Effect of cereal aphid Infestation on ascorbate content and ascorbate peroxidase activity in triticale

• Autorzy: Lukasik I. , Golawska S. , Wojcicka A.
• Języki publikacji: EN

Abstrakty

EN

The aim of the present study was to compare ascorbate (ASA) content and ascorbate peroxidase (APX) activity in seedlings of the less susceptible triticale cultivar Witon and the more susceptible triticale cultivar Tornado after infestation by the grain aphid Sitobion avenae (F). and the bird cherry-oat aphid Rhopalosiphum padi (L.). The content of ASA in triticale seedlings slightly decreased after 24 hrs of infestation by cereal aphids, but prolonged feeding (48 hrs and 72 hrs) resulted in significant losses in ASA dependent on cultivar and aphid species. The aphid infestation caused an increase in APX activity in triticale tissues throughout the test period. The aphid herbivores induced APX activity to a higher level in a less susceptible cultivar than in a more susceptible one. The oligophagous species R. padi caused a higher decrease of ASA and stronger induction of APX activity in tested triticale than the monophagous species S. avenae. The experiments carried out indicate that ascorbate and ascorbate peroxidase may play a significant role in the defense mechanism of aphid infested triticale.

• Wydawca: -
• Czasopismo: Polish Journal of Environmental Studies
• Rocznik: 2012
• Tom: 21
• Numer: 6
• Opis fizyczny: p.1937-1941,ref.

Twórcy

autor

Lukasik I.

• Department of Biochemistry and Molecular Biology, Siedlce University of Natural Sciences and Humanities, B. Prusa 12, 08-110 Siedlce, Poland

autor

Golawska S.

• Department of Biochemistry and Molecular Biology, Siedlce University of Natural Sciences and Humanities, B. Prusa 12, 08-110 Siedlce, Poland

autor

Wojcicka A.

• Department of Biochemistry and Molecular Biology, Siedlce University of Natural Sciences and Humanities, B. Prusa 12, 08-110 Siedlce, Poland

Bibliografia

• 1. GOGGIN F.L. Plant-aphid interactions: molecular and ecological perspectives. Curr. Opin. Plant Biol. 10, 399, 2007.
• 2. PARANIDHARAN V., PALANISWAMI A., VIDHYASEKARAN P., VELAZHAHAN R. Induction of enzymatic scavengers of active oxygen species in rice in response to infection by Rhizoctonia solani. Acta Physiol. Plant. 25, 91, 2003.
• 3. KUŹNIAK E., URBANEK H. The involvement of hydrogen peroxide in plant responses to stresses. Acta Physiol. Plant. 22, 195, 2000.
• 4. APEL K., HIRT H. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu. Rev. Plant Biol. 55, 373, 2004.
• 5. MOLOI M.J., VAN DER WESTHUIZEN A.J.The reactive oxygen species are involved in resistance responses of wheat to the Russian wheat aphid. J. Plant Physiol. 163, 1118, 2006.
• 6. HU Z.-H., SHEN Y.-B., SHEN F.-Y., SU X.-H. Effects of feeding Clostera anachoreta on hydrogen peroxide accumulation and activities of peroxidase, catalase, and ascorbate peroxidase in Populus simonii × P. pyramidalis ‘Opera 8277’ leaves. Acta Physiol. Plant. 31, 995, 2009.
• 7. OROZCO-CARDENAS M., RYAN C.A. Hydrogen peroxide is generated systematically in plant leaves by wounding and systemin via octadecanoid pathway. Proc. Natl. Acad. Sci. U.S.A. 96, (11), 6553, 1999.
• 8. VRANOVÁ E., INZÉ D., VAN BREUSEGEM F. Signal transduction during oxidative stress. J. Exp. Bot. 53, 1227, 2002.
• 9. MITTLER R., VANDERAUWERA S., GOLLERY M., VAN BREUSEGEM F. Reactive oxygen gene network of plants. Trends Plant Sci. 9, 490, 2004.
• 10. PUKACKA S., RATAJCZAK E. Antioxidative response of ascorbate-glutathione pathway enzymes and metabolites to desiccation of recalcitrant, Acer saccharinum seeds. J. Plant Physiol. 163, 1259, 2006.
• 11. SUMMERS C.B., FELTON G.W. Antioxidant role of dehydroascorbic acid reductase in insects. Biochim. Biophys. Acta, 1156, 235, 1993.
• 12. MAFFEI M.E., MITHOFER A., BOLAND W. Insects feeding on plants: rapid signals and responses preceding the induction of phytochemical release. Phytochemistry 68, 2946, 2007. 13. WALLING L.L. Myriad responses to herbivores. J. Plant Growth Regul. 19, 195, 2000.
• 14. JIANG Y., MILES P.W. Responses of a compatible Lucerne variety to attack by spotted alfalfa aphid: Changes in redox balance in affected tissues. Entomol. Exp. Appl. 67, 263, 1993.
• 15. ARGANDONA V.H. Effect of aphid infestation on enzyme activities in barley and wheat. Phytochemistry 35, 313, 1994.
• 16. GOMEZ S.K., OOSTERHUIS D.M., RAJGURU S.N., JOHNSON D.R. Foliar antioxidant enzyme responses in cotton after aphid herbivory. J. Cotton Sci. 8, 99, 2004.
• 17. HE J., CHEN F., CHEN S., LV G., DENG Y., FANG W., LIU Z., GUAN Z., HE C. Chrysanthemum leaf epidermal surface morphology and antioxidant and defense enzyme activity in response to aphid infestation. J. Plant Physiol. 168, 687, 2011.
• 18. OMAYE S.T., TURNBULL J.D., SAUBERLICH H.E. Selected methods for the determination of ascorbic acid in animal cells, tissues and fluids. Meth. Enzymol. 62, 3, 1979.
• 19. ASADA K. Chloroplasts: formation of active oxygen species and its scavenging. Meth. Enzymol. 105, 422, 1984.
• 20. BRADFORD M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72, 258, 1976.
• 21. FOYER C.H., NOCTOR G. Redox homeostasis and antioxidant signaling: a metabolic interface between stress perception and physiological responses. Plant Cell 17, 1866, 2005.
• 22. PANDHAIR V., SEKHON B.S. Reactive oxygen species and antioxidants in plants: an overview. J. Plant Biochem. Biotechnol. 15, 71, 2006.
• 23. GAPPER C., DOLAN L. Control of plant development by reactive oxygen species. Plant Physiol. 141, 341, 2006.
• 24. FOYER C.H., NOCTOR G. Redox sensing and signaling associated with reactive oxygen species in chloroplasts, peroxisomes and mitochondria. Physiol. Plant. 119, 355, 2003.
• 25. PATYKOWSKI J., URBANEK H. The activity of antioxidative enzymes, contents of H2O2 and of ascorbate in tomato leaves of cultivars more or less sensitive to infection with Botrytis cinerea. Acta Physiol. Plant. 27, 193, 2005.
• 26. ASADA K. Production and scavenging of reactive oxygen species in chloroplasts and their functions. Plant Physiol. 141, 39, 2006.
• 27. BI J.L., FELTON G.W. Foliar oxidative stress and insect herbivory: primary compounds, secondary metabolites, and reactive oxygen species as components of induced resistance. J. Chem. Ecol. 21, 1511, 1995.
• 28. BOYKO E.V., SMITH C.M., THARA V.K., BRUNO J.M., DENG Y., SHARON S.R., DARSEY K.L. Molecular basis of plant gene expression during aphid invasion: wheat Ptoand Pti-like sequences are involved in interactions between wheat and Russian wheat aphid (Homoptera: Aphididae). J. Econ. Entomol. 99, 1430, 2006.
• 29. MORKUNAS I., MAI V.C., GABRYŚ B. Phytohormonal signaling in plant responses to aphid feeding. Acta Physiol. Plant. 33, 2057, 2011.
• 30. GOGGIN F.L., AVILA C.A., LORENCE A. Vitamin C content in plants is modified by insects and influences susceptibility to herbivory. Bioessays 32, 777, 2010.
• 31. WRIGHT K.P., KADER A.A. Effect of slicing and controlled-atmosphere storage on the ascorbate content and quality of stawberries and persimmons. Post-harvest Biol. Technol. 10, 39, 1997.
• 32. REYES L.F., VILLAREAL J.E., CISNEROS-ZEVALLOS L. The increase in antioxidant capacity after wounding depends on the type of fruit or vegetable tissue. Food Chem. 101, 1254, 2007.
• 33. SUZA W.P., AVILA C.A., CARRUTHERS K., KULKARNI S., GOGGIN F.L., LORENCE A. Exploring the impact of wounding and jasmonates on ascorbate metabolism. Plant Physiol. Biochem. 48, 337, 2010.
• 34. CONKLIN P.L., WILLIAMS E.H., LAST R.L. Environmental stress sensitivity of an ascorbic acid-deficient Arabidopsis mutant. Proc. Natl. Acad. Sci. U.S.A. 93, 9970, 1996.
• 35. 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 Physiol. 140, 1022, 2006.
• 36. SEMPRUCH C., WÓJCICKA A., MAKOSZ M., LESZCZYŃSKI B. Changes in activity of ornithine decarboxylase in winter triticale seedlings stressed by grain aphid attack. Zesz. Probl. Post. Nauk Rol. 524, 401, 2008.
• 37. ŁUKASIK I., GOŁAWSKA S., WÓJCICKA A., POGONOWSKA M. Activity of cereal aphids enzymem towards scavenging hydrogen peroxide. Aphids and other Hemipterous Insects 14, 165, 2008.