Mechanisms of Antibiotic and Biocide Resistance That Contribute to Pseudomonas aeruginosa Persistence in the Hospital Environment

Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance

Magiorakos, A.-P., Srinivasan, A., Carey, R. B., Carmeli, Y., Falagas, M. E., Giske, C. G., Harbarth, S., Hindler, J. F., Kahlmeter, G., Olsson-Liljequist, B., et al. (2012) · Clinical Microbiology and Infection · doi:10.1111/j.1469-0691.2011.03570.x · Cited by 14,449 · see citing works

Emergence of plasmid-mediated colistin resistance mechanism MCR-1 in animals and human beings in China: a microbiological and molecular biological study.

Liu, Y.-Y., Wang, Y., Walsh, T., Yi, L.-X., Zhang, R., Spencer, J., Doi, Y., Tian, G.-B., Dong, B.-L., Huang, X.-H., et al. (2016) · Lancet. Infectious Diseases (Print) · doi:10.1016/s1473-3099(15)00424-7 · Cited by 4,920 · see citing works

Complete genome sequence of Pseudomonas aeruginosa PAO1, an opportunistic pathogen

Stover, C. K., Pham, X. Q., Erwin, A. L., Mizoguchi, S., Warrener, P., Hickey, M. J., Brinkman, F. S. L., HUFNAGLE, W. O., Kowalik, D., Mj, L., et al. (2000) · Nature · doi:10.1038/35023079 · Cited by 4,544 · see citing works

Molecular mechanisms of antibiotic resistance

Blair, J. M. A., Webber, M. A., Baylay, A. J., Ogbolu, D. O., & Piddock, L. J. V. (2015) · Nature Reviews Microbiology · doi:10.1038/nrmicro3380 · Cited by 4,092 · see citing works

Mechanisms of Antibiotic Resistance

Munita, J. M., & Arias, C. A. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.vmbf-0016-2015 · Cited by 2,782 · see citing works

Flagellar and twitching motility are necessary for <i>Pseudomonas aeruginosa</i> biofilm development

O'Toole, G. A., & Kolter, R. (1998) · Molecular Microbiology · doi:10.1046/j.1365-2958.1998.01062.x · Cited by 2,697 · see citing works

How long do nosocomial pathogens persist on inanimate surfaces? A systematic review

Krämer, A., Schwebke, I., & Kampf, G. (2006) · BMC Infectious Diseases · doi:10.1186/1471-2334-6-130 · Cited by 2,508 · see citing works

Antibiotic resistance in Pseudomonas aeruginosa: mechanisms and alternative therapeutic strategies

Pang, Z., Raudonis, R., Glick, B. R., Lin, T., & Cheng, Z. (2018) · Biotechnology Advances · doi:10.1016/j.biotechadv.2018.11.013 · Cited by 2,375 · see citing works

Antibacterial-Resistant Pseudomonas aeruginosa : Clinical Impact and Complex Regulation of Chromosomally Encoded Resistance Mechanisms

Lister, P., Wolter, D. J., & Hanson, N. D. (2009) · Clinical Microbiology Reviews · doi:10.1128/cmr.00040-09 · Cited by 1,798 · see citing works

Pseudomonas aeruginosa Lifestyle: A Paradigm for Adaptation, Survival, and Persistence

Moradali, M. F., Ghods, S., & Rehm, B. H. A. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00039 · Cited by 1,554 · see citing works

Pseudomonas aeruginosa: pathogenesis, virulence factors, antibiotic resistance, interaction with host, technology advances and emerging therapeutics

Qin, S., Xiao, W., Zhou, C., Pu, Q., Deng, X., Lan, L., Liang, H., Song, X., & Wu, M. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01056-1 · Cited by 1,553 · see citing works

Multidrug-resistance efflux pumps ? not just for resistance

Piddock, L. J. V. (2006) · Nature Reviews Microbiology · doi:10.1038/nrmicro1464 · Cited by 1,523 · see citing works

Aminoglycoside modifying enzymes

Ramirez, M. S., & Tolmasky, M. E. (2010) · Drug Resistance Updates · doi:10.1016/j.drup.2010.08.003 · Cited by 1,504 · see citing works

Mechanisms of antibiotic resistance in bacterial biofilms

Stewart, P. S. (2002) · International Journal of Medical Microbiology · doi:10.1078/1438-4221-00196 · Cited by 1,388 · see citing works

The hierarchy quorum sensing network in Pseudomonas aeruginosa

Lee, J., & Zhang, L. (2014) · Protein & Cell · doi:10.1007/s13238-014-0100-x · Cited by 1,344 · see citing works

Pseudomonas aeruginosa: all roads lead to resistance

Breidenstein, E. B. M., de la Fuente‐Núñez, C., & Hancock, R. E. W. (2011) · Trends in Microbiology · doi:10.1016/j.tim.2011.04.005 · Cited by 1,338 · see citing works

<i>Pseudomonas aeruginosa</i> : new insights into pathogenesis and host defenses

Gellatly, S. L., & Hancock, R. E. W. (2013) · Pathogens and Disease · doi:10.1111/2049-632x.12033 · Cited by 1,295 · see citing works

Persistent bacterial infections and persister cells

Fisher, R. A., Gollan, B., & Helaine, S. (2017) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2017.42 · Cited by 1,243 · see citing works

Bacterial Secretion Systems: An Overview

Green, E. R., & Mecsas, J. C. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.vmbf-0012-2015 · Cited by 1,090 · see citing works

β-Lactamases and β-Lactamase Inhibitors in the 21st Century

Tooke, C. L., Hinchliffe, P., Bragginton, É. C., Colenso, C. K., Hirvonen, V. H. A., Takebayashi, Y., & SPENCER, J. M. (2019) · Journal of Molecular Biology · doi:10.1016/j.jmb.2019.04.002 · Cited by 1,062 · see citing works

Contributions of Antibiotic Penetration, Oxygen Limitation, and Low Metabolic Activity to Tolerance of Pseudomonas aeruginosa Biofilms to Ciprofloxacin and Tobramycin

Walters, M. C., Roe, F., Bugnicourt, A., Franklin, M. J., & Stewart, P. S. (2002) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.47.1.317-323.2003 · Cited by 1,005 · see citing works

Pseudomonas genomes: diverse and adaptable

Silby, M. W., Winstanley, C., Godfrey, S. A. C., Levy, S. B., & Jackson, R. W. (2011) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2011.00269.x · Cited by 965 · see citing works

Pseudomonas aeruginosa Biofilms

Thi, M. T. T., Wibowo, D., & Rehm, B. H. A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21228671 · Cited by 923 · see citing works

The European Centre for Disease Prevention and Control (ECDC) pilot point prevalence survey of healthcare-associated infections and antimicrobial use

Zarb, P., Coignard, B., Griskeviciene, J., Müller, A., Vankerckhoven, V., Weist, K., Goossens, M. M., Vaerenberg, S., Hopkins, S., Catry, B., et al. (2012) · Eurosurveillance · doi:10.2807/ese.17.46.20316-en · Cited by 783 · see citing works

Epidemiologic Background of Hand Hygiene and Evaluation of the Most Important Agents for Scrubs and Rubs

Kampf, G., & Krämer, A. (2004) · Clinical Microbiology Reviews · doi:10.1128/cmr.17.4.863-893.2004 · Cited by 760 · see citing works

The role of pyocyanin in Pseudomonas aeruginosa infection

Lau, G. W., Hassett, D. J., Ran, H., & Kong, F. (2004) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2004.10.002 · Cited by 750 · see citing works

Bacterial multidrug efflux pumps: Mechanisms, physiology and pharmacological exploitations

Sun, J., Deng, Z., & Yan, A. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.05.090 · Cited by 747 · see citing works

Environmental contamination makes an important contribution to hospital infection

Boyce, J. M. (2007) · Journal of Hospital Infection · doi:10.1016/s0195-6701(07)60015-2 · Cited by 731 · see citing works

Type VI secretion system translocates a phage tail spike-like protein into target cells where it cross-links actin

Pukatzki, S. U., Ma, A. T., Revel, A. T., Sturtevant, D., & Mekalanos, J. J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706532104 · Cited by 730 · see citing works

Pseudomonas aeruginosa: An Audacious Pathogen with an Adaptable Arsenal of Virulence Factors

Jurado‐Martín, I., Sainz-Mejías, M., & McClean, S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22063128 · Cited by 722 · see citing works

Substrate Specificities of MexAB-OprM, MexCD-OprJ, and MexXY-OprM Efflux Pumps in Pseudomonas aeruginosa

Masuda, N., Sakagawa, E., Ohya, S., Gotoh, N., Tsujimoto, H., & Nishino, T. (2000) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.44.12.3322-3327.2000 · Cited by 720 · see citing works

Type VI secretion system effectors: poisons with a purpose

Russell, A. B., Peterson, S. B., & Mougous, J. D. (2014) · Nature Reviews Microbiology · doi:10.1038/nrmicro3185 · Cited by 718 · see citing works

The versatile bacterial type IV secretion systems

Cascalès, E., & Christie, P. J. (2003) · Nature Reviews Microbiology · doi:10.1038/nrmicro753 · Cited by 695 · see citing works

Controlling Hospital-Acquired Infection: Focus on the Role of the Environment and New Technologies for Decontamination

Dancer, S. J. (2014) · Clinical Microbiology Reviews · doi:10.1128/cmr.00020-14 · Cited by 693 · see citing works

Bacterial Multidrug Efflux Pumps: Much More Than Antibiotic Resistance Determinants

Blanco, P., Hernando‐Amado, S., Reales‐Calderón, J. A., Corona, F., Lira, F., Alcalde‐Rico, M., Bernardini, A., Sánchez, M. B., & Martínez, J. L. (2016) · Microorganisms · doi:10.3390/microorganisms4010014 · Cited by 667 · see citing works

The increasing threat of Pseudomonas aeruginosa high-risk clones

Oliver, A., Mulet, X., López-Causapé, C., & Juan, C. (2015) · Drug Resistance Updates · doi:10.1016/j.drup.2015.08.002 · Cited by 642 · see citing works

Biosynthesis of the Pseudomonas aeruginosa Extracellular Polysaccharides, Alginate, Pel, and Psl

Franklin, M. J., Nivens, D. E., Weadge, J. T., & Howell, P. L. (2011) · Frontiers in Microbiology · doi:10.3389/fmicb.2011.00167 · Cited by 581 · see citing works

The role of the surface environment in healthcare-associated infections

Weber, D. J., Anderson, D. J., & Rutala, W. A. (2013) · Current Opinion in Infectious Diseases · doi:10.1097/qco.0b013e3283630f04 · Cited by 568 · see citing works

Efflux pumps as antimicrobial resistance mechanisms

Poole, K. (2007) · Annals of Medicine · doi:10.1080/07853890701195262 · Cited by 561 · see citing works

Antibiotic resistance in Pseudomonas aeruginosa – Mechanisms, epidemiology and evolution

Botelho, J., Grosso, F., & Peixe, L. M. S. V. (2019) · Drug Resistance Updates · doi:10.1016/j.drup.2019.07.002 · Cited by 561 · see citing works

Quaternary Ammonium Biocides: Efficacy in Application

Gerba, C. P. (2015) · Applied and Environmental Microbiology · doi:10.1128/aem.02633-14 · Cited by 561 · see citing works

Role of Exopolysaccharides in Pseudomonas aeruginosa Biofilm Formation and Architecture

Ghafoor, A., Hay, I. D., & Rehm, B. H. A. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.00637-11 · Cited by 535 · see citing works

Aminoglycoside Resistance in Pseudomonas aeruginosa

Poole, K. (2005) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.49.2.479-487.2005 · Cited by 469 · see citing works

Microbe Profile: Pseudomonas aeruginosa: opportunistic pathogen and lab rat

Diggle, S. P., & Whiteley, M. (2019) · Microbiology · doi:10.1099/mic.0.000860 · Cited by 461 · see citing works

Pathogenesis of the Pseudomonas aeruginosa Biofilm: A Review

Tuon, F. F., Dantas, L. R., Suss, P. H., & Ribeiro, V. S. T. (2022) · Pathogens · doi:10.3390/pathogens11030300 · Cited by 430 · see citing works

Cross-Resistance between Triclosan and Antibiotics in Pseudomonas aeruginosa Is Mediated by Multidrug Efflux Pumps: Exposure of a Susceptible Mutant Strain to Triclosan Selects nfxB Mutants Overexpressing MexCD-OprJ

Chuanchuen, R., Beinlich, K., Hoang, T. T., Becher, A., Karkhoff-Schweizer, R. R., & Schweizer, H. P. (2001) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.45.2.428-432.2001 · Cited by 427 · see citing works

Cellular Effects of Pyocyanin, a Secreted Virulence Factor of Pseudomonas aeruginosa

Hall, S., McDermott, C., Anoopkumar‐Dukie, S., McFarland, A. J., Forbes, A., Perkins, A. V., Davey, A. K., Chess‐Williams, R., Kiefel, M. J., Arora, D. S., et al. (2016) · Toxins · doi:10.3390/toxins8080236 · Cited by 422 · see citing works

A cell-cell communication signal integrates quorum sensing and stress response

Lee, J., Wu, J., Deng, Y., Wang, J., Wang, C., Wang, J., Chang, C., Dong, Y., Williams, P. M., & Zhang, L. (2013) · Nature Chemical Biology · doi:10.1038/nchembio.1225 · Cited by 418 · see citing works

Colistin kills bacteria by targeting lipopolysaccharide in the cytoplasmic membrane

Sabnis, A., Hagart, K. L., Klöckner, A., Becce, M., Evans, L. E., Furniss, R. C. D., Mavridou, D. A. I., Murphy, R. A., Stevens, M. M., Davies, J. C., et al. (2021) · eLife · doi:10.7554/elife.65836 · Cited by 393 · see citing works

Quaternary ammonium disinfectants: microbial adaptation, degradation and ecology

Tezel, U., & Pavlostathis, S. G. (2015) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2015.03.018 · Cited by 389 · see citing works

Role of Efflux Pumps on Antimicrobial Resistance in Pseudomonas aeruginosa

Lorusso, A. B., Carrara, J. A., Barroso, C. D. N., Tuon, F. F., & Faoro, H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232415779 · Cited by 386 · see citing works

Updates on the pathogenicity status of Pseudomonas aeruginosa

Azam, M. W., & Khan, A. U. (2018) · Drug Discovery Today · doi:10.1016/j.drudis.2018.07.003 · Cited by 377 · see citing works

Pseudomonas aeruginosa epidemic high-risk clones and their association with horizontally-acquired β-lactamases: 2020 update

del Barrio-Tofiño, E., López-Causapé, C., & Oliver, A. (2020) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2020.106196 · Cited by 376 · see citing works

Antimicrobial Therapy in Veterinary Medicine

Giguère, S. (2013) · Wiley eBooks · doi:10.1002/9781118675014 · Cited by 373 · see citing works

Structure, function and regulation of Pseudomonas aeruginosa porins

Chevalier, S., Bouffartigues, E., Bodilis, J., Maillot, O., Lesouhaitier, O., Feuilloley, M., Orange, N., Dufour, A., & Cornelis, P. (2017) · FEMS Microbiology Reviews · doi:10.1093/femsre/fux020 · Cited by 370 · see citing works

Pseudomonas aeruginosa Genomic Structure and Diversity

Klockgether, J., Cramer, N., Wiehlmann, L., Davenport, C., & Tümmler, B. (2011) · Frontiers in Microbiology · doi:10.3389/fmicb.2011.00150 · Cited by 355 · see citing works

Overexpression ofmarA, soxS, oracrABproduces resistance to triclosan in laboratory and clinical strains ofEscherichia coli

McMurry, L. M., Oethinger, M. D., & Levy, S. B. (1998) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1998.tb13905.x · Cited by 346 · see citing works

Function of <i>Pseudomonas</i> Porins in Uptake and Efflux

Hancock, R. E. W., & Brinkman, F. S. L. (2002) · Annual Review of Microbiology · doi:10.1146/annurev.micro.56.012302.160310 · Cited by 319 · see citing works

Antibiotic resistance in Pseudomonas aeruginosa and alternative therapeutic options

Chatterjee, M., Anju, C., Biswas, L., Kumar, V. A., Mohan, C. G., & Biswas, R. (2015) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2015.11.004 · Cited by 313 · see citing works

Virulence Factors of Pseudomonas Aeruginosa and Antivirulence Strategies to Combat Its Drug Resistance

Liao, C., Huang, X., Wang, Q., Yao, D., & Lu, W. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.926758 · Cited by 313 · see citing works

Review: Lipopolysaccharide biosynthesis in Pseudomonas aeruginosa

King, J. D., Kocíncová, D., Westman, E. L., & Lam, J. S. (2009) · Innate Immunity · doi:10.1177/1753425909106436 · Cited by 312 · see citing works

A Prospective Study of Postoperative Surgical Site Infections in Dogs and Cats

Eugster, S., Schawalder, P., Gaschen, F. P., & Boerlin, P. (2004) · Veterinary Surgery · doi:10.1111/j.1532-950x.2004.04076.x · Cited by 310 · see citing works

Does improving surface cleaning and disinfection reduce health care-associated infections?

Donskey, C. J. (2013) · American Journal of Infection Control · doi:10.1016/j.ajic.2012.12.010 · Cited by 304 · see citing works

Relationship Between Quorum Sensing and Secretion Systems

Trastoy, R., Blasco, L., Ambroa, A., González‐Pedrajo, B., Fernández-García, L., López, M. C., Bleriot, I., Bou, G., García‐Contreras, R., Wood, T. K., et al. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01100 · Cited by 301 · see citing works

Small multidrug resistance proteins: A multidrug transporter family that continues to grow

Bay, D. C., Rommens, K. L., & Turner, R. J. (2007) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2007.08.015 · Cited by 300 · see citing works

History of Antibiotics Research

Mohr, K. I. (2016) · Current topics in microbiology and immunology · doi:10.1007/82_2016_499 · Cited by 296 · see citing works

Type IV secretion systems: tools of bacterial horizontal gene transfer and virulence

Juhas, M., Crook, D. W., & Hood, D. W. (2008) · Cellular Microbiology · doi:10.1111/j.1462-5822.2008.01187.x · Cited by 291 · see citing works

Ecology of Pseudomonas aeruginosa in the intensive care unit and the evolving role of water outlets as a reservoir of the organism

Trautmann, M., Lepper, P. M., & Haller, M. (2005) · American Journal of Infection Control · doi:10.1016/j.ajic.2005.03.006 · Cited by 279 · see citing works

The Pseudomonas Quinolone Signal (PQS): Not Just for Quorum Sensing Anymore

Lin, J., Cheng, J., Wang, Y., & Shen, X. (2018) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2018.00230 · Cited by 274 · see citing works

Epidemiology and Characteristics of Metallo-β-Lactamase-ProducingPseudomonas aeruginosa

Hong, D. J., Bae, I. K., Jang, I.-H., Jeong, S. H., Kang, H., & Lee, K. (2015) · Infection and Chemotherapy · doi:10.3947/ic.2015.47.2.81 · Cited by 273 · see citing works

Mutations in β-Lactamase AmpC Increase Resistance of Pseudomonas aeruginosa Isolates to Antipseudomonal Cephalosporins

Berrazeg, M., Jeannot, K., Enguéné, V. Y. N., Broutin, I., Loeffert, S. T., Fournier, P., & Plésiat, P. (2015) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00825-15 · Cited by 270 · see citing works

Structure and function of OprD protein in Pseudomonas aeruginosa: From antibiotic resistance to novel therapies

Li, H., Luo, Y., Williams, B. J., Blackwell, T. S., & Xie, C. (2012) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2011.10.001 · Cited by 268 · see citing works

Efficacy of common hospital biocides with biofilms of multi-drug resistant clinical isolates

Smith, K., & Hunter, I. S. (2008) · Journal of Medical Microbiology · doi:10.1099/jmm.0.47668-0 · Cited by 267 · see citing works

Pseudomonas aeruginosa: Infections, Animal Modeling, and Therapeutics

Wood, S. J., Kuzel, T. M., & Shafikhani, S. H. (2023) · Cells · doi:10.3390/cells12010199 · Cited by 267 · see citing works

Distribution of multi-resistant Gram-negative versus Gram-positive bacteria in the hospital inanimate environment

Lemmen, S., Häfner, H., Zolldann, D., Stanzel, S. F., & Lütticken, R. (2004) · Journal of Hospital Infection · doi:10.1016/j.jhin.2003.12.004 · Cited by 266 · see citing works

Interactions between Biocide Cationic Agents and Bacterial Biofilms

Campanac, C., Pineau, L., Payard, A., Baziard, G., & Roques, C. G. (2002) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.46.5.1469-1474.2002 · Cited by 265 · see citing works

Opportunistic Premise Plumbing Pathogens: Increasingly Important Pathogens in Drinking Water

Falkinham, J. O., Pruden, A. J., & Edwards, M. A. (2015) · Pathogens · doi:10.3390/pathogens4020373 · Cited by 264 · see citing works

PhoP–PhoQ homologues in Pseudomonas aeruginosa regulate expression of the outer‐membrane protein OprH and polymyxin B resistance

Macfarlane, E. L. A., Kwasnicka, A., Ochs, M. M., & Hancock, R. E. W. (1999) · Molecular Microbiology · doi:10.1046/j.1365-2958.1999.01600.x · Cited by 256 · see citing works

Transfer of multidrug-resistant bacteria to healthcare workers’ gloves and gowns after patient contact increases with environmental contamination*

Morgan, D. J., Rogawski, E., Thom, K. A., Johnson, J. K., Perencevich, E. N., Shardell, M. D., Leekha, S., & Harris, A. D. (2012) · Critical Care Medicine · doi:10.1097/ccm.0b013e31823bc7c8 · Cited by 249 · see citing works

Antibiotic resistance—consequences for animal health, welfare, and food production

Bengtsson, B., & Greko, C. (2014) · Upsala Journal of Medical Sciences · doi:10.3109/03009734.2014.901445 · Cited by 245 · see citing works

Pseudomonas aeruginosaIncreases Formation of Multidrug-Tolerant Persister Cells in Response to Quorum-Sensing Signaling Molecules

Möker, N., Dean, C. R., & Tao, J. (2010) · Journal of Bacteriology · doi:10.1128/jb.01231-09 · Cited by 243 · see citing works

Widely Used Benzalkonium Chloride Disinfectants Can Promote Antibiotic Resistance

Kim, M., Weigand, M. R., Oh, S., Hatt, J. K., Krishnan, R., Tezel, U., Pavlostathis, S. G., & Konstantinidis, K. T. (2018) · Applied and Environmental Microbiology · doi:10.1128/aem.01201-18 · Cited by 239 · see citing works

Long-Term Exposure to Benzalkonium Chloride Disinfectants Results in Change of Microbial Community Structure and Increased Antimicrobial Resistance

Tandukar, M., Oh, S., Tezel, U., Konstantinidis, K. T., & Pavlostathis, S. G. (2013) · Environmental Science & Technology · doi:10.1021/es401507k · Cited by 229 · see citing works

Protein Secretion Systems in Pseudomonas aeruginosa: An Essay on Diversity, Evolution, and Function

Filloux, A. (2011) · Frontiers in Microbiology · doi:10.3389/fmicb.2011.00155 · Cited by 229 · see citing works

It’s Not Easy Being Green: A Narrative Review on the Microbiology, Virulence and Therapeutic Prospects of Multidrug-Resistant Pseudomonas aeruginosa

Behzadi, P., Baráth, Z., & Gajdács, M. (2021) · Antibiotics · doi:10.3390/antibiotics10010042 · Cited by 229 · see citing works

The MexJK Efflux Pump of Pseudomonas aeruginosa Requires OprM for Antibiotic Efflux but Not for Efflux of Triclosan

Chuanchuen, R., Narasaki, C. T., & Schweizer, H. P. (2002) · Journal of Bacteriology · doi:10.1128/jb.184.18.5036-5044.2002 · Cited by 228 · see citing works

Growth and Laboratory Maintenance of Pseudomonas aeruginosa

LaBauve, A. E., & Wargo, M. J. (2012) · Current Protocols in Microbiology · doi:10.1002/9780471729259.mc06e01s25 · Cited by 224 · see citing works

The Second Type VI Secretion System of Pseudomonas aeruginosa Strain PAO1 Is Regulated by Quorum Sensing and Fur and Modulates Internalization in Epithelial Cells

Sana, T. G., Hachani, A., Bucior, I., Soscia, C., Garvis, S., Termine, E., Engel, J. N., Filloux, A., & Bleves, S. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.376368 · Cited by 224 · see citing works

Triclosan Resistance of Pseudomonas aeruginosa PAO1 Is Due to FabV, a Triclosan-Resistant Enoyl-Acyl Carrier Protein Reductase

Zhu, L., Lin, J., Ma, J., Cronan, J. E., & Wang, H. (2009) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01152-09 · Cited by 201 · see citing works

Biocide Use in the Antimicrobial Era: A Review

Jones, I. A., & Joshi, L. T. (2021) · Molecules · doi:10.3390/molecules26082276 · Cited by 193 · see citing works

Type V Secretion Systems: An Overview of Passenger Domain Functions

Meuskens, I., Saragliadis, A., Leo, J. C., & Linke, D. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01163 · Cited by 187 · see citing works

Association between healthcare water systems and Pseudomonas aeruginosa infections: a rapid systematic review

Loveday, H. P., Wilson, J. A., Kerr, K., Pitchers, R., Walker, J. T., & Browne, J. (2013) · Journal of Hospital Infection · doi:10.1016/j.jhin.2013.09.010 · Cited by 185 · see citing works

Effect of subinhibitory concentrations of benzalkonium chloride on the competitiveness of Pseudomonas aeruginosa grown in continuous culture

Cay, P. H. M., Ocampo-Sosa, A. A., & Fleming, G. T. A. (2009) · Microbiology · doi:10.1099/mic.0.029751-0 · Cited by 179 · see citing works

Resistance Mechanisms of Multiresistant Pseudomonas aeruginosa Strains from Germany and Correlation with Hypermutation

Henrichfreise, B., Wiegand, I., Pfister, W., & Wiedemann, B. (2007) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00148-07 · Cited by 179 · see citing works

Molecular Mechanisms of β-Lactam Resistance Mediated by AmpC Hyperproduction in Pseudomonas aeruginosa Clinical Strains

Juan, C., Macia, M. D., Gutiérrez, O., Vidal, C., Pérez, J. L., & Oliver, A. (2005) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.49.11.4733-4738.2005 · Cited by 176 · see citing works

Molecular analysis of beta-lactamase structure and function

Majiduddin, F. K., Materon, I. C., & Palzkill, T. G. (2002) · International Journal of Medical Microbiology · doi:10.1078/1438-4221-00198 · Cited by 175 · see citing works

Development of bacterial resistance to several biocides and effects on antibiotic susceptibility

Walsh, S. E., Maillard, J., Russell, A. D., Catrenich, C. E., Charbonneau, D. L., & Bartolo, R. G. (2003) · Journal of Hospital Infection · doi:10.1016/s0195-6701(03)00240-8 · Cited by 168 · see citing works

MexCD-OprJ Multidrug Efflux System of Pseudomonas aeruginosa : Involvement in Chlorhexidine Resistance and Induction by Membrane-Damaging Agents Dependent upon the AlgU Stress Response Sigma Factor

Fraud, S., Campigotto, A. J., Chen, Z., & Poole, K. (2008) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01072-08 · Cited by 166 · see citing works

Parallel evolutionary pathways to antibiotic resistance selected by biocide exposure

Webber, M. A., Whitehead, R. N., Mount, M., Loman, N. J., Pallen, M. J., & Piddock, L. J. V. (2015) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkv109 · Cited by 155 · see citing works

Pseudomonas aeruginosa and microbial keratitis

Hilliam, Y., Kaye, S., & Winstanley, C. (2020) · Journal of Medical Microbiology · doi:10.1099/jmm.0.001110 · Cited by 152 · see citing works

Reduced Susceptibility and Increased Resistance of Bacteria against Disinfectants: A Systematic Review

Rozman, U., Pušnik, M., Kmetec, S., Duh, D., & Turk, S. Š. (2021) · Microorganisms · doi:10.3390/microorganisms9122550 · Cited by 150 · see citing works

Resistance of Bacteria to Biocides

Maillard, J. (2018) · Microbiology Spectrum · doi:10.1128/microbiolspec.arba-0006-2017 · Cited by 147 · see citing works

Genomic and Metabolic Characteristics of the Pathogenicity in Pseudomonas aeruginosa

de Sousa, T., Hébraud, M., Dapkevicius, M. D. L. E., Maltez, L., Pereira, J. E., Capita, R., Alonso‐Calleja, C., Igrejas, G., & Poeta, P. A. C. Q. D. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222312892 · Cited by 145 · see citing works

Quantitative Contributions of Target Alteration and Decreased Drug Accumulation to Pseudomonas aeruginosa Fluoroquinolone Resistance

Bruchmann, S., Dötsch, A., Nouri, B., Chaberny, I. F., & Häußler, S. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01581-12 · Cited by 144 · see citing works

Overview of mechanisms of antibiotic resistance in Pseudomonas aeruginosa: an ocular perspective

Subedi, D., Vijay, A. K., & Willcox, M. D. P. (2017) · Clinical and Experimental Optometry · doi:10.1111/cxo.12621 · Cited by 142 · see citing works

Biocide-tolerance and antibiotic-resistance in community environments and risk of direct transfers to humans: Unintended consequences of community-wide surface disinfecting during COVID-19?

Chen, B., Han, J., Dai, H., & Jia, P. (2021) · Environmental Pollution · doi:10.1016/j.envpol.2021.117074 · Cited by 140 · see citing works

The third quorum-sensing system of Pseudomonas aeruginosa: Pseudomonas quinolone signal and the enigmatic PqsE protein

García‐Reyes, S., Soberón‐Chávez, G., & Cocotl‐Yañez, M. (2019) · Journal of Medical Microbiology · doi:10.1099/jmm.0.001116 · Cited by 138 · see citing works

Involvement of the MexXY-OprM Efflux System in Emergence of Cefepime Resistance in Clinical Strains of Pseudomonas aeruginosa

Hocquet, D., Nordmann, P., Garch, F. E., Cabanne, L., & Plésiat, P. (2006) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.50.4.1347-1351.2006 · Cited by 136 · see citing works

Biocides – resistance, cross-resistance mechanisms and assessment

Gnanadhas, D. P., Marathe, S. A., & Chakravortty, D. (2012) · Expert Opinion on Investigational Drugs · doi:10.1517/13543784.2013.748035 · Cited by 135 · see citing works

Pseudomonas aeruginosa quorum sensing modulates immune responses: An updated review article

Kariminik, A., Baserisalehi, M., & Kheirkhah, B. (2017) · Immunology Letters · doi:10.1016/j.imlet.2017.07.002 · Cited by 135 · see citing works

Induction of mexCD-oprJ operon for a multidrug efflux pump by disinfectants in wild-type Pseudomonas aeruginosa PAO1

Morita, Y. (2003) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkg173 · Cited by 134 · see citing works

Seeking the source ofPseudomonas aeruginosainfections in a recently opened hospital: an observational study using whole-genome sequencing

Quick, J., Cumley, N., Wearn, C. M., Niebel, M. O., Constantinidou, C., Thomas, C. M., Pallen, M. J., Moiemen, N. S., Bamford, A. L., Oppenheim, B. A., et al. (2014) · BMJ Open · doi:10.1136/bmjopen-2014-006278 · Cited by 130 · see citing works

Efflux Pump Induction by Quaternary Ammonium Compounds and Fluoroquinolone Resistance in Bacteria

Buffet‐Bataillon, S., Tattevin, P., Maillard, J., Bonnaure‐Mallet, M., & Jolivet‐Gougeon, A. (2015) · Future Microbiology · doi:10.2217/fmb.15.131 · Cited by 127 · see citing works

Exposure of Escherichia coli ATCC 12806 to Sublethal Concentrations of Food-Grade Biocides Influences Its Ability To Form Biofilm, Resistance to Antimicrobials, and Ultrastructure

Capita, R., Riesco-Peláez, F., Alonso-Hernando, A., & Alonso‐Calleja, C. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.02283-13 · Cited by 126 · see citing works

Role of the MexEF-OprN Efflux System in Low-Level Resistance of Pseudomonas aeruginosa to Ciprofloxacin

Llanes, C., Köhler, T., Patry, I., Dehecq, B., van Delden, C., & Plésiat, P. (2011) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00101-11 · Cited by 125 · see citing works

Frequency of urinary tract infection in catheterized dogs and comparison of bacterial culture and susceptibility testing results for catheterized and noncatheterized dogs with urinary tract infections

Bubenik, L. J., Hosgood, G. L., Waldron, D. R., & Snow, L. A. (2007) · Journal of the American Veterinary Medical Association · doi:10.2460/javma.231.6.893 · Cited by 124 · see citing works

Dynamics of the Action of Biocides in Pseudomonas aeruginosa Biofilms

Bridier, A., Dubois‐Brissonnet, F., Greub, G., Thomas, V., & Briandet, R. (2011) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01760-10 · Cited by 122 · see citing works

PilMNOPQ from the Pseudomonas aeruginosa Type IV Pilus System Form a Transenvelope Protein Interaction Network That Interacts with PilA

Tammam, S. D., Sampaleanu, L. M., Koo, J. T., Manoharan, K., Daubaras, M., Burrows, L. L., & Howell, P. L. (2013) · Journal of Bacteriology · doi:10.1128/jb.00032-13 · Cited by 119 · see citing works

The role of the hospital environment in the healthcare-associated infections: a general review of the literature.

Facciolà, A., Pellicanò, G. F., Visalli, G., Paolucci, I. A., Rullo, E. V., Ceccarelli, M., D’Aleo, F., Pietro, A. D., Squeri, R., Nunnari, G., et al. (2019) · PubMed · doi:10.26355/eurrev_201902_17020 · Cited by 119 · see citing works

Multiple Mutations Lead to MexXY-OprM-Dependent Aminoglycoside Resistance in Clinical Strains of Pseudomonas aeruginosa

Guénard, S., Muller, C., Monlezun, L., Bénas, P., Broutin, I., Jeannot, K., & Plésiat, P. (2013) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01252-13 · Cited by 115 · see citing works

Horizontal Gene Transfer among Bacteria and Its Role in Biological Evolution

Arber, W. (2014) · Life · doi:10.3390/life4020217 · Cited by 111 · see citing works

Mechanisms of bacterial insusceptibility to biocides

Russell, A. D. (2001) · American Journal of Infection Control · doi:10.1067/mic.2001.115671 · Cited by 111 · see citing works

Alterations in the GyrA and GyrB subunits of topoisomerase II and the ParC and ParE subunits of topoisomerase IV in ciprofloxacin-resistant clinical isolates of Pseudomonas aeruginosa

Lee, J., Lee, Y. S., Park, Y., & Kim, B. S. (2005) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2004.11.012 · Cited by 110 · see citing works

Persistence of microbial communities including Pseudomonas aeruginosa in a hospital environment: a potential health hazard

de Abreu, P. M., Farias, P., Paiva, G. E., de Almeida, A. M. S. F., & Morais, P. V. (2014) · BMC Microbiology · doi:10.1186/1471-2180-14-118 · Cited by 110 · see citing works

Contamination of the Surfaces of a Health Care Environment by Multidrug-Resistant (MDR) Bacteria

Chaoui, L., Mhand, R. A., Mellouki, F., & Rhallabi, N. (2019) · International Journal of Microbiology · doi:10.1155/2019/3236526 · Cited by 109 · see citing works

Risk factors for Pseudomonas aeruginosa acquisition in intensive care units: a prospective multicentre study

Venier, A.-G., Leroyer, C., Slekovec, C., Talon, D. R., Bertrand, X., Parer, S., Alfandari, S., Guérin, J. M., Mégarbane, B., Lawrence, C., et al. (2014) · Journal of Hospital Infection · doi:10.1016/j.jhin.2014.06.018 · Cited by 107 · see citing works

Genetic basis of resistance to quaternary ammonium compounds - the qac genes and their role: a review

Jaglic, Z., & Cervinkova, D. (2012) · Veterinární Medicína · doi:10.17221/6013-vetmed · Cited by 104 · see citing works

Isolation of Methicillin-Resistant Staphylococcus aureus from the Environment in a Veterinary Teaching Hospital

Weese, J. S., DaCosta, T., Button, L., Goth, K., Ethier, M., & Boehnke, K. (2004) · Journal of Veterinary Internal Medicine · doi:10.1892/0891-6640(2004)18 · Cited by 103 · see citing works

Pseudomonas aeruginosa in the healthcare facility setting

Spagnolo, A. M., Sartini, M., & Cristina, M. L. (2021) · Reviews in Medical Microbiology · doi:10.1097/mrm.0000000000000271 · Cited by 103 · see citing works

Pseudomonas Aeruginosa: Virulence Factors and Antibiotic Resistance Genes

Rocha, A. J., Barsottini, M. R. D. O., Rocha, R. R., Laurindo, M. V., de Moraes, F. L. L., & da Rocha, S. L. (2019) · Brazilian Archives of Biology and Technology · doi:10.1590/1678-4324-2019180503 · Cited by 100 · see citing works

Efficacy of Triclosan as an Antimicrobial Hand Soap and Its Potential Impact on Antimicrobial Resistance: A Focused Review

Giuliano, C. A., & Rybak, M. J. (2015) · Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy · doi:10.1002/phar.1553 · Cited by 98 · see citing works

Effects of exposure to quaternary-ammonium-based biocides on antimicrobial susceptibility and tolerance to physical stresses in bacteria from organic foods

Gadea, R., Fuentes, M. Á. F., Pulido, R. P., Gálvez, A., & Ortega, E. (2016) · Food Microbiology · doi:10.1016/j.fm.2016.10.037 · Cited by 96 · see citing works

New Drugs for the Treatment of Pseudomonas aeruginosa Infections with Limited Treatment Options: A Narrative Review

Losito, A. R., Raffaelli, F., Giacomo, P. D., & Tumbarello, M. (2022) · Antibiotics · doi:10.3390/antibiotics11050579 · Cited by 91 · see citing works

Effect of triclosan or a phenolic farm disinfectant on the selection of antibiotic-resistant Salmonella enterica

Randall, L. P., Cooles, S. W., Piddock, L. J. V., & Woodward, M. J. (2004) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkh376 · Cited by 89 · see citing works

Carbapenemase-producing bacteria in companion animals: a public health concern on the horizon

Abraham, S., Wong, H. S., Turnidge, J. D., Johnson, J. R., & Trott, D. J. (2014) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkt518 · Cited by 84 · see citing works

The Epidemiology of Pseudomonas aeruginosa in Oncology Patients in a General Hospital

Griffith, S. J., Nathan, C., Selander, R. K., Chamberlin, W., Gordon, S., Kabins, S. A., & Weinstein, R. A. (1989) · The Journal of Infectious Diseases · doi:10.1093/infdis/160.6.1030 · Cited by 83 · see citing works

The many antibiotic resistance and tolerance strategies of Pseudomonas aeruginosa

Sindeldecker, D. A., & Stoodley, P. (2021) · Biofilm · doi:10.1016/j.bioflm.2021.100056 · Cited by 83 · see citing works

Isolation of Methicillin-Resistant Staphylococcus aureus from the Environment in a Veterinary Teaching Hospital

Weese, J. S., DaCosta, T., Button, L., Goth, K., Ethier, M., & Boehnke, K. (2004) · Journal of Veterinary Internal Medicine · doi:10.1111/j.1939-1676.2004.tb02568.x · Cited by 82 · see citing works

Enterococcus Virulence and Resistant Traits Associated with Its Permanence in the Hospital Environment

Geraldes, C., Tavares, L. M., Gil, S., & Oliveira, M. (2022) · Antibiotics · doi:10.3390/antibiotics11070857 · Cited by 81 · see citing works

Diversity of -lactam resistance mechanisms in cystic fibrosis isolates of Pseudomonas aeruginosa: a French multicentre study

Llanes, C., Pourcel, C., Richardot, C., Plésiat, P., Fichant, G. A., Cavallo, J.-D., Mérens, A., on behalf of the GERPA Study Group, Vu-Thien, H., Leclercq, R., et al. (2013) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkt115 · Cited by 78 · see citing works

Outer membrane protein shifts in biocide-resistant Pseudomonas aeruginosa PAO1

Winder, C. L., Al-Adham, I. S. I., Malek, S. M. A. A., Büültjens, T. E. J., Horrocks, A. J., & Collier, P. J. (2000) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.2000.01119.x · Cited by 78 · see citing works

Pseudomonas aeruginosa in hospital water systems: biofilms, guidelines, and practicalities

Walker, J. T., & Moore, G. (2014) · Journal of Hospital Infection · doi:10.1016/j.jhin.2014.11.019 · Cited by 77 · see citing works

Genomics of antibiotic‐resistance prediction in Pseudomonas aeruginosa

Jeukens, J., Freschi, L., Kukavica‐Ibrulj, I., Emond-Rhéault, J.-G., Tucker, N. P., & Lévesque, R. C. (2017) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13358 · Cited by 74 · see citing works

Mechanisms of β-lactam Resistance Among Pseudomonas aeruginosa

Wolter, D. J., & Lister, P. (2012) · Current Pharmaceutical Design · doi:10.2174/138161213804070311 · Cited by 72 · see citing works

Colistin Resistance Gene mcr-1 Mediates Cell Permeability and Resistance to Hydrophobic Antibiotics

Li, B., Yin, F., Zhao, X., Guo, Y., Wang, W., Wang, P., Zhu, H., Yin, Y., & Wang, X. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.03015 · Cited by 72 · see citing works

Distribution of biocide resistant genes and biocides susceptibility in multidrug-resistant Klebsiella pneumoniae, Pseudomonas aeruginosa and Acinetobacter baumannii — A first report from the Kingdom of Saudi Arabia

Vijayakumar, R., Sandle, T., Al-Aboody, M. S., AlFonaisan, M. K., Alturaiki, W., Mickymaray, S., Premanathan, M., & Alsagaby, S. A. (2018) · Journal of Infection and Public Health · doi:10.1016/j.jiph.2018.05.011 · Cited by 71 · see citing works

High Prevalence of blaNDM-1, blaVIM, qacE, and qacEΔ1 Genes and Their Association with Decreased Susceptibility to Antibiotics and Common Hospital Biocides in Clinical Isolates of Acinetobacter baumannii

Gomaa, F. A. M., Helal, Z. H., & Khan, M. I. (2017) · Microorganisms · doi:10.3390/microorganisms5020018 · Cited by 69 · see citing works

Hospitalized Pets as a Source of Carbapenem-Resistance

Gentilini, F., Turba, M. E., Pasquali, F., Mion, D., Romagnoli, N., Zambon, E., Terni, D., Peirano, G., Pitout, J. D. D., Parisi, A., et al. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02872 · Cited by 68 · see citing works

Escherichia coli and selected veterinary and zoonotic pathogens isolated from environmental sites in companion animal veterinary hospitals in southern Ontario.

Murphy, C. P., Reid‐Smith, R. J., Boerlin, P., Weese, J. S., Prescott, J. F., Janecko, N., Hassard, L. E., & McEwen, S. A. (2010) · PubMed Central · Cited by 67 · see citing works

Resistance of Animal Strains of Pseudomonas aeruginosa to Carbapenems

Haenni, M., Bour, M., Châtre, P., Madec, J.-Y., Plésiat, P., & Jeannot, K. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01847 · Cited by 63 · see citing works

Evolution of biofilm-forming pathogenic bacteria in the presence of nanoparticles and antibiotic: adaptation phenomena and cross-resistance

Mann, R., Holmes, A. M., McNeilly, O., Cavaliere, R., Sotiriou, G. A., Rice, S. A., & Gunawan, C. (2021) · Journal of Nanobiotechnology · doi:10.1186/s12951-021-01027-8 · Cited by 63 · see citing works

Environmental surveillance for Salmonella enterica in a veterinary teaching hospital

Burgess, B. A., Morley, P. S., & Hyatt, D. R. (2004) · Journal of the American Veterinary Medical Association · doi:10.2460/javma.2004.225.1344 · Cited by 63 · see citing works

ESBL colonization and acquisition in a hospital population: The molecular epidemiology and transmission of resistance genes

Hagel, S., Makarewicz, O., Hartung, A., Weiß, D., Stein, C., Brandt, C., Schumacher, U., Ehricht, R., Patchev, V. K., & Pletz, M. W. (2019) · PLoS ONE · doi:10.1371/journal.pone.0208505 · Cited by 61 · see citing works

Effect of sub-lethal concentrations of biocides on the susceptibility to antibiotics of multi-drug resistant Salmonella enterica strains

Molina-González, D., Alonso‐Calleja, C., Alonso-Hernando, A., & Capita, R. (2013) · Food Control · doi:10.1016/j.foodcont.2013.11.046 · Cited by 60 · see citing works

Triclosan: antimicrobial mechanisms, antibiotics interactions, clinical applications, and human health

Shrestha, P., Zhang, Y., Chen, W., & Wong, T.-Y. (2020) · Journal of Environmental Science and Health Part C · doi:10.1080/26896583.2020.1809286 · Cited by 60 · see citing works

Hospital environment as a reservoir for cross transmission: cleaning and disinfection procedures.

Protano, C., Cammalleri, V., Spica, V. R., Valeriani, F., & Vitali, M. (2019) · PubMed · doi:10.7416/ai.2019.2305 · Cited by 59 · see citing works

Evidence‐based veterinary dermatology: a systematic review of interventions for treatment ofPseudomonasotitis in dogs

Nuttall, T. J., & Cole, L. K. (2007) · Veterinary Dermatology · doi:10.1111/j.1365-3164.2007.00575.x · Cited by 58 · see citing works

An inside look at a biofilm: Pseudomonas aeruginosa flagella biotracking

Ozer, E., Yaniv, K., Chetrit, E., Boyarski, A., Meijler, M. M., Berkovich, R., Kushmaro, A., & Alfonta, L. (2021) · Science Advances · doi:10.1126/sciadv.abg8581 · Cited by 58 · see citing works

Resident Cats in Small Animal Veterinary Hospitals Carry Multi-Drug Resistant Enterococci and are Likely Involved in Cross-Contamination of the Hospital Environment

Ghosh, A., KuKanich, K. S., Brown, C. E., & Žůrek, L. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00062 · Cited by 57 · see citing works

Tolerance of Clostridium perfringens biofilms to disinfectants commonly used in the food industry

Charlebois, A., Jacques, M., Boulianne, M., & Archambault, M. (2016) · Food Microbiology · doi:10.1016/j.fm.2016.09.009 · Cited by 57 · see citing works

Antimicrobial, Antibiofilm, and Anti-persister Activities of Penfluridol Against Staphylococcus aureus

Liu, Y., She, P., Xu, L., Chen, L., Li, Y., Liu, S., Li, Z., Hussain, Z. B., & Wu, Y. C. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.727692 · Cited by 56 · see citing works

Pseudomonas aeruginosa outer membrane protein OprH: expression from the cloned gene and function in EDTA and gentamicin resistance

Bell, A., Bains, M., & Hancock, R. E. W. (1991) · Journal of Bacteriology · doi:10.1128/jb.173.21.6657-6664.1991 · Cited by 55 · see citing works

Resistance and cross-resistance to oxidising agents of bacterial isolates from endoscope washer disinfectors

Martin, D. J. H., Denyer, S. P., McDonnell, G. E., & Maillard, J. (2008) · Journal of Hospital Infection · doi:10.1016/j.jhin.2008.04.010 · Cited by 55 · see citing works

SAAP-148 Eradicates MRSA Persisters Within Mature Biofilm Models Simulating Prosthetic Joint Infection

Scheper, H., Wubbolts, J. M., Verhagen, J. A. M., de Visser, A. W., van der Wal, R. J. P., Visser, L. G., de Boer, M. G. J., & Nibbering, P. H. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.625952 · Cited by 55 · see citing works

Environmental Cleaning and Disinfection

Traverse, M., & Aceto, H. W. (2014) · Veterinary Clinics of North America Small Animal Practice · doi:10.1016/j.cvsm.2014.11.011 · Cited by 54 · see citing works

Association between biofilm and multi/extensive drug resistance in diabetic foot infection

Vatan, A., Saltoğlu, N., Yemişen, M., Balkan, İ. İ., Sürme, S., Demiray, T., Mete, B., Tabak, F., & Study Group, C. D. F. (2018) · International Journal of Clinical Practice · doi:10.1111/ijcp.13060 · Cited by 53 · see citing works

Pseudomonas aeruginosa adapts to octenidine in the laboratory and a simulated clinical setting, leading to increased tolerance to chlorhexidine and other biocides

Shepherd, M. J., Moore, G., Wand, M. E., Sutton, J. M., & Bock, L. J. (2018) · Journal of Hospital Infection · doi:10.1016/j.jhin.2018.03.037 · Cited by 52 · see citing works

From Copper Tolerance to Resistance in Pseudomonas aeruginosa towards Patho-Adaptation and Hospital Success

Virieux-Petit, M., Hammer-Dedet, F., Aujoulat, F., Jumas‐Bilak, E., & Romano-Bertrand, S. (2022) · Genes · doi:10.3390/genes13020301 · Cited by 51 · see citing works

Acquisition and persistence of antimicrobial-resistant bacteria isolated from dogs and cats admitted to a veterinary teaching hospital

Hamilton, E., Kruger, J. M., Schall, W. D., Beal, M. W., Manning, S. D., & Kaneene, J. B. (2013) · Journal of the American Veterinary Medical Association · doi:10.2460/javma.243.7.990 · Cited by 51 · see citing works

Detection of Antiseptic-Resistance Genes in Pseudomonas and Acinetobacter spp. Isolated From Burn Patients

Mahzounieh, M., Khoshnood, S., Ebrahimi, A., Saied, H. D., & Yaghoubian, M. (2014) · Jundishapur Journal of Natural Pharmaceutical Products · doi:10.17795/jjnpp-15402 · Cited by 50 · see citing works

Antibiotic Resistance in Pseudomonas

Laborda, P., Hernando‐Amado, S., Martínez, J. L., & Sanz‐García, F. (2022) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-08491-1_5 · Cited by 50 · see citing works

Cardiovascular Device Infections in Dogs: Report of 8 Cases and Review of The Literature

Fine, D. M., & Tobias, A. H. (2007) · Journal of Veterinary Internal Medicine · doi:10.1111/j.1939-1676.2007.tb01948.x · Cited by 45 · see citing works

Bacteriostatic and bactericidal activities of eight fluoroquinolones against MexAB-OprM-overproducing clinical strains of Pseudomonas aeruginosa

Dupont, P., Hocquet, D., Jeannot, K., Chavanet, P., & Plésiat, P. (2005) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dki030 · Cited by 44 · see citing works

Antibiotic susceptibility of glutaraldehyde-tolerant Mycobacterium chelonae from bronchoscope washing machines

Nomura, K., Ogawa, M., Miyamoto, H., Muratani, T., & Taniguchi, H. (2004) · American Journal of Infection Control · doi:10.1016/j.ajic.2003.07.007 · Cited by 44 · see citing works

Prevalence of resistance genes to biocides in antibiotic-resistant Pseudomonas aeruginosa clinical isolates

Kheljan, M. N., Habibzadeh, S., Vaez, H., Arzanlou, M., Safarirad, S., Bazghandi, S. A., Sahebkar, A., & Khademi, F. (2021) · Molecular Biology Reports · doi:10.1007/s11033-021-07032-2 · Cited by 44 · see citing works

Chlorhexidine leads to the evolution of antibiotic-resistant Pseudomonas aeruginosa

TagElDein, M. A., Yassin, A. S., El‐Tayeb, O. M., & Kashef, M. T. (2021) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-021-04292-5 · Cited by 43 · see citing works

Nosocomial outbreak of Pseudomonas aeruginosa associated with a drinking water fountain

Costa, D., Bousseau, A., Ayraud-Thévenot, S., Dufour, X., Laland, C., Burucoa, C., & Castel, O. (2015) · Journal of Hospital Infection · doi:10.1016/j.jhin.2015.07.010 · Cited by 43 · see citing works

Pseudomonas otitis externa in dogs.

Pye, C. (2018) · PubMed Central · Cited by 41 · see citing works

Presence of qacEΔ1 Gene and Susceptibility to a Hospital Biocide in Clinical Isolates of Pseudomonas aeruginosa Resistant to Antibiotics

Romão, C. M. C. P. A., de Miranda, C. A. C., da Silva, J. W., Clementino, M. M., de Filippis, I., & Asensi, M. D. (2011) · Current Microbiology · doi:10.1007/s00284-011-9934-0 · Cited by 40 · see citing works

Benzyl Isothiocyanate Attenuates Inflammasome Activation in Pseudomonas aeruginosa LPS-Stimulated THP-1 Cells and Exerts Regulation through the MAPKs/NF-κB Pathway

Park, W. S., Lee, J. H., Na, G., Park, S.-G., Seo, S., Choi, J. S., Jung, W., & Choi, I. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031228 · Cited by 40 · see citing works

Rapid monitoring of Pseudomonas aeruginosa in hospital water systems: a key priority in prevention of nosocomial infection

Asghari, F. B., Nikaeen, M., & Mirhendi, H. (2013) · FEMS Microbiology Letters · doi:10.1111/1574-6968.12132 · Cited by 40 · see citing works

Resistance of Pseudomonas to Quaternary Ammonium Compounds

Adair, F. W., Geftic, S. G., & Gelzer, J. (1971) · Applied Microbiology · doi:10.1128/am.21.6.1058-1063.1971 · Cited by 39 · see citing works

Potential impact of biocide adaptation on selection of antibiotic resistance in bacterial isolates

Elekhnawy, E., Sonbol, F., Abdelaziz, A., & El-Banna, T. (2020) · Future Journal of Pharmaceutical Sciences · doi:10.1186/s43094-020-00119-w · Cited by 38 · see citing works

The prevalence and mechanism of triclosan resistance in Escherichia coli isolated from urine samples in Wenzhou, China

Zeng, W., Xu, W., Xu, Y., Liao, W., Zhao, Y., Zheng, X., Xu, C., Zhou, T., & Cao, J. (2020) · Antimicrobial Resistance and Infection Control · doi:10.1186/s13756-020-00823-5 · Cited by 37 · see citing works

Effect of MexXY Overexpression on Ceftobiprole Susceptibility in Pseudomonas aeruginosa

Baum, E. Z., Crespo‐Carbone, S. M., Morrow, B. J., Davies, T. A., Foleno, B. D., He, W., Queenan, A. M., & Bush, K. (2009) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00018-09 · Cited by 35 · see citing works

Antimicrobial resistance patterns of Pseudomonas aeruginosa isolated from canine clinical cases at a veterinary academic hospital in South Africa

Sebola, D. C., Eliasi, U. L., Oguttu, J. W., & Qekwana, D. N. (2020) · Journal of the South African Veterinary Association · doi:10.4102/jsava.v91i0.2052 · Cited by 34 · see citing works

Antimicrobial Susceptibility of Persister Biofilm Cells of Bacillus cereus and Pseudomonas fluorescens

Fernandes, S., Gomes, I. B., Sousa, S. F., & Simões, M. V. (2022) · Microorganisms · doi:10.3390/microorganisms10010160 · Cited by 30 · see citing works

Antimicrobial Resistance and Type III Secretion System Virulotypes of Pseudomonas aeruginosa Isolates from Dogs and Cats in Primary Veterinary Hospitals in Japan: Identification of the International High-Risk Clone Sequence Type 235

Hayashi, W., Izumi, K., Yoshida, S., Takizawa, S., Sakaguchi, K., Iyori, K., Minoshima, K.-I., Takano, S., Kitagawa, M., Nagano, Y., et al. (2021) · Microbiology Spectrum · doi:10.1128/spectrum.00408-21 · Cited by 29 · see citing works

Pseudomonas aeruginosa Pneumonia: Evolution of Antimicrobial Resistance and Implications for Therapy

Lynch, J. P., & Zhanel, G. G. (2022) · Seminars in Respiratory and Critical Care Medicine · doi:10.1055/s-0041-1740109 · Cited by 24 · see citing works

Guidelines for reducing pathogens in veterinary hospitals: disinfectant selection, cleaning protocols, and hand hygiene.

Portner, J. A., & Johnson, J. A. (2010) · PubMed · Cited by 23 · see citing works

Bacterial quorum‐sensing signal IQS induces host cell apoptosis by targeting POT1–p53 signalling pathway

Wang, J., Wang, C., Yu, H., Ahator, S. D., Wu, X., Lv, S., & Zhang, L. (2019) · Cellular Microbiology · doi:10.1111/cmi.13076 · Cited by 21 · see citing works

Tolerance to Glutaraldehyde in Escherichia coli Mediated by Overexpression of the Aldehyde Reductase YqhD by YqhC

Pereira, B. M. P., Salim, M. A., Rai, N., & Tagkopoulos, I. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.680553 · Cited by 21 · see citing works

Susceptibility to biocides and the prevalence of biocides resistance genes in clinical multidrug-resistant Pseudomonas aeruginosa isolates from Hamadan, Iran

Goodarzi, R., Yousefimashouf, R., Taheri‬, M., Nouri, F., & Asghari, B. (2021) · Molecular Biology Reports · doi:10.1007/s11033-021-06533-4 · Cited by 20 · see citing works

Exogenous acquisition of Pseudomonas aeruginosa in intensive care units: a prospective multi-centre study (DYNAPYO study)

Coppry, M., Leroyer, C., Saly, M., Venier, A.-G., Slekovec, C., Bertrand, X., Parer, S., Alfandari, S., Cambau, E., Mégarbane, B., et al. (2019) · Journal of Hospital Infection · doi:10.1016/j.jhin.2019.08.008 · Cited by 19 · see citing works

Evaluation of a Biocide Used in the Biological Isolation and Containment Unit of a Veterinary Teaching Hospital

Geraldes, C., Verdial, C., Cunha, E. S., Almeida, V., Tavares, L. M., Oliveira, M., & Gil, S. (2021) · Antibiotics · doi:10.3390/antibiotics10060639 · Cited by 17 · see citing works

Molecular epidemiology of antimicrobial-resistant Pseudomonas aeruginosa in a veterinary teaching hospital environment

Soonthornsit, J., Pimwaraluck, K., Kongmuang, N., Pratya, P., & Phumthanakorn, N. (2022) · Veterinary Research Communications · doi:10.1007/s11259-022-09929-0 · Cited by 17 · see citing works

Impact of intensive care unit relocation and role of tap water on an outbreak of Pseudomonas aeruginosa expressing OprD-mediated resistance to imipenem

Tran‐Dinh, A., Neulier, C., Amara, M., Nebot, N., Troché, G., Breton, N., Zuber, B., Cavelot, S., Pangon, B., Bedos, J. P., et al. (2018) · Journal of Hospital Infection · doi:10.1016/j.jhin.2018.05.016 · Cited by 16 · see citing works

Carbapenem Resistance Determinants Acquired through Novel Chromosomal Integrations in Extensively Drug-Resistant Pseudomonas aeruginosa

Janice, J., Agyepong, N., Owusu-Ofori, A. K., Govinden, U., Essack, S. Y., Samuelsen, Ø., Sundsfjord, A., & Pedersen, T. (2021) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00289-21 · Cited by 15 · see citing works

Quorum machinery: Effect of the las system in rhl regulation of P. aeruginosa

Alfiniyah, C., Bees, M. A., & Wood, A. J. (2019) · AIP conference proceedings · doi:10.1063/1.5139147 · Cited by 11 · see citing works

Controlling bacteriological contamination of environmental surfaces at the biological isolation and containment unit of a veterinary teaching hospital

Verdial, C., Carneiro, C., Machado, I., Tavares, L. M., Almeida, V., Oliveira, M., & Gil, S. (2021) · Irish Veterinary Journal · doi:10.1186/s13620-021-00197-z · Cited by 10 · see citing works

Biochemistry of Bacterial Biofilm: Insights into Antibiotic Resistance Mechanisms and Therapeutic Intervention

Azeem, K., Fatima, S., Ali, A., Ubaid, A., Husain, F. M., & Abid, M. (2025) · Life · doi:10.3390/life15010049 · Cited by 112 · see citing works

Prevalence of Infections and Antimicrobial Resistance of ESKAPE Group Bacteria Isolated from Patients Admitted to the Intensive Care Unit of a County Emergency Hospital in Romania

Bereanu, A. S., Bereanu, R., Mohor, C. I., Vintilă, B. I., Codru, I. R., Olteanu, C., & Sava, M. (2024) · Antibiotics · doi:10.3390/antibiotics13050400 · Cited by 70 · see citing works

A systematic review of diabetic foot infections: pathogenesis, diagnosis, and management strategies

Maity, S., Leton, N., Nayak, N., Jha, A. K., Anand, N., Thompson, K., Boothe, D., Cromer, A., Garcia, Y., Al-Islam, A., et al. (2024) · Frontiers in Clinical Diabetes and Healthcare · doi:10.3389/fcdhc.2024.1393309 · Cited by 79 · see citing works

Biocides as drivers of antibiotic resistance: A critical review of environmental implications and public health risks

Sousa, M., Machado, I., Simões, L. C., & Simões, M. V. (2025) · Environmental Science and Ecotechnology · doi:10.1016/j.ese.2025.100557 · Cited by 69 · see citing works

Impact of multidrug resistance on the virulence and fitness of Pseudomonas aeruginosa: a microbiological and clinical perspective

Sendra, E., Fernández-Muñoz, A., Zamorano, L., Oliver, A., Horcajada, J. P., Juan, C., & Gómez-Zorrilla, S. (2024) · Infection · doi:10.1007/s15010-024-02313-x · Cited by 59 · see citing works

A Systematic Review on Antimicrobial Resistance in Ghana from a One Health Perspective

Donkor, E. S., Odoom, A., Osman, A.-H., Darkwah, S., & Kotey, F. C. N. (2024) · Antibiotics · doi:10.3390/antibiotics13070662 · Cited by 52 · see citing works

P. aeruginosa interactions with other microbes in biofilms during co-infection

Oliveira, M., Cunha, E. S., Tavares, L. M., & Serrano, I. D. (2023) · AIMS Microbiology · doi:10.3934/microbiol.2023032 · Cited by 27 · see citing works

Orthopedic Implant Infection Management: Prevention, Barrier Breakthrough, and Immunomodulation

Yi, J., Chen, Z., Li, R., Xu, Z., Song, Y., Fan, Q., Wang, J., & Chai, W. (2025) · ACS Nano · doi:10.1021/acsnano.4c17509 · Cited by 27 · see citing works

Antimicrobial Resistance: What Lies Beneath This Complex Phenomenon?

Sakalauskienė, G. V., & Radzevičienė, A. (2024) · Diagnostics · doi:10.3390/diagnostics14202319 · Cited by 21 · see citing works

The chemical composition and the preservative, antimicrobial, and antioxidant effects of Thymus broussonetii Boiss. essential oil: an in vitro and in silico approach

Boukhira, S., Amrati, F. E., Chebaibi, M., Grafov, A., Mothana, R. A., Al-Yousef, H. M., & Bousta, D. (2024) · Frontiers in Chemistry · doi:10.3389/fchem.2024.1402310 · Cited by 17 · see citing works

Enzyme Production and Inhibitory Potential of Pseudomonas aeruginosa: Contrasting Clinical and Environmental Isolates

Aqel, H., Sannan, N., Foudah, R., & Al‐Hunaiti, A. (2023) · Antibiotics · doi:10.3390/antibiotics12091354 · Cited by 17 · see citing works

From disinfection to pathogenicity: Occurrence, resistome risks and assembly mechanism of biocide and metal resistance genes in hospital wastewaters

Xu, C., Zhang, Y., Hu, C., Shen, C., Li, F., Xu, Y., Liu, W., & Shi, D. (2024) · Environmental Pollution · doi:10.1016/j.envpol.2024.123910 · Cited by 16 · see citing works

Sublethal Sodium Hypochlorite Exposure: Impact on Resistance-Nodulation-Cell Division Efflux Pump Overexpression and Cross-Resistance to Imipenem

Nam, J.-H., & Yoo, J. S. (2024) · Antibiotics · doi:10.3390/antibiotics13090828 · Cited by 13 · see citing works

Mechanisms of Pseudomonas aeruginosa Resilience Against Antibiotic Treatment and Outlooks of Emerging Treatment Strategies

Krūmiņa, A., Zeltiņa, I., Simsone, P., Eulitz, E., Reinis, A., & Vīksna, L. (2026) · Medicina · doi:10.3390/medicina62010163 · Cited by 12 · see citing works

Antimicrobial resistance profile, biofilm forming capacity and associated factors of multidrug resistance in Pseudomonas aeruginosa among patients admitted at Tikur Anbessa Specialized Hospital and Yekatit 12 Hospital Medical College in Addis Ababa, Ethiopia

Olana, M. D., Asrat, D., & Swedberg, G. (2024) · BMC Infectious Diseases · doi:10.1186/s12879-024-10359-3 · Cited by 14 · see citing works

Comparative analysis of quorum sensing mechanisms in Pseudomonas aeruginosa and Klebsiella pneumoniae: implications for antibiotic resistance

Venkatesan, B. V., Anbarasu, A., & Muniyan, R. (2025) · Archives of Microbiology · doi:10.1007/s00203-025-04603-w · Cited by 11 · see citing works

Molecular and genomic insights into multidrug-resistant (MDR) and extensively drug-resistant (XDR) Pseudomonas aeruginosa causing burn wound infections in Bangladesh

Mondol, S. M., Islam, M. R., Mia, M. E., Hassan, M. H., Farhad, F., Akter, K., Shakil, S. K., Islam, I., Rakhi, N. N., Mustary, J. F., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-11614-6 · Cited by 15 · see citing works

Evolving trends among Pseudomonas aeruginosa: a 12-year retrospective study from the United Arab Emirates

Thomsen, J., Menezes, G. A., Abdulrazzaq, N. M., Moubareck, C. A., Senok, A. C., & Everett, D. (2023) · Frontiers in Public Health · doi:10.3389/fpubh.2023.1243973 · Cited by 12 · see citing works

Antimicrobial management of complex biofilms in diabetic foot ulcers: a microbiological perspective

Oliveira, M., Cunha, E. S., Tavares, L. M., & Serrano, I. D. (2025) · Expert Review of Anti-infective Therapy · doi:10.1080/14787210.2025.2538614 · Cited by 10 · see citing works

Veterinary Clinics as Reservoirs for Pseudomonas aeruginosa: A Neglected Pathway in One Health Surveillance

Nadăș, G., Manchon, A., Bouari, C., & Fiț, N. (2025) · Antibiotics · doi:10.3390/antibiotics14070720 · Cited by 13 · see citing works

Genomic Insights into Pluralibacter gergoviae Sheds Light on Emergence of a Multidrug-Resistant Species Circulating between Clinical and Environmental Settings

Furlan, J. P. R., & Stehling, E. G. (2023) · Pathogens · doi:10.3390/pathogens12111335 · Cited by 12 · see citing works

Impact of Antimicrobial Resistance of Pseudomonas aeruginosa in Urine of Small Companion Animals in Global Context: Comprehensive Analysis

Pereira, A. F., de Sousa, T., Silva, C., Igrejas, G., & Poeta, P. A. C. Q. D. (2025) · Veterinary Sciences · doi:10.3390/vetsci12020157 · Cited by 10 · see citing works

Antimicrobial Resistance Mechanisms in Carbapenem-Resistant Pseudomonas aeruginosa Clinical Strains Isolated in Shanghai, China

ZHU, K., LI, S., Guo, Z., Xiao, C., & Wei, Q. (2025) · Polish Journal of Microbiology · doi:10.33073/pjm-2025-022 · Cited by 9 · see citing works

PqsR-specific quorum sensing inhibitors targeting Pseudomonas aeruginosa : current advances and future directions

Aziz, M., Ahmed, K., & Ravichandran, V. (2025) · Journal of Chemotherapy · doi:10.1080/1120009x.2025.2510093 · Cited by 8 · see citing works

Genomic insights into five selected multidrug-resistant Pseudomonas aeruginosa isolated from Sodwana Bay, South Africa

Serepa‐Dlamini, M. H., Kondiah, K., Maumela, P., Ogofure, A. G., & Green, E. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1578578 · Cited by 8 · see citing works

Impact of disinfection methods used in the slaughterhouse environment on microbiome diversity throughout the meat production chain

Naim, W., Manetsberger, J., Lerma, L. L., Benomar, N., Gómez, N. C., Bertomeu, I. D. L. S. C., Díaz, J. Á. G., & Abriouel, H. (2024) · Current Research in Microbial Sciences · doi:10.1016/j.crmicr.2024.100336 · Cited by 7 · see citing works

Prevalence and Antimicrobial Resistance of Gram-Negative ESKAPE Pathogens Isolated from Tertiary Care Hospital in Eastern India

Rana, P., Routray, S. P., Mandal, S. D., Panigrahy, R., Sahoo, A. K., & Subudhi, E. (2025) · Applied Sciences · doi:10.3390/app15158171 · Cited by 7 · see citing works

Host-derived peptide signals regulate Pseudomonas aeruginosa virulence stress via the ParRS and CprRS two-component systems

Zhao, N., Zhu, Z., Feng, H., Song, Y., Huang, Q., Mou, X., Nong, C., He, Y., & Bao, R. (2023) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2023.132512 · Cited by 7 · see citing works

Characterization of Virulence Genes Associated with Type III Secretion System and Biofilm Formation in Pseudomonas aeruginosa Clinical Isolates

Ali, A. S. B. E., Ozler, B., & Baddal, B. (2023) · Current Microbiology · doi:10.1007/s00284-023-03498-4 · Cited by 6 · see citing works

Pseudomonas aeruginosa bloodstream infections in internal medicine wards: A large Italian multicenter retrospective study

Corcione, S., Pinna, S. M., Vena, A., Schenone, M., Sanino, M., Pascale, R., Pivetta, E. E., Giacobbe, D. R., Giannella, M., Shbaklo, N., et al. (2025) · PLoS ONE · doi:10.1371/journal.pone.0317540 · Cited by 4 · see citing works

Targeting antimicrobial resistance through vaccinology: a review of preclinical and clinical pipeline vaccines against WHO priority bacterial pathogens

Hetta, ‏. F., Alatawi, Z., Bukhari, S. Q., Atoom, A. M., Ellah, N. H. A., & Ramadan, Y. N. (2026) · Infection · doi:10.1007/s15010-026-02752-8 · Cited by 4 · see citing works

Prevalence and Multidrug Resistance of WHO-Priority Bacterial Pathogens in a Romanian Intensive Care Unit

Bereanu, A. S., Vintilă, B. I., Oprinca-Muja, L.-A., Bereanu, R., Codru, I. R., Bădilă, R. M., Neamțu, S. I., Mohor, C. I., Prodan, L., & Sava, M. (2026) · Journal of Clinical Medicine · doi:10.3390/jcm15072799 · Cited by 5 · see citing works

Integrating resistance biology, virulence networks, and precision therapeutics against multidrug-resistant Pseudomonas aeruginosa

Abdelmoneim, H. M., Alhudhaibi, A. M., Taha, R. H., Bendif, H., & Taha, T. H. (2026) · Infection · doi:10.1007/s15010-026-02817-8 · Cited by 3 · see citing works

Advancements in two-dimensional scanning sterilization utilizing high repetition rate laser-induced quasi-continuous plasmas

Chen, F., Wang, S., Zhang, W., Guo, Y. C., Zhang, Y., Liang, J., Zhang, L., Yin, W., Xiao, L., & Jia, S. (2024) · Optics & Laser Technology · doi:10.1016/j.optlastec.2024.111091 · Cited by 3 · see citing works

In Vivo Antimicrobial Activity of Nisin Z Against S. aureus and Polyurea Pharmadendrimer PUREG4OEI48 Against P. aeruginosa from Diabetic Foot Infections

Serrano, I. D., Mil‐Homens, D., Pires, R. F., Bonifácio, V. D. B., Guerreiro, J. F., Cunha, E. S., Costa, S. S., Tavares, L. M., & Oliveira, M. (2025) · Antibiotics · doi:10.3390/antibiotics14050444 · Cited by 3 · see citing works

Convergence of multidrug resistance and efflux-mediated biocide tolerance in klebsiella pneumoniae ST307: implications for nosocomial infection control in Iranian hospitals

Goodarzi, R., Kazemi, S., Nasershariati, M. H., & Asghari, B. (2025) · BMC Infectious Diseases · doi:10.1186/s12879-025-11178-w · Cited by 3 · see citing works

Companion Animals as Reservoirs of Multidrug Resistance—A Rare Case of an XDR, NDM-1-Producing Pseudomonas aeruginosa Strain of Feline Origin in Greece

Lysitsas, M., Triantafillou, E. A., Chatzipanagiotidou, I., Triantafillou, A., Agorou, G., Filippitzi, M., Giakountis, A., & Valiakos, G. (2025) · Veterinary Sciences · doi:10.3390/vetsci12060576 · Cited by 3 · see citing works

Antimicrobial Resistance Patterns and Epidemiological Distribution of Pathogenic Bacteria in the Pediatric Intensive Care Unit at Beijing Children’s Hospital: A Decade-Long Retrospective Analysis (2014–2023)

Luo, T., Maimaiti, W., & Lyu, Z. (2025) · Infection and Drug Resistance · doi:10.2147/idr.s571466 · Cited by 2 · see citing works

Prevalence and Antibiotic Resistance Patterns of Metallo-Beta-Lactamase-Producing Pseudomonas aeruginosa Isolated from Patients in a Hospital in Zabol, Southeast of Iran

Vaez, H., Yazdanpour, Z., Khademi, F., & Pishdadian, A. (2023) · Infection Epidemiology and Microbiology · doi:10.61186/iem.9.3.201 · Cited by 2 · see citing works

Transcriptome Analysis Reveals the Mechanism of Y0-C10-HSL on Biofilm Formation and Motility of Pseudomonas aeruginosa

Tang, D., Liu, Y., Yao, H., Lin, Y., Xi, Y., Li, M., & Mao, A. (2024) · Pharmaceuticals · doi:10.3390/ph17121719 · Cited by 2 · see citing works

Bacteriophages in Pseudomonas aeruginosa evade the CRISPR-Cas I-F system by depletion of PAM sequences

Ortega-Sanz, I., Rubio, A., & Pérez‐Pulido, A. J. (2025) · Microbial Genomics · doi:10.1099/mgen.0.001423 · Cited by 1 · see citing works

Evaluation of Combinatorial Efficacy of Nisin and Lactoferrin against Pseudomonas Aeruginosa Induced Experimental Pulmonary Infection Model

Preet, S., Kaur, J., Panjeta, A., Dogra, S., & Sharma, S. (2025) · Current Microbiology · doi:10.1007/s00284-025-04578-3 · Cited by 1 · see citing works

Pseudomonas aeruginosa LasI/RhlI quorum sensing system controls protease-mediated autoaggregation behavior, cell envelope characteristics and extracellular proteome responses

Eriksson, A., Turkina, M. V., Ntzouni, M. P., Magnusson, K., & Vikström, E. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1693814 · Cited by 2 · see citing works

Multifaceted antimicrobial mechanisms of NCR147-derived peptides from Medicago truncatula

Tiricz, H., Lima, R. M., Pfeiffer, I., Igaz, N., Domonkos, I., Jenei, S., Howan, D. H. O., Pál, A., Tímár, E., Hunyady-Gulyás, É., et al. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1720738 · Cited by 1 · see citing works

Parallel microevolution of multidrug resistance and hypermucoviscosity in two carbapenem-resistant Pseudomonas aeruginosa clinical isolates with strikingly divergent virulence outcomes

Yang, R., Zhu, R., Lai, C., Zeng, J., Zheng, A., Chen, P., Chen, X., Tian, X., Wang, X., Feng, S., et al. (2026) · BMC Microbiology · doi:10.1186/s12866-025-04703-z · Cited by 1 · see citing works

Integrated Phenotypic, Proteomic (MALDI-TOF MS), and Genomic (WGS) Investigation of a Prolonged Hospital Outbreak of Pseudomonas aeruginosa with High Biofilm-Forming Capacity

Panchi, S. C., Cangui-Panchi, D. S., Palacios, V. E., Becerra, E., Santamaría, A. L., Muñoz, D., Reyes, J., Machado, A., & Garzón-Chávez, D. (2026) · Antibiotics · doi:10.3390/antibiotics15030257 · Cited by 1 · see citing works

Multidrug Resistance and Biocide Susceptibility in Pseudomonas aeruginosa: Insights into Efflux Pump-Mediated Resistance

Nasershariati, M. H., Asghari, B., Zarnegarpour, H. A., & Saki, S. (2025) · Molecular Genetics Microbiology and Virology · doi:10.3103/s0891416825600105 · Cited by 1 · see citing works

Antimicrobial resistance in complicated urinary tract infections: A retrospective study from a rehabilitation centre in a resource-limited setting

Do, D. V., Tran, T. T. H., Tran, T. T. H., Nguyen, Q. H., Truong, T. P., Nguyen, T. T. M., Nong, V. M., & Nguyen, H. L. (2026) · Journal of Global Antimicrobial Resistance · doi:10.1016/j.jgar.2026.04.004 · Cited by 1 · see citing works

Targeting quorum sensing to combat bacterial biofilms: Natural biomass as emerging anti-virulence strategies

Shehabeldine, A. M., Basher, N. S., Hashem, A. H., Ibrahim, N. A., Dora, M. S., & Abdelaziz, A. M. (2026) · Microbial Pathogenesis · doi:10.1016/j.micpath.2026.108519 · Cited by 1 · see citing works

Molecular identification and hydrolase activity profiling of bacteria isolated from septic surface environments using 16S rRNA sequencing

Albayrak, E., & Uluçay, O. (2026) · Molecular Biology Reports · doi:10.1007/s11033-026-11957-x · Cited by 1 · see citing works

Reducing the Spreading of Human Pathogenic Bacteria with a Biomechanical Device

Symochko, L., Silva, J. R., Pinheiro, M. N. C., de Castro, L. M. M. N., & Roseiro, L. M. (2023) · Lecture notes in bioengineering · doi:10.1007/978-3-031-47790-4_30

Isolation, Sensitivity, and Tolerance of Pseudomonas aeruginosa from Canine Otitis

Neeraja, E., Anju, J. R., Kunnuchalil, S. M., Joy, L., Deepa, P. M., Janus, A., Bipin, K. C., Chandran, A., & Rathish, R. L. (2024) · Journal of Advances in Microbiology · doi:10.9734/jamb/2024/v24i7837

Biocide-resistant Pseudomonas oleovorans isolated from water-based coatings used in construction

Ali, M. L., Ferrières, L., Hyötyläinen, T., & Jaß, J. (2024) · Journal of Industrial Microbiology & Biotechnology · doi:10.1093/jimb/kuaf015

Sequential Phage Pretreatment and TiO2–Thyme Essential Oil Photocatalysis: A Synergistic Approach to Pseudomonas aeruginosa Biofilm Inhibition and Control

Said, M. B., Chekir-Jlizi, A., Bel-Haj-Amor, N., Bousselmı, L., & Orange, D. (2026) · Water · doi:10.3390/w18020213

Identification of a novel gene in Pseudomonas aeruginosa promotes persister formation by repressing translation and cell division

Feng, J., Bian, Y., Yin, L., Xu, C., Cheng, Z., Jin, Y., Jin, S., & Wu, W. (2026) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01274-25

Biocide efficacy against extensively drug-resistant (XDR) Pseudomonas aeruginosa patient isolates during planktonic and biofilm growth

Sierra, E., Johnson, J., Ilori, T., Carabetta, V. J., & Nahra, R. (2026) · American Journal of Infection Control · doi:10.1016/j.ajic.2026.04.006

Antimicrobial activity of echinacea-loaded metal-organic framework against Pseudomonas aeruginosa

Ashrafi, F., Moulavi, P., Jamalipanah, Z., Jafari, M., Zomorodi, A. R., & Asadi, S. (2026) · AMB Express · doi:10.1186/s13568-026-02073-x

Molecular and Cellular Mechanisms Underlying Recurrent Urinary Tract Infections Caused by Pseudomonas aeruginosa in Women

Naser, L. A. (2026) · Academia Open · doi:10.21070/acopen.11.2026.13984

Virulence and antimicrobial resistance mechanisms in Pseudomonas aeruginosa in dogs and cats: a review

Chambino, I., Menezes, J., & Belas, A. (2026) · Frontiers in Bacteriology · doi:10.3389/fbrio.2026.1891783

Biofilm and blaOXA-40 Co-Production: A Key Pathogenic Strategy in Hospital-Adapted Pseudomonas aeruginosa

Ghahremanpour, H., Abadi, A. T. B., & Fooladi, A. A. I. (2026) · Archives of Medical Research · doi:10.1016/j.arcmed.2026.103479

Metagenomic indications of potential pathogen-associated and antibiotic resistance risks following UV–chlorine disinfection in sprout production

Wei, Y., Zhu, L., Jin, X., Yao, H., He, S., Feng, P., Yu, F., Xiang, Y., Li, Z., & He, S. (2026) · Environmental Pollution · doi:10.1016/j.envpol.2026.128943

Prevalence and Antimicrobial Resistance of Pseudomonas aeruginosa Recovered from Respiratory and Urinary Specimens in a Lebanese Hospital (2020–2025)

Barakat, R., Ezzeddine, Z., Haidari, R. E., Hassan, S., & Ghssein, G. (2026) · Infectious Disease Reports · doi:10.3390/idr18040087

Long-Term Environmental Surveillance of Pseudomonas aeruginosa in a Hospital Water Distribution System: Trends in Prevalence, Biofilm Formation, and Antimicrobial Susceptibility

Cristina, M. L., Schinca, E., Piccinini, C., Cima, S., Ottria, G., Dupont, C., Carbone, A., & Sartini, M. (2026) · Pathogens · doi:10.3390/pathogens15080868

High-Risk Clones of Carbapenem-Resistant Pseudomonas aeruginosa in India: Genome and Traits

Sivasankar, S., Grobusch, M. P., Sriramajayam, L., & Jeyaraj, S. (2026) · Microbial Drug Resistance · doi:10.1177/10766294261480779

Comprehensive Genotypic Characterization of Antiseptic Resistance Determinants in Pseudomonas aeruginosa Clinical Isolates

Abdullah, S. A., Khalaf, B. H., & Jameel, N. Q. (2026) · The Open Biotechnology Journal · doi:10.2174/0118740707499534260825174015

Phage-first treatment results in subpopulation-driven collateral sensitivity to beta-lactams in an extensively drug-resistant Pseudomonas aeruginosa

Han, C., Patel, K., Gao, H., Sanborn, J. T., Nguyen, T. D., Klem, J. F., Ho, B. M., Kenney, P., Zhao, Y., Wood, T. D., et al. (2026) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00048-26

Artificial intelligence applications in biofilm research: computational approaches for biofilm analysis and antimicrobial prediction

Fortaleza, J. A. G., Cabuhat, K. S. P., Argüello-Ramos, E. D., Cruz, J. T. P., Matamis, J. G., Mamaat, J. E. R., Libres, A. C., Leon, C. S., & Nuevo, J. J. M. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1892814

Healthcare-Associated Infections with Pseudomonas spp. in a Neurosurgical Hospital: Epidemiological and Clinical Insights

Luchian, N., Guțu, C., Salim, C., Pleșea-Condratovici, A., Dabija, M. G., Ciuhodaru, M. I., Duceac, M. C., Marcu, C., Gurzu, I. L., Moraru, I. P., et al. (2026) · Medicina · doi:10.3390/medicina62102019

Emerging Molecular Mechanisms of Antimicrobial Resistance in ESKAPE Pathogens: A Comprehensive Review

Sharma, T., Maurya, I. K., & Chandley, P. (2026) · Journal of the Royal Society of New Zealand · doi:10.1002/snz2.70087

Impact of ESKAPE pathogens on the One Health framework considering epidemiology and environmental occurrence

Silva, C., de Sousa, T., Igrejas, G., Nunes, F. M., & Poeta, P. A. C. Q. D. (2026) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00145-26

Evaluating the qualitative characteristics and heavy elements of hospital water and their relationship with bioresistance in P. aeruginosa.

Al-Hashimi, O. A., Saeed, I. O., & Meani, S. A. L. A. (2024) · Technium BioChemMed · doi:10.47577/biochemmed.v8i.10934 · Cited by 1 · see citing works

The Prevalence of some biofilm formation and Biocide resistance genes of Pseudomonas aeruginosa strains isolated from hospital environments.

abdulmuayn, S., & Al-Saadi, A. G. M. (2026) · DOAJ (DOAJ: Directory of Open Access Journals)

ADAPTAÇÃO, PERSISTÊNCIA E RESISTÊNCIA ANTIMICROBIANA DE PSEUDOMONAS AERUGINOSA NO AMBIENTE HOSPITALAR

Sa, L. D. S. (2026) · Revista Ibero-Americana de Humanidades, Ciências e Educação · doi:10.51891/rease.v12i1.23967

The many antibiotic resistance and tolerance strategies of Pseudomonas aeruginosa

Sindeldecker, D. A., & Stoodley, P. (2021) · Biofilm · doi:10.1016/j.bioflm.2021.100056 · Cited by 83 · see citing works

Tolerance and Persistence of Pseudomonas aeruginosa in Biofilms Exposed to Antibiotics: Molecular Mechanisms, Antibiotic Strategies and Therapeutic Perspectives

Soares, A., Alexandre, K., & Etienne, M. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.02057 · Cited by 115 · see citing works