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Role of catalase, H2O2 and phenolics in resistance of pigeonpea towards Helicoverpa armigera (Hubner)

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Abstract

Rapid generation of superoxide radicals and accumulation of H2O2 is a characteristic early response of plants following perception of insect herbivory signals. Induction of oxidative burst on account of herbivory triggers various defense mechanisms in plants. Response of superoxide and H2O2-metabolizing enzymes and secondary metabolites in nine pigeonpea genotypes to Helicoverpa armigera feeding was investigated. Out of nine, four genotypes were found to be moderately resistant, three were intermediate and two were moderately susceptible. In general, H. armigera infestation resulted in increase in superoxide dismutase activity, H2O2 and phenolics content and decrease in catalase (CAT) activity in leaves, developing seeds and pod wall of pigeonpea genotypes. Peroxidase activity was found only in leaves. Among genotypes, the increase in phenolic constituents was found greater in moderately resistant genotypes than in moderately susceptible genotypes; this might determine their contribution in providing resistance to genotypes against H. armigera infestation. The capability of moderately resistant genotypes to maintain relatively lower H2O2 content and higher CAT activity in pod wall and developing seeds also appeared to determine resistance of genotypes towards H. armigera. Expression of resistance to H. armigera was found to be associated with a negative correlation of H2O2-metabolizing enzymes and phenolics with pod damage as well as with negative association between CAT activity and H2O2 content. A positive correlation found between H2O2 content and pod damage suggested the accumulation of H2O2 in response to pod borer attack. In addition, correlation analysis also revealed a positive association between CAT, phenolic compounds and DPPH radical scavenging activity following pod borer attack; this indicated their contribution in resistance mechanisms against H. armigera herbivory.

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Abbreviations

SOD:

Superoxide dismutase

CAT:

Catalase

POD:

Peroxidase

DPPH:

2,2-Diphenyl-1-picrylhydrozyl

ROS:

Reactive oxygen species

NOX:

NADPH oxidases

PSRR:

Pest susceptibility/resistance rating

PVP:

Polyvinyl pyrrolidone

SD:

Standard deviation

FW:

Fresh weight

I:

Infested

UI:

Uninfested

References

  • Abbott WS (1925) A method of computing the effectiveness of an insecticide. J Econ Entomol 18:265–267

    CAS  Google Scholar 

  • Anantharaju P, Muthiah AR (2008) Biochemical components in relation to pests incidence of pigeonpea spotted pod borer (Maruca vitrata) and blister beetle (Mylabris spp.). Legume Res 31:87–93

    Google Scholar 

  • Apel K, Hirt H (2004) Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu Rev Plant Biol 55:373–399

    Article  CAS  PubMed  Google Scholar 

  • Argandona VH, Chaman M, Cardemil L, Munoz O, Zuniga GE, Corcuera LJ (2001) Ethylene production and peroxidase activity in aphid-infested barley. J Chem Ecol 27:53–68

    Article  CAS  PubMed  Google Scholar 

  • Balbaa ST, Zaki AY, El-Shamy AM (1974) Total flavonoid and rutin content of the different organs of Sophora japonica L. J Assoc Off Anal Chem 57:752–755

    CAS  Google Scholar 

  • Banu MR, Muthiah AR, Ashok S (2005) Evaluation of pigeonpea (Cajanus cajan L.) genotypes against gram-pod borer (Helicoverpa armigera). Abstract in 4th international food legume research conference on food Legumes for nutritional security and sustainable agriculture, New Delhi, India, 317

  • Berglund T, Ohlsson AB (1995) Defensive and secondary metabolism in plant tissue cultures, with special reference to nicotinamide, glutathione and oxidative stress. Plant Cell Tiss Org Cult 43:137–145

    Article  CAS  Google Scholar 

  • Bernards MA, Bastrup-Spohr L (2008) Phenylpropanoid metabolism induced by wounding and insect herbivory. In: Schaller A (ed) Induced plant resistance to herbivory. Springer, Berlin, pp 189–211

    Chapter  Google Scholar 

  • Bhonwong A, Stout MJ, Attajarusit J, Tantasawat P (2009) Defensive role of tomato polyhenol oxidase against cotton bollworm (Helicoverpa armigera) and beet armyworm (Spodoptera exigua). J Chem Ecol 35:28–38

    Article  CAS  PubMed  Google Scholar 

  • Blois MS (1958) Antioxidant determinations by the use of a stable free radical. Nature 181:1199–1200

    Article  CAS  Google Scholar 

  • Broze AK, Broeckling CD, De-le-Pena C, Lewis MR, Greene E, Callaway RM, Sumner LW, Vivanco JM (2010) Plant neighbor identity influences plant biochemistry and physiology related to defense. BMC Plant Biol 10:115

    Article  Google Scholar 

  • Buettner GR (1993) The pecking order of free radicals and antioxidants: lipid peroxidation, α-tocopherol and ascorbate. Arch Biochem Biophys 300:535–543

    Article  CAS  PubMed  Google Scholar 

  • Chance B, Maehly AC (1955) Assay of catalases and peroxidases. Method Enzymol 2:764–775

    Article  Google Scholar 

  • Chen Y, Ni X, Buntin GD (2009) Physiological, nutritional and biochemical bases of corn resistance to foliage-feeding fall armyworm. J Chem Ecol 35:297–306

    Article  PubMed  Google Scholar 

  • Chougule NP, Hivrale VK, Chhabda PJ, Giri AP (2003) Differential inhibition of Helicoverpa armigera gut proteinases by proteinase inhibitors of pigeonpea (Cajanus cajan) and its wild relatives. Phytochemistry 64:681–687

    Article  CAS  PubMed  Google Scholar 

  • Foreman J, Demidchik V, Bothwell JHF, Mylona P, Miedema H, Torres MA, Linstead P, Costa S, Brownlee C, Jones JDG, Davies JM, Dolan L (2003) Reactive oxygen species produced by NADPH oxidase regulate plant cell growth. Nature 422:442–446

    Article  CAS  PubMed  Google Scholar 

  • Foyer CH, Noctor G (2005) Oxidant and antioxidant signaling in plants: a re-evaluation of the concept of oxidative stress in a physiological context. Plant, Cell Environ 28:1056–1071

    Article  CAS  Google Scholar 

  • Gaspar T, Penel C, Hagege D, Greppin H (1991) Peroxidases in plant growth, differentiation, and developmental processes. In: Lobarzewski J, Greppin H, Penel C, Gaspar T (eds) Biochemical, molecular and physiological aspects of plant peroxidases. University M Curie Sklodowska, Lublin, pp 249–280

    Google Scholar 

  • Gechev T, Gadjev I, Van Breusegem F, Inze D, Dukiandjiev S, Toneva V, Minkov I (2002) Hydrogen peroxide protects tobacco from oxidative stress by inducing a set of antioxidant enzymes. Cell Mol Life Sci 59:708–714

    Article  CAS  PubMed  Google Scholar 

  • Gill RS, Gupta AK, Taggar GK, Taggar MS (2010) Role of oxidative enzymes in plant defenses against insect herbivory. Acta Phytopathol Hun 45:277–290

    Article  CAS  Google Scholar 

  • Grayer RJ, Kimmins FM, Padgham DE, Harborne JB, Ranga Rao DV (1992) Condensed tannin levels and resistance in groundnuts Arachis hypogoea (L.) against Aphis craccivora (Koch). Phytochemistry 31:3795–3799

    Article  CAS  Google Scholar 

  • Hancock JT, Desikan R, Clarke A, Hurst RD, Neill SJ (2002) Cell signaling following plant/pathogen interactions involves the generation of reactive oxygen and reactive nitrogen species. Plant Physiol Biochem 40:611–617

    Article  CAS  Google Scholar 

  • Heng-Moss TM, Sarath G, Baxendale F, Novak D, Bose S, Ni X, Quisenberry S (2004) Characterization of oxidative enzyme change changes in buffalograsses challenged by Blissus occidus. J Econ Entomol 97:1086–1095

    Article  CAS  PubMed  Google Scholar 

  • Kaur H, Gupta AK, Kaur N, Sandhu JS (2009) Differential response of the antioxidant system in wild and cultivated genotypes of chickpea. Plant Growth Regul 57:109–114

    Article  CAS  Google Scholar 

  • Khattab H (2007) The defense mechanism of cabbage plant against phloem-sucking aphid (Brevicoryne brassicae L.). Aust J Basic Appl Sci 1:56–62

    CAS  Google Scholar 

  • Khattab H, Khattab I (2005) Responses of Eucalypt trees to the insect feeding (Gall forming Psyllid). Int J Agric Biol 7:979–984

    Google Scholar 

  • Kono Y, Fridovich I (1982) Superoxide radical inhibits catalase. J Biol Chem 257:5751–5754

    CAS  PubMed  Google Scholar 

  • Kooner BS, Cheema HK (2006) Evaluation of pigeon pea genotypes for resistance to pod borer complex. Indian J Crop Sci 1:194–196

    Google Scholar 

  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with folin-phenol reagent. J Biol Chem 193:265–275

    CAS  PubMed  Google Scholar 

  • Maffei ME, Mithofer A, Arimura GI, Uchtenhagen H, Bossi S, Bertea CM, Cucuzza LS, Novero M, Volpe V, Quadro S, Boland W (2006) Effects of feeding Spodoptera littoralis on Lima bean leaves. III. Membrane depolarization and involvement of hydrogen peroxide. Plant Physiol 140:1022–1035

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Maffei ME, Mithofer A, Boland W (2007) Insects feeding on plants: rapid signals and responses preceding the induction of phytochemical release. Phytochemistry 68:2946–2959

    Article  CAS  PubMed  Google Scholar 

  • Marklund S, Marklund G (1974) Involvement of superoxide anion radical in the autoxidation of pyragallol and a convenient assay for superoxide dismutase. Eur J Biochem 47:169–174

    Article  Google Scholar 

  • Moloi MJ, van der Westhuizen AJ (2006) The reactive oxygen species are involved in resistance responses of wheat to the Russian wheat aphid. J Plant Physiol 163:1118–1125

    Article  CAS  PubMed  Google Scholar 

  • Nagaraja M (2006) Evaluation of pigeonpea and cowpea genotypes for bruchid resistance (Bruchidae). Dissertation, University of Agricultural Sciences

  • Nair PM, Vaidyanathan CS (1964) A colorimetric method for determination of pyrocatechol and related substances. Anal Biochem 7:315–321

    Article  CAS  PubMed  Google Scholar 

  • Ni X, Quisenberry SS, Heng-Moss T, Markwell J, Sarath G, Klucas R, Baxendale FP (2001) Oxidative responses of resistant and susceptible cereal leaves to symptomatic and nonsymptomatic cereal aphid (Hemiptera: Aphididae) feeding. J Econ Entomol 94:743–751

    Article  CAS  PubMed  Google Scholar 

  • Noreen Z, Ashraf M (2009) Change in antioxidant enzymes and some key metabolites in some genetically diverse cultivars of radish (Raphanus sativus L). Environ Exp Bot 67:395–402

    Article  CAS  Google Scholar 

  • Orozco-Cardenas M, Ryan CA (1999) Hydrogen peroxide is generated systemically in plant leaves by wounding and systemin via the octadecanoid pathway. Proc Natl Acad Sci USA 96:6553–6557

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Price ML, Van Scoyoc S, Butler LG (1978) A critical evaluation of the vanillin reaction: an assay for tannins in sorghum grain. J Agric Food Chem 26:1214–1218

    Article  CAS  Google Scholar 

  • Rani PU, Jyothsna Y (2010) Biochemical and enzymatic changes in rice as a mechanism of defense. Acta Physiol Plant 32:695–701

    Article  CAS  Google Scholar 

  • Raychaudhuri S, Deng XW (2000) The role of superoxide dismutase in combating stress in higher plants. Bot Rev 66:89–98

    Article  Google Scholar 

  • Shannon LM, Kay E, Lew JY (1966) Peroxidase isozymes from horseradish roots I. Isolation and physical properties. J Biol Chem 241:2166–2172

    CAS  PubMed  Google Scholar 

  • Sharma KK, Sreelatha G, Dayal S (2006) Pigeonpea (Cajanus cajan L. Millsp.). Methods Mol Biol 343:359–367

    PubMed  Google Scholar 

  • Sharma HC, Sujana G, Rao DM (2009) Morphological and chemical components of resistance to pod borer Helicoverpa armigera in wild relatives of pigeonpea. Arthropod Plant Interact 3:151–161

    Article  Google Scholar 

  • Smith CM, Clement SL (2012) Molecular bases of plant resistance to arthropods. Annu Rev Entomol 57:309–328

    Article  CAS  PubMed  Google Scholar 

  • Sunitha V, Ranga Rao GV, Vijaya Lakshmi K, Saxena KB, Rameshwar Rao V, Reddy YVR (2008) Morphological and biochemical factors associated with resistance to Maruca vitrata (Lepidoptera: Pyralidae) in short-duration pigeonpea. Int J Trop Insect Sci 28:45–52

    Article  Google Scholar 

  • Swain T, Hillis WE (1959) Phenolic constituents of Prunus domestica. The qualitative analysis of phenolic constituents. J Sci Food Agric 10:63–68

    Article  CAS  Google Scholar 

  • Swamy SVSG (2005) Assessment of transgenic pigeonpea for resistance against legume pod borer, Helicoverpa armigera (Hubner) (Noctuidae:Lepidoptera). Dissertation, Acharya NG Ranga Agricultural University

  • Taggar GK, Gill RS, Gupta AK, Sandhu JS (2012) Fluctuations in peroxidase and catalase activities of resistant and susceptible blackgram (Vigna mungo (L.) Hepper) genotypes elicited by Bemisia tabaci (Gennadius) feeding. Plant Signal Behav 7:1321–1329

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Walling LL (2000) The myriad plant responses to herbivores. J Plant Growth Regul 19:195–216

    CAS  PubMed  Google Scholar 

  • War AR, Paulraj MG, War MY, Ignacimuthu S (2011) Jasmonic acid-mediated induced resistance in groundnut (Arachis hypogaea L.) against Helicoverpa armigera (Hubner) (Lepidoptera: Noctuidae). J Plant Growth Regul 30:512–523

    Article  CAS  Google Scholar 

  • War AR, Paulraj MG, War MY, Ignacimuthu S (2012a) Differential defensive response of groundnut germplasms of Helicoverpa armigera (Hubner) (Lepidoptera: Noctuidae). J Plant Interact 7:45–55

    Article  Google Scholar 

  • War AR, Paulraj MG, War MY, Ignacimuthu S (2012b) Herbivore induced resistance in different groundnut germplasm lines to Asian armyworm, Spodoptera litura (Fab.) (Lepidoptera: Noctuidae). Acta Physiol Plant 34:343–352

    Article  CAS  Google Scholar 

  • War AR, Paulraj MG, War MY, Ignacimuthu S, Sharma HC (2013) Defensive responses in groundnut against chewing and sap-sucking insects. J Plant Growth Regul 32:259–272

    Article  CAS  Google Scholar 

  • Wu J, Baldwin IT (2010) New insights into plant responses to attack from insect herbivores. Annu Rev Genet 44:1–24

    Article  CAS  PubMed  Google Scholar 

  • Zhang SZ, Hau BZ, Zhang F (2008) Induction of the activities of antioxidative enzymes and the levels of malonidialdehyde in cucumber seedlings as a consequence of Bemisia tabaci (Hemiptera: Aleyrodidae) infestation. Arthropod-Plant Interact 2:209–213

    Article  Google Scholar 

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Correspondence to Anil Kumar Gupta.

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Communicated by B. Barna.

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Kaur, R., Gupta, A.K. & Taggar, G.K. Role of catalase, H2O2 and phenolics in resistance of pigeonpea towards Helicoverpa armigera (Hubner). Acta Physiol Plant 36, 1513–1527 (2014). https://doi.org/10.1007/s11738-014-1528-6

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  • DOI: https://doi.org/10.1007/s11738-014-1528-6

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