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2014 | 36 | 01 |

Tytuł artykułu

The participation of plant cell organelles in compatible and incompatible potato virus Y-tobacco and -potato plant interaction

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Potyviruses replicate and express their genomes in the cytoplasm in closely related membranous structures such as the endoplasmic reticulum or in the vicinity of the ER. The present research demonstrates the participation of plant cell organelles based on ultrastructural examination of compatible and incompatible interactions in tobacco- and potato-potato virus Y (PVY) necrotic strains. In two interaction types, PVYN Wi and PVYNTN particles were documented inside cell nuclei. Virus cytoplasmic inclusions and particles were associated with nuclear envelope pore complexes. Moreover, the PVY capsid protein was immunolocalised in the cell nucleus and nucleolus. Our results for the first time show PVY particles and capsid proteins inside the mitochondrion in compatible interactions, whereas in hypersensitive responses these interactions were identified inside chloroplasts. The PVY particles attached to mitochondria caused association groups of these organelles. The ultrastructural analysis clearly demonstrated both the dynamics of the endoplasmatic reticulum in two types of PVY interactions and connections between PVY cytoplasmic inclusions and particles with its membranous structures. Moreover, we demonstrated strongly localised immunodetection of the PVY capsid protein on the surface and in the vicinity of ER in cases of hypersensitive response as well as in compatible interaction.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

36

Numer

01

Opis fizyczny

p.85-99,fig.,ref.

Twórcy

autor
  • Department of Botany, Faculty of Agriculture and Biology, Warsaw University of Life Sciences-SGGW, Nowoursynowska 159, 02-776 Warsaw, Poland
  • Department of Botany, Faculty of Agriculture and Biology, Warsaw University of Life Sciences-SGGW, Nowoursynowska 159, 02-776 Warsaw, Poland

Bibliografia

  • Almási A, Gáborjányi R, Ekés M (1996) Ultrastructural changes of tobacco plants in different compatible host–parasite relations. Acta Phytopathol Entomol Hung 31:181–190.
  • Balachandran S, Hurry VM, Kelley SE, Osmond CB, Robinson SA, Rohozinski J, Seaton GGR, Sims DA (1997) Concepts of plant biotic stress. Some insights into the stress physiology of virusinfected plants, from the perspective of photosynthesis. Physiol Plant 100:203–212.
  • Beczner L, Horvath J, Romhanyi I, Forster H (1984) Studies on the etiology of tuber necrotic ringspot disease in potato. Potato Res 27:339–352.
  • Channarayappa Muniyappa V, Schwegler-Berry D, Shivashankar G (1992) Ultrastructural changes in tomato infected with tomato leaf curl virus, a whitefly-transmitted geminivirus. Can J Bot 70:1747–1753.
  • Chrzanowska M (1991) New isolates of the necrotic strain of potato virus Y (PVY N) found recently in Poland. Potato Res 34:179–182.
  • Chrzanowska M (1994) Differentiation of potato virus Y (PVY) isolates. Phytopathol Pol 8:15–20.
  • Chrzanowska M, Doroszewska T (1997) Comparison between PVY isolates obtained from potato and tobacco plants grown in Poland. Phytopathol Polon 8:15–20.
  • Chung BY, Miller WJ, Atkins JF, Firth AE (2008) An overlapping essential gene in the Potyviridae. Proc Natl Acad Sci USA 105:5897–5902.
  • 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.
  • Fauquet CM, Mayo MA, Maniloff J, Desselberger U, Ball LA (eds) (2005) Virus taxonomy. In: Eight report of the ICTV. Elsevier Academic Press, London.
  • Galili G (2004) ER-derived compartments are formed by highly regulated processes and have special functions in plants. Plant Physiol 136:3411–3413.
  • Goodman RN, Kiraly Z, Wood KR (1986) Photosynthesis. The biochemistry and physiology of plant disease. University Missouri Press, Columbia Hara-Nishimura I, Hatsugai N, Nakaune S, Kuroyanagi M, Nishimura M (2005) Vacuolar processing enzyme: an executor of plant cell death. Curr Opin Plant Biol 8:404–408.
  • Heath MC, Nimchuk ZL, Xu H (1997) Plant nuclear migrations as indications of critical interactions between resistant and susceptible cowpea epidermal cells and invasion hyphae of the cowpea rust fungus. New Phytol 135:689–700.
  • Hinrichs-Berger J, Harold M, Berger S, Buchenauer H (1999) Cytological responses of susceptible and extremely resistant potato plants to inoculation with potato virus Y. Physiol Mol Plant Pathol 55:143–150.
  • Hodgson RAJ, Beachy RN, Pakrasi HB (1989) Selective inhibition of photosystem II in spinach by tobacco mosaic virus: an effect of the viral coat protein. FEBS Lett 245:267–270.
  • Hong Y, Hunt AG (1996) RNA polymerase activity catalyzed by a potyvirus-encoded RNA-dependent RNA polymerase. Virology 226:146–151.
  • Hüttner S, Strasser R (2012) Endoplasmic reticulum-associated degradation of glycoproteins in plants. Front Plant Sci 3:67. doi:10.3389/fpls.2012.00067
  • Jelitto-Van Dooren EP, Vidal S, Denecke J (1999) Anticipating endoplasmic reticulum stress. A novel early response before pathogenesis related gene induction. Plant Cell 11:1935–1944.
  • Karnovsky MJ (1965) A formaldehyde–glutaraldehyde fixative of high osmolarity for use in electron microscopy. J Cell Biol 27:137A.
  • Kerlan C, Le Romancer M (1992) In: Ritter E, Perez de San Roman C (compilers) Proceedings of the 11th EAPR virology section meeting, Vitoria-Gasteiz, pp 77–80, 29 June–3 July 1992.
  • Kopek BG, Perkins G, Miller DJ, Ellisman MH, Ahlquist P (2007) Three-dimensional analysis of a viral RNA replication complex reveals a virus-induced mini-organelle. PLoS Biol 5:e220. doi:10.1371/journal.pbio.0050220
  • Krichevsky A, Kozlovsky SV, Gafni Y, Citovsky V (2006) Nuclear import and export of plant virus proteins and genomes. Mol Plant Pathol 7:131–146.
  • Lam E, Kato N, Lawton M (2001) Programmed cell death, mitochondria and the plant hypersensitive response. Nature 411:848–853.
  • Levine A, Pennell RI, Alvarez ME, Palmer R, Lamb C (1996) Calcium mediated apoptosis in plant hypersensitive disease resistance response. Curr Biol 6:427–437.
  • Li J, Zhao-Hui C, Batoux M, Nekrasov V, Roux M, Chinchilla D, Zipfel C, Jones JD (2009) Specific ER quality control components required for biogenesis of the plant innate immune receptor EFR. Proc Natl Acad Sci USA 106:15973–15978.
  • Lohaus G, Heldt HW, Osmond CB (2000) Infection with phloem limited abutilon mosaic virus causes localized carbohydrate accumulation in leaves of Abutilon striatum: relationships to symptom development and effects on chlorophyll fluorescence quenching during photosynthetic induction. Plant Biol 2:161–167.
  • McCartney AW, Greenwood JS, Fabian MR, White KA, Mullen RT (2005) Localization of the tomato bushy stunt virus replication protein p33 reveals a peroxisome-to-endoplasmic reticulum sorting pathway. Plant Cell 17:3513–3531.
  • Mittler R, Lam E (1995) Identification, characterization, and purification of a tobacco endonuclease activity induced upon hypersensitive response cell death. Plant Cell 7:1951–1962.
  • Mould MJR, Heath MC (1999) Ultrastructural evidence of differential changes in transcription, translation and cortical microtubule during in planta penetration of cells resistant and susceptible to rust infection. Physiol Mol Plant Pathol 55:225–236.
  • Otulak K, Garbaczewska G (2010) Ultrastructural events during hypersensitive response of potato cv. Rywal infected with necrotic strains of potato virus Y. Acta Physiol Plantarum 32:635–644.
  • Otulak K, Garbaczewska G (2012) Cytopathological potato virus Y structures during Solanaceous plants infection. Micron 43:839–850.
  • Prod’homme D, Le Panse S, Drugeon G, Jupin I (2001) Detection and subcellular localization of the Turnip yellow mosaic virus 66K replication protein in infected cells. Virology 281:88–101.
  • Rahoutei J, Garcia-Luque I, Baron M (2000) Inhibition of photosynthesis by viral infection: effect on PSII structure and function. Physiol Plant 110:286–292.
  • Reinero A, Beachy RN (1989) Reduced photosystem II activity and accumulation of viral coat protein in chloroplasts of leaves infected with tobacco mosaic virus. Plant Physiol 89:111–116.
  • 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.
  • Riechmann L, Lain S, Garcia JA (1992) Highlights and prospects of potyvirus molecular biology. J Gen Virol 73:1–16.
  • 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.
  • Robert Y, Woodford JAT, Ducray-Bourdin DG (2000) Some epidemiological approaches to the control of aphid-borne virus diseases in seed potato crops in northern Europe. Virus Res 71:33–47.
  • Saijo Y, Tintor N, Lu X, Rauf P, Pajerowska-Mukhtar K, Häweker H, Dong X, Robatzek S, Schulze-Lefert P (2009) Receptor quality control in the endoplasmic reticulum for plant innate immunity. EMBO J 28:3439–3449.
  • Selga T, Selga M (1993) Effect of ethylene producer camposan M on the genome and morphogenesis of plants. Proc Latv Acad Sci B12:71–73.
  • Selga T, Selga M, Pavila V (2005) Death of mitochondria during programmed cell death of leaf mesophyll cells. Cell Biol Int 29:1050–1056.
  • Shalitin D, Wolf S (2000) Cucumber mosaic virus infection affects sugar transport in melon plants. Plant Physiol 123:597–604.
  • Staehelin LA (1997) The plant ER: a dynamic organelle composed of a large number of discrete functional domains. Plant J 11:1151–1165.
  • Szajko K, Chrzanowska M, Witek K, Strzelczyk-Zyta D, Zagórska H, Gebhardt C, Hennig J, Marczewski W (2008) The novel gene Ny-1 on potato chromosome IX confers hypersensitive resistance to potato virus Y and is an alternative to Ry genes in potato breeding for PVY resistance. Theor Appl Genet 116:297–303.
  • Tiwari BS, Belenghi B, Levine A (2002) Oxidative stress increases respiration and generation of reactive oxygen species, resulting in ATP depletion, opening of mitochondria permeability transition and programmed cell death. Plant Physiol 128:1271–1281.
  • Urcuqui-Inchima S, Haenni AL, Bernardi F (2001) Potyvirus proteins: a wealth of functions. Virus Res 74:157–175.
  • Valkonen JPT (2007) Viruses: economical losses and biotechnological potential. In: Vreugdenhil D, Bradshaw J, Gebhardt C, Govers F, Taylor M, MacKerron D, Ross H (eds) Potato biology and biotechnology: advances and perspectives. Elsevier, Amsterdam, pp 619–641.
  • van Lent WM, Verduin BJM (1986) Detection of viral protein and particles in thin section of infected plant tissue using immunogold labeling. Dev Appl Biol 1:193–211.
  • Wang D, Weaver ND, Kesarwani M, Dong X (2005) Induction of protein secretory pathway is required for systemic acquired resistance. Science 308:1036–1040.
  • Wei T, Zhang C, Hong J, Xiong R, Kasschau KD et al (2010) Formation of complexes at plasmodesmata for potyvirus intercellular movement is mediated by the viral protein P3NPIPO. PLoS Pathog 6:e1000962. doi:10.1371/journal.ppat.1000962.
  • Yu F, Finley RL, Raz A, Kim HRC (2002) Galectin-3 translocates to the perinuclear membranes and inhibits cytochrome c release from the mitochondria A role for synexin in galectin-3 translocation. J Biol Chem 277:15819–15827.
  • Zechmann B, Muller M, Zellnig G (2003) Cytological modifications in zucchini yellow mosaic virus (ZYMV)-infected Styrian pumpkin plants. Arch Virol 148:1119–1133.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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