On the move: induced resistance in monocots

The plant immune system

Jones, J. D. G., & Dangl, J. L. (2006) · Nature · doi:10.1038/nature05286 · Cited by 13,177 · see citing works

Quorum Sensing in Bacteria

Miller, M. B., & Bassler, B. L. (2001) · Annual Review of Microbiology · doi:10.1146/annurev.micro.55.1.165 · Cited by 5,127 · see citing works

The map-based sequence of the rice genome

International Rice Genome Sequencing Project, & Sasaki, T. (2005) · Nature · doi:10.1038/nature03895 · Cited by 3,784 · see citing works

Networking by small-molecule hormones in plant immunity

Pieterse, C. M. J., León-Reyes, A., der Ent, S. V., & Wees, S. C. M. V. (2009) · Nature Chemical Biology · doi:10.1038/nchembio.164 · Cited by 2,334 · see citing works

A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence

Chinchilla, D., Zipfel, C., Robatzek, S., Kemmerling, B., Nürnberger, T., Jones, J. D. G., Felix, G., & Boller, T. (2007) · Nature · doi:10.1038/nature05999 · Cited by 1,923 · see citing works

Inducers of Plant Systemic Acquired Resistance Regulate NPR1 Function through Redox Changes

Mou, Z., Fan, W., & Dong, X. (2003) · Cell · doi:10.1016/s0092-8674(03)00429-x · Cited by 1,588 · see citing works

The Arabidopsis NPR1 Gene That Controls Systemic Acquired Resistance Encodes a Novel Protein Containing Ankyrin Repeats

Cao, H., Glazebrook, J., Clarke, J. D., Volko, S. M., & Dong, X. (1997) · Cell · doi:10.1016/s0092-8674(00)81858-9 · Cited by 1,572 · see citing works

The endophytic fungus Piriformospora indica reprograms barley to salt-stress tolerance, disease resistance, and higher yield

Waller, F., Achatz, B., Baltruschat, H., Fodor, J., Becker, K., Fischer, M., Heier, T., Hückelhoven, R., Neumann, C., von WETTSTEIN, D., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504423102 · Cited by 1,325 · see citing works

Unraveling mycorrhiza-induced resistance

Pozo, M. J., & Azcón‐Aguilar, C. (2007) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2007.05.004 · Cited by 1,178 · see citing works

Direct interaction of resistance gene and avirulence gene products confers rice blast resistance

Jia, Y., McAdams, S. A., Bryan, G. T., et al. (2000) · The EMBO Journal · doi:10.1093/emboj/19.15.4004 · Cited by 1,154 · see citing works

How do plants achieve immunity? Defence without specialized immune cells

Spoel, S. H., & Dong, X. (2012) · Nature reviews. Immunology · doi:10.1038/nri3141 · Cited by 1,114 · see citing works

Innate Immunity in Plants: An Arms Race Between Pattern Recognition Receptors in Plants and Effectors in Microbial Pathogens

Boller, T., & He, S. Y. (2009) · Science · doi:10.1126/science.1171647 · Cited by 1,088 · see citing works

Benzothiadiazole, a novel class of inducers of systemic acquired resistance, activates gene expression and disease resistance in wheat.

Görlach, J., Volrath, S., Knauf-Beiter, G., Hengy, G., Beckhove, U., Kogel, K.-H., Oostendorp, M., Staub, T. H., Ward, E., Keßmann, H., et al. (1996) · The Plant Cell · doi:10.1105/tpc.8.4.629 · Cited by 1,066 · see citing works

Methyl Salicylate Is a Critical Mobile Signal for Plant Systemic Acquired Resistance

Park, S., Kaimoyo, E., Kumar, D., Mosher, S., & Klessig, D. F. (2007) · Science · doi:10.1126/science.1147113 · Cited by 1,045 · see citing works

The transcriptome of Arabidopsis thaliana during systemic acquired resistance

Maleck, K., Levine, A., Eulgem, T., Morgan, A., Schmid, J., Lawton, K. A., Dangl, J. L., & Dietrich, R. A. (2000) · Nature Genetics · doi:10.1038/82521 · Cited by 1,021 · see citing works

An Elicitor of Plant Volatiles from Beet Armyworm Oral Secretion

Alborn, H. T., Turlings, T. C. J., Jones, T. H., Stenhagen, G., Loughrin, J. H., & Tumlinson, J. H. (1997) · Science · doi:10.1126/science.276.5314.945 · Cited by 998 · see citing works

Increase in Salicylic Acid at the Onset of Systemic Acquired Resistance in Cucumber

Métraux, J., Signer, H., Ryals, J. A., Ward, E. R., Wyss‐Benz, M., Gaudin, J., Raschdorf, K., Schmid, E., Blum, W., & Inverardi, B. (1990) · Science · doi:10.1126/science.250.4983.1004 · Cited by 984 · see citing works

NPR3 and NPR4 are receptors for the immune signal salicylic acid in plants

Fu, Z. Q., Yan, S., Saleh, A., Wang, W., Ruble, J., Oka, N., Mohan, R., Spoel, S. H., Tada, Y., Zheng, N., et al. (2012) · Nature · doi:10.1038/nature11162 · Cited by 984 · see citing works

Priming in Systemic Plant Immunity

Jung, H. W., Tschaplinski, T. J., Wang, L., Glazebrook, J., & Greenberg, J. T. (2009) · Science · doi:10.1126/science.1170025 · Cited by 929 · see citing works

Plant immune responses triggered by beneficial microbes

Wees, S. C. M. V., der Ent, S. V., & Pieterse, C. M. J. (2008) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2008.05.005 · Cited by 919 · see citing works

Plant responses to plant growth-promoting rhizobacteria

van Loon, L. C. (2007) · European Journal of Plant Pathology · doi:10.1007/s10658-007-9165-1 · Cited by 915 · see citing works

Comparing signaling mechanisms engaged in pattern-triggered and effector-triggered immunity

Tsuda, K., & Katagiri, F. (2010) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2010.04.006 · Cited by 886 · see citing works

A Kinase-START Gene Confers Temperature-Dependent Resistance to Wheat Stripe Rust

Fu, D., Uauy, C., Distelfeld, A., Blechl, A. E., Epstein, L., Chen, X., Sela, H., Fahima, T., & Dubcovsky, J. (2009) · Science · doi:10.1126/science.1166289 · Cited by 769 · see citing works

The role and regulation of programmed cell death in plant-pathogen interactions

Greenberg, J. T., & Yao, N. (2004) · Cellular Microbiology · doi:10.1111/j.1462-5822.2004.00361.x · Cited by 743 · see citing works

Two LysM receptor molecules, CEBiP and OsCERK1, cooperatively regulate chitin elicitor signaling in rice

Shimizu, T., Nakano, T., Takamizawa, D., Desaki, Y., Ishii-Minami, N., Nishizawa, Y., Minami, E., Okada, K., Yamane, H., Kaku, H., et al. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04324.x · Cited by 736 · see citing works

Expression of Xa1 , a bacterial blight-resistance gene in rice, is induced by bacterial inoculation

Yoshimura, S., Yamanouchi, U., Katayose, Y., Toki, S., Wang, Z., Kono, I., Kurata, N., Yano, M., Iwata, N., & Sasaki, T. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.4.1663 · Cited by 663 · see citing works

Helping plants to deal with insects: the role of beneficial soil-borne microbes

Pineda, A., Zheng, S., van Loon, J. J. A., Pieterse, C. M. J., & Dicke, M. (2010) · Trends in Plant Science · doi:10.1016/j.tplants.2010.05.007 · Cited by 640 · see citing works

The Broad-Spectrum Blast Resistance Gene Pi9 Encodes a Nucleotide-Binding Site–Leucine-Rich Repeat Protein and Is a Member of a Multigene Family in Rice

Qu, S., Liu, G., Zhou, B., Bellizzi, M. D. R., Zeng, L., Dai, L., Han, B., & Wang, G. (2005) · Genetics · doi:10.1534/genetics.105.044891 · Cited by 628 · see citing works

R gene expression induced by a type-III effector triggers disease resistance in rice

Gu, K., Yang, B., Tian, D., et al. (2005) · Nature · doi:10.1038/nature03630 · Cited by 578 · see citing works

A B‐lectin receptor kinase gene conferring rice blast resistance

Chen, X., Shang, J., Chen, D., Lei, C., Zou, Y., Zhai, W., Liu, G., Xu, J., ZhongZhuan, L., Cao, G., et al. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02739.x · Cited by 575 · see citing works

A unique wheat disease resistance-like gene governs effector-triggered susceptibility to necrotrophic pathogens

Faris, J. D., Zhang, Z., Lu, H., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1004090107 · Cited by 548 · see citing works

Early molecular events in PAMP-triggered immunity

Zipfel, C. (2009) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2009.06.003 · Cited by 545 · see citing works

Identification and characterization of Bph14 , a gene conferring resistance to brown planthopper in rice

Du, B., Zhang, W., Liu, B., Hu, J., Wei, Z., Shi, Z., He, R., Zhu, L., Chen, R., Han, B., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0912139106 · Cited by 542 · see citing works

Priming by airborne signals boosts direct and indirect resistance in maize

Ton, J., D’Alessandro, M., Jourdie, V., Jakab, G., Karlen, D., Held, M., Mauch‐Mani, B., & Turlings, T. C. J. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02935.x · Cited by 515 · see citing works

Rice xa13 Recessive Resistance to Bacterial Blight Is Defeated by Induction of the Disease Susceptibility Gene Os- 11N3

Antony, G., Zhou, J., Huang, S., Li, T., Liu, B., White, F. F., & Yang, B. (2010) · The Plant Cell · doi:10.1105/tpc.110.078964 · Cited by 502 · see citing works

Induction of systemic resistance in tomato by N ‐acyl‐L‐homoserine lactone‐producing rhizosphere bacteria

Schuhegger, R., Ihring, A., Gantner, S., Bahnweg, G., Knappe, C., Vogg, G., Hutzler, P., Schmid, M., Breusegem, F. V., Eberl, L., et al. (2006) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2005.01471.x · Cited by 474 · see citing works

Protein kinase signaling networks in plant innate immunity

Tena, G., Boudsocq, M., & Sheen, J. (2011) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2011.05.006 · Cited by 454 · see citing works

Localized versus systemic effect of arbuscular mycorrhizal fungi on defence responses to Phytophthora infection in tomato plants

Pozo, M. J., Cordier, C., Dumas‐Gaudot, E., Gianinazzi, S., Barea, J. M., & Azcón‐Aguilar, C. (2002) · Journal of Experimental Botany · doi:10.1093/jexbot/53.368.525 · Cited by 449 · see citing works

Unlocking the Barley Genome by Chromosomal and Comparative Genomics

Mayer, K., Martis, M. M., Hedley, P. E., Šimková, H., Liu, H., Morris, J., Steuernagel, B., Taudien, S., Roessner, S. K., Gundlach, H., et al. (2011) · The Plant Cell · doi:10.1105/tpc.110.082537 · Cited by 448 · see citing works

Inducible direct plant defense against insect herbivores: A review

Chen, M. (2008) · Insect Science · doi:10.1111/j.1744-7917.2008.00190.x · Cited by 447 · see citing works

Endogenous salicylic acid protects rice plants from oxidative damage caused by aging as well as biotic and abiotic stress

Yang, Y., Qi, M., & Mei, C. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02267.x · Cited by 444 · see citing works

Salicylic Acid in Rice (Biosynthesis, Conjugation, and Possible Role)

Silverman, P., Seskar, M., Kanter, D., Schweizer, P., Métraux, J., & Raskin, I. (1995) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.2.633 · Cited by 442 · see citing works

The barley stem rust-resistance gene Rpg1 is a novel disease-resistance gene with homology to receptor kinases

Brueggeman, R. S., Rostoks, N., Kudrna, D. A., Kilian, A., Han, F., Chen, J., Druka, A., Steffenson, B. J., & Kleinhofs, A. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.142284999 · Cited by 437 · see citing works

Glycerol-3-phosphate is a critical mobile inducer of systemic immunity in plants

Chanda, B., Xia, Y., Mandal, M. K., Yu, K., Sekine, K., Gao, Q.-M., Selote, D. S., Hu, Y., Stromberg, A. J., Navarre, D. A., et al. (2011) · Nature Genetics · doi:10.1038/ng.798 · Cited by 406 · see citing works

Hypersensitive Cell Death and Papilla Formation in Barley Attacked by the Powdery Mildew Fungus Are Associated with Hydrogen Peroxide but Not with Salicylic Acid Accumulation1

Hückelhoven, R., Fodor, J., Preis, C., & Kogel, K. (1999) · PLANT PHYSIOLOGY · doi:10.1104/pp.119.4.1251 · Cited by 401 · see citing works

Overexpression of a Rice NPR1 Homolog Leads to Constitutive Activation of Defense Response and Hypersensitivity to Light

Chern, M., Fitzgerald, H. A., Canlas, P. E., Navarre, D. A., & Ronald, P. C. (2005) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-18-0511 · Cited by 400 · see citing works

Evidence for a disease‐resistance pathway in rice similar to the NPR1‐mediated signaling pathway in Arabidopsis

Chern, M., Fitzgerald, H. A., Yadav, R. C., Canlas, P. E., Dong, X., & Ronald, P. C. (2001) · The Plant Journal · doi:10.1046/j.1365-313x.2001.01070.x · Cited by 353 · see citing works

SOS – too many signals for systemic acquired resistance?

Dempsey, D. A., & Klessig, D. F. (2012) · Trends in Plant Science · doi:10.1016/j.tplants.2012.05.011 · Cited by 345 · see citing works

Systemic acquired resistance: the elusive signal(s)

Vlot, A. C., Klessig, D. F., & Park, S. (2008) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2008.05.003 · Cited by 330 · see citing works

A Proteinaceous Elicitor Sm1 from the Beneficial Fungus Trichoderma virens Is Required for Induced Systemic Resistance in Maize

Djonović, S., Vargas, W. A., Kolomiets, M. V., et al. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.103689 · Cited by 329 · see citing works

Herbivore-Induced Callose Deposition on the Sieve Plates of Rice: An Important Mechanism for Host Resistance

Hao, P., Liu, C., Wang, Y., Chen, R., Tang, M., Du, B., Zhu, L., & He, G. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.111484 · Cited by 322 · see citing works

Silencing OsHI‐LOX makes rice more susceptible to chewing herbivores, but enhances resistance to a phloem feeder

Zhou, G., Qi, J., Ren, N., et al. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03988.x · Cited by 281 · see citing works

The Magnaporthe oryzae Avirulence Gene AvrPiz-t Encodes a Predicted Secreted Protein That Triggers the Immunity in Rice Mediated by the Blast Resistance Gene Piz-t

Li, W., Wang, B., Wu, J., Lu, G., Hu, Y., Zhang, X., Zhang, Z., Zhao, Q., Feng, Q. M., Zhang, H., et al. (2009) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-22-4-0411 · Cited by 281 · see citing works

Plant and Animal Pathogen Recognition Receptors Signal through Non-RD Kinases

Dardick, C. D., & Ronald, P. C. (2006) · PLoS Pathogens · doi:10.1371/journal.ppat.0020002 · Cited by 275 · see citing works

Pseudomonas fluorescens WCS374r-Induced Systemic Resistance in Rice against Magnaporthe oryzae Is Based on Pseudobactin-Mediated Priming for a Salicylic Acid-Repressible Multifaceted Defense Response

Vleesschauwer, D. D., Djavaheri, M., Bakker, P. A. H. M., & Höfte, M. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.127878 · Cited by 275 · see citing works

Chapter 6 Rhizobacteria-Induced Systemic Resistance

Vleesschauwer, D. D., & Höfte, M. (2009) · Advances in botanical research · doi:10.1016/s0065-2296(09)51006-3 · Cited by 271 · see citing works

Signal signature of aboveground‐induced resistance upon belowground herbivory in maize

Erb, M., Flors, V., Karlen, D., et al. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03868.x · Cited by 268 · see citing works

The Downy Mildew Effector Proteins ATR1 and ATR13 Promote Disease Susceptibility in Arabidopsis thaliana

Sohn, K. H., Lei, R., Nemri, A., et al. (2007) · The Plant Cell · doi:10.1105/tpc.107.054262 · Cited by 268 · see citing works

Signal signature of aboveground induced resistance upon belowground herbivory in maize

Erb, M., Flors, V., Karlen, D., et al. (2009) · reroDoc Digital Library · doi:10.7892/boris.73047 · Cited by 267 · see citing works

Induced Resistance Responses in Maize

Morris, S. W., Vernooij, B., Titatarn, S., Starrett, M., Thomas, S., Wiltse, C. C., Frederiksen, R. A., Bhandhufalck, A., Hulbert, S. H., & Uknes, S. J. (1998) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.1998.11.7.643 · Cited by 242 · see citing works

Disulfooxy fatty acids from the American bird grasshopper Schistocerca americana , elicitors of plant volatiles

Alborn, H. T., Hansen, T. V., Jones, T. H., Bennett, D. C., Tumlinson, J. H., Schmelz, E. A., & Teal, P. E. A. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705947104 · Cited by 239 · see citing works

Light conditions influence specific defence responses in incompatible plant?pathogen interactions: uncoupling systemic resistance from salicylic acid and PR-1 accumulation

Zeier, J., Pink, B., Mueller, M. J., et al. (2004) · Planta · doi:10.1007/s00425-004-1272-z · Cited by 237 · see citing works

Herbivore-associated elicitors: FAC signaling and metabolism

Bonaventure, G., VanDoorn, A., & Baldwin, I. T. (2011) · Trends in Plant Science · doi:10.1016/j.tplants.2011.01.006 · Cited by 232 · see citing works

Analysis of Flagellin Perception Mediated by flg22 Receptor OsFLS2 in Rice

Takai, R., Isogai, A., Takayama, S., & Che, F. (2008) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-21-12-1635 · Cited by 226 · see citing works

An abietane diterpenoid is a potent activator of systemic acquired resistance

Chaturvedi, R., Venables, B. J., Petros, R. A., Nalam, V. J., Li, M., Wang, X., TAKEMOTO, L. J., & Shah, J. (2012) · The Plant Journal · doi:10.1111/j.1365-313x.2012.04981.x · Cited by 225 · see citing works

ZmPep1, an Ortholog of Arabidopsis Elicitor Peptide 1, Regulates Maize Innate Immunity and Enhances Disease Resistance

Huffaker, A., Dafoe, N. J., & Schmelz, E. A. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.166710 · Cited by 223 · see citing works

Identification of a New Rice Blast Resistance Gene, Pid3, by Genomewide Comparison of Paired Nucleotide-Binding Site–Leucine-Rich Repeat Genes and Their Pseudogene Alleles Between the Two Sequenced Rice Genomes

Shang, J., Tao, Y., Chen, X., et al. (2009) · Genetics · doi:10.1534/genetics.109.102871 · Cited by 212 · see citing works

Plants under attack: systemic signals in defence

Shah, J. (2009) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2009.05.011 · Cited by 211 · see citing works

Pseudomonas fluorescens based bio-formulation for the management of sheath blight disease and leaffolder insect in rice

Commare, R. R., Nandakumar, R., Kandan, A., Suresh, S., Bharathi, M. J., Raguchander, T., & Samiyappan, R. (2002) · Crop Protection · doi:10.1016/s0261-2194(02)00020-0 · Cited by 208 · see citing works

Control of Fusarium Wilt of Radish by Combining Pseudomonas putida Strains that have Different Disease-Suppressive Mechanisms

de Boer, M., Bom, P., Kindt, F., et al. (2003) · Phytopathology · doi:10.1094/phyto.2003.93.5.626 · Cited by 200 · see citing works

An EAR‐motif‐containing ERF transcription factor affects herbivore‐induced signaling, defense and resistance in rice

Lü, J., Ju, H., Zhou, G., et al. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04709.x · Cited by 198 · see citing works

Probenazole induces systemic acquired resistance in Arabidopsis with a novel type of action

Yoshioka, K., Nakashita, H., Klessig, D. F., et al. (2001) · The Plant Journal · doi:10.1046/j.1365-313x.2001.00952.x · Cited by 197 · see citing works

Chapter 7 Plant Growth-Promoting Actions of Rhizobacteria

Spaepen, S., Vanderleyden, J., & Okon, Y. (2009) · Advances in botanical research · doi:10.1016/s0065-2296(09)51007-5 · Cited by 194 · see citing works

Plant growth-promoting rhizobacteria mediate induced systemic resistance in rice against bacterial leaf blight caused by Xanthomonas oryzae pv. oryzae

Chithrashree, C., Udayashankar, A. C., Nayaka, S. C., Reddy, M. S., & Srinivas, C. (2011) · Biological Control · doi:10.1016/j.biocontrol.2011.06.010 · Cited by 187 · see citing works

Detection and identification of bacteria intimately associated with fungi of the orderSebacinales

Sharma, M., Schmid, M., Rothballer, M., et al. (2008) · Cellular Microbiology · doi:10.1111/j.1462-5822.2008.01202.x · Cited by 172 · see citing works

Redox-Active Pyocyanin Secreted by Pseudomonas aeruginosa 7NSK2 Triggers Systemic Resistance to Magnaporthe grisea but Enhances Rhizoctonia solani Susceptibility in Rice

Vleesschauwer, D. D., Cornélis, P., & Höfte, M. (2006) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-19-1406 · Cited by 168 · see citing works

Plant NB-LRR signaling: upstreams and downstreams

Elmore, J. M., Lin, Z.-J. D., & Coaker, G. (2011) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2011.03.011 · Cited by 163 · see citing works

Perception of the chitin oligosaccharides contributes to disease resistance to blast fungus Magnaporthe oryzae in rice

Kishimoto, K., Kouzai, Y., Kaku, H., Shibuya, N., Minami, E., & Nishizawa, Y. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04328.x · Cited by 163 · see citing works

Innate immunity in rice

Chen, X., & Ronald, P. C. (2011) · Trends in Plant Science · doi:10.1016/j.tplants.2011.04.003 · Cited by 159 · see citing works

A Plasma Membrane Protein from Zea mays Binds with the Herbivore Elicitor Volicitin

Truitt, C. L., Wei, H., & Paré, P. W. (2004) · The Plant Cell · doi:10.1105/tpc.017723 · Cited by 145 · see citing works

Bacterial Lipopolysaccharides Induce Defense Responses Associated with Programmed Cell Death in Rice Cells

Desaki, Y., Miya, A., Venkatesh, B., et al. (2006) · Plant and Cell Physiology · doi:10.1093/pcp/pcl019 · Cited by 143 · see citing works

Plants on Constant Alert: Elevated Levels of Jasmonic Acid and Jasmonate-Induced Transcripts in Caterpillar-Resistant Maize

Shivaji, R., Camas, A., Ankala, A., et al. (2010) · Journal of Chemical Ecology · doi:10.1007/s10886-010-9752-z · Cited by 142 · see citing works

Barley Leaf Transcriptome and Metabolite Analysis Reveals New Aspects of Compatibility and Piriformospora indica –Mediated Systemic Induced Resistance to Powdery Mildew

Molitor, A., Zajic, D., Voll, L. M., et al. (2011) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-06-11-0177 · Cited by 137 · see citing works

Role of OsNPR1 in rice defense program as revealed by genome-wide expression analysis

Sugano, S., Jiang, C., Miyazawa, S., et al. (2010) · Plant Molecular Biology · doi:10.1007/s11103-010-9695-3 · Cited by 137 · see citing works

Seed bio-priming withPseudomonas fluorescensisolates enhances growth of pearl millet plants and induces resistance against downy mildew

Raj, S. N., Shetty, N., & Shetty, H. S. (2004) · International Journal of Pest Management · doi:10.1080/09670870310001626365 · Cited by 136 · see citing works

The Extent to Which Methyl Salicylate Is Required for Signaling Systemic Acquired Resistance Is Dependent on Exposure to Light after Infection

Liu, P., von Dahl, C. C., & Klessig, D. F. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.187773 · Cited by 129 · see citing works

Acquired Resistance in Barley (The Resistance Mechanism Induced by 2,6-Dichloroisonicotinic Acid Is a Phenocopy of a Genetically Based Mechanism Governing Race-Specific Powdery Mildew Resistance)

Kogel, K. H., Beckhove, U., Dreschers, J., Münch, S., & Romme, Y. (1994) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.4.1269 · Cited by 126 · see citing works

Pseudomonas syringae pv. syringae induces systemic resistance to Pyricularia oryzae in rice

Smith, J. A., & Métraux, J. (1991) · Physiological and Molecular Plant Pathology · doi:10.1016/0885-5765(91)90011-6 · Cited by 125 · see citing works

Use of two PGPR strains in the integrated management of blast disease in rice (Oryza sativa) in Southern Spain

Lucas, J. A., Ramos‐Solano, B., Montes, F., et al. (2009) · Field Crops Research · doi:10.1016/j.fcr.2009.09.013 · Cited by 119 · see citing works

Probenazole induces systemic acquired resistance in tobacco through salicylic acid accumulation

Nakashita, H., Yoshioka, K., Yasuda, M., et al. (2002) · Physiological and Molecular Plant Pathology · doi:10.1006/pmpp.2002.0426 · Cited by 111 · see citing works

Differential inducible defense mechanisms against bacterial speck pathogen in Arabidopsis thaliana by plant-growth-promoting-fungus Penicillium sp. GP16-2 and its cell free filtrate

Hossain, M. M., Sultana, F., Kubota, M., et al. (2008) · Plant and Soil · doi:10.1007/s11104-008-9542-3 · Cited by 109 · see citing works

Induced disease resistance and gene expression in cereals

Kogel, K., & Langen, G. (2005) · Cellular Microbiology · doi:10.1111/j.1462-5822.2005.00592.x · Cited by 108 · see citing works

Some endophytic fungi reduce the density of pustules of Puccinia recondita f. sp. tritici in wheat

Dingle, J., & McGee, P. A. (2003) · Mycological Research · doi:10.1017/s0953756203007512 · Cited by 104 · see citing works

Contribution of salicylic acid glucosyltransferase, OsSGT1, to chemically induced disease resistance in rice plants

Umemura, K., Satou, J., Iwata, M., et al. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03697.x · Cited by 96 · see citing works

Induction of DIMBOA accumulation and systemic defense responses as a mechanism of enhanced resistance of mycorrhizal corn (Zea mays L.) to sheath blight

Song, Y., Cao, M., Xie, L., et al. (2011) · Mycorrhiza · doi:10.1007/s00572-011-0380-4 · Cited by 92 · see citing works

The role of secreted proteins in diseases of plants caused by rust, powdery mildew and smut fungi

Ellis, J. G., Dodds, P. N., & Lawrence, G. J. (2007) · Current Opinion in Microbiology · doi:10.1016/j.mib.2007.05.015 · Cited by 89 · see citing works

Induced systemic resistance against three foliar diseases of Agrostis stolonifera by (2R,3R)‐butanediol or an isoparaffin mixture

Cortes‐Barco, A. M., Hsiang, T., & Goodwin, P. H. (2010) · Annals of Applied Biology · doi:10.1111/j.1744-7348.2010.00417.x · Cited by 86 · see citing works

EndophyticChaetomium globosumreduces development of tan spot in wheat caused byPyrenophora tritici-repentis

Istifadah, N., & McGee, P. A. (2006) · Australasian Plant Pathology · doi:10.1071/ap06038 · Cited by 86 · see citing works

Mir1-CP, a novel defense cysteine protease accumulates in maize vascular tissues in response to herbivory

Lopez, L., Camas, A., Shivaji, R., et al. (2007) · Planta · doi:10.1007/s00425-007-0501-7 · Cited by 85 · see citing works

Induction of Growth Promotion and Resistance Against Downy Mildew on Pearl Millet (Pennisetum glaucum) by Rhizobacteria

Raj, S. N., Chaluvaraju, G., Amruthesh, K. N., et al. (2003) · Plant Disease · doi:10.1094/pdis.2003.87.4.380 · Cited by 83 · see citing works

Induction of systemic resistance in banana (Musa spp.) against Banana bunchy top virus (BBTV) by combining chitin with root-colonizing Pseudomonas fluorescens strain CHA0

Kavino, M., Harish, S., Kumar, N., et al. (2007) · European Journal of Plant Pathology · doi:10.1007/s10658-007-9223-8 · Cited by 78 · see citing works

Differential effectiveness of Serratia plymuthica IC1270-induced systemic resistance against hemibiotrophic and necrotrophic leaf pathogens in rice

De Vleesschauwer, D., Chernin, L., & Höfte, M. M. (2009) · BMC Plant Biology · doi:10.1186/1471-2229-9-9 · Cited by 77 · see citing works

Ethylene Signaling Mediates a Maize Defense Response to Insect Herbivory

Harfouche, A. L., Shivaji, R., Stocker, R. S., Williams, P. W., & Luthe, D. S. (2006) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-19-0189 · Cited by 77 · see citing works

Concerted action of two avirulent spore effectors activates Reaction to Puccinia graminis 1 ( Rpg1 ) - mediated cereal stem rust resistance

Nirmala, J., Drader, T., Lawrence, P. K., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1111771108 · Cited by 76 · see citing works

Pseudomonas aeruginosa inducing rice resistance againstRhizoctonia solani: Production of salicylic acid and peroxidases

Saikia, R., Kumar, R., Arora, D. K., et al. (2006) · Folia Microbiologica · doi:10.1007/bf02931579 · Cited by 74 · see citing works

Jasmonic acid induces resistance to economically important insect pests in winter wheat

El-Wakeil, N. E., Volkmar, C., & Sallam, A. A. (2010) · Pest Management Science · doi:10.1002/ps.1906 · Cited by 72 · see citing works

Molecular characterization and genomic mapping of the pathogenesis-related protein 1 (PR-1) gene family in hexaploid wheat (Triticum aestivum L.)

Lu, S., Friesen, T. L., & Faris, J. D. (2011) · Molecular Genetics and Genomics · doi:10.1007/s00438-011-0618-z · Cited by 70 · see citing works

Tiadinil, a Novel Class of Activator of Systemic Acquired Resistance, Induces Defense Gene Expression and Disease Resistance in Tobacco

Yasuda, M., Nakashita, H., & Yoshida, S. (2004) · Journal of Pesticide Science · doi:10.1584/jpestics.29.46 · Cited by 68 · see citing works

HvCEBiP, a gene homologous to rice chitin receptor CEBiP, contributes to basal resistance of barley to Magnaporthe oryzae

TANAKA, S., Ichikawa, A., Yamada, K. H., et al. (2010) · BMC Plant Biology · doi:10.1186/1471-2229-10-288 · Cited by 68 · see citing works

Biocontrol of vascular wilt and corm rot of gladiolus caused by Fusarium oxysporum f. sp. gladioli using plant growth promoting rhizobacterial mixture

Shanmugam, V., Kanoujia, N., Singh, M., et al. (2011) · Crop Protection · doi:10.1016/j.cropro.2011.02.033 · Cited by 68 · see citing works

The CC-NB-LRR-Type Rdg2a Resistance Gene Confers Immunity to the Seed-Borne Barley Leaf Stripe Pathogen in the Absence of Hypersensitive Cell Death

Bulgarelli, D., Biselli, C., Collins, N. C., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012599 · Cited by 66 · see citing works

Association of the Hydrolytic Enzyme Chitinase against Rhizoctonia solani in Rhizobacteria‐treated Rice Plants

Radjacommare, R., Kandan, A., Nandakumar, R., et al. (2004) · Journal of Phytopathology · doi:10.1111/j.1439-0434.2004.00857.x · Cited by 64 · see citing works

The wheat Mla homologue TmMla1 exhibits an evolutionarily conserved function against powdery mildew in both wheat and barley

Jordan, T., Seeholzer, S., Schwizer, S., et al. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04445.x · Cited by 64 · see citing works

Pseudomonas‐induced defence molecules in rice plants against leaffolder (Cnaphalocrocis medinalis) pest

Saravanakumar, D., Muthumeena, K., Lavanya, N., et al. (2007) · Pest Management Science · doi:10.1002/ps.1381 · Cited by 64 · see citing works

Genome‐wide transcriptional changes and defence‐related chemical profiling of rice in response to infestation by the rice striped stem borer Chilo suppressalis

Zhou, G., Wang, X., Yan, F., et al. (2011) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2011.01483.x · Cited by 61 · see citing works

Comparison of resistance‐inducing abilities of virulent and avirulent races of Erysiphe graminis f.sp. hordei and a race of Erysiphe graminis f.sp. tritici in barley

Thordal‐Christensen, H., & Smedegård-Petersen, V. (1988) · Plant Pathology · doi:10.1111/j.1365-3059.1988.tb02191.x · Cited by 57 · see citing works

Emission of Herbivore-induced Volatiles in Absence of a Herbivore - Response of Zea mays to Green Leaf Volatiles and Terpenoids

Rüther, J., & Fürstenau, B. (2005) · Zeitschrift für Naturforschung C · doi:10.1515/znc-2005-9-1014 · Cited by 57 · see citing works

Suppression of Pythium ultimum root rot of sorghum by rhizobacterial isolates from Ethiopia and South Africa

Idris, H. A., Labuschagne, N., & Korsten, L. (2007) · Biological Control · doi:10.1016/j.biocontrol.2007.11.004 · Cited by 56 · see citing works

Chloroisonicotinamide Derivative Induces a Broad Range of Disease Resistance in Rice and Tobacco

Nakashita, H., Yasuda, M., Nishioka, M., et al. (2002) · Plant and Cell Physiology · doi:10.1093/pcp/pcf097 · Cited by 53 · see citing works

Enhancement of Defence Responses against Bayoud Disease by Treatment of Date Palm Seedlings with an Hypoaggressive Fusarium oxysporum Isolate

Hassni, M. E., Jaiti, F., Dihazi, A., et al. (2004) · Journal of Phytopathology · doi:10.1111/j.1439-0434.2004.00824.x · Cited by 52 · see citing works

A Genome-Wide Comparison of NB-LRR Type of Resistance Gene Analogs (RGA) in the Plant Kingdom

Kim, J., Lim, C. J., Lee, B., et al. (2012) · Molecules and Cells · doi:10.1007/s10059-012-0003-8 · Cited by 51 · see citing works

Herbivore- and Elicitor-Induced Resistance in Rice to the Rice Water Weevil (Lissorhoptrus oryzophilus Kuschel) in the Laboratory and Field

Hamm, J. C., Stout, M. J., & Riggio, R. M. (2010) · Journal of Chemical Ecology · doi:10.1007/s10886-010-9751-0 · Cited by 48 · see citing works

Lipid transfer proteins and protease inhibitors as key factors in the priming of barley responses to Fusarium head blight disease by a biocontrol strain of Pseudomonas fluorescens

Petti, C., Khan, M. R., & Doohan, F. M. (2010) · Functional & Integrative Genomics · doi:10.1007/s10142-010-0177-0 · Cited by 48 · see citing works

Spent growth medium of Pantoea agglomerans primes wheat suspension cells for augmented accumulation of hydrogen peroxide and enhanced peroxidase activity upon elicitation

Ortmann, I., & Moerschbacher, B. M. (2006) · Planta · doi:10.1007/s00425-006-0271-7 · Cited by 47 · see citing works

Pseudomonas fluorescens CHA0 maintains carbon delivery to Fusarium graminearum-infected roots and prevents reduction in biomass of barley shoots through systemic interactions

Henkes, G. J., Jousset, A., Bonkowski, M., et al. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err149 · Cited by 46 · see citing works

Feeding by Hessian fly [ Mayetiola destructor (Say)] larvae does not induce plant indirect defences

Tooker, J. F., & Moraes, C. Μ. D. (2007) · Ecological Entomology · doi:10.1111/j.1365-2311.2007.00852.x · Cited by 43 · see citing works

A highly conserved NB-LRR encoding gene cluster effective against Setosphaeria turcica in sorghum

Martin, T., Biruma, M., Fridborg, I., et al. (2011) · BMC Plant Biology · doi:10.1186/1471-2229-11-151 · Cited by 41 · see citing works

β-Glucosidase treatment and infestation by the rice brown planthopper Nilaparvata lugens elicit similar signaling pathways in rice plants

Wang, X., Zhou, G., Xiang, C., et al. (2008) · Chinese Science Bulletin · doi:10.1007/s11434-008-0048-4 · Cited by 40 · see citing works

Two loci in sorghum with NB-LRR encoding genes confer resistance to Colletotrichum sublineolum

Biruma, M., Martin, T., Fridborg, I., Okori, P., & Dixelius, C. (2011) · Theoretical and Applied Genetics · doi:10.1007/s00122-011-1764-8 · Cited by 38 · see citing works

Mechanisms of Induced Resistance in Barley Against Drechslera teres

Jørgensen, H. J. L., Lübeck, P. S., Thordal‐Christensen, H., et al. (1998) · Phytopathology · doi:10.1094/phyto.1998.88.7.698 · Cited by 38 · see citing works

Suppression of southern corn leaf blight by a plant growth‐promoting rhizobacterium Bacillus cereus C1L

Huang, C., Yang, K., Liu, Y., Lin, Y., & Chen, C. (2010) · Annals of Applied Biology · doi:10.1111/j.1744-7348.2010.00408.x · Cited by 34 · see citing works

The temporal and spatial fluctuation of the groundwater level along the Tarim Desert Highway

Fan, J., Xu, X., Lei, J., et al. (2008) · 中国科学通报：英文版 · doi:10.1007/s11434-008-6005-4 · Cited by 33 · see citing works

Chapter 8 Interactions Between Nonpathogenic Fungi and Plants

Trillas, M. I., & Segarra, G. (2009) · Advances in botanical research · doi:10.1016/s0065-2296(09)51008-7 · Cited by 32 · see citing works

Evidence of Induced Systemic Resistance Against Botrytis elliptica in Lily

Liu, Y., Huang, C., & Chen, C. (2008) · Phytopathology · doi:10.1094/phyto-98-7-0830 · Cited by 31 · see citing works

Induction of systemic resistance by mixtures of antagonist bacteria for the management of crown rot complex on banana

Sangeetha, G., Thangavelu, R., Rani, S. U., Muthukumar, A., & Udayakumar, R. (2010) · Acta Physiologiae Plantarum · doi:10.1007/s11738-010-0513-y · Cited by 30 · see citing works

Broad-Spectrum Acquired Resistance in Barley Induced by thePseudomonasPathosystem Shares Transcriptional Components withArabidopsisSystemic Acquired Resistance

Colebrook, E. H., Creissen, G. P., MCGRANN, G. R. D., et al. (2012) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-09-11-0246 · Cited by 26 · see citing works

Adaptive evolution of Xa21 homologs in Gramineae

Tan, S., Wang, D., Ding, J., et al. (2011) · Genetica · doi:10.1007/s10709-012-9645-x · Cited by 24 · see citing works

Effect of Acibenzolar-S-methyl (ASM) pre-treatment in inducing resistance against Pythium aphanidermatum infection in Curcuma longa

Radhakrishnan, N., Alphonse, A. J., & Balasubramanian, R. (2010) · Crop Protection · doi:10.1016/j.cropro.2010.08.020 · Cited by 23 · see citing works

Stomatal closure, callose deposition, and increase of LsGRP1-corresponding transcript in probenazole-induced resistance against Botrytis elliptica in lily

Lu, Y.-Y., Liu, Y., & Chen, C. (2007) · Plant Science · doi:10.1016/j.plantsci.2006.12.020 · Cited by 20 · see citing works

The Role of Chitinase Gene Expression in the Defense of Harvested Banana Against Anthracnose Disease

Ma, B., Tang, W.-L., Ma, L., et al. (2009) · Journal of the American Society for Horticultural Science · doi:10.21273/jashs.134.3.379 · Cited by 20 · see citing works

Feeding‐induced changes in defence enzymes and PR proteins and their implications in host resistance to Nilaparvata lugens

Alagar, M., Suresh, S., Saravanakumar, D., et al. (2009) · Journal of Applied Entomology · doi:10.1111/j.1439-0418.2009.01461.x · Cited by 19 · see citing works

Mechanism of resistance induced by plant activators againstColletotrichum falcatumin sugarcane

Sundar, A. R., Viswanathan, R., Malathi, P., et al. (2006) · Archives of Phytopathology and Plant Protection · doi:10.1080/03235400500181154 · Cited by 17 · see citing works

Effects of Pseudomonas fluorescens CHA0 on the Resistance of Wheat Seedling Roots to the Take-all Fungus Gaeumannomyces graminis var. tritici

Sari, E., Etebarian, H. R., & Aminian, H. (2008) · Plant Production Science · doi:10.1626/pps.11.298 · Cited by 17 · see citing works

Biosynthesis, Conjugation, and Possible Role

Silverman, P., Seskar, M., Kanter, D., et al. (1995) · Cited by 11 · see citing works

Fusarium oxysporum f. sp. radicis‐lycopersici can Induce Systemic Resistance in Barley Against Powdery Mildew

Nelson, H. (2005) · Journal of Phytopathology · doi:10.1111/j.1439-0434.2005.00986.x · Cited by 8 · see citing works

Plant Hormones and Metabolites as Universal Vocabulary in Plant Defense Signaling

Balmer, D., & Mauch‐Mani, B. (2011) · Signaling and communication in plants · doi:10.1007/978-3-642-23524-5_3 · Cited by 6 · see citing works

The protection of Pseudomonas aeruginosa wheat seeds treated against powdery mildew and leaf blight correlates with up-regulated expression of a subtilisin-like gene in leaves : research letter

Muyanga, S. C., Nembaware, V., & Gehring, C. (2005) · South African Journal of Science · Cited by 6 · see citing works

Study of priming for callose accumulation in Allium cepa during treatment with biotic inducers

Poliakovskiy, S. O., & Дмитриев, А. П. (2011) · Cytology and Genetics · doi:10.3103/s0095452711040086 · Cited by 6 · see citing works

Psychological Development in Children

Romanes, G. J. (1882) · Nature · doi:10.1038/026497a0 · Cited by 5 · see citing works

Birdcraft, a Field Book of Two Hundred Song, Game, and Water Birds . By Mabel Osgood Wright. New York, The Macmillan Co. November, 1897. With 80 full-page plates by Louis Agassiz Fuertes. 8mo, pp. 317. Price, $2.50.

Merriam, C. H. (1897) · Science · doi:10.1126/science.6.153.850.b · Cited by 3 · see citing works

Investigating the mechanisms underpinning bacterium-mediated control of FHB disease

Petti, C., Mojibur, K., & Doohan, F. M. (2008) · Cereal Research Communications · doi:10.1556/crc.36.2008.suppl.b.61 · Cited by 2 · see citing works

Intensify production, transform biomass to energy and novel goods and protect soils in Europe—A vision how to mobilize marginal lands

Schröder, P., Beckers, B., Daniels, S., Gnädinger, F., Maestri, E., Marmiroli, N., Mench, M., Millan, R., Obermeier, M. M., Oustriere, N., et al. (2018) · Science of The Total Environment · doi:10.1016/j.scitotenv.2017.10.209 · Cited by 151 · see citing works

Diffuse interactions between two herbivores and constraints on the evolution of resistance in horsenettle (Solanum carolinense)

Wise, M. J. (2010) · Arthropod-Plant Interactions · doi:10.1007/s11829-010-9094-3 · Cited by 11 · see citing works

Population Consequences of Constitutive and Inducible Plant Resistance: Herbivore Spatial Spread

Morris, W. F., & Dwyer, G. (1997) · The American Naturalist · doi:10.1086/286039 · Cited by 35 · see citing works

Bringing Fundamental Insights of Induced Resistance to Agricultural Management of Herbivore Pests

Poelman, E. H., Bourne, M. E., Croijmans, L., Cuny, M. A. C., Delamore, Z., Joachim, G., Kalisvaart, S. N., Kamps, B. B. J., Longuemare, M., Suijkerbuijk, H. A. C., et al. (2023) · Journal of Chemical Ecology · doi:10.1007/s10886-023-01432-3 · Cited by 18 · see citing works

Indirect plant defense against insect herbivores: a review

Aljbory, Z., & Chen, M. (2016) · Insect Science · doi:10.1111/1744-7917.12436 · Cited by 444 · see citing works

Current understanding of maize and rice defense against insect herbivores

Qi, J., Malook, S. U., Shen, G., Gao, L., Zhang, C., Li, J., Zhang, J., Wang, L., & Wu, J. (2018) · Acta Botanica Yunnanica · doi:10.1016/j.pld.2018.06.006 · Cited by 71 · see citing works