky ME, Drampyan AH, Kaplan IB, Turka IE (1984) Systemic infection by a phloem-restricted virus in parenchyma cells in a mixed infection (in Russian). Biol Nauki 10:28–31Google Scholar
  4. Barker H (1987) Invasion of non-phloem tissue in Nicotiana clevelandii by potato leafroll virus is enhanced in plants also infected with potato Y potyvirus. J Gen Virol 68:1223–1227CrossRefGoogle Scholar
  5. Barker H (1989) Specificity of the effect of sap-transmissible viruses in increasing the accumulation of luteoviruses in co-infected plants. Ann Appl Biol 155:in press.Google Scholar
  6. Barker H, Harrison BD (1985) Restricted multiplication of potato leafroll virus in resistant potato genotypes. Ann Appl Biol 107:205–212CrossRefGoogle Scholar
  7. 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 109:595–604CrossRefGoogle Scholar
  8. Beier H, Bruening G, Russell ML, Tucker CL (1979) Replication of cowpea mosaic virus in protoplasts isolated from immune lines of cowpeas. Virology 95:165–175PubMedCrossRefGoogle Scholar
  9. Boccara M, Hamilton WDO, Baulcombe DC (1986) The organisation and interviral homologies of genes at the 3’ end of tobacco rattle virus RNA1. EMBO J 5:223–229PubMedGoogle Scholar
  10. Cadnian CH, Harrison BD (1959) Studies on the properties of soil-borne viruses of the tobacco-rattle type occurring in Scotland. Ann Appl Biol 47:542–556CrossRefGoogle Scholar
  11. Derrick PM, Barker H, Oparka KJ (1989) Effects of virus infection on plasmodesmatal permeability. Rep Scott Crop Res Inst for 1988, in pressGoogle Scholar
  12. Frost RR, Harrison BD, Woods RD (1967) Apparent symbiotic interaction between particles of tobacco rattle virus. J Gen Virol 1:57–70CrossRefGoogle Scholar
  13. Goodwin PB (1983) Molecular size limit for movement in the symplast of the Elodea leaf. Planta 157:124–130CrossRefGoogle Scholar
  14. Kassanis B, Welkie GW (1963) The nature and behaviour of unstable variants of tobacco necrosis virus. Virology 21:540–550PubMedCrossRefGoogle Scholar
  15. Kojima M, Shikata E, Sugawara M, Murayama D (1969) Purification and electron microscopy of potato leafroll virus. Virology 39:162–174PubMedCrossRefGoogle Scholar
  16. Kubo S, Takanami Y (1979) Infection of tobacco mesophyll protoplasts with tobacco necrotic dwarf virus, a phloem-limited virus. J Gen Virol 42:387–398CrossRefGoogle Scholar
  17. Mayo MA, Robinson DJ, Jolly CA, Hyman L (1989) Nucleotide sequence of potato leafroll luteovirus RNA. J Gen Virol 70:1037–1051PubMedCrossRefGoogle Scholar
  18. Miller WA, Waterhouse PM, Gerlach WL (1988) Sequence and organization of barley yellow dwarf virus genomic RNA, Nucleic Acids Res 16:6097–6111PubMedCrossRefGoogle Scholar
  19. Murant AF, Roberts IM, Goold RA (1973) Cytopathological changes and extractable infectivity in Nicotiana clevelandii leaves infected with carrot mottle virus. J Gen Virol 21:269–283CrossRefGoogle Scholar
  20. Nishiguchi M, Motoyoshi F (1987) Resistance mechanisms of tobacco mosaic virus strains in tomato and tobacco. In: Evered D, Harnett S (eds) Plant resistance to viruses. Ciba Foundation Symposium 133. John Wiley & Sons, Chichester, New York p 38Google Scholar
  21. Roberts IM, Harrison BD (1970) Inclusion bodies and tubular structures in Chenopodium amaranticolor plants infected with strawberry latent ringspot virus. J Gen Virol 7:47–54PubMedCrossRefGoogle Scholar
  22. Sanger H (1968) Characteristics of tobacco rattle virus. I. Evidence that its two particles are functionally defective and mutually complementing. Mol Gen Genet 101:346–367PubMedCrossRefGoogle Scholar
  23. Siegel A, Zaitlin M, Sehgal OP (1962) The isolation of defective tobacco mosaic virus strains. Proc Natl Acad Sci USA 48:1845–1851PubMedCrossRefGoogle Scholar
  24. Stussi-Garaud C, Garaud J-C, Berna A, Godefroy-Colburn T (1987) In situ location of an alfalfa mosaic virus non-structural protein in plant cell walls: correlation with virus transport. J Gen Virol 68:1779–1784CrossRefGoogle Scholar
  25. Taliansky ME, Malyshenko SI, Pshennikova ES, Atabekov JG (1982) Plant virus-specific transport function. II. A factor controlling virus host range. Virology 122:327–331PubMedCrossRefGoogle Scholar
  26. Tomenius K, Clapham D, Meshi T (1987) Localization by immunogold cytochemistry of the virus-coded 30K protein in plasmodesmata of leaves infected with tobacco mosaic virus. Virology 160:363–371PubMedCrossRefGoogle Scholar
  27. Veidt I, Lot H, Leiser M, Scheidecker D, Guilley H, Richards K, Jonard G (1988) Nucleotide sequence of beet western yellows virus RNA. Nucleic Acids Res 16:9917–9932PubMedCrossRefGoogle Scholar
  28. Waterhouse PM, Murant AF (1983) Further evidence on the nature of the dependence of carrot mottle virus on carrot red leaf virus for transmission by aphids. Ann Appl Biol 103:455–464CrossRefGoogle Scholar
  29. Waterhouse PM, Gildow FE, Johnstone GR (1988) Luteovirus group. AAB Descriptions of Plant Viruses No 339Google Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 1990

Authors and Affiliations

  • B. D. Harrison
    • 1
  • H. Barker
    • 1
  • P. M. Derrick
    • 1
  1. 1.Scottish Crop Research InstituteInvergowrie, DundeeUK

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