Use of plant growth-promoting bacteria for biocontrol of plant diseases: principles, mechanisms of action, and future prospects

Compant, Stéphane; Duffy, Brion; Nowak, Jerzy; Clément, Christophe; Barka, Essaïd Ait

doi:10.1128/aem.71.9.4951-4959.2005

Cited by 2,640Plant-Microbe Interactions and ImmunityPlant Pathogenic Bacteria StudiesPlant Disease Management Techniques

Use of plant growth-promoting bacteria for biocontrol of plant diseases: principles, mechanisms of action, and future prospects

Open access

Compant, Stéphane, Duffy, Brion, Nowak, Jerzy, Clément, Christophe, Barka, Essaïd Ait·2005·Applied and Environmental Microbiology

DOI 10.1128/aem.71.9.4951-4959.2005PMC PMC1214602

Open this paper in CoChat — free account

Abstract

Pathogenic microorganisms affecting plant health are a major and chronic threat to food production and ecosystem stability worldwide. As agricultural production intensified over the past few decades, producers became more and more dependent on agrochemicals as a relatively reliable method of crop

Integrity signals

Registry

Crossref · 10.1128/aem.71.9.4951-4959.2005

Cites

194 of 194 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

The production of siderophores may deprive pathogenic bacteria and fungi from iron thereby limiting their pathogenicity.
“For example, the production of siderophores may deprive pathogenic bacteria and fungi from iron thereby limiting their pathogenicity (Sharma and Johri, 2003;Compant et al., 2005).”
From Intensify production, transform biomass to energy and novel goods and protect soils in Europe—A vision how to mobilize marginal lands (2018) · cites this paper as Compant et al., 2005

The enhancement of plant growth by free-living bacteria
Glick, B. R. (1995) · Canadian Journal of Microbiology · doi:10.1139/m95-015 · Cited by 2,669 · 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
Bacterial endophytes in agricultural crops
Hallmann, J., Quadt-Hallmann, A., Mahaffee, W. F., & Kloepper, J. W. (1997) · Canadian Journal of Microbiology · doi:10.1139/m97-131 · Cited by 2,018 · see citing works
Microbial interactions and biocontrol in the rhizosphere
Whipps, J. M. (2001) · Journal of Experimental Botany · doi:10.1093/jexbot/52.suppl_1.487 · Cited by 1,934 · see citing works
Biological Control of Soilborne Plant Pathogens in the Rhizosphere with Bacteria
Weller, D. M. (1988) · Annual Review of Phytopathology · doi:10.1146/annurev.py.26.090188.002115 · Cited by 1,765 · see citing works
A model for the lowering of plant ethylene concentrations by plant growth-promoting bacteria
Glick, B. R., Penrose, D. M., & Li, J. (1998) · Journal of Theoretical Biology · doi:10.1006/jtbi.1997.0532 · Cited by 1,466 · cited 1× · see citing works
“For example, transforming the 1-aminocyclopropane-1-carboxylic acid deaminase gene, which directly stimulates plant growth by cleaving the immediate precursor of plant ethylene (64) into P.”
Background
F UNCTION AND M ECHANISM OF O RGANIC A NION E XUDATION FROM P LANT R OOTS
Ryan, P., Delhaize, E., & Jones, D. (2001) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.52.1.527 · Cited by 1,443 · see citing works
Bacterial Volatiles Induce Systemic Resistance in Arabidopsis
Ryu, C.-M., Farag, M. A., Hu, C.-H., Reddy, M. S., Kloepper, J. W., & Paré, P. W. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.026583 · Cited by 1,308 · see citing works
Plant growth-promoting bacteria confer resistance in tomato plants to salt stress
Mayak, S., Tirosh, T., & Glick, B. R. (2004) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2004.05.009 · Cited by 1,257 · 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
Plant Growth-Promoting Effects of Diazotrophs in the Rhizosphere
Dobbelaere, S., Vanderleyden, J., & Okon, Y. (2003) · Critical Reviews in Plant Sciences · doi:10.1080/713610853 · Cited by 1,116 · see citing works
Molecular basis of plant growth promotion and biocontrol by rhizobacteria
Bloemberg, G. V., & Lugtenberg, B. J. J. (2001) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(00)00183-7 · Cited by 1,049 · see citing works
Intracellular and extracellular PGPR: commonalities and distinctions in the plant–bacterium signaling processes
Gray, E. J., & Smith, D. L. (2004) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2004.08.030 · Cited by 1,007 · see citing works
The chalcone synthase superfamily of type III polyketide synthases
Austin, M. B., & Noel, J. P. (2002) · Natural Product Reports · doi:10.1039/b100917f · Cited by 991 · see citing works
Azospirillum , a free-living nitrogen-fixing bacterium closely associated with grasses: genetic, biochemical and ecological aspects
Steenhoudt, O., & Vanderleyden, J. (2000) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2000.tb00552.x · Cited by 940 · see citing works
How plants communicate using the underground information superhighway
Bais, H. P., Park, S.-W., Weir, T. L., Callaway, R. M., & Vivanco, J. M. (2003) · Trends in Plant Science · doi:10.1016/j.tplants.2003.11.008 · Cited by 890 · see citing works
Antibiotic production by bacterial biocontrol agents
Raaijmakers, J. M., Vlami, M., & de Souza, J. T. (2002) · Antonie van Leeuwenhoek · doi:10.1023/a:1020501420831 · Cited by 870 · see citing works
Bacterial Endophytes: Potential Role in Developing Sustainable Systems of Crop Production
Sturz, A. V., Christie, B. R., & Nowak, J. (2000) · Critical Reviews in Plant Sciences · doi:10.1016/s0735-2689(01)80001-0 · Cited by 857 · see citing works
Self-citation
Endophytic Colonization of Vitis vinifera L. by Plant Growth-Promoting Bacterium Burkholderia sp. Strain PsJN
Compant, S., Reiter, B., Sessitsch, A., et al. (2005) · Applied and Environmental Microbiology · doi:10.1128/aem.71.4.1685-1693.2005 · Cited by 830 · see citing works
Self-citation
R EGULATION OF A NTIBIOTIC P RODUCTION IN R OOT -C OLONIZING P SEUDOMONAS SPP. AND R ELEVANCE FOR B IOLOGICAL C ONTROL OF P LANT D ISEASE
Haas, D., & Keel, C. (2003) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.41.052002.095656 · Cited by 824 · see citing works
M OLECULAR D ETERMINANTS OF R HIZOSPHERE C OLONIZATION BY P SEUDOMONAS
Lugtenberg, B. J. J., Dekkers, L. C., & Bloemberg, G. V. (2001) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.39.1.461 · Cited by 807 · see citing works
AiiA, an enzyme that inactivates the acylhomoserine lactone quorum-sensing signal and attenuates the virulence of Erwinia carotovora
Dong, Y.-H., Xu, J., Li, X., & Zhang, L. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.7.3526 · Cited by 803 · see citing works
AiiA, an enzyme that inactivates the acylhomoserine lactone quorum-sensing signal and attenuates the virulence of Erwinia carotovora
Dong, Y. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.060023897 · Cited by 783 · 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
Induced Resistance and Phytoalexin Accumulation in Biological Control of Fusarium Wilt of Carnation byPseudomonassp. Strain WCS417r
van Peer, R. (1991) · Phytopathology · doi:10.1094/phyto-81-728 · Cited by 774 · see citing works
Endophytic Bacteria and Their Potential Applications
Lodewyckx, C., Vangronsveld, J., Porteous, F., et al. (2002) · Critical Reviews in Plant Sciences · doi:10.1080/0735-260291044377 · Cited by 761 · see citing works
Enzymes in the Environment
Burns, R. G., & Dick, R. P. (2002) · CRC Press eBooks · doi:10.1201/9780203904039 · Cited by 717 · see citing works
Induction of systemic resistance by plant growth promoting rhizobacteria in crop plants against pests and diseases
Ramamoorthy, V., Viswanathan, R., Raguchander, T., et al. (2001) · Crop Protection · doi:10.1016/s0261-2194(00)00056-9 · Cited by 717 · see citing works
Plant growth-promoting rhizobacteria on radishes
Kloepper, J. W. (1978) · Medical Entomology and Zoology · Cited by 666 · see citing works
Traits of fluorescent Pseudomonas spp. involved in suppression of plant root pathogens
O’Sullivan, D. J., & O’Gara, F. (1992) · Microbiological Reviews · doi:10.1128/mr.56.4.662-676.1992 · Cited by 664 · see citing works
Salicylic acid-independent plant defence pathways
Pieterse, C. M. J., & van Loon, L. C. (1999) · Trends in Plant Science · doi:10.1016/s1360-1385(98)01364-8 · Cited by 646 · see citing works
Mixtures of Plant Growth-Promoting Rhizobacteria Enhance Biological Control of Multiple Cucumber Pathogens
Raupach, G. S., & Kloepper, J. W. (1998) · Phytopathology · doi:10.1094/phyto.1998.88.11.1158 · Cited by 634 · see citing works
Induction of Systemic Resistance of Cucumber toColletotrichum orbiculareby Select Strains of Plant Growth-Promoting Rhizobacteria
Wei, G. (1991) · Phytopathology · doi:10.1094/phyto-81-1508 · Cited by 616 · see citing works
Q UORUM S ENSING IN P LANT -P ATHOGENIC B ACTERIA
von Bodman, S. B., Bauer, W. D., & Coplin, D. L. (2003) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.41.052002.095652 · Cited by 588 · see citing works
Flagella-Driven Chemotaxis Towards Exudate Components Is an Important Trait for Tomato Root Colonization by Pseudomonas fluorescens
de Weert, S., Vermeiren, H., Mulders, I. H. M., et al. (2002) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2002.15.11.1173 · Cited by 573 · see citing works
Rhizosphere Interactions and the Exploitation of Microbial Agents for the Biological Control of Plant-Parasitic Nematodes
Kerry, B. R. (2000) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.38.1.423 · Cited by 555 · see citing works
Defense enzymes induced in cucumber roots by treatment with plant growth-promoting rhizobacteria (PGPR) and Pythium aphanidermatum
Chen, C., Bélanger, R. R., Benhamou, N., et al. (2000) · Physiological and Molecular Plant Pathology · doi:10.1006/pmpp.1999.0243 · Cited by 537 · see citing works
Induction of Systemic Resistance of Tobacco to Tobacco Necrosis Virus by the Root-ColonizingPseudomonas fluorescensStrain CHA0: Influence of thegacAGene and of Pyoverdine Production
Maurhofer, M. (1994) · Phytopathology · doi:10.1094/phyto-84-139 · Cited by 537 · see citing works
Extensive and specific responses of a eukaryote to bacterial quorum-sensing signals
Mathesius, U., Mulders, S., Gao, M., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.262672599 · Cited by 535 · see citing works
STRUCTURE-FUNCTION AND BIOGENESIS OF THE TYPE IV PILI
Strom, M. S., & Lory, S. (1993) · Annual Review of Microbiology · doi:10.1146/annurev.mi.47.100193.003025 · Cited by 498 · see citing works
Bacterial Endophytes: Potential Role in Developing Sustainable Systems of Crop Production
Sturz, A. V., Christie, B. R., & Nowak, J. (2000) · Critical Reviews in Plant Sciences · doi:10.1080/07352680091139169 · Cited by 496 · see citing works
Self-citation
Environmental Factors Modulating Antibiotic and Siderophore Biosynthesis by Pseudomonas fluorescens Biocontrol Strains
Duffy, B. K., & Défago, G. (1999) · Applied and Environmental Microbiology · doi:10.1128/aem.65.6.2429-2438.1999 · Cited by 488 · see citing works
Self-citation
The Rhizosphere and Plant Growth.
Nicolson, T. H., Keister, D. L., & Cregan, P. B. (1992) · Journal of Applied Ecology · doi:10.2307/2404369 · Cited by 440 · see citing works
Proposal for the division of plant growth-promoting rhizobacteria into two classifications: biocontrol-PGPB (plant growth-promoting bacteria) and PGPB
Bashan, Y., & Holguín, G. (1998) · Soil Biology and Biochemistry · doi:10.1016/s0038-0717(97)00187-9 · Cited by 439 · see citing works
Biological Control of Fusarium Wilt of Cucumber by Chitinolytic Bacteria
Singh, P. P., Shin, Y. C., Park, C.-S., et al. (1999) · Phytopathology · doi:10.1094/phyto.1999.89.1.92 · Cited by 435 · see citing works
MICROBIAL DYNAMICS AND INTERACTIONS IN THE SPERMOSPHERE
Nelson, E. B. (2004) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.42.121603.131041 · Cited by 422 · see citing works
Managing Soil Microorganisms to Improve Productivity of Agro-Ecosystems
Welbaum, G. E., Sturz, A. V., Dong, Z., & Nowak, J. (2004) · Critical Reviews in Plant Sciences · doi:10.1080/07352680490433295 · Cited by 411 · see citing works
Self-citation
Differential Induction of Systemic Resistance in Arabidopsis by Biocontrol Bacteria
Wees, S. C. M. V., Pieterse, C. M. J., Trijssenaar, A., et al. (1997) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.1997.10.6.716 · Cited by 410 · see citing works
Munumbicins, wide-spectrum antibiotics produced by Streptomyces NRRL 30562, endophytic on Kennedia nigriscans a aThe GenBank accession number for the sequence determined in this work is AY127079.
Castillo, U. F., Strobel, G. A., Ford, E. J., Hess, W. M., Porter, H., Jensen, J. B., Albert, H., Robison, R. A., Condron, M. A. M., Teplow, D. B., et al. (2002) · Microbiology · doi:10.1099/00221287-148-9-2675 · Cited by 406 · see citing works
Gnotobiotic System for Studying Rhizosphere Colonization by Plant Growth-PromotingPseudomonasBacteria Gnotobiotic System for Studying Rhizosphere
Simons, M. (1996) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-9-0600 · Cited by 399 · see citing works
Endophytic bacterial communities of field-grown potato plants and their plant-growth-promoting and antagonistic abilities
Sessitsch, A., Reiter, B., & Berg, G. (2004) · Canadian Journal of Microbiology · doi:10.1139/w03-118 · Cited by 376 · see citing works
Burkholderia phytofirmans sp. nov., a novel plant-associated bacterium with plant-beneficial properties.
Sessitsch, A., Coenye, T., Sturz, A. V., Vandamme, P., Barka, E. A., Salles, J. F., Van Elsas, J. D., Faure, D., Reiter, B., Glick, B. R., et al. (2005) · International Journal of Systematic and Evolutionary Microbiology · doi:10.1099/ijs.0.63149-0 · Cited by 375 · see citing works
Self-citation
Biological substitutes for pesticides
Gerhardson, B. (2002) · Trends in biotechnology · doi:10.1016/s0167-7799(02)02021-8 · Cited by 369 · see citing works
Identification and Characterization of a Gene Cluster for Synthesis of the Polyketide Antibiotic 2,4-Diacetylphloroglucinol from Pseudomonas fluorescens Q2-87
Bangera, M. G., & Thomashow, L. S. (1999) · Journal of Bacteriology · doi:10.1128/jb.181.10.3155-3163.1999 · Cited by 356 · see citing works
Effect of transferring 1-aminocyclopropane-1-carboxylic acid (ACC) deaminase genes intoPseudomonas fluorescensstrain CHA0 and itsgacA derivative CHA96 on their growth-promoting and disease-suppressive capacities
Wang, C., Knill, E., Glick, B. R., et al. (2000) · Canadian Journal of Microbiology · doi:10.1139/w00-071 · Cited by 349 · see citing works
Endophytic nitrogen fixation in sugarcane: present knowledge and future applications
Boddey, R. M., Urquiaga, S. S., Alves, B. J. R., & Reis, V. M. (2003) · Plant and Soil · doi:10.1023/a:1024152126541 · Cited by 346 · 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
Induction of Systemic Resistance Against Fusarium Wilt of Radish by Lipopolysaccharides ofPseudomonas fluorescens
Leeman, M. (1995) · Phytopathology · doi:10.1094/phyto-85-1021 · Cited by 340 · see citing works
Autoinduction of 2,4-Diacetylphloroglucinol Biosynthesis in the Biocontrol Agent Pseudomonas fluorescens CHA0 and Repression by the Bacterial Metabolites Salicylate and Pyoluteorin
Schnider‐Keel, U., Seematter, A., Maurhofer, M., et al. (2000) · Journal of Bacteriology · doi:10.1128/jb.182.5.1215-1225.2000 · Cited by 340 · see citing works
What makes Pseudomonas bacteria rhizosphere competent?
Lugtenberg, B. J. J., & Dekkers, L. C. (1999) · Environmental Microbiology · doi:10.1046/j.1462-2920.1999.00005.x · Cited by 339 · see citing works
The type-4 pilus is the major virulence-associated adhesin of Pseudomonas aeruginosa – a review
Hahn, H. P. (1997) · Gene · doi:10.1016/s0378-1119(97)00116-9 · Cited by 335 · see citing works
Salicylic Acid Produced by the Rhizobacterium Pseudomonas aeruginosa 7NSK2 Induces Resistance to Leaf Infection by Botrytis cinerea on Bean
Meyer, G. D., & Höfte, M. (1997) · Phytopathology · doi:10.1094/phyto.1997.87.6.588 · Cited by 335 · 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
Biological Control of Fusarium Wilt on Cotton by Use of Endophytic Bacteria
Chen, C., Bauske, E. M., Musson, G., et al. (1995) · Biological Control · doi:10.1006/bcon.1995.1009 · Cited by 331 · see citing works
Flagella of a plant-growth-stimulating Pseudomonas fluorescens strain are required for colonization of potato roots
de Weger, L. A., van der Vlugt, C. I., Wijfjes, A. H. M., Bakker, P. A. H. M., Schippers, B., & Lugtenberg, B. J. J. (1987) · Journal of Bacteriology · doi:10.1128/jb.169.6.2769-2773.1987 · Cited by 322 · see citing works
Plant root-bacterial interactions in biological control of soilborne diseases and potential extension to systemic and foliar diseases
Kloepper, J. W., Rodríguez-Kábana, R., Zehnder, G. W., Murphy, J. F., Sikora, E. J., & Fernández, C. (1999) · Australasian Plant Pathology · doi:10.1071/ap99003 · Cited by 320 · see citing works
Biological control of soilborne plant pathogens by a β-1,3 glucanase-producing Pseudomonas cepacia
Fridlender, M., Inbar, J., & Chet, I. (1993) · Soil Biology and Biochemistry · doi:10.1016/0038-0717(93)90217-y · Cited by 319 · see citing works
Chemical characterization of root exudates from rice (Oryza sativa) and their effects on the chemotactic response of endophytic bacteria
Bacilio, M., Aguilar-Flores, S., Ventura-Zapata, E., Pérez‐Campos, E., Bouquelet, S., & Zenteno, E. (2003) · Plant and Soil · doi:10.1023/a:1022888900465 · Cited by 317 · see citing works
Interactions Between Plant Roots and Soil Microorganisms
Rovira, A. (1965) · Annual Review of Microbiology · doi:10.1146/annurev.mi.19.100165.001325 · Cited by 316 · see citing works
Pseudomonas for biocontrol of phytopathogens: from functional genomics to commercial exploitation
Walsh, U. F., Morrissey, J. P., & O’Gara, F. (2001) · Current Opinion in Biotechnology · doi:10.1016/s0958-1669(00)00212-3 · Cited by 316 · see citing works
The role of chitinase of Serratia marcescens in biocontrol of Sclerotium rolfsii
Ordentlich, A., Elad, Y., & Chet, I. (1988) · Phytopathology · Cited by 315 · see citing works
Iron Availability Affects Induction of Systemic Resistance to Fusarium Wilt of Radish byPseudomonas fluorescens
Leeman, M. (1996) · Phytopathology · doi:10.1094/phyto-86-149 · Cited by 299 · see citing works
Developments in the Biological Control of Soil-borne Plant Pathogens
Whipps, J. M. (1997) · Advances in botanical research · doi:10.1016/s0065-2296(08)60119-6 · Cited by 286 · see citing works
Induction of resistance against Fusarium wilt of tomato by combination of chitosan with an endophytic bacterial strain: ultrastructure and cytochemistry of the host response
Benhamou, N., Kloepper, J. W., & Tuzun, S. (1998) · Planta · doi:10.1007/s004250050242 · Cited by 286 · see citing works
Degradation of pathogen quorum-sensing molecules by soil bacteria: a preventive and curative biological control mechanism
Molina, L., CONSTANTINESCU, F., Michel, L., et al. (2003) · FEMS Microbiology Ecology · doi:10.1016/s0168-6496(03)00125-9 · Cited by 285 · see citing works
Attracting friends to feast on foes: engineering terpene emission to make crop plants more attractive to herbivore enemies
Degenhardt, J., Gershenzon, J., Baldwin, I. T., & Keßler, A. (2003) · Current Opinion in Biotechnology · doi:10.1016/s0958-1669(03)00025-9 · Cited by 284 · see citing works
Utilization of Heterologous Siderophores Enhances Levels of Iron Available to Pseudomonas putida in the Rhizosphere
Loper, J. E., & Henkels, M. D. (1999) · Applied and Environmental Microbiology · doi:10.1128/aem.65.12.5357-5363.1999 · Cited by 283 · see citing works
Tomato seed and root exudate sugars: composition, utilization by Pseudomonas biocontrol strains and role in rhizosphere colonization
Lugtenberg, B. J. J., Lv, K., & Simons, M. (1999) · Environmental Microbiology · doi:10.1046/j.1462-2920.1999.00054.x · Cited by 280 · see citing works
Diversity of siderophore‐mediated iron uptake systems in fluorescent pseudomonads: not only pyoverdines
Cornelis, P., & Matthijs, S. (2002) · Environmental Microbiology · doi:10.1046/j.1462-2920.2002.00369.x · Cited by 278 · see citing works
P ATHOGEN S ELF -D EFENSE : Mechanisms to Counteract Microbial Antagonism
Duffy, B. K., Schouten, A., & Raaijmakers, J. M. (2003) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.41.052002.095606 · Cited by 273 · see citing works
Self-citation
Inhibitory effect of endophyte bacteria on Botrytis cinerea and its influence to promote the grapevine growth
Barka, E. A., Gognies, S., Nowak, J., et al. (2002) · Biological Control · doi:10.1016/s1049-9644(02)00034-8 · Cited by 271 · see citing works
Self-citation
Increased resistance toFusarium oxysporumf. sp.radicis-lycopersiciin tomato plants treated with the endophytic bacteriumPseudomonas fluorescensstrain 63-28
M'piga, P., Bélanger, R. R., Paulitz, T. C., et al. (1997) · Physiological and Molecular Plant Pathology · doi:10.1006/pmpp.1997.0088 · Cited by 267 · see citing works
Root Mucilage from Pea and Its Utilization by Rhizosphere Bacteria as a Sole Carbon Source
Knee, E. M., Gong, F.-C., Gao, M., et al. (2001) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2001.14.6.775 · Cited by 266 · see citing works
Endophytic bacteria in grapevine
Bell, C. R., Dickie, G. A., Harvey, W. L. G., et al. (1995) · Canadian Journal of Microbiology · doi:10.1139/m95-006 · Cited by 266 · see citing works
Genomics of pyoverdine-mediated iron uptake in pseudomonads
Ravel, J., & Cornélis, P. (2003) · Trends in Microbiology · doi:10.1016/s0966-842x(03)00076-3 · Cited by 260 · see citing works
Encyclopedia of plant pathology
(2001) · Choice Reviews Online · doi:10.5860/choice.39-0036 · Cited by 254 · see citing works
Insecticidal Bacillus thuringiensis Silences Erwinia carotovora Virulence by a New Form of Microbial Antagonism, Signal Interference
Dong, Y.-H., Zhang, X., Xu, J.-L., & Zhang, L. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.2.954-960.2004 · Cited by 254 · see citing works
Signals from the underground: bacterial volatiles promote growth in Arabidopsis
Ping, L. (2004) · Trends in Plant Science · doi:10.1016/j.tplants.2004.04.008 · Cited by 251 · see citing works
Pseudomonas stutzeri YPL-1 Genetic Transformation and Antifungal Mechanism against Fusarium solani , an Agent of Plant Root Rot
Lim, H.-S., Kim, Y., & Kim, S.-D. (1991) · Applied and Environmental Microbiology · doi:10.1128/aem.57.2.510-516.1991 · Cited by 250 · see citing works
Zinc Improves Biocontrol of Fusarium Crown and Root Rot of Tomato by Pseudomonas fluorescens and Represses the Production of Pathogen Metabolites Inhibitory to Bacterial Antibiotic Biosynthesis
Duffy, B. K., & Défago, G. (1997) · Phytopathology · doi:10.1094/phyto.1997.87.12.1250 · Cited by 249 · see citing works
Self-citation
Plant growth‐promoting rhizobacteria systemically protect Arabidopsis thaliana against Cucumber mosaic virus by a salicylic acid and NPR1‐independent and jasmonic acid‐dependent signaling pathway
Ryu, C., Murphy, J. F., Mysore, K. S., et al. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02142.x · Cited by 244 · see citing works
Biochemical, Genetic, and Zoosporicidal Properties of Cyclic Lipopeptide Surfactants Produced by Pseudomonas fluorescens
de Souza, J. T., de Boer, M., de Waard, P., et al. (2003) · Applied and Environmental Microbiology · doi:10.1128/aem.69.12.7161-7172.2003 · Cited by 239 · see citing works
H OST V ARIATION FOR I NTERACTIONS WITH B ENEFICIAL P LANT -A SSOCIATED M ICROBES
Smith, K. P., & Goodman, R. M. (1999) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.37.1.473 · Cited by 237 · see citing works
Novel bacteria degrading N-acylhomoserine lactones and their use as quenchers of quorum-sensing-regulated functions of plant-pathogenic bacteria
Uroz, S., D’Angelo‐Picard, C., Carlier, A. L., et al. (2003) · Microbiology · doi:10.1099/mic.0.26375-0 · Cited by 234 · see citing works
Purification and properties of two chitinolytic enzymes of Serratia plymuthica HRO-C48
Frankowski, J., Lorito, M., Scala, F., et al. (2001) · Archives of Microbiology · doi:10.1007/s002030100347 · Cited by 226 · see citing works
Antibiotic and Biosurfactant Properties of Cyclic Lipopeptides Produced by Fluorescent Pseudomonas spp. from the Sugar Beet Rhizosphere
Nielsen, T. H., Sørensen, D., Tobiasen, C., et al. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.7.3416-3423.2002 · Cited by 224 · see citing works
Beneficial microbial allelopathies in the root zone: the management of soil quality and plant disease with rhizobacteria
Sturz, A. V., & Christie, B. R. (2003) · Soil and Tillage Research · doi:10.1016/s0167-1987(03)00082-5 · Cited by 220 · see citing works
Evidence for direct utilization of a siderophore, ferrioxamine B, in axenically grown cucumber
Wang, Y., Brown, H., Crowley, D. E., et al. (1993) · Plant Cell & Environment · doi:10.1111/j.1365-3040.1993.tb00906.x · Cited by 215 · see citing works
Genetic basis in plants for interactions with disease-suppressive bacteria
Smith, K. P., Handelsman, J., & Goodman, R. M. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.9.4786 · Cited by 211 · see citing works
Frequency and Biodiversity of 2,4-Diacetylphloroglucinol-Producing Bacteria Isolated from the Maize Rhizosphere at Different Stages of Plant Growth
Picard, C., Cello, F. D., Ventura, M., et al. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.3.948-955.2000 · Cited by 210 · see citing works
Involvement of the outer membrane lipopolysaccharides in the endophytic colonization of tomato roots by biocontrol Pseudomonas fluorescens strain WCS417r
Duijff, B. J., Gianinazzi-Pearson, V., & Lemanceau, P. (1997) · New Phytologist · doi:10.1046/j.1469-8137.1997.00646.x · Cited by 206 · see citing works
Amino Acid Synthesis Is Necessary for Tomato Root Colonization by Pseudomonas fluorescens Strain WCS365
Simons, M., Permentier, H. P., de Weger, L. A., et al. (1997) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.1997.10.1.102 · Cited by 198 · see citing works
Combination ofTrichoderma koningiiwith Fluorescent Pseudomonads for Control of Take-all on Wheat
Duffy, B. K. (1996) · Phytopathology · doi:10.1094/phyto-86-188 · Cited by 196 · see citing works
Self-citation
Type IV pili are involved in plant–microbe and fungus–microbe interactions
Dörr, J., Hurek, T., & Reinhold‐Hurek, B. (1998) · Molecular Microbiology · doi:10.1046/j.1365-2958.1998.01010.x · Cited by 192 · see citing works
Production of kanosamine by Bacillus cereus UW85
Milner, J. L., Silo-Suh, L., Lee, J. C., et al. (1996) · Applied and Environmental Microbiology · doi:10.1128/aem.62.8.3061-3065.1996 · Cited by 188 · see citing works
Utilization of heterologous siderophores and rhizosphere competence of fluorescentPseudomonasspp.
Raaijmakers, J. M., van der Sluis, L., Bakker, P. A. H. M., Schippers, B., Koster, M. C., & Weisbeek, P. J. (1995) · Canadian Journal of Microbiology · doi:10.1139/m95-017 · Cited by 188 · see citing works
Selected Topics in Biological Control
Schroth, M. N., & Hancock, J. G. (1981) · Annual Review of Microbiology · doi:10.1146/annurev.mi.35.100181.002321 · Cited by 188 · see citing works
Are microbes at the root of a solution to world food production?
Morrissey, J. P., Dow, J. M., Mark, G. L., et al. (2004) · EMBO Reports · doi:10.1038/sj.embor.7400263 · Cited by 187 · see citing works
Introduction of the phzH Gene of Pseudomonas chlororaphis PCL1391 Extends the Range of Biocontrol Ability of Phenazine-1-Carboxylic Acid-Producing Pseudomonas spp. Strains
Chin‐A‐Woeng, T. F. C., THOMAS‐OATES, J. E., Lugtenberg, B. J. J., et al. (2001) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2001.14.8.1006 · Cited by 182 · see citing works
Interpopulation Signaling via N-Acyl-Homoserine Lactones among Bacteria in the Wheat Rhizosphere
Pierson, E. A., Wood, D. W., Cannon, J. A., et al. (1998) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.1998.11.11.1078 · Cited by 181 · see citing works
Possible Role of Xanthobaccins Produced by Stenotrophomonas sp. Strain SB-K88 in Suppression of Sugar Beet Damping-Off Disease
Nakayama, T., Homma, Y., Hashidoko, Y., et al. (1999) · Applied and Environmental Microbiology · doi:10.1128/aem.65.10.4334-4339.1999 · Cited by 177 · see citing works
Enhancement of in vitro growth and resistance to gray mould ofVitis viniferaco-cultured with plant growth-promoting rhizobacteria
Barka, E. A., Belarbi, A., Hachet, C., et al. (2000) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2000.tb09087.x · Cited by 176 · see citing works
Self-citation
Soil-borne strain IC14 of Serratia plymuthica with multiple mechanisms of antifungal activity provides biocontrol of Botrytis cinerea and Sclerotinia sclerotiorum diseases
Kamensky, M., Ovadis, M. I., Chet, I., et al. (2003) · Soil Biology and Biochemistry · doi:10.1016/s0038-0717(02)00283-3 · Cited by 174 · see citing works
Availability of iron to Pseudomonas fluorescens in rhizosphere and bulk soil evaluated with an ice nucleation reporter gene
Loper, J. E., & Henkels, M. D. (1997) · Applied and Environmental Microbiology · doi:10.1128/aem.63.1.99-105.1997 · Cited by 168 · see citing works
Extracellular protease and phospholipase C are controlled by the global regulatory gene gacA in the biocontrol strainPseudomonas fluorescensCHA0
Sacherer, P., DÃ©fago, G., & Haas, D. (1994) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1994.tb06694.x · Cited by 168 · see citing works
Iron Sufficiency, a Prerequisite for the Suppression of Tobacco Black Root Rot byPseudomonas fluorescensStrain CHA0 under Gnotobiotic Conditions
Keel, C. (1989) · Phytopathology · doi:10.1094/phyto-79-584 · Cited by 166 · see citing works
Microbial enrichment to enhance the disease suppressive activity of compost
Postma, J., Montanari, M., & van den Boogert, P. H. J. F. (2003) · European Journal of Soil Biology · doi:10.1016/s1164-5563(03)00031-1 · Cited by 166 · see citing works
Strain-specific chemotaxis of Azospirillum spp
Reinhold, B., Hurek, T., & Fendrik, I. (1985) · Journal of Bacteriology · doi:10.1128/jb.162.1.190-195.1985 · Cited by 165 · see citing works
Endophytic bacterial communities in the periderm of potato tubers and their potential to improve resistance to soil‐borne plant pathogens
Sturz, Christie, Matheson, et al. (1999) · Plant Pathology · doi:10.1046/j.1365-3059.1999.00351.x · Cited by 162 · see citing works
Two-Component Transcriptional Regulation of N -Acyl-Homoserine Lactone Production in Pseudomonas aureofaciens
Chancey, S. T., Wood, D. W., & Pierson, L. S. (1999) · Applied and Environmental Microbiology · doi:10.1128/aem.65.6.2294-2299.1999 · Cited by 160 · see citing works
Induced systemic resistance in radish is not associated with accumulation of pathogenesis-related proteins
Hoffland, E., Pieterse, C. M. J., Bik, L., & van Pelt, J. A. (1995) · Physiological and Molecular Plant Pathology · doi:10.1006/pmpp.1995.1024 · Cited by 159 · see citing works
A global regulator of secondary metabolite production in Pseudomonas fluorescens Pf-5
Corbell, N., & Loper, J. E. (1995) · Journal of Bacteriology · doi:10.1128/jb.177.21.6230-6236.1995 · Cited by 158 · see citing works
The role of bacterial motility in the survival and spread of Pseudomonas fluorescens in soil and in the attachment and colonisation of wheat roots
Turnbull, G. A., Morgan, J. A. W., Whipps, J. M., et al. (2001) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2001.tb00822.x · Cited by 158 · see citing works
The sss Colonization Gene of the Tomato-Fusarium oxysporum f. sp. radicis-lycopersici Biocontrol Strain Pseudomonas fluorescens WCS365 Can Improve Root Colonization of Other Wild-type Pseudomonas spp. Bacteria
Dekkers, L. C., Mulders, I. H. M., Phoelich, C. C., Chin‐A‐Woeng, T. F. C., Wijfjes, A. H. M., & Lugtenberg, B. J. J. (2000) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2000.13.11.1177 · Cited by 157 · see citing works
Involvement ofgacSandrpoSin enhancement of the plant growth-promoting capabilities ofEnterobacter cloacaeCAL2 and UW4
Saleh, S. S., & Glick, B. R. (2001) · Canadian Journal of Microbiology · doi:10.1139/w01-072 · Cited by 156 · see citing works
Pseudomonas aeruginosa 7NSK2-induced Systemic Resistance in Tobacco Depends on in planta Salicylic Acid Accumulation but is not Associated with PR1a Expression
Meyer, G. D., Audenaert, K., & Höfte, M. (1999) · European Journal of Plant Pathology · doi:10.1023/a:1008741015912 · Cited by 154 · see citing works
HOMOSERINE LACTONE-MEDIATED GENE REGULATION IN PLANT-ASSOCIATED BACTERIA
Pierson, L. S., Wood, D. W., & Pierson, E. A. (1998) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.36.1.207 · Cited by 154 · see citing works
Phenotypic Selection and Phase Variation Occur during Alfalfa Root Colonization by Pseudomonas fluorescens F113
Sánchez-Contreras, M., Martín, M., Durbán, M. V., et al. (2002) · Journal of Bacteriology · doi:10.1128/jb.184.6.1587-1596.2002 · Cited by 153 · see citing works
Biotic Factors Affecting Expression of the 2,4-Diacetylphloroglucinol Biosynthesis Gene phlA in Pseudomonas fluorescens Biocontrol Strain CHA0 in the Rhizosphere
Notz, R., Maurhofer, M., Schnider‐Keel, U., et al. (2001) · Phytopathology · doi:10.1094/phyto.2001.91.9.873 · Cited by 151 · see citing works
Effects of Antagonist Cell Concentration and Two-Strain Mixtures on Biological Control of Fusarium Dry Rot of Potatoes
Schisler, D. A., Slininger, P. J., & Bothast, R. J. (1997) · Phytopathology · doi:10.1094/phyto.1997.87.2.177 · Cited by 144 · see citing works
Evaluation of Endophytic Bacteria as Potential Biological-Control Agents for Oak Wilt
Brooks, D. S., Gonzalez, C. F., Appel, D. N., et al. (1994) · Biological Control · doi:10.1006/bcon.1994.1047 · Cited by 144 · see citing works
A site-specific recombinase is required for competitive root colonization by Pseudomonas fluorescens WCS365
Dekkers, L. C., Phoelich, C. C., van der Fits, L., et al. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.12.7051 · Cited by 139 · see citing works
Population dynamics of endophytic bacteria in field-grown sweet corn and cotton
McInroy, J. A., & Kloepper, J. W. (1995) · Canadian Journal of Microbiology · doi:10.1139/m95-123 · Cited by 139 · see citing works
Global Regulation of Expression of Antifungal Factors by aPseudomonas fluorescensBiological Control Strain
Gaffney, T. D. (1994) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-7-0455 · Cited by 137 · see citing works
Identification and Manipulation of Soil Properties To Improve the Biological Control Performance of Phenazine-Producing Pseudomonas fluorescens
Ownley, B. H., Duffy, B. K., & Weller, D. M. (2003) · Applied and Environmental Microbiology · doi:10.1128/aem.69.6.3333-3343.2003 · Cited by 136 · see citing works
Self-citation
Combining Fluorescent Pseudomonas spp. Strains to Enhance Suppression of Fusarium Wilt of Radish
de Boer, M., van der Sluis, I., van Loon, L. C., et al. (1999) · European Journal of Plant Pathology · doi:10.1023/a:1008761729073 · Cited by 136 · see citing works
Activation of PR-1a Promoter by Rhizobacteria That Induce Systemic Resistance in Tobacco against Pseudomonas syringae pv. tabaci
Park, K. S., & Kloepper, J. W. (2000) · Biological Control · doi:10.1006/bcon.2000.0815 · Cited by 135 · see citing works
Biological control of plant root pathogens
Thomashow, L. S. (1996) · Current Opinion in Biotechnology · doi:10.1016/s0958-1669(96)80042-5 · Cited by 133 · see citing works
Endophytic colonization and field responses of hybrid spruce seedlings after inoculation with plant growth-promoting rhizobacteria
Chanway, C. P., Shishido, M., Nairn, J. D., et al. (2000) · Forest Ecology and Management · doi:10.1016/s0378-1127(99)00300-x · Cited by 130 · see citing works
Characterization of Root Surface and Endorhizosphere Pseudomonads in Relation to Their Colonization of Roots
van Peer, R., Punte, H. L. M., de Weger, L. A., et al. (1990) · Applied and Environmental Microbiology · doi:10.1128/aem.56.8.2462-2470.1990 · Cited by 129 · see citing works
Colonization of the rhizosphere of crop plants by plant-beneficial pseudomonads
de Weger, L. A., van der Bij, A. J., Dekkers, L. C., et al. (1995) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.1995.tb00146.x · Cited by 125 · see citing works
Production of Cyclic Lipopeptides byPseudomonas fluorescensStrains in Bulk Soil and in the Sugar Beet Rhizosphere
Nielsen, T. H., & Sørensen, J. (2003) · Applied and Environmental Microbiology · doi:10.1128/aem.69.2.861-868.2003 · Cited by 124 · see citing works
Enhancement of verticillium wilt resistance in tomato transplants by in vitro co-culture of seedlings with a plant growth promoting rhizobacterium (Pseudomonas sp. strain PsJN)
Sharma, V. K., & Nowak, J. (1998) · Canadian Journal of Microbiology · doi:10.1139/cjm-44-6-528 · Cited by 123 · see citing works
Self-citation
Role of the O-Antigen of Lipopolysaccharide, and Possible Roles of Growth Rate and of NADH:ubiquinone Oxidoreductase (nuo) in Competitive Tomato Root-Tip Colonization by Pseudomonas fluorescens WCS365
Dekkers, L. C., van der Bij, A. J., Mulders, I. H. M., Phoelich, C. C., Wentwoord, R. A. R., Glandorf, B., Wijffelman, C. A., & Lugtenberg, B. J. J. (1998) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.1998.11.8.763 · Cited by 123 · see citing works
Biocontrol ability of fluorescent pseudomonads genetically dissected: importance of positive feedback regulation
Haas, D., Blumer, C., & Keel, C. (2000) · Current Opinion in Biotechnology · doi:10.1016/s0958-1669(00)00098-7 · Cited by 122 · see citing works
Controlling Instability in gacS-gacA Regulatory Genes during Inoculant Production of Pseudomonas fluorescens Biocontrol Strains
Duffy, B. K., & Défago, G. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.8.3142-3150.2000 · Cited by 122 · see citing works
Self-citation
Suppression of fusarium wilt of radish by co-inoculation of fluorescentPseudomonas spp. and root-colonizing fungi
(1996) · doi:10.1007/bf01877112 · Cited by 122 · see citing works
Defense Responses of Fusarium oxysporum to 2,4-Diacetylphloroglucinol, a Broad-Spectrum Antibiotic Produced by Pseudomonas fluorescens
Schouten, A., Berg, G. V. D., Edel‐Hermann, V., et al. (2004) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2004.17.11.1201 · Cited by 121 · see citing works
P OLYKETIDE P RODUCTION BY P LANT -A SSOCIATED P SEUDOMONADS
Bender, C. L., Rangaswamy, V., & Loper, J. E. (1999) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.37.1.175 · Cited by 119 · see citing works
Priming for transplant stress resistance in In vitro propagation
Nowak, J., & Shulaev, V. (2003) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1079/ivp2002403 · Cited by 118 · see citing works
Self-citation
Positive Autoregulation and Signaling Properties of Pyoluteorin, an Antibiotic Produced by the Biological Control Organism Pseudomonas fluorescens Pf-5
Brodhagen, M., Henkels, M. D., & Loper, J. E. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.3.1758-1766.2004 · Cited by 118 · see citing works
Potential Role of Pathogen Signaling in Multitrophic Plant-Microbe Interactions Involved in Disease Protection
Duffy, B. K., Keel, C., & Défago, G. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.3.1836-1842.2004 · Cited by 117 · see citing works
Self-citation
Integration of environmental and host-derived signals with quorum sensing during plant-microbe interactions
Newton, J. A., & Fray, R. G. (2004) · Cellular Microbiology · doi:10.1111/j.1462-5822.2004.00362.x · Cited by 116 · see citing works
Systemic induction of phytoalexins in cucumber in response to treatments with fluorescent pseudomonads
Ongena, M., Daayf, F., Jacques, P., et al. (2000) · Plant Pathology · doi:10.1046/j.1365-3059.2000.00468.x · Cited by 106 · see citing works
Increased Uptake of Putrescine in the Rhizosphere Inhibits Competitive Root Colonization by Pseudomonas fluorescens Strain WCS365
Kuiper, I., Bloemberg, G. V., Noreen, S., et al. (2001) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2001.14.9.1096 · Cited by 103 · see citing works
The gene for albicidin detoxification from Pantoea dispersa encodes an esterase and attenuates pathogenicity of Xanthomonas albilineans to sugarcane
Zhang, L., & Birch, R. G. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.18.9984 · Cited by 102 · see citing works
Signaling between bacterial and fungal biocontrol agents in a strain mixture
Lutz, M. P., Wenger, S., Maurhofer, M., et al. (2004) · FEMS Microbiology Ecology · doi:10.1016/j.femsec.2004.03.002 · Cited by 101 · see citing works
Root colonization by indigenous and introduced microorganisms
Parke, J. L. (1991) · Springer eBooks · doi:10.1007/978-94-011-3336-4_4 · Cited by 100 · see citing works
Induction of Differential Host Responses byPseudomonas fluorescensin Ri T DNA Transformed Pea Roots After Challenge withFusarium oxysporumf. sp.pisiandPythium ultimum
Benhamou, N. (1996) · Phytopathology · doi:10.1094/phyto-86-1174 · Cited by 100 · see citing works
Contribution of the Global Regulator Gene gacA to Persistence and Dissemination of Pseudomonas fluorescens Biocontrol Strain CHA0 Introduced into Soil Microcosms
Natsch, A., Keel, C., Pfirter, H. A., et al. (1994) · Applied and Environmental Microbiology · doi:10.1128/aem.60.7.2553-2560.1994 · Cited by 95 · see citing works
Influence of In Situ and In Vitro pH on Suppression ofGaeumannomyces graminisvar.triticibyPseudomonas fluorescens2-79
Ownley, B. H. (1992) · Phytopathology · doi:10.1094/phyto-82-178 · Cited by 95 · see citing works
Enhancement of verticillium wilt resistance in tomato transplants by in vitro co-culture of seedlings with a plant growth promoting rhizobacterium (Pseudomonas sp. strain PsJN)
Sharma, V. K., & Nowak, J. (1998) · Canadian Journal of Microbiology · doi:10.1139/w98-017 · Cited by 95 · see citing works
Self-citation
Culture conditions that influence accumulation of zwittermicin A by Bacillus cereus UW85
Milner, J. L., Raffel, S. J., Lethbridge, B. J., et al. (1995) · Applied Microbiology and Biotechnology · doi:10.1007/bf00164774 · Cited by 94 · see citing works
Transformation of Pseudomonas fluorescens with genes for biosynthesis of phenazine-1-carboxylic acid improves biocontrol of rhizoctonia root rot and in situ antibiotic production
Huang, Z., Bonsall, R. F., Mavrodi, D. V., et al. (2004) · FEMS Microbiology Ecology · doi:10.1016/j.femsec.2004.03.010 · Cited by 94 · see citing works
Cytological observations of cucumber plants during induced resistance elicited by rhizobacteria
Jeun, Y. C., Park, K. S., Kim, C. H., et al. (2003) · Biological Control · doi:10.1016/s1049-9644(03)00082-3 · Cited by 94 · see citing works
Chromosomal Insertion of Phenazine-1-Carboxylic Acid Biosynthetic Pathway Enhances Efficacy of Damping-off Disease Control by Pseudomonas fluorescens
Timms‐Wilson, T. M., Ellis, R. J., Renwick, A., et al. (2000) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2000.13.12.1293 · Cited by 93 · see citing works
Root Exudate-Induced Promoter Activity in Pseudomonas fluorescens Mutants in the Wheat Rhizosphere
van Overbeek, L. S., & van Elsas, J. D. (1995) · Applied and Environmental Microbiology · doi:10.1128/aem.61.3.890-898.1995 · 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
Signal transduction in plant-beneficial rhizobacteria with biocontrol properties
Haas, D., Keel, C., & Reimmann, C. (2002) · Antonie van Leeuwenhoek · doi:10.1023/a:1020549019981 · Cited by 87 · see citing works
Antibacterial activity of 2,4-diacetylphloroglucinol produced by Pseudomonas sp. AMSN isolated from a marine alga, against vancomycin-resistant Staphylococcus aureus
Isnansetyo, A. (2003) · International Journal of Antimicrobial Agents · doi:10.1016/s0924-8579(03)00155-9 · Cited by 79 · see citing works
A gnotobiotic bioassay for studying interactions between potatoes and plant growth-promoting rhizobacteria
Conn, K. L., Lazarovits, G., & Nowak, J. (1997) · Canadian Journal of Microbiology · doi:10.1139/m97-117 · Cited by 77 · see citing works
Self-citation
Detoxification of Fusaric Acid by a Fusaric Acid-Resistant Mutant ofPseudomonas solanacearumand its Application to Biological Control of Fusarium Wilt of Tomato
Toyoda, H. (1988) · Phytopathology · doi:10.1094/phyto-78-1307 · Cited by 77 · see citing works
Biocontrol Traits of Pseudomonas spp. Are Regulated by Phase Variation
van den Broek, D., Chin‐A‐Woeng, T. F. C., Eijkemans, K., et al. (2003) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2003.16.11.1003 · Cited by 75 · see citing works
Exploitation of genetically modified inoculants for industrial ecology applications
Morrissey, J. P., Walsh, U. F., O'Donnell, A., Moënne‐Loccoz, Y., & O’Gara, F. (2002) · Antonie van Leeuwenhoek · doi:10.1023/a:1020522025374 · Cited by 74 · see citing works
Colonization of Arabidopsis roots by Pseudomonas fluorescens primes the plant to produce higher levels of ethylene upon pathogen infection
Hase, S., van Pelt, J. A., van Loon, L. C., et al. (2003) · Physiological and Molecular Plant Pathology · doi:10.1016/s0885-5765(03)00059-6 · Cited by 74 · see citing works
Isolation, identification, and antifungal activity of a macrolide antibiotic, oligomycin A, produced by Streptomyces libani
Kim, B. S., Moon, S., & Hwang, B. K. (1999) · Canadian Journal of Botany · doi:10.1139/b99-044 · Cited by 72 · see citing works
Comparison of strains of Lysobacter enzymogenes and PGPR for induction of resistance against Bipolaris sorokiniana in tall fescue
Kilic-Ekici, O., & Yuen, G. Y. (2004) · Biological Control · doi:10.1016/j.biocontrol.2004.01.014 · Cited by 68 · see citing works
Pseudomonas spp. with Mutational Changes in the O-Antigenic Side Chain of their Lipopolysaccharide are Affected in their Ability to Colonize Potato Roots
de Weger, L. A., Bakker, P. A. H. M., Schippers, B., et al. (1989) · NATO ASI series. Series H. Cell biology · doi:10.1007/978-3-642-74158-6_23 · Cited by 65 · see citing works
Pyrrolnitrin and related pyrroles endowed with antibacterial activities against Mycobacterium tuberculosis
Santo, R. D., Costi, R., Artico, M., et al. (1998) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/s0960-894x(98)00526-5 · Cited by 59 · see citing works
Structure elucidation of xanthobaccin A, a new antibiotic produced from Stenotrophomonas sp. strain SB-K88
Hashidoko, Y., Nakayama, T., Homma, Y., et al. (1999) · Tetrahedron Letters · doi:10.1016/s0040-4039(99)00336-6 · Cited by 58 · see citing works
The role of motility in the in vitro attachment of Pseudomonas putida PaW8 to wheat roots
Turnbull, G. A., Morgan, J. A. W., Whipps, J. M., et al. (2001) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2001.tb00788.x · Cited by 56 · see citing works
Negative Cross-Communication among Wheat Rhizosphere Bacteria: Effect on Antibiotic Production by the Biological Control Bacterium Pseudomonas aureofaciens 30-84
Morello, J. E., Pierson, E. A., & Pierson, L. S. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.5.3103-3109.2004 · Cited by 56 · see citing works
Siderophores, the iron nutrition of plants, and nitrate reductase
Castignetti, D., & Smarrelli, J. (1986) · FEBS Letters · doi:10.1016/0014-5793(86)81100-0 · Cited by 54 · see citing works
Timing Pseudomonas chlororaphis applications to control Pythium aphanidermatum, Pythium dissotocum, and root rot in hydroponic peppers
Chatterton, S., Sutton, J. C., & Boland, G. J. (2003) · Biological Control · doi:10.1016/j.biocontrol.2003.11.001 · Cited by 52 · see citing works
Cloning and characterization of an albicidin resistance gene from Klebsiella oxytoca
Walker, M. J., Birch, R. G., & Pemberton, J. (1988) · Molecular Microbiology · doi:10.1111/j.1365-2958.1988.tb00050.x · Cited by 51 · see citing works
Cloning of a phenazine biosynthetic locus of Pseudomonas aureofaciens PGS12 and analysis of its expression in vitro with the ice nucleation reporter gene
Georgakopoulos, D. G., Hendson, M., Panopoulos, N. J., et al. (1994) · Applied and Environmental Microbiology · doi:10.1128/aem.60.8.2931-2938.1994 · Cited by 48 · see citing works
2,4‐Diacetylphloroglucinol, a promising compound in biocontrol
Défago, G. (1993) · Plant Pathology · doi:10.1111/j.1365-3059.1993.tb01506.x · Cited by 47 · see citing works
Biocontrol of sugar cane leaf scald disease by an isolate of Pantoea dispersa which detoxifies albicidin phytotoxins
Zhang, L., & Birch, R. G. (1996) · Letters in Applied Microbiology · doi:10.1111/j.1472-765x.1996.tb01126.x · Cited by 45 · see citing works
Rhizosphere colonization of hexaploid wheat by Pseudomonas fluorescens strains Q8r1-96 and Q2-87 is cultivar-variable and associated with changes in gross root morphology
Okubara, P. A., Kornoely, J. P., & Landa, B. B. (2004) · Biological Control · doi:10.1016/j.biocontrol.2003.11.003 · Cited by 43 · see citing works
A gene from Alcaligenes denitrificans that confers albicidin resistance by reversible antibiotic binding
Basnayake, W. V. S., & Birch, R. G. (1995) · Microbiology · doi:10.1099/13500872-141-3-551 · Cited by 40 · see citing works
Cloning and characterisation of the rpoS gene from plant growth-promoting Pseudomonas putida WCS358: RpoS is not involved in siderophore and homoserine lactone production
Kojić, M., Degrassi, G., & Venturi, V. (1999) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/s0167-4781(99)00210-9 · Cited by 38 · see citing works
Production of a Mixed Inoculum ofFusarium oxysporumFo47 andPseudomonas fluorescensC7 to Control Fusarium Diseases
Olivain, C., Alabouvette, C., & Steinberg, C. (2004) · Biocontrol Science and Technology · doi:10.1080/09583150310001655657 · Cited by 35 · see citing works
Antimicrobial activity of naturally occurring and synthetic phloroglucinols against Staphylococcus aureus
Yamaki, M., Miwa, M., Ishiguro, K., et al. (1994) · Phytotherapy Research · doi:10.1002/ptr.2650080214 · Cited by 34 · see citing works
Effects of the properties of the bacterial community on pH adaptation during recolonisation of a humus soil
Pettersson, M., & Bååth, E. (2004) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2004.02.028 · Cited by 29 · see citing works

Flagged first, then by citations

Sorted by citations

Plant growth-promoting bacteria in the rhizo- and endosphere of plants: Their role, colonization, mechanisms involved and prospects for utilization
Compant, S., Clément, C., & Sessitsch, A. (2010) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2009.11.024 · Cited by 2,318 · see citing works
Self-citation
Plant–microbe interactions promoting plant growth and health: perspectives for controlled use of microorganisms in agriculture
Berg, G. (2009) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-009-2092-7 · Cited by 1,648 · see citing works
Exploiting plant–microbe partnerships to improve biomass production and remediation
Weyens, N., van der Lelie, D., Taghavi, S., Newman, L., & Vangronsveld, J. (2009) · Trends in Biotechnology · doi:10.1016/j.tibtech.2009.07.006 · Cited by 592 · see citing works
Bacillus velezensis: A Valuable Member of Bioactive Molecules within Plant Microbiomes
Rabbee, M. F., Ali, M. S., Choi, J., Hwang, B. S., Jeong, S. C., & Baek, K.-H. (2019) · Molecules · doi:10.3390/molecules24061046 · Cited by 550 · see citing works
Understanding and enhancing soil biological health: the solution for reversing soil degradation
Lehman, R., Cambardella, C., Stott, D., Acosta-Martinez, V., Manter, D., Buyer, J., Maul, J., Smith, J., Collins, H., Halvorson, J., et al. (2015) · Sustainability · doi:10.3390/su7010988 · Cited by 449 · see citing works
Plant growth-promoting rhizobacteria modulate root-system architecture in Arabidopsis thaliana through volatile organic compound emission
Gutiérrez-Luna, F. M., López-Bucio, J., Altamirano-Hernández, J., Valencia-Cantero, E., de la Cruz, H. R., & Macías-Rodríguez, L. (2010) · Symbiosis · doi:10.1007/s13199-010-0066-2 · Cited by 246 · see citing works
How effective are ‘Effective microorganisms® (EM)’? Results from a field study in temperate climate
Mayer, J., Scheid, S., Widmer, F., Fließbach, A., & Oberholzer, H.-R. (2010) · Applied Soil Ecology · doi:10.1016/j.apsoil.2010.08.007 · Cited by 161 · 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

Plant Beneficial Bacteria
Davison, J. (1988) · Nature Biotechnology · doi:10.1038/nbt0388-282 · Cited by 276 · see citing works
Plant Growth-Promoting Bacterial Consortia Render Biological Control of Plant Pathogens: A Review
Pellegrini, M., Djebaili, R., Pagnani, G., et al. (2023) · Microorganisms for sustainability · doi:10.1007/978-981-19-9570-5_4 · Cited by 7 · see citing works
Association of L-form Bacteria with Plants and their Application in Biological Control of Phytopathogenic Fungi and Bacteria: A Review
Daulagala, P. W. H. K. P. (2021) · Journal of Advances in Microbiology · doi:10.9734/jamb/2021/v21i1030395 · Cited by 5 · see citing works
Advances in Engineering of Trichoderma for Improvement of Adaption to Adverse Environment and Efficiency of Biological Control Against Plant Pathogen
Chen, Y., Ting-heng, Z., Wang, K., et al. (2012) · Zhongguo shengwu gongcheng zazhi
Role of Trichoderma as a biocontrol agent (BCA) of phytoparasitic nematodes and plant growth inducer
Tariqjaveed, M., Farooq, T., Al-Hazmi, A. S., et al. (2021) · Journal of Invertebrate Pathology · doi:10.1016/j.jip.2021.107626 · Cited by 74 · see citing works

Authors: Compant, S., Duffy, B., Nowak, J., Clément, C., & Barka, E. A.
Affiliations: Laboratoire de Stress, Défenses et Reproduction des Plantes, Unité de Recherche Vignes et Vins de Champagne, UPRES EA 2069, UFR Sciences, Université de Reims Champagne-Ardenne, 51687 Reims Cedex 2, France
Agroscope (CH)
Virginia Tech (US)
Venue: Applied and Environmental Microbiology
Publisher: American Society for Microbiology
Published: 2005-09
Volume: 71
Issue: 9
Pages: 4951-4959
ISSN: 0099-2240 (ISSN-L)
1098-5336
DOI: 10.1128/aem.71.9.4951-4959.2005
PMC: PMC1214602
OpenAlex: W2135333204
Cited by: 2,640
References: 194
Citations by year: 2026: 126 · 2025: 140 · 2024: 131 · 2023: 146 · 2022: 185 · 2021: 209 · 2020: 194 · 2019: 202 · 2018: 152 · 2017: 179 · 2016: 133 · 2015: 120 · 2014: 127 · 2013: 110 · 2012: 139
FWCI: 3.84
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: journals.asm.org/non-commercial-tdm-license (tdm)
Locations: Applied and Environmental Microbiology (publishedVersion)
Europe PMC (PubMed Central) (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant-Microbe Interactions and Immunity
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Pathogenic Bacteria Studies
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Disease Management Techniques
Keywords: plant growth-promoting bacteria, biological control, plant disease, mechanism of action, plant pathogens, agrochemical dependence, crop protection
MeSH terms: Bacteria, Pest Control, Biological, Plant Diseases, Plants, Plant Development

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Use of plant growth-promoting bacteria for biocontrol of plant diseases: principles, mechanisms of action, and future prospects

Abstract

Integrity signals

Claims the paper makes

Claims other papers make about this one

Cites

Cited by

Related

Record

About these checks