Cited by 184Bacterial biofilms and quorum sensingAntimicrobial Resistance in StaphylococcusBacterial Genetics and Biotechnology

The DOI matches its Crossref record; 19 of the 19 references it cites were found in a registry or an index.

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

Open access

Biswas, Lalitha, Biswas, Raja, Schlag, Martin, Bertram, Ralph, Götz, Friedrich·2009·Applied and Environmental Microbiology

DOI 10.1128/aem.01211-09PMC PMC2772425

Open this paper in CoChat — free account

Abstract

Previously it has been demonstrated that Staphylococcus aureus is sensitive toward Pseudomonas -secreted exotoxins, which preferentially target the electron transport chain in staphylococci. Here it is shown that a subpopulation of S. aureus survives these respiratory toxins of P seudomonas aeruginosa by selection of the small-colony variant (SCV) phenotype. Purified pyocyanin alone causes the same effect. A hem B mutant of S. aureus survives cocultivation with P. aeruginosa without a decrease in CFU.

Integrity signals

Registry

Crossref · 10.1128/aem.01211-09

Cites

19 of 19 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

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 1,655
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
Staphyloxanthin Plays a Role in the Fitness of Staphylococcus aureus 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
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 489
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
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
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
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
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
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×
“aureus hemB, which is auxotrophic for hemin (18), was tested for its sensitivity toward the culture supernatant of P.”
Background

Flagged first, then by citations

Show all 19 references

Sorted by citations

Items 101–184 of 184

Mutations in the Staphylococcus aureus Global Regulator CodY confer tolerance to an interspecies redox-active antimicrobial
Martini, A. M., Alexander, S. A., & Khare, A. (2025) · PLoS Genetics · doi:10.1371/journal.pgen.1011610 · Cited by 14
The transcription factors ActR and SoxR differentially affect the phenazine tolerance of Agrobacterium tumefaciens
Perry, E. K., & Newman, D. K. (2019) · Molecular Microbiology · doi:10.1111/mmi.14263 · Cited by 15
Bacterial brothers in arms: cooperation of Staphylococcus aureus and Pseudomonas aeruginosa during antimicrobial exposure
Lenhard, J. R., Smith, N. M., Quach, C. D., Nguyen, T. Q., Doan, L. H., & Chau, J. (2019) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkz247 · Cited by 15
The Mla system and its role in maintaining outer membrane barrier function in Stenotrophomonas maltophilia
Coves, X., Mamat, U., Conchillo‐Solé, O., Huedo, P., Bravo, M., Gómez, A.-C., Krohn, I., Streit, W. R., Schaible, U. E., Gibert, I., et al. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1346565 · Cited by 13
Functional variation reflects intra-strain diversity of Staphylococcus aureus small colony variants in the host–pathogen interaction
Hilmi, D., Parčina, M., Bode, K. A., Ostrop, J., Schuett, S., Heeg, K. M., Ziebuhr, W., Sommerburg, O., & Bekeredjian‐Ding, I. (2013) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2012.12.008 · Cited by 13
Biofilm Formation of Staphylococcus aureus
Vázquez‐Sánchez, D., & Rodríguez-López, P. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809671-0.00005-x · Cited by 16
Genetic Dissection of Cyclic di‐ GMP Signalling in Pseudomonas aeruginosa via Systematic Diguanylate Cyclase Disruption
Martino, R. A., Volke, D. C., Tenaglia, A. H., Tribelli, P. M., Nikel, P. I., & Smania, A. M. (2025) · Microbial Biotechnology · doi:10.1111/1751-7915.70137 · Cited by 12
Subinhibitory Cefotaxime and Levofloxacin Concentrations Contribute to Selection of Pseudomonas aeruginosa in Coculture with Staphylococcus aureus
Zhao, K., Li, J., Yang, X., Zeng, Q., Liu, W., Wu, Y., Zhou, H., Prithiviraj, B., Wang, X., Zhou, X., et al. (2022) · Applied and Environmental Microbiology · doi:10.1128/aem.00592-22 · Cited by 12
Development, characterization, and evaluation of a simple polymicrobial colony biofilm model for testing of antimicrobial wound dressings
Robertson, S. N., Romero, M., Fenn, S. J., Riedi, P. L. K., & Cámara, M. (2024) · Journal of Applied Microbiology · doi:10.1093/jambio/lxae042 · Cited by 15
Evolution of Resistance to Phenazine Antibiotics in Staphylococcus aureus and Its Role During Coinfection with Pseudomonas aeruginosa
Fu, T., Cai, Z., Yue, Z., Yang, H., Fang, B., Zhang, X., Fan, Z., Pan, X., Yang, F., Jin, Y., et al. (2021) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.0c00837 · Cited by 12
Hitchhiking motility of Staphylococcus aureus involves the interaction between its wall teichoic acids and lipopolysaccharide of Pseudomonas aeruginosa
Liu, C., & Lin, M. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1068251 · Cited by 11
Colonization of CF patients’ upper airways with S. aureus contributes more decisively to upper airway inflammation than P. aeruginosa
Janhsen, W. K., Arnold, C., Hentschel, J., Lehmann, T., Pfister, W., Baier, M., Böer, K., Hünniger, K., Kurzai, O., Hipler, U., et al. (2016) · Medical Microbiology and Immunology · doi:10.1007/s00430-016-0463-0 · Cited by 10
Crucial Role for Lipoteichoic Acid Assembly in the Metabolic Versatility and Antibiotic Resistance of Staphylococcus aureus
Burtchett, T. A., Shook, J. C., Hesse, L. E., Delekta, P. C., Brzozowski, R., Nouri, A., Calas, A. J., Spanoudis, C. M., Eswara, P. J., & Hammer, N. D. (2023) · Infection and Immunity · doi:10.1128/iai.00550-22 · Cited by 9
Antibiotic intervention redisposes bacterial interspecific interacting dynamics in competitive environments
Li, J., Chen, X., Lin, J., Yuan, Y., Huang, T. L., Du, L., Prithiviraj, B., Zhang, A., Wang, X., Chu, Y., et al. (2021) · Environmental Microbiology · doi:10.1111/1462-2920.15461 · Cited by 8
The great divide: rhamnolipids mediate separation between P. aeruginosa and S. aureus
Bru, J.-L., Kasallis, S. J., Chang, R., Zhuo, Q., Nguyen, J., Pham, P., Warren, E., Whiteson, K., Høyland‐Kroghsbo, N. M., Limoli, D. H., et al. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1245874 · Cited by 7
Functional and Proteomic Dissection of the Contributions of CodY, SigB and the Hibernation Promoting Factor HPF to Interactions of Staphylococcus aureus USA300 with Human Lung Epithelial Cells
Li, X., Busch, L. M., Piersma, S., Wang, M., Liu, L., Salazar, M. G., Surmann, K., Mäder, U., Völker, U., Buist, G., et al. (2024) · Journal of Proteome Research · doi:10.1021/acs.jproteome.4c00724 · Cited by 8
Long-Term Coexistence of Pseudomonas Aeruginosa and Staphylococcus Aureus Using an In Vitro Cystic Fibrosis Model
Monteiro, R., Magalhães, A. P., Pereira, M. O., & Sousa, A. M. (2021) · Future Microbiology · doi:10.2217/fmb-2021-0025 · Cited by 7
Outcome and Prevention of Pseudomonas aeruginosa-Staphylococcus aureus Interactions During Pulmonary Infections in Cystic Fibrosis
Mitchell, G., & Maloui, F. (2012) · InTech eBooks · doi:10.5772/31527 · Cited by 7
Examination of a first-in-class bis-dialkylnorspermidine-terphenyl antibiotic in topical formulation against mono and polymicrobial biofilms
Miller, M., Rogers, J. C., Badham, M. A., Cadenas, L., Brightwell, E., Adams, J., Tyler, C., Sebahar, P. R., Haussener, T. J., Reddy, H. R. K., et al. (2020) · PLoS ONE · doi:10.1371/journal.pone.0234832 · Cited by 7
Staphylococcus aureus and Pseudomonas aeruginosa Respiratory Tract Coinfection—What Can We Learn From Animal Models?
Kahl, B. C. (2017) · The Journal of Infectious Diseases · doi:10.1093/infdis/jix624 · Cited by 7
Treatment of Mixed Infections in Wounds
Ahmed, A., & Boateng, J. S. (2020) · Wiley eBooks · doi:10.1002/9781119433316.ch5 · Cited by 7
Phenotypic Variation in Staphylococcus aureus during Colonisation Involves Antibiotic-Tolerant Cell Types
Burford-Gorst, C. M., & Kidd, S. P. (2024) · Antibiotics · doi:10.3390/antibiotics13090845 · Cited by 7
Allelic polymorphism shapes community function in evolving Pseudomonas aeruginosa populationsPreprint
Azimi, S., Roberts, A. E. L., Peng, S., Weitz, J. S., McNally, A., Brown, S. P., & Diggle, S. P. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/644724 · Cited by 6
Quorum-sensing effector pyocyanin but not farnesol & acyl homoserine lactone exhibit antibacterial activity
Kahlon, N. K., Sharma, A., Dogra, H., & Singh, &. R. (2022) · The Indian Journal of Medical Research · doi:10.4103/ijmr.ijmr_1576_19 · Cited by 5
Evaluating the effects of ivacaftor exposure on Staphylococcus aureus small colony variant development and antibiotic tolerance
Bollar, G. E., Shaffer, K. M., Keith, J. D., Oden, A. M., Dowell, A. E., Ryan, K. J., Acosta, E. P., Guimbellot, J. S., Kiedrowski, M. R., & Birket, S. E. (2024) · JAC-Antimicrobial Resistance · doi:10.1093/jacamr/dlae185 · Cited by 4
Altering the interfacial rheology of Pseudomonas aeruginosa and Staphylococcus aureus with N-acetyl cysteine and cysteamine
Balmuri, S. R., Noaman, S., Usman, H., & Niepa, T. H. R. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1338477 · Cited by 4
Contribution of the infection ecosystem and biogeography to antibiotic failure in vivo
Nazeer, R. R., Askenasy, I., Swain, J. E. V., & Welch, M. (2024) · npj Antimicrobials and Resistance · doi:10.1038/s44259-024-00063-2 · Cited by 5
Mechanical properties of Staphylococcus aureus and Pseudomonas aeruginosa dual-species biofilms grown in chronic wound-based models
Bhattarai, B., & Christopher, G. F. (2025) · Soft Matter · doi:10.1039/d4sm01441c · Cited by 4
Respiration and Small Colony Variants ofStaphylococcus aureus
Proctor, R. A. (2019) · ASM Press eBooks · doi:10.1128/9781683670131.ch34 · Cited by 4
Pseudomonas aeruginosa- secreted respiratory toxin HQNO triggers fatty acid accumulation in respiring Staphylococcus aureus, decreasing SaeRS-dependent transcriptional regulation
Román‐Rodríguez, F., Tyagi, N., Al‐Tameemi, H., & Boyd, J. M. (2025) · Journal of Bacteriology · doi:10.1128/jb.00395-25 · Cited by 3
Detection and Impact of Staphylococcus aureus Small Colony Variants in Chronic Wounds: A Pilot Study
Carris, E., Keim, K. C., Reynolds, L., George, I. K., Sanford, N. E., Navarro-Garcia, R., Lenzmeier, T. D., & Smith, A. C. (2025) · Pathogens · doi:10.3390/pathogens14101023 · Cited by 4
A quorum-sensing molecule from Pseudomonas aeruginosa induces defensive multicellularity in a coinfecting pathogen
Katharios-Lanwermeyer, S., Zarrella, T. M., Godsil, M., Severin, S., Casiano, A. E., Tai, C., & Khare, A. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2513122123 · Cited by 4
A Review on Survival Strategies and Social Dynamics of Microbial Communities in Biofilm
Jafar, T., Saha, S. R., Alam, S., Saha, O., & Sultana, K. F. (2025) · Indian Journal of Microbiology · doi:10.1007/s12088-025-01501-z · Cited by 3
An effective response to respiratory inhibition by a Pseudomonas aeruginosa excreted quinoline promotes Staphylococcus aureus fitness and survival in co-culture
Román‐Rodríguez, F., Tyagi, N., Kim, J., Parker, D., & Boyd, J. M. (2025) · Journal of Bacteriology · doi:10.1128/jb.00101-25 · Cited by 3
Resistance to aminoglycoside, tetracycline and macrolides
Samanta, I., & Bandyopadhyay, S. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-815770-1.00009-2 · Cited by 3
Co-infection with Pseudomonas aeruginosa impacts virulence of Staphylococcus aureus and intensifies the severity of infection.
Shoaib, A., Lone, N. A., & Yi, X. (2020) · PubMed · Cited by 3
A combination of phenotypic responses and genetic adaptations enables Staphylococcus aureus to withstand inhibitory molecules secreted by Pseudomonas aeruginosa
Schwyter, L., Niggli, S., Zajac, N., Poveda, L., Wolski, W., Panse, C., Schlapbach, R., Kümmerli, R., & Grossmann, J. (2025) · mSystems · doi:10.1128/msystems.00262-25 · Cited by 2
Metabolic responses to Staphylococcus aureus airway infection
Bünsow, D., & Winstel, V. (2025) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00612.2025 · Cited by 2
Contribution of viable but non culturable cells and small colony variants in antibiotic insusceptibility and therapeutic failure against S. aureus and P. aeruginosa biofilm co-infections
Magalhães, A. P., Jorge, P., Neiva, J., Sousa, A. M., Cerca, N., & Pereira, M. O. (2026) · Microbial Pathogenesis · doi:10.1016/j.micpath.2026.108312 · Cited by 2
Characterization of β-lactam resistance in dual-species biofilms of Pseudomonas aeruginosa and methicillin-sensitive Staphylococcus aureus
Nizer, W. S. D. C., Allison, K. N., Beaulieu, C., Montgomery, M. C., Cassol, E., & Overhage, J. (2026) · Biofouling · doi:10.1080/08927014.2026.2620072 · Cited by 2
Microbial dormancy evolution in the environments: Environmental adaptation and health risks of small colony variants
Sun, T. S., Cai, Y., Huang, P., Li, G., Wong, P. K., & An, T. (2025) · Critical Reviews in Environmental Science and Technology · doi:10.1080/10643389.2025.2566174 · Cited by 2
Author response: 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.sa2 · Cited by 2
Pathogen Partnerships or Power Struggles? Pseudomonas aeruginosa, and Staphylococcus aureus Dynamics in Cystic Fibrosis
Saleh, N. M., Sudan, E. S. F., Mohamed, S., Elshahed, M. M. S., Hamouda, R. E., EL-Gendy, A. O., & Farag, A. A. (2025) · Current Microbiology · doi:10.1007/s00284-025-04167-4 · Cited by 1
Engineered Mycoplasma pneumoniae targeting dual-species bacterial biofilms: a novel strategy against infections
Mazzolini, R., Garrido, V., Gómez, A.-C., Collantes, M., Grilló, M. J., Piñero‐Lambea, C., Gibert, I., Yero, D., & Lluch‐Senar, M. (2025) · npj Biofilms and Microbiomes · doi:10.1038/s41522-025-00835-2 · Cited by 1
Microbial and host innate immune factors affecting the persistence of Staphylococcus aureus in cystic fibrosis airways
Fairholm, J. D., Paul, G. T., Birket, S. E., & Rada, B. (2026) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2026.1797869 · Cited by 1
The Clinical Significance ofStaphylococcus aureusSmall Colony Variants
Keim, K. C., George, I. K., Reynolds, L., & Smith, A. C. (2021) · American Society for Clinical Laboratory Science · doi:10.29074/ascls.2020002691 · Cited by 1
The past, present and future of polymicrobial infection research: Modelling, eavesdropping, terraforming and other stories
Bényei, É. B., Nazeer, R. R., Askenasy, I., Mancini, L., Ho, P.-M., Sivarajan, G. A. C., Swain, J. E. V., & Welch, M. (2024) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/bs.ampbs.2024.04.002 · Cited by 1
Pyochelin biotransformation by Staphylococcus aureus shapes bacterial competition with Pseudomonas aeruginosa in polymicrobial infectionsPreprint
Jenul, C., Keim, K. C., Jens, J. N., Zeiler, M. J., Schilcher, K., Schurr, M. J., Melander, C., Phelan, V. V., & Horswill, A. R. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.04.18.486787 · Cited by 1
Iron content of commercial mucin contributes to compositional stability of a cystic fibrosis airway synthetic microbiota communityPreprint
Giedraitis, E., Neve, R. L., & Phelan, V. V. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.06.611695 · Cited by 1
Stenotrophomonas maltophilia exhibits defensive multicellularity in response to a Pseudomonas aeruginosa quorum sensing moleculePreprint
Katharios-Lanwermeyer, S., Zarrella, T. M., Godsil, M., Severin, E. S., Casiano, A. E., Tai, C., & Khare, A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.02.651457 · Cited by 1
Dynamique réactionnelle d'antibiotiques au sein des biofilms de Staphylococcus aureus : apport de la microscopie de fluorescence multimodale
Oubekka, S. D. (2012) · doi:10.70675/9d8dc787zd26ez48b4z9beczceb548d34c8d · Cited by 1
The Membrane as a Novel Target Site for Antibiotics to Kill Persisting Bacterial Pathogens
Wu, X., & Hurdle, J. G. (2013) · Antibiotics · doi:10.1002/9783527659685.ch8
SCV'S: FORMATION AND CHARACTERISATION IN STAPHYLOCOCCUS SP
Alharbi, N. S. H. A. (2013) · ORCA Online Research @Cardiff (Cardiff University)
Interspecific interactions of heterotrophic bacteria during chitin degradation
Jagmann, N. (2012) · KOPS (University of Konstanz)
Interspecific interactions of heterotrophic bacteria during chitin degradation
Schink, B., Philipp, B., & Hauck, C. R. (2012)
Effect of Oxygen on the Competition between Pseudomonas aeruginosa and Staphylococcus aureus
Barrera, L., & Alexandra, M. (2014)
Évaluation du potentiel d'action de l'utilisation combinée de la tomatidine (ou son analogue : FC04-100) et d'aminoglycosides contre Staphylococcus aureus et Pseudomomas aeruginosa
Boulanger, S. (2015)
A 3-D Computational Model to Investigate the Role of Small Colony Variants (SCVs) in the Antibiotic Susceptibility of a Polymicrobial Biofilm
Joy, N. (2016) · Research Archive of Indian Institute of Technology Hyderabad (Indian Institute of Technology Hyderabad)
Effects of plasmid acquisition by Pseudomonas aeruginosa clinical isolates on methicillin-resistant Staphylococcus aureus biofilm formation
Sarra, E. S., Khaled, M. A., Mohammad, M. A., & Nadia, A. H. (2015) · African Journal of Microbiology Research · doi:10.5897/ajmr2015.7789
New Genomics Tools and Strategies for Studying Antibiotics and Antibiotic-Resistance in Staphylococcus Aureus
Santiago, M. (2016) · Digital Access to Scholarship at Harvard (DASH) (Harvard University)
Towards New Topical Treatments For Bacterial Infection
Lee, V. E. (2018) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York)
Small Colony Variant Selection, Biofilm Induction, and Interspecies Interactions of Ocular Clinical Pseudomonas aeruginosa
Sagar, S. S., & Kaistha, S. D. (2019) · Springer eBooks · doi:10.1007/978-981-13-6321-4_14
Adverse effects of adaptive mutation to survive static culture conditions on successful fitness of the rice pathogen Burkholderia glumae in a host
Kwak, G.-Y., Goo, E., Jeong, H., & Hwang, I. (2020) · PLoS ONE · doi:10.1371/journal.pone.0238151
Rapid and strain-specific resistance evolution of Staphylococcus aureus against inhibitory molecules secreted by Pseudomonas aeruginosaPreprint
Niggli, S., Schwyter, L., Poveda, L., Grossmann, J., & Kümmerli, R. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.10.455797
Quorum sensing relationship analysis of microbial symbionts
Thirunavukkarasu, R., Pandi, P., Pushparaj, S., Subramanian, K., & Arokiarajan, M. S. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-99334-0.00031-1
Interspecies Interaction between Pseudomonas aeruginosa, Staphylococcus aureus and E. coli in vitro
Abdelwahab, I. A., Abozahra, R., Sultan, S. A., Abd-elaal, H. M., & Abdelhamid, S. M. (2023) · Journal of Pure and Applied Microbiology · doi:10.22207/jpam.17.1.39
Factors Associated with the Development of Adrenal Insufficiency in Patients with Juvenile Idiopathic Arthritis Who Received Systemic Corticosteroids
Ersoy, G. Z., Ergüven, M., & Yıldız, M. (2023) · The Journal of Pediatric Research · doi:10.4274/jpr.galenos.2022.04207
Eisenträger mit Doppelfunktion
Hille‐Rehfeld, A. (2023) · Chemie in unserer Zeit · doi:10.1002/ciuz.202310015
Genetic dissection of cyclic di-GMP signaling in Pseudomonas aeruginosa via diguanylate cyclase disruptionPreprint
Martino, R. A., Volke, D. C., Tenaglia, A. H., Tribelli, P. M., Nikel, P. I., & Smania, A. M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.26.634905
Proteomics and its Applications in Biofilm Research
Ahmed, Z. H. T., Singh, P., Haque, M. R., Vasudevan, D., Rajesh, V., Ravichandran, S. S., Srinivasan, D., Maqbool, M., & Hassan, S. (2025) · Springer eBooks · doi:10.1007/978-3-031-91863-6_6
Pseudomonas aeruginosa differentially influences antibiotic-resistant Staphylococcus aureus emergence and expansion in hyperglycemic environments
Darwitz, B. P., Lifschin, Z. J., Miller, C. M., Genito, C. J., Gossett, C. A., Augustine, K. E., & Thurlow, L. R. (2025) · Journal of Bacteriology · doi:10.1128/jb.00333-25
Additional file 1 of The effect of nisin on the biofilm production, antimicrobial susceptibility and biofilm formation of Staphylococcus aureus and Pseudomonas aeruginosa
Ghapanvari, P., Taheri, M., Jalilian, F. A., Dehbashi, S., Dezfuli, A. A. Z., & Arabestani, M. R. (2022) · Figshare · doi:10.6084/m9.figshare.21069605
Additional file 3 of 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) · Figshare · doi:10.6084/m9.figshare.26677277
Additional file 4 of 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) · Figshare · doi:10.6084/m9.figshare.26677280
Additional file 2 of 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) · Figshare · doi:10.6084/m9.figshare.25150719
Additional file 1 of 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) · Figshare · doi:10.6084/m9.figshare.25150510
A three-component logic gate governs quorum sensing-regulated killing of Stenotrophomonas maltophilia by Pseudomonas aeruginosaPreprint
Frando, A., Parsek, R. S., Roberts, G. W., & Dandekar, A. A. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.27.702039
Tracking eco-evolutionary dynamics among lung pathobiome members from children with cystic fibrosisPreprint
Schwyter, L., Kuratli, R., Provveduto, S., Silva, P. D. C., Latzin, P., Harrison, F., Hilty, M., & Kümmerli, R. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.29.702708
Unlocking the potential of Pseudomonas aeruginosa QS intermediates as antimicrobial synergists against three multidrug-resistant enteric bacteria
Kiran, S., Alhegaili, A. S., Al‐Dayan, N., Naseem, Z., Siddique, W., Ayoub, I., Iqbal, S., Jabeen, S., Habib, F.-E., Taj, S., et al. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1726554
Microbiotes Pulmonaires des patients atteints de mucoviscidose : interactions avec Pseudomonas aeruginosa
Pagès, L. (2016) · theses.fr (ABES) · doi:10.70675/9d450abbzb581z49cez9268z17379d9c31b5
PhoPQ is an upstream regulator of quorum sensing in small colony variant subpopulations of Pseudomonas aeruginosaPreprint
Simanek, K. A., Kurtz, A. F., Schumacher, M. L., Pope, A. N., Mendoza, A. G., & Paczkowski, J. E. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.10.723372
Analysis of mono, duo and multispecies biofilms of Enterococcus faecalis, Pseudomonas aeruginosa, and Staphylococcus aureus
Guerra, N. D. S., Rodrigues, B. Á., Loureiro, I. P., Maboni, L. J., & Zimmer, K. R. (2026) · Microbial Pathogenesis · doi:10.1016/j.micpath.2026.108604
Microenvironment shapes Staphylococcus aureus phenotypes in children with cystic fibrosis over time
Robaldi, S. A., Pereda, R., Pautasso, M. C., Blasko, E., Fretes, A., Jaureguialzo, T., Appella, M. N. D., Galeano, M. B., Rial, M. J., Smith, S., et al. (2026) · iScience · doi:10.1016/j.isci.2026.117708
Tracking eco-evolutionary patterns among oropharyngeal pathobiome members in a pediatric cystic fibrosis cohort
Schwyter, L., Kuratli, R., Provveduto, S., Silva, P. D. C., Latzin, P., Harrison, F., Hilty, M., & Kümmerli, R. (2026) · Microbiology Spectrum · doi:10.1128/spectrum.01577-26

Authors: Biswas, L., Biswas, R., Schlag, M., Bertram, R., & Götz, F.
Affiliations: University of Tübingen (DE)
Institute of Microbial Genetics, University of Tübingen, 72076 Tübingen, Germany
ORCID: Biswas, Lalitha
Biswas, Raja
Bertram, Ralph
Venue: Applied and Environmental Microbiology
Publisher: American Society for Microbiology
Published: 2009-11
Volume: 75
Issue: 21
Pages: 6910-6912
ISSN: 0099-2240 (ISSN-L)
1098-5336
DOI: 10.1128/aem.01211-09
PMC: PMC2772425
OpenAlex: W2145292900
Cited by: 182
References: 19
Citations by year: 2026: 12 · 2025: 17 · 2024: 14 · 2023: 15 · 2022: 13 · 2021: 12 · 2020: 8 · 2019: 18 · 2018: 5 · 2017: 10 · 2016: 10 · 2015: 8 · 2014: 10 · 2013: 12 · 2012: 9
FWCI: 2.42
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: journals.asm.org/non-commercial-tdm-license (tdm)
Locations: Applied and Environmental Microbiology (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Funders: Deutsche Forschungsgemeinschaft (SPP 1316)
Bundesministerium für Bildung und Forschung
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacterial biofilms and quorum sensing
Health Sciences › Medicine › Infectious Diseases › Antimicrobial Resistance in Staphylococcus
Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
Keywords: Staphylococcus aureus, Pseudomonas aeruginosa, small colony variants, pyocyanin, electron transport chain, bacterial survival, coexistence, bacterial virulence factors
MeSH terms: Antibiosis, Pseudomonas aeruginosa, Pyocyanine, Staphylococcus aureus, Stress, Physiological, Microbial Viability

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

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

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks