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

The plant immune system

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

Reactive oxygen species: Metabolism, oxidative stress, and signal transduction

Apel, K., & Hirt, H. (2004) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.55.031903.141701 · Cited by 11,723 · see citing works

Two simple media for the demonstration of pyocyanin and fluorescin.

Eo, K., WARD, M. K., & De, R. (1954) · PubMed · Cited by 5,209 · see citing works

Contrasting Mechanisms of Defense Against Biotrophic and Necrotrophic Pathogens

Glazebrook, J. (2005) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.43.040204.135923 · Cited by 4,380 · see citing works

SYSTEMIC ACQUIRED RESISTANCE

Durrant, W. E., & Dong, X. (2004) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.42.040803.140421 · Cited by 3,184 · see citing works

Host-Microbe Interactions: Shaping the Evolution of the Plant Immune Response

Chisholm, S. T., Coaker, G., Day, B., & Staskawicz, B. J. (2006) · Cell · doi:10.1016/j.cell.2006.02.008 · Cited by 2,957 · see citing works

H2O2 from the oxidative burst orchestrates the plant hypersensitive disease resistance response

Levine, A., Tenhaken, R., Dixon, R. A., & Lamb, C. J. (1994) · Cell · doi:10.1016/0092-8674(94)90544-4 · Cited by 2,767 · see citing works

Subcellular localization of H2O2 in plants. H2O2 accumulation in papillae and hypersensitive response during the barley—powdery mildew interaction

Thordal‐Christensen, H., Zhang, Z., Wei, Y., & Collinge, D. B. (1997) · The Plant Journal · doi:10.1046/j.1365-313x.1997.11061187.x · Cited by 2,680 · see citing works

SYSTEMIC RESISTANCE INDUCED BY RHIZOSPHERE BACTERIA

van Loon, L. C., Bakker, P. A. H. M., & Pieterse, C. M. J. (1998) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.36.1.453 · Cited by 2,366 · see citing works

Reactive Oxygen Species Signaling in Response to Pathogens

Torres, M. Á. M., Jones, J. D. G., & Dangl, J. L. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.079467 · Cited by 1,733 · see citing works

Priming: Getting Ready for Battle

Conrath, U., Beckers, G. J. M., Flors, V., García‐Agustín, P., Jakab, G., Mauch, F., Newman, M., Pieterse, C. M. J., Poinssot, B., Pozo, M. J., et al. (2006) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-19-1062 · Cited by 1,534 · see citing works

Networks of WRKY transcription factors in defense signaling

Eulgem, T., & Somssich, I. E. (2007) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2007.04.020 · Cited by 1,337 · see citing works

A Novel Signaling Pathway Controlling Induced Systemic Resistance in Arabidopsis

Pieterse, C. M. J., Wees, S. C. M. V., van Pelt, J. A., Knoester, M., Laan, R., Gerrits, H., Weisbeek, P. J., & van Loon, L. C. (1998) · The Plant Cell · doi:10.1105/tpc.10.9.1571 · Cited by 1,207 · see citing works

The hypersensitive response facilitates plant infection by the necrotrophic pathogen Botrytis cinerea

Govrin, E. M., & Levine, A. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00560-1 · Cited by 1,196 · see citing works

Reactive Oxygen Intermediates Mediate a Systemic Signal Network in the Establishment of Plant Immunity

Álvarez, M. E., Pennell, R. I., Meijer, P., Ishikawa, A., Dixon, R. A., & Lamb, C. (1998) · Cell · doi:10.1016/s0092-8674(00)81405-1 · Cited by 1,154 · see citing works

Signal interactions between nitric oxide and reactive oxygen intermediates in the plant hypersensitive disease resistance response

Delledonne, M., Zeier, J., Marocco, A., & Lamb, C. J. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.231178298 · Cited by 1,083 · see citing works

Reactive Oxygen Species in Plant Cell Death

Breusegem, F. V., & Dat, J. F. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.078295 · Cited by 1,002 · see citing works

Priming in plant–pathogen interactions

Conrath, U., Pieterse, C. M. J., & Mauch‐Mani, B. (2002) · Trends in Plant Science · doi:10.1016/s1360-1385(02)02244-6 · Cited by 985 · see citing works

Hydrogen Peroxide Acts as a Second Messenger for the Induction of Defense Genes in Tomato Plants in Response to Wounding, Systemin, and Methyl Jasmonate

Orozco-Cárdenas, M. L., Narváez-Vásquez, J., & Ryan, C. A. (2001) · The Plant Cell · doi:10.1105/tpc.13.1.179 · Cited by 889 · see citing works

Costs and benefits of priming for defense in Arabidopsis

van Hulten, M. H. A., Pelser, M., van Loon, L. C., Pieterse, C. M. J., & Ton, J. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510213103 · Cited by 860 · see citing works

Systemic resistance in Arabidopsis induced by biocontrol bacteria is independent of salicylic acid accumulation and pathogenesis-related gene expression.

Pieterse, C. M. J., Wees, S. C. M. V., Hoffland, E., van Pelt, J. A., & van Loon, L. C. (1996) · The Plant Cell · doi:10.1105/tpc.8.8.1225 · Cited by 777 · 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

Quantitative Nature of Arabidopsis Responses during Compatible and Incompatible Interactions with the Bacterial PathogenPseudomonas syringae [W]

Tao, Y., Xie, Z., Chen, W., Glazebrook, J., Chang, H.-S., Han, B., Zhu, T., Zou, G., & Katagiri, F. (2003) · The Plant Cell · doi:10.1105/tpc.007591 · Cited by 703 · see citing works

Rice WRKY45 Plays a Crucial Role in Benzothiadiazole-Inducible Blast Resistance

Shimono, M., Sugano, S., Nakayama, A., Jiang, C., Ono, K., Toki, S., & Takatsuji, H. (2007) · The Plant Cell · doi:10.1105/tpc.106.046250 · Cited by 635 · see citing works

Signal Crosstalk and Induced Resistance: Straddling the Line Between Cost and Benefit

Bostock, R. M. (2005) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.41.052002.095505 · Cited by 611 · see citing works

The Transcriptional Innate Immune Response to flg22. Interplay and Overlap with Avr Gene-Dependent Defense Responses and Bacterial Pathogenesis

Navarro, L., Zipfel, C., Rowland, O., Keller, I., Robatzek, S., Boller, T., & Jones, J. D. G. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.036749 · Cited by 605 · see citing works

Roles for Rice Membrane Dynamics and Plasmodesmata during Biotrophic Invasion by the Blast Fungus

Kankanala, P., Czymmek, K. J., & Valent, B. S. (2007) · The Plant Cell · doi:10.1105/tpc.106.046300 · Cited by 596 · see citing works

Brassinosteroid functions in a broad range of disease resistance in tobacco and rice

Nakashita, H., Yasuda, M., Nitta, T., Asami, T., Fujioka, S., Arai, Y. O., Sekimata, K., Takatsuto, S., Yamaguchi, I., & Yoshida, S. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01675.x · Cited by 576 · see citing works

The Transcriptome of Rhizobacteria-Induced Systemic Resistance in Arabidopsis

Verhagen, B. W. M., Glazebrook, J., Zhu, T., Chang, H.-S., van Loon, L. C., & Pieterse, C. M. J. (2004) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2004.17.8.895 · Cited by 558 · see citing works

Induced Systemic Resistance by Fluorescent Pseudomonas spp.

Bakker, P. A. H. M., Pieterse, C. M. J., & van Loon, L. C. (2007) · Phytopathology · doi:10.1094/phyto-97-2-0239 · Cited by 529 · see citing works

Pathogen‐associated molecular pattern recognition rather than development of tissue necrosis contributes to bacterial induction of systemic acquired resistance in Arabidopsis

Mishina, T. E., & Zeier, J. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03067.x · Cited by 444 · see citing works

Regulation of the Arabidopsis defense transcriptome

Eulgem, T. (2004) · Trends in Plant Science · doi:10.1016/j.tplants.2004.12.006 · Cited by 440 · see citing works

Priming for stress resistance: from the lab to the field

Beckers, G. J. M., & Conrath, U. (2007) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2007.06.002 · Cited by 416 · see citing works

Breaking the Barriers: Microbial Effector Molecules Subvert Plant Immunity

Göhre, V., & Robatzek, S. (2008) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.46.120407.110050 · Cited by 405 · 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

Essential role of the small GTPase Rac in disease resistance of rice

Ono, E., Wong, H. L., Kawasaki, T., Hasegawa, M., Kodama, O., & Shimamoto, K. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.759 · Cited by 389 · see citing works

Functional analysis of rice NPR1‐like genes reveals that OsNPR1/NH1 is the rice orthologue conferring disease resistance with enhanced herbivore susceptibility†

Yuan, Y., Zhong, S., Li, Q., Zhu, Z., Lou, Y., Wang, L., Wang, J., Wang, M., Li, Q., Yang, D., et al. (2007) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2007.00243.x · Cited by 388 · see citing works

Interplay between MAMP‐triggered and SA‐mediated defense responses

Tsuda, K., Sato, M., Glazebrook, J., Cohen, J. D., & Katagiri, F. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03369.x · Cited by 380 · see citing works

Chitinolytic Enterobacter agglomerans Antagonistic to Fungal Plant Pathogens

Chernin, L. S., Ismailov, Z. F., Haran, S., & Chet, I. (1995) · Applied and Environmental Microbiology · doi:10.1128/aem.61.5.1720-1726.1995 · Cited by 375 · see citing works

Inheritance of Blast Resistance in Near-Isogenic Lines of Rice

Mackill, D. J. (1992) · Phytopathology · doi:10.1094/phyto-82-746 · Cited by 375 · see citing works

Cinnamoyl-CoA reductase, a key enzyme in lignin biosynthesis, is an effector of small GTPase Rac in defense signaling in rice

Kawasaki, T., Koita, H., Nakatsubo, T., Hasegawa, K., Wakabayashi, K., Takahashi, H., Umemura, K., Umezawa, T., & Shimamoto, K. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0509875103 · Cited by 373 · 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

Induction of Defense-Related Ultrastructural Modifications in Pea Root Tissues Inoculated with Endophytic Bacteria

Benhamou, N., Kloepper, J. W., Quadt-Hallmann, A., & Tuzun, S. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.112.3.919 · Cited by 345 · see citing works

Determinants of Pseudomonas putida WCS358 involved in inducing systemic resistance in plants

Meziane, H., van der Sluis, I., van Loon, L. C., Höfte, M., & Bakker, P. A. H. M. (2005) · Molecular Plant Pathology · doi:10.1111/j.1364-3703.2005.00276.x · Cited by 340 · see citing works

Rhizobacteria-mediated induced systemic resistance (ISR) in Arabidopsis is not associated with a direct effect on expression of known defense-related genes but stimulates the expression of the jasmonate-inducible gene Atvsp upon challenge

Wees, S. C. M. V., Luijendijk, M. C. M., Smoorenburg, I., van Loon, L. C., & Pieterse, C. M. J. (1999) · Plant Molecular Biology · doi:10.1023/a:1006319216982 · Cited by 332 · see citing works

Induction of systemic resistance in rice against sheath blight disease by Pseudomonas fluorescens

Nandakumar, R., Babu, S., Viswanathan, R., Raguchander, T., & Samiyappan, R. (2001) · Soil Biology and Biochemistry · doi:10.1016/s0038-0717(00)00202-9 · Cited by 321 · 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

Rhizobacteria-mediated induced systemic resistance (ISR) in Arabidopsis requires sensitivity to jasmonate and ethylene but is not accompanied by an increase in their production

Pieterse, C. M. J., van Pelt, J. A., Ton, J., Parchmann, S., Mueller, M. J., Buchala, A. J., Métraux, J., & van Loon, L. C. (2000) · Physiological and Molecular Plant Pathology · doi:10.1006/pmpp.2000.0291 · Cited by 270 · see citing works

CAB Reviews: Perspectives in Agriculture, Veterinary Science, Nutrition and Natural Resources

(2006) · CABI Reviews · doi:10.1079/pavsnnr · Cited by 265 · see citing works

Induction of Resistance to Verticillium dahliae in Arabidopsis thaliana by the Biocontrol Agent K-165 and Pathogenesis-Related Proteins Gene Expression

Tjamos, S. E., Flemetakis, E., Paplomatas, E. J., & Katinakis, P. K. (2005) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-18-0555 · Cited by 225 · see citing works

Silicon influences cytological and molecular events in compatible and incompatible rice-Magnaporthe grisea interactions

Rodrigues, F. Á., Jurick, W. M., Datnoff, L. E., Jones, J. B., & Rollins, J. A. (2005) · Physiological and Molecular Plant Pathology · doi:10.1016/j.pmpp.2005.06.002 · Cited by 213 · see citing works

A Compromised Mlo Pathway Affects the Response of Barley to the Necrotrophic Fungus Bipolaris sorokiniana (Teleomorph: Cochliobolus sativus) and Its Toxins

Kumar, J., Hückelhoven, R., Beckhove, U., Nagarajan, S., & Kogel, K. (2001) · Phytopathology · doi:10.1094/phyto.2001.91.2.127 · Cited by 206 · see citing works

Nitric Oxide- and Hydrogen Peroxide-Responsive Gene Regulation during Cell Death Induction in Tobacco

Zago, E. D., Morsa, S., Dat, J. F., Alard, P., Ferrarini, A., Inzé, D., Delledonne, M., & Breusegem, F. V. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.078444 · Cited by 194 · see citing works

Cross Talk between Reactive Nitrogen and Oxygen Species during the Hypersensitive Disease Resistance Response

Zaninotto, F., Camera, S. L., Polverari, A., & Delledonne, M. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.078857 · Cited by 186 · see citing works

Identification and fine mapping of Pi33, the rice resistance gene corresponding to the Magnaporthe grisea avirulence gene ACE1

Berruyer, R., Adreit, H., Milazzo, J., Gaillard, S., Berger, A., Dioh, W., Lebrun, M., & Tharreau, D. (2003) · Theoretical and Applied Genetics · doi:10.1007/s00122-003-1349-2 · Cited by 179 · 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

Rhizobacteria-Induced Priming in Arabidopsis Is Dependent on Ethylene, Jasmonic Acid, and NPR1

Ahn, I., Lee, S.-W., & Suh, S. (2007) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-20-7-0759 · Cited by 162 · see citing works

A global view of defense gene expression regulation – a highly interconnected signaling network

Katagiri, F. (2004) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2004.07.013 · Cited by 153 · see citing works

Salicylic acid response in rice: influence of salicylic acid on H2O2 accumulation and oxidative stress

Ganesan, V., & THOMAS, G. V. (2001) · Plant Science · doi:10.1016/s0168-9452(01)00327-2 · Cited by 128 · see citing works

An Elicitor from Botrytis cinerea Induces the Hypersensitive Response in Arabidopsis thaliana and Other Plants and Promotes the Gray Mold Disease

Govrin, E. M., Rachmilevitch, S., Tiwari, B. S., Solomon, M., & Levine, A. (2006) · Phytopathology · doi:10.1094/phyto-96-0299 · Cited by 127 · 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

A novel inoculation method of Magnaporthe grisea for cytological observation of the infection process using intact leaf sheaths of rice plants

Koga, H., Dohi, K., Nakayachi, O., & Mori, M. (2004) · Physiological and Molecular Plant Pathology · doi:10.1016/j.pmpp.2004.07.002 · Cited by 114 · 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

Characterization, Genetic Structure, and Pathogenicity of Rhizoctonia spp. Associated with Rice Sheath Diseases in India

Taheri, P., Gnanamanickam, S., & Höfte, M. (2007) · Phytopathology · doi:10.1094/phyto-97-3-0373 · Cited by 107 · see citing works

Effect of Rice Growth Stages and Silicon on Sheath Blight Development

Rodrigues, F. Á., do Vale, F. X. R., Datnoff, L. E., Prabhu, A. S., & Korndörfer, G. H. (2003) · Phytopathology · doi:10.1094/phyto.2003.93.3.256 · Cited by 100 · see citing works

Rhizobacteria-induced Resistance Perturbs Viral Disease Progress and Triggers Defense-related Gene Expression

Ahn, I., Park, K., & Kim, C.-H. (2002) · Molecules and Cells · doi:10.1016/s1016-8478(23)15037-0 · Cited by 92 · see citing works

The Global Regulator Genes from Biocontrol Strain Serratia plymuthica IC1270: Cloning, Sequencing, and Functional Studies

Ovadis, M. I., Liu, X., Gavriel, S., Ismailov, Z. F., Chet, I., & Chernin, L. S. (2004) · Journal of Bacteriology · doi:10.1128/jb.186.15.4986-4993.2004 · Cited by 90 · see citing works

Hypersensitive death, autofluorescence, and ultrastructural changes in cells of leaf sheaths of susceptible and resistant near-isogenic lines of rice (Pi-zt) in relation to penetration and growth of Pyricularia oryzae

Koga, H. (1994) · Canadian Journal of Botany · doi:10.1139/b94-180 · Cited by 85 · see citing works

The oomycete response gene LURP1 is required for defense against Hyaloperonospora parasitica in Arabidopsis thaliana

Knoth, C., & Eulgem, T. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03486.x · Cited by 81 · see citing works

Induction of H2O2 in Transgenic Rice Leads to Cell Death and Enhanced Resistance to Both Bacterial and Fungal Pathogens

Kachroo, A., He, Z., Patkar, R., Zhu, Q., Zhong, J., Li, D., Ronald, P. C., Lamb, C. J., & Chattoo, B. B. (2003) · Transgenic Research · doi:10.1023/a:1025896513472 · Cited by 78 · see citing works

Using Serratia plymuthica to control fungal pathogens of plants.

Vleesschauwer, D. D., & Höfte, M. (2007) · CABI Reviews · doi:10.1079/pavsnnr20072046 · Cited by 75 · see citing works

Cellular differentiation and host invasion by the rice blast fungus Magnaporthe grisea

Caracuel‐Rios, Z., & Talbot, N. J. (2007) · Current Opinion in Microbiology · doi:10.1016/j.mib.2007.05.019 · Cited by 74 · see citing works

Essential role of the small GTPase Rac in disease resistance of rice

Ono, E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.021273498 · Cited by 71 · see citing works

Rice Defense Mechanisms AgainstCochliobolus miyabeanusandMagnaporthe griseaAre Distinct

Ahn, I., Kim, S., Kang, S., Suh, S., & Lee, Y. (2005) · Phytopathology · doi:10.1094/phyto-95-1248 · Cited by 69 · see citing works

Gene Expression Analysis in Cucumber Leaves Primed by Root Colonization with Pseudomonas chlororaphis O6 upon Challenge‐Inoculation with Corynespora cassiicola

Kim, M. S., Kim, Y. C., & Cho, B. H. (2004) · Plant Biology · doi:10.1055/s-2004-817803 · Cited by 66 · see citing works

Detoxification of oxalic acid by Pseudomonas fluorescens strain PfMDU2: Implications for the biological control of rice sheath blight caused by Rhizoctonia solani

Kumar, M. N., Jayaraj, J., Muthukrishnan, S., BHASKARAN, R., & Velazhahan, R. (2005) · Microbiological Research · doi:10.1016/j.micres.2005.02.002 · Cited by 65 · see citing works

Potential ofSerratia marcescensstrain B2 for biological control of rice sheath blight

Someya, N., Nakajima, M., Watanabe, K., Hibi, T., & AKUTSU, K. (2004) · Biocontrol Science and Technology · doi:10.1080/09583150400016092 · Cited by 64 · see citing works

Foliar application of Bacillus subtilis AUBS1 reduces sheath blight and triggers defense mechanisms in rice

Jayaraj, J., Yi, H.-S., Liang, G. H., Muthukrishnan, S., & Velazhahan, R. (2004) · Journal of Plant Diseases and Protection · doi:10.1007/bf03356138 · Cited by 64 · see citing works

Molecular and Pathotype Analysis of the Rice Blast Fungus in North Vietnam

Thuan, N. T. N., Bigirimana, J., Roumen, E. C., Straeten, D. V. D., & Höfte, M. (2006) · European Journal of Plant Pathology · doi:10.1007/s10658-006-0002-8 · Cited by 61 · see citing works

Effect of seed inoculation with the rhizopseudomonad strain 7NSK2 on the root microbiota of maize (Zea mays) and barley (Hordeum vulgare)

Iswandi, A., Bossier, P., Vandenabeele, J., & Verstraete, W. (1987) · Biology and Fertility of Soils · doi:10.1007/bf00255776 · Cited by 58 · see citing works

Early and specific gene expression triggered by rice resistance genePi33in response to infection byACE1avirulent blast fungus

Vergne, E., Ballini, E., Marques, S., Mammar, B. S., Droc, G., Gaillard, S., Bourot, S., DeRose, R. T., Tharreau, D., Notteghem, J. L., et al. (2007) · New Phytologist · doi:10.1111/j.1469-8137.2007.01971.x · Cited by 57 · see citing works

In planta measurements of oxidative bursts elicited by avirulent and virulent bacterial pathogens suggests that H2O2 is insufficient to elicit cell death in tobacco

Mur, L. A. J., Kenton, P., & Draper, J. (2005) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2005.01301.x · Cited by 53 · see citing works

Advances in Rice Blast Research

(2000) · Developments in plant pathology · doi:10.1007/978-94-015-9430-1 · Cited by 44 · see citing works

Phospholipase C/diacylglycerol kinase-mediated signalling is required for benzothiadiazole-induced oxidative burst and hypersensitive cell death in rice suspension-cultured cells

Chen, J., Zhang, W., Song, F., & Zheng, Z. (2006) · PROTOPLASMA · doi:10.1007/s00709-006-0195-x · Cited by 32 · see citing works

Correction

(2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03589.x · Cited by 29 · see citing works

Induced Resistance Against Rice Blast

Manandhar, H. K., Jørgensen, H. J. L., Mathur, S. B., & Smedegaard-Petersen, V. (2000) · Developments in plant pathology · doi:10.1007/978-94-015-9430-1_12 · Cited by 5 · see citing works

In Posidonia oceanica cadmium induces changes in DNA methylation and chromatin patterning

Greco, M., Chiappetta, A. A. C., Bruno, L., & Bitonti, M. B. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err313 · Cited by 533 · see citing works

Comparison of the toxicity of silver nanoparticles and silver ions on the growth of terrestrial plant model Arabidopsis thaliana

Qian, H., Peng, X., Xiao, H., Ren, J., Sun, L., & Fu, Z. (2013) · Journal of Environmental Sciences · doi:10.1016/s1001-0742(12)60301-5 · Cited by 448 · see citing works

Towards establishing broad-spectrum disease resistance in plants: silicon leads the way

Bockhaven, J. V., Vleesschauwer, D. D., & Höfte, M. (2012) · Journal of Experimental Botany · doi:10.1093/jxb/ers329 · Cited by 372 · see citing works

Genome-Wide Characterization of ISR Induced in Arabidopsis thaliana by Trichoderma hamatum T382 Against Botrytis cinerea Infection

Mathys, J., Cremer, K. D., Timmermans, P., Kerckhove, S. V., Lievens, B., Vanhaecke, M., Cammue, B. P. A., & Coninck, B. D. (2012) · Frontiers in Plant Science · doi:10.3389/fpls.2012.00108 · Cited by 239 · see citing works

Biocontrol of Bacterial Leaf Blight of Rice and Profiling of Secondary Metabolites Produced by Rhizospheric Pseudomonas aeruginosa BRp3

Yasmin, S., Hafeez, F. Y., Mirza, M. S., Rasul, M., Arshad, H. M. I., Zubair, M., & Iqbal, M. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01895 · Cited by 236 · see citing works

The Janus face of reactive oxygen species in resistance and susceptibility of plants to necrotrophic and biotrophic pathogens

Barna, B., Fodor, J., Harrach, B. D., Pogány, M., & Király, Z. (2012) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2012.01.014 · Cited by 229 · 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

Broad-range antagonistic rhizobacteria Pseudomonas fluorescens and Serratia plymuthica suppress Agrobacterium crown gall tumours on tomato plants

Dandurishvili, N., Toklikishvili, N., Ovadis, M. I., Eliashvili, P., Giorgobiani, N., Keshelava, R. F., Tediashvili, M., Vainstein, A., Khmel, I. A., Szegedi, E., et al. (2010) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2010.04891.x · Cited by 180 · see citing works

Root inoculation with Pseudomonas putida KT2440 induces transcriptional and metabolic changes and systemic resistance in maize plants

Planchamp, C., Glauser, G., & Mauch‐Mani, B. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00719 · Cited by 174 · see citing works

Overexpression of CaWRKY27 , a subgroup IIe WRKY transcription factor ofCapsicum annuum, positively regulates tobacco resistance toRalstonia solanacearuminfection

Dang, F., Wang, Y., She, J., Lei, Y., Liu, Z., Eulgem, T., Lai, Y., Lin, J., Yu, L., Lei, D., et al. (2013) · Physiologia Plantarum · doi:10.1111/ppl.12093 · Cited by 164 · 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

Community- and Genome-Based Views of Plant-Associated Bacteria: Plant–Bacterial Interactions in Soybean and Rice

Ikeda, S., Okubo, T., Anda, M., Nakashita, H., Yasuda, M., Sato, S., Kaneko, T., Tabata, S., Eda, S., Momiyama, A., et al. (2010) · Plant and Cell Physiology · doi:10.1093/pcp/pcq119 · Cited by 121 · see citing works

C a WRKY 58 , encoding a group I WRKY transcription factor of C apsicum annuum , negatively regulates resistance to R alstonia solanacearum infection

Wang, Y., Dang, F., Liu, Z., Wang, X., Eulgem, T., Lai, Y., Yu, L., She, J., Shi, Y., Lin, J., et al. (2012) · Molecular Plant Pathology · doi:10.1111/j.1364-3703.2012.00836.x · Cited by 109 · see citing works

Effects of Colonization of a Bacterial Endophyte,Azospirillumsp. B510, on Disease Resistance in Rice

Yasuda, M., ISAWA, T., 篠崎, 聰., Minamisawa, K., & Nakashita, H. (2009) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.90402 · Cited by 108 · see citing works

Tomato partial resistance to Rhizoctonia solani involves antioxidative defense mechanisms

Nikraftar, F., Taheri, P., Rastegar, M. F., & Tarighi, S. (2012) · Physiological and Molecular Plant Pathology · doi:10.1016/j.pmpp.2012.11.004 · Cited by 95 · see citing works

Role of phenazines and cyclic lipopeptides produced by pseudomonas sp. CMR12a in induced systemic resistance on rice and bean

Ma, Z., Hua, G. K. H., Ongena, M., & Höfte, M. (2016) · Environmental Microbiology Reports · doi:10.1111/1758-2229.12454 · Cited by 92 · see citing works

On the move: induced resistance in monocots

Balmer, D., Planchamp, C., & Mauch-Mani, B. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ers248 · Cited by 77 · see citing works

Reactive oxygen species accumulation and homeostasis are involved in plant immunity to an opportunistic fungal pathogen

Taheri, P., & Kakooee, T. (2017) · Journal of Plant Physiology · doi:10.1016/j.jplph.2017.04.018 · Cited by 63 · see citing works

The cyclic lipopeptide orfamide induces systemic resistance in rice to Cochliobolus miyabeanus but not to Magnaporthe oryzae

Ma, Z., Ongena, M., & Höfte, M. (2017) · Plant Cell Reports · doi:10.1007/s00299-017-2187-z · Cited by 59 · see citing works

DNA methylation changes and TE activity induced in tissue cultures of barley (Hordeum vulgare L.)

Orłowska, R., Machczyńska, J., Oleszczuk, S., Zimny, J., & Bednarek, P. T. (2016) · Journal of Biological Research-Thessaloniki · doi:10.1186/s40709-016-0056-5 · Cited by 53 · see citing works

Isolation and selection of plant growth-promoting rhizobacteria as inducers of systemic resistance in melon

García‐Gutiérrez, L., Romero, D., Zeriouh, H., Cazorla, F. M., Torés, J. A., de Vicente, A., & Pérez‐García, A. (2012) · Plant and Soil · doi:10.1007/s11104-012-1173-z · Cited by 53 · see citing works

Genome-wide identification and characterization of aquaporin gene family in Beta vulgaris

Kong, W., Yang, S., Wang, Y., Bendahmane, M., & Fu, X. (2017) · PeerJ · doi:10.7717/peerj.3747 · Cited by 51 · see citing works

Biocontrol of Rhizoctonia solani: complex interaction of biocontrol strains, pathogen and indigenous microbial community in the rhizosphere of lettuce shown by molecular methods

Grosch, R., Dealtry, S., Schreiter, S., Berg, G., Mendonça-Hagler, L. C., & Smalla, K. (2012) · Plant and Soil · doi:10.1007/s11104-012-1239-y · Cited by 50 · see citing works

Bio-priming of rice seeds with novel bacterial strains, for management of seedborne Magnaporthe oryzae L.

Amruta, N., Kumar, M. K. P., Kandikattu, H. K., Sarika, G., Puneeth, M. E., Ranjitha, H. P., Vishwanath, K., Manjunatha, C., Pramesh, D., Mahesh, H. B., et al. (2019) · Plant Physiology Reports · doi:10.1007/s40502-019-00492-6 · Cited by 42 · see citing works

Bacillus spp.-Mediated Growth Promotion of Rice Seedlings and Suppression of Bacterial Blight Disease under Greenhouse Conditions

Rajer, F. U., Samma, M. K., Ali, Q., Rajar, W. A., Wu, H., Raza, W., Xie, Y., Tahir, H. A. S., & Gao, X. (2022) · Pathogens · doi:10.3390/pathogens11111251 · Cited by 40 · see citing works

Studies on the interaction between the biocontrol agent, Serratia plymuthica A30, and blackleg‐causing Dickeya sp. (biovar 3) in potato ( Solanum tuberosum )

Czajkowski, R., de Boer, W. J., van Veen, J. A., & van der Wolf, J. M. (2011) · Plant Pathology · doi:10.1111/j.1365-3059.2011.02565.x · Cited by 33 · see citing works

Reactive oxygen species and antioxidant system responses in wheat cultivars during interaction with Fusarium species

Khaledi, N., Taheri, P., & Falahati‐Rastegar, M. (2016) · Australasian Plant Pathology · doi:10.1007/s13313-016-0455-y · Cited by 33 · see citing works

Oxidative burst and enzymatic antioxidant systems in rice plants during interaction with Alternaria alternata

Taheri, P., Irannejad, A., Goldani, M., & Tarighi, S. (2014) · European Journal of Plant Pathology · doi:10.1007/s10658-014-0512-8 · Cited by 32 · see citing works

The plant growth promoting bacterium Azospirillum brasilense is vertically transmitted in Phaseolus vulgaris (common bean)

Malinich, E. A., & Bauer, C. E. (2018) · Symbiosis · doi:10.1007/s13199-018-0539-2 · Cited by 30 · see citing works

Authentication and characterization of a candidate antagonistic bacterium against soft rot of Amorphophallus konjac

Wu, J., Liu, X., Diao, Y., Ding, Z., & Hu, Z. (2012) · Crop Protection · doi:10.1016/j.cropro.2011.12.008 · Cited by 27 · see citing works

Biopriming for induction of disease resistance against pathogens in rice

Shasmita, Swain, B. B., Mohapatra, P. K., Naik, S. K., & Mukherjee, A. K. (2022) · Planta · doi:10.1007/s00425-022-03900-8 · Cited by 26 · see citing works

Draft Genome Sequence of Serratia sp. Strain M24T3, Isolated from Pinewood Disease Nematode Bursaphelenchus xylophilus

Proença, D. N., Santo, C. E., Grass, G., & Morais, P. V. (2012) · Journal of Bacteriology · doi:10.1128/jb.00670-12 · Cited by 24 · see citing works

Dual stimuli-responsive prodrug co-delivery nanosystem of salicylic acid and bioavailable silicon for long-term immunity in plant

Liang, Y., Du, Y., Song, Y., Wang, S., Zhao, C., Feng, Z., Zuo, S., Yang, F., Xu, K., & Huo, Z. (2025) · Journal of Nanobiotechnology · doi:10.1186/s12951-025-03416-9 · Cited by 23 · see citing works

Contrasting Regulation of NO and ROS in Potato Defense-Associated Metabolism in Response to Pathogens of Different Lifestyles

Floryszak‐Wieczorek, J., & Arasimowicz‐Jelonek, M. (2016) · PLoS ONE · doi:10.1371/journal.pone.0163546 · Cited by 23 · see citing works

Rhizoctonia solani and Bacterial Inoculants Stimulate Root Exudation of Antifungal Compounds in Lettuce in a Soil-Type Specific Manner

Windisch, S., Bott, S., Ohler, M.-A., Mock, H., Lippmann, R., Grosch, R., Smalla, K., Ludewig, U., & Neumann, G. (2017) · Agronomy · doi:10.3390/agronomy7020044 · Cited by 23 · see citing works

Role of plant-associated microbes in plant health and development: the case of the Serratia genus

Trinh, L. L., & Nguyen, H. H. (2024) · Technology in Agronomy · doi:10.48130/tia-0024-0025 · Cited by 20 · see citing works

Draft Genome Sequence of a Plant Growth-Promoting Rhizobacterium, Serratia fonticola Strain AU-P3(3)

Devi, U., Khatri, I., Kumar, N., Kumar, L., Sharma, D., Subramanian, S., & Saini, A. K. (2013) · Genome Announcements · doi:10.1128/genomea.00946-13 · Cited by 20 · see citing works

Epidemiological and histological components of crown rust resistance in oat genotypes

Graichen, F. A. S., Martinelli, J. A., Wesp, C. D. L., Federizzi, L. C., & Chaves, M. S. (2011) · European Journal of Plant Pathology · doi:10.1007/s10658-011-9825-z · Cited by 20 · see citing works

Metallomic study of selenium biomolecules metabolized by the microalgae Chlorella sorkiniana in the biotechnological production of functional foods enriched in selenium

Gómez-Jacinto, V., García‐Barrera, T., Garbayo, I., Vı́lchez, C., & Gómez‐Ariza, J. L. (2012) · Pure and Applied Chemistry · doi:10.1351/pac-con-11-09-18 · Cited by 20 · see citing works

Mechanisms of Action of Bacterial Biological Control Agents

Narayanasamy, P. (2013) · Springer eBooks · doi:10.1007/978-94-007-6380-7_5 · Cited by 18 · see citing works

Transcriptional behavior of EUL-related rice lectins toward important abiotic and biotic stresses

Atalah, B. A., Vleesschauwer, D. D., Xu, J., Fouquaert, E., Höfte, M., & Damme, E. J. M. V. (2014) · Journal of Plant Physiology · doi:10.1016/j.jplph.2014.04.004 · Cited by 19 · see citing works

Identification of a toxic serralysin family protease with unique thermostable property from S. marcescens FS14

Wu, D., Li, P., Zhou, J., Gao, M., Lou, X., Ran, T., Wu, S., Wang, W., & Xu, D. (2016) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2016.08.041 · Cited by 18 · see citing works

Induced Systemic Resistance in Rice

Nadarajah, K. K. (2016) · Springer eBooks · doi:10.1007/978-981-10-0388-2_7 · Cited by 17 · see citing works

Developing Plant-Growth-Promoting Rhizobacteria: A Crucial Approach for Achieving Sustainable Agriculture

Wang, D., Wang, C., Chen, Y., & Xie, Z. (2023) · Agronomy · doi:10.3390/agronomy13071835 · Cited by 13 · see citing works

Antagonistic and plant growth promotion of rhizobacteria against Phytophthora colocasiae in taro

Kelbessa, B. G., Ghadamgahi, F., Kumar, P. L., Ortiz, R. O., Whisson, S. C., Bhattacharjee, R., & Vetukuri, R. R. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.1035549 · Cited by 13 · see citing works

Improvement of fitness and biocontrol properties of Pseudomonas putida via an extracellular heme peroxidase

Santamaría‐Hernando, S., Bruyne, L. D., Höfte, M., & Ramos‐González, M. I. (2022) · Microbial Biotechnology · doi:10.1111/1751-7915.14123 · Cited by 11 · see citing works

Chemicobiological Insight into Anti-phytopathogenic Properties of Rhizospheric Serratia plymuthica R51

John, C. J., & Radhakrishnan, E. K. (2017) · Proceedings of the National Academy of Sciences India Section B Biological Sciences · doi:10.1007/s40011-017-0909-1 · Cited by 12 · see citing works

Diagonal two-dimensional electrophoresis (D-2DE): a new approach to study the effect of osmotic stress induced by polyethylene glycol in durum wheat (Triticum durum Desf.)

Kacem, N. S., Mauro, S., Muhovski, Y., Delporte, F., Renaut, J., Djekoun, A., & Watillon, B. (2016) · Molecular Biology Reports · doi:10.1007/s11033-016-4028-5 · Cited by 12 · see citing works

The role of oxidative burst, antioxidant genes and enzymes in association with callose in tomato reaction to various taxonomic groups of Rhizoctonia spp.

Hosseini-Zahani, F., & Taheri, P. (2023) · Physiological and Molecular Plant Pathology · doi:10.1016/j.pmpp.2023.102174 · Cited by 11 · see citing works

Physiological response of Bacillus cereus C1L-induced systemic resistance in lily against Botrytis leaf blight

Huang, C., Liu, Y., Yang, K., & Chen, C. (2012) · European Journal of Plant Pathology · doi:10.1007/s10658-012-0013-6 · Cited by 11 · see citing works

Augmenting Plant Immune Responses and Biological Control by Microbial Determinants

Lee, S., Chung, J.-H., & Ryu, C. (2015) · Research in Plant Disease · doi:10.5423/rpd.2015.21.3.161 · Cited by 11 · see citing works

Polymorphism of high M r glutenin subunits in wild emmer Triticum turgidum subsp. dicoccoides: chromatographic, electrophoretic separations and PCR analysis of their encoding genes

Margiotta, B., Colaprico, G., & Urbano, M. (2013) · Genetic Resources and Crop Evolution · doi:10.1007/s10722-013-0037-6 · Cited by 10 · see citing works

Efficacies of Some Fungicides and Antagonists in Controlling Northern Corn Leaf Blight Disease

Wathaneeyawech, S., Kirdsiri, K., Sirithunya, P., & Smitamana, P. (2015) · International Journal of Agricultural Technology · Cited by 8 · see citing works

Induction of Systemic Resistance for Disease Suppression

Nadarajah, K. K. (2017) · Springer eBooks · doi:10.1007/978-3-319-65079-1_15 · Cited by 7 · see citing works

Rhizospheric bacteria as soil health engineer promoting plant growth

Vyas, P., Rana, A. K., & Kaur, M. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-89973-4.00017-x · Cited by 7 · see citing works

Serratia

Barman, S., Bhattacharya, S. S., & Mandal, N. C. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-823414-3.00003-4 · Cited by 7 · see citing works

Draft Genome Sequence of Plant-Growth-Promoting Rhizobacterium Serratia fonticola Strain AU-AP2C, Isolated from the Pea Rhizosphere

Devi, U., Khatri, I., Kumar, N., Sharma, D., Subramanian, S., & Saini, A. K. (2013) · Genome Announcements · doi:10.1128/genomea.01022-13 · Cited by 6 · see citing works

Serratia rhizosphaerae sp. nov., a novel plant resistance inducer against soft rot disease in tobacco

Son, J., Hwang, Y.-J., Lee, S.-Y., & Ghim, S. (2021) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijsem.0.004788 · Cited by 5 · see citing works

CaZingipain2 Acts Positively in Pepper (Capsicum annuum L.) Immunity against R. solanacearum

Wu, R., Wu, Z., Qing, Y., Duan, C., Guo, Y., Zhang, X., Huang, R., He, S., & Qiu, A. (2024) · Plants · doi:10.3390/plants13182552 · Cited by 5 · see citing works

Root Colonization and ISR-mediated Anthracnose Disease Control in Cucumber by Strain Enterobacter asburiae B1

Bharathkumar, S., Park, J.-W., Han, J.-H., & Park, K. S. (2009) · The Plant Pathology Journal · doi:10.5423/ppj.2009.25.4.333 · Cited by 5 · see citing works

Quantitative and specific detection of the biocontrol agent, Serratia plymuthica, in plant extracts using a real-time TaqMan® assay

Czajkowski, R., & van der Wolf, J. M. (2012) · Journal of Applied Genetics · doi:10.1007/s13353-012-0106-0 · Cited by 5 · see citing works

Manipulation of Reactive Oxygen Species, Redox and Nitric Oxide Signaling Systems to Activate Plant Innate Immunity for Crop Disease Management

Vidhyasekaran, P. (2020) · Signaling and communication in plants · doi:10.1007/978-94-024-1940-5_3 · Cited by 5 · see citing works

The Effects of Plant Breeding on Soil Microbes

Marschner, P., & Rengel, Z. (2010) · Springer eBooks · doi:10.1007/978-90-481-9479-7_8 · Cited by 5 · see citing works

Activation of disease resistance and defense gene expression in Agrostis stolonifera and Nicotiana benthamiana by a copper-containing pigment and a benzothiadiazole derivative

Nash, B. T. (2011) · The Atrium (University of Guelph) · Cited by 5 · see citing works

Spongospora subterranea f. sp. subterranea Affects Plant Susceptibility to Subsequent Pathogen Infections Under Controlled-Environment Conditions

Ozturk, I. K., Buchholz, E., Bentley, A., Halterman, D., & Rioux, R. A. (2024) · Plant Disease · doi:10.1094/pdis-02-24-0276-re · Cited by 2 · see citing works

Suppression of Crown Gall Disease by Rhizosphere Bacteria andAgrobacterium‐Specific Bacteriophages

Chernin, L. S., Toklikishvili, N., Dandurishvili, N., Tediashvili, M., & Vainstein, A. (2013) · doi:10.1002/9781118297674.ch57 · Cited by 2 · see citing works

Direct and indirect effect of the rhizobacteria Pseudomonas putida KT2440 on maize plants

Planchamp, C. (2013) · doi:10.35662/unine-thesis-2343 · Cited by 3 · see citing works

Multi-Phyto Beneficial Mechanisms and Applications of Serratia spp.

Aswani, R., & Radhakrishnan, E. K. (2017) · Global Journal of Agricultural Innovation Research & Development · doi:10.15377/2409-9813.2017.04.01.2 · Cited by 1 · see citing works

RNA-sequencing for transcriptomic analysis of chili peppers induced by Serratia plymuthica strain UBCF_13

Gozalia, E. N., Tjong, D. H., Renfiyeni, R., Jamsari, J., & Nova, B. (2021) · IOP Conference Series Earth and Environmental Science · doi:10.1088/1755-1315/741/1/012044 · Cited by 1 · see citing works

Plant growth promotion by Pseudomonas fluorescens : mechanisms, genes and regulation

Cheng, X. (2016) · doi:10.18174/387191

Genome of Serratia plymuthica UBCF_13, Insight into diverse unique traits

Fatiah, R., Suliansyah, I., Tjong, D. H., Syukriani, L., Yunita, R., Trivano, R., Azizah, N., & Jamsari, J. (2021) · F1000Research · doi:10.12688/f1000research.54402.1

Introduction

Vidhyasekaran, P. (2020) · Signaling and communication in plants · doi:10.1007/978-94-024-1940-5_1

Insights into the Metabolites Conferring Pathogenicity of Xanthomonas oryzae and Its Inhibition by Trichoderma longibrachiatum EF5

Sridharan, A. P., Thankappan, S., KARTHIKEYAN, G., & Uthandi, S. (2022) · Current Journal of Applied Science and Technology · doi:10.9734/cjast/2022/v41i1631727

The role of oxidative burst and cell wall in tomato interaction with various taxonomic groups of Rhizoctonia sppPreprint

Taheri, P., Hosseini-Zahani, F., & Tarighi, S. (2023) · Research Square · doi:10.21203/rs.3.rs-3127941/v1

Improve the principles for selecting new bacterial biocontrol agents for FHB

Besset-Manzoni, Y. (2018) · doi:10.70675/6f838ff3z76faz4f1ezb358zf37e099d6a38

Caractérisation et rôle du microbiote rhizosphérique fonctionnel dans la résistance de la vigne à Plasmopara viticola

Duret, M. (2024) · doi:10.70675/3abf8bcdzf0d6z4a56za162zf0eef1a59260

Unraveling rhizobacteria- and abscisic acid-induced pathogen resistance in rice (Oryza sativa L.)

Vleesschauwer, D. D. (2008) · Ghent University Academic Bibliography (Ghent University) · Cited by 2 · see citing works

Bacterial Determinants and Host Defense Responses Underpinning Rhizobacteria - Mediated Systemic Resistance in Rice

Vleesschauwer, D. D., & Höfte, M. (2009) · Springer eBooks · doi:10.1007/978-1-4020-9500-9_20 · Cited by 3 · 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

Induced systemic resistance (ISR) in plants: mechanism of action

Choudhary, D. K., Prakash, A., & Johri, B. N. (2007) · Indian Journal of Microbiology · doi:10.1007/s12088-007-0054-2 · Cited by 551 · see citing works

Induced Systemic Resistance in Rice

Nadarajah, K. K. (2016) · Springer eBooks · doi:10.1007/978-981-10-0388-2_7 · Cited by 17 · see citing works