Bacterial siderophores in community and host interactions

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Biofilms: an emergent form of bacterial life

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Induced systemic resistance by beneficial microbes

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Bacterial iron homeostasis

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Siderophore-Based Iron Acquisition and Pathogen Control

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The non-ribosomal peptide synthetase-independent siderophore (NIS) rhizobactin produced by Caballeronia mineralivorans PML1(12) confers the ability to weather minerals

Nouche, C. B., Paris, C., Dhalleine, T., Oger, P., Turpault, M., & Uroz, S. (2023) · Applied and Environmental Microbiology · doi:10.1128/aem.00453-23 · Cited by 17

The diversity and utility of arylthiazoline and aryloxazoline siderophores: Challenges of coordination chemistry, biological activity and selected applications

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Plant‐derived virulence arresting drugs as novel antimicrobial agents: Discovery, perspective, and challenges in clinical use

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Distinctive species interaction patterns under high nitrite stress shape inefficient denitrifying phosphorus removal performance

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A New Biocontrol Agent Bacillus velezensis SF334 against Rubber Tree Fungal Leaf Anthracnose and Its Genome Analysis of Versatile Plant Probiotic Traits

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Microbial iron limitation in the ocean’s twilight zone

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GNPS‐Guided Discovery of Madurastatin Siderophores from the Termite‐Associated Actinomadura sp. RB99**

Lee, S. R., Schalk, F., Schwitalla, J. W., Guo, H., Yu, J. S., Song, M., Jung, W. H., de Beer, Z. W., Beemelmanns, C., & Kim, K. H. (2022) · Chemistry - A European Journal · doi:10.1002/chem.202200612 · Cited by 17

Rhizosphere microbes facilitate the break of chlamydospore dormancy and root colonization of rice false smut fungi

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Avian Pathogenic Escherichia coli: Advances in Pathogenesis, Diagnosis, and Control

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Organic complexation of iron by strong ligands and siderophores in the eastern tropical North Pacific oxygen deficient zone

Moore, L. E., Heller, M. I., Barbeau, K. A., Moffett, J. W., & Bundy, R. M. (2021) · Marine Chemistry · doi:10.1016/j.marchem.2021.104021 · Cited by 17

Genetic variation is associated with differences in facilitative and competitive interactions in the Rhizobium leguminosarum species complex

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Thermophilic bacteria from Peruvian hot springs with high potential application in environmental biotechnology

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Host subversion of bacterial metallophore usage drives copper intoxication

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Siderophores and competition for iron govern myxobacterial predation dynamics

Contreras-Moreno, F. J., Moraleda‐Muñoz, A., Marcos‐Torres, F. J., Cuéllar, V., Soto, M. J., Pérez, J., & Muñoz‐Dorado, J. (2024) · The ISME Journal · doi:10.1093/ismejo/wrae077 · Cited by 16

Elucidation of Chalkophomycin Biosynthesis Reveals N-Hydroxypyrrole-Forming Enzymes

Crooke, A. M., Chand, A. K., Cui, Z., & Balskus, E. P. (2024) · Journal of the American Chemical Society · doi:10.1021/jacs.4c04712 · Cited by 17

Exploring the Potential of Purple Non-Sulfur Bacteria Strains A3-5 and F3-3 in Sustainable Agriculture: A Study on Nutrient Solubilization, Plant Growth Promotion, and Acidic Stress Tolerance

Wu, J., Chen, H.-W., Sundar, L. S., Tu, Y.-K., & Chao, Y.-Y. (2025) · Journal of soil science and plant nutrition · doi:10.1007/s42729-025-02268-4 · Cited by 16

Beyond tug-of-war: Iron metabolism in cooperative host–microbe interactions

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Recent developments in plant growth-promoting rhizobacteria (PGPR) for sustainable agriculture

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Natural combinatorial genetics and prolific polyamine production enable siderophore diversification in Serratia plymuthica

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Evolution of cooperation in costly institutions exhibits Red Queen and Black Queen dynamics in heterogeneous public goods

Salahshour, M. (2021) · Communications Biology · doi:10.1038/s42003-021-02865-w · Cited by 16

A Salvaging Strategy Enables Stable Metabolite Provisioning among Free-Living Bacteria

Gude, S., Pherribo, G. J., & Taga, M. E. (2022) · mSystems · doi:10.1128/msystems.00288-22 · Cited by 16

Fostering climate-resilient agriculture with ACC-deaminase producing rhizobacterial biostimulants from the cold deserts of the Indian Himalayas

Gulati, A., Thakur, R., Vyas, P., Sharma, A., Dhar, H., Pal, M., Thakur, N., Kaushal, K., Chawla, A., Sharma, K. C., et al. (2024) · Journal of Environmental Management · doi:10.1016/j.jenvman.2024.123075 · Cited by 15

The diversity and utility of arylthiazoline and aryloxazoline siderophores: challenges of total synthesis

Kamińska, K., Mular, A., Olshvang, E., Metzler‐Nolte, N., Kozłowski, H., Wojaczyńska, E., & Gumienna‐Kontecka, E. (2022) · RSC Advances · doi:10.1039/d2ra03841b · Cited by 15

Catechol siderophores framed on 2,3-dihydroxybenzoyl-L-serine from Streptomyces varsoviensis

Liu, Z., Huang, T., Shi, Q., Deng, Z., & Lin, S. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1182449 · Cited by 15

Siderophore-producingBacillus amyloliquefaciensBM3 mitigate arsenic contamination and suppressFusariumwilt in brinjal plants

Pradhan, S., Choudhury, A., Dey, S., Hossain, M. F., Saha, A., & Saha, D. (2023) · Journal of Applied Microbiology · doi:10.1093/jambio/lxad217 · Cited by 15

Antifungal mechanism of volatile compounds emitted by Actinomycetota Paenarthrobacter ureafaciens from a disease-suppressive soil on Saccharomyces cerevisiae

Nguyen, T.-P., Meng, D.-R., Chang, C., Su, P., Ou, C.-A., Hou, P.-F., Sung, H., Chou, C., Ohme‐Takagi, M., & Huang, H.-J. (2023) · mSphere · doi:10.1128/msphere.00324-23 · Cited by 15

Taxonomic distribution of metabolic functions in bacteria associated with Trichodesmium consortia

Koedooder, C., Zhang, F., Wang, S., Basu, S., Haley, S. T., Tolić, N., Nicora, C., del Rio, T. G., Dyhrman, S. T., Gledhill, M., et al. (2023) · mSystems · doi:10.1128/msystems.00742-23 · Cited by 15

Multifaceted regulation of siderophore synthesis by multiple regulatory systems in Shewanella oneidensis

Xie, P., Xu, Y., Tang, J., Wu, S., & Gao, H. (2024) · Communications Biology · doi:10.1038/s42003-024-06193-7 · Cited by 16

New Insights into the Organic Complexation of Bioactive Trace Metals in the Global Ocean from the GEOTRACES Era

Whitby, H., Park, J., Shaked, Y., Boiteau, R. M., Buck, K. N., & Bundy, R. M. (2024) · Oceanography · doi:10.5670/oceanog.2024.419 · Cited by 15

Parallel ecological and evolutionary responses to selection in a natural bacterial community

Hesse, E., Luján, A. M., O’Brien, S., Newbury, A., McAvoy, T., Pascual, J. S., Bayer, F., Hodgson, D. J., & Buckling, A. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2403577121 · Cited by 15

Significance of zinc-solubilizing plant growth-promoting rhizobacterial strains in nutrient acquisition, enhancement of growth, yield, and oil content of canola (Brassica napus L.)

Jalaluddin, S., Elahi, N. N., & Mubeen, F. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1446064 · Cited by 16

Targeting Siderophore Biosynthesis to Thwart Microbial Growth

da Rocha, B. M., Pinto, E., Sousa, E., & Resende, D. I. S. P. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26083611 · Cited by 15

Iron acquisition system of Sphingobium sp. strain SYK-6, a degrader of lignin-derived aromatic compounds

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Saccharochelins A–H, Cytotoxic Amphiphilic Siderophores from the Rare Marine Actinomycete Saccharothrix sp. D09

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Marine macroalga-associated heterotrophic Bacillus velezensis: a novel antimicrobial agent with siderophore mode of action against drug-resistant nosocomial pathogens

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Infection metallomics for critical care in the post‐COVID era

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Weathered granites and soils harbour microbes with lanthanide-dependent methylotrophic enzymes

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Targeting the epigenetic regulation of ferroptosis: a potential therapeutic approach for sepsis-associated acute kidney injury

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Iron Modulates the Growth and Activity of Nitrate-Dependent Methanotrophic Bacteria by Reprogramming Carbon Metabolism

Yao, X., Zhang, M., Jetten, M. S. M., Zhu, L., & Hu, B. (2025) · Environmental Science & Technology · doi:10.1021/acs.est.5c01275 · Cited by 14

Viruses hijack FPN1 to disrupt iron withholding and suppress host defense

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Legionella pneumophila Rhizoferrin Promotes Bacterial Biofilm Formation and Growth within Amoebae and Macrophages

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Microbial interaction-induced siderophore dynamics lead to phenotypic differentiation of Staphylococcus aureus

Rajapitamahuni, S., Lyou, E. S., Kang, B. R., & Lee, T. K. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1277176 · Cited by 14

Spatiotemporal dynamics during niche remodeling by super-colonizing microbiota in the mammalian gut

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Evaluation of Apple Root-Associated Endophytic Streptomyces pulveraceus Strain ES16 by an OSMAC-Assisted Metabolomics Approach

Armin, R., Zühlke, S., Mahnkopp-Dirks, F., Winkelmann, T., & Kusari, S. (2021) · Frontiers in Sustainable Food Systems · doi:10.3389/fsufs.2021.643225 · Cited by 14

Seaweed-associated heterotrophic bacteria: are they future novel sources of antimicrobial agents against drug-resistant pathogens?

Asharaf, S., Chakraborty, K., & Chakraborty, R. D. (2022) · Archives of Microbiology · doi:10.1007/s00203-022-02835-8 · Cited by 14

Pseudomonas Species in Soil as a Natural Resource for Plant Growth Promotion and Biocontrol Characteristics - An Overview

Anuroopa, N., RAM, A. B., Ranadev, P., Bagyaraj, D. J., & Ashwin, R. (2021) · Madras Agricultural Journal · doi:10.29321/maj.10.000571 · Cited by 14

Bacillus velezensis SQR9: a model biofertilizer strain for beneficial plant root-rhizobacterium interaction

Sun, X., Xu, Z., Zhang, N., Liu, Y., Xun, W., Miao, Y., Shao, J., Zhang, R., & Shen, Q. (2025) · Science China Life Sciences · doi:10.1007/s11427-025-3112-x · Cited by 13

Evolution-proof inhibitors of public good cooperation: a screening strategy inspired by social evolution theory

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The Role of the Respiratory Microbiome in the Pathogenesis of Aspiration Pneumonia: Implications for Diagnosis and Potential Therapeutic Choices

Vallianou, N. G., Skourtis, A., Kounatidis, D. C., Margellou, E., Panagopoulos, F., Geladari, E. V., Evangelopoulos, A. A., & Jahaj, E. (2023) · Antibiotics · doi:10.3390/antibiotics12010140 · Cited by 13

Facilitating effects of the reductive soil disinfestation process combined with Paenibacillus sp. amendment on soil health and physiological properties of Momordica charantia

Liu, L., Xie, Y., Zhong, X., Deng, Q., Shao, Q., Cai, Z., & Huang, X. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2022.1095656 · Cited by 13

PGPR Promotes the Recovery of Submerged Macrophytes via Indigenous Microbiome Modulations under Combined Abiotic Stress

Li, Y., Liu, X., Li, Q., Guo, Y., Zhang, Y., Wang, C., Zhou, Q., & Wu, Z. (2023) · Water · doi:10.3390/w15030590 · Cited by 13

Microbiota-derived metabolites in regulating the development and physiology of Caenorhabditis elegans

Feng, M., Gao, B., Garcia, L. R., & Sun, Q. H. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1035582 · Cited by 13

Cyanobacterial blooms, iron, and environmental pollutants

Ghio, A. J., & Hilborn, E. D. (2023) · BioMetals · doi:10.1007/s10534-023-00553-2 · Cited by 15

Plant Invasion and Soil Processes: A Mechanistic Understanding

Afreen, T., Kumari, S., Bhadouria, R., Devi, R. S., Singh, S., & Tripathi, S. (2023) · Springer eBooks · doi:10.1007/978-981-99-5910-5_10 · Cited by 13

Population-level control of two manganese oxidases expands the niche for bacterial manganese biomineralization

Gehin, G., Carraro, N., van der Meer, J. R., & Peña, J. (2025) · npj Biofilms and Microbiomes · doi:10.1038/s41522-025-00670-5 · Cited by 13

Stress Responses and Mechanisms of Phytopathogens Infecting Humans: Threats, Drivers, and Recommendations

Hossain, M. M., Sultana, F., Mostafa, M., Ferdus, H., Kundu, M., Adhikary, S., Akter, N., Saha, A., & Sabbir, M. A. A. (2025) · Stresses · doi:10.3390/stresses5020028 · Cited by 13

Competition and cooperation: The plasticity of bacterial interactions across environments

Solowiej-Wedderburn, J., Pentz, J. T., Lizana, L., Schroeder, B. O., Lind, P. A., & Libby, E. (2025) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1013213 · Cited by 14

FUNCTIONING OF PLANT GROWTH PROMOTING RHIZOBACTERIA (PGPR) AND THEIR MODE OF ACTIONS: AN OVERVIEW FROM CHEMISTRY POINT OF VIEW

Sukul, P., Kumar, J., Rani, A., Abdillahi, A. M., Rakesh, R. B., & Kumar, M. H. (2021) · PLANT ARCHIVES · doi:10.51470/plantarchives.2021.v21.s1.096 · Cited by 13

Microbial vesicle-mediated communication: convergence to understand interactions within and between domains of life

McMillan, H. M., Rogers, N. M. K., Wadle, A., Hsu‐Kim, H., Wiesner, M. R., Kuehn, M. J., & Hendren, C. O. (2021) · Environmental Science Processes & Impacts · doi:10.1039/d1em00022e · Cited by 13

Draft genome and description of Waterburya agarophytonicola gen. nov. sp. nov. (Pleurocapsales, Cyanobacteria): a seaweed symbiont

Bonthond, G., Shalygin, S. S., Bayer, T., & Weinberger, F. (2021) · Antonie van Leeuwenhoek · doi:10.1007/s10482-021-01672-x · Cited by 13

Serratia plymuthica MBSA-MJ1 Increases Shoot Growth and Tissue Nutrient Concentration in Containerized Ornamentals Grown Under Low-Nutrient Conditions

Nordstedt, N. P., & Jones, M. L. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.788198 · Cited by 13

Rhizobiales -Specific RirA Represses a Naturally “Synthetic” Foreign Siderophore Gene Cluster To Maintain Sinorhizobium -Legume Mutualism

Liu, K., Zhang, B., Yang, B.-S., Shi, W.-T., Li, Y., Yin, W., Zhang, P., Jiao, J., & Tian, C. F. (2022) · mBio · doi:10.1128/mbio.02900-21 · Cited by 13

Halogenated Metal-Binding Compounds from Shipworm Symbionts

Miller, B. W., Schmidt, E. W., Concepción, G. P., & Haygood, M. G. (2022) · Journal of Natural Products · doi:10.1021/acs.jnatprod.1c01049 · Cited by 13

Investigation of Streptomyces sp. Strain EMB24 Secondary Metabolite Profile Has Unraveled Its Extraordinary Antibacterial Potency Against Drug-Resistant Bacteria

Goel, N., Singh, R., Sood, S., & Khare, S. K. (2022) · Marine Biotechnology · doi:10.1007/s10126-022-10168-2 · Cited by 13

Siccibacter colletis as a member of the plant growth-promoting rhizobacteria consortium to improve faba-bean growth and alleviate phosphorus deficiency stress

Chamkhi, I., Zwanzig, J., Ibnyasser, A., Cheto, S., Geistlinger, J., Saidi, R., Zeroual, Y., Kouisni, L., Bargaz, A., & Ghoulam, C. (2023) · Frontiers in Sustainable Food Systems · doi:10.3389/fsufs.2023.1134809 · Cited by 13

Phytoremediation proficiency of Jatropha gossypifolia under the influence of Pseudomonas aeruginosa on metal contaminated soil

Lan, N. T., Hương, Đ. T. T., Đạo, P., & Lapčík, V. (2023) · Environmental Research · doi:10.1016/j.envres.2023.116295 · Cited by 13

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

Transcript Profiling of Nitroxoline-Treated Biofilms Shows Rapid Up-regulation of Iron Acquisition Gene Clusters

Liu, K., Abouelhassan, Y., Zhang, Y., Jin, S., & Huigens, R. W. (2022) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.2c00206 · Cited by 12

Ferrichrome, a fungal-type siderophore, confers high ammonium tolerance to fission yeast

Chiu, P.-C., Nakamura, Y., Nishimura, S., Tabuchi, T., Yashiroda, Y., Hirai, G., Matsuyama, A., & Yoshida, M. (2022) · Scientific Reports · doi:10.1038/s41598-022-22108-0 · Cited by 12

The potential to produce tropodithietic acid by Phaeobacter inhibens affects the assembly of microbial biofilm communities in natural seawater

Bech, P. K., Zhang, S., Henriksen, N. N. S. E., Bentzon‐Tilia, M., Strube, M. L., & Gram, L. (2023) · npj Biofilms and Microbiomes · doi:10.1038/s41522-023-00379-3 · Cited by 12

Iron, Copper, and Zinc Homeostasis in the Battle between Macrophage and Mycobacterium Tuberculosis

Yang, Z., Zhang, L., Wang, Y., Pi, J., Peng, D., Yao, Y., Xu, J., & Zhao, Y. (2024) · Current Medicinal Chemistry · doi:10.2174/0109298673283407231225140659 · Cited by 12

Transcriptomic and biochemical analysis of metabolic remodeling in Bacillus subtilis MSC4 under Benzo[a]pyrene stress

Chen, R., Liu, N., Ren, Y., & Cui, T. (2024) · Chemosphere · doi:10.1016/j.chemosphere.2024.141637 · Cited by 12

Interactions between Pseudomonas aeruginosa and six opportunistic pathogens cover a broad spectrum from mutualism to antagonism

Laffont, C., Wechsler, T., & Kümmerli, R. (2024) · Environmental Microbiology Reports · doi:10.1111/1758-2229.70015 · Cited by 12

Patterns of siderophore production and utilization at Station ALOHA from the surface to mesopelagic waters

Bundy, R. M., Manck, L. E., Repeta, D. J., Church, M. J., Hawco, N. J., Boiteau, R. M., Park, J., DeLong, E. F., & Saito, M. A. (2024) · Limnology and Oceanography · doi:10.1002/lno.12746 · Cited by 15

Skin Microbiome and Radiation-Induced Skin Injury: Unraveling the Relationship, Mechanisms, and Therapeutic Implications

Bratborska, A. W., Głuszak, P., Joks, M. M., Kaźmierska, J., Pazdrowski, J., Polańska, A., Jain, S., Yadav, H., Masternak, M. M., & Dańczak‐Pazdrowska, A. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26115022 · Cited by 14

Cooperation between a root fungal endophyte and host‐derived coumarin scopoletin mediates Arabidopsis iron nutrition

Dijck, L. V., Esposto, D., Huelsmann, C., Malisic, M., Piro, A. S., Giehl, R. F. H., Balcke, G. U., Tissier, A. F., & Parker, J. E. (2025) · New Phytologist · doi:10.1111/nph.70476 · Cited by 12

Akkermansia muciniphila MucT harnesses dietary polyphenols as xenosiderophores for enhanced iron uptake

Rodríguez-Daza, M.-C., Boeren, S. A., Tytgat, H. L. P., Desjardins, Y., & de Vos, W. M. (2025) · Nature Communications · doi:10.1038/s41467-025-64477-w · Cited by 12

The marine bivalve molluscs pathogen Vibrio neptunius produces the siderophore amphibactin, which is widespread in molluscs microbiota

Galvis, F., Ageitos, L., Martínez‐Matamoros, D., Barja, J. L., Rodrı́guez, J., Lemos, M. L., Jiménez, C., & Balado, M. (2020) · Environmental Microbiology · doi:10.1111/1462-2920.15312 · Cited by 12

Radionuclide Imaging of Fungal Infections and Correlation with the Host Defense Response

Ankrah, A. O., Sathekge, M. M., Dierckx, R., & Glaudemans, A. W. J. M. (2021) · Journal of Fungi · doi:10.3390/jof7060407 · Cited by 12

Evolutionary genomics and biosynthetic potential of novel environmental Actinobacteria

Caicedo-Montoya, C., Gómez-Román, M. P., Vázquez‐Hernández, M., Mora-Rincón, R. A., Rodríguez-Luna, S. D., Rodrı́guez-Sanoja, R., & Sánchez, S. (2021) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-021-11659-3 · Cited by 12

Siderophores and iron transport

Codd, R. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823144-9.00044-3 · Cited by 13

Genomic insight into iron acquisition by sulfate-reducing bacteria in microaerophilic environments

Barton, L. L., Duarte, A. G., & Staicu, L. C. (2022) · BioMetals · doi:10.1007/s10534-022-00410-8 · Cited by 12

Altered fecal microbial and metabolic profile reveals potential mechanisms underlying iron deficiency anemia in pregnant women in China

Chen, H., Wu, W., Tang, S., Fu, R., Gong, X., Hou, H., & Xu, J.-F. (2022) · Biomolecules and Biomedicine · doi:10.17305/bjbms.2022.7091 · Cited by 12

Genetic diversity of siderophores and hypermucoviscosity phenotype in Klebsiella pneumoniae

Lan, P., Yan, R., Lu, Y., Zhao, D., Shi, Q., Jiang, Y., Yu, Y., & Zhou, J. (2021) · Microbial Pathogenesis · doi:10.1016/j.micpath.2021.105014 · Cited by 12

Diverse soil protists show auxin regulated growth in partnership with auxin-producing bacteria

Patel, R., Triplett, L. R., Taerum, S. J., Nason, S. L., Wilson, C. O., & Steven, B. T. (2025) · The ISME Journal · doi:10.1093/ismejo/wraf234 · Cited by 11

The small RNA PrrH of Pseudomonas aeruginosa regulates hemolysis and oxidative resistance in bloodstream infection

Zeng, S., Shi, Q., Liu, Y., Li, M., Li, M., Zhang, S., Li, Q., Pu, J., Shen, C., Huang, B., et al. (2023) · Microbial Pathogenesis · doi:10.1016/j.micpath.2023.106124 · Cited by 11

Regulation of virulence mechanisms in plant-pathogenic Streptomyces

Vincent, C. V., & Bignell, D. R. D. (2024) · Canadian Journal of Microbiology · doi:10.1139/cjm-2023-0171 · Cited by 11

Heme sequestration by hemophilin from Haemophilus haemolyticus reduces respiratory tract colonization and infection with non-typeable Haemophilus influenzae

Fulte, S., Atto, B., McCarty, A., Horn, K. J., Redzic, J. S., Eisenmesser, E. Z., Yang, M., Marsh, R. L., Tristram, S. G., & Clark, S. E. (2024) · mSphere · doi:10.1128/msphere.00006-24 · Cited by 11

Citrate serves as a signal molecule to modulate carbon metabolism and iron homeostasis in Staphylococcus aureus

Chen, F., Zhao, Q., Yang, Z., Chen, R., Pan, H., Wang, Y., Liu, H., Cao, Q., Gan, J., Liu, X., et al. (2024) · PLoS Pathogens · doi:10.1371/journal.ppat.1012425 · Cited by 11

Combating plant diseases through transition metal allocation

De, A., Hoang, C. V., Escudero, V., Armas, A. M., Echávarri‐Erasun, C., González‐Guerrero, M., & Jordá, L. (2024) · New Phytologist · doi:10.1111/nph.20366 · Cited by 12

Initial gut microbiota composition is a determining factor in the promotion of colorectal cancer by oral iron supplementation: evidence from a murine model

Cuisiniere, T., Hajjar, R., Oliero, M., Calvé, A., Fragoso, G., Rendos, H. V., Gerkins, C., Taleb, N., Gagnon-Konamna, M., Dagbert, F., et al. (2025) · Microbiome · doi:10.1186/s40168-025-02101-1 · Cited by 11

Сolloidal probe based on iron(III)-doped calcium phytate nanoparticles for 31P NMR monitoring of bacterial siderophores

Pechrová, Z., Lobaz, V., Konefał, M., Konefał, R., & Hrubý, M. (2021) · Colloids and Interface Science Communications · doi:10.1016/j.colcom.2021.100427 · Cited by 11

FoxR is an AraC ‐like transcriptional regulator of ferrioxamine uptake in Salmonella enterica

Saldaña‐Ahuactzi, Z., & Knodler, L. A. (2022) · Molecular Microbiology · doi:10.1111/mmi.14970 · Cited by 11

The potential of novel bacterial isolates from healthy ginseng for the control of ginseng root rot disease (Fusarium oxysporum)

Li, Q., Yan, N., Miao, X., Yu, Z., & Chen, C. (2022) · PLoS ONE · doi:10.1371/journal.pone.0277191 · Cited by 11

Iron acquisition and mineral transformation by cyanobacteria living in extreme environments

Huang, W. D., Wang, T., Pérez-Fernández, C. A., DiRuggiero, J., & Kisailus, D. (2022) · Materials Today Bio · doi:10.1016/j.mtbio.2022.100493 · Cited by 11

A Disturbed Siderophore Transport Inhibits Myxobacterial Predation

Dong, Y., Dong, H., Feng, Z., Wang, X., Yao, Q., & Zhu, H. (2022) · Cells · doi:10.3390/cells11233718 · Cited by 11

Diversification of Ubiquinone Biosynthesis via Gene Duplications, Transfers, Losses, and Parallel Evolution

Kazemzadeh, K., Pélosi, L., Chenal, C., Chobert, S.-C., Chehade, M. H., Jullien, M., Flandrin, L., Schmitt, W., He, Q., Bouvet, E., et al. (2023) · Molecular Biology and Evolution · doi:10.1093/molbev/msad219 · Cited by 11

Ecological dependencies and the illusion of cooperation in microbial communities

Hesse, E., & O’Brien, S. (2024) · Microbiology · doi:10.1099/mic.0.001442 · Cited by 11

RNA-Seq reveals that Pseudomonas aeruginosa mounts growth medium-dependent competitive responses when sensing diffusible cues from Burkholderia cenocepacia

Leinweber, A., Laffont, C., Lardi, M., Eberl, L., Pessi, G., & Kümmerli, R. (2024) · Communications Biology · doi:10.1038/s42003-024-06618-3 · Cited by 11

Iron biofortification of crop food by symbiosis with beneficial microorganisms

Liu, C., Ye, Y., Liu, J., Pu, Y., & Wu, C. L. (2021) · Journal of Plant Nutrition · doi:10.1080/01904167.2021.1927089 · Cited by 11

The role of siderophores for bacterial community building

Maréchal, S., & Kümmerli, R. (2026) · Current Opinion in Microbiology · doi:10.1016/j.mib.2026.102825 · Cited by 1

The Ecology and Evolution of Bacterial Social Interactions and How They Shape Microbial Communities and Interactions with Hosts

Figueiredo, A. R. T. (2021) · Zurich Open Repository and Archive (University of Zurich) · doi:10.5167/uzh-217033

Siderophore synthetase-receptor gene coevolution reveals habitat- and pathogen-specific bacterial iron interaction networks

Gu, S., Shao, Z., Qu, Z., Zhu, S., Shao, Y., Zhang, D., Allen, R., He, R., Shao, J., Xiong, G., et al. (2025) · Science Advances · doi:10.1126/sciadv.adq5038 · Cited by 31

Context-dependent siderophore exploitability shapes microbial community structure

Krüger, A., Paik, S., Bund, M., Pesch, M., Krueger, S., Lückel, B., Papadopoulos, A., Wiechert, J., Hassan, T., Weber, U., et al. (2026) · The ISME Journal · doi:10.1093/ismejo/wrag247 · Cited by 1

Siderophore-mediated iron acquisition and modulation of host-bacterial interactions

Ellermann, M., & Arthur, J. C. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.10.489 · Cited by 186