Reactive oxygen species in pathogen clearance: The killing mechanisms, the adaption response, and the side effects
Open accessAbstract
Reactive oxygen species (ROS) are attractive weapons in both antibiotic-mediated killing and host-mediated killing. However, the involvement of ROS in antibiotic-mediated killing and complexities in host environments challenge the paradigm. In the case of bacterial pathogens, the examples of some certain pathogens thriving under ROS conditions prompt us to focus on the adaption mechanism that pathogens evolve to cope with ROS. Based on these, we here summarized the mechanisms of ROS-mediated killing of either antibiotics or the host, the examples of bacterial adaption that successful pathogens evolved to defend or thrive under ROS conditions, and the potential side effects of ROS in pathogen clearance. A brief section for new antibacterial strategies centered around ROS was also addressed.
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In the recognition and response process of phagocytosis, reactive oxygen species ROS and reactive nitrogen species RNS are produced.
“In the recognition and response process of phagocytosis, reactive oxygen species ROS and reactive nitrogen species RNS are produced [5].”
From The Role of Reactive Species on Innate Immunity (2022) · cites this paper as [5]
Under non-lethal levels of ROS, certain pathogens have evolved mechanisms to adapt and thrive, and may even use ROS as a cornerstone for increasing tolerance and resistance to antibiotics.
“However, they are a double-edged sword and must be regulated with care, as under non-lethal levels of ROS, certain pathogens have evolved mechanisms to adapt and thrive, and may even use ROS as a cornerstone for increasing tolerance and resistance to antibiotics.”
From The Role of Reactive Species on Innate Immunity (2022) · cites this paper as [5]
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Cites
Mittler, R. (2017) · Trends in Plant Science · doi:10.1016/j.tplants.2016.08.002 · Cited by 3,499 · see citing works
A Common Mechanism of Cellular Death Induced by Bactericidal Antibiotics
Kohanski, M. A., Dwyer, D. J., Hayete, B., Lawrence, C. A., & Collins, J. J. (2007) · Cell · doi:10.1016/j.cell.2007.06.049 · Cited by 2,982 · see citing works
Mills, E. L., Kelly, B., Logan, A., Costa, A. S. H., Varma, M., Bryant, C. E., Tourlomousis, P., Däbritz, J. H. M., Gottlieb, E., Latorre, I., et al. (2016) · Cell · doi:10.1016/j.cell.2016.08.064 · Cited by 2,291 · see citing works
Myeloperoxidase: friend and foe
Klebanoff, S. J. (2005) · Journal of Leukocyte Biology · doi:10.1189/jlb.1204697 · Cited by 2,282 · see citing works
How antibiotics kill bacteria: from targets to networks
Kohanski, M. A., Dwyer, D. J., & Collins, J. J. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2333 · Cited by 2,266 · see citing works
Neutrophil elastase and myeloperoxidase regulate the formation of neutrophil extracellular traps
Papayannopoulos, V., Metzler, K. D., Hakkim, A., & Zychlinsky, A. (2010) · Journal of Cell Biology · doi:10.1083/jcb.201006052 · Cited by 2,103 · see citing works
Tlr signalling augments macrophage bactericidal activity through mitochondrial ros
West, A. P., Brodsky, I. E., Rahner, C., Woo, D. K., Erdjument-Bromage, H., Tempst, P., Walsh, M. C., Choi, Y., Shadel, G. S., & Ghosh, S. (2011) · Nature · doi:10.1038/nature09973 · Cited by 1,659 · see citing works
Distinguishing between resistance, tolerance and persistence to antibiotic treatment
Brauner, A., Fridman, O., Gefen, O., & Balaban, N. Q. (2016) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2016.34 · Cited by 1,612 · see citing works
Cellular Defenses against Superoxide and Hydrogen Peroxide
Imlay, J. A. (2008) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.77.061606.161055 · Cited by 1,563 · see citing works
Interactions between the microbiota and pathogenic bacteria in the gut
Bäumler, A. J., & Sperandio, V. (2016) · Nature · doi:10.1038/nature18849 · Cited by 1,420 · see citing works
Gut inflammation provides a respiratory electron acceptor for Salmonella
Winter, S., Thiennimitr, P., Winter, M. G., Butler, B. P., Huseby, D. L., Crawford, R. W., Russell, J. M., Bevins, C. L., Adams, L. G., Tsolis, R. M., et al. (2010) · Nature · doi:10.1038/nature09415 · Cited by 1,271 · see citing works
Vatansever, F., Melo, W., Avci, P., Vecchio, D., Sadasivam, M., Gupta, A., Chandran, R., Karimi, M., Parizotto, N. A., Yin, R., et al. (2013) · FEMS Microbiology Reviews · doi:10.1111/1574-6976.12026 · Cited by 1,134 · see citing works
Oxidative stress, protein damage and repair in bacteria
Ezraty, B., Gennaris, A., Barras, F., & Collet, J. (2017) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2017.26 · Cited by 1,042 · see citing works
The physics, biophysics and technology of photodynamic therapy
Wilson, B. C., & Patterson, M. S. (2008) · Physics in Medicine and Biology · doi:10.1088/0031-9155/53/9/r01 · Cited by 1,009 · see citing works
Sublethal Antibiotic Treatment Leads to Multidrug Resistance via Radical-Induced Mutagenesis
Kohanski, M. A., DePristo, M. A., & Collins, J. J. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.01.003 · Cited by 985 · see citing works
NADPH oxidases: An overview from structure to innate immunity-associated pathologies
Panday, A., Sahoo, M. K., Osorio, D., & Batra, S. (2015) · Cellular & Molecular Immunology · doi:10.1038/cmi.2014.89 · Cited by 944 · see citing works
Antibiotic efficacy is linked to bacterial cellular respiration
Lobritz, M. A., Belenky, P. A., Porter, C. B. M., Gutierrez, A., Yang, J. H., Schwarz, E. G., Dwyer, D. J., Khalil, A. S., & Collins, J. J. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1509743112 · Cited by 756 · see citing works
Neutrophils to the ROScue: Mechanisms of NADPH oxidase activation and bacterial resistance
Nguyen, G. T., Green, E. R., & Mecsas, J. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00373 · Cited by 741 · see citing works
The Role of Reactive Oxygen Species in Antibiotic-Mediated Killing of Bacteria
Acker, H. V., & Coenye, T. (2017) · Trends in Microbiology · doi:10.1016/j.tim.2016.12.008 · Cited by 615 · see citing works
Bacterial Metabolism and Antibiotic Efficacy
Stokes, J. M., Lopatkin, A. J., Lobritz, M. A., & Collins, J. J. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.06.009 · Cited by 611 · see citing works
Kohanski, M. A., Dwyer, D. J., Wierzbowski, J., Cottarel, G., & Collins, J. J. (2008) · Cell · doi:10.1016/j.cell.2008.09.038 · Cited by 576 · see citing works
Quinolone-Mediated Bacterial Death
Drlica, K., Malik, M., Kerns, R. J., & Zhao, X. (2007) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01617-06 · Cited by 569 · see citing works
Activation of antibacterial autophagy by NADPH oxidases
Huang, J., Canadien, V., Lam, G. Y., Steinberg, B. E., Dinauer, M. C., Magalhaes, M. A. O., Glogauer, M., Grinstein, S., & Brumell, J. H. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811045106 · Cited by 556 · see citing works
Killing by Bactericidal Antibiotics Does Not Depend on Reactive Oxygen Species
Keren, I., Wu, Y., Inocencio, J. F., Mulcahy, L. R., & Lewis, K. (2013) · Science · doi:10.1126/science.1232688 · Cited by 551 · see citing works
Post-stress bacterial cell death mediated by reactive oxygen species
Hong, Y., Zeng, J., Wang, X., Drlica, K., & Zhao, X. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1901730116 · Cited by 520 · see citing works
Bactericidal Antibiotics Induce Toxic Metabolic Perturbations that Lead to Cellular Damage
Belenky, P. A., Ye, J. D., Porter, C. B. M., Cohen, N. R., Lobritz, M. A., Ferrante, T. C., Jain, S. R., Korry, B. J., Schwarz, E. G., Walker, G. C., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.09.059 · Cited by 512 · see citing works
Antimicrobial Photodynamic Therapy to Control Clinically Relevant Biofilm Infections
Hu, X., Huang, Y., Wang, Y., Wang, X., & Hamblin, M. R. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01299 · Cited by 508 · see citing works
Self-citationTranscriptional 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
Gyrase inhibitors induce an oxidative damage cellular death pathway in Escherichia coli
Dwyer, D. J., Kohanski, M. A., Hayete, B., & Collins, J. J. (2007) · Molecular Systems Biology · doi:10.1038/msb4100135 · Cited by 470 · see citing works
Reactive oxygen species and the bacterial response to lethal stress
Zhao, X., & Drlica, K. (2014) · Current Opinion in Microbiology · doi:10.1016/j.mib.2014.06.008 · Cited by 445 · see citing works
How does the oxidative burst of macrophages kill bacteria? Still an open question
Slauch, J. M. (2011) · Molecular Microbiology · doi:10.1111/j.1365-2958.2011.07612.x · Cited by 436 · see citing works
Tavares, A., Carvalho, C. M. B., Faustino, M. A. F., Neves, M. G. P. M. S., Tomé, J. P. C., Tomé, A. C., Cavaleiro, J. A. S., Cunha, Â., Gomes, N. C. M., Alves, E., et al. (2010) · Marine Drugs · doi:10.3390/md8010091 · Cited by 421 · see citing works
Meylan, S., Porter, C. B. M., Yang, J. H., Belenky, P. A., Gutierrez, A., Lobritz, M. A., Park, J., Kim, S. H., Moskowitz, S. M., & Collins, J. J. (2017) · Cell chemical biology · doi:10.1016/j.chembiol.2016.12.015 · Cited by 384 · see citing works
Chiang, S. M., & Schellhorn, H. E. (2012) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2012.02.007 · Cited by 381 · see citing works
Cold Atmospheric Plasma: A Powerful Tool for Modern Medicine
Braný, D., Dvorská, D., Halášová, E., & Škovierová, H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21082932 · Cited by 357 · see citing works
A White-Box Machine Learning Approach for Revealing Antibiotic Mechanisms of Action
Yang, J. H., Wright, S. N., Hamblin, M., McCloskey, D., Alcantar, M. A., Schrübbers, L. C., Lopatkin, A. J., Satish, S., Nili, A., Palsson, B. Ø., et al. (2019) · Cell · doi:10.1016/j.cell.2019.04.016 · Cited by 317 · see citing works
de Luca, A., Smeekens, S. P., Casagrande, A., Iannitti, R., Conway, K. L., Gresnigt, M. S., Begun, J., Plantinga, T. S., Joosten, L. A. B., van der Meer, J. W. M., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1322831111 · Cited by 313 · see citing works
Mitochondrial respiratory-chain adaptations in macrophages contribute to antibacterial host defense
Garaude, J., Acín-Pérez, R., Martínez-Cano, S., Enamorado, M., Ugolini, M., Nistal-Villán, E., Hervás-Stubbs, S., Pelegrín, P., Sander, L. E., Enríquez, J. A., et al. (2016) · Nature Immunology · doi:10.1038/ni.3509 · Cited by 313 · see citing works
Bacterial Stress Responses during Host Infection
Fang, F. C., Frawley, E. R., Tapscott, T., & Vázquez‐Torres, A. (2016) · Cell Host & Microbe · doi:10.1016/j.chom.2016.07.009 · Cited by 313 · see citing works
Where in the world do bacteria experience oxidative stress?
Imlay, J. A. (2018) · Environmental Microbiology · doi:10.1111/1462-2920.14445 · Cited by 311 · see citing works
Reactive oxygen species induce antibiotic tolerance during systemic Staphylococcus aureus infection
Rowe, S. E., Wagner, N. J., Li, L., Beam, J. E., Wilkinson, A. D., Radlinski, L. C., Zhang, Q., Miao, E. A., & Conlon, B. P. (2019) · Nature Microbiology · doi:10.1038/s41564-019-0627-y · Cited by 305 · see citing works
Wang, Y., Lu, J., Engelstädter, J., Zhang, S., Ding, P., Mao, L., Yuan, Z., Bond, P. L., & Guo, J. (2020) · The ISME Journal · doi:10.1038/s41396-020-0679-2 · Cited by 305 · see citing works
Isocitrate lyase mediates broad antibiotic tolerance in Mycobacterium tuberculosis
Nandakumar, M., Nathan, C., & Rhee, K. Y. (2014) · Nature Communications · doi:10.1038/ncomms5306 · Cited by 298 · see citing works
Advancing antimicrobial strategies for managing oral biofilm infections
Jiao, Y., Tay, F. R., Niu, L.-N., & Chen, J.-H. (2019) · International Journal of Oral Science · doi:10.1038/s41368-019-0062-1 · Cited by 280 · see citing works
Glutathione activates virulence gene expression of an intracellular pathogen
Reniere, M. L., Whiteley, A. T., Hamilton, K. L., John, S. M., Lauer, P., Brennan, R. G., & Portnoy, D. A. (2015) · Nature · doi:10.1038/nature14029 · Cited by 277 · see citing works
Role of oxidative stress in persister tolerance
Wu, Y., Vulić, M., Keren, I., & Lewis, K. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00921-12 · Cited by 276 · see citing works
Diagnosing oxidative stress in bacteria: not as easy as you might think
Imlay, J. A. (2015) · Current Opinion in Microbiology · doi:10.1016/j.mib.2015.01.004 · Cited by 264 · see citing works
The Role of Reactive Oxygen Species (ROS) in the Formation of Extracellular Traps (ETs) in Humans
Stoiber, W., Obermayer, A., Steinbacher, P., & Krautgartner, W.-D. (2015) · Biomolecules · doi:10.3390/biom5020702 · Cited by 250 · see citing works
Abuaita, B. H., Schultz, T. L., & O’Riordan, M. X. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2018.10.005 · Cited by 223 · see citing works
Global regulation of gene expression by OxyR in an important human opportunistic pathogen
Wei, Q., Minh, P. N. L., Dötsch, A., Hildebrand, F., Panmanee, W., Elfarash, A. E. M., Schulz, S., Plaisance, S., Charlier, D., Hassett, D. J., et al. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks017 · Cited by 220 · see citing works
Nuclear receptor ERRα and coactivator PGC-1β are effectors of IFN-γ-induced host defensePreprint
Sonoda, J., Laganière, J., Mehl, I. R., Barish, G. D., Chong, L.-W., Li, X., Scheffler, I. E., Mock, D. C., Bataille, A. R., Robert, F., et al. (2007) · Genes & Development · doi:10.1101/gad.1553007 · Cited by 217 · see citing works
Christodoulou, D., Link, H., Fuhrer, T., Kochanowski, K., Gerosa, L., & Sauer, U. (2018) · Cell Systems · doi:10.1016/j.cels.2018.04.009 · Cited by 214 · see citing works
Reactive Oxygen Species Localization Programs Inflammation to Clear Microbes of Different Size
Warnatsch, A., Tsourouktsoglou, T.-D., Branzk, N., Wang, Q., Reincke, S., Herbst, S., Gutierrez, M. G., & Papayannopoulos, V. (2017) · Immunity · doi:10.1016/j.immuni.2017.02.013 · Cited by 183 · see citing works
The glyoxylate shunt, 60 years on
Dolan, S. K., & Welch, M. (2018) · Annual Review of Microbiology · doi:10.1146/annurev-micro-090817-062257 · Cited by 180 · see citing works
Kvam, E., Davis, B., Mondello, F. J., & Garner, A. L. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.05642-11 · Cited by 173 · see citing works
Metabolic defence against oxidative stress: the road less travelled so far
Lemire, J. A., Alhasawi, A. A., Appanna, V. D., Tharmalingam, S., & Appanna, V. D. (2017) · Journal of Applied Microbiology · doi:10.1111/jam.13509 · Cited by 148 · see citing works
Van Acker, H., Sass, A., Bazzini, S., De Roy, K., Udine, C., Messiaen, T., Riccardi, G., Boon, N., Nelis, H. J., Mahenthiralingam, E., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058943 · Cited by 135 · see citing works
Photodynamic Inactivation of Bacterial and Yeast Biofilms With a Cationic Porphyrin
Beirão, S., Fernandes, S., Coelho, J., Faustino, M. A. F., Tomé, J. P. C., Neves, M. G. P. M. S., Tomé, A. C., Almeida, A., & Cunha, Â. (2014) · Photochemistry and Photobiology · doi:10.1111/php.12331 · Cited by 128 · see citing works
Khademian, M., & Imlay, J. A. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1701587114 · Cited by 126 · see citing works
Herb, M., Gluschko, A., Wiegmann, K., Farid, A., Wolf, A., Utermöhlen, O., Krut, O., Krönke, M., & Schramm, M. (2019) · Science Signaling · doi:10.1126/scisignal.aar5926 · Cited by 119 · see citing works
Amaral, E. P., Conceição, E. L., Costa, D. L., Rocha, M. S., Marinho, J. M., Cordeiro‐Santos, M., Lima, M. R. D., Barbosa, T., Sher, A., & Andrade, B. B. (2016) · BMC Microbiology · doi:10.1186/s12866-016-0872-7 · Cited by 118 · see citing works
Non-lethal exposure to H2O2 boosts bacterial survival and evolvability against oxidative stress
Rodríguez-Rojas, A., Kim, J. J., Johnston, P. R., Makarova, O., Eravci, M., Weise, C., Hengge, R., & Rolff, J. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1008649 · Cited by 114 · see citing works
Redanz, S., Cheng, X., Giacaman, R. A., Pfeifer, C. S., Merritt, J. L., & Kreth, J. (2018) · Molecular Oral Microbiology · doi:10.1111/omi.12231 · Cited by 111 · see citing works
Reduce, Induce, Thrive: Bacterial Redox Sensing during Pathogenesis
Reniere, M. L. (2018) · Journal of Bacteriology · doi:10.1128/jb.00128-18 · Cited by 106 · see citing works
The role of mitochondrial ROS in antibacterial immunity
Pinegin, B. V., Vorobjeva, N. V., Pashenkov, M. V., & Chernyak, B. V. (2017) · Journal of Cellular Physiology · doi:10.1002/jcp.26117 · Cited by 105 · see citing works
Chronic Granulomatous Disease and Other Disorders of Phagocyte Function
Dinauer, M. C. (2005) · Hematology · doi:10.1182/asheducation-2005.1.89 · Cited by 94 · see citing works
Moving forward with reactive oxygen species involvement in antimicrobial lethality
Zhao, X., Hong, Y., & Drlica, K. (2014) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dku463 · Cited by 89 · see citing works
Fighting Mixed-Species Microbial Biofilms With Cold Atmospheric Plasma
Rao, Y., Shang, W., Yang, Y., Zhou, R., & Rao, X. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01000 · Cited by 86 · see citing works
Li, X., & Imlay, J. A. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.03.025 · Cited by 83 · see citing works
YihE Kinase Is a Central Regulator of Programmed Cell Death in Bacteria
Dorsey‐Oresto, A., Lu, T., Mosel, M., Wang, X., Salz, T., Drlica, K., & Zhao, X. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.01.026 · Cited by 80 · see citing works
Lau, G. W., Britigan, B. E., & Hassett, D. J. (2005) · Infection and Immunity · doi:10.1128/iai.73.4.2550-2553.2005 · Cited by 77 · see citing works
Hall, J. W., Yang, J., Guo, H., & Ji, Y. (2016) · Infection and Immunity · doi:10.1128/iai.00838-16 · Cited by 77 · see citing works
Wong, J., Chen, Y., & Gan, Y. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.06.002 · Cited by 74 · see citing works
Itzek, A., Zheng, L., Chen, Z., Merritt, J. L., & Kreth, J. (2011) · Journal of Bacteriology · doi:10.1128/jb.05791-11 · Cited by 67 · see citing works
Lemire, J. A., Milandu, Y., Auger, C., Bignucolo, A., Appanna, V. D., & Appanna, V. D. (2010) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2010.02034.x · Cited by 66 · see citing works
Grunenwald, C. M., Choby, J. E., Juttukonda, L. J., Beavers, W. N., Weiss, A., Torres, V. J., & Skaar, E. P. (2019) · mBio · doi:10.1128/mbio.02915-18 · Cited by 66 · see citing works
Shen, F., Tang, X., Cheng, W., Wang, Y., Wang, C., Shi, X., An, Y., Zhang, Q., Liu, M., Liu, B., et al. (2016) · Scientific Reports · doi:10.1038/srep19262 · Cited by 64 · see citing works
Superoxide-Mediated Protection of Escherichia coli from Antimicrobials
Mosel, M., Li, L., Drlica, K., & Zhao, X. (2013) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00754-13 · Cited by 61 · see citing works
Helicobacter pylori senses bleach (HOCl) as a chemoattractant using a cytosolic chemoreceptor
Perkins, A., Tudorica, D. A., Amieva, M. R., Remington, S. J., & Guillemin, K. J. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000395 · Cited by 61 · see citing works
Bignucolo, A., Appanna, V. P., Thomas, S. C., Auger, C., Han, S., Omri, A., & Appanna, V. D. (2013) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2013.07.002 · Cited by 59 · see citing works
Takahashi, N. K., Gruber, C. C., Yang, J. H., Liu, X., Braff, D., Yashaswini, C. N., Bhubhanil, S., Furuta, Y., Andreescu, S., Collins, J. J., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1707466114 · Cited by 57 · see citing works
Activation of the Listeria monocytogenes Virulence Program by a Reducing Environment
Portman, J. L., Dubensky, T. B., Peterson, B. N., Whiteley, A. T., & Portnoy, D. A. (2017) · mBio · doi:10.1128/mbio.01595-17 · Cited by 57 · see citing works
Luan, G., Hong, Y., Drlica, K., & Zhao, X. (2017) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01622-17 · Cited by 50 · see citing works
Resveratrol amelioratesSerratia marcescens-induced acute pneumonia in rats
Lu, C., Lai, H., Hsieh, S.-C., & Chen, J. (2008) · Journal of Leukocyte Biology · doi:10.1189/jlb.0907647 · Cited by 46 · see citing works
Influence of Reactive Oxygen Species onDe NovoAcquisition of Resistance to Bactericidal Antibiotics
Hoeksema, M., Brul, S., & ter Kuile, B. H. (2018) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02354-17 · Cited by 45 · see citing works
Mahakalkar, S. M., Nagrale, D., Gaur, S., Urade, C. S., Murhar, B., & Turankar, A. V. (2017) · Perspectives in Clinical Research · doi:10.4103/2229-3485.210450 · Cited by 34 · see citing works
Activity of Antibiotics in Chronic Granulomatous Disease Leukocytes
Jacobs, R. F., & Wilson, C. B. (1983) · Pediatric Research · doi:10.1203/00006450-198311000-00016 · Cited by 32 · see citing works
Collins, K. D., Hu, S., Grasberger, H., Kao, J. Y., & Ottemann, K. M. (2018) · Infection and Immunity · doi:10.1128/iai.00878-17 · Cited by 32 · see citing works
Superoxide protects Escherichia coli from bleomycin mediated lethality
Burger, R. M., & Drlica, K. (2009) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2009.07.009 · Cited by 27 · see citing works
Melo, T., Santos, N. F., Lopes, D., Alves, E., Maciel, E. A., Faustino, M. A. F., Tomé, J. P. C., Neves, M. G. P. M. S., Almeida, A., Domingues, P. M., et al. (2013) · Journal of Mass Spectrometry · doi:10.1002/jms.3301 · Cited by 26 · see citing works
Metabolic networks to generate pyruvate, PEP and ATP from glycerol in Pseudomonas fluorescens
Alhasawi, A. A., Thomas, S. C., & Appanna, V. D. (2016) · Enzyme and Microbial Technology · doi:10.1016/j.enzmictec.2016.01.007 · Cited by 25 · see citing works
Wang, P., Zhang, H., Liu, Y., Lv, R., Liu, X., Song, X., Wang, J., & Jiang, L. (2019) · Microbial Pathogenesis · doi:10.1016/j.micpath.2019.103925 · Cited by 16 · see citing works
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Alfei, S., Schito, G. C., Schito, A. M., & Zuccari, G. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25137182 · Cited by 316 · see citing works
Antimicrobials Functioning through ROS-Mediated Mechanisms: Current Insights
Vaishampayan, A., & Grohmann, E. (2021) · Microorganisms · doi:10.3390/microorganisms10010061 · Cited by 181 · see citing works
The Role of Reactive Species on Innate Immunity
Andrés, C., Pérez de la Lastra, J., Juan, C., Plou, F., & Pérez-Lebeña, E. (2022) · Vaccines · doi:10.3390/vaccines10101735 · Cited by 142 · see citing works
Modi, S. K., Gaur, S., Sengupta, M., & Singh, M. S. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1135579 · Cited by 146 · see citing works
Priatama, R. A., Pervitasari, A. N., Park, S., Park, S. J., & Lee, Y. K. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094609 · Cited by 139 · see citing works
Šimat, V., Rathod, N. B., Čagalj, M., Hamed, I., & Mekinić, I. G. (2022) · Marine Drugs · doi:10.3390/md20030206 · Cited by 124 · see citing works
Antibiotic adjuvants: synergistic tool to combat multi-drug resistant pathogens
Kumar, V., Yasmeen, N., Pandey, A., Chaudhary, A. A., Alawam, A. S., Rudayni, H. A., Islam, A., Lakhawat, S. S., Sharma, P. K., & Shahid, M. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1293633 · Cited by 121 · see citing works
Titanium dioxide nanoparticles: Recent progress in antimicrobial applications
Younis, A. B., Haddad, Y., Košarišťanová, L., & Šmerková, K. (2022) · Wiley Interdisciplinary Reviews Nanomedicine and Nanobiotechnology · doi:10.1002/wnan.1860 · Cited by 117 · see citing works
Forcados, G. E., Muhammad, A. I., Oladipo, O. O., Makama, S., & Meseko, C. A. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.654813 · Cited by 98 · see citing works
Shahalaei, M., Azad, A. K., Sulaiman, W. M. A. W., Derakhshani, A., Mofakham, E. B., Mallandrich, M., Kumarasamy, V., & Subramaniyan, V. (2024) · Frontiers in Chemistry · doi:10.3389/fchem.2024.1398979 · Cited by 93 · see citing works
Su, H., Wang, Y., Xu, J. H., Omar, A. A., Grosser, J. W., Ćalović, M., Zhang, L., Yu, F., Vakulskas, C. A., & Wang, N. (2023) · Nature Communications · doi:10.1038/s41467-023-39714-9 · Cited by 87 · see citing works
Yong, S.-S., Lee, J.-I., & Kang, D. (2022) · Food Microbiology · doi:10.1016/j.fm.2022.104119 · Cited by 78 · see citing works
Edge, R., & Truscott, T. (2021) · Oxygen · doi:10.3390/oxygen1020009 · Cited by 64 · see citing works
Nutritional and lifestyle management of the aging journey: A narrative review
Kassis, A. N., Fichot, M., Horcajada, M.-N., Horstman, A. M. H., Duncan, P. I., Bergonzelli, G. E., Preitner, N., Zimmermann, D., Bosco, N., Vidal, K., et al. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2022.1087505 · Cited by 75 · see citing works
Majumder, A., Sarkar, C., Das, I., Sk, S., Bandyopadhyay, S., Mandal, S., & Bera, M. (2023) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.2c21899 · Cited by 64 · see citing works
Zhao, W., Zhang, Y. L., Chen, J., & Hu, D. (2024) · Redox Biology · doi:10.1016/j.redox.2024.103451 · Cited by 61 · see citing works
Anti- and Pro-Oxidant Properties of Essential Oils against Antimicrobial Resistance
Kong, A. S.-Y., Maran, S., Yap, P. S. X., Lim, S. E., Yang, S.-K., Cheng, W.-H., Tan, Y.-H., & Lai, K. (2022) · Antioxidants · doi:10.3390/antiox11091819 · Cited by 57 · see citing works
Ginsenosides for therapeutically targeting inflammation through modulation of oxidative stress
Paik, S., Song, G., & Jo, E. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.110461 · Cited by 58 · see citing works
Yoo, W., Shealy, N. G., Zieba, J. K., Torres, T. P., Baltagulov, M., Thomas, J., Shelton, C. D., McGovern, A. G., Foegeding, N. J., Olsan, E. E., et al. (2024) · Cell Host & Microbe · doi:10.1016/j.chom.2024.05.001 · Cited by 56 · see citing works
Modulation of reactive oxygen species to enhance sonodynamic therapy
Liu, X., Pan, X., Wang, C., & Liu, H. (2022) · Particuology · doi:10.1016/j.partic.2022.08.001 · Cited by 53 · see citing works
Dayyih, A. A., Gutberlet, B., Preis, E., Engelhardt, K. H., Amin, M. U., Abdelsalam, A. M., Bonsu, M., & Bakowsky, U. (2022) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.2c02741 · Cited by 52 · see citing works
The Redox Properties of Polyphenols and Their Role in ROS Generation for Biomedical Applications
Bolaños‐Cardet, J., Pepió‐Tárrega, B., Saiz‐Poseu, J., López‐Moral, A., Ullah, F., Yuste, V. J., Ruiz‐Molina, D., & Suárez–García, S. (2025) · Angewandte Chemie International Edition · doi:10.1002/anie.202513698 · Cited by 54 · see citing works
Singh, S. K., Mazumder, S., Vincy, A., Hiremath, N., Kumar, R., Banerjee, I., & Vankayala, R. (2023) · ACS Applied Nano Materials · doi:10.1021/acsanm.2c04551 · Cited by 48 · see citing works
Zhang, J., Cheng, L., Li, H., Chen, X., Zhang, L., Shan, T., Wang, J., Chen, D., Shen, J., Zhou, X., et al. (2024) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2024.178020 · Cited by 44 · see citing works
Self-citationHost Immune Responses to Clostridioides difficile: Toxins and Beyond
Nibbering, B., Gerding, D. N., Kuijper, E. J., Zwittink, R. D., & Smits, W. K. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.804949 · Cited by 44 · see citing works
Thi, P. L., Tran, D. L., Thi, T. T. H., Lee, Y., & Park, K. D. (2022) · Regenerative Biomaterials · doi:10.1093/rb/rbac069 · Cited by 43 · see citing works
Polyamine-mediated mechanisms contribute to oxidative stress tolerance in Pseudomonas syringae
Solmi, L., Rossi, F. R., Romero, F. M., Bach‐Pages, M., Preston, G. M., Ruiz, O. A., & Gárriz, A. (2023) · Scientific Reports · doi:10.1038/s41598-023-31239-x · Cited by 43 · see citing works
Surface Chemistry of Biologically Active Reducible Oxide Nanozymes
Neal, C. J., Kolanthai, E., Wei, F., Coathup, M. J., & Seal, S. (2023) · Advanced Materials · doi:10.1002/adma.202211261 · Cited by 43 · see citing works
Galhano, J., Capelo, J. L., Lorenzo, J., Lodeiro, C., & Oliveira, E. (2025) · ACS Nano · doi:10.1021/acsnano.5c08822 · Cited by 41 · see citing works
Yan, B., Fung, K., Ye, S., Lai, P.-M., Wei, Y., Sze, K. H., Yang, D., Gao, P., & Kao, R. Y. T. (2022) · Chemical Science · doi:10.1039/d2sc04307f · Cited by 38 · see citing works
Li, H., Xu, J., Hu, J., Hu, Q.-Y., Fang, X., Sun, Z., Xu, Z., & Zhang, L. (2022) · Biomaterials Science · doi:10.1039/d2bm01099b · Cited by 37 · see citing works
Self-citationThe Role of Microbiota-Derived Metabolites in Colorectal Cancer
Duizer, C., & de Zoete, M. R. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24098024 · Cited by 37 · see citing works
Manna, B., Zhou, X., & Singhal, N. (2025) · Water Research · doi:10.1016/j.watres.2025.123366 · Cited by 37 · see citing works
Self-citationAribisala, . O., & Sabiu, S. (2022) · Biomolecules · doi:10.3390/biom12111545 · Cited by 36 · see citing works
Rebelo, A., Almeida, A. A., Peixe, L. M. S. V., Antunes, P., & Novais, C. (2023) · Antibiotics · doi:10.3390/antibiotics12091474 · Cited by 34 · see citing works
Awassa, J., Cornu, D., Ruby, C., & El‐Kirat‐Chatel, S. (2022) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2022.112623 · Cited by 35 · see citing works
Birhanu, R., Afrasa, M. A., & Hone, F. G. (2023) · Journal of Nanomaterials · doi:10.1155/2023/8435480 · Cited by 34 · see citing works
Tănase, D. M., Apostol, A. G., Costea, C. F., Tărniceriu, C. C., Tudorancea, I., Maranducă, M. A., Floria, M., & Șerban, I. L. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14030534 · Cited by 34 · see citing works
Antunes, J. C., Moreira, I. P., Gomes, F., Cunha, F., Henriques, M., & Fangueiro, R. M. E. S. (2022) · Polymers · doi:10.3390/polym14081599 · Cited by 32 · see citing works
Ranathunga, K., Yapa, P. N., Munaweera, I., Weerasekera, M. M., & Sandaruwan, C. (2024) · RSC Advances · doi:10.1039/d4ra03136a · Cited by 31 · see citing works
Margarita, V., Bailey, N. P., Rappelli, P., Diaz, N., Dessì, D., Fettweis, J. M., Hirt, R. P., & Fiori, P. L. (2022) · mBio · doi:10.1128/mbio.00918-22 · Cited by 32 · see citing works
Antibacterial and Antibiofilm Potency of Menadione Against Multidrug-Resistant S. aureus
Mone, N., Kamble, E. E., Pardesi, K. R., & Satpute, S. (2022) · Current Microbiology · doi:10.1007/s00284-022-02975-6 · Cited by 23 · see citing works
From ubiquity to specificity: The diverse functions of bacterial thioredoxin systems
Anjou, C., Lotoux, A., Morvan, C., & Martin‐Verstraete, I. (2024) · Environmental Microbiology · doi:10.1111/1462-2920.16668 · Cited by 26 · see citing works
Amrhar, R., Singh, J., Eesaee, M., Carrière, P., Saïdi, A., & Nguyen‐Tri, P. (2025) · Results in Surfaces and Interfaces · doi:10.1016/j.rsurfi.2025.100497 · Cited by 27 · see citing works
Day, N. J., Zhang, T., Gaffrey, M. J., Zhao, R., Fillmore, T., Moore, R. J., Rodney, G. G., & Qian, W. (2022) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2022.10.300 · Cited by 26 · see citing works
Ouyang, Y., Tang, X., Zhao, Y. H., Zuo, X., Ren, X., Wang, J., Zou, L., & Lu, J. (2023) · Antioxidants · doi:10.3390/antiox12061180 · Cited by 25 · see citing works
Promila, L., Joshi, A., Khan, S., Aggarwal, A., & Lahiri, A. (2023) · Mitochondrion · doi:10.1016/j.mito.2023.10.004 · Cited by 25 · see citing works
Arbuscular mycorrhizal fungus alleviates anthracnose disease in tea seedlings
Chen, W., Ye, T., Sun, Q., Niu, T., & Zhang, J. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2022.1058092 · Cited by 25 · see citing works
Abdel-Hakeem, M. A., Maksoud, A. I. A. E., Aladhadh, M. A., Almuryif, K. A., Elsanhoty, R. M., & Elebeedy, D. (2022) · Antibiotics · doi:10.3390/antibiotics11111530 · Cited by 22 · see citing works
pH-activated antibiofilm strategies for controlling dental caries
Wang, X., Li, J., Zhang, S. J., Zhou, W., Zhang, L., & Huang, X. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1130506 · Cited by 22 · see citing works
Mistretta, M., Cimino, M., Campagne, P., Volant, S., Kornobis, É., Hebert, O., Rochais, C., Dallemagne, P., Lecoutey, C., Tisnerat, C., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-48269-2 · Cited by 22 · see citing works
A Short Tale of the Origin of Proteins and Ribosome Evolution
Farías‐Rico, J. A., & Mourra-Díaz, C. M. (2022) · Microorganisms · doi:10.3390/microorganisms10112115 · Cited by 21 · see citing works
Liang, P., Wang, L., Yang, S., Pan, X., Li, J., Liang, Y., Li, J., Li, J., & Zhou, B. (2022) · Journal of Inflammation · doi:10.1186/s12950-022-00319-6 · Cited by 21 · see citing works
Immunometabolic Regulation of Bacterial Infection, Biofilms, and Antibiotic Susceptibility
Chen, Y.-T., Lohia, G. K., Chen, S., & Riquelme, S. A. (2024) · Journal of Innate Immunity · doi:10.1159/000536649 · Cited by 21 · see citing works
Kim, S., Park, H., Pandey, S., Jeong, D., Lee, C.-T., Yeon, J., Park, S., & Kang, M. (2022) · Nanomaterials · doi:10.3390/nano12244417 · Cited by 20 · see citing works
A novel aquaporin Aagp contributes to Streptococcus suis H 2 O 2 efflux and virulence
Zhu, X., Wang, S., Du, Y., Liang, Z., Yao, H., Chen, X., & Wu, Z. (2023) · Virulence · doi:10.1080/21505594.2023.2249789 · Cited by 20 · see citing works
Human DNA Mutations and their Impact on Genetic Disorders
Samir, S. (2023) · Recent Patents on Biotechnology · doi:10.2174/0118722083255081231020055309 · Cited by 20 · see citing works
Nikolaou, A., Salvador, M., Wright, I. P., Wantock, T., Sandison, G., Harle, T., Carta, D., & Gutierrez‐Merino, J. (2024) · Microbiological Research · doi:10.1016/j.micres.2024.127986 · Cited by 20 · see citing works
Role of Reactive Oxygen Species against Pathogens in Relation to Postharvest Disease of Papaya Fruit
Feng, L., Sun, J., Jiang, Y., & Duan, X. (2022) · Horticulturae · doi:10.3390/horticulturae8030205 · Cited by 19 · see citing works
Relationship between mineral nutrition, plant diseases, and pests
Weinmann, M., Bradáčová, K., & Nikolić, M. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-819773-8.00009-5 · Cited by 19 · see citing works
Aluta, U. P., Aderolu, A. Z., Ishola, I. O., Alyassin, M., Morris, G. A., & Olajide, O. A. (2023) · Food Hydrocolloids for Health · doi:10.1016/j.fhfh.2023.100135 · Cited by 19 · see citing works
Zhang, X., Cao, L., Li, H., Xiong, Z., Fu, Z., Zhang, Z., Xie, W., Cui, H., Zhang, S., Tang, Y., et al. (2023) · Journal of Materials Chemistry B · doi:10.1039/d2tb02797f · Cited by 19 · see citing works
Self-citationNovel Aptamer Strategies in Combating Bacterial Infections: From Diagnostics to Therapeutics
Ye, Z., Chen, H., Weinans, H., van der Wal, B., & Rios, J. L. (2024) · Pharmaceutics · doi:10.3390/pharmaceutics16091140 · Cited by 18 · see citing works
Ledger, E. V. K., Lau, K., Tate, E. W., & Edwards, A. M. (2023) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01206-22 · Cited by 17 · see citing works
Burgeoning Single-Atom Nanozymes for Efficient Bacterial Elimination
Shi, T., Cui, Y., Yuan, H., Qi, R., & Yu, Y. (2023) · Nanomaterials · doi:10.3390/nano13202760 · Cited by 18 · see citing works
Yang, Y., Ma, S., Li, T., He, J., Liu, S., Liu, H., Zhang, J., Zhou, X., Liu, L., & Yang, S. (2023) · Frontiers of Chemical Science and Engineering · doi:10.1007/s11705-023-2361-5 · Cited by 18 · see citing works
Self-citationThe Redox Properties of Polyphenols and Their Role in ROS Generation for Biomedical Applications
Bolaños‐Cardet, J., Pepió‐Tárrega, B., Saiz‐Poseu, J., López‐Moral, A., Ullah, F., Yuste, V. J., Ruiz‐Molina, D., & Suárez–García, S. (2025) · Angewandte Chemie · doi:10.1002/ange.202513698 · Cited by 16 · see citing works
Li, Y., Li, B., Guo, X. D., Wang, H., & Cheng, L. (2023) · Journal of Dentistry · doi:10.1016/j.jdent.2023.104678 · Cited by 16 · see citing works
Self-citationJayaseelan, E., Nixon, P., Bewyn Joseph., P., Gnanaraj, M. A., Kalivel, P., & Ananthi, N. (2024) · Nano-Structures & Nano-Objects · doi:10.1016/j.nanoso.2024.101119 · Cited by 16 · see citing works
Singh, S. S., Jena, B., Roy, S., Nayak, S., Behera, S. K., Chakrabortty, S., Tripathy, S. K., Khan, M. A., Kumar, R., Jeon, B., et al. (2024) · Chemical Engineering Journal · doi:10.1016/j.cej.2024.151788 · Cited by 16 · see citing works
Dereje, D. M., Pontremoli, C., García, A., Galliano, S., Colilla, M., González, B., Vallet‐Regí, M., Izquierdo‐Barba, I., & Barbero, N. (2024) · Polymers · doi:10.3390/polym16141962 · Cited by 17 · see citing works
Bhattacharya, S., Gupta, N., Dutta, A., Bonomo, M. G., Milella, L., Sarker, S. D., & Nahar, L. (2025) · Phytochemistry Reviews · doi:10.1007/s11101-025-10179-6 · Cited by 17 · see citing works
He, W., Xu, T., Wang, M., Ni, N., Su, Y., & Fan, X. (2025) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2025.09.040 · Cited by 19 · see citing works
Mendez, D. F. G., Rengifo‐Herrera, J. A., Sanabria, J., & Wist, J. (2022) · Microorganisms · doi:10.3390/microorganisms10071323 · Cited by 14 · see citing works
Wardell, S. J. T., Yung, D. B. Y., Gupta, A., Bostina, M., Overhage, J., Hancock, R. E. W., & Pletzer, D. (2025) · npj Biofilms and Microbiomes · doi:10.1038/s41522-024-00637-y · Cited by 14 · see citing works
Kim, J. Y., Kim, J. Y., Park, J. Y., Kim, J.-S., Seo, M.-K., Shin, M., & Kim, J. (2023) · Applied Biological Chemistry · doi:10.1186/s13765-023-00803-4 · Cited by 14 · see citing works
Manaa, A. O., Baghdadi, H. H., Heikal, L., & El‐Hosseiny, L. S. (2025) · Scientific Reports · doi:10.1038/s41598-025-18967-y · Cited by 13 · see citing works
Fusobacterium nucleatum elicits subspecies-specific responses in human neutrophils
Muchova, M., Kuehne, S. A., Grant, M. M., Smith, P. P., Nagi, M., Chapple, I., & Hirschfeld, J. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1449539 · Cited by 13 · see citing works
Zhou, Y., Zhou, X., Zhang, J., Zhao, Y., Ye, Z., Xu, F., & Li, F. (2025) · Analytical Chemistry · doi:10.1021/acs.analchem.4c05503 · Cited by 13 · see citing works
Self-citationStimulus-responsive nanomaterials for ocular antimicrobial therapy
Zhang, T., & Luo, Z. (2025) · Nanoscale · doi:10.1039/d4nr05462h · Cited by 13 · see citing works
Alghamdi, A. I., Ababutain, I. M., Alonizan, N., Hjiri, M., Hammad, A. H., Zerrad, B., & Aïda, M. S. (2022) · Applied Nanoscience · doi:10.1007/s13204-021-02274-9 · Cited by 13 · see citing works
Gurushantha, K., Swetha, B. N., Chinnam, S., Keshavamurthy, K., Meena, S., Surendra, B. S., Malini, S., & Roopa, K. P. (2023) · Inorganic Chemistry Communications · doi:10.1016/j.inoche.2023.111162 · Cited by 13 · see citing works
Ikram, M., Butt, A. R., Fatima, A., Shahzadi, I., Haider, A., Ul‐Hamid, A., Alshahrani, T. M., & Nabgan, W. (2023) · Journal of Photochemistry and Photobiology A Chemistry · doi:10.1016/j.jphotochem.2023.114835 · Cited by 12 · see citing works
The 2D Ti3C2T MXene-enabled self-cleaning and self-sterilizing lacquer coatings for offset printing
Jakubczak, M., Bury, D., Rozmysłowska‐Wojciechowska, A., Mitrzak, J., Budnik, K., Moszczyńska, D., & Jastrzębska, A. M. (2023) · Journal of Alloys and Compounds · doi:10.1016/j.jallcom.2023.173318 · Cited by 12 · see citing works
Johnson, A., Wu, J., Zhou, Z., Li, Y., Yin, Y., Ponder, M. A., Kim, Y., Shuai, D., & Huang, H. (2024) · ACS Food Science & Technology · doi:10.1021/acsfoodscitech.4c00040 · Cited by 12 · see citing works
Rawat, S. S., Keshri, A. K., Arora, N., Kaur, R., Mishra, A., Kumar, R., & Prasad, A. (2024) · Journal of Extracellular Vesicles · doi:10.1002/jev2.12448 · Cited by 12 · see citing works
Priyanka, P., Sharma, S., & Sharma, M. (2024) · Microbial Pathogenesis · doi:10.1016/j.micpath.2024.106757 · Cited by 12 · see citing works
Devaraji, M., Thanikachalam, P. V., Rajalakshmi, A. S., Rohan, S., & Bhagyalakshmi, J. (2024) · Nano-Structures & Nano-Objects · doi:10.1016/j.nanoso.2024.101376 · Cited by 12 · see citing works
Fadda, H., Khan, R. H., Shqair, Y., Uslu, C., Panov, A. V., & Lyakhovich, A. (2025) · Aquatic Toxicology · doi:10.1016/j.aquatox.2025.107284 · Cited by 12 · see citing works
Li, Z., Jiang, J., Sun, K., & Ye, S. (2025) · Food Microbiology · doi:10.1016/j.fm.2025.104784 · Cited by 12 · see citing works
Shao, Y., Wang, C., Lu, T., Jiang, J., Li, C., & Wang, X. (2023) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2023.109237 · Cited by 12 · see citing works
Narita, K., Fukushi, R., Yamane, K., Okumura, Y., Koi, T., Asano, K., & Nakane, A. (2025) · Applied and Environmental Microbiology · doi:10.1128/aem.01886-24 · Cited by 12 · see citing works
Khan, A., Khan, R. A., Anas, M., Qadri, T. A., Ashiq, B., Younis, T., Ullah, N., Khan, A. M., Nasreen, Z., & Shinwari, Z. K. (2026) · Nano-Horizons Journal of Nanosciences and Nanotechnologies · doi:10.25159/3005-2602/20247 · Cited by 12 · see citing works
Chen, Y., Liu, P., Tang, K., Liu, H., & Liao, T. (2022) · Microbiology Spectrum · doi:10.1128/spectrum.03172-22 · Cited by 12 · see citing works
Hameed, R. K., Al‐Jawad, S. M. H., & Imran, N. J. (2024) · Optical and Quantum Electronics · doi:10.1007/s11082-024-07043-w · Cited by 11 · see citing works
Manna, B., Jay, E., Zhang, W., Zhou, X., Lyu, B., Thomas, G. M., & Singhal, N. (2024) · Water · doi:10.3390/w16182655 · Cited by 11 · see citing works
Self-citationZhang, R., Hartline, C. J., & Zhang, F. (2024) · mSystems · doi:10.1128/msystems.01295-24 · Cited by 11 · see citing works
Zirconium-Coated β-Cyclodextrin Nanomaterials for Biofilm Eradication
Gupta, A., Luong, J. H. T., & Gedanken, A. (2023) · ACS Applied Bio Materials · doi:10.1021/acsabm.3c00679 · Cited by 10 · see citing works
Mohammed, A. E., Aldahasi, R. M., Rahman, I., Shami, A., Alotaibi, M. O., BinShabaib, M. S., ALHarthi, S. S., & Aabed, K. (2024) · PeerJ · doi:10.7717/peerj.17241 · Cited by 10 · see citing works
Dias-Souza, M. V., Alves, A. L., Pagnin, S., Veiga, A. A., Haq, I. U., Alonazi, W. B., & dos Santos, V. L. (2024) · Microbial Cell Factories · doi:10.1186/s12934-024-02502-1 · Cited by 10 · see citing works
- Authors
- Li, H., Zhou, X., Huang, Y., Liao, B., Cheng, L., & Ren, B.
- Affiliations
- Sichuan University (CN)
- Corresponding author
- Cheng, Lei
- Ren, Biao
- Venue
- Frontiers in Microbiology
- Publisher
- Frontiers Media SA
- Published
- 2021-02-04
- Volume
- 11
- Pages
- 622534-622534
- ISSN
- 1664-302X (ISSN-L)
- PMC
- PMC7889972
- OpenAlex
- W4206764679
- Cited by
- 284
- References
- 92
- Citations by year
- 2026: 39 · 2025: 79 · 2024: 65 · 2023: 52 · 2022: 41 · 2021: 8
- FWCI
- 4.35
- Type
- journal article
- Language
- en
- Update notices
- corrigendum (2021-05-13)
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Microbiology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Natural Science Foundation of China
- Applied Basic Research Program of Sichuan Province
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Keywords
- reactive oxygen species, pathogen clearance, antibacterial strategies, pathogenic bacteria
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 ›
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