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The Acinetobacter baumannii Znu System Overcomes Host-Imposed Nutrient Zinc Limitation

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Multidrug-resistant Acinetobacter baumannii resists reactive oxygen species and survives in macrophages

Sato, Y., Unno, Y., 千鶴, 宮., Ubagai, T., & Ono, Y. (2019) · Scientific Reports · doi:10.1038/s41598-019-53846-3 · Cited by 56 · see citing works

The Response of Acinetobacter baumannii to Hydrogen Sulfide Reveals Two Independent Persulfide-Sensing Systems and a Connection to Biofilm Regulation

Walsh, B. J. C., Wang, J., Edmonds, K. A., Palmer, L. D., Zhang, Y., Trinidad, J. C., Skaar, E. P., & Giedroc, D. P. (2020) · mBio · doi:10.1128/mbio.01254-20 · Cited by 55 · see citing works

Identification of Two Variants of Acinetobacter baumannii Strain ATCC 17978 with Distinct Genotypes and Phenotypes

Wijers, C. D. M., Pham, L., Menon, S., Boyd, K. L., Noel, H. R., Skaar, E. P., Gaddy, J. A., Palmer, L. D., & Noto, M. J. (2021) · Infection and Immunity · doi:10.1128/iai.00454-21 · Cited by 46 · see citing works

The intracellular life of Acinetobacter baumannii

Maure, A., Robino, E., & der Henst, C. V. (2023) · Trends in Microbiology · doi:10.1016/j.tim.2023.06.007 · Cited by 46 · see citing works

Developing new therapeutic approaches for treating infections caused by multi-drug resistant Acinetobacter baumannii

Gallagher, P., & Baker, S. G. (2020) · Journal of Infection · doi:10.1016/j.jinf.2020.10.016 · Cited by 45 · see citing works

Activity-Based NIR Bioluminescence Probe Enables Discovery of Diet-Induced Modulation of the Tumor Microenvironment via Nitric Oxide

Yadav, A. K., Lee, M., Lucero, M. Y., Su, S., Reinhardt, C. J., & Chan, J. (2022) · ACS Central Science · doi:10.1021/acscentsci.1c00317 · Cited by 44 · see citing works

Histidine Utilization Is a Critical Determinant of Acinetobacter Pathogenesis

Lonergan, Z. R., Palmer, L. D., & Skaar, E. P. (2020) · Infection and Immunity · doi:10.1128/iai.00118-20 · Cited by 40 · see citing works

Promising Acinetobacter baumannii Vaccine Candidates and Drug Targets in Recent Years

Tan, Y. C., & Lahiri, C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.900509 · Cited by 40 · see citing works

Capsule mutations serve as a key strategy of phage resistance evolution of K54 hypervirulent Klebsiella pneumoniae

Fu, Y., Yin, M., Cao, L., Lu, Y., Li, Y., & Zhang, L. (2025) · Communications Biology · doi:10.1038/s42003-025-07687-8 · Cited by 41 · see citing works

The Manganese-Responsive Transcriptional Regulator MumR Protects Acinetobacter baumannii from Oxidative Stress

Green, E. R., Juttukonda, L. J., & Skaar, E. P. (2019) · Infection and Immunity · doi:10.1128/iai.00762-19 · Cited by 37 · see citing works

Depletion of Alveolar Macrophages Increases Pulmonary Neutrophil Infiltration, Tissue Damage, and Sepsis in a Murine Model of Acinetobacter baumannii Pneumonia

Lee, H. H., Aslanyan, L., Vidyasagar, A., Brennan, M. B., Tauber, M. S., Carrillo-Sepúlveda, M. A., Dores, M. R., Rigel, N. W., & Martinez, L. R. (2020) · Infection and Immunity · doi:10.1128/iai.00128-20 · Cited by 37 · see citing works

Stress responses linked to antimicrobial resistance in Acinetobacter species

Shin, B., Park, C., & Park, W. (2020) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-10317-z · Cited by 34 · see citing works

An insight into MDR Acinetobacter baumannii infection and its pathogenesis: Potential therapeutic targets and challenges

Singh, S., Singh, S., Trivedi, M., & Dwivedi, M. (2024) · Microbial Pathogenesis · doi:10.1016/j.micpath.2024.106674 · Cited by 33 · see citing works

Quantifying the Fast Dynamics of HClO in Living Cells by a Fluorescence Probe Capable of Responding to Oxidation and Reduction Events within the Time Scale of Milliseconds

Li, P., Jia, Y., Zhao, N., Zhang, Y., Zhou, P., Lou, Z., Qiao, Y., Zhang, P., Wen, S., & Han, K. (2020) · Analytical Chemistry · doi:10.1021/acs.analchem.0c01703 · Cited by 32 · see citing works

The Molecular Basis of Acinetobacter baumannii Cadmium Toxicity and Resistance

Alquethamy, S. F., Adams, F. G., Maharjan, R. P., Delgado, N. N., Zang, M., Ganio, K., Paton, J. C., Hassan, K. A., Paulsen, I. T., McDevitt, C. A., et al. (2021) · Applied and Environmental Microbiology · doi:10.1128/aem.01718-21 · Cited by 28 · see citing works

Nitrogen Metabolism in Pseudomonas putida: Functional Analysis Using Random Barcode Transposon Sequencing

Schmidt, M., Pearson, A. N., Incha, M. R., Thompson, M. G., Baidoo, E. E. K., Kakumanu, R., Mukhopadhyay, A., Shih, P. M., Deutschbauer, A. M., Blank, L. M., et al. (2022) · Applied and Environmental Microbiology · doi:10.1128/aem.02430-21 · Cited by 28 · see citing works

CsrA-Controlled Proteins Reveal New Dimensions of Acinetobacter baumannii Desiccation Tolerance

Oda, Y., Shapiro, M. M., Lewis, N. M., Zhong, X., Huse, H., Zhong, W., Bruce, J. E., Manoil, C., & Harwood, C. S. (2022) · Journal of Bacteriology · doi:10.1128/jb.00479-21 · Cited by 27 · see citing works

Evolutionarily stable gene clusters shed light on the common grounds of pathogenicity in the Acinetobacter calcoaceticus-baumannii complex

Djahanschiri, B., Venanzio, G. D., Distel, J. S., Breisch, J., Dieckmann, M. A., Goesmann, A., Averhoff, B., Göttig, S., Wilharm, G., Feldman, M. F., et al. (2022) · PLoS Genetics · doi:10.1371/journal.pgen.1010020 · Cited by 27 · see citing works

DksA is a conserved master regulator of stress response in Acinetobacter baumannii

Maharjan, R. P., Sullivan, G. J., Adams, F. G., Shah, B. S., Hawkey, J., Delgado, N. N., Semenec, L., Dinh, H., Li, L., Short, F. L., et al. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad341 · Cited by 26 · see citing works

The tRNA methyltransferase TrmB is critical for Acinetobacter baumannii stress responses and pulmonary infection

McGuffey, J. C., Jackson-Litteken, C. D., Venanzio, G. D., Zimmer, A. A., Lewis, J. M., Distel, J. S., Kim, K. Q., Zaher, H. S., Alfonzo, J. D., Scott, N. E., et al. (2023) · mBio · doi:10.1128/mbio.01416-23 · Cited by 24 · see citing works

Tightly controlled response to oxidative stress; an important factor in the tolerance of Bacteroides fragilis

Yekani, M., Baghi, H. B., Vahed, S. Z., Ghanbari, H., Hoseinpur, R., Azargun, R., Azimi, S., & Memar, M. Y. (2021) · Research in Microbiology · doi:10.1016/j.resmic.2021.103798 · Cited by 22 · see citing works

Proteomic and Systematic Functional Profiling Unveils Citral Targeting Antibiotic Resistance, Antioxidant Defense, and Biofilm-Associated Two-Component Systems of Acinetobacter baumannii To Encumber Biofilm and Virulence Traits

Selvaraj, A., Valliammai, A., Muthuramalingam, P., Sethupathy, S., Ganapathy, A. S., Ramesh, M., & Pandian, S. K. (2020) · mSystems · doi:10.1128/msystems.00986-20 · Cited by 20 · see citing works

Coordinated interaction between Lon protease and catalase-peroxidase regulates virulence and oxidative stress management during Salmonellosis

Kirthika, P., Jawalagatti, V., Senevirathne, A., & Lee, J. H. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2064705 · Cited by 16 · see citing works

Genomics-guided identification of a conserved CptBA-like toxin-antitoxin system in Acinetobacter baumannii

ElBanna, S. A., Moneib, N. A., Aziz, R. K., & Samir, R. (2020) · Journal of Advanced Research · doi:10.1016/j.jare.2020.11.007 · Cited by 16 · see citing works

Diclofenac sensitizes multi-drug resistant Acinetobacter baumannii to colistin

Bisaro, F., Jackson-Litteken, C. D., McGuffey, J. C., Hooppaw, A. J., Bodrog, S., Jebeli, L., Janet-Maitre, M., Ortiz-Marquez, J. C. F., van Opijnen, T., Scott, N. E., et al. (2024) · PLoS Pathogens · doi:10.1371/journal.ppat.1012705 · Cited by 13 · see citing works

Assessing the Role of Cold-Shock Protein C: a Novel Regulator of Acinetobacter baumannii Biofilm Formation and Virulence

Tomlinson, B. R., Denham, G. A., Torres, N. J., Brzozowski, R. S., Allen, J. L., Jackson, J. K., Eswara, P. J., & Shaw, L. N. (2022) · Infection and Immunity · doi:10.1128/iai.00376-22 · Cited by 13 · see citing works

Bacillus anthracis Responds to Targocil-Induced Envelope Damage through EdsRS Activation of Cardiolipin Synthesis

Laut, C. L., Perry, W., Metzger, A. L., Weiss, A., Stauff, D. L., Walker, S., Caprioli, R. M., & Skaar, E. P. (2020) · mBio · doi:10.1128/mbio.03375-19 · Cited by 12 · see citing works

The Influence of Blue Light and the BlsA Photoreceptor on the Oxidative Stress Resistance Mechanisms of Acinetobacter baumannii

Squire, M. S., Townsend, H. A., & Actis, L. A. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.856953 · Cited by 12 · see citing works

Catalases of the polyextremophylic Andean isolate Acinetobacter sp. Ver 3 confer adaptive response to H2O2 and UV radiation

Sartorio, M. G., Repizo, G. D., & Cortez, N. (2020) · FEBS Journal · doi:10.1111/febs.15244 · Cited by 12 · see citing works

OxyR-controlled surface polysaccharide production and biofilm formation in Acinetobacter oleivorans DR1

Shin, B., Park, C., & Park, W. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-10303-5 · Cited by 11 · see citing works

Mechanistic and structural insights into the bifunctional enzyme PaaY from Acinetobacter baumannii

Jiao, M., He, W., Ouyang, Z., Qin, Q., Guo, Y.-C., Zhang, J., Bai, Y., Guo, X., Yu, Q., She, J., et al. (2023) · Structure · doi:10.1016/j.str.2023.05.015 · Cited by 10 · see citing works

Molybdate uptake interplay with ROS tolerance modulates bacterial pathogenesis

Jiao, M., He, W., Ouyang, Z., Yu, Q., Zhang, J., Qian, Q., Wang, R., Guo, X., Liu, R., He, X., et al. (2025) · Science Advances · doi:10.1126/sciadv.adq9686 · Cited by 9 · see citing works

Feature architecture aware phylogenetic profiling indicates a functional diversification of type IVa pili in the nosocomial pathogen Acinetobacter baumannii

Iruegas, R., Pfefferle, K., Göttig, S., Averhoff, B., & Ebersberger, I. (2023) · PLoS Genetics · doi:10.1371/journal.pgen.1010646 · Cited by 12 · see citing works

Systems-level exploitation of OxyR regulon unravels a potential antibacterial target in Pseudomonas aeruginosa

Cui, K., Fu, Z., Sun, R., You, Q., Wang, F., Sun, X., Tan, Y. C., Xia, Y., Wang, P., Wei, Q., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-08770-w · Cited by 7 · see citing works

Dihydrophenazine: a multifunctional new weapon that kills multidrug-resistant Acinetobacter baumannii and restores carbapenem and oxidative stress susceptibilities

Mahdally, N. H., El‐Shiekh, R. A., Thissera, B., Eltaher, A., Osama, A., Mokhtar, M., Elhosseiny, N. M., Kashef, M. T., Magdeldin, S., Halawany, A. M. E., et al. (2024) · Journal of Applied Microbiology · doi:10.1093/jambio/lxae100 · Cited by 7 · see citing works

Innovations in Nuclear Medicine Imaging for Reactive Oxygen Species: Applications and Radiopharmaceuticals

Park, J. Y., Park, S. M., Lee, T. S., Lee, S. J., Kim, J. H., Oh, S. J., Yoon, H., Kim, B. S., & Moon, B. S. (2024) · Antioxidants · doi:10.3390/antiox13101254 · Cited by 6 · see citing works

Cecal Microbial Diversity and Metabolome Reveal a Reduction in Growth Due to Oxidative Stress Caused by a Low-Energy Diet in Donkeys

Li, L., Guo, X., Zhao, Y., Guo, Y., Shi, B., Zhou, Y., Zhang, Y., & Yan, S. (2024) · Antioxidants · doi:10.3390/antiox13111377 · Cited by 6 · see citing works

Characterization of the oxidative stress response regulatory network in Bacteroides fragilis: An interaction between BmoR and OxyR regulons promotes abscess formation in a model of intra-abdominal infection

Teixeira, F. L., da Costa, S. B., Pauer, H., de Almeida, B. J., Oliveira, A. C., Smith, C. J., Domingues, R. M. C. P., Rocha, E. R., & Lobo, L. A. (2022) · Anaerobe · doi:10.1016/j.anaerobe.2022.102668 · Cited by 6 · see citing works

In vitro selection of cefiderocol-resistant mutants in Acinetobacter baumannii harbouring the most common carbapenemase genes

Raro, O. H. F., Findlay, J., Poirel, L., Decousser, J., & Nordmann, P. (2025) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkaf462 · Cited by 5 · see citing works

Two redox-responsive LysR-type transcription factors control the oxidative stress response of Agrobacterium tumefaciens

Schmidt, J. J., Brandenburg, V. B., Elders, H., Shahzad, S., Schäkermann, S., Fiedler, R., Knoke, L. R., Pfänder, Y., Dietze, P., Bille, H., et al. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf267 · Cited by 5 · see citing works

Physiological roles of an Acinetobacter -specific σ factor

Bacon, E. E., Myers, K. S., Iruegas, R., Banta, A. B., Place, M., Ebersberger, I., & Peters, J. M. (2025) · mBio · doi:10.1128/mbio.00968-25 · Cited by 5 · see citing works

Draft genome sequence of novel Candidatus Ornithobacterium hominis carrying antimicrobial resistance genes in Egypt

Ahmed, N., Azab, M., Enany, S., & Hanora, A. (2024) · BMC Microbiology · doi:10.1186/s12866-023-03172-6 · Cited by 5 · see citing works

Inside Enemy Lines: Adhesion, Invasion, and Intracellular Persistence of Acinetobacter baumannii in the Respiratory Epithelium

Limongi, D., Scribano, D., Palamara, A. T., & Ambrosi, C. (2026) · Pathogens · doi:10.3390/pathogens15010102 · Cited by 4 · see citing works

Wax Ester and Triacylglycerol Production in Acinetobacter baumannii: Role in Osmostress Protection, Reactive Oxygen Species, and Antibiotic Sensitivity

Pfefferle, K., & Averhoff, B. (2023) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.3c00214 · Cited by 4 · see citing works

DksA is a central regulatory switch for stress protection and virulence in Acinetobacter baumanniiPreprint

Maharjan, R. P., Sullivan, G. J., Adams, F. G., Delgado, N. N., Semenec, L., Dinh, H., Li, L., Short, F. L., Parkhill, J., Paulsen, I. T., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-449513/v1 · Cited by 3 · see citing works

Characterization of a Novel Oxidative Stress Responsive Transcription Regulator in Mycobacterium bovis

Jiang, Q., Hu, R., Liu, F., Huang, F., Zhang, L., & Zhang, H. (2024) · Biomedicines · doi:10.3390/biomedicines12081872 · Cited by 3 · see citing works

Imaging Infection Across Scales of Size: From Whole Animals to Single Molecules

Skaar, E. P. (2021) · Annual Review of Microbiology · doi:10.1146/annurev-micro-041521-121457 · Cited by 3 · see citing works

Domain-architecture aware phylogenetic profiling indicates a functional diversification of type IVa pili in the nosocomial pathogen Acinetobacter baumanniiPreprint

Iruegas, R., Pfefferle, K., Goettig, S., Averhoff, B., & Ebersberger, I. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.01.526601 · Cited by 3 · see citing works

Acinetobacter baumannii in food safety: emerging threats and control strategies

Lee, J. Y., & Kim, J. (2025) · Food Science and Biotechnology · doi:10.1007/s10068-025-02008-5 · Cited by 2 · see citing works

Reduced glutathione levels in Enterococcus faecalis trigger metabolic and transcriptional compensatory adjustments during iron exposure

Aliaga-Tobar, V., Torres, J., Mendoza, S. N., Gálvez, G., Ortega, J., Gómez, S. U., Parra, V., Arenas, F., Maass, A., Siegel, A., et al. (2025) · mSystems · doi:10.1128/msystems.01240-25 · Cited by 2 · see citing works

Genomic and phenotypic analysis of ST25 A. baumannii identifies virulence-associated clades and capsular/outer core locus types

Migliaccio, A., Destanque, T., Haenni, M., Madec, J.-Y., Jolley, K. A., Stabile, M. R., Gregorio, E. D., Lupo, A., & Zarrilli, R. (2025) · mSphere · doi:10.1128/msphere.00717-25 · Cited by 2 · see citing works

A novel type of hemoglobin confers host-derived nitric oxide resistance to the opportunistic pathogen Acinetobacter baumannii

Beas, J. Z., Folgosa, F., Karavaeva, V., Sousa, F. L., & Saraiva, L. M. (2025) · Scientific Reports · doi:10.1038/s41598-025-88123-z · Cited by 2 · see citing works

Nitrogen metabolism in <i>Pseudomonas putida</i> : functional analysis using random barcode transposon sequencing

Schmidt, M., Pearson, A. N., Incha, M. R., Thompson, M. G., Baidoo, E. E. K., Kakumanu, R., Mukhopadhyay, A., Shih, P. M., Deutschbauer, A. M., Blank, L. M., et al. (2021) · doi:10.1101/2021.12.09.472016 · Cited by 2 · see citing works

Acinetobacter baumannii utilizes a novel protective factor to combat desiccation-induced oxidative stress

Farrow, J. M., Wells, G., & Pesci, E. C. (2026) · PLoS ONE · doi:10.1371/journal.pone.0350814 · Cited by 1 · see citing works

Chloramphenicol stress triggers oxidative adaptation in Acinetobacter baumannii ATCC19606 devoid of RND efflux pumps AdeAB or AdeIJ

Foong, W. E., Xiang, X., He, W., Xuan, Y., Huang, J., Pos, K. M., & Tam, H.-K. (2026) · mSystems · doi:10.1128/msystems.00009-26 · Cited by 1 · see citing works

NIR Bioluminescence Probe Enables Discovery of Diet-Induced Modulation of the Tumor Microenvironment via Nitric OxidePreprint

Yadav, A. K., Lee, M., Lucero, M. Y., Reinhardt, C. J., Su, S., & Chan, J. (2021) · ChemRxiv · doi:10.26434/chemrxiv.14176835

Time-course proteomic study of Acinetobacter baumannii after exposure to oxidative stress

Gallo, V. (2022) · doi:10.22215/etd/2022-15390

Short-term bacterioplankton responses to black carbon-derived dissolved organic matter additions in Mediterranean seawater

Cuny, P., Martinot, P. L., Guigue, C., Chifflet, S., Didry, M., Pringault, O., Vu, C. T., Mari, X., Pradel, N., & Tedetti, M. (2026) · Marine Ecology Progress Series · doi:10.3354/meps15146

A novel GntR-ABC efflux system mediates oxidative stress response, drug resistance, motility and virulence in Acinetobacter baumannii ATCC 17978

Corral, J., Pérez−Varela, M., Sánchez−Osuna, M., Gaona, M., Campoy, S., Barbé, J., & Aranda, J. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1748186

The Overlooked Role of Biocides in Driving Antibiotic Resistance in Acinetobacter baumannii

Muhtar, U. N., Yusuf, I., Inuwa, A. B., & Saleh, K. J. (2026) · Infectious diseases · doi:10.5772/intechopen.1014262

Decoding the genome of Acinetobacter baumannii from a urinary tract infection case: A comprehensive analysis of resistance, virulence, and genetic mobility attributes

Girija, A. S. S., & Kannan, K. P. (2026) · Brazilian Journal of Microbiology · doi:10.1007/s42770-026-02036-1

Molecular determinants of adhesion and biofilm formation in Acinetobacter baumannii: genetic basis and clinical relevance

Materniak, M., Krakowiak, N., Maciocha, M., & Andrzejczuk, S. (2026) · Diagnostyka Laboratoryjna · doi:10.5604/01.3001.0055.8645

A minimalist opportunist: the emergence of Acinetobacter baumannii

Janet-Maitre, M., & Feldman, M. F. (2026) · Journal of Bacteriology · doi:10.1128/jb.00360-26

The Interplay Between Molybdopterin Synthase and Metal Metabolism Contributes to Pathogenicity in Acinetobacter baumannii

Jiao, M., He, W., Ouyang, Z., Wang, R., Zhang, J., Liu, X., Jing, Y.-R., Yu, Q., He, X., Qin, Q., et al. (2026) · Advanced Science · doi:10.1002/advs.78547

2-Hydroxylation of Acinetobacter baumannii Lipid A Contributes to Virulence

Bartholomew, T. L., Kidd, T. J., Sá‐Pessoa, J., Conde-Álvarez, R., & Bengoechea, J. A. (2019) · Infection and Immunity · doi:10.1128/iai.00066-19 · Cited by 47 · see citing works

Stress Responses in the Opportunistic Pathogen Acinetobacter Baumannii

Fiester, S. E., & Actis, L. A. (2013) · Future Microbiology · doi:10.2217/fmb.12.150 · Cited by 64 · see citing works

Insights into Acinetobacter baumannii: A Review of Microbiological, Virulence, and Resistance Traits in a Threatening Nosocomial Pathogen

Moubareck, C. A., & Halat, D. H. (2020) · Antibiotics · doi:10.3390/antibiotics9030119 · Cited by 629 · see citing works

Editorial

Jenkins, R. O. (2000) · Biochemistry and Molecular Biology Education · doi:10.1016/s1470-8175(00)00056-4

Targeting virulence regulation to disarm Acinetobacter baumannii pathogenesis

Trebosc, V., Lucchini, V., Narwal, M., Wicki, B., Gartenmann, S., Schellhorn, B., Schill, J., Bourotte, M., FREY, D. J., Grünberg, J., et al. (2022) · Virulence · doi:10.1080/21505594.2022.2135273 · Cited by 10 · see citing works