Effects of mechanical damage and herbivore wounding on H2O2 metabolism and antioxidant enzyme activities in hybrid poplar leaves

Yu An , Ying-bai Shen , Zhi-xiang Zhang

Journal of Forestry Research ›› 2009, Vol. 20 ›› Issue (2) : 156 -160.

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Journal of Forestry Research ›› 2009, Vol. 20 ›› Issue (2) : 156 -160. DOI: 10.1007/s11676-009-0027-x
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Effects of mechanical damage and herbivore wounding on H2O2 metabolism and antioxidant enzyme activities in hybrid poplar leaves

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Abstract

The changes of hydrogen peroxide (H2O2) metabolism and antioxidant enzyme activities in a hybrid poplar (Populus simonii × P. pyramidalis ‘Opera 8277’) in response to mechanical damage (MD) and herbivore wounding (HW) were investigated to determine whether H2O2 could function as the secondary messenger in the signaling of systemic resistance. Results show that H2O2 was generated in wounded leaves through MD and HW treatments and systemically in unwounded leaves around the wounded leaves. The activities of antioxidant enzymes such as superoxide dismutase (SOD), catalase (CAT) and ascorbate peroxidase (APX) were also enhanced. However, the H2O2 accumulation and antioxidant enzyme activities were inhibited in MD leaves through the pretreatment with DPI (which is a specific inhibitor of NADPH oxidase). The results of this study suggest that H2O2 could be systemically induced by MD and HW treatments, and H2O2 metabolism was closely related to the change in SOD, APX and CAT activities. A high level of antioxidant enzymes could decrease membrane lipid peroxidation levels and effectively induce plant defense responses.

Keywords

antioxidant enzymes / herbivore wound / induced resistance / mechanical damage / reactive oxygen species

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Yu An, Ying-bai Shen, Zhi-xiang Zhang. Effects of mechanical damage and herbivore wounding on H2O2 metabolism and antioxidant enzyme activities in hybrid poplar leaves. Journal of Forestry Research, 2009, 20(2): 156-160 DOI:10.1007/s11676-009-0027-x

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References

[1]

Blokhina O., Virolainen E., Fagerstedt K.V.. Antioxidants, oxidative damage and oxygen deprivation stress: a review. Annals of Botany, 2003, 91: 179-194.

[2]

Bochkov V.N., Kadl A., Huber J., Gruber F., Binder B.R., Leitinger N.. Protection role of phospholipids oxidation products in endotoxin-induced tissue damage. Nature, 2002, 419: 77-81.

[3]

Bolwell G.P., Blee K.A., Butt V.S., Davies D.R., Gardner S.L., Gerrish C., Minibayeva F., Rowntree E.G., Wojtaszek P.. Recent advances in understanding the origin of the apoplastic oxidative burst in plant cells. Free Radical Research, 1999, 31: 137-145.

[4]

Bostock R.M., Karban R., Thaler J.S., Weyman P.D., Gilchrist D.. Signal interactions in induced resistance to pathogens and insect herbivores. European Journal of Plant Pathology, 2001, 107: 103-111.

[5]

Bowler C., Fluhr R.. The role of calcium and activated oxygen as signals for controlling cross-tolerance. Trends in Plant Science, 2000, 5: 241-246.

[6]

Bowler C., Van Montagu M., Inzé D.. Superoxide dismutase and stress tolerance. Annual Review of Plant Physiology and Plant Molecular Biology, 1992, 43: 83-116.

[7]

Chandru H.K., Kim E., Kuk Y., Cho K., Han O.. Kinetics of wound-induced activation of antioxidative enzymes in Oryza Sativa: differential activation at different growth stages. Plant Science, 2003, 164: 935-941.

[8]

Chang C.C., Ball L., Fryer M.J., Baker N.R., Karpinski S., Mullineaux P.M.. Induction of ascorbate peroxidase 2 expression in wounded Arabidopsis leaves does not involve known wound-signalling pathways but is associated with changes in photosynthesis. Plant Journal, 2004, 38: 499-511.

[9]

Chen J., Wang Q., Zhang J.. The change of superoxide dismutase’s activity in bean sprout under stress circumstance. Journal of Shanghai Normal University (Natural Sciences), 2007, 36: 49-53.

[10]

Costet L., Cordilier S., Dorey S., Baillieul F., Fritig B., Kauffmann S.. Relationship between localized acquired resistance (LAR) and the hypersensitive response (HR): HR is necessary for LAR to occur and salicylic acid is not sufficient to trigger LAR. Molecular Plant Microbe Interactions, 1999, 8: 655-662.

[11]

Dat J.F., Vandenabeele S., Vranová E., Van Montagu M., Inzé D., Van Breuseqem F.. Dual action of the active oxygen species during plant stress responses. Cellular and Molecular Life Sciences, 2000, 57: 779-795.

[12]

De Vos M., Van Zaanen W., Koornneef A., Korzelius J.P., Dicke M., Van Loon L.C., Pieterse C.M.J.. Herbivore-induced resistance against microbial pathogens in Arabidopsis. Plant Physiology, 2006, 142: 352-363.

[13]

del Río L.A., Corpas F.J., Sandalio L.M., Palma J.M., Gómez M., Barroso J.B.. Reactive oxygen species, antioxidant systems, and nitric oxide in peroxisomes. Journal of Experimental Botany, 2002, 53: 1255-1272.

[14]

Doke N., Miura Y., Sanchez L.M., Park H.J., Noritake T., Yoshioka H., Kavakita K.. The oxidative burst protects plants against pathogen attack: mechanism and role as an emergency signal for plant bio-defence. Gene, 1996, 179: 45-51.

[15]

Fath A., Bethke P., Belligni V., Jones R.. Active oxygen and cell death in cereal aleurone cells. Journal of Experiment Botany, 2002, 53: 1273-1282.

[16]

Guan L.M., Scandalios J.G.. Hydrogen peroxide-mediated catalase gene expression in response to wounding. Free Radical Biology and Medicine, 2000, 28: 1182-1190.

[17]

Lamb C.J., Dixon R.A.. The oxidative burst in plant resistance. Annual Review of Plant Physiology and Plant Molecular Biology, 1997, 48: 251-275.

[18]

Leitner M., Boland W., Mithöfer A.. Direct and indirect defences induced by piercing-sucking and chewing herbivores in Medicago truncatula. New Phytologist, 2005, 167: 597-606.

[19]

León J., Rojo E., Sánchez-Serrano J.J.. Wound signalling in plants. Journal of Experiment Botany, 2001, 52: 1-9.

[20]

Liu J., B., Xu L.. An improved method for the determination of hydrogen peroxide in leaves. Progress in Biochemistry and Biophysics, 2000, 27: 548-551.

[21]

Maffei M.E., Mithöfer A., Arimura G., Uchtenhagen H., Bossi S., Bertea C.M., Cucuzza L.S., Novero M., Volpe V., Quadro S., Boland W.. Effects of feeding Spodoptera littoralis on lima bean leaves. III. Membrane depolarization and involvement of hydrogen peroxide. Plant Physiology, 2006, 140: 1022-1035.

[22]

Mehdy M.C.. Active oxygen species in plant defence against pathogens. Plant Physiology, 1994, 105: 467-472.

[23]

Mithöfer A., Schulze B., Boland W.. Biotic and heavy metal stress response in plants: evidence for common signals. FEBS Lettesr, 2004, 566: 1-5.

[24]

O’Donel V.S., Tew D.G., Jones O.T.G., England P.J.. Studies on the inhibitory mechanism of iodonium compounds with special reference to neutrophil NADPH oxidase. Biochemisty Journal, 1993, 290: 41-49.

[25]

Orozco-Cárdenas M., Ryan C.A.. Hydrogen peroxide is generated systemically in plant leaves by wounding and systemin via the octadecanoid pathway. Proceedings of National Academy Science of the United States of America, 1999, 96: 6553-6557.

[26]

Paul N.D., Paul Hatcher P.E., Taylor J.E.. Coping with multiple enemies: an integration of molecular and ecological perspectives. Trends in Plant Science, 2000, 5: 220-225.

[27]

Sairam R.K., Srivastava G.C., Agarwal S., Meena R.C.. Differences in antioxidant activity in response to salinity stress in tolerant and susceptible wheat genotypes. Biologia Plantarum, 2005, 49: 85-81.

[28]

Shen W., Xu L., Ye M., Zhang R.. Study on determination of ASP activity. Plant Physiology Communication, 1996, 32: 203-205.

[29]

Somssich I.E., Hahlbrock K.. Pathogen defense in plants-a paradigm of biological complexity. Trends in Plant Science, 1998, 3: 86-90.

[30]

Song F., Ge X., Zheng Z.. The roles of active oxygen species and lipid peroxidation in the resistance of cotton seedling to fusarium wilt. Acta Phytopathologica Sinica, 2001, 31: 110-116.

[31]

Vandenabeele S., Van Der Kelen K., Dat J., Gadjev I., Boonefaes T., Morsa S., Rottiers P., Slooten L., Van Montagu M., Zabeau M., Inzé D., Van Breusegem F.. A comprehensive analysis of hydrogen peroxide-induced gene expression in tobacco. Proceedings of National Academy Science of the United States of America, 2003, 23: 16113-16118.

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