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Impact of Salicylic Acid on the Transport and Distribution of Sugars in Plants

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SALICYLIC ACID
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Abstract

The article discusses the ways of salicylic acid influence on transport of sucrose and its distribution in plants. The intercellular and long-distance transport along phloem depends on the presence or absence of SA. As a result of sucrose influx in heterotrophic tissues the content of sucrose in the sink organs may increase. Complex interactions between SA, sucrose, Ca2+, ROS and transmembrane electrical potential that occur in the apoplast and at the level of plasma membrane are discussed.

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References

  • Aaziz, R., Dinant, S., & Epel, B. L. (2001). Plasmodesmata and plant cytoskeleton. Trends in Plant Science, 6, 326–330.

    PubMed  CAS  Google Scholar 

  • Abdel-Wahed, M. S. A., Amin, A. A., & El-Rashad, S. M. (2006). Physiological effect of some bioregulators on vegetative growth, yield and chemical constituents of yellow maize plants. World Journal of Agricultural Science, 2, 149–155.

    Google Scholar 

  • Aldesuquy, H. S., Abo-Hamed, S. A., Abbas, M. A., & Elhakem, A. H. (2012). Role of glycine betaine and salicylic acid in improving growth vigour and physiological aspects of droughted wheat cultivars. Journal of Stress Physiology and Biochemistry, 8, 149–171.

    Google Scholar 

  • Al-Hakimi, A. M. A., & Alghalibis, S. M. S. (2007). Thiamin and salicylic acid as biological alternatives for controlling broad bean rot disease. Journal of Applied Science and Environmental Management, 11, 125–131.

    Google Scholar 

  • Allen, G. J., Chu, S. P., Harrington, C. L., Schumacher, K., Hoffmann, T., Tang, Y. Y., et al. (2001). A defined range of guard cell calcium oscillation parameters encodes stomatal movements. Nature, 411, 1053–1057.

    PubMed  CAS  Google Scholar 

  • Alpaslan, M., & Gunes, A. (2001). Interactive effects of boron and salinity stress on the growth, membrane permeability and mineral composition of tomato and cucumber plants. Plant and Soil, 236, 123–128.

    CAS  Google Scholar 

  • Amin, A. A., Rashad, E.-S. M., & Gharib, F. A. E. (2008). Changes in morphological, physiological and reproductive characters of wheat plants as affected by foliar application with salicylic acid and ascorbic acid. Australian Journal of Basic and Applied Sciences, 2, 252–261.

    CAS  Google Scholar 

  • Anderson, J. M. (1983). Release of sucrose from Vicia faba L. leaf discs. Plant Physiology, 71, 333–340.

    Google Scholar 

  • Amin, A. A., Rashad, E.-S. M., & El-Abagy, H. M. H. (2007). Physiological effect of indole-3-butyric acid and salicylic acid on growth, yield and chemical constituents of onion plants. Journal of Applied Science Research, 3, 1554–1563.

    CAS  Google Scholar 

  • Arfan, M., Athar, H. R., & Ashraf, M. (2007). Does exogenous application of salicylic acid through the rooting medium modulate growth and photosynthetic capacity in two differently adapted spring wheat cultivars under salt stress? Journal of Plant Physiology, 164, 685–694.

    PubMed  CAS  Google Scholar 

  • Arimura, G., & Maffei, M. E. (2010). Calcium and secondary CPK signaling in plants in response to herbivore attack. Biochemical and Biophysical Research Communications, 400, 455–460.

    PubMed  CAS  Google Scholar 

  • Ayre, B. G. (2011). Membrane-transport systems for sucrose in relation to whole-plant carbon partitioning. Molecular plant, 4, 377–394.

    PubMed  CAS  Google Scholar 

  • Baghizadeh, G. A., Haj, R. M., & Mozafarih, H. (2009). Evaluation of interaction effect of drought stress with ascorbate and salicylic acid on some of physiological and biochemical parameters in Okra (Hibiscus esculentus L.). Research Journal of Biological Sciences, 4, 380–387.

    Google Scholar 

  • BaluÅ¡ka, F., Å amaj, J., Napier, R., & Volkmann, D. (1999). Maize calreticulin localizes preferentially to plasmodesmata in root apex. The Plant Journal, 19, 481–488.

    PubMed  Google Scholar 

  • BaluÅ¡ka, F., Cvrckova, F., Kendrick-Jones, J., & Volkmann, D. (2001). Sink plasmodesmata as gateways for phloem unloading. Myosin VIII and calreticulin as molecular determinants of sink strength? Plant Physiology, 126, 39–46.

    PubMed  Google Scholar 

  • BaluÅ¡ka, F., Hlavacka, A., Volkmann, D., & Menzel, D. (2004). Getting connected: Actinbased cell-to-cell channels in plants and animals. Trends in Cell Biology, 14, 404–408.

    PubMed  Google Scholar 

  • Barakat, N. A. M. (2011). Oxidative stress markers and antioxidant potential of wheat treated with phytohormones under salinity stress. Journal of Stress Physiology and Biochemistry, 7, 250–267.

    Google Scholar 

  • Barratt, D. H., Kölling, K., Graf, A., Pike, M., Calder, G., Findlay, K., et al. (2011). Callose synthase GSL7 is necessary for normal phloem transport and inflorescence growth in Arabidopsis. Plant Physiology, 155, 328–341.

    PubMed  CAS  Google Scholar 

  • Bayat, H., Alirezaie, M., & Neamati, H. (2012). Impact of exogenous salicylic acid on growth and ornamental characteristics of calendula (Calendula officinalis L.) under salinity stress. Journal of Stress Physiology and Biochemistry, 8, 258–267.

    Google Scholar 

  • Bayer, E., Thomas, C., & Maule, A. (2008). Symplastic domains in the Arabidopsis shoot apical meristem correlate with PDLP1 expression patterns. Plant Signaling & Behavior, 3, 853–855

    Google Scholar 

  • Benitez-Alfonso, Y., Faulkner, C., Ritzenthaler, C., & Maule, A. J. (2010). Plasmodesmata: Gateways to local and systemic virus infection. Molecular Plant-Microbe Interactions, 23, 1403–1412.

    PubMed  CAS  Google Scholar 

  • Bernard, F., Baghai, M., & Kaveh, S. H. (2012). In vitro carbohydrate stress: Salicylic acid increases soluble invertase activity in Pestacia vera L. in vitro plantlets. Iranian Journal of Plant Physiology, 2, 355–360.

    Google Scholar 

  • Bhuja, P., McLachlan, K., Stephens, J., & Taylor, G. (2004). Accumulation of ß-1,3-glucans, in response to aluminum and cytosolic calcium in Triticum aestivum. Plant and Cell Physiology, 45, 543–549.

    PubMed  CAS  Google Scholar 

  • Blackman, L. M., & Overall, R. L. (1998). Immunolocalization of the cytoskeleton to plasmodesmata of Chara coralline. The Plant Journal, 14, 733–741.

    CAS  Google Scholar 

  • Botha, C. E. J., & Cross, R. H. M. (2000). Toward reconciliation of structure with function in plasmodesmata: Who is the gatekeeper. Micron, 31, 713–721.

    PubMed  CAS  Google Scholar 

  • Burch-Smith, T. M., Stonebloom, S., Xu, M., & Zambryski, P. C. (2011). Plasmodesmata during development: Re-examination of the importance of primary, secondary, and branched plasmodesmata structure versus function. Protoplasma, 248, 61–74.

    PubMed  CAS  Google Scholar 

  • Burch-Smith, T. M., & Zambryski, P. C. (2012). Plasmodesmata paradigm shift: Regulation from without versus within. Annual Review of Plant Biology, 63, 239–260.

    PubMed  CAS  Google Scholar 

  • Burmistrova, N. A., Krasavina, M. S., & Akanov, E. N. (2009). Salicylic acid can regulate phloem unloading in the root tip. Russian Journal of Plant Physiology, 56, 627–634.

    CAS  Google Scholar 

  • Carpaneto, A., Geiger, D., Bamberg, E., Sauer, N., Fromm, J., & Hedrich, R. (2005). Phloem-localized, proton-coupled sucrose carrier ZmSUT1 mediates sucrose efflux under the control of the sucrose gradient and the proton motive force. Journal of Biological Chemistry, 280, 21437–21443.

    PubMed  CAS  Google Scholar 

  • Chapleo, S., & Hall, J. L. (1989). Sugar unloading in roots of Ricinus communis L. II. Characteristics of the extravascular apoplast. New Phytologist, 111, 381–390.

    CAS  Google Scholar 

  • Chaudhuri, B., Hormann, F., Lalonde, S., Brady, S. M., Orlando, D. A., Benfey, P., et al. (2008). Protonophore- and pH insensitive glucose and sucrose accumulation detected by FRET nanosensors in Arabidopsis root tips. The Plant Journal, 56, 948–962.

    PubMed  CAS  Google Scholar 

  • Chen, L. Q., Qu, X. Q., Hou, B. H., Sosso, D., Osorio, S., Fernie, A. R., et al. (2012). Sucrose efflux mediated by SWEET proteins as a key step for phloem transport. Science, 335, 207–211.

    PubMed  CAS  Google Scholar 

  • Couée, I., Sulmon, C., Gouesbet, G., & El Amrani, A. (2006). Involvement of soluble sugars in reactive oxygen species balance and responses to oxidative stress in plants. Journal of Experimental Botany, 57, 449–459.

    PubMed  Google Scholar 

  • Cronshaw, J., & Esau, K. (1968). P-protein in the phloem of Cucurbita. II. The P-protein of mature sieve elements. Journal of Cell Biology, 38, 292–303.

    PubMed  CAS  Google Scholar 

  • Currier, H., & Webster, D. H. (1964). Callose formation and subsequent disappearance: Studies in ultrasound stimulation. Plant Physiology, 39, 843–847.

    PubMed  CAS  Google Scholar 

  • Ding, B., Kwon, M. O., & Warnberg, L. (1996). Evidence that actin filaments are involved in controlling the permeability of plasmodesmata in tobacco mesophyll. The Plant Journal, 10, 157–164.

    Google Scholar 

  • Dong, M. A., Farréb, E. M., & Thomashow, M. F. (2011). CIRCADIAN CLOCK-ASSOCIATED 1 and LATE ELONGATED HYPOCOTYL regulate expression of the C-REPEAT BINDING FACTOR (CBF) pathway in Arabidopsis. PNAS, 108, 7241–7246.

    PubMed  CAS  Google Scholar 

  • Dong, X., Hong, Z., Chatterjee, J., Kim, S., & Verma, D. P. (2008). Expression of callose synthase genes and its connection with Npr1 signaling pathway during pathogen infection. Planta, 229, 87–98.

    PubMed  CAS  Google Scholar 

  • Ehlers, K., & van Bel, A. J. (2010). Dynamics of plasmodesmal connectivity in successive interfaces of the cambial zone. Planta, 231, 371–385.

    PubMed  CAS  Google Scholar 

  • El Tayeb, M. A., & Ahmed, N. L. (2010). Response of wheat cultivars to drought and salicylic acid. American-Eurasian Journal of Agronomy, 3, 1–7.

    Google Scholar 

  • Esau, K., & Thorsch, J. (1985). Sieve plate pores and plasmodesmata, the communication channels of the symplast: Ultrastructural aspects and developmental relations. American Journal of Botany, 72, 1641–1653.

    Google Scholar 

  • Eschrich, W. (1965). Physiologie der Siebröhren callose. Planta, 65, 280–300.

    Google Scholar 

  • Evert, R. F., & Derr, W. F. (1964). Callose substance in sieve elements. American Journal of Botany, 51, 552–559.

    CAS  Google Scholar 

  • Farouk, S., & Osman, M. A. (2011). The effect of plant defense elicitors on common bean (Phaseolus vulgaris L.) growth and yield in absence or presence of spider mite (Tetranychus urticae Koch) infestation. Journal of Stress Physiology and Biochemistry, 7, 5–22.

    Google Scholar 

  • Farouk, S., Ghoneem, K. M., & Abeer, A. (2008). Induction and expression of systematic resistance to downy mildew disease in cucumber plant by elicitors. Egyptian Journal of Phytopathology, 1–2, 95–111.

    Google Scholar 

  • Fernandez-Calvino, L., Faulkner, C., Walshaw, J., Saalbach, G., Bayer, E., Benitez-Alfonco, Y., et al. (2011). Arabidopsis plasmodesmal proteome. PLoS ONE, 6, 1–13.

    Google Scholar 

  • Foyer, C. H., & Noctor, G. (2003). Redox sensing and signaling associated with reactive oxygen in chloroplasts, peroxisomes and mitochondria. Physiologia Plantarum, 119, 355–364.

    CAS  Google Scholar 

  • Froelich, D. R., Mullendore, D. L., Jensen, K. H., Ross-Elliott, T. J., Anstead, J. A., Thompson, G. A., et al. (2011). Phloem ultrastructure and pressure flow: Sieve-element-occlusion-related agglomerations do not affect translocation. Plant Cell, 23, 428–445.

    Google Scholar 

  • Furch, A. C. U., Zimmermann, M. R., Will, T., Hafke, J. B., & van Bel, A. J. E. (2010). Remote controlled stop of mass flow by biphasic occlusion in Cucurbita maxima. Journal of Experimental Botany, 61, 3697–3708.

    PubMed  CAS  Google Scholar 

  • Gadi, B. R., & Laxmi, V. (2012). Effect of salicylic acid and moisture stress on sugar content and sucrose synthase activity in Ziziphus seedlings. Biochemical and Cellular Archives, 12, 21–23.

    CAS  Google Scholar 

  • Gamalei, Yu.V. (2004). Transport system of vascular plants. Publ. House S.-Petersburg State Uni, 422p.

    Google Scholar 

  • Gharib, F. A., & Hegazi, A. Z. (2010). Salicylic acid ameliorates germination, seedling growth, phytohormone and enzyme activity in bean (Phaseolus vulgaris L.) under cold stress. Journal of the American Science, 6, 675–683.

    Google Scholar 

  • Ghasemzadeh, A., & Jaafar, H. Z. E. (2012). Effect of salicylic acid application on biochemical changes in ginger (Zingiber officinale Roscoe). Journal of Medicinal Plants Research, 6, 790–795.

    CAS  Google Scholar 

  • Glass, A. D. M., & Dunlop, J. (1974). Influence of phenolic acids on ion uptake. IV. Depolarization of the membrane potentials. Plant Physiology, 54, 855–858.

    Google Scholar 

  • Giaquinta, R. T. (1977). Phloem loading of sucrose: pH dependence and selectivity. Plant Physiology, 59, 750–753.

    PubMed  CAS  Google Scholar 

  • Giaquinta, R. T. (1979). Phloem loading of sucrose: Involvement of membrane ATPase and proton transport. Plant Physiology, 63, 744–748.

    PubMed  CAS  Google Scholar 

  • Gordon, L. Kh., Minibayeva, F. V., Ogorodnikova, T. I., Rakhmatullina, D. F., Tzentzevitzky, A. N., Kolesnikov, O. P., et al. (2002). Salicylic acid induces dissipation of the proton gradient on the plant cell plasma membrane. Doklady Biological Sciences, 387, 581–583.

    PubMed  CAS  Google Scholar 

  • Guan, H. P., & Janes, H. W. (1989). Sugar uptake in the protoplasts isolated from tomato leaves. Journal of Plant Physiology, 134, 327–330.

    CAS  Google Scholar 

  • Gunes, A., Inal, A., Alpaslan, M., Cicek, N., Guneri, E., Eraslan, F., et al. (2005). Effects of exogenously applied salicylic acid on the induction of multiple stress tolerance and mineral nutrition in maize (Zea mays L.). Archives of Agronomy and Soil Science, 51, 687–695.

    CAS  Google Scholar 

  • Gutierrez–Coronado, M. A., Trejo-Lopez, C., & Larque-Saavedra, A. (1998). Effects of salicylic acid on growth of roots and shoots in soybean. Plant Physiology and Biochemistry, 36, 653–665.

    Google Scholar 

  • Hafke, J. B., Furch, A. C., Fricker, M. D., & van Bel, A. J. (2009). Forisome dispersion in Vicia faba is triggered by Ca(2+) hotspots created by concerted action of diverse Ca2+ channels in sieve elements. Plant Signaling & Behavior, 4, 968–972.

    CAS  Google Scholar 

  • Haroun, S. A., Aldesuqy, H. S., Shukry, W. M., & Gaber, A. M. (1998). Regulation of growth and metabolism in Lupinus termis plant by sodium salicylate. Egyptian Journal of Physiology Sciences, 22, 75–95.

    CAS  Google Scholar 

  • Hayat, S., Ali B., & Ahmad, A. (2007). Salicylic acid: Biosynthesis, metabolism and physiological role in plants. In: S. Hayat, A. & Ahmad (Eds.), Salicylic acid: A plant hormone (pp. 1–14). Dordrecht: Springer.

    Google Scholar 

  • Hayat, Q., Hayat, S., Irfan, M., & Ahmad, A. (2010). Effect of exogenous salicylic acid under changing environment. A review. Environmental and Experimental Botany, 68, 14–25.

    CAS  Google Scholar 

  • Hayat, S., Fariduddin, Q., Ali, B., & Ahmad, A. (2005). Effect of salicylic acid on growth and enzyme activities of wheat seedlings. Acta Agronomica Hungarica, 53, 433–437.

    CAS  Google Scholar 

  • Heinlein, M., & Epel, B. L. (2004). Macromolecular transport and signaling through plasmodesmata. International Review of Cytology, 235, 93–164.

    PubMed  CAS  Google Scholar 

  • Herbers, K., Meuwly, P., Métraux, J.-P., & Sonnewald, U. (1996). Salicylic acid-independent induction of pathogenesis-related protein transcripts by sugars is dependent on leaf developmental stage. FEBS Letters, 397, 239–244.

    PubMed  CAS  Google Scholar 

  • Holdaway-Clarke, T. L., Walker, N. A., Hepler, P. K., & Overall, R. L. (2000). Physiological elevations in cytoplasmic free calcium by cold or ion injection result in transient closure of higher plant plasmodesmata. Planta, 210, 329–335.

    PubMed  CAS  Google Scholar 

  • Hunt, J. V., Dean, R. T., & Wolff, S. P. (1988). Hydroxyl radical production and autoxidative glycosylation. Glucose autoxidation as the cause of protein damage in the experimental glycation model of diabetes mellitus and ageing. Biochemical Journal, 256, 205–212.

    PubMed  CAS  Google Scholar 

  • Hussain, K., Nawaz, K., Majeed, A., Ilyas, U., Lin, F., Ali, K., et al. (2011). Role of exogenous salicylic acid applications for salt tolerance in violet. Sarhad Journal of Agriculture, 27, 171–175.

    Google Scholar 

  • Iqbal, M., & Ashraf, M. (2005). Changes in growth, Role of glycine betaine and salicylic acid, photosynthetic capacity and ionic relations in spring wheat (Triticum aestivum L.). Plant Growth Regulation, 60, 41–52.

    Google Scholar 

  • Iqbal, M., & Ashraf, M. (2006). Wheat seed priming in relation to salt toleration: Growth, yield and levels of free salicylic acid and polyamines. Annales Botanici Fennici, 43, 250–259.

    CAS  Google Scholar 

  • Jacobs, A. K., Lipka, V., Burton, R. A., Panstruga, R., Strizhov, N., Schulze-Lefert, P., et al. (2003). An Arabidopsis callose synthase, GSL 5, is required for wound and papillary callose formation. Plant Cell, 15, 2503–2513.

    PubMed  CAS  Google Scholar 

  • Jayalakshmi, P., Suvarnalatha, D. P., Prasanna, N. D., Revathi, G., & Shaheen, S. K. (2010). Morphological and physiological changes of groundnut plants by foliar application with salicylic acid. Biosean, 5, 193–195.

    CAS  Google Scholar 

  • Kang, M. K., Park, K. S., & Choi, D. (1998). Coordinated expression of defense-related genes by TMV infection or salicylic acid treatment in tobacco. Molecules and Cells, 31, 388–392.

    Google Scholar 

  • Kartusch, R. (2003). On the mechanism of callose synthesis induction by metal ions in onion epidermal cells. Protoplasma, 220, 219–225.

    PubMed  CAS  Google Scholar 

  • Kauss, H. (1985). Callose biosynthesis as a Ca2+-regulated process and possible relations to the induction of other metabolic changes. Journal of Cell Science. Supplement, 2, 89–103.

    PubMed  CAS  Google Scholar 

  • Kaveh, S. H., Bernard, F., & Samiee, K. (2004). Growth stimulation and enhanced invertase activity induced by salicylic acid in tea cuttings (Camellia sinensis L.). In Proceedings of IV International Iran-Russia Conference (pp. 113–116).

    Google Scholar 

  • Kawano, T. (2003). Roles of the reactive oxygen species-generating peroxidase reactions in plant defense and growth induction. Plant Cell Reports, 21, 829–837.

    PubMed  CAS  Google Scholar 

  • Kawano, T., & Furuichi, T. (2007). Salicylic acid as a defense-related plant hormone. Roles of oxidative and calcium signaling paths in salicylic acid biology. In: S. Hayat & A. Ahmad (Eds.) Salicylic acid: A plant hormone (pp. 277–321). Dordrecht: Springer.

    Google Scholar 

  • Kawano, T., Nobuya, S., Takahashi, S., Uozumi, N., & Muto, S. (1998). Salicylic acid induces extracellular superoxide generation followed by an increase in cytosolic calcium ion in tobacco suspension culture: The earliest events in salicylic acid signal transduction. Plant and Cell Physiology, 39, 721–730.

    CAS  Google Scholar 

  • Keller, C. P., Barkosky, R. R., Seil, J. E., Mazurek, S. A., & Grundstad, M. L. (2008). The electrical response of Phaseolus vulgaris roots to abrupt exposure to hydroquinone. Plant Signaling & Behavior, 3, 633–640.

    Google Scholar 

  • Kempers, R., Ammerlaan, A., & van Bel, A. J. E. (1998). Symplasmic constriction and ultrastructural features of the sieve element/companion cell complex in the transport phloem of apoplasmically and symplasmically loading species. Plant Physiology, 116, 271–278.

    CAS  Google Scholar 

  • Khan, S. U., Bano, A., & Jalal-ud-Din, G. A. (2012). Abscisic acid and salicylic acid seed treatment as potent inducer of drought tolerance in wheat (Triticum aestivum L.). Pakistan Journal of Botany, 44, 43–49, Special issue.

    Google Scholar 

  • Khan, W., Prithviraj, B., & Smith, D. L. (2003). Photosynthetic responses of corn and soybean to foliar application of salicylates. Journal of Plant Physiology, 160, 485–492.

    PubMed  CAS  Google Scholar 

  • Khodary, S. E. A. (2004). Effect of salicylic acid on the growth, photosynthesis and carbohydrate metabolism in salt stressed maize plants. International Journal of Agriculture & Biology, 6, 5–8.

    CAS  Google Scholar 

  • Klessig, D. F., & Malamy, J. (1994). The salicylic acid signal in plants. Plant Molecular Biology, 26, 1439–1458.

    PubMed  CAS  Google Scholar 

  • Knoblauch, M., & van Bel, A. J. E. (1998). Sieve tubes in action. Plant Cell, 10, 35–50.

    CAS  Google Scholar 

  • Knoblauch, M., Stubenrauch, M., van Bel, A. J. E., & Peters, W. S. (2012). Forisome performance in artificial sieve tubes. Plant, Cell and Environment, 35, 1419–1427.

    PubMed  Google Scholar 

  • Kobayashi, I., & Hakuno, H. (2003). Actin-related defense mechanism to reject penetration attempt by a non-pathogen is maintained in tobacco BY-2 cells. Planta, 217, 340–345.

    PubMed  CAS  Google Scholar 

  • Köhle, H., Jeblick, W., Poten, F., Blaschek, W., & Kauss, H. (1985). Chitosan-elicited callose synthesis in soybean cells as a Ca2+-dependent process. Plant Physiology, 77, 544–551.

    PubMed  Google Scholar 

  • Krasavina, M. S. (2007). Effect of salicylic acid on solute transport in plants. In: S. Hayat & A. Ahmad (eds.) Salicylic acid: A plant hormone (pp. 25–68). Dordrecht: Springer.

    Google Scholar 

  • Krasavina, M. S., Ktitorova, I. N., & Burmistrova, N. A. (2001). Electrical conductance of cell-to-cell junctions and cytoskeleton of plant cells. Russian Journal of Plant Physiology, 48, 741–748.

    CAS  Google Scholar 

  • Krasavina, M. S., Malyshenko, S. I., Raldugina, G. N., Burmistrova, N. A., & Nosov, A. V. (2002). Can salicylic acid affect the intercellular transport of the tobacco mosaic virus by changing plasmodesmal permeability? Russian Journal of Plant Physiology, 49, 61–67.

    CAS  Google Scholar 

  • Kuhn, C., & Grof, C. P. L. (2010). Sucrose transporters of higher plants. Current Opinion in Plant Biology, 13, 288–298.

    PubMed  Google Scholar 

  • Kuhn, C., Hajirezaei, M. R., Fernie, A. R., Roessner-Tunali, U., Czechowski, T., Hirner, B., et al. (2003). The sucrose transporter StSUT1 localizes to sieve elements in potato tuber phloem and influences tuber physiology and development. Plant Physiology, 131, 102–113.

    PubMed  CAS  Google Scholar 

  • Ladyzhenskaya, E. P., & Korablyova, N. P. (2011). Effect of salicylic acid on the proton translocation activity of plasmalemma of potato tuber cells. Applied Biochemistry and Microbiology, 47, 479–483. (in Russian).

    Google Scholar 

  • Lalonde, S., Wipf, D., & Frommer, W.B. (2004). Transport mechanisms for organic forms of carbon and nitrogen between source and sink. Annual Review of Plant Biology, 55, 341–372.

    Google Scholar 

  • Lalonde, S., Tegeder, M., Throne-Holst, M., Frommer, W. B., & Patrick, J. W. (2003). Phloem loading and unloading of sugars and amino acids. Plant, Cell and Environment, 26, 37–56.

    CAS  Google Scholar 

  • Lee, J. Y., Wang, X., Cui, W., Sage, R., Modla, S., Czymmek, K., et al. (2011). A plasmodesmata-localized protein mediates crosstalk between cell-to-cell communication and innate immunity in Arabidopsis. Plant Cell, 23, 3353–3373.

    PubMed  CAS  Google Scholar 

  • Lee, J. Y., & Lu, H. (2011). Plasmodesmata: The battle ground against intruders. Trends in Plant Science, 16, 201–210.

    PubMed  CAS  Google Scholar 

  • Levy, A., Erlanger, M., Rosenthal, M., & Epel, B. L. (2007). A plasmodesmata-associated beta-1,3-glucanase in Arabidopsis. The Plant Journal, 49, 669–682.

    PubMed  CAS  Google Scholar 

  • Liesche, J., & Schulz, A. (2012). In vivo quantification of cell coupling in plants with different phloem-loading strategies. Plant Physiology, 159, 355–365.

    PubMed  CAS  Google Scholar 

  • Liu, Y., Liu, H., Pan, Q., Yang, H., Zhanm, J., & Huang, W. (2009a). The plasma membrane H+-ATPase is related to the development of salicylic acid-induced thermotolerance in pea leaves. Planta, 229, 1087–1098.

    PubMed  CAS  Google Scholar 

  • Liu, Y., Zhang, J., Liu, H., & Huang, W. (2008). Salicylic acid or heat acclimation pre-treatment enhances the plasmamembrane-associated ATPase activities in young grape plants under heat shock. Scientia Horticulturae, 119, 21–27.

    CAS  Google Scholar 

  • Loutfy, N., El-Tayeb, M. A., Hassanen, A. M., Moustafa, M. F., Sakuma, Y., & Inouhe, M. (2012). Changes in the water status and osmotic solute contents in response to drought and salicylic acid treatments in four different cultivars of wheat (Triticum aestivum). Journal of Plant Research, 125, 173–184.

    PubMed  CAS  Google Scholar 

  • Lucas, W. J., & Lee, J.-Y. (2004). Plasmodesmata as a supracellular control network in plants. Nature Reviews Molecular Cell Biology, 5, 712–726.

    PubMed  CAS  Google Scholar 

  • Lucas, W. J., Ham, B. K., & Kim, J. Y. (2009). Plasmodesmata—bridging the gap between neighboring plant cells. Trends in Cell Biology, 19, 495–503.

    PubMed  CAS  Google Scholar 

  • Lyalin, O. O., Ktitorova, I. N., Barmicheva, E. M., & Achmedov, N. I. (1986). Intercellular connections in submersed trichomes of Salvinia. Fiziologia Rastenij, 33, 432–446. (in Russian).

    Google Scholar 

  • Maria, E. B., José, D. A., Maria, C. B., & Francisco, P. A. (2000). Carbon partitioning and sucrose metabolism in tomato plants growing under salinity. Physiologia Plantarum, 110, 503–511.

    Google Scholar 

  • Maslenkova, L., Peeva, V., Stojnova, Zh., & Popova, L. (2009). Salicylic acid-induced changes in photosystem II reactions in barley plants. Biotechnology and Biotechnological Equipment, 23, 297–300.

    Google Scholar 

  • Mathur, N., & Vyas, A. (2007). Physiological effect of some bioregulators on vegetative growth, yield and chemical constituents of pearl millet (Pennisetum typhoides (Burm) Stapf. and Hubb). International Journal of Agricultural Research, 2, 238–245.

    CAS  Google Scholar 

  • McAinsh, M. R., & Pittman, J. K. (2009). Shaping the calcium signature. New Phytologist, 181, 275–294.

    PubMed  CAS  Google Scholar 

  • McNairn, R. B., & Currier, H. B. (1968). Translocation blockage by sieve plate callose. Planta, 82, 369–380.

    Google Scholar 

  • Minchin, P. E. H., & Thorpe, M. R. (1987). Measurement of unloading and reloading of photo-assimilate within the stem of bean. Journal of Experimental Botany, 38, 211–220.

    Google Scholar 

  • Mishra, A., & Choudhuri, M. A. (1999). Effect of salicylic acid on heavy metal-induced membrane deterioration mediated by lipoxygenase in rice. Biologia Plantarum, 42, 409–415.

    CAS  Google Scholar 

  • Misra, N., & Saxena, P. (2009). Effect of salicylic acid on proline metabolism in lentil grown under salinity stress. Plant Science, 177, 181–189.

    CAS  Google Scholar 

  • Morgan, J. M. (1994). Osmoregulation and water-stress in higher-plants. Annual Review of Plant Physiology, Plant Molecular Biology, 35, 299–319.

    Google Scholar 

  • Mostajeran, A., & Rahimi-Eichi, V. (2009). Effects of drought on growth and yield of rice (Oryza sativa L.) cultivars and accumulation of proline and soluble sugars in sheath and blades of their different age leaves. American-Eurasian Journal of Environmental Sciences, 5, 264–272.

    CAS  Google Scholar 

  • Mullendore, D. L., Windt, C. W., van As, H., & Knoblauch, M. (2010). Sieve tube geometry in relation to phloem flow. Plant Cell, 22, 579–593.

    Google Scholar 

  • Murphy, A. M., & Carr, J. P. (2002). Salicylic acid has cell-specific effects on Tobacco mosaic virus replication and cell-to-cell movement. Plant Physiology, 128, 552–563.

    PubMed  CAS  Google Scholar 

  • Najafian, S., Khoshkhui, M., Tavallali, V., & Saharkhiz, M. J. (2009). Effect of salicylic acid and salinity in thyme (Thymus vulgaris L.): Investigation on changes in gas exchange, water relations, and membrane stabilization and biomass accumulation. Australian Journal of Basic and Applied Sciences, 3, 2620–2626.

    CAS  Google Scholar 

  • Neuenschwander, U., Vernooij, B., Friedrich, L., Uknes, S., Kessmann, H., & Ryals, J. (1995). Is hydrogen peroxide a second messenger of salicylic acid in systemic acquired resistance? The Plant Journal, 8, 227–233.

    CAS  Google Scholar 

  • Nishimura, M. T., Stein, M., Hou, B., Vogel, J. P., Edwards, H., & Somerville, S. C. (2003). Loss of a callose synthase results in salicylic acid-dependent disease resistance. Science, 301, 969–972.

    PubMed  CAS  Google Scholar 

  • Oparka, K. J., Duckett, C. M., Prior, D. A. M., & Fisher, D. M. (1994). Real time imaging of phloem unloading in the root tip of Arabidopsis. The Plant Journal, 5, 756–766.

    Google Scholar 

  • Oparka, K. J., & Roberts, A. G. (2001). Plasmodesmata. A not so open-and-shut case. Plant Physiology, 125, 123–126.

    PubMed  CAS  Google Scholar 

  • Ostergaard, L., Petersen, M., Mattsson, O., & Mundy, J. (2002). An Arabidopsis callose synthase. Plant Molecular Biology, 49, 559–566.

    PubMed  CAS  Google Scholar 

  • Patrick, J. W. (1997). Phloem unloading: sieve element unloading and post-sieve element transport. Annual Review of Plant Physiology, Plant Molecular Biology, 28, 165–190.

    Google Scholar 

  • Pei, Z. M., Murata, Y., Benning, G., Thomine, S., Klusener, B., Allen, G. J., et al. (2000). Calcium channels activated by hydrogen peroxidase mediate abscisic acid signaling in guard cells. Nature, 406, 731–734.

    PubMed  CAS  Google Scholar 

  • Petersen, M., Brodersen, P., Naested, H., Andreasson, E., Lindhart, U., Johansen, B., Nielsen, H. B., Lacy, M., Austin, M. J., Parker, J. E., Sharma, S. B., Klessig, D. F., Martienssen, R., Mattsson, O., Jensen, A. B., & Mundy, J. (2000). Arabidopsis map kinase 4 negatively regulates systemic acquired resistance. Cell, 103, 1111–1120.

    Google Scholar 

  • Prudnikov, G. A., Panichkin, L. A., & Krasavina, M. S. (2010). Effect of ion channel blockers and H+-ATPase inhibitors on generation of local electrical response in a cucumber leaf. Russian Journal of Plant Physiology, 57, 865–874.

    CAS  Google Scholar 

  • Qudeimat, E., & Frank, W. (2009). Ca2+ signatures: the role of Ca2+-ATPases. Plant Signaling & Behavior, 4, 350–352.

    CAS  Google Scholar 

  • Radford, J. E., Vesk, M., & Overall, R. L. (1998). Callose deposition at plasmodesmata. Protoplasma, 201, 30–37.

    CAS  Google Scholar 

  • Rai, V. K., Sharma, S. S., & Sharma, S. (1986). Reversal of ABA–induced stomatal closure by phenolic compounds. Journal of Experimental Botany, 37, 129–134.

    CAS  Google Scholar 

  • Reinders, A., Schulze, W., Kuhn, C., Barker, L., Schulz, A., Ward, J. M., et al. (2002). Protein–protein interactions between sucrose transporters of different affinities colocalized in the same enucleate sieve element. Plant Cell, 14, 1567–1577.

    PubMed  CAS  Google Scholar 

  • Rennie, E. A., & Turgeon, R. (2009). A comprehensive picture of phloem loading strategies. Proceedings of the National Academy of Sciences of the United States of America, 106, 14162–14167.

    PubMed  CAS  Google Scholar 

  • Roberts, A. G., & Oparka, K. J. (2003). Plasmodesmata and the control of symplasmic transport. Plant, Cell and Environment, 26, 103–124.

    Google Scholar 

  • Ruan, Y. L., & Patrick, J. W. (1995). The cellular pathway of postphloem sugar-transport in developing tomato fruit. Planta, 196, 434–444.

    CAS  Google Scholar 

  • Ruiz-Medrano, R., Xoconostle-Cazares, B., & Kragler, F. (2004). The plasmodesmatal transport pathway for homeotic proteins, silencing signals and viruses. Current Opinion in Plant Biology, 7, 641–650.

    PubMed  CAS  Google Scholar 

  • Russell, J. W., Golovoy, D., Vincent, A. M., Mahendru, P., Olzmann, J. A., Mentzer, A., et al. (2002). High glucose-induced oxidative stress and mitochondrial dysfunction in neurons. The FASEB Journal, 16, 1738–1748.

    CAS  Google Scholar 

  • Sahar, K., Amin, B., & Taher, N. M. (2011). The salicylic acid effect on the Salvia officinalis L. sugar protein and prolin contents under salinity (NaCl) stress. Journal of Stress Physiology and Biochemistry, 7, 80–87.

    Google Scholar 

  • Samardakiewicz, S., KrzesÅ‚owska, M., Bilski, H., Bartosiewicz, R., & Woźny, A. (2012). Is callose a barrier for lead ions entering Lemna minor L. root cells? Protoplasma, 249, 347–351.

    PubMed  CAS  Google Scholar 

  • Sauer, N. (2007). Molecular physiology of higher plant sucrose transporters. FEBS Letters, 581, 2309–2317.

    PubMed  CAS  Google Scholar 

  • Scholthof, H. B. (2005). Plant virus transport: motions of functional equivalence. Trends in Plant Science, 10, 376–382.

    PubMed  CAS  Google Scholar 

  • Schroeder, J. I., & Hagiwara, S. (1989). Cytosolic calcium regulates ion channels in plasma membrane of Vicia faba guard cells. Nature, 338, 427–430.

    Google Scholar 

  • Schulz, A. (2005) Role of plasmodesmata in solute loading and unloading. In: K. J. Oparka (Ed.) Plasmodesmata. Annual Plant Reviews (Vol. 18, pp. 135–161). Oxford: Blackwell Science.

    Google Scholar 

  • Serova, V. V., Raldugina, G. N., & Krasavina, M. S. (2006). Inhibition of callose hydrolysis by salicylic acid disturbs transport of tobacco mosaic virus. Doklady Biochemistry and Biophysics, 406, 36–39.

    PubMed  CAS  Google Scholar 

  • Shah, J., & Klessig, D. F. (1996). Identification of a salicylic acid-responsive element in the promoter of the tobacco pathogenesis-related β-1,3-glucanase gene, PR-2d. The Plant Journal, 10, 1089–1101.

    PubMed  CAS  Google Scholar 

  • Shaaban, M. M., Abd El-Aal A. M. K., & Ahmed, F. F. (2011). Insight into the effect of salicylic acid on apple trees growing under sandy saline. Soil Research Journal of Agricultural and Biological Science, 7, 150–156.

    Google Scholar 

  • Shakirova, F. M., Sakhabutdinova, D. R., Bezrukova, M. V., Fatkhutdinova, R. F., & Fatkhutdinova, D. R. (2003). Changes in the hormonal status of wheat seedlings induced by salicylic acid and salinity. Plant Science, 164, 317–322.

    CAS  Google Scholar 

  • Shehata, S. A. M., Ibrahim, S. I., & Zaghlool, S. A. M. (2001). Physiological response of flag leaf and ears of maize plant induced by foliar application of kinetin and acetyl salicylic acid. Annals of Agricultural Science, Ain Shams University Cairo, 46, 435–449.

    Google Scholar 

  • Shimoura, T., & Dijkstra, J. (1975). The occurrence of callose during the process of local lesion formation. Netherlands Journal of Plant Pathology, 81, 107–121.

    Google Scholar 

  • Siegel, R. S., Xue, S., Murata, Y., Yang, Y., Nishimura, N., Wang, A., et al. (2009). Calcium elevation-dependent and attenuated resting calcium-dependent abscisic acid induction of stomatal closure and abscisic acid-induced enhancement of calcium sensitivities of S-type anion and inward-rectifying K channels in Arabidopsis guard cells. The Plant Journal, 59, 207–220.

    PubMed  CAS  Google Scholar 

  • Simpson, C., Thomas, C., Findlay, K., Bayer, E., & Maule, A. J. (2009). An Arabidopsis GPI-anchor plasmodesmal neck protein with callose binding activity and potential to regulate cell-to-cell trafficking. Plant Cell, 21, 581–594.

    PubMed  CAS  Google Scholar 

  • Singh, B., & Usha, K. (2003). Salicylic acid induced physiological and biochemical changes in wheat seedlings under water stress. Plant Growth Regulation, 39, 137–141.

    CAS  Google Scholar 

  • Sinha, S. K., Srivastava, H. S., & Tripathi, R. B. (1993). Influence of some growth regulators and cations on inhibition of chlorophyll biosynthesis by lead in Maize. Bulletin of Environmental Contamination and Toxicology, 51, 241–246.

    PubMed  CAS  Google Scholar 

  • Slewinski, T. L., & Braun, D. M. (2010). Current perspectives on the regulation of whole-plant carbohydrate partitioning. Plant Science, 178, 341–349.

    CAS  Google Scholar 

  • Sondergaard, T. E., Schulz, A., & Palmgren, M. G. (2004). Energization of transport processes in plants. Roles of the plasma membrane H+-ATPase. Plant Physiology, 136, 2475–2482.

    PubMed  CAS  Google Scholar 

  • Srivastava, A. C., Ganesan, S., Ismail, I. O., & Ayre, B. G. (2008). Functional characterization of the Arabidopsis AtSUC2 sucrose/H+ symporter by tissue-specific complementation. Reveals an essential role in phloem loading but not in long-distance transport. Plant Physiology, 148, 200–211.

    PubMed  CAS  Google Scholar 

  • Srivastava, A. C., Dasgupta, K., Ajieren, E., Costilla, G., McGarry, R. C., & Ayre, B. G. (2009). Arabidopsis plants harbouring a mutation in AtSUC2, encoding the predominant sucrose/proton symporter necessary for efficient phloem transport, are able to complete their life cycle and produce viable seed. Annals of Botany, 104, 1121–1128.

    PubMed  CAS  Google Scholar 

  • Stadler, R., Lauterbach, C., & Sauer, N. (2005a). Cell-to-cell movement of green fluorescent protein reveals post-phloem transport in the outer integument and identifies symplastic domains in Arabidopsis seeds and embryos. Plant Physiology, 139, 701–712.

    PubMed  CAS  Google Scholar 

  • Stadler, R., Wright, K. M., Lauterbach, C., Amon, G., Gahrtz, M., Feuerstein, A., et al. (2005b). Expression of GFP-fusions in Arabidopsis companion cells reveals nonspecific protein trafficking into sieve elements and identifies a novel post-phloem domain in roots. The Plant Journal, 41, 319–331.

    PubMed  CAS  Google Scholar 

  • Stonebloom, S., Brunkard, J., Cheung, A., Jiang, K., Feldman, L., & Zambryski, P. (2012). Redox states of plastids and mitochondria differentially regulate intercellular transport via plasmodesmata. Plant Physiology, 158, 190–199.

    PubMed  CAS  Google Scholar 

  • Stonebloom, S., Burch-Smith, T., Kim, I., Meinke, D., Mindrinos, M., & Zambryski, P. (2009). Loss of the plant DEAD-box protein ISE1 leads to defective mitochondria and increased cell-to-cell transport via plasmodesmata. Proceedings of the National Academy of Sciences of the United States of America, 106, 17229–17234.

    PubMed  CAS  Google Scholar 

  • Summermatter, K., Sticher, L., & Metraux, J. P. (1995). Systemic responses in Arabidopsis thaliana infected and challenged with Pseudomonas syringae pv syringae. Plant Physiology, 108, 1379-1385.

    Google Scholar 

  • Thompson, M. V. (2006). Phloem: The long and the short of it. Trends in Plant Science, 11, 26–32.

    PubMed  CAS  Google Scholar 

  • Truernit, E., & Sauer, N. (1995). The promoter of the Arabidopsis thaliana SUC2 sucrose–H+ symporter gene directs expression of beta-glucuronidase to the phloem: Evidence for phloem loading and unloading by SUC2. Planta, 196, 564–570.

    PubMed  CAS  Google Scholar 

  • Turgeon, R., & Gowan, E. (1990). Phloem loading in Coleus blumei in the absence of carrier-mediated uptake of export sugar from the apoplast. Plant Physiology, 94, 1244–1249.

    PubMed  CAS  Google Scholar 

  • Turgeon, R., & Medville, R. (2011). Amborella trichopoda, plasmodesmata, and the evolution of phloem loading. Protoplasma, 248, 173–180.

    PubMed  Google Scholar 

  • Ueki, S., & Citovsky, V. (2011). To gate, or not to gate: regulatory mechanisms for intercellular protein transport and virus movement in plants. Molecular Plant, 4, 782–793.

    PubMed  CAS  Google Scholar 

  • Ueki, S., Spektor, R., Natale, D. M., & Citovsky, V. (2010). ANK, a host cytoplasmic receptor for the tobacco mosaic virus cell-to-cell movement protein, facilitates intercellular transport through plasmodesmata. PLoS Pathogens, 6, 1–13.

    Google Scholar 

  • Uzunova, A. N., & Popova, L. P. (2000). Effect of salicylic acid on leaf anatomy and chloroplast ultrastructure of barley plants. Photosynthetica, 38, 243–250.

    CAS  Google Scholar 

  • Van Bel, A. J. (2003a). The phloem, a miracle of ingenuity. Plant, Cell and Environment, 26, 125–149.

    Google Scholar 

  • Van Bel, A. J. (2003b). Transport phloem: Low profile, high impact. Plant Physiology, 131, 1509–1510.

    PubMed  Google Scholar 

  • White, R.G., Badelt, K., Overall, R.L., & Vesk, M. (1994). Actin associated with plasmodesmata. Protoplasma, 180, 169–184.

    Google Scholar 

  • White, R. G., & Barton, D. A. (2011). The cytoskeleton in plasmodesmata: a role in intercellular transport? Journal of Experimental Botany, 62, 5249–5266.

    PubMed  CAS  Google Scholar 

  • Wolff, S. P., & Dean, R. T. (1987). Glucose autoxidation and protein modification. The potential role of ‘autoxidative glycosylation’ in diabetes. Biochemical Journal, 245, 243–250.

    PubMed  CAS  Google Scholar 

  • Yarullina, L. G., Troshina, N. B., Cherepanova, E. A., Zaikina, E. A., & Maksimov, I. V. (2011). Salicylic and jasmonic acids in regulation of the proantooxidant state in wheat leaves infected by Septoria nodorum Berk. Applied Biochemistry and Microbiology, 47, 602–608.

    Google Scholar 

  • Zahra, S., Amin, B., Ali, M. V. S., Ali, Y., & Mehdi, Y. (2010). The salicylic acid effect on the tomato Lycopersicum esculentum Mill.) sugar, protein and proline contents under salinity stress (NaCl). Journal of Biophysics and Structural Biology, 2, 35–41.

    Google Scholar 

  • Zavaliev, R., Ueki, S., Epel, B. L., & Citovsky, V. (2011). Biology of callose (beta-1,3-glucan) turnover at plasmodesmata. Protoplasma, 248, 117–130.

    PubMed  CAS  Google Scholar 

  • Zeidne, G., Sadja, R., & Reuveny, E. (2001). Redox-dependent gating of G protein-coupled inwardly rectifying K+ channels. Journal of Biological Chemistry, 276, 35564–35570.

    Google Scholar 

  • Zhang, W.-H., Zhou, Y., Dibley, K. E., Tyerman, S. D., Furbank, R. T., & Patrick, J. W. (2007). Nutrient loading of developing seeds. Functional Plant Biology, 34, 314–331.

    CAS  Google Scholar 

  • Zhang, X.-Y., Wang, X.-L., Wang, X.-F., Xia, G.-H., Pan, Q.-H., Fan, R.-C., et al. (2006). A shift of phloem unloading from symplasmic to apoplasmic pathway is involved in developmental onset of ripening in grape berry. Plant Physiology, 142, 220–232.

    PubMed  CAS  Google Scholar 

  • Zhen, X.-H., & Li, Y.-Z. (2004). Ultrastructural changes and location of ß-1,3-glucanase in resistant and susceptible cotton callus cells in response to treatment with toxin of Verticillium dahliae and salicylic acid. Journal of Plant Physiology, 161, 1367–1377.

    PubMed  CAS  Google Scholar 

  • Zhao, H. J., Lin, X. W., Shi, H. Z., & Chang, S. M. (1995). The regulating effects of phenolic compounds on the physiological characteristics and yield of soybeans. Acta Agronomica Sinica, 21, 351–355.

    Google Scholar 

  • Zhou, Y., Qu, H., Dibley, K. E., Offler, C. E., & Patrick, J. W. (2007). A suite of sucrose transporters expressed in coats of developing legume seeds includes novel pH-independent facilitators. The Plant Journal, 49, 750–764.

    PubMed  CAS  Google Scholar 

  • Zippel, R., & Ehwald, R. (1980). Accumulation of 2-deoxy-d-glucose in the maize radicle after import via the phloem. Biochemie und Physiologie der Pflanzen, 175, 676–680.

    CAS  Google Scholar 

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Krasavina, M.S., Burmistrova, N.A. (2013). Impact of Salicylic Acid on the Transport and Distribution of Sugars in Plants. In: Hayat, S., Ahmad, A., Alyemeni, M. (eds) SALICYLIC ACID. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-6428-6_6

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