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Next article No AccessThe Problem of Acquired Physiological Immunity in PlantsKenneth S. ChesterKenneth S. Chester Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The Quarterly Review of Biology Volume 8, Number 2Jun., 1933 Published in association with Stony Brook University Article DOIhttps://doi.org/10.1086/394430 Views: 4Total views on this site Citations: 89Citations are reported from Crossref PDF download Crossref reports the following articles citing this article:Palina V. Hryvusevich, Veranika V. Samokhina, Vadim V. Demidchik Stress-induced electrolyte leakage from root cells of higher plants: background, mechanism and physiological role, Experimental Biology and Biotechnology , no.22 (Jul 2022): 4–18.https://doi.org/10.33581/2957-5060-2022-2-4-18Lisa David, Jianing Kang, Josh Nicklay, Craig Dufresne, Sixue Chen Identification of DIR1-Dependant Cellular Responses in Guard Cell Systemic Acquired Resistance, Frontiers in Molecular Biosciences 8 (Dec 2021).https://doi.org/10.3389/fmolb.2021.746523Hachiro Oku Systemic Induced Resistance as a Tool for Disease Control, (Oct 2020): 143–162.https://doi.org/10.1201/9781003070085-6Rui Li, Jiping Sheng, Lin Shen Nitric Oxide Plays an Important Role in β-Aminobutyric Acid-Induced Resistance to Botrytis cinerea in Tomato Plants, The Plant Pathology Journal 36, no.22 (Apr 2020): 121–132.https://doi.org/10.5423/PPJ.OA.11.2019.0274David Langan, Noel R. Rose, Kamal D. Moudgil Common innate pathways to autoimmune disease, Clinical Immunology 212 (Mar 2020): 108361.https://doi.org/10.1016/j.clim.2020.108361Jessica Sharrock, Joseph C Sun Innate immunological memory: from plants to animals, Current Opinion in Immunology 62 (Feb 2020): 69–78.https://doi.org/10.1016/j.coi.2019.12.001Shyam Singh, L.P. Awasthi, H.N. Verma Systemic resistance inducers from plants—an ecofriendly approach for the management of viral diseases of crops, (Jan 2020): 603–617.https://doi.org/10.1016/B978-0-12-818654-1.00042-6Lisa David, Alice C. Harmon, Sixue Chen Plant immune responses - from guard cells and local responses to systemic defense against bacterial pathogens, Plant Signaling & Behavior 14, no.55 (Mar 2019): e1588667.https://doi.org/10.1080/15592324.2019.1588667Mohammad Tofajjal Hossain, Young Ryun Chung Endophytic Bacillus Species Induce Systemic Resistance to Plant Diseases, (Jan 2020): 151–160.https://doi.org/10.1007/978-3-030-15175-1_9Thomas Pradeu, Louis Du Pasquier Immunological memory: What's in a name?, Immunological Reviews 283, no.11 (Apr 2018): 7–20.https://doi.org/10.1111/imr.12652T. Marimuthu, M. Suganthy, S. Nakkeeran Common Pests and Diseases of Medicinal Plants and Strategies to Manage Them, (Apr 2018): 289–312.https://doi.org/10.1007/978-981-10-8291-7_14Baliah V. David, Govindan Chandrasehar, Pamila N. Selvam Pseudomonas fluorescens : A Plant-Growth-Promoting Rhizobacterium (PGPR) With Potential Role in Biocontrol of Pests of Crops, (Jan 2018): 221–243.https://doi.org/10.1016/B978-0-444-63987-5.00010-4Vivek Kumar, Ajit Varma, Narendra Tuteja, Anfal Arshi, Manoj Kumar Combinations of Plant Growth-Promoting Rhizobacteria (PGPR) for Initiation of Systemic Resistance Against Tree Diseases: A Glimpse, (Mar 2016): 207–212.https://doi.org/10.1007/978-981-10-0388-2_14F. L. Lukezic, G. C. M. Latch, F. S. Hay, K. Sivasithamparam Prospects of Biological Control of Diseases in Pasture Crops, (Nov 2015): 509–531.https://doi.org/10.2134/1996.pastureforagecroppathol.c29Shalini Srivastava, Vivek Prasad Induction of Defence Responses for Biological Control of Plant Diseases, (Jul 2014): 321–339.https://doi.org/10.1002/9781118533024.ch14Saskia C. M. Van Wees, Johan A. Van Pelt, Peter A. H. M. Bakker, Corné M. J. Pieterse Bioassays for Assessing Jasmonate-Dependent Defenses Triggered by Pathogens, Herbivorous Insects, or Beneficial Rhizobacteria, (Apr 2013): 35–49.https://doi.org/10.1007/978-1-62703-414-2_4Nicole Benhamou, Patrice Rey Stimulateurs des défenses naturelles des plantes : une nouvelle stratégie phytosanitaire dans un contexte d’écoproduction durable., Phytoprotection 92, no.11 (Sep 2012): 1–23.https://doi.org/10.7202/1012399arRay Hammerschmidt, Jennifer Smith Becker Acquired Resistance to Disease in Plants, (Jul 2010): 247–289.https://doi.org/10.1002/9780470650608.ch5Alieta Eyles, Pierluigi Bonello, Rebecca Ganley, Caroline Mohammed Induced resistance to pests and pathogens in trees, New Phytologist 185, no.44 (Dec 2009): 893–908.https://doi.org/10.1111/j.1469-8137.2009.03127.xLubomir Vechet, Lenka Burketova, Milada Sindelarova A comparative study of the efficiency of several sources of induced resistance to powdery mildew (Blumeria graminis f. sp. tritici) in wheat under field conditions, Crop Protection 28, no.22 (Feb 2009): 151–154.https://doi.org/10.1016/j.cropro.2008.09.009Michiko Yasuda, Atsushi Ishikawa, Yusuke Jikumaru, Motoaki Seki, Taishi Umezawa, Tadao Asami, Akiko Maruyama-Nakashita, Toshiaki Kudo, Kazuo Shinozaki, Shigeo Yoshida, Hideo Nakashita Antagonistic Interaction between Systemic Acquired Resistance and the Abscisic Acid–Mediated Abiotic Stress Response in Arabidopsis , The Plant Cell 20, no.66 (Jun 2008): 1678–1692.https://doi.org/10.1105/tpc.107.054296R. J. Scheffer, J. G. W. F. Voeten, R. P. Guries Biological Control of Dutch Elm Disease, Plant Disease 92, no.22 (Feb 2008): 192–200.https://doi.org/10.1094/PDIS-92-2-0192RICARDO B. FERREIRA, SARA MONTEIRO, REGINA FREITAS, CLÁUDIA N. SANTOS, ZHENJIA CHEN, LUÍS M. BATISTA, JOÃO DUARTE, ALEXANDRE BORGES, ARTUR R. TEIXEIRA The role of plant defence proteins in fungal pathogenesis, Molecular Plant Pathology 8, no.55 (Sep 2007): 677–700.https://doi.org/10.1111/j.1364-3703.2007.00419.xR. Karban, Y. Chen Induced resistance in rice against insects, Bulletin of Entomological Research 97, no.44 (Jul 2007): 327–335.https://doi.org/10.1017/S0007485307005056Ralf R Weigel Salicylic Acid, (Jul 2007).https://doi.org/10.1002/9780470015902.a0020137Murray Grant, Chris Lamb Systemic immunity, Current Opinion in Plant Biology 9, no.44 (Aug 2006): 414–420.https://doi.org/10.1016/j.pbi.2006.05.013F. Paul Silverman, Peter D. Petracek, Daniel F. Heiman, Christina M. Fledderman, Prem Warrior Salicylate Activity. 3. Structure Relationship to Systemic Acquired Resistance, Journal of Agricultural and Food Chemistry 53, no.2525 (Nov 2005): 9775–9780.https://doi.org/10.1021/jf051383tGary E. Vallad, Robert M. Goodman Systemic Acquired Resistance and Induced Systemic Resistance in Conventional Agriculture, Crop Science 44, no.66 (Nov 2004): 1920–1934.https://doi.org/10.2135/cropsci2004.1920Holger B. Deising, Sven Reimann, Andreas Peil, W. Eberhard Weber Disease Management of Rusts and Powdery Mildews, (Jan 2002): 243–269.https://doi.org/10.1007/978-3-662-03059-2_13Jolanta Floryszak-Wieczorek, Halina Gniazdowska-Skoczek Ribonuclease and proteinase activities in potato leaves immunized against Phytophthora infestans, Acta Physiologiae Plantarum 23, no.22 (Jun 2001): 207–212.https://doi.org/10.1007/s11738-001-0010-4V Ramamoorthy, R Viswanathan, T Raguchander, V Prakasam, R Samiyappan Induction of systemic resistance by plant growth promoting rhizobacteria in crop plants against pests and diseases, Crop Protection 20, no.11 (Feb 2001): 1–11.https://doi.org/10.1016/S0261-2194(00)00056-9Martin Heil Induced systemic resistance (ISR) against pathogens – a promising field for ecological research, Perspectives in Plant Ecology, Evolution and Systematics 4, no.22 (Jan 2001): 65–79.https://doi.org/10.1078/1433-8319-00015Joseph Kuć Development and future direction of induced systemic resistance in plants, Crop Protection 19, no.8-108-10 (Sep 2000): 859–861.https://doi.org/10.1016/S0261-2194(00)00122-8Katrin Beßer, Birgit Jarosch, Gregor Langen, Karl-Heinz Kogel Expression analysis of genes induced in barley after chemical activation reveals distinct disease resistance pathways, Molecular Plant Pathology 1, no.55 (Dec 2001): 277–286.https://doi.org/10.1046/j.1364-3703.2000.00031.x The Response of Plant Cell Wall Hydroxyproline-Rich Glycoproteins to Microbial Pathogens and Their Elicitors, (Apr 1999): 163–176.https://doi.org/10.1201/9781420049299-11D Mazau, Marie-Th√©r√®se Esquerr√©-Tugay√©, C Campargue The Response of Plant Cell Wall Hydroxyproline-Rich Glycoproteins to Microbial Pathogens and Their Elicitors, (Nov 2009).https://doi.org/10.1201/9781420049299.ch7John A Lucas Plant immunisation: from myth to SAR, Pesticide Science 55, no.22 (Mar 1999): 193–196.https://doi.org/10.1002/(SICI)1096-9063(199902)55:2<193::AID-PS883>3.0.CO;2-5Timothy C. Paulitz, Alberto Matta The Role of the Host in Biological Control of Diseases, (Jan 1999): 394–410.https://doi.org/10.1007/0-306-47585-5_28David M. Ribnicky, Vladimir Shulaev, Ilya Raskin Intermediates of Salicylic Acid Biosynthesis in Tobacco, Plant Physiology 118, no.22 (Oct 1998): 565–572.https://doi.org/10.1104/pp.118.2.565Mirjana Seskar, Vladimir Shulaev, Ilya Raskin Endogenous Methyl Salicylate in Pathogen-Inoculated Tobacco Plants, Plant Physiology 116, no.11 (Jan 1998): 387–392.https://doi.org/10.1104/pp.116.1.387Ken Shirasu, Richard A Dixon, Chris Lamb Signal transduction in plant immunity, Current Opinion in Immunology 8, no.11 (Feb 1996): 3–7.https://doi.org/10.1016/S0952-7915(96)80097-5K. Engstrom, A. Strömberg Changes in Sugar Content During Induction of Systemic Acquired Resistance to Late Blight Caused by Phytophthora infestans (Mont.) de Bary in Potato, Journal of Phytopathology 144, no.11 (Jan 1996): 33–36.https://doi.org/10.1111/j.1439-0434.1996.tb01485.xKarl-Heinz Kogel, Birgit Ortel, Birgit Jarosch, Rainer Atzorn, Ruth Schiffer, Claus Wasternack Resistance in barley against the powdery mildew fungus (Erysiphe graminis f.sp.hordei) is not associated with enhanced levels of endogenous jasmonates, European Journal of Plant Pathology 101, no.33 (May 1995): 319–332.https://doi.org/10.1007/BF01874788Joseph Kuć Induced Systemic Resistance — An Overview, (Jan 1995): 169–175.https://doi.org/10.1007/978-94-015-8420-3_8C. Wasternack, R. Atzorn, B. Jarosch, K. H. Kogel Induction of a Thionin, the Jasmonate-Induced 6 kDa Protein of Barley by 2,6-Dechloroisonicotinic acid, Journal of Phytopathology 140, no.33 (Mar 1994): 280–284.https://doi.org/10.1111/j.1439-0434.1994.tb04817.xJeffry R. Borgmeyer, Christine E. Smith, Q. Khai Huynh Isolation and characterization of a 25 kDa antifungal protein from flax seeds, Biochemical and Biophysical Research Communications 187, no.11 (Aug 1992): 480–487.https://doi.org/10.1016/S0006-291X(05)81519-0Amira A. El-Gammal, R.M.A. Mansour Antimicrobial Activities of Some Flavonoid Compounds, Zentralblatt für Mikrobiologie 141, no.77 (Jan 1986): 561–565.https://doi.org/10.1016/S0232-4393(86)80010-5K. Stenzel, Ulrke Steiner, F. Schönbeck Effect of induced resistance on the efficiency of powdery mildew haustoria in wheat and barley, Physiological Plant Pathology 27, no.33 (Nov 1985): 357–367.https://doi.org/10.1016/0048-4059(85)90048-7Ralph A. Dean, Joseph Kuć Induced systemic protection in plants, Trends in Biotechnology 3, no.55 (May 1985): 125–129.https://doi.org/10.1016/0167-7799(85)90128-3P. J. G. M. De Wit Induced Resistance to Fungal and Bacterial Diseases, (Jan 1985): 405–424.https://doi.org/10.1007/978-94-009-5145-7_10F.L. Caruso, R.H. Cody Potential for induced resistance in apple against infection by Venturia inaequalis, Canadian Journal of Plant Pathology 6, no.22 (Dec 2009): 151–159.https://doi.org/10.1080/07060668409501576R. Rohringer, R. Heitefuss Histology and Molecular Biology of Host–Parasite Specificity, (Jan 1984): 193–229.https://doi.org/10.1016/B978-0-12-148401-9.50013-3Albertus B. Eskes Expression of Incomplete Resistance to Pathogens, (Jan 1983): 169–195.https://doi.org/10.1007/978-1-4615-9305-8_15 Induced Immunity to Plant Disease, BioScience 32, no.1111 (Dec 1982): 854–860.https://doi.org/10.2307/1309008J. Kuc Plant Immunization-Mechanisms and Practical Implications, (Jan 1982): 157–178.https://doi.org/10.1007/978-1-4615-8309-7_9R.N. GOODMAN Defenses Triggered by Previous Invaders: Bacteria, (Jan 1980): 305–317.https://doi.org/10.1016/B978-0-12-356405-4.50023-XHans Grisebach, Jürgen Ebel Phytoalexine, chemische Abwehrstoffe höherer Pflanzen?, Angewandte Chemie 90, no.99 (Sep 1978): 668–681.https://doi.org/10.1002/ange.19780900906Hans Grisebach, J�rgen Ebel Phytoalexins, Chemical Defense Substances of Higher Plants?, Angewandte Chemie International Edition in English 17, no.99 (Sep 1978): 635–647.https://doi.org/10.1002/anie.197806351 Proceedings of the Association of Applied Biologists, Annals of Applied Biology 89, no.22 (Jul 1978): 287–378.https://doi.org/10.1111/j.1744-7348.1978.tb07702.xDonald F. Schoeneweiss WATER STRESS AS A PREDISPOSING FACTOR IN PLANT DISEASE, (Jan 1978): 61–99.https://doi.org/10.1016/B978-0-12-424155-8.50008-0J. Kuć Plant protection by the activation of latent mechanisms for resistance, Netherlands Journal of Plant Pathology 83, no.S1S1 (Jan 1977): 463–471.https://doi.org/10.1007/BF03041464A. Hilda, S. Suryanarayanan Cross-protection in the blast disease ofPanicum repens L., Proceedings / Indian Academy of Sciences 84, no.66 (Dec 1976).https://doi.org/10.1007/BF03045544Joseph Kuć Phytoalexins and the Specificity of Plant-Parasite Interaction, (Jan 1976): 253–271.https://doi.org/10.1007/978-1-4684-2769-1_16J. A. Kuć Phytoalexins, (Jan 1976): 632–652.https://doi.org/10.1007/978-3-642-66279-9_23J. Kuć, G. Shockley, K. Kearney Protection of cucumber against Colletotrichum lagenarium by Colletotrichum lagenarium, Physiological Plant Pathology 7, no.22 (Nov 1975): 195–199.https://doi.org/10.1016/0048-4059(75)90010-7S. Ouchi, H. Oku, C. Hibino, I. Akiyama Induction of Accessibility to a Nonpathogen by Preliminary Inoculation with a Pathogen, Journal of Phytopathology 79, no.22 (Feb 1974): 142–154.https://doi.org/10.1111/j.1439-0434.1974.tb02695.xMICHAEL A. MCCLURE, IRAJ MISAGHI, EDWARD L. NIGH Shared Antigens of Parasitic Nematodes and Host Plants, Nature 244, no.54145414 (Aug 1973): 306–307.https://doi.org/10.1038/244306a0 James E. DeVay , R. Charudattan , and D. L. S. Wimalajeewa Common Antigenic Determinants as a Possible Regulator of Host-Pathogen Compatibility, The American Naturalist 106, no.948948 (Oct 2015): 185–194.https://doi.org/10.1086/282761Sadik Tuzun Terminology Related to Induced Systemic Resistance: Incorrect Use of Synonyms may Lead to a Scientific Dilemma by Misleading Interpretation of Results, (): 1–8.https://doi.org/10.1007/0-387-23266-4_1Joseph Kuć What’s Old and What’s New in Concepts of Induced Systemic Resistance in Plants, and its Application, (): 9–20.https://doi.org/10.1007/0-387-23266-4_2Ulrike Steiner Induced Resistance as a Means of Plant Disease Control, (): 495–512.https://doi.org/10.1201/9781351075459-27D. Hocking Disease Resistance in Coffee Berries, East African Agricultural and Forestry Journal 32, no.44 (Dec 2015): 365–366.https://doi.org/10.1080/00128325.1967.11662145Robert C. Hare Physiology of resistance to fungal diseases in plants, The Botanical Review 32, no.22 (Apr 1966): 95–137.https://doi.org/10.1007/BF02858657D. Atanasoff Universality of Interferon Formation, Journal of Phytopathology 50, no.44 (Jun 1964): 336–358.https://doi.org/10.1111/j.1439-0434.1964.tb02932.xD. Atanasoff Interferon and Plant Viruses, Journal of Phytopathology 47, no.33 (May 1963): 207–214.https://doi.org/10.1111/j.1439-0434.1963.tb02099.xJ. G. Dickson Chemical control of cereal rusts, The Botanical Review 25, no.33 (Jul 1959): 486–513.https://doi.org/10.1007/BF02860028PAUL J. ALLEN Physiology and Biochemistry of Defense, (Jan 1959): 435–467.https://doi.org/10.1016/B978-0-12-395677-4.50018-6K.O. MÜLLER Hypersensitivity, (Jan 1959): 469–519.https://doi.org/10.1016/B978-0-12-395677-4.50019-8 Ralph W. Lewis An Outline of the Balance Hypothesis of Parasitism, The American Naturalist 87, no.836836 (Sep 2015): 273–281.https://doi.org/10.1086/281785Ethel K. Allen, O. N. Allen BIOCHEMICAL AND SYMBIOTIC PROPERTIES OF THE RHIZOBIA, Bacteriological Reviews 14, no.44 (Dec 1950): 273–330.https://doi.org/10.1128/br.14.4.273-330.1950Ralph O. Snelling Resistance of plants to insect attack, The Botanical Review 7, no.1010 (Oct 1941): 543–586.https://doi.org/10.1007/BF02872411S. A. Wingard The nature of disease resistance in plants. I, The Botanical Review 7, no.22 (Feb 1941): 59–109.https://doi.org/10.1007/BF02872445H. R. X. D'AETH A SURVEY OF INTERACTION BETWEEN FUNGI, Biological Reviews 14, no.22 (Apr 1939): 105–131.https://doi.org/10.1111/j.1469-185X.1939.tb00927.x Frances Louise Jewett Relation of Soil Temperature and Nutrition to the Resistance of Tobacco to Thielavia basicola, Botanical Gazette 100, no.22 (Oct 2015): 276–297.https://doi.org/10.1086/334785R. Doerr, C. Hallauer, J. Craigie, G. M. Findlay, K. M. Smith, O. Thomsen Classification, (Jan 1938): 1334–1342.https://doi.org/10.1007/978-3-662-42438-4_19D. W. Thorne, P. E. Brown The Growth and Respiration of Some Soil Bacteria in Juices of Leguminous and Non-Leguminous Plants, Journal of Bacteriology 34, no.66 (Dec 1937): 567–580.https://doi.org/10.1128/jb.34.6.567-580.1937W. F. Loehwing Root interactions of plants, The Botanical Review 3, no.44 (Apr 1937): 195–239.https://doi.org/10.1007/BF02872308William Brown The physiology of host-parasite relations, The Botanical Review 2, no.55 (May 1936).https://doi.org/10.1007/BF02867931 On the interactions of two strains of a plant virus; experiments on induced immunity in plants, Proceedings of the Royal Society of London. Series B - Biological Sciences 117, no.803803 (Mar 1935): 120–139.https://doi.org/10.1098/rspb.1935.0019

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