Skip to main content

Advertisement

Log in

Characterization of a vacuolar processing enzyme expressed in Arachis diogoi in resistance responses against late leaf spot pathogen, Phaeoisariopsis personata

  • Published:
Plant Molecular Biology Aims and scope Submit manuscript

Abstract

Vacuolar processing enzymes are cysteine proteases responsible for maturation of vacuolar proteins. They have been shown to possess caspase-1-like activity, mediate cell death and display increased activity during pathogen infections. A transcript derived fragment corresponding to VPE was found to be up-regulated in a cDNA-AFLP analysis of host responses of a wild peanut, Arachis diogoi upon challenge from the late leaf spot pathogen Phaeoisariopsis personata, which was subsequently validated by q-PCR in a time course analysis, where susceptible peanut did not show its upregulation. In transient conditional and constitutive expression studies in tobacco leaves using agroinfiltration, we have observed that expression of AdVPE was associated with hypersensitive response (HR) like cell death. AdVPE expression was found to be high at 24 h post estradiol application and this was associated with the enhanced co-expression of molecular markers of HR cell death genes and genes for pathogenesis related proteins indicating that AdVPE positively regulates defense responses and its estradiol induced expression is sufficient for HR-like cell death in tobacco. We found that AdVPE expression was very strongly induced in response to sodium nitroprusside, which indicates its involvement in stress signaling. Induced expression of AdVPE in response to jasmonic acid and ethylene also indicates its involvement in an interconnected network of signaling. Transgenic tobacco plants ectopically expressing AdVPE exhibited enhanced resistance against Phytophthora parasitica var. nicotianae, Alternaria alternata var.  nicotianae and Rhizoctonia solani. To our knowledge, this is the first report on the heterologous expression of a pathogen induced VPE enhancing resistance to fungal pathogens with cell death phenomenon under transient expression.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7

Similar content being viewed by others

References

  • Abdou YAM, Gregory WC, Cooper WE (1974) Sources and nature of resistance to Cercospora arachidicola Hori and Cercosporidium personatum (Beck & Curtis) Deighton in Arachis species 1. Peanut Sci 1:6–11

    Article  Google Scholar 

  • Anderson NA (1982) The genetics and pathology of Rhizoctonia solani. Annu Rev Phytopathol 20:329–347

    Article  Google Scholar 

  • Ayliffe M, Periyannan SK, Feechan A, Dry I, Schumann U, Ming-Bo Wang, Pryor A, Lagudah E (2013) A simple method for comparing fungal biomass in infected plant tissues. MPMI 26(6):658–667

    Article  CAS  PubMed  Google Scholar 

  • Baker CJ, Mock N (1994) An improved method for monitoring cell death in cell suspension and leaf disc assays using Evans blue. Plant Cell, Tissue Organ Cult 39:7–12

    Article  Google Scholar 

  • Belenghi B, Acconcia F, Trovato M, Perazzolli M, Bocedi A, Polticelli F, Ascenzi P, Delledonne M (2003) AtCYS1, a cystatin from Arabidopsis thaliana, suppresses hypersensitive cell death. Eur J Biochem/FEBS 270(12):2593–2604

    Article  CAS  Google Scholar 

  • Brand Y, Hovav R (2010) Identification of suitable internal control genes for quantitative real-time PCR expression analyses in peanut (Arachis hypogaea). Peanut Sci 37:12–19

    Article  Google Scholar 

  • Bright J, Desikan R, Hancock JT, Weir IS, Neill SJ (2006) ABA-induced NO generation and stomatal closure in Arabidopsis are dependent on H2O2 synthesis. Plant J 45:113–122

    Article  CAS  PubMed  Google Scholar 

  • Brouwer M, Lievens B, Van Hemelrijck W, Van den Ackerveken G, Cammue BPA, Thomma BPHJ (2003) Quantification of disease progression of several microbial pathogens on Arabidopsis thaliana using real-time fluorescence PCR. FEMS Microbiol Lett 228:241–248

    Article  CAS  PubMed  Google Scholar 

  • Calo L, Garcia I, Gotor C, Romero LC (2006) Leaf hairs influence phytopathogenic fungus infection and confer an increased resistance when expressing a Trichoderma α-1,3-glucanase. J Exp Bot 57(14):3911–3920

    Article  CAS  PubMed  Google Scholar 

  • Chang S, Puryear J, Cairney J (1993) A simple and efficient method for isolating RNA from pine trees. Plant Mol Biol Rep 11:113–116

    Article  CAS  Google Scholar 

  • Courtois C, Besson A, Dahan J, Bourque S, Dobrowolska G, Pugin A, Wendehenne D (2008) Nitric oxide signalling in plants: interplays with Ca2+ and protein kinases. J Exp Bot 59:155–163

    Article  CAS  PubMed  Google Scholar 

  • Creelman RA, Mullet JE (1997) Biosynthesis and action of jasmonates in plants. Ann Rev Plant Physiol Plant Mol Biol 48:355–381

    Article  CAS  Google Scholar 

  • Delledonne M, Xia Y, Dixon RA, Lamb C (1998) Nitric oxide functions as a signal in plant disease resistance. Nature 394:585–588

    Article  CAS  PubMed  Google Scholar 

  • Delledonne M, Polverari A, Murgia I (2003) The functions of nitric oxide-mediated signaling and changes in gene expression during the hypersensitive response. Antioxid Redox Signal 5:33–41

    Article  CAS  PubMed  Google Scholar 

  • Dhondt S, Geoffroy P, Stelmach BA, Legrand M, Heitz T (2000) Soluble phospholipase A2 activity is induced before oxylipin accumulation in tobacco mosaic virus-infected tobacco leaves and is contributed by patatin-like enzymes. Plant J 23:431–440

    Article  CAS  PubMed  Google Scholar 

  • Doyle JJ, Doyle JL (1990) Isolation of plant DNA from fresh tissues. Focus 12:13–15

    Google Scholar 

  • Durrant WE, Dong X (2004) Systemic acquired resistance. Ann Rev Phytopathol 42:185–209

    Article  CAS  Google Scholar 

  • Gruis DF, Selinger DA, Curran JM, Jung R (2002) Redundant proteolytic mechanisms process seed storage proteins in the absence of seed-type members of the vacuolar processing enzyme family of cysteine proteases. Plant Cell 14:2863–2882

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Hara-Nishimura I, Hatsugai N (2011) The role of vacuole in plant cell death. Cell Death Differ 18:1298–1304

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Hara-Nishimura I, Nishimura M (1987) Proglobulin processing enzyme in vacuoles isolated from developing pumpkin cotyledons. Plant Physiol 85:440–445

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Hara-Nishimura I, Nishimura M, Akazawa T (1985) Biosynthesis and intracellular transport of 11S globulin in developing pumpkin cotyledons. Plant Physiol 77:747–752

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Hatsugai N, Kuroyanagi M, Yamada K, Meshi T, Tsuda S, Kondo M, Nishimura M, Hara-Nishimura I (2004) A plant vacuolar protease, VPE, mediates virus-induced hypersensitive cell death. Science 305:855–858

    Article  CAS  PubMed  Google Scholar 

  • Hatsugai N, Kuroyanagi M, Nishimura M, Hara-Nishimura I (2006) A cellular suicide strategy of plants: vacuole-mediated cell death. Apoptosis 11:905–911

    Article  CAS  PubMed  Google Scholar 

  • Hiraiwa N, Nishimura M, Hara-Nishimura I (1997) Expression and activation of the vacuolar processing enzyme in Saccharomyces cerevisiae. Plant J 12:819–829

    Article  CAS  PubMed  Google Scholar 

  • Hoepflinger MC, Reitsamer J, Geretschlaeger AM, Mehlmer N, Tenhaken R (2013) The effect of translationally controlled tumour protein (TCTP) on programmed cell death in plants. BMC Plant Biol 13:135

    Article  PubMed Central  PubMed  Google Scholar 

  • Horsch RB, Fry JE, Hoffman NL, Eichholtz D, Rogers SG, Fraley RT (1985) A simple and general method for transferring genes into plants. Science 227:1229–1231

    Article  CAS  Google Scholar 

  • Igarashi D, Bethke G, Xu Y, Tsuda K, Glazebrook J, Katagiri F (2013) Pattern-triggered immunity suppresses programmed cell death triggered by fumonisin b1. PLoS ONE 8(4):e60769. doi:10.1371/journal.pone.0060769

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Jang EK, Min KH, Kim SH, Nam SH, Zhang S, Kim YC, Cho BH, Yang KY (2009) Mitogen-activated protein kinase cascade in the signaling for polyamine biosynthesis in tobacco. Plant Cell Physiol 50:658–664

    Article  CAS  PubMed  Google Scholar 

  • Jones JD, Dangl JL (2006) The plant immune system. Nature 444:323–329

    Article  CAS  PubMed  Google Scholar 

  • Kessler A, Baldwin IT (2001) Defensive function of herbivore-induced plant volatile emissions in nature. Science 291:2141–2144

    Article  CAS  PubMed  Google Scholar 

  • Kinoshita T, Yamada K, Hiraiwa N, Kondo M, Nishimura M, Hara-Nishimura I (1999) Vacuolar processing enzyme is up-regulated in the lytic vacuoles of vegetative tissues during senescence and under various stressed conditions. Plant J 19:43–53

    Article  CAS  PubMed  Google Scholar 

  • Kobae Y, Sekino T, Yoshioka H, Nakagawa T, Martinoia E, Maeshima M (2006) Loss of AtPDR8, a plasma membrane ABC transporter of Arabidopsis thaliana, causes hypersensitive cell death upon pathogen infection. Plant Cell Physiol 47:309–318

    Article  CAS  PubMed  Google Scholar 

  • Kumamaru T, Uemura Y, Inoue Y, Takemoto Y, Siddiqui SU, Ogawa M, Hara-Nishimura I, Satoh H (2010) Vacuolar processing enzyme plays an essential role in the crystalline structure of glutelin in rice seed. Plant Cell Physiol 51:38–46

    Article  CAS  PubMed  Google Scholar 

  • Kumar KR, Kirti PB (2010) A mitogen-activated protein kinase, AhMPK6 from peanut localizes to the nucleus and also induces defense responses upon transient expression in tobacco. Plant Physiol Biochem 48:481–486

    Article  CAS  PubMed  Google Scholar 

  • Kumar KR, Kirti PB (2011) Differential gene expression in Arachis diogoi upon interaction with peanut late leaf spot pathogen Phaeoisariopsis personata and characterization of a pathogen induced cyclophilin. Plant Mol Biol 75:497–513

    Article  CAS  PubMed  Google Scholar 

  • Kumar KR, Kirti PB (2012) Novel role for a serine/arginine-rich splicing factor, AdRSZ21 in plant defense and HR-like cell death. Plant Mol Biol 80:461–476

    Article  CAS  PubMed  Google Scholar 

  • Kumar D, Kirti PB (2015a) Pathogen-induced SGT1 of Arachis diogoi induces cell death and enhanced disease resistance in tobacco and peanut. Plant Biotechnol J 13:73–84

    Article  CAS  PubMed  Google Scholar 

  • Kumar D, Kirti PB (2015b) Transcriptomic and proteomic analyses of resistant host responses in Arachis diogoi challenged with late leaf spot pathogen, Phaeoisariopsis personata. PLoS ONE 10(2):e0117559. doi:10.1371/journal.pone.0117559

    Article  PubMed Central  PubMed  Google Scholar 

  • Kuroyanagi M, Yamada K, Hatsugai N, Kondo M, Nishimura M, Hara-Nishimura I (2005) Vacuolar processing enzyme is essential for mycotoxin-induced cell death in Arabidopsis thaliana. J Biol Chem 280:32914–32920

    Article  CAS  PubMed  Google Scholar 

  • La Camera S, Balague C, Gobel C, Geoffroy P, Legrand M, Feussner I, Roby D, Heitz T (2009) The Arabidopsis patatin-like protein 2 (PLP2) plays an essential role in cell death execution and differentially affects biosynthesis of oxylipins and resistance to pathogens. Mol Plant Microbe Interact 22:469–481

    Article  PubMed  Google Scholar 

  • Lam E, Kato N, Lawton M (2001) Programmed cell death, mitochondria and the plant hypersensitive response. Nature 411:848–853

    Article  CAS  PubMed  Google Scholar 

  • Lee SB, Taylor JW (1990) Isolation of DNA from fungal mycelia and single cells. In: Innis MA, Gelfand DH, Sninsky JJ, White TJ (eds) PCR protocols, a guide to methods and applications. Academic Press, San Diego, pp 282–287

    Chapter  Google Scholar 

  • Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method. Methods 25:402–408

    Article  CAS  PubMed  Google Scholar 

  • Lorito M, Woo SL, Garcia I, Colucci G, Harman GE, Pintor-Toro JA, Filippone E, Muccifora S, Lawrence CB, Zoina A, Tuzun S, Scala F (1998) Genes from mycoparasitic fungi as a source for improving plant resistance to fungal pathogens. Proc Natl Acad Sci USA 95:7860–7865

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Mims CW, Luttrell ES, Alderman SC (1989) Ultrastructure of the haustorium of the peanut late leaf spot fungus Cercosporidium personatum. Can J Bot 67(4):1198–1202

    Google Scholar 

  • Misas-Villamil JC, Toenges G, Kolodziejek I, Sadaghiani AM, Kaschani F, Colby T, Bogyo M, van der Hoorn RA (2013) Activity profiling of vacuolar processing enzymes reveals a role for VPE during oomycete infection. Plant J 73:689–700

    Article  CAS  PubMed  Google Scholar 

  • Morgante CV, Guimaraes PM, Martins ACQ, Araujo ACG, Leal-Bertioli SCM, Bertioli DJ, Brasileiro ACM (2011) Reference genes for quantitative reverse transcription-polymerase chain reaction expression studies in wild and cultivated peanut. BMC Res Notes 4:339

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Neill SJ, Desikan R, Clarke A, Hancock JT (2002) Nitric oxide is a novel component of abscisic acid signaling in stomatal guard cells. Plant Physiol 128:13–16

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Oh C-S, Pedley KF, Martin GB (2010) Tomato 14-3-3 protein 7 positively regulates immunity-associated programmed cell death by enhancing protein abundance and signaling ability of MAPKKKα. Plant Cell 22:260–272

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Okamoto T, Minamikawa T (1999) Molecular cloning and characterization of Vigna mungo processing enzyme 1 (VmPE-1), an asparaginyl endopeptidase possibly involved in post-translational processing of a vacuolar cysteine endopeptidase (SH-EP). Plant Mol Biol 39:63–73

    Article  CAS  PubMed  Google Scholar 

  • Pasche JS, Mallik I, Anderson NR, Gudmestad NC (2013) Development and validation of a real-time PCR assay for the quantification of Verticillium dahliae in potato. Plant Dis 97:608–618

    Article  CAS  Google Scholar 

  • Pernas M, Sanchez-Monge R, Salcedo G (2000) Biotic and abiotic stress can induce cystatin expression in chestnut. FEBS Lett 467:206–210

    Article  CAS  PubMed  Google Scholar 

  • Pontier D, Gan S, Amasino RM, Roby D, Lam E (1999) Markers for hypersensitive response and senescence show distinct patterns of expression. Plant Mol Biol 39:1243–1255

    Article  CAS  PubMed  Google Scholar 

  • Qiao W, Fan LM (2008) Nitric oxide signaling in plant responses to abiotic stresses. J Integr Plant Biol 50:1238–1246

    Article  CAS  PubMed  Google Scholar 

  • Rao NK, Reddy LJ, Bramel PJ (2003) Potential of wild species for genetic enhancement of some semi-arid food crops. Genetic Res Crop Evol 50:707–721

    Article  Google Scholar 

  • Rawlings ND, Barrett AJ, Bateman A (2012) MEROPS: the database of proteolytic enzymes, their substrates and inhibitors. Nucl Acids Res 40(Database issue):D343–D350

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Rojo E, Martin R, Carter C, Zouhar J, Pan S, Plotnikova J, Jin H, Paneque M, Sanchez-Serrano JJ, Baker B, Ausubel FM, Raikhel NV (2004) VPEγ exhibits a caspase-like activity that contributes to defense against pathogens. Curr Biol 14:1897–1906

    Article  CAS  PubMed  Google Scholar 

  • Santos-Silva LK, Soares-Costa A, Gerald LT, Meneghin SP, Henrique-Silva F (2012) Recombinant expression and biochemical characterization of sugarcane legumain. Plant Physiol Biochem 57:181–192

    Article  CAS  PubMed  Google Scholar 

  • Shimada T, Yamada K, Kataoka M, Nakaune S, Koumoto Y, Kuroyanagi M, Tabata S, Kato T, Shinozaki K, Seki M, Kobayashi M, Kondo M, Nishimura M, Hara-Nishimura I (2003) Vacuolar processing enzymes are essential for proper processing of seed storage proteins in Arabidopsis thaliana. J Biol Chem 278:32292–32299

    Article  CAS  PubMed  Google Scholar 

  • Shokes FM, Culbreath AK (1997) Early and late leaf spots. In: Kokalis-Burelle N, Porter DM, Rodriguez-Kabana R, Smith DH, Subrahmanyam P (eds) Compendium of peanut diseases, 2nd edn. American Phytopathological Society, St. Paul, pp 17–20

    Google Scholar 

  • Su’udi M, Jong-Mi Park, Sang-Ryeol Park, Duk-Ju Hwang, Shin-Chul Bae, Kim S, Il-Pyung Ahn (2013) Quantification of Alternaria brassicicola infection in the Arabidopsis thaliana and Brassica rapa subsp. pekinensis. Microbiology 159:1946–1955

    Article  PubMed  Google Scholar 

  • Tae Hoon K, Dae Yeon K, Yong Weon S (2013) Identification and expression analysis of wheat vacuolar processing enzymes (VPEs). Plant Breed Biotechnol 1:148–161

    Article  Google Scholar 

  • Takahashi Y, Uehara Y, Berberich T, Ito A, Saitoh H, Miyazaki A, Terauchi R, Kusano T (2004) A subset of hypersensitive response marker genes, including HSR203 J, is the downstream target of a spermine signal transduction pathway in tobacco. Plant J 40:586–595

    Article  CAS  PubMed  Google Scholar 

  • Tedford EC, Miller TL, Nielsen MT (1990) A detached-leaves technique for detecting Phytophthora parasitica var. nicotianae in tobacco. Plant Dis 74:313–316

    Article  Google Scholar 

  • Thomma BP, Penninckx IA, Broekaert WF, Cammue BP (2001) The complexity of disease signaling in Arabidopsis. Curr Opin Immunol 13:63–68

    Article  CAS  PubMed  Google Scholar 

  • Tsiatsiani L, Van Breusegem F, Gallois P, Zavialov A, Lam E, Bozhkov PV (2011) Metacaspases. Cell Death Differ 18:1279–1288

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Wang Y, Zhu S, Liu S, Jiang L, Chen L, Ren Y, Han X, Liu F, Ji S, Liu X, Wan J (2009) The vacuolar processing enzyme OsVPE1 is required for efficient glutelin processing in rice. Plant J 58:606–617

    Article  CAS  PubMed  Google Scholar 

  • Wasilewska A, Vlad F, Sirichandra C, Redko Y, Jammes F, Valon C, Frei dit Frey N, Leung J (2008) An update on abscisic acid signaling in plants and more. Mol Plant 1:198–217

    Article  CAS  PubMed  Google Scholar 

  • Yamada K, Nishimura M, Hara-Nishimura I (2004) The slow wound-response of γVPE is regulated by endogenous salicylic acid in Arabidopsis. Planta 218:599–605

    Article  CAS  PubMed  Google Scholar 

  • Zhang H, Dong S, Wang M, Wang W, Song W, Dou X, Zheng X, Zhang Z (2010) The role of vacuolar processing enzyme (VPE) from Nicotiana benthamiana in the elicitor-triggered hypersensitive response and stomatal closure. J Exp Bot 61:3799–3812

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Zhang J, Li QF, Huang WW, Xu XY, Zhang XL, Hui MX, Zhang MK, Zhang LG (2013) A vacuolar processing enzyme RsVPE1 gene of radish is involved in floral bud abortion under heat stress. Int J Mol Sci 14(7):13346–13359

    Article  PubMed Central  PubMed  Google Scholar 

Download references

Acknowledgments

This work has been supported by the Department of Biotechnology, Government of India in the form of a research project to PBK with the reference BT/PR6853/PBD/16/627/2005. Facilities from the Department of Plant Sciences, University of Hyderabad under UGC-CAS, DST-FIST and DBT-CREBB are acknowledged. The germplasm of A. diogoi was kindly provided by ICRISAT, Patancheru, India.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to P. B. Kirti.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (DOC 4198 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kumar, D., Rampuria, S., Singh, N.K. et al. Characterization of a vacuolar processing enzyme expressed in Arachis diogoi in resistance responses against late leaf spot pathogen, Phaeoisariopsis personata . Plant Mol Biol 88, 177–191 (2015). https://doi.org/10.1007/s11103-015-0318-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11103-015-0318-x

Keywords

Navigation