Abstract
Short-time direct and indirect effects of 25 μM Cd on the growth of dicotyledon (Phaseolus coccineus) and monocotyledon (Allium cepa) plants were investigated in the presence of inhibitors of ethylene synthesis, NADPH oxidase, and the octadecanoid pathway. Only 5 min-long action of Cd was enough for inhibition of growth in bean roots, but its recovery time was extended to several days. After 7 h treatment, Cd was significantly accumulated in bean roots, but maximum H2O2 accumulation was seen after 1 h. Cd-induced H2O2 accumulation decreased especially after addition of ethylene inhibitor silver thiosulphate (STS). Low Cd accumulation and high growth inhibition were observed also in bean leaves and in A. cepa roots. The inhibitors of the octadecanoid pathway greatly weakened the inhibitory effect of Cd in P. coccineus roots, while no significant effect was observed in A. cepa. NADPH oxidase and ethylene blockade reversed (in the case of bean plants and indirectly treated A. cepa plants) or significantly diminished Cd action. Cd-induced growth inhibition of P. coccineus leaves was also alleviated by most inhibitors of the jasmonate pathway and by STS. These results indicate that Cd may have indirect and direct effects on growth processes.
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Abbreviations
- IB:
-
ibuprofen
- IM:
-
imidazole
- MJ:
-
methyl jasmonate
- PG:
-
propyl gallate
- ROS:
-
reactive oxygen species
- SHAM:
-
salicylhydroxamic acid
- STS:
-
silver thiosulphate
References
Cho, U.H., Seo, N.H.: Oxidative stress in Arabidopsis thaliana exposed to cadmium is due to hydrogen peroxide accumulation. — Plant Sci. 168: 113–120, 2005.
Cockcroft, C.E., Den Boer, B.G.W., Healy, J.M.S., Murray, J.A.: Cyclin D control of growth rate in plants. — Nature 404: 575–579, 2000.
Ďurčeková, K., Huttová, J., Mistrík, I., Ollé, M., Tamás, L.: Cadmium induces premature xylogenesis in barley roots. — Plant Soil 290: 61–68, 2007.
Enyedi, A.J., Yalpani, N., Silverman, P., Raskin, I.: Signal molecules in systemic plant resistance to pathogens and pests. — Cell 70: 879–886, 1992.
Fusconi, A., Gallo, C., Camusso, W.: Effects of cadmium on root apical meristems of Pisum sativum L.: cell viability, cell proliferation and microtubule pattern as suitable markers for assessment of stress pollution. — Mutat. Res. 632: 9–19, 2007.
Gianazza, E., Wait, R., Sozzi, A., Regondi, S., Saco, D., Labra, M., Agradi, E.: Growth and protein profile changes in Lepidium sativum L. plantlets exposed to cadmium. — Environ. exp. Bot. 59: 179–187, 2007.
Greger, M., Bertel, G.: Effects of Ca2+ and Cd2+ on the carbohydrate metabolism in sugar beet (Beta vulgaris). — J. exp. Bot. 247: 167–173, 1992.
Groppa, M.D., Rosales, E.P., Iannone, M.F., Benavides, M.P.: Nitric oxide, polyamines and Cd-induced phytotoxicity in wheat roots. — Phytochemistry 69: 2609–2615, 2008.
Guo, B., Liang, Y.C., Zhu, Y.G., Zhao, F.J.: Role of salicylic acid in alleviating oxidative damage in rice roots (Oryza sativa) subjected to cadmium stress. — Environ. Pollut. 147: 743–749, 2007.
Herbette, S., Taconnat, L., Hugouvieux, V., Piette, L., Magniette, M.-L.M., Cuine, S., Auroy, P., Richaud, P., Forestier, C., Bourguignon, J., Renou, J.-P., Vavasseur, A., Leonhardt, N.: Genome-wide transcriptome profiling of the early cadmium response of Arabidopsis roots and shoots. — Biochimie 88: 1751–1765, 2006.
Iakimova, E.T., Woltering, E.J., Kapchina-Toteva, V.M., Harren, F.J.M., Cristescu, S.M.: Cadmium toxicity in cultured tomato cells - role of ethylene. Proteases and oxidative stress in cell death signaling. — Cell Biol. Internat. 32: 1521–1529, 2008.
Irving, H.R., Dyson, G., McConchie, R., Parish, R.W., Gehring, C.A.: Effects of exogenously applied jasmonates on growth and intracellular pH in maize coleoptile segments. — J. Plant Growth Regul. 18: 93–100, 1999.
Karcz, W., Kurtyka, R.: Effect of cadmium on growth, proton extrusion and membrane potential in maize coleoptile segments. — Biol. Plant. 51: 713–719, 2007.
Lamb, C., Dixon, R.: The oxidative burst in plant disease resistance. — Annu. Rev. Plant Physiol. Plant mol. Biol. 48: 251–275, 1997.
Lin, C.-C., Chen, L.-M., Liu, Z.-H.: Rapid effect of copper on lignin biosynthesis in soybean roots. — Plant Sci. 168: 855–861, 2005.
Liszkay, A., Kenk, B., Schopfer, P.: Evidence for the involvement of cell wall peroxidase in the generation of hydroxyl radicals mediating extension growth. — Planta 217: 658–667, 2003.
Maciejewska, B., Kopcewicz, J.: Inhibitory effect of methyl jasmonate on flowering and elongation growth in Pharbitis nil. — J. Plant Growth Regul. 21: 216–223, 2003.
Maksymiec, W.: Effect of copper on cellular processes in higher plants. — Photosynthetica 34: 321–342, 1997.
Maksymiec, W.: Signaling responses in plants to heavy metal stress. — Acta Physiol. Plant. 29: 177–187, 2007.
Maksymiec, W., Baszyński, T.: Different susceptibility of runner bean plants to excess copper as a function of the growth stage of primary leaves. — J. Plant Physiol. 149: 217–221, 1996.
Maksymiec, W., Krupa Z.: The effects of short term exposition to Cd, excess Cu ions and jasmonate on oxidative stress appearing in Arabidopsis thaliana. — Environ. exp. Bot. 57: 187–194, 2006.
Maksymiec, W., Krupa, Z.: Effects of methyl jasmonate and excess copper on root and leaf growth. — Biol. Plant. 51: 322–326, 2007.
Maksymiec, W., Wianowska, D., Dawidowicz, A.L., Radkiewicz, S., Mardarowicz, M., Krupa, Z.: The level of jasmonic acid in Arabidopsis thaliana and Phaseolus coccineus plants under heavy metal stress. — J. Plant Physiol. 162: 1338–1346, 2005.
Merkouropoulos, G., Shirsat, A.H.: The unusual Arabidopsis extensin gene atExt1 is expressed throughout plant development and is induced by a variety of biotic and abiotic stresses. — Planta 217: 356–366, 2003.
Miyamoto, K., Oka, M., Ueda, J.: Update on the possible mode of action of the jasmonates: focus on the metabolism of cell wall polysaccharides in relation to growth and development. — Physiol. Plant. 100: 631–638, 1997.
Moya, J.L., Ros, R., Picazo, I.: Influence of cadmium and nickel on growth, net photosynthesis and carbohydrate distribution on rice plants. — Photosynth. Res. 36: 75–80, 1993.
Orozco-Cárdenas, M.L., Narváez-Vásquez, J., Ryan, C.A.: Hydrogen peroxide acts as a second messenger for the induction of defense genes in tomato plants in response to wounding, systemin, and methyl jasmonate. — Plant Cell 13: 179–191, 2001.
Ortega-Villasante, C., Hernández, L.E., Rellán-Álvarez, R., Del Campo, F., Carpena-Ruiz, R.O.: Rapid alteration of cellular redox homeostasis upon exposure to cadmium and mercury in alfalfa seedlings. — New Phytol. 176: 96–107, 2007.
Papadakis, A.K., Roubelakis-Angelakis, K.A.: The generation of active oxygen species differs in tobacco and grapevine mesophyll protoplasts. — Plant Physiol. 121: 197–205, 1999.
Pasternak, T., Rudas, V., Potters, G., Jansen, M.A.K.: Morphogenic effects of abiotic stress: reorientation of growth in Arabidopsis thaliana seedlings. — Environ. exp. Bot. 53: 299–314, 2005.
Pick, E.: Microassays for superoxide and hydrogen peroxide production and nitroblue tetrazolium reduction using an enzyme immunoassay microplate reader. — Methods Enzymol. 132: 407–421, 1986.
Poschenrieder, C., Gunsé, B., Barceló, J.: Influence of cadmium on water relations, stomatal resistance, an abscisic acid content in expanding bean leaves. — Plant Physiol. 90: 1365–1371, 1989.
Quartacci, M.F., Cosi, E., Navari-Izzo, F.: Lipids and NADPH-dependent superoxide production in plasma membrane vesicles from roots of wheat grown under copper deficiency or excess. — J. exp. Bot. 52: 77–84, 2001.
Ranieri, A., Castagna, A., Scebba, F., Careri, M., Zagnoni, I., Predieri, G., Pagliari, M., Sanità di Toppi, L.: Oxidative stress and phytochelatin characterisation in bread wheat exposed to cadmium excess. — Plant Physiol. Biochem. 43: 45–54, 2005.
Sabreen, S., Sugiyama, S.: Trade-off between cadmium tolerance and relative growth rate in 10 grass species. — Environ. exp. Bot. 63: 327–332, 2008.
Sandalio, L.M., Dalurzo, H.C., Gómez, M., Romero-Puertas, M.C., del Río, L.A.: Cadmium-induced changes in the growth and oxidative metabolism of pea plants. — J. exp. Bot. 52: 2115–2126, 2001.
Saniewski, M., Ueda, J., Miyamoto, K.: Relationships between jasmonates and auxin in regulation of some physiological processes in higher plants. — Acta Physiol. Plant. 24: 211–220, 2002.
Saniewski, M., Urbanek, H., Czapski, J.: Effects of methyl jasmonate on ethylene production, chlorophyll degradation, and polygalacturonase activity in tomatoes. — J. Plant Physiol. 127: 177–181, 1987.
Schützendübel, A., Schwanz, P., Teichmann, T., Gross, K., Langenfeld-Heyser, R., Godbold, D.L., Polle, A.: Cadmium-induced changes in antioxidateive systems, hydrogen peroxide content, and differentiation in Scots pine roots. — Plant Physiol. 127: 887–898, 2001.
Skórzyńska, E., Baszyński, T.: The modifying effect of calcium on Cd-treated runner bean plants. The level of carbohydrates. — In: Garab, G. (ed.): Photosynthesis: Mechanisms and Effects. Pp. 2673–2676. Kluwer Academic Publishers, Dordrecht - Boston - London 1998.
Sobkowiak, R., Dekert, J.: Cadmium-induced changes in growth and cell cycle gene expression in suspension-culture cells of soybean. — Plant Physiol. Biochem. 41: 767–772, 2003.
Świątek, A., Lenjou, M., Van Bockstaele, D., Inzé, D., Van Onckelen, H.: Differential effect of jasmonic acid and abscisic acid on cell cycle progression in tobacco BY-2 cells. — Plant Physiol. 128: 201–211, 2002.
Trivedi, S., Erdei, L.: Effects of cadmium and lead on the accumulation of Ca2+ and K+ and on the influx and translocation of K+ in wheat of low and high K+ status. — Physiol. Plant. 84: 94–100, 1992.
Ueda, J., Miyamamoto, K., Kamisaka, S.: Inhibition of the synthesis of cell wall polysaccharides in oat coleoptile segments by jasmonic acid. Relevance to its growth inhibition. — J. Plant Growth Regul. 14: 69–76, 1995.
Vassiliev, A., Lidon, F., Da Graca, M., Yordanov, I.: Cadmiuminduced changes in chloroplast lipids and photosystem activities in barley plants. — Biol. Plant. 48: 153–156, 2004.
Vecchia, F.D., La Rocca, N., Moro, I., De Faveri, S., Andreoli, C., Rascio, N.: Morphogenetic, utrastructural and physiological damages suffered by submerged leaves of Elodea canadensis exposed to cadmium. — Plant Sci. 168: 329–338, 2005.
Yeh, C.-M., Chien, P.-S., Huang, H.-J.: Distinct signalling pahways for induction of MAP kinase activities by cadmium and copper in rice roots. — J. exp. Bot. 58: 659–671, 2007.
Zawoznik, M.S., Groppa, M.D., Tomaro, M.L., Benavides, M.P.: Endogenous salicylic acid potentiates cadmiuminduced oxidative stress in Arabidopsis thaliana. — Plant Sci. 173: 190–197, 2007.
Xu, P., Liu, D., Jiang, W.: Cadmium effects on the organization of microtubular cytoskeleton in interphase and mitotic cells of Allium sativum. — Biol. Plant. 53: 387–390, 2009.
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Maksymiec, W. Effects of jasmonate and some other signalling factors on bean and onion growth during the initial phase of cadmium action. Biol Plant 55, 112–118 (2011). https://doi.org/10.1007/s10535-011-0015-9
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DOI: https://doi.org/10.1007/s10535-011-0015-9