Relationship of Resistance-Related Enzyme Activity and Salicylic Acid Content in Phalaenopsis Species with Different Levels of Resistance to Dickeya dadantii
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Aeny T.N., Suharjo R., Ginting C., Hapsoro D., Niswati A. 2020. Characterization and host range assessment of Dickeya zeae associated with pineapple soft rot disease in East Lampung, Indonesia. Biodiversitas 21(2): 587–595. DOI: 10.13057/biodiv/d210221.AenyT.N.SuharjoR.GintingC.HapsoroD.NiswatiA.2020Characterization and host range assessment of Dickeya zeae associated with pineapple soft rot disease in East Lampung, IndonesiaBiodiversitas21258759510.13057/biodiv/d210221Open DOISearch in Google Scholar
Agyemang P.A., Kabir M.N., Kersey C.M., Dumenyo C.K. 2020. The bacterial soft rot pathogens, Pectobacterium carotovorum and P. atrosepticum, respond to different classes of virulence-inducing host chemical signals. Horticulturae 6(1); 13; 13 p. DOI: 10.3390/horticulturae6010013.AgyemangP.A.KabirM.N.KerseyC.M.DumenyoC.K.2020The bacterial soft rot pathogens, Pectobacterium carotovorum and P. atrosepticum, respond to different classes of virulence-inducing host chemical signalsHorticulturae611313 p.10.3390/horticulturae6010013Open DOISearch in Google Scholar
Andersen E.J., Ali S., Byamukama E., Yen Y., Nepal M.P. 2018. Disease resistance mechanisms in plants. Genes 9(7); 339; 30 p. DOI: 10.3390/genes9070339.AndersenE.J.AliS.ByamukamaE.YenY.NepalM.P.2018Disease resistance mechanisms in plantsGenes9733930 p.10.3390/genes9070339607110329973557Open DOISearch in Google Scholar
Asai S., Mase K., Yoshioka H. 2010. Role of nitric oxide and reactive oxygen species in disease resistance to necrotrophic pathogens. Plant Signaling and Behavior 5(7): 872–874. DOI: 10.4161/psb.5.7.11899.AsaiS.MaseK.YoshiokaH.2010Role of nitric oxide and reactive oxygen species in disease resistance to necrotrophic pathogensPlant Signaling and Behavior5787287410.4161/psb.5.7.11899301454120448455Open DOISearch in Google Scholar
Bhuiyan N.H., Selvaraj G., Wei Y., King J. 2009. Role of lignification in plant defense. Plant Signaling and Behavior 4(2): 158–159. DOI: 10.4161/psb.4.2.7688.BhuiyanN.H.SelvarajG.WeiY.KingJ.2009Role of lignification in plant defensePlant Signaling and Behavior4215815910.4161/psb.4.2.7688263751019649200Open DOISearch in Google Scholar
Bindschedler L.V., Dewdney J., Blee K.A., Stone J.M., Asai T., Plotnikov J. et al. 2006. Peroxidase-dependent apoplastic oxidative burst in Arabidopsis required for pathogen resistance. Plant Journal 47(6): 851–863. DOI: 10.1111/j.1365-313x.2006.02837.x.BindschedlerL.V.DewdneyJ.BleeK.A.StoneJ.M.AsaiT.PlotnikovJ.2006Peroxidase-dependent apoplastic oxidative burst in Arabidopsis required for pathogen resistancePlant Journal47685186310.1111/j.1365-313x.2006.02837.xOpen DOISearch in Google Scholar
Bolwell G.P., Wojtaszek P. 1997. Mechanisms for the generation of reactive oxygen species in plant defense – a broad perspective. Physiological and Molecular Plant Pathology 51(6): 347–366. DOI: 10.1006/pmpp.1997.0129.BolwellG.P.WojtaszekP.1997Mechanisms for the generation of reactive oxygen species in plant defense – a broad perspectivePhysiological and Molecular Plant Pathology51634736610.1006/pmpp.1997.0129Open DOISearch in Google Scholar
Chandrashekar B.S., Prasannakumar M.K., Puneeth M.E., Teli K., Priyanka K., Mahesh H.B., Desai R.U. 2018. First report of bacterial soft rot of carrot caused by Klebsiella variicola in India. New Disease Reports 37(1): 21. DOI: 10.5197/j.2044-0588.2018.037.021.ChandrashekarB.S.PrasannakumarM.K.PuneethM.E.TeliK.PriyankaK.MaheshH.B.DesaiR.U.2018First report of bacterial soft rot of carrot caused by Klebsiella variicola in IndiaNew Disease Reports3712110.5197/j.2044-0588.2018.037.021Open DOISearch in Google Scholar
Charkowski A.O. 2018. The changing face of bacterial soft-rot diseases. Annual Review of Phytopathology 56(1): 269–288. DOI: 10.1146/annurev-phyto-080417-045906.CharkowskiA.O.2018The changing face of bacterial soft-rot diseasesAnnual Review of Phytopathology56126928810.1146/annurev-phyto-080417-04590629958075Open DOISearch in Google Scholar
Chowdhury S., Basu A., Kundu S. 2017. Biotrophy-necrotrophy switch in pathogen evoke differential response in resistant and susceptible sesame involving multiple signaling pathways at different phases. Scientific Reports 7(1); 17251; 17 p. DOI: 10.1038/s41598-017-17248-7.ChowdhuryS.BasuA.KunduS.2017Biotrophy-necrotrophy switch in pathogen evoke differential response in resistant and susceptible sesame involving multiple signaling pathways at different phasesScientific Reports711725117 p.10.1038/s41598-017-17248-7572281329222513Open DOISearch in Google Scholar
Czajkowski R., Pérombelon M.C.M., van Veen J.A., van der Wolf J.M. 2011. Control of blackleg and tuber soft rot of potato caused by Pectobacterium and Dickeya species: a review. Plant Pathology 60(6): 999–1013. DOI: 10.1111/j.1365-3059.2011.02470.x.CzajkowskiR.PérombelonM.C.M.van VeenJ.A.van der WolfJ.M.2011Control of blackleg and tuber soft rot of potato caused by Pectobacterium and Dickeya species: a reviewPlant Pathology606999101310.1111/j.1365-3059.2011.02470.xOpen DOISearch in Google Scholar
Dangcham S., Bowen J., Ferguson I.B., Ketsa S. 2008. Effect of temperature and low oxygen on pericarp hardening of mangosteen fruit stored at low temperature. Postharvest Biology and Technology 50(1): 37–44. DOI: 10.1016/j.postharvbio.2008.02.005.DangchamS.BowenJ.FergusonI.B.KetsaS.2008Effect of temperature and low oxygen on pericarp hardening of mangosteen fruit stored at low temperaturePostharvest Biology and Technology501374410.1016/j.postharvbio.2008.02.005Open DOISearch in Google Scholar
Datta R. 1981. Acidogenic fermentation of lignocellulose – acid yield and conversion of components. Biotechnology and Bioengineering 23(9): 2167–2170. DOI: 10.1002/bit.260230921.DattaR.1981Acidogenic fermentation of lignocellulose – acid yield and conversion of componentsBiotechnology and Bioengineering2392167217010.1002/bit.260230921Open DOISearch in Google Scholar
Davidsson P.R., Kariola T., Niemi O., Palva E.T. 2013. Pathogenicity of and plant immunity to soft rot pectobacteria. Frontiers in Plant Science 4; 191; 13 p. DOI: 10.3389/fpls.2013.00191.DavidssonP.R.KariolaT.NiemiO.PalvaE.T.2013Pathogenicity of and plant immunity to soft rot pectobacteriaFrontiers in Plant Science419113 p.10.3389/fpls.2013.00191367830123781227Open DOISearch in Google Scholar
Dey N., Roy U.K., Aditya M., Bhattacharjee S. 2020. Defensive strategies of ROS in Programmed Cell Death associated with hypertensive response in plant pathogenesis. Annals of Systems Biology 3(1): 1–9. DOI: 10.17352/asb.000004.DeyN.RoyU.K.AdityaM.BhattacharjeeS.2020Defensive strategies of ROS in Programmed Cell Death associated with hypertensive response in plant pathogenesisAnnals of Systems Biology311910.17352/asb.000004Open DOISearch in Google Scholar
Durner J., Klessig D.F. 1995. Inhibition of ascorbate peroxidase by salicylic acid and 2,6-dichloroisonicotinic acid, two inducers of plant defense responses. Proceedings of the National Academy of Sciences 92(24): 11312–11316. DOI: 10.1073/pnas.92.24.11312.DurnerJ.KlessigD.F.1995Inhibition of ascorbate peroxidase by salicylic acid and 2,6-dichloroisonicotinic acid, two inducers of plant defense responsesProceedings of the National Academy of Sciences9224113121131610.1073/pnas.92.24.11312406227479986Open DOISearch in Google Scholar
Expert D., Patrit O., Shevchik V.E., Perino C., Boucher V., Creze C. et al. 2018. Dickeya dadantii pectic enzymes necessary for virulence are also responsible for activation of the Arabidopsis thaliana innate immune system. Molecular Plant Pathology 19(2): 313–327. DOI: 10.1111/mpp.12522.ExpertD.PatritO.ShevchikV.E.PerinoC.BoucherV.CrezeC.2018Dickeya dadantii pectic enzymes necessary for virulence are also responsible for activation of the Arabidopsis thaliana innate immune systemMolecular Plant Pathology19231332710.1111/mpp.12522663812227925401Open DOISearch in Google Scholar
Fatima U., Senthil-Kumar M. 2015. Plant and pathogen nutrient acquisition strategies. Frontiers in Plant Science 6; 750; 12 p. DOI: 10.3389/fpls.2015.00750.FatimaU.Senthil-KumarM.2015Plant and pathogen nutrient acquisition strategiesFrontiers in Plant Science675012 p.10.3389/fpls.2015.00750458525326442063Open DOISearch in Google Scholar
Freeman B.C., Beattie G.A. 2009. Bacterial growth restriction during host resistance to Pseudomonas syringae is associated with leaf water loss and localized cessation of vascular activity in Arabidopsis thaliana. Molecular Plant-Microbe Interactions 22(7): 857–867. DOI: 10.1094/mpmi-22-7-0857.FreemanB.C.BeattieG.A.2009Bacterial growth restriction during host resistance to Pseudomonas syringae is associated with leaf water loss and localized cessation of vascular activity in Arabidopsis thalianaMolecular Plant-Microbe Interactions22785786710.1094/mpmi-22-7-085719522568Open DOISearch in Google Scholar
Fu S.-F., Tsai T.-M., Chen Y.-R., Liu C.-P., Haiso L.-J., Syue L.-H. et al. 2012. Characterization of the early response of the orchid, Phalaenopsis amabilis, to Erwinia chrysanthemi infection using expression profiling. Physiologia Plantarum 145(3): 406–425. DOI: 10.1111/j.1399-3054.2012.01582.x.FuS.-F.TsaiT.-M.ChenY.-R.LiuC.-P.HaisoL.-J.SyueL.-H.2012Characterization of the early response of the orchid, Phalaenopsis amabilis, to Erwinia chrysanthemi infection using expression profilingPhysiologia Plantarum145340642510.1111/j.1399-3054.2012.01582.x22268629Open DOISearch in Google Scholar
Ganapathy G., Keerthi D., Nair R.A., Pillai P. 2016. Correlation of phenylalanine ammonia lyase (PAL) and tyrosine ammonia lyase (TAL) activities to phenolics and curcuminoid content in ginger and its wild congener, Zingiber zerumbet following Pythium myriotylum infection. European Journal of Plant Pathology 145(4): 777–785. DOI: 10.1007/s10658-016-0865-2.GanapathyG.KeerthiD.NairR.A.PillaiP.2016Correlation of phenylalanine ammonia lyase (PAL) and tyrosine ammonia lyase (TAL) activities to phenolics and curcuminoid content in ginger and its wild congener, Zingiber zerumbet following Pythium myriotylum infectionEuropean Journal of Plant Pathology145477778510.1007/s10658-016-0865-2Open DOISearch in Google Scholar
Garcion C., Lohmann A., Lamodière E., Catinot J., Buchala A., Doermann P., Mètraux J.-P. 2008. Characterization and biological function of the ISOCHORISMATE SYNTHASE2 gene of Arabidopsis. Plant Physiology 147(3): 1279–1287. DOI: 10.1104/pp.108.119420.GarcionC.LohmannA.LamodièreE.CatinotJ.BuchalaA.DoermannP.MètrauxJ.-P.2008Characterization and biological function of the ISOCHORISMATE SYNTHASE2 gene of ArabidopsisPlant Physiology14731279128710.1104/pp.108.119420244254018451262Open DOISearch in Google Scholar
Gechev T.S., Van Breusegem F., Stone J.M., Denev I., Laloi C. 2006. Reactive oxygen species as signals that modulate plant stress responses and programmed cell death. BioEssays 28(11): 1091–1101. DOI: 10.1002/bies.20493.GechevT.S.Van BreusegemF.StoneJ.M.DenevI.LaloiC.2006Reactive oxygen species as signals that modulate plant stress responses and programmed cell deathBioEssays28111091110110.1002/bies.2049317041898Open DOISearch in Google Scholar
Gill S.S., Tuteja N. 2010. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry 48(12): 909–930. DOI: 10.1016/j.plaphy.2010.08.016.GillS.S.TutejaN.2010Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plantsPlant Physiology and Biochemistry481290993010.1016/j.plaphy.2010.08.01620870416Open DOISearch in Google Scholar
Giorgio M., Trinei M., Migliaccio E., Pelicci P.G. 2007. Hydrogen peroxide: a metabolic by-product or a common mediator of ageing signals? Nature Reviews Molecular Cell Biology 8(9): 722–728. DOI: 10.1038/nrm2240.GiorgioM.TrineiM.MigliaccioE.PelicciP.G.2007Hydrogen peroxide: a metabolic by-product or a common mediator of ageing signals?Nature Reviews Molecular Cell Biology8972272810.1038/nrm224017700625Open DOISearch in Google Scholar
Golubenko Z., Akhunov A., Khashimova N., Beresneva Y., Mustakimova E., Ibragimov F., Abdurashidova N., Stipanovic R. 2007. Induction of peroxidase as a disease resistance response in resistant (Hibiscus trionum) and susceptible (Althea armeniaca) species in the family Malvaceae. Phytoparasitica 35(4): 401–413. DOI: 10.1007/bf02980704.GolubenkoZ.AkhunovA.KhashimovaN.BeresnevaY.MustakimovaE.IbragimovF.AbdurashidovaN.StipanovicR.2007Induction of peroxidase as a disease resistance response in resistant (Hibiscus trionum) and susceptible (Althea armeniaca) species in the family MalvaceaePhytoparasitica35440141310.1007/bf02980704Open DOISearch in Google Scholar
Göhre V., Robatzek S. 2008. Breaking the barriers: Microbial effector molecules subvert plant immunity. Annual Review of Phytopathology 46: 189–215. DOI: 10.1146/annurev.phyto.46.120407.110050.GöhreV.RobatzekS.2008Breaking the barriers: Microbial effector molecules subvert plant immunityAnnual Review of Phytopathology4618921510.1146/annurev.phyto.46.120407.11005018422429Open DOISearch in Google Scholar
Hanudin, Suhardi 2009. Praevaluasi karakter ketahanan terhadap penyakit busuk lunak pada anggrek Phalaenopsis. Laporan Hasil Penelitian Balai Penelitian Tanaman Hias, Segunung, Indonesia, 14 p. [in Indonesian]HanudinSuhardi2009Praevaluasi karakter ketahanan terhadap penyakit busuk lunak pada anggrek PhalaenopsisLaporan Hasil Penelitian Balai Penelitian Tanaman HiasSegunung, Indonesia14[in Indonesian]Search in Google Scholar
Hasanuzzaman M., Bhuyan M.H.M.B., Zulfiqar F., Raza A., Mohsin S.M., Al Mahmud J. et al. 2020. Reactive oxygen species and antioxidant defense in plants under abiotic stress: Revisiting the crucial role of a universal defense regulator. Antioxidants 9(8); 681; 52 p. DOI: 10.3390/antiox9080681.HasanuzzamanM.BhuyanM.H.M.B.ZulfiqarF.RazaA.MohsinS.M.Al MahmudJ.2020Reactive oxygen species and antioxidant defense in plants under abiotic stress: Revisiting the crucial role of a universal defense regulatorAntioxidants9868152 p.10.3390/antiox9080681746562632751256Open DOISearch in Google Scholar
Herrera-Vásquez A., Salinas P., Holuigue L. 2015. Salicylic acid and reactive oxygen species interplay in the transcriptional control of defense genes expression. Frontiers in Plant Science 6; 171; 9. DOI: 10.3389/fpls.2015.00171.Herrera-VásquezA.SalinasP.HoluigueL.2015Salicylic acid and reactive oxygen species interplay in the transcriptional control of defense genes expressionFrontiers in Plant Science61719.10.3389/fpls.2015.00171436554825852720Open DOISearch in Google Scholar
Honty K., Hevesi M., Tóth M., Sárdi É., Stefanovits-Bányai É. 2008. Effect of Erwinia amylovora infection in biochemical changes of different pear fruits. Acta Horticulturae 800: 879–884. DOI: 10.17660/actahortic.2008.800.119.HontyK.HevesiM.TóthM.SárdiÉ.Stefanovits-BányaiÉ.2008Effect of Erwinia amylovora infection in biochemical changes of different pear fruitsActa Horticulturae80087988410.17660/actahortic.2008.800.119Open DOISearch in Google Scholar
Huang J., Gu M., Lai Z., Fan B., Shi K., Zhou Y.-H. et al. 2010. Functional analysis of the Arabidopsis PAL gene family in plant growth, development, and response to environmental stress. Plant Physiology 153(4): 1526–1538. DOI: 10.1104/pp.110.157370.HuangJ.GuM.LaiZ.FanB.ShiK.ZhouY.-H.2010Functional analysis of the Arabidopsis PAL gene family in plant growth, development, and response to environmental stressPlant Physiology15341526153810.1104/pp.110.157370292390920566705Open DOISearch in Google Scholar
Huang H., Ullah F., Zhou D.-X., Yi M., Zhao Y. 2019. Mechanisms of ROS regulation of plant development and stress responses. Frontiers in Plant Science 10; 800; 10 p. DOI: 10.3389/fpls.2019.00800.HuangH.UllahF.ZhouD.-X.YiM.ZhaoY.2019Mechanisms of ROS regulation of plant development and stress responsesFrontiers in Plant Science1080010 p.10.3389/fpls.2019.00800660315031293607Open DOISearch in Google Scholar
Huang S., Zhang X., Fernando W.G.D. 2020. Directing trophic divergence in plant-pathogen interactions: Antagonistic phytohormones with NO doubt? Frontiers in Plant Science 11; 600063; 9 p. DOI: 10.3389/fpls.2020.600063.HuangS.ZhangX.FernandoW.G.D.2020Directing trophic divergence in plant-pathogen interactions: Antagonistic phytohormones with NO doubt?Frontiers in Plant Science116000639 p.10.3389/fpls.2020.600063774431033343601Open DOISearch in Google Scholar
Kumari Y.S.M.A.I., Vengadaramana A. 2017. Stimulation of defense enzymes in tomato (Solanum lycopersicum L.) and chilli (Capsicum annuum L.) in response to exogenous application of different chemical elicitors. Universal Journal of Plant Science 5(1): 10–15. DOI: 10.13189/ujps.2017.050102.KumariY.S.M.A.I.VengadaramanaA.2017Stimulation of defense enzymes in tomato (Solanum lycopersicum L.) and chilli (Capsicum annuum L.) in response to exogenous application of different chemical elicitorsUniversal Journal of Plant Science51101510.13189/ujps.2017.050102Open DOISearch in Google Scholar
Jayanna S.K., Umesha S. 2017. Enhancement of the expression of defense genes in tomato against Ralstonia solanacearum by N-octanoyl-L-homoserine lactone. African Journal of Microbiology Research 11(5): 194–203. DOI: 10.5897/ajmr2016.8370.JayannaS.K.UmeshaS.2017Enhancement of the expression of defense genes in tomato against Ralstonia solanacearum by N-octanoyl-L-homoserine lactoneAfrican Journal of Microbiology Research11519420310.5897/ajmr2016.8370Open DOISearch in Google Scholar
Kapoor D., Singh S., Kumar V., Romero R., Prasad R., Singh J. 2019. Antioxidant enzymes regulation in plants in reference to reactive oxygen species (ROS) and reactive nitrogen species (RNS). Plant Gene 19; 100182; 13 p. DOI: 10.1016/j.plgene.2019.100182.KapoorD.SinghS.KumarV.RomeroR.PrasadR.SinghJ.2019Antioxidant enzymes regulation in plants in reference to reactive oxygen species (ROS) and reactive nitrogen species (RNS)Plant Gene1910018213 p.10.1016/j.plgene.2019.100182Open DOISearch in Google Scholar
Kar M., Mishra D. 1976. Catalase, peroxidase, and polyphenoloxidase activities during rice leaf senescence. Plant Physiology 57(2): 315–319. DOI: 10.1104/pp.57.2.315.KarM.MishraD.1976Catalase, peroxidase, and polyphenoloxidase activities during rice leaf senescencePlant Physiology57231531910.1104/pp.57.2.31554201516659474Open DOISearch in Google Scholar
Kobayashi M., Yoshioka M., Asai S., Nomura H., Kuchimura K., Mori H. et al. 2012. StCDPK5 confers resistance to late blight pathogen but increases susceptibility to early blight pathogen in potato via reactive oxygen species burst. New Phytologist 196(1): 223–237. DOI: 10.1111/j.1469-8137.2012.04226.x.KobayashiM.YoshiokaM.AsaiS.NomuraH.KuchimuraK.MoriH.2012StCDPK5 confers resistance to late blight pathogen but increases susceptibility to early blight pathogen in potato via reactive oxygen species burstNew Phytologist196122323710.1111/j.1469-8137.2012.04226.x22783903Open DOISearch in Google Scholar
Lee M-H., Jeon H.S., Kim S.H., Chung J.H., Roppolo D., Lee H.-J. et al. 2019. Lignin-based barrier restricts pathogens to the infection site and confers resistance in plants. EMBO Journal 38(23); e101948; 17 p. DOI: 10.15252/embj.2019101948.LeeM-H.JeonH.S.KimS.H.ChungJ.H.RoppoloD.LeeH.-J.2019Lignin-based barrier restricts pathogens to the infection site and confers resistance in plantsEMBO Journal3823e10194817 p.10.15252/embj.2019101948688573631559647Open DOISearch in Google Scholar
Lefevere H., Bauters L., Gheysen G. 2020. Salicylic acid biosynthesis in plants. Frontiers in Plant Science 11; 338; 7 p. DOI: 10.3389/fpls.2020.00338.LefevereH.BautersL.GheysenG.2020Salicylic acid biosynthesis in plantsFrontiers in Plant Science113387 p.10.3389/fpls.2020.00338718200132362901Open DOISearch in Google Scholar
Li X., Xing X., Tian P., Zhang M., Huo Z., Zhao K. et al. 2018. Comparative transcriptome profiling reveals defense-related genes against Meloidogyne incognita invasion in tobacco. Molecules 23(8); 2081; 16 p. DOI: 10.3390/molecules23082081.LiX.XingX.TianP.ZhangM.HuoZ.ZhaoK.2018Comparative transcriptome profiling reveals defense-related genes against Meloidogyne incognita invasion in tobaccoMolecules238208116 p.10.3390/molecules23082081Open DOISearch in Google Scholar
Liu Q., Luo L., Zheng L. 2018. Lignins: Biosynthesis and biological functions in plants. International Journal of Molecular Sciences 19(2); 335; 16 p. DOI: 10.3390/ijms19020335.LiuQ.LuoL.ZhengL.2018Lignins: Biosynthesis and biological functions in plantsInternational Journal of Molecular Sciences19233516 p.10.3390/ijms19020335Open DOISearch in Google Scholar
Liu L., Gueguen-Chaignon V., Gonçalves I.R., Rascle C., Rigault M., Dellagi A. et al. 2019a. A secreted metal-binding protein protects necrotrophic phytopathogens from reactive oxygen species. Nature Communications 10; 4853; 15 p. DOI: 10.1038/s41467-019-12826-x.LiuL.Gueguen-ChaignonV.GonçalvesI.R.RascleC.RigaultM.DellagiA.2019aA secreted metal-binding protein protects necrotrophic phytopathogens from reactive oxygen speciesNature Communications10485315 p.10.1038/s41467-019-12826-xOpen DOISearch in Google Scholar
Liu M., Wu F., Wang S., Lu Y., Chen X., Wang Y. et al. 2019b. Comparative transcriptome analysis reveals defense responses against soft rot in Chinese cabbage. Horticulture Research 6; 68; 18 p. DOI: 10.1038/s41438-019-0149-z.LiuM.WuF.WangS.LuY.ChenX.WangY.2019bComparative transcriptome analysis reveals defense responses against soft rot in Chinese cabbageHorticulture Research66818 p.10.1038/s41438-019-0149-zOpen DOISearch in Google Scholar
Lowry O.H., Rosebrough N.J., Farr A.L., Randall R.J. 1951. Protein measurement with the Folin phenol reagent. Journal of Biological Chemistry 193(1): 265–275. DOI: 10.1016/s0021-9258(19)52451-6.LowryO.H.RosebroughN.J.FarrA.L.RandallR.J.1951Protein measurement with the Folin phenol reagentJournal of Biological Chemistry193126527510.1016/s0021-9258(19)52451-6Open DOISearch in Google Scholar
Lubis U.N.Q., Sukma D., Sudarsono 2020. Response of in vitro plantlets and induced resistance of Phalaenopsis amabilis seedling to Dickeya dadantii using salicylic acid. Jurnal Agronomi Indonesia 48(3): 331–338. DOI: 10.24831/jai.v48i3.32014. [in Indonesian with English abstract]LubisU.N.Q.SudarsonoSukma D.2020Response of in vitro plantlets and induced resistance of Phalaenopsis amabilis seedling to Dickeya dadantii using salicylic acidJurnal Agronomi Indonesia48333133810.24831/jai.v48i3.32014[in Indonesian with English abstract]Open DOISearch in Google Scholar
Luna E., Pastor V., Robert J., Flors V., Mauch-Mani B., Ton J. 2011. Callose deposition: A multifaceted plant defense response. Molecular Plant-Microbe Interactions 24(2): 183–193. DOI: 10.1094/mpmi-07-10-0149.LunaE.PastorV.RobertJ.FlorsV.Mauch-ManiB.TonJ.2011Callose deposition: A multifaceted plant defense responseMolecular Plant-Microbe Interactions24218319310.1094/mpmi-07-10-014920955078Open DOISearch in Google Scholar
Luzzatto T., Yishay M., Lipsky A., Ion A., Belausov E., Yedidia I. 2007. Efficient, long-lasting resistance against the soft rot bacterium Pectobacterium carotovorum in calla lily provided by the plant activator methyl jasmonate. Plant Pathology 56(4): 692–701. DOI: 10.1111/j.1365-3059.2007.01622.x.LuzzattoT.YishayM.LipskyA.IonA.BelausovE.YedidiaI.2007Efficient, long-lasting resistance against the soft rot bacterium Pectobacterium carotovorum in calla lily provided by the plant activator methyl jasmonatePlant Pathology56469270110.1111/j.1365-3059.2007.01622.xOpen DOISearch in Google Scholar
Łojkowska E., Hołubowska M. 1992. The role of polyphenol oxidase and peroxidase in potato tuber resistance to soft rot caused by Erwinia carotovora. Journal of Phytopathology 136(4): 319–328. DOI: 10.1111/j.1439-0434.1992.tb01314.x.ŁojkowskaE.HołubowskaM.1992The role of polyphenol oxidase and peroxidase in potato tuber resistance to soft rot caused by Erwinia carotovoraJournal of Phytopathology136431932810.1111/j.1439-0434.1992.tb01314.xOpen DOISearch in Google Scholar
Łojkowska E., Kelman A. 1994. Comparison of the effectiveness of different methods of screening for bacterial soft rot resistance of potato tubers. American Potato Journal 71: 99–113. DOI: 10.1007/bf02849113.ŁojkowskaE.KelmanA.1994Comparison of the effectiveness of different methods of screening for bacterial soft rot resistance of potato tubersAmerican Potato Journal719911310.1007/bf02849113Open DOISearch in Google Scholar
Meng X., Chai A., Shi Y., Xie X., Ma Z., Li B. 2017. Emergence of bacterial soft rot in cucumber caused by Pectobacterium carotovorum subsp. brasiliense in China. Plant Disease 101(2): 279–287. DOI: 10.1094/pdis-05-16-0763-re.MengX.ChaiA.ShiY.XieX.MaZ.LiB.2017Emergence of bacterial soft rot in cucumber caused by Pectobacterium carotovorum subsp. brasiliense in ChinaPlant Disease101227928710.1094/pdis-05-16-0763-re30681927Open DOISearch in Google Scholar
Mengiste T. 2012. Plant immunity to necrotrophs. Annual Review of Phytopathology 50: 267–294. DOI: 10.1146/annurev-phyto-081211-172955.MengisteT.2012Plant immunity to necrotrophsAnnual Review of Phytopathology5026729410.1146/annurev-phyto-081211-17295522726121Open DOISearch in Google Scholar
Mithöfer A., Maffei M.E. 2017. General mechanisms of plant defense and plant toxins. Plant Toxins, pp. 3–24. DOI: 10.1007/978-94-007-6464-4_21.MithöferA.MaffeiM.E.2017General mechanisms of plant defense and plant toxinsPlant Toxins32410.1007/978-94-007-6464-4_21Open DOISearch in Google Scholar
Mittler R. 2017. ROS are good. Trends in Plant Science 22(1): 11–19. DOI: 10.1016/j.tplants.2016.08.002.MittlerR.2017ROS are goodTrends in Plant Science221111910.1016/j.tplants.2016.08.00227666517Open DOISearch in Google Scholar
Motyka A., Zoledowska S., Sledz W., Lojkowska E. 2017. Molecular methods as tools to control plant diseases caused by Dickeya and Pectobacterium spp: A minireview. New Biotechnology 39: 181–189. DOI: 10.1016/j.nbt.2017.08.010.MotykaA.ZoledowskaS.SledzW.LojkowskaE.2017Molecular methods as tools to control plant diseases caused by Dickeya and Pectobacterium spp: A minireviewNew Biotechnology3918118910.1016/j.nbt.2017.08.01028847714Open DOISearch in Google Scholar
Pervez Z., Alam M.S., Islam M.S. 2016. First report of bacterial soft rot of Aloe vera (Aloe barbadensis) caused by Pectobacterium chrysanthemi in Bangladesh. Journal of Plant Pathology and Microbiology 7(12); e110. DOI: 10.4172/2157-7471.1000e110.PervezZ.AlamM.S.IslamM.S.2016First report of bacterial soft rot of Aloe vera (Aloe barbadensis) caused by Pectobacterium chrysanthemi in BangladeshJournal of Plant Pathology and Microbiology712e11010.4172/2157-7471.1000e110Open DOISearch in Google Scholar
Pérombelon M.C.M. 1992. Potato blackleg: Epidemiology, host–pathogen interaction and control. Netherlands Journal of Plant Pathology 98: 135–146. DOI: 10.1007/bf01974480.PérombelonM.C.M.1992Potato blackleg: Epidemiology, host–pathogen interaction and controlNetherlands Journal of Plant Pathology9813514610.1007/bf01974480Open DOISearch in Google Scholar
Pérombelon M.C.M. 2002. Potato diseases caused by soft rot erwinias: an overview of pathogenesis. Plant Pathology 51(1): 1–12. DOI: 10.1046/j.0032-0862.2001.shorttitle.doc.x.PérombelonM.C.M.2002Potato diseases caused by soft rot erwinias: an overview of pathogenesisPlant Pathology51111210.1046/j.0032-0862.2001.shorttitle.doc.xOpen DOISearch in Google Scholar
Potrykus M., Hugouvieux-Cotte-Pattat N., Lojkowska E. 2018. Interplay of classic Exp and specific Vfm quorum sensing systems on the phenotypic features of Dickeya solani strains exhibiting different virulence levels. Molecular Plant Pathology 19(5): 1238–1251. DOI: 10.1111/mpp.12614.PotrykusM.Hugouvieux-Cotte-PattatN.LojkowskaE.2018Interplay of classic Exp and specific Vfm quorum sensing systems on the phenotypic features of Dickeya solani strains exhibiting different virulence levelsMolecular Plant Pathology1951238125110.1111/mpp.12614663815628921772Open DOISearch in Google Scholar
Prasannath K. 2017. Plant defense-related enzymes against pathogens: A review. AGRIEAST 11(1): 38–48. DOI: 10.4038/agrieast.v11i1.33.PrasannathK.2017Plant defense-related enzymes against pathogens: A reviewAGRIEAST111384810.4038/agrieast.v11i1.33Open DOISearch in Google Scholar
Putri H.A., Purwito A., Sudarsono, Sukma D. 2021. Morphological, molecular and resistance responses to soft-rot disease variability among plantlets of Phalaenopsis amabilis regenerated from irradiated protocorms. Biodiversitas 22(3): 1077–1090. DOI: 10.13057/biodiv/d220301.PutriH.A.PurwitoA.SudarsonoSukma D.2021Morphological, molecular and resistance responses to soft-rot disease variability among plantlets of Phalaenopsis amabilis regenerated from irradiated protocormsBiodiversitas2231077109010.13057/biodiv/d220301Open DOISearch in Google Scholar
Reverchon S., Nasser W. 2013. Dickeya ecology, environment sensing and regulation of virulence programme. Environmental Microbiology Reports 5(5): 622–636. DOI: 10.1111/1758-2229.12073.ReverchonS.NasserW.2013Dickeya ecology, environment sensing and regulation of virulence programmeEnvironmental Microbiology Reports5562263610.1111/1758-2229.1207324115612Open DOISearch in Google Scholar
Rossmann S., Dees M.W., Perminow J., Meadow R., Brurberg M.B. 2018. Soft rot Enterobacteriaceae are carried by a large range of insect species in potato fields. Applied and Environmental Microbiology 84(12); e00281-18. DOI: 10.1128/aem.00281-18.RossmannS.DeesM.W.PerminowJ.MeadowR.BrurbergM.B.2018Soft rot Enterobacteriaceae are carried by a large range of insect species in potato fieldsApplied and Environmental Microbiology8412e00281-1810.1128/aem.00281-18598108529625979Open DOISearch in Google Scholar
Sanjaya I P.W., Sukma D., Sudarsono, Chan M.-T. 2020. Effect of genotype, concentration and timing of salicylic acid application to Phalaenopsis against Dickeya dadantii infection. Biodiversitas 21(9): 4317–4324. DOI: 10.13057/biodiv/d210950.SanjayaI P.W.SukmaD.SudarsonoChanM.-T.2020Effect of genotype, concentration and timing of salicylic acid application to Phalaenopsis against Dickeya dadantii infectionBiodiversitas2194317432410.13057/biodiv/d210950Open DOISearch in Google Scholar
Schippers J.H.M., Foyer C.H., van Dongen J.T. 2016. Redox regulation in shoot growth, SAM maintenance and flowering. Current Opinion in Plant Biology 29: 121–128. DOI: 10.1016/j.pbi.2015.11.009.SchippersJ.H.M.FoyerC.H.van DongenJ.T.2016Redox regulation in shoot growth, SAM maintenance and floweringCurrent Opinion in Plant Biology2912112810.1016/j.pbi.2015.11.00926799134Open DOISearch in Google Scholar
Simons T.J., Ross A.F. 1971. Metabolic changes associated with systemic induced resistance to tobacco mosaic virus in Samsun NN tobacco. Phytopathology 61: 293–300. DOI: 10.1094/phyto-61-293.SimonsT.J.RossA.F.1971Metabolic changes associated with systemic induced resistance to tobacco mosaic virus in Samsun NN tobaccoPhytopathology6129330010.1094/phyto-61-293Open DOISearch in Google Scholar
Singh Y., Nair A.M., Verma P.K. 2021. Surviving the odds: From perception to survival of fungal phytopathogens under host-generated oxidative burst. Plant Communications 2(3); 100142; 17 p. DOI: 10.1016/j.xplc.2021.100142.SinghY.NairA.M.VermaP.K.2021Surviving the odds: From perception to survival of fungal phytopathogens under host-generated oxidative burstPlant Communications2310014217 p.10.1016/j.xplc.2021.100142813212434027389Open DOISearch in Google Scholar
Pedras M.S.C., Yaya E.E. 2015. Plant chemical defenses: Are all constitutive antimicrobial metabolites phytoanticipins? Natural Product Communications 10(1): 209–218. DOI: 10.1177/1934578x1501000142.PedrasM.S.C.YayaE.E.2015Plant chemical defenses: Are all constitutive antimicrobial metabolites phytoanticipins?Natural Product Communications10120921810.1177/1934578x1501000142Open DOISearch in Google Scholar
Sudarsono S., Elina J., Giyanto, Sukma D. 2018. Pathogen causing Phalaenopsis soft rot disease – 16S rDNA and virulence characterisation. Plant Protection Science 54(1): 1–8. DOI: 10.17221/18/2017-pps.SudarsonoS.ElinaJ.GiyantoSukma D.2018Pathogen causing Phalaenopsis soft rot disease – 16S rDNA and virulence characterisationPlant Protection Science5411810.17221/18/2017-ppsOpen DOISearch in Google Scholar
Sukma D., Poerwanto R., Sudarsono, Khumaida N., Artika I M., Wiyono S. 2012. Chitinase and peroxydase activities of crude protein extracts from callus and Trichosanthes cucumerina var. anguina tissues. Jurnal Agronomi Indonesia 40(3): 225–231. [in Indonesian with English abstract]SukmaD.PoerwantoR.SudarsonoKhumaida N.ArtikaI M.WiyonoS.2012Chitinase and peroxydase activities of crude protein extracts from callus and Trichosanthes cucumerina var. anguina tissuesJurnal Agronomi Indonesia403225231[in Indonesian with English abstract]Search in Google Scholar
Sukma D., Elina J., Giyanto, Sudarsono 2017. Disease resistance breeding of Phalaenopsis spp. for tropical environment and molecular marker development for plant selection. Acta Horticulturae 1167: 237–244. DOI: 10.17660/actahortic.2017.1167.36.SukmaD.ElinaJ.GiyantoSudarsono2017Disease resistance breeding of Phalaenopsis spp. for tropical environment and molecular marker development for plant selectionActa Horticulturae116723724410.17660/actahortic.2017.1167.36Open DOISearch in Google Scholar
Tenhaken R., Rübel C. 1997. Salicylic acid is needed in hypersensitive cell death in soybean but does not act as a catalase inhibitor. Plant Physiology 115(1): 291–298. DOI: 10.1104/pp.115.1.291.TenhakenR.RübelC.1997Salicylic acid is needed in hypersensitive cell death in soybean but does not act as a catalase inhibitorPlant Physiology115129129810.1104/pp.115.1.29115848512223807Open DOISearch in Google Scholar
Toth I.K, Bell K.S., Holeva M.C., Birch P.R.J. 2003. Soft rot erwiniae: from genes to genomes. Molecular Plant Pathology 4(1): 17–30. DOI: 10.1046/j.1364-3703.2003.00149.x.TothI.KBellK.S.HolevaM.C.BirchP.R.J.2003Soft rot erwiniae: from genes to genomesMolecular Plant Pathology41173010.1046/j.1364-3703.2003.00149.x20569359Open DOISearch in Google Scholar
Tsers I., Gorshkov V., Gogoleva N., Parfirova O., Petrova O., Gogolev Y. 2020. Plant soft rot development and regulation from the viewpoint of transcriptomic profiling. Plants 9(9); 1176; 30 p. DOI: 10.3390/plants9091176.TsersI.GorshkovV.GogolevaN.ParfirovaO.PetrovaO.GogolevY.2020Plant soft rot development and regulation from the viewpoint of transcriptomic profilingPlants99117630 p.10.3390/plants9091176757024732927917Open DOISearch in Google Scholar
Walters D., Cowley T., Mitchell A. 2002. Methyl jasmonate alters polyamine metabolism and induces systemic protection against powdery mildew infection in barley seedlings. Journal of Experimental Botany 53(369): 747–756. DOI: 10.1093/jexbot/53.369.747.WaltersD.CowleyT.MitchellA.2002Methyl jasmonate alters polyamine metabolism and induces systemic protection against powdery mildew infection in barley seedlingsJournal of Experimental Botany5336974775610.1093/jexbot/53.369.74711886895Open DOISearch in Google Scholar
Wang S., Wu X.-M., Liu C.-H., Shang J.-Y., Gao F., Guo H.-S. 2020. Verticillium dahliae chromatin remodeling facilitates the DNA damage repair in response to plant ROS stress. PLoS Pathogens 16(4); e1008481; 22 p. DOI: 10.1371/journal.ppat.1008481.WangS.WuX.-M.LiuC.-H.ShangJ.-Y.GaoF.GuoH.-S.2020Verticillium dahliae chromatin remodeling facilitates the DNA damage repair in response to plant ROS stressPLoS Pathogens164e100848122 p.10.1371/journal.ppat.1008481718829832298394Open DOISearch in Google Scholar
Wang Y., Li X., Fan B., Zhu C., Chen Z. 2021. Regulation and function of defense-related callose deposition in plants. International Journal of Molecular Sciences 22(5); 2393; 15 p. DOI: 10.3390/ijms22052393.WangY.LiX.FanB.ZhuC.ChenZ.2021Regulation and function of defense-related callose deposition in plantsInternational Journal of Molecular Sciences225239315 p.10.3390/ijms22052393795782033673633Open DOISearch in Google Scholar
Xu L., Zhu L., Tu L., Liu L., Yuan D., Jin L. et al. 2011. Lignin metabolism has a central role in the resistance of cotton to the wilt fungus Verticillium dahliae as revealed by RNA-Seq-dependent transcriptional analysis and histochemistry. Journal of Experimental Botany 62(15): 5607–5621. DOI: 10.1093/jxb/err245.XuL.ZhuL.TuL.LiuL.YuanD.JinL.2011Lignin metabolism has a central role in the resistance of cotton to the wilt fungus Verticillium dahliae as revealed by RNA-Seq-dependent transcriptional analysis and histochemistryJournal of Experimental Botany62155607562110.1093/jxb/err245322305421862479Open DOISearch in Google Scholar
Zhang X., Liu C.-J. 2015. Multifaceted regulations of gateway enzyme phenylalanine ammonia-lyase in the biosynthesis of phenylpropanoids. Molecular Plant 8(1): 17–27. DOI: 10.1016/j.molp.2014.11.001.ZhangX.LiuC.-J.2015Multifaceted regulations of gateway enzyme phenylalanine ammonia-lyase in the biosynthesis of phenylpropanoidsMolecular Plant81172710.1016/j.molp.2014.11.00125578269Open DOISearch in Google Scholar