The Involvement of Cell-to-Cell Signals in the Development of a Bacterial Biofilm

Colorimetric Method for Determination of Sugars and Related Substances

DuBois, M., Gilles, K. A., Hamilton, J. K., Rebers, P. A., & Smith, F. (1956) · Analytical Chemistry · doi:10.1021/ac60111a017 · Cited by 52,269 · see citing works

MICROBIAL BIOFILMS

Costerton, J. W., Lewandowski, Z., Caldwell, D. E., Korber, D. R., & Lappin-Scott, H. M. (1995) · Annual Review of Microbiology · doi:10.1146/annurev.mi.49.100195.003431 · Cited by 4,718 · see citing works

Quorum sensing in bacteria: the LuxR-LuxI family of cell density-responsive transcriptional regulators

Fuqua, W. C., Winans, S. C., & Greenberg, E. P. (1994) · Journal of Bacteriology · doi:10.1128/jb.176.2.269-275.1994 · Cited by 2,941 · see citing works

FACS-optimized mutants of the green fluorescent protein (GFP)

Cormack, B. P., Valdivia, R. H., & Falkow, S. (1996) · Gene · doi:10.1016/0378-1119(95)00685-0 · Cited by 2,621 · see citing works

Roles of Pseudomonas aeruginosa las and rhl quorum-sensing systems in control of elastase and rhamnolipid biosynthesis genes

Pearson, J. P., Pesci, E. C., & Iglewski, B. H. (1997) · Journal of Bacteriology · doi:10.1128/jb.179.18.5756-5767.1997 · Cited by 1,049 · see citing works

Structure of the autoinducer required for expression of Pseudomonas aeruginosa virulence genes.

Pearson, J. P., Gray, K. M., Passador, L., Tucker, K. D., Eberhard, A., Iglewski, B. H., & Greenberg, E. P. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.1.197 · Cited by 992 · see citing works

Regulation of las and rhl quorum sensing in Pseudomonas aeruginosa

Pesci, E. C., Pearson, J. P., Seed, P. C., & Iglewski, B. H. (1997) · Journal of Bacteriology · doi:10.1128/jb.179.10.3127-3132.1997 · Cited by 892 · see citing works

Expression of Pseudomonas aeruginosa Virulence Genes Requires Cell-to-Cell Communication

Passador, L., Cook, J. M., Gambello, M. J., et al. (1993) · Science · doi:10.1126/science.8493556 · Cited by 876 · see citing works

Optical sectioning of microbial biofilms

Lawrence, J. R., Korber, D. R., Hoyle, B. D., Costerton, J. W., & Caldwell, D. E. (1991) · Journal of Bacteriology · doi:10.1128/jb.173.20.6558-6567.1991 · Cited by 828 · see citing works

A second N-acylhomoserine lactone signal produced by Pseudomonas aeruginosa.

Pearson, J. P., Passador, L., Iglewski, B. H., & Greenberg, E. P. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.5.1490 · Cited by 786 · see citing works

A hierarchical quorum‐sensing cascade in Pseudomonas aeruginosa links the transcriptional activators LasR and RhIR (VsmR) to expression of the stationary‐phase sigma factor RpoS

Latifi, A., Foglino, M., Tanaka, K., et al. (1996) · Molecular Microbiology · doi:10.1046/j.1365-2958.1996.00063.x · Cited by 727 · see citing works

Cloning and characterization of the Pseudomonas aeruginosa lasR gene, a transcriptional activator of elastase expression

Gambello, M. J., & Iglewski, B. H. (1991) · Journal of Bacteriology · doi:10.1128/jb.173.9.3000-3009.1991 · Cited by 710 · see citing works

Synthesis of multiple exoproducts in Pseudomonas aeruginosa is under the control of RhlR-RhlI, another set of regulators in strain PAO1 with homology to the autoinducer-responsive LuxR-LuxI family

Brint, J. M., & Ohman, D. E. (1995) · Journal of Bacteriology · doi:10.1128/jb.177.24.7155-7163.1995 · Cited by 579 · see citing works

Autoinducer-mediated regulation of rhamnolipid biosurfactant synthesis in Pseudomonas aeruginosa.

Ochsner, U. A., & Reiser, J. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.14.6424 · Cited by 579 · see citing works

Multiple homologues of LuxR and LuxI control expression of virulence determinants and secondary metabolites through quorum sensing in Pseudomonas aeruginosa PAO1

Latifi, A., Winson, M. K., Foglino, M., et al. (1995) · Molecular Microbiology · doi:10.1111/j.1365-2958.1995.mmi_17020333.x · Cited by 492 · see citing works

Production and Characterization of the Slime Polysaccharide of Pseudomonas aeruginosa

Evans, L. R., & Linker, A. (1973) · Journal of Bacteriology · doi:10.1128/jb.116.2.915-924.1973 · Cited by 429 · see citing works

Isolation and characterization of a regulatory gene affecting rhamnolipid biosurfactant synthesis in Pseudomonas aeruginosa

Ochsner, U. A., Koch, A., Fiechter, A., & Reiser, J. (1994) · Journal of Bacteriology · doi:10.1128/jb.176.7.2044-2054.1994 · Cited by 429 · see citing works

Exopolysaccharide production in biofilms: substratum activation of alginate gene expression by Pseudomonas aeruginosa

Davies, D. G., Chakrabarty, A. M., & Geesey, G. G. (1993) · Applied and Environmental Microbiology · doi:10.1128/aem.59.4.1181-1186.1993 · Cited by 427 · see citing works

Liquid flow in heterogeneous biofilms

de Beer, D., Stoodley, P., & Lewandowski, Z. (1994) · Biotechnology and Bioengineering · doi:10.1002/bit.260440510 · Cited by 291 · see citing works

Evidence of autoinducer activity in naturally occurring biofilms

McLean, R. J. C., Whiteley, M., Stickler, D. J., & Fuqua, W. C. (1997) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1997.tb12653.x · Cited by 290 · see citing works

Carbohydrate Interference and Its Correction in Pectin Analysis Using the m‐Hydroxydiphenyl Method

KINTNER, P. K., & Buren, J. P. V. (1982) · Journal of Food Science · doi:10.1111/j.1365-2621.1982.tb12708.x · Cited by 286 · see citing works

Prevention and Control of Bacterial Infections Associated with Medical Devices

Khoury, A. E., LAM, K., Ellis, B. D., et al. (1992) · ASAIO Journal · doi:10.1097/00002480-199207000-00013 · Cited by 269 · see citing works

An atypical Pseudomonas aeruginosa associated with cystic fibrosis of the pancreas

Doggett, R. G., Harrison, G. M., Stillwell, R. N., et al. (1966) · The Journal of Pediatrics · doi:10.1016/s0022-3476(66)80152-x · Cited by 153 · see citing works

The chain of command in Pseudomonas quorum sensing

Pesci, E. C., & Iglewski, B. H. (1997) · Trends in Microbiology · doi:10.1016/s0966-842x(97)01008-1 · Cited by 131 · see citing works

Relationship between glycocalyx and povidone-iodine resistance in Pseudomonas aeruginosa (ATCC 27853) biofilms

Brown, M. L., Aldrich, H. C., & Gauthier, J. J. (1995) · Applied and Environmental Microbiology · doi:10.1128/aem.61.1.187-193.1995 · Cited by 72 · see citing works

Why and How Bacteria Communicate

Losick, R. M., & Kaiser, D. (1997) · Scientific American · doi:10.1038/scientificamerican0297-68 · Cited by 70 · see citing works

Comparison of Alcian blue and ruthenium red effects on preservation of outer envelope ultrastructure in methanotrophic bacteria

Fassel, T. A., Schaller, M. J., & Remsen, C. C. (1992) · Microscopy Research and Technique · doi:10.1002/jemt.1070200109 · Cited by 17 · see citing works

Indonesian Studies and the Social Sciences

Sutherland, H. (1977) · Itinerario · doi:10.1017/s016511530001651x · Cited by 8 · see citing works

Bacterial Biofilms: A Common Cause of Persistent Infections

Costerton, J. W., Stewart, P. S., & Greenberg, E. P. (1999) · Science · doi:10.1126/science.284.5418.1318 · Cited by 12,167 · see citing works

Biofilms: Survival Mechanisms of Clinically Relevant Microorganisms

Donlan, R. M., & Costerton, J. W. (2002) · Clinical Microbiology Reviews · doi:10.1128/cmr.15.2.167-193.2002 · Cited by 6,644 · see citing works

Biofilm formation as microbial development

O'Toole, G., Kaplan, H. B., & Kolter, R. (2000) · Annual Review of Microbiology · doi:10.1146/annurev.micro.54.1.49 · Cited by 3,571 · see citing works

Biological roles of glycans

Varki, A. (2017) · Glycobiology · doi:10.1093/glycob/cww086 · Cited by 2,635 · 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

The Calgary Biofilm Device: New Technology for Rapid Determination of Antibiotic Susceptibilities of Bacterial Biofilms

Ceri, H., Olson, M. E., Stremick, C., Read, R. R., Morck, D., & Buret, A. (1999) · Journal of Clinical Microbiology · doi:10.1128/jcm.37.6.1771-1776.1999 · Cited by 2,155 · see citing works

<i>Pseudomonas aeruginosa</i> Displays Multiple Phenotypes during Development as a Biofilm

Sauer, K., Camper, A. K., Ehrlich, G. D., Costerton, J. W., & Davies, D. G. (2002) · Journal of Bacteriology · doi:10.1128/jb.184.4.1140-1154.2002 · Cited by 1,691 · see citing works

Biofilm Formation by the Fungal Pathogen <i>Candida albicans</i> : Development, Architecture, and Drug Resistance

Chandra, J., Kuhn, D. M., Mukherjee, P. K., Hoyer, L. L., McCormick, T., & Ghannoum, M. A. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.18.5385-5394.2001 · Cited by 1,578 · see citing works

Bacterial adhesion: seen any good biofilms lately

Dunne, W. M. (2002) · Clinical Microbiology Reviews · doi:10.1128/cmr.15.2.155-166.2002 · Cited by 1,516 · see citing works

Candida biofilms and their role in infection

Douglas, L. J. (2003) · Trends in Microbiology · doi:10.1016/s0966-842x(02)00002-1 · Cited by 1,150 · see citing works

A component of innate immunity prevents bacterial biofilm development

Singh, P. K., Parsek, M. R., Greenberg, E. P., & Welsh, M. J. (2002) · Nature · doi:10.1038/417552a · Cited by 1,026 · see citing works

Thinking about Bacterial Populations as Multicellular Organisms

Shapiro, J. A. (1998) · Annual Review of Microbiology · doi:10.1146/annurev.micro.52.1.81 · Cited by 876 · see citing works

What are Bacterial Extracellular Polymeric Substances?

Wingender, J., Neu, T. R., & Flemming, H.-C. (1999) · Microbial Extracellular Polymeric Substances · doi:10.1007/978-3-642-60147-7_1 · Cited by 655 · see citing works

Dental plaque formation

Rosan, B., & Lamont, R. J. (2000) · Microbes and Infection · doi:10.1016/s1286-4579(00)01316-2 · Cited by 561 · see citing works

Engineered probiotic Escherichia coli can eliminate and prevent Pseudomonas aeruginosa gut infection in animal models

Hwang, I. Y., Koh, E., Wong, A., March, J. C., Bentley, W. E., Lee, Y. S., & Chang, M. W. (2017) · Nature Communications · doi:10.1038/ncomms15028 · Cited by 472 · see citing works

Biofilms and Inflammation in Chronic Wounds

Zhao, G., Usui, M. L., Lippman, S. I., James, G. A., Stewart, P. S., Fleckman, P., & Olerud, J. E. (2013) · Advances in Wound Care · doi:10.1089/wound.2012.0381 · Cited by 448 · see citing works

Environmental factors that shape biofilm formation

Toyofuku, M., Inaba, T., Kiyokawa, T., Obana, N., Yawata, Y., & Nomura, N. (2016) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2015.1058701 · Cited by 429 · see citing works

Matrix polymers of Candida biofilms and their possible role in biofilm resistance to antifungal agents

Baillie, G. S. (2000) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/46.3.397 · Cited by 389 · see citing works

Exploitation of marine algae: biogenic compounds for potential antifouling applications

Bhadury, P., & Wright, P. (2004) · Planta · doi:10.1007/s00425-004-1307-5 · Cited by 327 · see citing works

Role of dimorphism in the development of Candida albicans biofilms

BAILLIE, G. S., & DOUGLAS, L. J. (1999) · Journal of Medical Microbiology · doi:10.1099/00222615-48-7-671 · Cited by 304 · see citing works

Mechanisms of removing pollutants from aqueous solutions by microorganisms and their aggregates: a review

Wu, Y., Li, T., & Yang, L. (2012) · Bioresource Technology · doi:10.1016/j.biortech.2011.12.088 · Cited by 294 · see citing works

Beneficial biofilm formation by industrial bacteria Bacillus subtilis and related species

Morikawa, M. (2006) · Journal of Bioscience and Bioengineering · doi:10.1263/jbb.101.1 · Cited by 265 · see citing works

Fungal Biofilms, Drug Resistance, and Recurrent Infection

Desai, J. V., Mitchell, A. P., & Andes, D. R. (2014) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a019729 · Cited by 252 · see citing works

Brominated Furanones Inhibit Biofilm Formation by <i>Salmonella enterica</i> Serovar Typhimurium

Janssens, J. C. A., Steenackers, H., Robijns, S., Gellens, E., Levin, J., Zhao, H., Hermans, K., De Coster, D., Verhoeven, T. L., Marchal, K., et al. (2008) · Applied and Environmental Microbiology · doi:10.1128/aem.01262-08 · Cited by 223 · see citing works

Analysis of quorum sensing-deficient clinical isolates of Pseudomonas aeruginosa

Schaber, J. A., Carty, N. L., McDonald, N. A., Graham, E. D., Cheluvappa, R., Griswold, J. A., & Hamood, A. N. (2004) · Journal of Medical Microbiology · doi:10.1099/jmm.0.45617-0 · Cited by 224 · see citing works

Quorum Sensing in the Context of Food Microbiology

Skandamis, P. N., & Nychas, G.-J. E. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.00468-12 · Cited by 215 · see citing works

Nitric oxide regulation of bacterial biofilms

Arora, D. P., Hossain, S., Xu, Y., & Boon, E. M. (2015) · Biochemistry · doi:10.1021/bi501476n · Cited by 206 · see citing works

Microcolonies, quorum sensing and cytotoxicity determine the survival of <i>Pseudomonas aeruginosa</i> biofilms exposed to protozoan grazing

Matz, C., Bergfeld, T., Rice, S. A., & Kjelleberg, S. (2004) · Environmental Microbiology · doi:10.1111/j.1462-2920.2004.00556.x · Cited by 200 · see citing works

S <scp>upragingival</scp> C <scp>alculus:</scp> F <scp>ormation and</scp> C <scp>ontrol</scp>

Jin, Y., & Yip, H.-K. (2002) · Critical Reviews in Oral Biology &amp; Medicine · doi:10.1177/154411130201300506 · Cited by 181 · see citing works

Loss of microbicidal activity and increased formation of biofilm due to decreased lactoferrin activity in patients with cystic fibrosis

Rogan, M. P., Taggart, C. C., Greene, C. M., Murphy, P. G., O’Neill, S. J., & McElvaney, N. G. (2004) · The Journal of Infectious Diseases · doi:10.1086/423821 · Cited by 171 · see citing works

Antibiofilm Activity of an Exopolysaccharide from Marine Bacterium Vibrio sp. QY101

Jiang, P., Li, J., Han, F., Duan, G., Lu, X., Gu, Y., & Yu, W. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018514 · Cited by 165 · see citing works

Should the biofilm mode of life be taken into consideration for microbial biocontrol agents?

Pandin, C., Le Coq, D., Canette, A., Aymerich, S., & Briandet, R. (2017) · Microbial Biotechnology · doi:10.1111/1751-7915.12693 · Cited by 157 · see citing works

Genetic control of bacterial biofilms

Wolska, K. I., Grudniak, A. M., Rudnicka, Z., & Markowska, K. (2016) · Journal of Applied Genetics · doi:10.1007/s13353-015-0309-2 · Cited by 154 · see citing works

Laser-induced vapour nanobubbles improve drug diffusion and efficiency in bacterial biofilms

Teirlinck, E., Xiong, R., Brans, T., Forier, K., Fraire, J., Van Acker, H., Matthijs, N., De Rycke, R., De Smedt, S. C., Coenye, T., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06884-w · Cited by 154 · see citing works

Physical Morphology and Surface Properties of Unsaturated <i>Pseudomonas putida</i> Biofilms

Auerbach, I. D., Sorensen, C., Hansma, H. G., & Holden, P. A. (2000) · Journal of Bacteriology · doi:10.1128/jb.182.13.3809-3815.2000 · Cited by 144 · see citing works

Stochastic expression of a multiple antibiotic resistance activator confers transient resistance in single cells

El Meouche, I., Siu, Y., & Dunlop, M. J. (2016) · Scientific Reports · doi:10.1038/srep19538 · Cited by 120 · see citing works

Recent developments in the use of nanoparticles for treatment of biofilms

Han, C., Romero, N., Fischer, S., Dookran, J., Berger, A., & Doiron, A. L. (2017) · Nanotechnology Reviews · doi:10.1515/ntrev-2016-0054 · Cited by 114 · see citing works

Prevention of catheter-associated urinary tract infection

Trautner, B. W., Hull, R. A., & Darouiche, R. O. (2005) · Current Opinion in Infectious Diseases · doi:10.1097/00001432-200502000-00007 · Cited by 99 · see citing works

Shaping the growth behaviour of biofilms initiated from bacterial aggregates

Melaugh, G., Hutchison, J., Kragh, K. N., Irie, Y., Roberts, A., Bjarnsholt, T., Diggle, S. P., Gordon, V. D., & Allen, R. J. (2016) · PLoS ONE · doi:10.1371/journal.pone.0149683 · Cited by 93 · see citing works

Antibacterial and biofilm-disrupting coatings from resin acid-derived materials

Ganewatta, M. S., Miller, K. P., Singleton, S. P., Mehrpouya-Bahrami, P., Chen, Y. P., Yan, Y., Nagarkatti, M., Nagarkatti, P., Decho, A. W., & Tang, C. (2015) · Biomacromolecules · doi:10.1021/acs.biomac.5b01005 · Cited by 84 · see citing works

Bundle-Forming Pili and EspA Are Involved in Biofilm Formation by Enteropathogenic<i>Escherichia coli</i>

Moreira, C. G., Palmer, K., Whiteley, M., Sircili, M. P., Trabulsi, L. R., Castro, A. F. P., & Sperandio, V. (2006) · Journal of Bacteriology · doi:10.1128/jb.00177-06 · Cited by 77 · see citing works

LuxR Homologue SmcR Is Essential for Vibrio vulnificus Pathogenesis and Biofilm Detachment, and Its Expression is Induced by Host Cells

Kim, S. M., Park, J. H., Lee, H. S., Kim, W. B., Ryu, J. M., Han, H. J., & Choi, S. H. (2013) · Infection and Immunity · doi:10.1128/iai.00561-13 · Cited by 75 · see citing works

Impact of Hydrodynamics on Oral Biofilm Strength

Paramonova, E., Kalmykowa, O. J., van der Mei, H. C., Busscher, H. J., & Sharma, P. K. (2009) · Journal of Dental Research · doi:10.1177/0022034509344569 · Cited by 74 · see citing works

Quantitative Comparison and Analysis of Species-Specific Wound Biofilm Virulence Using an In Vivo, Rabbit-Ear Model

Seth, A. K., Geringer, M. R., Galiano, R. D., Leung, K. P., Mustoe, T. A., & Hong, S. J. (2012) · Journal of the American College of Surgeons · doi:10.1016/j.jamcollsurg.2012.05.028 · Cited by 65 · see citing works

Flexible survival strategies of Pseudomonas aeruginosa in biofilms result in increased fitness compared with Candida albicans

Purschke, F. G., Hiller, E., Trick, I., & Rupp, S. (2012) · Molecular &amp; Cellular Proteomics · doi:10.1074/mcp.m112.017673 · Cited by 60 · see citing works

Contribution of quorum sensing to the virulence of <i>Pseudomonas aeruginosa</i> in pressure ulcer infection in rats

Nakagami, G., Morohoshi, T., Ikeda, T., Ohta, Y., Sagara, H., Huang, L., Nagase, T., Sugama, J., & Sanada, H. (2011) · Wound Repair and Regeneration · doi:10.1111/j.1524-475x.2010.00653.x · Cited by 34 · see citing works

The Interplay between the Microbiota and Enterohemorrhagic <i>Escherichia coli</i>

Pifer, R., & Sperandio, V. (2014) · Microbiology Spectrum · doi:10.1128/microbiolspec.ehec-0015-2013 · Cited by 32 · see citing works

Bacterial biofilms associated with food particles in the human large bowel

Van Wey, A. S., Cookson, A. L., Roy, N. C., McNabb, W. C., Soboleva, T. K., & Shorten, P. R. (2011) · Molecular Nutrition &amp; Food Research · doi:10.1002/mnfr.201000589 · Cited by 31 · see citing works

[Increase in the ecological danger upon the use of biocides for fighting corrosion induced by microorganisms].

Zhigletsova, S. K., Rodin, V. B., Kobelev, V. S., et al. (2001) · PubMed · Cited by 3 · see citing works

Application of the New Biocide: FA-101

Ma, L. (2005) · Fine and Specialty Chemicals

Influence of Al(III) on biofilm and its extracellular polymeric substances in sequencing batch biofilm reactors

Hu, X., Yang, L., Lai, X., et al. (2017) · Environmental Technology · doi:10.1080/09593330.2017.1378268 · Cited by 15 · see citing works

Numerical Evaluation of Biocide Treatment against Sulfate Reducing Bacteria in Oilfield Water Pipelines

Vilcáez, J., Miyazawa, S., Suto, K., et al. (2007) · Journal of the Japan Petroleum Institute · doi:10.1627/jpi.50.208 · Cited by 5 · see citing works

Sub-minimum inhibitory concentrations of biocides induced biofilm formation in Pseudomonas aeruginosa

Hemati, S., Kouhsari, E., Sadeghifard, N., et al. (2020) · New Microbes and New Infections · doi:10.1016/j.nmni.2020.100794 · Cited by 43 · see citing works