Virus interference with trans-plasma membrane activity in infected grapevine leaves

• Autorzy: Rinaldelli E. , Luvisi A. , Panattoni A.
• Języki publikacji: EN

Abstrakty

EN

The trans-plasma membrane behavior in virus-infected grapevine leaves was investigated and the effects of six viruses included in European and Italian certification protocols of grapevine on trans-plasma membrane potential (t-PMEP) or electron transport (t-PMET) activity were evaluated. Electrophysiological tests were carried out on leaf samples of virus-infected Vitis vinifera cv. Sangiovese. Microelectrodes were placed in the central zone of the mesophyll for membrane potential measurement, while carbon fiber microelectrodes were used to estimate the membrane reductase activity of virus-infected resting cells. Viruses, the presence of which increased the NADH content, interfere differently with t-PMEP and t-PMET. Those that did not interfere negatively with membrane potential caused an increment in cell reductase activity, while virus-infected samples which showed a stressed status—as suggested by low energy availability and difficulty in the impalement procedure—were characterized by a lower t-PMET activity despite NADH content.

• Wydawca: -
• Czasopismo: Acta Physiologiae Plantarum
• Rocznik: 2014
• Tom: 36
• Numer: 12
• Opis fizyczny: p.3345-3349,fig.,ref.

Twórcy

autor

Rinaldelli E.

• Laboratory of Electrophysiology, Section Arboriculture, Department of Agrifood Production and Environmental Sciences, University of Florence, Viale delle Idee, 30, 50019, Sesto Fiorentino, Florence, Italy

autor

Luvisi A.

• Department of Agriculture, Food and Environment, University of Pisa, Via del Borghetto, 80, 56124, Pisa, Italy

autor

Panattoni A.

• Department of Agriculture, Food and Environment, University of Pisa, Via del Borghetto, 80, 56124, Pisa, Italy

Bibliografia

• Akeson M, Scharff J, Sharp CM, Neville DM (1992) Evidence that plasma membrane electrical potential is required for Vesicular Stomatitis Virus infection of MDCK cells: a study using fluorescence measurements through polycarbonate supports. J Membr Biol 125:81–91
• Atkinson MM, Midland SL, Keen NT (1996) Syringolide 1 triggers Ca²⁺ influx, K’ efflux, and extracellular alkalization in soybean cells carrying the disease-resistance gene Rpg4. Plant Physiol 112:297–302
• Del Principe D, Avigliano L, Savini I, Catani MV (2011) Transplasma membrane electron transport in mammalian: functional significance in healthy and disease. Antioxid Redox Sign 14:2289–2317
• Elmore JM, Coaker G (2011) The role of the plasma membrane H⁺-ATPase in plant-microbe interactions. Mol Plant 4:416–427
• Gray JP, Eisen T, Cline GW, Smith PJS, Heart E (2011) Plasma membrane electron transport in pancreatic B-cells is mediated in part by NQO1. Am J Physiol Endovasc 301:113–121
• Helenius A, Kielien M, Wellsteed J, Mellman L, Rudnick G (1985) Effect of monovalent cations on Semliki Forest virus entry into BHK-21 cells. J Biol Chem 260:5691–5697
• Herst PM, Berridge MV (2006) Plasma membrane electron transport: a new target for cancer drug development. Curr Mol Med 6:895–904
• Luvisi A, Rinaldelli E, Panattoni A, Triolo E (2012) Membrane transport of antiviral drugs in plants: an electrophysiological study in grapevine explants infected by Grapevine leafroll associated virus 1. Acta Physiol Planta 34:2115–2123
• Ly JD, Lawen A (2003) Transplasma membrane electron transport: enzymes involved and biological function. Redox Rep 8:3–21
• Martelli GP (2014) Directory of virus and virus-like diseases in grapevine and their agents. J Plant Pathol 96S:1–136
• Nakaune R, Nakano M (2006) Efficient methods for sample processing and cDNA synthesis by RT-PCR for the detection of grapevine viruses and viroids. J Virol Methods 134:244–249
• Novacky A, Ullrich-Eberius CI (1982) Relationship between membrane potential and ATP level in Xanthomonas campestris pv. Malvacearum infected cotton cotyledons. Physiol Plant Pathol 21:237–249
• Ober ES, Sharp RE (2003) Electrophysiological responses of maize roots to low water potential: relationship to growth and ABA accumulation. J Exp Bot 54:813–824
• Panattoni A, Rinaldelli E, Triolo E, Luvisi A (2013) In vivo inhibition of trans-plasma membrane electron transport by antiviral drugs in grapevine. J Membrane Biol 246:513–518
• Rawyler A, Arpagaus S, Braendle R (2002) Impact of oxygen stress and energy availability on membrane stability of plant cells. Ann Bot 90:499–507
• Rinaldelli E, Panattoni A, Luvisi A, Triolo E (2012) Effect of mycophenolic acid on trans-plasma membrane electron transport and electric potential in virus-infected plant tissue. Plant Physiol Bioch 60:137–140
• Schvarzstein M (1997) Changes in host plasma membrane ion fluxes during the Gomphrena globosa Papaya Mosaic Virus interaction. MSc Thesis, Department of Botany, University of Toronto, Canada
• Shabala S, Babourina O, Rengel Z, Nemchinov LG (2010) Non-invasive microelectrode potassium flux measurements as a potential tool for early recognition of virus-host compatibility in plants. Planta 232:807–815
• Sholthof H (2005) Plant virus transport: motions of functional equivalence. Trends Plant Sci 10:376–382
• Sondergaard TE, Schulz A, Palmgreen MG (2004) Energization of transport processes in plants. Role of the plasma membrane H⁺-ATPase. Plant Physiol 136:2475–2482
• Stack JP, Tattar TA (1978) Measurement of transmembrane electropotentials of Vigna sinensis leaf cells infected with tobacco ringspot virus. Physiol Plant Pathol 12:173–178
• Taylor AR, Chow RH (2001) A microelectrochemical technique to measure trans-plasma membrane electron transport in plant tissue and cells in vivo. Plant Cell Environ 24:749–754
• Vuletic M, Radenovic C, Vucinic Z (1987) The role of calcium in the generation of membrane potential oscillations in Nitella cells. Gen Physiol Byophis 6:203–207
• Wiley DC, Skedel JJ (1987) The structure and function of the hemagglutinin membrane glycoprotein of influenza virus. Annu Rev Biochem 56:365–394

Identyfikatory

DOI

10.1007/s11738-014-1695-5