Small-Colony Variant Selection as a Survival Strategy for Staphylococcus aureus in the Presence of Pseudomonas aeruginosa

Lung Infections Associated with Cystic Fibrosis

Lyczak, J. B., Cannon, C. L., & Pier, G. B. (2002) · Clinical Microbiology Reviews · doi:10.1128/cmr.15.2.194-222.2002 · Cited by 1,634 · see citing works

Small colony variants: a pathogenic form of bacteria that facilitates persistent and recurrent infections

Proctor, R. A., von Eiff, C., Kahl, B. C., Becker, K., McNamara, P., Herrmann, M., & Peters, G. (2006) · Nature Reviews Microbiology · doi:10.1038/nrmicro1384 · Cited by 1,175 · see citing works

Staphyloxanthin Plays a Role in the Fitness of <i>Staphylococcus aureus</i> and Its Ability To Cope with Oxidative Stress

Clauditz, A., Resch, A., Wieland, K.-P., Peschel, A., & Götz, F. (2006) · Infection and Immunity · doi:10.1128/iai.00204-06 · Cited by 509 · see citing works

Selection for Staphylococcus aureus small-colony variants due to growth in the presence of Pseudomonas aeruginosa

Hoffman, L. R., Déziel, É., D’Argenio, D. A., Lepine, F. L., Emerson, J., McNamara, S., Gibson, R. L., Ramsey, B. W., & Miller, S. I. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0606756104 · Cited by 470 · see citing works

The global activator GacA of Pseudomonas aeruginosa PAO positively controls the production of the autoinducer N‐butyryl‐homoserine lactone and the formation of the virulence factors pyocyanin, cyanide, and lipase

Reimmann, C., Beyeler, M., Latifi, A., Winteler, H., Foglino, M., Lazdunski, A. M., & Haas, D. (1997) · Molecular Microbiology · doi:10.1046/j.1365-2958.1997.3291701.x · Cited by 440 · see citing works

Persistent and Relapsing Infections Associated with Small-Colony Variants of Staphylococcus aureus

Proctor, R. A., van Langevelde, P., Kristjansson, M., Maslow, J. N., & Arbeit, R. D. (1995) · Clinical Infectious Diseases · doi:10.1093/clinids/20.1.95 · Cited by 437 · see citing works

Microbiology of Sputum from Patients at Cystic Fibrosis Centers in the United States

Burns, J. L., Emerson, J., Stapp, J. R., Yim, D. L., Krzewinski, J., Louden, L., Ramsey, B. W., & Clausen, C. R. (1998) · Clinical Infectious Diseases · doi:10.1086/514631 · Cited by 420 · see citing works

Structure and Biosynthesis of Staphyloxanthin from Staphylococcus aureus

Pelz, A., Wieland, K.-P., Putzbach, K., Hentschel, P., Albert, K., & Götz, F. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m505070200 · Cited by 378 · see citing works

Mechanism of the antibiotic action pyocyanine

Hassan, H. M., & Fridovich, I. (1980) · Journal of Bacteriology · doi:10.1128/jb.141.1.156-163.1980 · Cited by 371 · see citing works

A site-directed Staphylococcus aureus hemB mutant is a small-colony variant which persists intracellularly

von Eiff, C., Heilmann, C., Proctor, R. A., Woltz, C., Peters, G., & Götz, F. (1997) · Journal of Bacteriology · doi:10.1128/jb.179.15.4706-4712.1997 · Cited by 310 · cited 1× · see citing works

Hydrogen cyanide, a secondary metabolite of Pseudomonas aeruginosa

Castric, P. A. (1975) · Canadian Journal of Microbiology · doi:10.1139/m75-088 · Cited by 304 · see citing works

2-Heptyl-4-hydroxyquinoline N -oxide, an antistaphylococcal agent produced by Pseudomonas aeruginosa

Machan, Z. A., Taylor, G. W., Pitt, T. L., COLE, P. J., & Wilson, R. (1992) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/30.5.615 · Cited by 190 · see citing works

Role of pyocyanin in the acquisition of iron from transferrin

Cox, C. D. (1986) · Infection and Immunity · doi:10.1128/iai.52.1.263-270.1986 · Cited by 189 · see citing works

Microevolution of Cytochrome bd Oxidase in Staphylococci and Its Implication in Resistance to Respiratory Toxins Released by Pseudomonas

Voggu, L., Schlag, S., Biswas, R., Rosenstein, R., Rausch, C. R., & Götz, F. (2006) · Journal of Bacteriology · doi:10.1128/jb.00858-06 · Cited by 136 · see citing works

Staphylococcus aureus small colony variants, electron transport and persistent infections

McNamara, P. J., & Proctor, R. A. (2000) · International Journal of Antimicrobial Agents · doi:10.1016/s0924-8579(99)00170-3 · Cited by 127 · see citing works

Role of physical fitness training in the fibrositis/fibromyalgia syndrome

McCain, G. A. (1986) · The American Journal of Medicine · doi:10.1016/0002-9343(86)90881-8 · Cited by 112 · see citing works

Clinical significance of Staphylococcus aureus in cystic fibrosis

Marks, M. I. (1990) · Infection · doi:10.1007/bf01644186 · Cited by 46 · see citing works

Infection in patients with cystic fibrosis

Rubio, T. T. (1986) · The American Journal of Medicine · doi:10.1016/0002-9343(86)90516-4 · Cited by 26 · see citing works

Selective inhibition by 2-heptyl-4-hydroxyquinoline N-oxide of certain oxidation-reduction reactions

Kogut, M. H., & Lightbown, J. W. (1962) · Biochemical Journal · doi:10.1042/bj0840368 · Cited by 18 · see citing works

Targeting bacterial membrane function: an underexploited mechanism for treating persistent infections

Hurdle, J. G., O’Neill, A. J., Chopra, I., & Lee, R. E., Jr. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2474 · Cited by 871 · see citing works

Multi-species biofilms: living with friendly neighbors

Elias, S., & Banin, E. (2012) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2012.00325.x · Cited by 764 · see citing works

Bacterial Quorum Sensing and Microbial Community Interactions

Abisado, R. G., Benomar, S., Klaus, J. R., Dandekar, A. A., & Chandler, J. R. (2018) · mBio · doi:10.1128/mbio.02331-17 · Cited by 681 · see citing works

Quinolones: from antibiotics to autoinducers

Heeb, S., Fletcher, M. P., Chhabra, S. R., Diggle, S. P., Williams, P. M., & Cámara, M. (2010) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2010.00247.x · Cited by 597 · see citing works

Insights into Cystic Fibrosis Polymicrobial Consortia: The Role of Species Interactions in Biofilm Development, Phenotype, and Response to In-Use Antibiotics

Magalhães, A. P., Lopes, S. P., & Pereira, M. O. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.02146 · Cited by 578 · see citing works

Clinical Significance of Microbial Infection and Adaptation in Cystic Fibrosis

Hauser, A. R., Jain, M., Bar‐Meir, M., & McColley, S. A. (2011) · Clinical Microbiology Reviews · doi:10.1128/cmr.00036-10 · Cited by 408 · see citing works

Ecology and evolution of antimicrobial resistance in bacterial communities

Bottery, M. J., Pitchford, J. W., & Friman, V. (2020) · The ISME Journal · doi:10.1038/s41396-020-00832-7 · Cited by 393 · see citing works

Interactions of Methicillin Resistant Staphylococcus aureus USA300 and Pseudomonas aeruginosa in Polymicrobial Wound Infection

Pastar, I., Nusbaum, A. G., Gil, J., Patel, S. B., Chen, J., Valdes, J., Stojadinovic, O., Plano, L. R., Tomic-Canic, M., & Davis, S. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056846 · Cited by 391 · see citing works

Coculture of Staphylococcus aureus with Pseudomonas aeruginosa Drives S. aureus towards Fermentative Metabolism and Reduced Viability in a Cystic Fibrosis Model

Filkins, L., Graber, J. A., Olson, D. G., Dolben, E. L., Lynd, L. R., Bhuju, S., & O’Toole, G. A. (2015) · Journal of Bacteriology · doi:10.1128/jb.00059-15 · Cited by 342 · see citing works

Clinical Significance and Pathogenesis of Staphylococcal Small Colony Variants in Persistent Infections

Kahl, B. C., Becker, K., & Löffler, B. (2016) · Clinical Microbiology Reviews · doi:10.1128/cmr.00069-15 · Cited by 325 · see citing works

In vivo and In vitro Interactions between Pseudomonas aeruginosa and Staphylococcus spp.

Hotterbeekx, A., Kumar‐Singh, S., Goossens, H., & Malhotra‐Kumar, S. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00106 · Cited by 265 · see citing works

Pseudomonas aeruginosa Alters Staphylococcus aureus Sensitivity to Vancomycin in a Biofilm Model of Cystic Fibrosis Infection

Orazi, G., & O’Toole, G. A. (2017) · mBio · doi:10.1128/mbio.00873-17 · Cited by 224 · see citing works

Staphylococcus aureus Small-Colony Variants Are Independently Associated With Worse Lung Disease in Children With Cystic Fibrosis

Wolter, D. J., Emerson, J., McNamara, S., Buccat, A. M., Qin, X. G., Cochrane, E., Houston, L. S., Rogers, G. B., Marsh, P., Prehar, K., et al. (2013) · Clinical Infectious Diseases · doi:10.1093/cid/cit270 · Cited by 191 · see citing works

Quorum Quenching Agents: Resources for Antivirulence Therapy

Tang, K., & Zhang, X. (2014) · Marine Drugs · doi:10.3390/md12063245 · Cited by 184 · see citing works

Pseudomonas aeruginosa biofilms and their partners in crime

Cendra, M. D. M., & Torrents, E. (2021) · Biotechnology Advances · doi:10.1016/j.biotechadv.2021.107734 · Cited by 179 · see citing works

Staphylococcus aureus sigma B-dependent emergence of small-colony variants and biofilm production following exposure to Pseudomonas aeruginosa 4-hydroxy-2-heptylquinoline-N-oxide

Mitchell, G., Séguin, D. L., Asselin, A.-E., Déziel, E., Cantin, A. M., Frost, E. H., Michaud, S., & Malouin, F. (2010) · BMC Microbiology · doi:10.1186/1471-2180-10-33 · Cited by 165 · see citing works

Two heme-dependent terminal oxidases power Staphylococcus aureus organ-specific colonization of the vertebrate host

Hammer, N. D., Reniere, M. L., Cassat, J. E., Zhang, Y., Hirsch, A. O., Indriati Hood, M., & Skaar, E. P. (2013) · mBio · doi:10.1128/mbio.00241-13 · Cited by 155 · see citing works

Adaptation of Pseudomonas aeruginosa in Cystic Fibrosis Airways Influences Virulence of Staphylococcus aureus In Vitro and Murine Models of Co-Infection

Baldan, R., Cigana, C., Testa, F., Bianconi, I., Simone, M. D., Pellin, D., Serio, C. D., Bragonzi, A., & Cirillo, D. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0089614 · Cited by 163 · see citing works

Impact of Staphylococcus aureus on Pathogenesis in Polymicrobial Infections

Nair, N., Biswas, R., Götz, F., & Biswas, L. (2014) · Infection and Immunity · doi:10.1128/iai.00059-14 · Cited by 154 · see citing works

From the soil to the clinic: the impact of microbial secondary metabolites on antibiotic tolerance and resistance

Perry, E. K., Meirelles, L. A., & Newman, D. K. (2021) · Nature Reviews Microbiology · doi:10.1038/s41579-021-00620-w · Cited by 145 · see citing works

Adaptation of Staphylococcus aureus to the cystic fibrosis lung

Goerke, C., & Wolz, C. (2010) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2010.08.003 · Cited by 134 · see citing works

Help, hinder, hide and harm: what can we learn from the interactions betweenPseudomonas aeruginosaandStaphylococcus aureusduring respiratory infections?

Limoli, D. H., & Hoffman, L. R. (2019) · Thorax · doi:10.1136/thoraxjnl-2018-212616 · Cited by 130 · see citing works

Interactions between Pseudomonas aeruginosa and Staphylococcus aureus during co-cultivations and polymicrobial infections

Nguyen, A. T., & Oglesby, A. G. (2016) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-016-7596-3 · Cited by 123 · see citing works

The role of multispecies social interactions in shaping Pseudomonas aeruginosa pathogenicity in the cystic fibrosis lung

O’Brien, S., & Fothergill, J. L. (2017) · FEMS Microbiology Letters · doi:10.1093/femsle/fnx128 · Cited by 118 · see citing works

Small colony variants (SCVs) of Staphylococcus aureus – A bacterial survival strategy

Kahl, B. C. (2014) · Infection, Genetics and Evolution · doi:10.1016/j.meegid.2013.05.016 · Cited by 118 · see citing works

Methicillin-resistant food-related Staphylococcus aureus: a review of current knowledge and biofilm formation for future studies and applications

Doulgeraki, A. I., Ciccio, P. A. D., Ianieri, A., & Nychas, G. E. (2016) · Research in Microbiology · doi:10.1016/j.resmic.2016.08.001 · Cited by 118 · see citing works

Triple threat: how diabetes results in worsened bacterial infections

Darwitz, B. P., Genito, C. J., & Thurlow, L. R. (2024) · Infection and Immunity · doi:10.1128/iai.00509-23 · Cited by 122 · see citing works

Differential adaptation of microbial pathogens to airways of patients with cystic fibrosis and chronic obstructive pulmonary disease

Döring, G., Parameswaran, G. I., & Murphy, T. F. (2010) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2010.00237.x · Cited by 107 · see citing works

Inactivation of <i>thyA</i> in Staphylococcus aureus Attenuates Virulence and Has a Strong Impact on Metabolism and Virulence Gene Expression

Kriegeskorte, A., Block, D., Drescher, M., Windmüller, N., Mellmann, A., Baum, C., Neumann, C., Lorè, N. I., Bragonzi, A., Liebau, E., et al. (2014) · mBio · doi:10.1128/mbio.01447-14 · Cited by 89 · see citing works

Bovine mastitis bacteria resolved by MALDI-TOF mass spectrometry

Nonnemann, B., Lyhs, U., Svennesen, L., Kristensen, K. A., Klaas, I. C., & Pedersen, K. (2019) · Journal of Dairy Science · doi:10.3168/jds.2018-15424 · Cited by 99 · see citing works

A new platform for ultra-high density Staphylococcus aureus transposon libraries

Santiago, M., Matano, L. M., Moussa, S. H., Gilmore, M. S., Walker, S., & Meredith, T. C. (2015) · BMC Genomics · doi:10.1186/s12864-015-1361-3 · Cited by 93 · see citing works

Bidirectional alterations in antibiotics susceptibility in Staphylococcus aureus—Pseudomonas aeruginosa dual-species biofilm

Trizna, E. Y., Yarullina, M. N., Baidamshina, D. R., Миронова, А. В., Akhatova, F. S., Rozhina, E. V., Fakhrullin, R. F., Мунавировна, Х. А., Рафаэловна, К. А., Bogachev, M. I., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-71834-w · Cited by 92 · see citing works

Molecular Mechanisms of Staphylococcus and Pseudomonas Interactions in Cystic Fibrosis

Biswas, L., & Götz, F. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.824042 · Cited by 89 · see citing works

Mechanisms of Pyocyanin Toxicity and Genetic Determinants of Resistance in Staphylococcus aureus

Noto, M. J., Burns, W. J., Beavers, W. N., & Skaar, E. P. (2017) · Journal of Bacteriology · doi:10.1128/jb.00221-17 · Cited by 85 · see citing works

Bacterial Interactions in the Context of Chronic Wound Biofilm: A Review

Durand, B. A. R. N., Pouget, C., Magnan, C., Molle, V., Lavigne, J., & Dunyach‐Remy, C. (2022) · Microorganisms · doi:10.3390/microorganisms10081500 · Cited by 85 · see citing works

Respiration and Small Colony Variants of Staphylococcus aureus

Proctor, R. A. (2019) · Microbiology Spectrum · doi:10.1128/microbiolspec.gpp3-0069-2019 · Cited by 80 · see citing works

Parasitic growth of Pseudomonas aeruginosa in co‐culture with the chitinolytic bacterium Aeromonas hydrophila

Jagmann, N., Brachvogel, H., & Philipp, B. (2010) · Environmental Microbiology · doi:10.1111/j.1462-2920.2010.02271.x · Cited by 80 · see citing works

Inter- and intraspecies metabolite exchange promotes virulence of antibiotic-resistant Staphylococcus aureus

Hammer, N. D., Cassat, J. E., Noto, M. J., Lojek, L. J., Chadha, A. D., Schmitz, J. E., Creech, C. B., & Skaar, E. P. (2014) · Cell Host &amp; Microbe · doi:10.1016/j.chom.2014.09.002 · Cited by 72 · see citing works

Quorum-Sensing Regulation of Virulence Factors in Bacterial Biofilm

Warrier, A., Satyamoorthy, K., & Murali, T. S. (2021) · Future Microbiology · doi:10.2217/fmb-2020-0301 · Cited by 77 · see citing works

Microbial ecology and adaptation in cystic fibrosis airways

Yang, L., Jelsbak, L., & Molin, S. (2011) · Environmental Microbiology · doi:10.1111/j.1462-2920.2011.02459.x · Cited by 76 · see citing works

Heme cross-feeding can augment Staphylococcus aureus and Enterococcus faecalis dual species biofilms

Ch’ng, J.-H., Muthu, M., Chong, K. K. L., Wong, J. J., Tan, C. A. Z., Koh, Z. J. S., López, D., Matysik, A. S., Nair, Z. J., Barkham, T., et al. (2022) · The ISME Journal · doi:10.1038/s41396-022-01248-1 · Cited by 74 · see citing works

Lactobacillus Fermentum Isolated from Human Colonic Mucosal Biopsy Inhibits the Growth and Adhesion of Enteric and Foodborne Pathogens

Varma, P., Dinesh, K. R., Menon, K. N., & Biswas, R. (2010) · Journal of Food Science · doi:10.1111/j.1750-3841.2010.01818.x · Cited by 74 · see citing works

The social life of microbes in chronic infection

Ibberson, C. B., & Whiteley, M. (2020) · Current Opinion in Microbiology · doi:10.1016/j.mib.2020.02.003 · Cited by 73 · see citing works

What Distinguishes Highly Pathogenic Staphylococci from Medium- and Non-pathogenic?

Rosenstein, R., & Götz, F. (2012) · Current topics in microbiology and immunology · doi:10.1007/82_2012_286 · Cited by 79 · see citing works

Maintenance of S. aureus in Co-culture With P. aeruginosa While Growing as Biofilms

Woods, P. W., Haynes, Z. M., Mina, E. G., & Marques, C. N. H. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.03291 · Cited by 67 · see citing works

In vitro Multi-Species Biofilms of Methicillin-Resistant Staphylococcus aureus and Pseudomonas aeruginosa and Their Host Interaction during In vivo Colonization of an Otitis Media Rat Model

Yadav, M., Chae, S. W., Go, Y. Y., Im, G. J., & Song, J. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00125 · Cited by 61 · see citing works

Influence of the lung microbiome on antibiotic susceptibility of cystic fibrosis pathogens

Vandeplassche, E., Tavernier, S., Coenye, T., & Crabbé, A. (2019) · European Respiratory Review · doi:10.1183/16000617.0041-2019 · Cited by 57 · see citing works

Antibiotic tolerance and the alternative lifestyles of Staphylococcus aureus

Bui, L. M. G., Conlon, B. P., & Kidd, S. P. (2017) · Essays in Biochemistry · doi:10.1042/ebc20160061 · Cited by 56 · see citing works

A Novel Silver Bioactive Glass Elicits Antimicrobial Efficacy Against Pseudomonas aeruginosa and Staphylococcus aureus in an ex Vivo Skin Wound Biofilm Model

Wilkinson, H. N., Iveson, S., Catherall, P., & Hardman, M. J. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01450 · Cited by 56 · see citing works

Polymicrobial Interactions in the Cystic Fibrosis Airway Microbiome Impact the Antimicrobial Susceptibility of Pseudomonas aeruginosa

Reece, E., Bettio, P. H. D. A., & Renwick, J. (2021) · Antibiotics · doi:10.3390/antibiotics10070827 · Cited by 51 · see citing works

Pharmacokinetics and Pharmacodynamics of Aerosolized Antibacterial Agents in Chronically Infected Cystic Fibrosis Patients

Dalhoff, A. (2014) · Clinical Microbiology Reviews · doi:10.1128/cmr.00022-14 · Cited by 55 · see citing works

A New Class of Quorum Quenching Molecules from Staphylococcus Species Affects Communication and Growth of Gram-Negative Bacteria

Chu, Y., Nega, M., Wölfle, M., Plener, L., Grond, S., Jung, K., & Götz, F. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003654 · Cited by 54 · see citing works

Pseudomonas aeruginosa induces pigment production and enhances virulence in a white phenotypic variant of Staphylococcus aureus

Alavi, M., Antonic, V., Stojadinovic, A., Zhang, B., & Izadjoo, M. J. (2013) · Infection and Drug Resistance · doi:10.2147/idr.s49039 · Cited by 52 · see citing works

Anaerobiosis influences virulence properties of Pseudomonas aeruginosa cystic fibrosis isolates and the interaction with Staphylococcus aureus

Pallett, R., Leslie, L. J., Lambert, P. A., Milic, I., Devitt, A., & Marshall, L. J. (2019) · Scientific Reports · doi:10.1038/s41598-019-42952-x · Cited by 52 · see citing works

Precise spatial structure impacts antimicrobial susceptibility of S. aureus in polymicrobial wound infections

Ibberson, C. B., Barraza, J. P., Holmes, A. L., Cao, P., & Whiteley, M. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2212340119 · Cited by 46 · see citing works

Activity of disinfectants against multispecies biofilms formed byStaphylococcus aureus,Candida albicansandPseudomonas aeruginosa

Kart, D., Tavernier, S., Acker, H. V., Nelis, H. J. C. F., & Coenye, T. (2014) · Biofouling · doi:10.1080/08927014.2013.878333 · Cited by 49 · see citing works

Environmental Heme Utilization by Heme-Auxotrophic Bacteria

Gruss, A., Borezée‐Durant, E., & Lechardeur, D. (2012) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/b978-0-12-394423-8.00003-2 · Cited by 47 · see citing works

Collagen and hyaluronan at wound sites influence early polymicrobial biofilm adhesive events

Birkenhauer, E., Neethirajan, S. R., & Weese, J. S. (2014) · BMC Microbiology · doi:10.1186/1471-2180-14-191 · Cited by 47 · see citing works

Polymicrobial community‐acquired pneumonia: An emerging entity

Cillóniz, C., Čivljak, R., Nicolini, A., & Torres, A. (2015) · Respirology · doi:10.1111/resp.12663 · Cited by 45 · see citing works

Staphylococcus aureus induces DNA damage in host cell

Deplanche, M., Mouhali, N., Nguyen, M., Cauty, C., Ezan, F., Diot, A., Raulin, L., Dutertre, S., Langouët, S., Legembre, P., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-44213-3 · Cited by 45 · see citing works

Pyochelin biotransformation by Staphylococcus aureus shapes bacterial competition with Pseudomonas aeruginosa in polymicrobial infections

Jenul, C., Keim, K. C., Jens, J. N., Zeiler, M. J., Schilcher, K., Schurr, M. J., Melander, C., Phelan, V. V., & Horswill, A. R. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112540 · Cited by 44 · see citing works

Matrix Polysaccharides and SiaD Diguanylate Cyclase Alter Community Structure and Competitiveness of Pseudomonas aeruginosa during Dual-Species Biofilm Development with Staphylococcus aureus

Chew, S. C., Yam, J. K. H., Matysik, A. S., Seng, Z. J., Klebensberger, J., Givskov, M., Doyle, P. S., Rice, S. A., Yang, L., & Kjelleberg, S. J. (2018) · mBio · doi:10.1128/mbio.00585-18 · Cited by 45 · see citing works

Population dynamics and transcriptomic responses of Pseudomonas aeruginosa in a complex laboratory microbial community

Cheng, Y., Yam, J. K. H., Cai, Z., Ding, Y., Zhang, L., Deng, Y., & Yang, L. (2019) · npj Biofilms and Microbiomes · doi:10.1038/s41522-018-0076-z · Cited by 42 · see citing works

Yeast Petites and Small Colony Variants

Day, M. (2013) · Advances in applied microbiology · doi:10.1016/b978-0-12-407672-3.00001-0 · Cited by 39 · see citing works

Immune Response Modulation by Pseudomonas aeruginosa Persister Cells

Hastings, C. J., Himmler, G. E., Patel, A., & Marques, C. N. H. (2023) · mBio · doi:10.1128/mbio.00056-23 · Cited by 40 · see citing works

Evolution in Fast Forward: a Potential Role for Mutators in Accelerating Staphylococcus aureus Pathoadaptation

Canfield, G. S., Schwingel, J. M., Foley, M. H., Vore, K. L., Boonanantanasarn, K., Gill, A. L., Sutton, M. D., & Gill, S. R. (2012) · Journal of Bacteriology · doi:10.1128/jb.00733-12 · Cited by 38 · see citing works

Global transcriptome responses including small RNAs during mixed‐species interactions with methicillin‐resistant Staphylococcus aureus and Pseudomonas aeruginosa

Miller, C. L., Laar, T. A. V., Chen, T., Karna, S. L. R., Chen, P., You, T., & Leung, K. P. (2016) · MicrobiologyOpen · doi:10.1002/mbo3.427 · Cited by 38 · see citing works

Species-specific viability analysis of Pseudomonas aeruginosa, Burkholderia cepacia and Staphylococcus aureus in mixed culture by flow cytometry

Rüger, M., Ackermann, M., & Reichl, U. (2014) · BMC Microbiology · doi:10.1186/1471-2180-14-56 · Cited by 37 · see citing works

Pseudomonas aeruginosa and Staphylococcus aureus communication in biofilm infections: insights through network and database construction

Magalhães, A. P., Jorge, P., & Pereira, M. O. (2019) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2019.1700209 · Cited by 36 · see citing works

The effect of nisin on the biofilm production, antimicrobial susceptibility and biofilm formation of Staphylococcus aureus and Pseudomonas aeruginosa

Ghapanvari, P., Taheri, M. N., Jalilian, F. A., Dehbashi, S., Dezfuli, A. A. Z., & Arabestani, M. R. (2022) · European journal of medical research · doi:10.1186/s40001-022-00804-x · Cited by 34 · see citing works

Staphylococcus aureus in Polymicrobial Skinand Soft Tissue Infections: Impact of Inter-Species Interactionsin Disease Outcome

Mariani, F., & Galván, E. M. (2023) · Antibiotics · doi:10.3390/antibiotics12071164 · Cited by 34 · see citing works

Presence of P seudomonas aeruginosa influences biofilm formation and surface protein expression of S taphylococcus aureus

Kumar, A., & Ting, Y. (2015) · Environmental Microbiology · doi:10.1111/1462-2920.12890 · Cited by 34 · see citing works

Mixed Populations and Co-Infection: Pseudomonas aeruginosa and Staphylococcus aureus

Camus, L., Briaud, P., Vandenesch, F., Doléans-Jordheim, A., & Moreau, K. (2022) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-08491-1_15 · Cited by 28 · see citing works

Interactions between metabolism and growth can determine the co-existence of Staphylococcus aureus and Pseudomonas aeruginosa

Pajon, C., Fortoul, M. C., Diaz-Tang, G., Meneses, E. M., Kalifa, A. R., Sevy, E., Mariah, T., Toscan, B., Marcelin, M., Hernandez, D. M., et al. (2023) · eLife · doi:10.7554/elife.83664 · Cited by 27 · see citing works

Denture stomatitis associated with small-colony variants of Staphylococcus aureus: a case report

Garbacz, K., Kwapisz, E., & Wierzbowska, M. (2019) · BMC Oral Health · doi:10.1186/s12903-019-0910-6 · Cited by 27 · see citing works

Understanding Pseudomonas aeruginosa Biofilms: Quorum Sensing, c-di-GMP Signaling, and Emerging Antibiofilm Approaches

Elbehiry, A., Marzouk, E., Edrees, H. M., Ibrahem, M. D., Alzahrani, S., Anagreyyah, S. A., Abualola, H., AlGhamdi, S. A., Alzahrani, A. F., Jaber, M., et al. (2026) · Microorganisms · doi:10.3390/microorganisms14010109 · Cited by 26 · see citing works

Interaction of Staphylococcus aureus and Acinetobacter baumannii during In Vitro β-Lactam Exposure

Smith, N. M., Ang, A., Tan, F., Macias, K., James, S. L., Sidhu, J., & Lenhard, J. R. (2021) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02414-20 · Cited by 26 · see citing works

Surfaceome and Exoproteome Dynamics in Dual-Species Pseudomonas aeruginosa and Staphylococcus aureus Biofilms

Reigada, I., San-Martin-Galindo, P., Gilbert-Girard, S., Chiaro, J., Cerullo, V., Savijoki, K., Nyman, T. A., Fallarero, A., & Miettinen, I. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.672975 · Cited by 26 · see citing works

Strain-specific interspecies interactions between co-isolated pairs of Staphylococcus aureus and Pseudomonas aeruginosa from patients with tracheobronchitis or bronchial colonization

Gomes-Fernandes, M., Gómez, A.-C., Bravo, M., Huedo, P., Coves, X., Prat, C., Gibert, I., Lacoma, A., & Yero, D. (2022) · Scientific Reports · doi:10.1038/s41598-022-07018-5 · Cited by 26 · see citing works

Bactericidal Effect of Tomatidine-Tobramycin Combination against Methicillin-Resistant Staphylococcus aureus and Pseudomonas aeruginosa Is Enhanced by Interspecific Small-Molecule Interactions

Boulanger, S., Mitchell, G., Bouarab, K., Marsault, É., Cantin, A. M., Frost, E. H., Déziel, É., & Malouin, F. (2015) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01711-15 · Cited by 26 · see citing works

Investigation of the Mechanism and Chemistry Underlying Staphylococcus aureus ' Ability to Inhibit Pseudomonas aeruginosa Growth In Vitro

Kvich, L., Crone, S. G., Christensen, M. H., Lima, R. D. C. L., Alhede, M., Alhede, M., Stærk, D., & Bjarnsholt, T. (2022) · Journal of Bacteriology · doi:10.1128/jb.00174-22 · Cited by 23 · see citing works

Impact of mixed Staphylococcus aureus-Pseudomonas aeruginosa biofilm on susceptibility to antimicrobial treatments in a 3D in vitro model

Landa, G., Clarhaut, J. A., Buyck, J. M., Mendoza, G., Arruebo, M., & Tewes, F. (2024) · Scientific Reports · doi:10.1038/s41598-024-79573-y · Cited by 23 · see citing works

Strain Background, Species Frequency, and Environmental Conditions Are Important in Determining Pseudomonas aeruginosa and Staphylococcus aureus Population Dynamics and Species Coexistence

Niggli, S., & Kümmerli, R. (2020) · Applied and Environmental Microbiology · doi:10.1128/aem.00962-20 · Cited by 22 · see citing works

Pseudomonas aeruginosa behaviour in polymicrobial communities: The competitive and cooperative interactions conducting to the exacerbation of infections

Al-Wrafy, F. A., Reem, A., Noman, E. A., Al-Gheethi, A. A. S., & Mutahar, M. (2023) · Microbiological Research · doi:10.1016/j.micres.2022.127298 · Cited by 22 · see citing works

Small-Colony Variants in Persistent and Recurrent Staphylococcus aureus Bacteremia

Kim, N., Kang, Y. M., Han, W. D., Park, K. U., Park, K., Yoo, J. I., Lee, D., Park, C., Song, K., Kim, E. S., et al. (2016) · Microbial Drug Resistance · doi:10.1089/mdr.2015.0262 · Cited by 22 · see citing works

Small colony variants are more susceptible to copper-mediated contact killing for Pseudomonas aeruginosa and Staphylococcus aureus

Liu, S., & Zhang, X. (2016) · Journal of Medical Microbiology · doi:10.1099/jmm.0.000348 · Cited by 22 · see citing works

A Continuous-Flow Model for in vitro Cultivation of Mixed Microbial Populations Associated With Cystic Fibrosis Airway Infections

O’Brien, T. J., & Welch, M. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.02713 · Cited by 21 · see citing works

Fever-like temperature impacts on Staphylococcus aureus and Pseudomonas aeruginosa interaction, physiology, and virulence both in vitro and in vivo

Venero, E. C. S., Galeano, M. B., Luqman, A., Ricardi, M. M., Serral, F., Porto, D. F. D., Robaldi, S. A., Ashari, B. A. Z., Munif, T. H., Egoburo, D. E., et al. (2024) · BMC Biology · doi:10.1186/s12915-024-01830-3 · Cited by 21 · see citing works

Effects of low intensity laser irradiation during healing of infected skin wounds in the rat

Nussbaum, E. L., Heras, F. L., Pritzker, K. P. H., Mazzulli, T., & Lilge, L. D. (2013) · Photonics and Lasers in Medicine · doi:10.1515/plm-2013-0049 · Cited by 21 · see citing works

Biofilm Inhibitor Taurolithocholic Acid Alters Colony Morphology, Specialized Metabolism, and Virulence of Pseudomonas aeruginosa

Condren, A. R., Kahl, L. J., Boelter, G., Kritikos, G., Banzhaf, M., Dietrich, L. E. P., & Sanchez, L. M. (2019) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.9b00424 · Cited by 21 · see citing works

Pseudomonas aeruginosa DesB Promotes Staphylococcus aureus Growth Inhibition in Coculture by Controlling the Synthesis of HAQs

Kim, S., Yoon, Y., & Choi, K. (2015) · PLoS ONE · doi:10.1371/journal.pone.0134624 · Cited by 20 · see citing works

Heme-Dependent Siderophore Utilization Promotes Iron-Restricted Growth of the Staphylococcus aureus <i>hemB</i> Small-Colony Variant

Batko, I. Z., Flannagan, R. S., Guariglia-Oropeza, V., Sheldon, J. R., & Heinrichs, D. E. (2021) · Journal of Bacteriology · doi:10.1128/jb.00458-21 · Cited by 19 · see citing works

Rapid and strain-specific resistance evolution of Staphylococcus aureus against inhibitory molecules secreted by Pseudomonas aeruginosa

Niggli, S., Schwyter, L., Poveda, L., Grossmann, J., & Kümmerli, R. (2023) · mBio · doi:10.1128/mbio.03153-22 · Cited by 19 · see citing works

AMPEROMETRIC DETECTION OF PYOCYANIN IN NANOFLUIDIC CHANNELS

Webster, T. A., Sismaet, H. J., & Goluch, E. D. (2013) · Nano LIFE · doi:10.1142/s1793984413400114 · Cited by 19 · see citing works

Microbial phenazines: biosynthesis, structural diversity, evolution, regulation, and biological significance

Mavrodi, D. V., Blankenfeldt, W., Mavrodi, O. V., Weller, D. M., & Thomashow, L. S. (2025) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00147-23 · Cited by 16 · see citing works

The Clinical Significance of Staphylococcus aureus Small Colony Variants

Keim, K. C., George, I. K., Reynolds, L., & Smith, A. C. (2022) · Laboratory Medicine · doi:10.1093/labmed/lmac101 · Cited by 16 · see citing works

Observation with microcalorimetry: Behaviour of P. aeruginosa in mixed cultures with S. aureus and E. coli

Fredua‐Agyeman, M., Gaisford, S., & Beezer, A. E. (2018) · Thermochimica Acta · doi:10.1016/j.tca.2018.03.009 · Cited by 16 · see citing works

Role of Biofilms in Environment Pollution and Control

Yadav, M. (2017) · Springer eBooks · doi:10.1007/978-981-10-6847-8_16 · Cited by 16 · see citing works

Biofilms: A Survival and Resistance Mechanism of Microorganisms

Estela, C. R. L., & Ramos, P. (2012) · InTech eBooks · doi:10.5772/28504 · Cited by 16 · see citing works

Hyperglycemia potentiates increased Staphylococcus aureus virulence and resistance to growth inhibition by Pseudomonas aeruginosa

Genito, C. J., Darwitz, B. P., Greenwald, M. A., Wolfgang, M. C., & Thurlow, L. R. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.02299-23 · Cited by 15 · see citing works

Emergence of Small Colony Variants (SCVs) is an adaptive strategy used by Pseudomonas aeruginosa to palliate O 2 limitationsPreprint

Besse, A., Groleau, M., & Déziel, É. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.07.20.500912

Selection for Staphylococcus aureus small-colony variants due to growth in the presence of Pseudomonas aeruginosa

Hoffman, L. R., Déziel, É., D’Argenio, D. A., Lepine, F. L., Emerson, J., McNamara, S., Gibson, R. L., Ramsey, B. W., & Miller, S. I. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0606756104 · Cited by 470 · see citing works

Haem toxicity provides a competitive advantage to the clinically relevant Staphylococcus aureus small colony variant phenotype

Herrin, B. E., Islam, S., Rentschler, K. N., Pert, L. H., Kopanski, S. P., & Wakeman, C. A. (2021) · Microbiology · doi:10.1099/mic.0.001044 · Cited by 4 · see citing works

Emergence of Small Colony Variants Is an Adaptive Strategy Used by Pseudomonas aeruginosa to Mitigate the Effects of Redox Imbalance

Besse, A., Groleau, M., & Déziel, É. (2023) · mSphere · doi:10.1128/msphere.00057-23 · Cited by 26 · see citing works

The ability of Pseudomonas aeruginosa to adopt a Small Colony Variant (SCV) phenotype is conserved, and not restricted to clinical isolatesPreprint

Besse, A., Trottier, M. C., Groleau, M., & Déziel, É. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.05.430018 · Cited by 2 · see citing works