Iron and Immunity

MYB transcription factors in Arabidopsis

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Trichoderma species — opportunistic, avirulent plant symbionts

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Plant-Growth-Promoting Rhizobacteria

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Induced systemic resistance by beneficial microbes

Pieterse, C. M. J., Zamioudis, C., Berendsen, R. L., Weller, D. M., Van Wees, S. C. M., & Bakker, P. A. H. M. (2014) · Annual Review of Phytopathology · doi:10.1146/annurev-phyto-082712-102340 · Cited by 3,272 · see citing works

LXXIII.—Oxidation of tartaric acid in presence of iron

Fenton, H. J. H. (1894) · J. Chem. Soc., Trans. · doi:10.1039/ct8946500899 · Cited by 3,179 · see citing works

Phenylpropanoid Biosynthesis

Vogt, T. (2009) · Molecular Plant · doi:10.1093/mp/ssp106 · Cited by 3,100 · see citing works

Hormonal Modulation of Plant Immunity

Pieterse, C. M. J., van der Does, D., Zamioudis, C., León-Reyes, A., & Wees, S. C. M. V. (2011) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-092910-154055 · Cited by 3,021 · see citing works

The catalytic decomposition of hydrogen peroxide by iron salts

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Microbial populations responsible for specific soil suppressiveness to plant pathogens.

Weller, D., Raaijmakers, J., Gardener, B. M. M., & Thomashow, L. (2002) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.40.030402.110010 · Cited by 1,800 · see citing works

Natural products and plant disease resistance

Dixon, R. A. (2001) · Nature · doi:10.1038/35081178 · Cited by 1,796 · see citing works

Siderophore-Based Iron Acquisition and Pathogen Control

Miethke, M., & Marahiel, M. A. (2007) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00012-07 · Cited by 1,774 · see citing works

Chemistry and biology of siderophores

Hider, R. C., & Kong, X. (2010) · Natural Product Reports · doi:10.1039/b906679a · Cited by 1,722 · see citing works

IRT1, an Arabidopsis Transporter Essential for Iron Uptake from the Soil and for Plant Growth

Vert, G., Grotz, N., Dédaldéchamp, F., Gaymard, F., Guerinot, M. L., Briat, J.-F., & Curie, C. (2002) · The Plant Cell · doi:10.1105/tpc.001388 · Cited by 1,679 · see citing works

A novel iron-regulated metal transporter from plants identified by functional expression in yeast.

Eide, D. J., Broderius, M. A., Fett, J. P., & Guerinot, M. L. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.11.5624 · Cited by 1,403 · see citing works

Iron Uptake, Translocation, and Regulation in Higher Plants

Kobayashi, T., & Nishizawa, N. K. (2012) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042811-105522 · Cited by 1,346 · see citing works

FERRITIN: STRUCTURE, GENE REGULATION, AND CELLULAR FUNCTION IN ANIMALS, PLANTS, AND MICROORGANISMS

Theil, E. C. (1987) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.56.070187.001445 · Cited by 1,337 · 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

A ferric-chelate reductase for iron uptake from soils

Robinson, N. J., Procter, C. M., Connolly, E. L., & Guerinot, M. L. (1999) · Nature · doi:10.1038/17800 · Cited by 1,271 · see citing works

Iron in infection and immunity

Cassat, J. E., & Skaar, E. P. (2013) · Cell Host & Microbe · doi:10.1016/j.chom.2013.04.010 · Cited by 1,214 · 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

Salicylic acid modulates colonization of the root microbiome by specific bacterial taxa

Lebeis, S. L., Paredes, S. H., Lundberg, D. S., Breakfield, N. W., Gehring, J., McDonald, M., Malfatti, S., del Rio, T. G., Jones, C. D., Tringe, S. G., et al. (2015) · Science · doi:10.1126/science.aaa8764 · Cited by 1,205 · see citing works

Root-Secreted Malic Acid Recruits Beneficial Soil Bacteria

Rudrappa, T., Czymmek, K. J., Paré, P. W., & Bais, H. P. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.127613 · Cited by 1,147 · see citing works

Siderophores in environmental research: roles and applications

Ahmed, E., & Holmström, S. (2014) · Microbial Biotechnology · doi:10.1111/1751-7915.12117 · Cited by 1,103 · see citing works

Maize yellow stripe1 encodes a membrane protein directly involved in Fe(III) uptake

Curie, C., Panaviene, Z., Loulergue, C., Dellaporta, S. L., Briat, J., & Walker, E. L. (2001) · Nature · doi:10.1038/35053080 · Cited by 1,033 · see citing works

MYB Transcription Factors as Regulators of Phenylpropanoid Metabolism in Plants

Liu, J., Osbourn, A., & Ma, P. (2015) · Molecular Plant · doi:10.1016/j.molp.2015.03.012 · Cited by 960 · see citing works

Iron homeostasis in host defence and inflammation

Ganz, T., & Nemeth, E. (2015) · Nature Reviews Immunology · doi:10.1038/nri3863 · Cited by 843 · see citing works

Iron: Nutritious, Noxious, and Not Readily Available

Guerinot, M. L., & Yi, Y. (1994) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.3.815 · Cited by 818 · see citing works

Opening the Iron Box: Transcriptional Metalloregulation by the Fur Protein

Escolar, L., Pérez-Martín, J., & de Lorenzo, V. (1999) · Journal of Bacteriology · doi:10.1128/jb.181.20.6223-6229.1999 · Cited by 815 · see citing works

The Battle for Iron between Bacterial Pathogens and Their Vertebrate Hosts

Skaar, E. P. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000949 · Cited by 796 · see citing works

The Essential Basic Helix-Loop-Helix Protein FIT1 Is Required for the Iron Deficiency Response

Colangelo, E. P., & Guerinot, M. L. (2004) · The Plant Cell · doi:10.1105/tpc.104.024315 · Cited by 791 · see citing works

Recognizing Plant Defense Priming

Martínez‐Medina, A., Flors, V., Heil, M., et al. (2016) · Trends in Plant Science · doi:10.1016/j.tplants.2016.07.009 · Cited by 759 · see citing works

Cell Identity Mediates the Response of Arabidopsis Roots to Abiotic Stress

Dinneny, J. R., Long, T. A., Wang, J. Y., Jung, J. W., Mace, D., Pointer, S., Barron, C., Brady, S. M., Schiefelbein, J., & Benfey, P. N. (2008) · Science · doi:10.1126/science.1153795 · Cited by 746 · see citing works

Iron uptake, translocation, and regulation in higher plants

Wang, Z., Sun, Y., Li, J., Shangguan, Y., Liu, Z., & Xuwu, S. (2017) · DOAJ (DOAJ: Directory of Open Access Journals) · doi:10.3969/j.issn.1000-5137.2017.05.018 · Cited by 724 · see citing works

Interactions of Deleterious and Beneficial Rhizosphere Microorganisms and the Effect of Cropping Practices

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Oxalate production by fungi: its role in pathogenicity and ecology in the soil environment

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Plant root-microbe communication in shaping root microbiomes

Lareen, A., Burton, F., & Schäfer, P. (2016) · Plant Molecular Biology · doi:10.1007/s11103-015-0417-8 · Cited by 664 · see citing works

Root Endophyte Colletotrichum tofieldiae Confers Plant Fitness Benefits that Are Phosphate Status Dependent

Hiruma, K., Gerlach, N., Sacristán, S., Nakano, R. T., Hacquard, S., Kracher, B., Neumann, U., Ramírez, D., Bucher, M., O’Connell, R. J., et al. (2016) · Cell · doi:10.1016/j.cell.2016.02.028 · Cited by 652 · see citing works

Facing the challenges of Cu, Fe and Zn homeostasis in plants

Palmer, C. M., & Guerinot, M. L. (2009) · Nature Chemical Biology · doi:10.1038/nchembio.166 · Cited by 633 · see citing works

Mobilization of vacuolar iron by AtNRAMP3 and AtNRAMP4 is essential for seed germination on low iron

Lanquar, V., Lelièvre, F., Bolte, S., Hamès, C., Alcon, C., Neumann, D., Vansuyt, G., Curie, C., Schröder, A., Krämer, U., et al. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600864 · Cited by 631 · see citing works

FIT interacts with AtbHLH38 and AtbHLH39 in regulating iron uptake gene expression for iron homeostasis in Arabidopsis

Yuan, Y., Wu, H., Wang, N., Li, J., Zhao, W., Du, J., Wang, D., & Ling, H. (2008) · Cell Research · doi:10.1038/cr.2008.26 · Cited by 609 · see citing works

Dissecting iron deficiency‐induced proton extrusion in Arabidopsis roots

Santi, S., & Schmidt, W. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2009.02908.x · Cited by 609 · see citing works

Root exudation of sugars, amino acids, and organic acids by maize as affected by nitrogen, phosphorus, potassium, and iron deficiency

Carvalhais, L. C., Dennis, P. G., Fedoseyenko, D., Hajirezaei, M., Borriss, R., & Nicolaus Von Wirén, A. (2010) · Journal of Plant Nutrition and Soil Science · doi:10.1002/jpln.201000085 · Cited by 604 · see citing works

The bHLH Transcription Factor POPEYE Regulates Response to Iron Deficiency in Arabidopsis Roots

Long, T. A., Tsukagoshi, H., Busch, W., Lahner, B., Salt, D. E., & Benfey, P. N. (2010) · The Plant Cell · doi:10.1105/tpc.110.074096 · Cited by 599 · see citing works

Siderophore-mediated signaling regulates virulence factor production in <i>Pseudomonas</i> <i>aeruginosa</i>

Lamont, I. L., Beare, P. A., Ochsner, U., Vasil, A. I., & Vasil, M. L. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.092016999 · Cited by 584 · see citing works

Pseudomonas siderophores: A mechanism explaining disease-suppressive soils

Kloepper, J. W., Leong, J. M., Teintze, M., et al. (1980) · Current Microbiology · doi:10.1007/bf02602840 · Cited by 574 · see citing works

Rhizosphere Microbial Community Structure in Relation to Root Location and Plant Iron Nutritional Status

Yang, C., & Crowley, D. E. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.1.345-351.2000 · Cited by 573 · see citing works

Phytosiderophore Efflux Transporters Are Crucial for Iron Acquisition in Graminaceous Plants

Nozoye, T., Nagasaka, S., Kobayashi, T., Takahashi, M., Sato, Y., Sato, Y., Uozumi, N., Nakanishi, H., & Nishizawa, N. K. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.180026 · Cited by 563 · see citing works

Rice OsYSL15 Is an Iron-regulated Iron(III)-Deoxymugineic Acid Transporter Expressed in the Roots and Is Essential for Iron Uptake in Early Growth of the Seedlings

Inoue, H., Kobayashi, T., Nozoye, T., Takahashi, M., Kakei, Y., Suzuki, K., Nakazono, M., Nakanishi, H., Mori, S., & Nishizawa, N. K. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m806042200 · Cited by 560 · 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

Involvement of NRAMP1 from Arabidopsis thaliana in iron transport

Curie, C., Alonso, J. M., Jean, M. L., Ecker, J. R., & Briat, J. (2000) · Biochemical Journal · doi:10.1042/bj3470749 · Cited by 552 · see citing works

β-Glucosidases as detonators of plant chemical defense

Morant, A. V., Jørgensen, K., Jørgensen, C., Paquette, S. M., Sánchez‐Pérez, R., Møller, B. L., & Bak, S. (2008) · Phytochemistry · doi:10.1016/j.phytochem.2008.03.006 · Cited by 550 · see citing works

Transcriptional regulation by Ferric Uptake Regulator (Fur) in pathogenic bacteria

Troxell, B., & Hassan, H. M. (2013) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2013.00059 · Cited by 500 · see citing works

Monoubiquitin-dependent endocytosis of the IRON-REGULATED TRANSPORTER 1 (IRT1) transporter controls iron uptake in plants

Barberon, M., Zelazny, E., Robert, S., Conéjéro, G., Curie, C., Friml, J., & Vert, G. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1100659108 · Cited by 469 · see citing works

Associations with rhizosphere bacteria can confer an adaptive advantage to plants

Haney, C. H., Samuel, B. S., Bush, J., & Ausubel, F. M. (2015) · Nature Plants · doi:10.1038/nplants.2015.51 · Cited by 462 · see citing works

Siderophores in Fungal Physiology and Virulence

Haas, H., Eisendle, M., & Turgeon, B. G. (2008) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.45.062806.094338 · Cited by 451 · see citing works

Overexpression of the FRO2 Ferric Chelate Reductase Confers Tolerance to Growth on Low Iron and Uncovers Posttranscriptional Control

Connolly, E. L., Campbell, N. H., Grotz, N., Prichard, C. L., & Guerinot, M. L. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.025122 · Cited by 451 · see citing works

Jasmonate signaling in plant interactions with resistance-inducing beneficial microbes

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Iron uptake and metabolism in pseudomonads

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Mechanisms and regulation of reduction‐based iron uptake in plants

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Current ReviewSiderophores in Microbial Interactions on Plant Surfaces

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Beneficial Microbes Affect Endogenous Mechanisms Controlling Root Development

Verbon, E. H., & Liberman, L. M. (2016) · Trends in Plant Science · doi:10.1016/j.tplants.2016.01.013 · Cited by 391 · see citing works

Different strategies for iron acquisition in higher plants

Römheld, V. (1987) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1987.tb06137.x · Cited by 380 · see citing works

Fungal invasion of the rhizosphere microbiome

Chapelle, E., Mendes, R., Bakker, P. A. H. M., & Raaijmakers, J. M. (2016) · The ISME Journal · doi:10.1038/ismej.2015.82 · Cited by 378 · see citing works

Involvement of the ABCG 37 transporter in secretion of scopoletin and derivatives by Arabidopsis roots in response to iron deficiency

Fourcroy, P., Sisó‐Terraza, P., Sudre, D., Savirón, M., Reyt, G., Gaymard, F., Abadı́a, A., Abadı́a, J., Álvarez‐Fernández, A., & Briat, J. (2013) · New Phytologist · doi:10.1111/nph.12471 · Cited by 378 · see citing works

A soil bacterium regulates plant acquisition of iron via deficiency‐inducible mechanisms

Zhang, H., Sun, Y., Xie, X., Kim, M., Dowd, S. E., & Paré, P. W. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03803.x · Cited by 371 · see citing works

Arabidopsis Yellow Stripe‐Like2 (YSL2) : a metal‐regulated gene encoding a plasma membrane transporter of nicotianamine–metal complexes

DiDonato, R. J., Roberts, L. A., Sanderson, T., Eisley, R. B., & Walker, E. L. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02128.x · Cited by 369 · see citing works

Requirement and Functional Redundancy of Ib Subgroup bHLH Proteins for Iron Deficiency Responses and Uptake in Arabidopsis thaliana

Wang, N., Cui, Y., Liu, Y., Fan, H., Du, J., Huang, Z.-A., Yuan, Y., Wu, H., & Ling, H. (2012) · Molecular Plant · doi:10.1093/mp/sss089 · Cited by 355 · see citing works

NPS6, Encoding a Nonribosomal Peptide Synthetase Involved in Siderophore-Mediated Iron Metabolism, Is a Conserved Virulence Determinant of Plant Pathogenic Ascomycetes

Oide, S., Moeder, W., Krasnoff, S. B., Gibson, D. M., Haas, H., Yoshioka, K., & Turgeon, B. G. (2006) · The Plant Cell · doi:10.1105/tpc.106.045633 · Cited by 350 · see citing works

FRU (BHLH029) is required for induction of iron mobilization genes in Arabidopsis thaliana

Jakoby, M. J., Wang, H.-Y., Reidt, W., Weißhaar, B., & Bauer, P. (2004) · FEBS Letters · doi:10.1016/j.febslet.2004.10.062 · Cited by 349 · see citing works

Unraveling Root Developmental Programs Initiated by Beneficial Pseudomonas spp. Bacteria

Zamioudis, C., Mastranesti, P., Dhonukshe, P., Blilou, I., & Pieterse, C. M. J. (2013) · PLANT PHYSIOLOGY · doi:10.1104/pp.112.212597 · Cited by 347 · 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

Feruloyl-CoA 6'-Hydroxylase1-Dependent Coumarins Mediate Iron Acquisition from Alkaline Substrates in Arabidopsis

Schmid, N. B., Giehl, R. F. H., Doll, S., Mock, H.-P., Strehmel, N., Scheel, D., Kong, X., Hider, R. C., & von Wiren, N. (2014) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.228544 · Cited by 334 · see citing works

MYB72 Is Required in Early Signaling Steps of Rhizobacteria-Induced Systemic Resistance in Arabidopsis

der Ent, S. V., Verhagen, B. W. M., Doorn, R. V., Bakker, D., Verlaan, M. G., Pel, M. J. C., Joosten, R. G., Proveniers, M. C. G., van Loon, L. C., Ton, J., et al. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.113829 · Cited by 324 · see citing works

New insights into ferritin synthesis and function highlight a link between iron homeostasis and oxidative stress in plants

Briat, J., Ravet, K., Arnaud, N., Duc, C., Boucherez, J., Touraine, B., Cellier, F., & Gaymard, F. (2009) · Annals of Botany · doi:10.1093/aob/mcp128 · Cited by 314 · see citing works

MYB72, a node of convergence in induced systemic resistance triggered by a fungal and a bacterial beneficial microbe

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Time to pump iron: iron-deficiency-signaling mechanisms of higher plants

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Iron Availability Affects Induction of Systemic Resistance to Fusarium Wilt of Radish byPseudomonas fluorescens

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Bacterial siderophores efficiently provide iron to iron-starved tomato plants in hydroponics culture

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Transcription factor MYC2 is involved in priming for enhanced defense during rhizobacteria‐induced systemic resistance in Arabidopsis thaliana

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Association of Piriformospora indica with Arabidopsis thaliana roots represents a novel system to study beneficial plant–microbe interactions and involves early plant protein modifications in the endoplasmic reticulum and at the plasma membrane

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Metabolic and Transcriptomic Changes Induced in Arabidopsis by the Rhizobacterium Pseudomonas fluorescens SS101

van de Mortel, J. E., de Vos, R. C. H., Dekkers, E., Pineda, A., Guillod, L., Bouwmeester, K., van Loon, J. J. A., Dicke, M., & Raaijmakers, J. M. (2012) · PLANT PHYSIOLOGY · doi:10.1104/pp.112.207324 · Cited by 290 · see citing works

The Analysis of Arabidopsis Nicotianamine Synthase Mutants Reveals Functions for Nicotianamine in Seed Iron Loading and Iron Deficiency Responses

Klatte, M., Schuler, M., Wirtz, M., Fink‐Straube, C., Hell, R., & Bauer, P. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.136374 · Cited by 285 · see citing works

Dual Regulation of the Arabidopsis High-Affinity Root Iron Uptake System by Local and Long-Distance Signals

Vert, G., Briat, J., & Curie, C. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.102.016089 · Cited by 283 · see citing works

Iron-Binding E3 Ligase Mediates Iron Response in Plants by Targeting Basic Helix-Loop-Helix Transcription Factors

Selote, D. S., Samira, R., Matthiadis, A., Gillikin, J. W., & Long, T. A. (2014) · PLANT PHYSIOLOGY · doi:10.1104/pp.114.250837 · Cited by 279 · see citing works

Survival trade-offs in plant roots during colonization by closely related beneficial and pathogenic fungi

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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

AtbHLH29 of Arabidopsis thaliana is a functional ortholog of tomato FER involved in controlling iron acquisition in strategy I plants

You Xi, Y. U. A. N., ZHANG, J., Dao Wen, W. A. N. G., & Ling, H. (2005) · Cell Research · doi:10.1038/sj.cr.7290331 · Cited by 269 · see citing works

Iron-withholding strategy in innate immunity

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Ethylene and nitric oxide involvement in the up-regulation of key genes related to iron acquisition and homeostasis in Arabidopsis

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Iron Acquisition from Fe-Pyoverdine by Arabidopsis thaliana

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Fitting into the Harsh Reality: Regulation of Iron-deficiency Responses in Dicotyledonous Plants

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