Bacterial siderophores in community and host interactions

The Tragedy of the Commons: The population problem has no technical solution; it requires a fundamental extension in morality.

Hardin, G. (1968) · Science · doi:10.1126/science.162.3859.1243 · Cited by 25,167

Biofilms: an emergent form of bacterial life

Flemming, H.-C., Wingender, J., Szewzyk, U., Steinberg, P., Rice, S. A., & Kjelleberg, S. (2016) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2016.94 · Cited by 5,979

On aims and methods of ethology

Tinbergen, N. (1963) · Zeitschrift für Tierpsychologie · doi:10.1111/j.1439-0310.1963.tb01161.x · Cited by 4,551

Embracing the unknown: disentangling the complexities of the soil microbiome

Fierer, N. (2017) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2017.87 · Cited by 3,579

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

Bacterial iron homeostasis

Andrews, S. C., Robinson, A. K., & Rodríguez-Quiñones, F. (2003) · FEMS Microbiology Reviews · doi:10.1016/s0168-6445(03)00055-x · Cited by 2,702

Arms races between and within species

Dawkins, R., & Krebs, J. R. (1979) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1979.0081 · Cited by 2,214

Toxicity of heavy metals to microorganisms and microbial processes in agricultural soils: a review

Giller, K. E., Witter, E., & McGrath, S. P. (1998) · Soil Biology and Biochemistry · doi:10.1016/s0038-0717(97)00270-8 · Cited by 1,987

Social semantics: altruism, cooperation, mutualism, strong reciprocity and group selection.

WEST, S. A., GRIFFIN, A. S., & GARDNER, A. (2007) · Journal of Evolutionary Biology · doi:10.1111/j.1420-9101.2006.01258.x · Cited by 1,889

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

Exploring the Potential of Four Novel Halotolerant Bacterial Strains as Plant-Growth-Promoting Rhizobacteria (PGPR) under Saline Conditions

Oliva, G., Stasio, L. D., Vigliottá, G., Guarino, F., Cicatelli, A., & Castiglione, S. (2023) · Applied Sciences · doi:10.3390/app13074320 · Cited by 27

Biocontrol in built environments to reduce pathogen exposure and infection risk

Gottel, N., Hill, M., Neal, M. J., Allard, S. M., Zengler, K., & Gilbert, J. A. (2024) · The ISME Journal · doi:10.1093/ismejo/wrad024 · Cited by 28

Iron at the crossroads of host–microbiome interactions in health and disease

Choi, G., & Bessman, N. J. (2025) · Nature Microbiology · doi:10.1038/s41564-025-02001-y · Cited by 28

The Pneumococcal Iron Uptake Protein A (PiuA) Specifically Recognizes Tetradentate FeIIIbis- and Mono-Catechol Complexes

Zhang, Y., Edmonds, K. A., Raines, D. J., Murphy, B. A., Wu, H., Guo, C., Nolan, E. M., VanNieuwenhze, M. S., Duhme‐Klair, A., & Giedroc, D. P. (2020) · Journal of Molecular Biology · doi:10.1016/j.jmb.2020.08.005 · Cited by 27

Recent developments in siderotyping: procedure and application

Singh, P., Khan, A., Kumar, R. K., Kumar, R., Singh, V. K., & Srivastava, A. (2020) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-020-02955-7 · Cited by 27

Enterococcus faecalis thrives in dual-species biofilm models under iron-rich conditions

Govindarajan, D. K., Meghanathan, Y., Sivaramakrishnan, M., Kothandan, R., Ananthasubramanian, M., Seviour, T. W., & Kandaswamy, K. (2022) · Archives of Microbiology · doi:10.1007/s00203-022-03309-7 · Cited by 27

Biological magnetic ion exchange resin on advanced treatment of synthetic wastewater

Xu, S., Yan, Y., Shuang, C., Zhou, Q., Ji, R., & Li, A. (2023) · Bioresource Technology · doi:10.1016/j.biortech.2023.128613 · Cited by 27

Lactoferrin receptors in Gram-negative bacteria: an evolutionary perspective

Ostan, N., Moraes, T. F., & Schryvers, A. B. (2021) · Biochemistry and Cell Biology · doi:10.1139/bcb-2020-0079 · Cited by 28

Harnessing regulatory networks in Actinobacteria for natural product discovery

Augustijn, H. E., Roseboom, A. M., Medema, M. H., & van Wezel, G. P. (2024) · Journal of Industrial Microbiology & Biotechnology · doi:10.1093/jimb/kuae011 · Cited by 26

Long-term cover crop monocultures and mixtures improve soil multifunctionality and shift microbial communities and functions

Ding, K., Zhang, Y., Ge, S., Zhang, Y., Lu, M., Shen, Z., Tong, Z., & Zhang, J. (2024) · European Journal of Agronomy · doi:10.1016/j.eja.2024.127188 · Cited by 28

Metabolic relationships between marine red algae and algae-associated bacteria

Kim, K. H., Kim, J., Baek, J. H., Jeong, S. E., Kim, H., Yoon, H. S., & Jeon, C. O. (2024) · Marine Life Science & Technology · doi:10.1007/s42995-024-00227-z · Cited by 26

Pseudomonas in the spotlight: emerging roles in the nodule microbiome

Yu, Y., Crosbie, D. B., & Marín, M. (2025) · Trends in Plant Science · doi:10.1016/j.tplants.2024.12.002 · Cited by 26

Microbial siderophores for One Health

Wei, Z., Gu, S., Vollenweider, V., Zuo, Y., Li, Z., & Kümmerli, R. (2025) · Trends in Microbiology · doi:10.1016/j.tim.2025.05.002 · Cited by 26

Antimicrobial roles of probiotics: Molecular mechanisms and application prospects

Yu, X., Liu, Z., Liu, Y., Li, X., Wang, B., & Yin, J. (2025) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2025.105146 · Cited by 27

Molecular, biochemical, and comparative genome analysis of a rhizobacterial strain Klebsiella Sp. KBG6.2 imparting salt stress tolerance to Oryza sativa L.

Girma, B., Panda, A. N., Roy, P. C., Ray, L. B., Mohanty, S., & Chowdhary, G. (2022) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2022.105066 · Cited by 26

Efflux-linked accelerated evolution of antibiotic resistance at a population edge

Bhattacharyya, S., Bhattacharyya, M., Pfannenstiel, D. M., Nandi, A. K., Hwang, Y., Ho, K., & Harshey, R. M. (2022) · Molecular Cell · doi:10.1016/j.molcel.2022.10.024 · Cited by 27

The Life Cycle of Aurelia aurita Depends on the Presence of a Microbiome in Polyps Prior to Onset of Strobilation

Jensen, N., Weiland‐Bräuer, N., Joel, S., Chibani, C. M., & Schmitz, R. A. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.00262-23 · Cited by 26

Bacillibactins E and F from a Marine Sponge-Associated Bacillus sp.

Wu, Q., Throckmorton, K., Maity, M., Chevrette, M. G., Braun, D. R., Rajski, S. R., Currie, C. R., Thomas, M. G., & Bugni, T. S. (2020) · Journal of Natural Products · doi:10.1021/acs.jnatprod.0c01170 · Cited by 25

Inductive Production of the Iron-Chelating 2-Pyridones Benefits the Producing Fungus To Compete for Diverse Niches

Chen, B., Sun, Y., Li, S., Yin, Y., & Wang, C. (2021) · mBio · doi:10.1128/mbio.03279-21 · Cited by 25

Enhancing Stevia rebaudiana growth and yield through exploring beneficial plant-microbe interactions and their impact on the underlying mechanisms and crop sustainability

Abdelsattar, A. M., Elsayed, A. A., El-Esawi, M. A., & Heikal, Y. M. (2023) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2023.107673 · Cited by 25

Biophysical and proteomic analyses of Pseudomonas syringae pv. tomato DC3000 extracellular vesicles suggest adaptive functions during plant infection

Janda, M., Rybak, K., Krassini, L., Meng, C., Feitosa-Junior, O. R., Stigliano, E., Szulc, B., Sklenář, J., Menke, F. L. H., Malone, J. G., et al. (2023) · mBio · doi:10.1128/mbio.03589-22 · Cited by 25

Chelating Effect of Siderophore Desferrioxamine-B on Uranyl Biomineralization Mediated by Shewanella putrefaciens

Lü, X., Zhang, Y., Cheng, W., Liu, Y., Li, Q., Li, X., Dong, F., Li, J., & Nie, X. (2024) · Environmental Science & Technology · doi:10.1021/acs.est.3c05753 · Cited by 25

Bacillus cereus sensu lato antimicrobial arsenal: An overview

Morandini, L., Caulier, S., Bragard, C., & Mahillon, J. (2024) · Microbiological Research · doi:10.1016/j.micres.2024.127697 · Cited by 25

In vivo development of cefiderocol resistance in carbapenem-resistant Acinetobacter baumannii associated with the downregulation of a TonB-dependent siderophore receptor, PiuA

Findlay, J., Bianco, G., Boattini, M., & Nordmann, P. (2024) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkae018 · Cited by 24

Siderophore-mediated iron enrichment in the biofilm matrix enhances plant iron nutrition

Tan, T., Xu, Z., Tao, L., Sun, X., Xie, J., Miao, Y., Zhang, N., Xun, W., Beauregard, P. B., Kovács, Á. T., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116481 · Cited by 24

Wolf in Sheep’s Clothing: Clostridioides difficile Biofilm as a Reservoir for Recurrent Infections

Meza‐Torres, J., Auria, E., Dupuy, B., & Tremblay, Y. D. N. (2021) · Microorganisms · doi:10.3390/microorganisms9091922 · Cited by 24

Trojan horselike T6SS effector TepC mediates both interference competition and exploitative competition

Li, S., Xu, L., Wu, T., Shi, Z., Kareem, H. A., Wang, Z., Dai, Q., Guo, C., Pan, J., Yang, M., et al. (2024) · The ISME Journal · doi:10.1093/ismejo/wrad028 · Cited by 24

Feature sequence-based genome mining uncovers the hidden diversity of bacterial siderophore pathwaysPreprint

Gu, S., Shao, Y., Rehm, K., Bigler, L., Zhang, D., He, R., Xu, R., Shao, J., Jousset, A., Friman, V., et al. (2024) · eLife · doi:10.7554/elife.96719 · Cited by 24

Type I Interferons Ameliorate Zinc Intoxication of Candida glabrata by Macrophages and Promote Fungal Immune Evasion

Riedelberger, M., Penninger, P., Tscherner, M., Hadriga, B., Brunnhofer, C., Jenull, S., Stoiber, A., Bourgeois, C., Petryshyn, A., Glaser, W., et al. (2020) · iScience · doi:10.1016/j.isci.2020.101121 · Cited by 23

Siderophore-mediated iron partition promotes dynamical coexistence between cooperators and cheaters

Shao, J., Rong, N., Wu, Z., Gu, S., Liu, B., Shen, N., & Li, Z. (2023) · iScience · doi:10.1016/j.isci.2023.107396 · Cited by 23

Genome sequence-based species classification of Enterobacter cloacae complex: a study among clinical isolates

Qiu, X., Ye, K., Ma, Y., Zhao, Q., Wang, L., & Yang, J. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.04312-23 · Cited by 23

Metal-antimicrobial peptides combo: promising weapons to combat bacteria invaders

Falcigno, L., Braccia, S., Bellavita, R., D’Auria, G., Falanga, A., & Galdiero, S. (2024) · Frontiers in Drug Discovery · doi:10.3389/fddsv.2024.1440378 · Cited by 23

Pantoea brenneri AS3 and Bacillus ginsengihumi M2.11 as Potential Biocontrol and Plant Growth-Promoting Agents

Itkina, D., Сулейманова, А. Д., & Sharipova, M. R. (2021) · Microbiology · doi:10.1134/s0026261721020053 · Cited by 23

Beyond the List: Bioagent-Agnostic Signatures Could Enable a More Flexible and Resilient Biodefense Posture Than an Approach Based on Priority Agent Lists Alone

Leiser, O. P., Hobbs, E. C., Sims, A. M., Korch, G. W., & Taylor, K. (2021) · Pathogens · doi:10.3390/pathogens10111497 · Cited by 23

Nutritional Interactions between Bacterial Species Colonising the Human Nasal Cavity: Current Knowledge and Future Prospects

Adolf, L. A., & Heilbronner, S. (2022) · Metabolites · doi:10.3390/metabo12060489 · Cited by 24

Endophytic Paenibacillus polymyxa LMG27872 inhibits Meloidogyne incognita parasitism, promoting tomato growth through a dose-dependent effect

Singh, R. R., & Wesemael, W. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.961085 · Cited by 23

Genome insights into the plant growth-promoting bacterium Saccharibacillus brassicae ATSA2T

Jiang, L., Seo, J., Peng, Y., Jeon, D., Park, S. J., Kim, C. Y., Kim, P. I., Kim, C. H., Lee, J. H., & Lee, J. (2023) · AMB Express · doi:10.1186/s13568-023-01514-1 · Cited by 23

Iron Acquisition and Metabolism as a Promising Target for Antimicrobials (Bottlenecks and Opportunities): Where Do We Stand?

Stelitano, G., Cocorullo, M., Mori, M., Villa, S., Meneghetti, F., & Chiarelli, L. R. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076181 · Cited by 23

Isolation and Characterization of Bacterial Endophytes from Small Nodules of Field-Grown Peanut

Hossain, M. S., Frith, C., Bhattacharyya, S. S., DeLaune, P. B., & Gentry, T. J. (2023) · Microorganisms · doi:10.3390/microorganisms11081941 · Cited by 23

Roles of Pseudomonas aeruginosa siderophores in interaction with prokaryotic and eukaryotic organisms

Jeong, G., Khan, F., Tabassum, N., Jo, D., Jung, W., & Kim, Y. (2024) · Research in Microbiology · doi:10.1016/j.resmic.2024.104211 · Cited by 23

Production of Siderophores by an Apple Root-Associated Streptomyces ciscaucasicus Strain GS2 Using Chemical and Biological OSMAC Approaches

Armin, R., Zühlke, S., Grunewaldt‐Stöcker, G., Mahnkopp-Dirks, F., & Kusari, S. (2021) · Molecules · doi:10.3390/molecules26123517 · Cited by 23

Soil warming increases the active antibiotic resistome in the gut of invasive giant African snails

Zhang, Y., Li, H.-Z., Breed, M. F., Tang, Z., Li, C., Zhu, Y., & Sun, X. (2025) · Microbiome · doi:10.1186/s40168-025-02044-7 · Cited by 22

Enterobactin: A key player in bacterial iron acquisition and virulence and its implications for vaccine development and antimicrobial strategies

Amiri, M., Golchin, M., Jamshidian-Mojaver, M., Farzin, H., & Hajizadeh, A. (2025) · Virulence · doi:10.1080/21505594.2025.2563018 · Cited by 23

Siderophore piracy enhances Vibrio cholerae environmental survival and pathogenesis

Byun, H., Jung, I.-J., Chen, J., Larios‐Valencia, J., & Zhu, J. (2020) · Microbiology · doi:10.1099/mic.0.000975 · Cited by 24

Cyclic Analogs of Desferrioxamine E Siderophore for 68 Ga Nuclear Imaging: Coordination Chemistry and Biological Activity in Staphylococcus aureus

Mular, A., Shanzer, A., Kozłowski, H., Hubmann, I., Misslinger, M., Krzywik, J., Decristoforo, C., & Gumienna‐Kontecka, E. (2021) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.1c02453 · Cited by 22

Characterization of Bacillus velezensis RDA1 as a Biological Control Agent against White Root Rot Disease Caused by Rosellinia necatrix

Sawant, S. S., Song, J.-H., & Seo, H.-J. (2022) · Plants · doi:10.3390/plants11192486 · Cited by 22

Chryseochelins—structural characterization of novel citrate-based siderophores produced by plant protecting Chryseobacterium spp.

Rehm, K., Vollenweider, V., Gu, S., Friman, V., Kümmerli, R., Wei, Z., & Bigler, L. (2023) · Metallomics · doi:10.1093/mtomcs/mfad008 · Cited by 22

Temperature-induced modulation of stress-tolerant PGP genes bioprospected from Bacillus sp. IHBT-705 associated with saffron (Crocus sativus) rhizosphere: A natural -treasure trove of microbial biostimulants

Ali, N., Swarnkar, M. K., Veer, R., Kaushal, P., & Pati, A. M. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1141538 · Cited by 22

Bioactive Compounds from and against Yeasts in the One Health Context: A Comprehensive Review

Tadioto, V., Giehl, A., Cadamuro, R. D., Guterres, I. Z., dos Santos, Â. A., Bressan, S. K., Werlang, L., Stambuk, B. U., Fongaro, G., Silva, I. T., et al. (2023) · Fermentation · doi:10.3390/fermentation9040363 · Cited by 22

Growth promotion and biological control of fungal diseases in tomato by a versatile rhizobacterium, Pseudomonas chlororaphis subsp. aureofaciens SPS-41

Shi, X.-Q., Zhu, D.-H., Chen, J.-L., Qin, Y.-Y., Li, X.-W., Qin, S., & 邢柯 (2024) · Physiological and Molecular Plant Pathology · doi:10.1016/j.pmpp.2024.102274 · Cited by 23

Coordination of siderophore gene expression among clonal cells of the bacterium Pseudomonas aeruginosa

Mridha, S., & Kümmerli, R. (2022) · Communications Biology · doi:10.1038/s42003-022-03493-8 · Cited by 23

Mikania micrantha Kunth and its derived biochar impacts on heavy metal bioavailability and siderophore-related genes during chicken manure composting

Abdellah, Y. A. Y., Chen, H.-Y., Deng, S.-W., Li, W., Ren, R.-J., Yang, X., Rana, M. S., Sun, S., Liu, J., & Wang, R. (2024) · Biochar · doi:10.1007/s42773-024-00347-w · Cited by 21

Periphytic Microbial Response to Environmental Phosphate (P) Bioavailability and Its Relevance to P Management in Paddy Fields

Zhang, J., Su, J., Ma, C., Hu, X., & Teng, H. H. (2021) · Applied and Environmental Microbiology · doi:10.1128/aem.01201-21 · Cited by 21

Vibrio neptunius Produces Piscibactin and Amphibactin and Both Siderophores Contribute Significantly to Virulence for Clams

Galvis, F., Ageitos, L., Rodrı́guez, J., Jiménez, C., Barja, J. L., Lemos, M. L., & Balado, M. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.750567 · Cited by 21

Insights on plant–microbe interactions in soil in relation to iron dynamics

Dhankhar, R., Gupta, S., & Gulati, P. (2022) · Vegetos · doi:10.1007/s42535-022-00467-3 · Cited by 21

How public can public goods be? Environmental context shapes the evolutionary ecology of partially private goods

Lerch, B. A., Smith, D. A., Koffel, T., Bagby, S. C., & Abbott, K. C. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010666 · Cited by 21

Molecular mechanism of Cu metal and drought stress resistance triggered by Porostereum spadiceum AGH786 in Solanum lycopersicum L.

Naz, F., Hamayun, M., Rauf, M., Arif, M., Khan, S. A., Ud-Din, J., Gul, H., Hussain, A., Iqbal, A., Kim, H., et al. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.1029836 · Cited by 21

Rejuvenating the Activity of Usual Antibiotics on Resistant Gram-Negative Bacteria: Recent Issues and Perspectives

Tabcheh, J., Vergalli, J., Davin‐Regli, A., Ghanem, N., Pagès, J., Al-Bayssari, C., & Brunel, J. M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021515 · Cited by 21

Community composition drives siderophore dynamics in multispecies bacterial communities

O’Brien, S., Culbert, C. T., & Barraclough, T. G. (2023) · BMC Ecology and Evolution · doi:10.1186/s12862-023-02152-8 · Cited by 21

Utilization of Rhodopseudomonas palustris in Crop Rotation Practice Boosts Rice Productivity and Soil Nutrient Dynamics

Sundar, L. S., Yen, K.-S., Chang, Y.-T., & Chao, Y.-Y. (2024) · Agriculture · doi:10.3390/agriculture14050758 · Cited by 21

Alteration of protein homeostasis mediates the interaction of Pseudomonas aeruginosa with Staphylococcus aureus

Yang, N., Cao, Q., Hu, S., Xu, C., Fan, K., Chen, F., Yang, C., Liang, H., Wu, M., Bae, T., et al. (2020) · Molecular Microbiology · doi:10.1111/mmi.14519 · Cited by 21

Harnessing Chemical Ecology for Environment-Friendly Crop Protection

Kang, S., Lumactud, R. A., Li, N., Bell, T. H., Kim, H.-S., Park, S., & Lee, Y. (2021) · Phytopathology · doi:10.1094/phyto-01-21-0035-rvw · Cited by 21

Siderophores of Bacillus pumilus promote 2‐keto‐L‐gulonic acid production in a vitamin C microbial fermentation system

Zhang, Q., Lin, Y., Shen, G., Zhang, H., & Lyu, S. (2022) · Journal of Basic Microbiology · doi:10.1002/jobm.202200237 · Cited by 21

Next-generation diagnostics of bloodstream infections enabled by rapid whole-genome sequencing of bacterial cells purified from blood cultures

Pilato, V. D., Bonaiuto, C., Morecchiato, F., Antonelli, A., Giani, T., & Rossolini, G. M. (2025) · EBioMedicine · doi:10.1016/j.ebiom.2025.105633 · Cited by 20

An inhalable gallium-polyphenol nanoparticle blocks bacterial electron transport chain and signal transduction for anti-biofilm therapy

Ni, Y., Huang, Y., Chen, Y., Li, Y., Liu, F., Ji, J., & Jin, Q. (2025) · Bioactive Materials · doi:10.1016/j.bioactmat.2025.10.043 · Cited by 20

Targeting bacterial transferrin and lactoferrin receptors for vaccines

Schryvers, A. B. (2022) · Trends in Microbiology · doi:10.1016/j.tim.2022.01.017 · Cited by 20

Eco-evolutionary modelling of microbial syntrophy indicates the robustness of cross-feeding over cross-facilitation

Boza, G., Barabás, G., Scheuring, I., & Zachar, I. (2023) · Scientific Reports · doi:10.1038/s41598-023-27421-w · Cited by 20

Secondary Metabolite Production Potential in a Microbiome of the Freshwater Sponge Spongilla lacustris

Graffius, S., Garzón, J. F. G., Zehl, M., Pjevac, P., Kirkegaard, R. H., Flieder, M., Loy, A., Rattei, T., Ostrovsky, A. N., & Zotchev, S. B. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.04353-22 · Cited by 21

Proximity-based defensive mutualism between Streptomyces and Mesorhizobium by sharing and sequestering iron

Du, X., Liu, N., Yan, B., Li, Y., Liu, M., & Huang, Y. (2024) · The ISME Journal · doi:10.1093/ismejo/wrad041 · Cited by 20

Phosphate solubilizing Aspergillus Niger PH1 ameliorates growth and alleviates lead stress in maize through improved photosynthetic and antioxidant response

Hussain, I., Irshad, M. S., Hussain, A., Qadir, M., Mehmood, A., Rahman, M., Alrefaei, A. F., Almutairi, M. H., Ali, S., & Hamayun, M. (2024) · BMC Plant Biology · doi:10.1186/s12870-024-05361-5 · Cited by 20

Harnessing rhizobacteria to fulfil inter-linked nutrient dependency on soil and alleviate stresses in plants

Neemisha, Kumar, A., Sharma, P., Kaur, A., Sharma, S., & Jain, R. (2022) · Journal of Applied Microbiology · doi:10.1111/jam.15649 · Cited by 20

Bacteria from the gut influence the host micronutrient status

Kouadio, D. K. D., Wieringa, F. T., Greffeuille, V., & Humblot, C. (2023) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2023.2227888 · Cited by 19

Navigating Antibiotic Resistance in Gram‐Negative Bacteria: Current Challenges and Emerging Therapeutic Strategies

Kumari, R., & Saraogi, I. (2025) · ChemPhysChem · doi:10.1002/cphc.202401057 · Cited by 19

Secondary Metabolites from Bacillus spp. probiotics as potential treatments for multidrug-resistant pathogens: A comprehensive review

Nicolas, G. M. (2025) · Current Research in Microbial Sciences · doi:10.1016/j.crmicr.2025.100392 · Cited by 19

Ecology drives the evolution of diverse social strategies in Pseudomonas aeruginosa

Figueiredo, A. R. T., Wagner, A., & Kümmerli, R. (2021) · Molecular Ecology · doi:10.1111/mec.16119 · Cited by 19

Understanding roles of humic substance and protein on iron phosphate transformation during anaerobic fermentation of waste activated sludge

Lu, K., Ping, Q., Lu, Q., & Li, Y. (2022) · Bioresource Technology · doi:10.1016/j.biortech.2022.127242 · Cited by 19

Battle for Metals: Regulatory RNAs at the Front Line

Charbonnier, M., González-Espinoza, G., Kehl‐Fie, T. E., & Lalaouna, D. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.952948 · Cited by 21

Synthesis and Characterization of DOTAM-Based Sideromycins for Bacterial Imaging and Antimicrobial Therapy

Peukert, C., Rox, K., Karge, B., Hotop, S., & Brönstrup, M. (2023) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.2c00523 · Cited by 19

Siderophore conjugation with cleavable linkers boosts the potency of RNA polymerase inhibitors against multidrug-resistant E. coli

Peukert, C., Vetter, A. C., Fuchs, H. L. S., Harmrolfs, K., Karge, B., Stadler, M., & Brönstrup, M. (2023) · Chemical Science · doi:10.1039/d2sc06850h · Cited by 19

Discovery and Biosynthesis of Anthrochelin, a Growth‐Promoting Metallophore of the Human Pathogen Luteibacter anthropi

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