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2012 | 34 | 3 |

Tytuł artykułu

Ultrastructural studies of plasmodesmatal and vascular translocation of tobacco rattle virus (TRV) in tobacco and potato

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The studies focus on an ultrastructural analysis of the phenomenon of intercellular and systemic (vascular) transport of tobacco rattle virus (TRV) in tissues of the infected plants. TRV is a dangerous pathogen of cultivated and ornamental plants due to its wide range of plant hosts and continuous transmission by vectors—ectoparasitic nematodes. Two weeks after infection with the PSG strain of TRV, tobacco plants of the Samsun variety and potato plants of the Glada variety responded with spot surface necroses on inoculated leaf blades. Four weeks after the infection a typical systemic response was observed on tobacco and potato leaves, necroses on stems and lesions referred to as corky ringspot. Ultrastructural analysis revealed the presence of two types of TRV virions: capsidated and non-capsidated forms in tobacco and potato tissues. In the protoplast area, viral particles either occurred in a dispersed form or they formed organised inclusions of virions. We demonstrated for the first time the presence of non-capsidated-type TRV in the vicinity of and inside plasmodesmata. Capsidated particles of TRV were observed in intercellular spaces of the tissues of aboveground and underground organs. Expanded apoplast area was noted at the cell wall, with numerous dispersed noncapsidated-type TRV particles. These phenomena suggest active intercellular transport. Our ultrastructure studies showed for the first time that xylem can be a possible route of TRV systemic transport. We demonstrated that both capsidated and non-capsidated virions, of varied length, participate in long-distance transport. TRV virions were more often documented in xylem (tracheary elements and parenchyma) than in phloem. Non-capsidated TRV particles were observed inside tracheary elements in a dispersed form and in regular arrangements in potato and tobacco xylem. The presence of TRV virions inside the bordered pits was demonstrated in aboveground organs and in the root of the tested plants. We documented that both forms of TRV virions can be transported systemically via tracheary elements of xylem.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

34

Numer

3

Opis fizyczny

p.1229-1238,fig.,ref.

Twórcy

  • Department of Botany, Faculty of Agriculture and Biology, Warsaw University of Life Sciences- SGGW, Nowoursynowska 159, 02-776 Warsaw, Poland
autor
  • Department of Botany, Faculty of Agriculture and Biology, Warsaw University of Life Sciences- SGGW, Nowoursynowska 159, 02-776 Warsaw, Poland
autor
  • Department of Botany, Faculty of Agriculture and Biology, Warsaw University of Life Sciences- SGGW, Nowoursynowska 159, 02-776 Warsaw, Poland
  • Research Division at Mlochow, Plant Breeding and Acclimatization Institute, National Research Institute, Platanowa 9, 05-831 Mlochow, Poland

Bibliografia

  • Allen TC (1963) A strain of tobacco rattle virus from Oregon grown potatoes. Plant Dis Rep 47:920–923
  • Bergh ST, Koziel MG, Huang S-C, Thomas RA, Gilley DP, Siegel A (1985) The nucleotide sequence of tobacco rattle virus RNA2 (CAM strain). Nucleic Acids Res 13:8507–8518
  • Carrington JC, Kasschau KD, Mahajan SK, Schaad MC (1996) Cellto-cell and long-distance transport of viruses in plants. Plant Cell 8:1669–1681
  • Clark MF, Adams AN (1977) Characteristics of the microplate method of enzyme-linked immunosorbent assay for the detection of plant viruses. J Gen Virol 34:475–483
  • Cornelissen BJC, Linthorst HJM, Brederode FT, Bol JF (1986) Analysis of the genome structure of tobacco rattle virus strain PSG. Nucleic Acids Res 14:2157–2169
  • Dubois F, Sangwan RS, Sangwan-Norreel BS (1994) Spread of Beet necrotic yellow vein virus in infected seedlings and plants of sugar beet (Beta vulgaris). Protoplasma 179:72–82
  • Frost RR, Harrisom BD, Woods RD (1967) Apparent symbiotic interaction between particles of tobacco rattle virus. J Gen Virol 1:57–70
  • Hamilton WDO, Baulcombe DC (1989) Infectious RNA produced by in vitro transcription of a full-length tobacco rattle virus RNA-1 cDNA. J Gen Virol 70:963–968
  • Harrison BD, Robinson DJ (1978) The tobraviruses. Adv Virus Res 23:25–77
  • Holeva RC, MacFarlane SA (2006) Yeast two-hybrid study of tobacco rattle virus coat protein and 2b protein interactions. Arch Virol 151:2123–2132
  • Huth W, Lesemann DE (1984) Natural occurrence of tobacco rattle virus in rye (Secale cereale) in the Federal Republic of Germany. Phytopathologische Zeitschrift 111:1–4
  • Karnovsky MJ (1965) A formaldehyde–glutaraldehyde fixative of high osmolarity for use in electron microscopy. J Cell Biol 27:137A
  • Lister RM, Bracker CE (1969) Defectiveness and dependence in three related strains of tobacco rattle virus. Virology 37:262–275
  • MacFarlane SA (1999) Molecular biology of the tobraviruses. J Gen Virol 80:2799–2807
  • MacFarlane SA (2010) Tobraviruses—plant pathogens and tools for biotechnology. Mol Plant Pathol 11:577–583
  • MacFarlane SA, Brown DJF (1995) Sequence comparison of RNA2 of nematode-transmissible and nematode-non-transmissible isolates of pea early-browning virus suggests that the gene encoding the 29 kDa protein may be involved in nematode transmission. J Gen Virol 76:1299–1304
  • 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 membrane. Proceedings of the National Academy of Science USA 95:3323–3328
  • Otulak K, Garbaczewska G (2010) Ultrastructural events during hypersensitive response of potato cv. Rywal infected with necrotic strains of potato virus Y. Acta Physiologia Plantarum 32:635–644
  • Ploeg AT, Robinson DJ, Brown DJF (1993) RNA-2 of tobacco rattle virus encodes the determinants of transmissibility by trichodorid vector nematodes. J Gen Virol 74:1463–1466
  • Swanson M, Barker H, MacFarlane SA (2002) Rapid vascular movement of tobraviruses does not require coat protein: evidence from mutated and wild-type viruses. Ann Appl Biol 141:259–266
  • Urban LA, Ramsdell DC, Klomparens KL, Lynch T, Hancock JF (1989) Detection of Blueberry shoestring virus in xylem and phloem tissues of high bush blueberry. Phytopathology 79:488–493
  • Valentine T, Shaw J, Block VC, Philipps MS, Oparka KJ, Lacomme C (2004) Efficient virus-induced gene silencing in roots using a modified tobacco rattle virus vector. Plant Physiol 136:3999–4009
  • 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
  • Verchot-Lubicz J (2003) Soilborne viruses: advances in virus movement, virus induced gene silencing, and engineered resistance. Physiol Mol Plant Pathol 62:55–63
  • Ziegler-Graff V, Guilford PJ, Baulcombe DC (1991) Tobacco rattle virus RNA-1 29 K gene product potentiates viral movement and also affects symptom induction in tobacco. Virology 182:145–155

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