Patients with Long-Term Oral Carriage Harbor High-Persister Mutants of Candida albicans

Persister cells, dormancy and infectious disease

Lewis, K. (2007) · Nature Reviews Microbiology · doi:10.1038/nrmicro1557 · Cited by 2,052

Isogenic strain construction and gene mapping in Candida albicans.

Fonzi, W. A., & Irwin, M. Y. (1993) · Genetics · doi:10.1093/genetics/134.3.717 · Cited by 1,695

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

Biofilms and Planktonic Cells of Pseudomonas aeruginosa Have Similar Resistance to Killing by Antimicrobials

Spoering, A. L., & Lewis, K. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.23.6746-6751.2001 · Cited by 907

Specialized Persister Cells and the Mechanism of Multidrug Tolerance in Escherichia coli

Keren, I., Shah, D., Spoering, A. L., Kaldalu, N., & Lewis, K. (2004) · Journal of Bacteriology · doi:10.1128/jb.186.24.8172-8180.2004 · Cited by 848

Standardized Method for In Vitro Antifungal Susceptibility Testing of Candida albicans Biofilms

Ramage, G., Vande Walle, K., Wickes, B. L., & López-Ribot, J. L. (2001) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.45.9.2475-2479.2001 · Cited by 753

hipA, a newly recognized gene of Escherichia coli K-12 that affects frequency of persistence after inhibition of murein synthesis

Moyed, H. S., & Bertrand, K. P. (1983) · Journal of Bacteriology · doi:10.1128/jb.155.2.768-775.1983 · Cited by 641

CHROMagar Candida, a new differential isolation medium for presumptive identification of clinically important Candida species

Odds, F. C., & Bernaerts, R. (1994) · Journal of Clinical Microbiology · doi:10.1128/jcm.32.8.1923-1929.1994 · Cited by 631

Persisters: a distinct physiological state of E. coli

Khodursky, A. B., Zhang, Z., Devang, S., Kaldalu, N., Kurg, K., & Lewis, K. (2006) · Digital Repository Service (Northeastern University) · doi:10.1186/1471-2180-6-53 · Cited by 630

Persister cells and the riddle of biofilm survival

Lewis, K. (2005) · Biochemistry (Moscow) · doi:10.1007/s10541-005-0111-6 · Cited by 524

Persister cells

Lewis, K. (2010) · Annual Review of Microbiology · doi:10.1146/annurev.micro.112408.134306 · Cited by 1,858

Platforms for antibiotic discovery

Lewis, K. (2013) · Nature Reviews Drug Discovery · doi:10.1038/nrd3975 · Cited by 1,527

Definitions and guidelines for research on antibiotic persistence

Balaban, N. Q., Helaine, S., Lewis, K., Ackermann, M., Aldridge, B., Andersson, D. I., Brynildsen, M. P., Bumann, D., Camilli, A., Collins, J. J., et al. (2019) · Nature Reviews Microbiology · doi:10.1038/s41579-019-0196-3 · Cited by 1,313

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

Antimicrobial Resistance and Virulence: a Successful or Deleterious Association in the Bacterial World?

Beceiro, A., Tomás, M., & Bou, G. (2013) · Clinical Microbiology Reviews · doi:10.1128/cmr.00059-12 · Cited by 1,118

Biofilm-specific antibiotic tolerance and resistance

Olsen, I. (2015) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-015-2323-z · Cited by 742

Activated ClpP kills persisters and eradicates a chronic biofilm infection

Conlon, B. P., Nakayasu, E. S., Fleck, L. E., LaFleur, M. D., Isabella, V. M., Coleman, K., Leonard, S. N., Smith, R. D., Adkins, J., & Lewis, K. (2013) · Nature · doi:10.1038/nature12790 · Cited by 675

Persister formation in Staphylococcus aureus is associated with ATP depletion

Conlon, B. P., Rowe, S. E., Gandt, A. B., Nuxoll, A. S., Donegan, N. P., Zalis, E. A., Clair, G., Adkins, J., Cheung, A. L., & Lewis, K. (2016) · Nature Microbiology · doi:10.1038/nmicrobiol.2016.51 · Cited by 656

Molecular Mechanisms Underlying Bacterial Persisters

Maisonneuve, E., & Gerdes, K. (2014) · Cell · doi:10.1016/j.cell.2014.02.050 · Cited by 668

Emergence of Pseudomonas aeruginosa Strains Producing High Levels of Persister Cells in Patients with Cystic Fibrosis

Mulcahy, L. R., Burns, J. L., Lory, S. J., & Lewis, K. (2010) · Journal of Bacteriology · doi:10.1128/jb.01651-09 · Cited by 621

Genetic control of Candida albicans biofilm development

Finkel, J. S., & Mitchell, A. P. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2475 · Cited by 641

Fungal Biofilm Resistance

Ramage, G., Rajendran, R., Sherry, L., & Williams, C. (2012) · International Journal of Microbiology · doi:10.1155/2012/528521 · Cited by 583

ATP-Dependent Persister Formation in Escherichia coli

Shan, Y., Brown Gandt, A., Rowe, S. E., Deisinger, J. P., Conlon, B. P., & Lewis, K. (2017) · mBio · doi:10.1128/mbio.02267-16 · Cited by 508

Effect of tolerance on the evolution of antibiotic resistance under drug combinations

Liu, J., Gefen, O., Ronin, I., Bar‐Meir, M., & Balaban, N. Q. (2020) · Science · doi:10.1126/science.aay3041 · Cited by 489

Microbial Persistence and the Road to Drug Resistance

Cohen, N. R., Lobritz, M. A., & Collins, J. J. (2013) · Cell Host & Microbe · doi:10.1016/j.chom.2013.05.009 · Cited by 475

Role of persister cells in chronic infections: clinical relevance and perspectives on anti-persister therapies

Fauvart, M., De Groote, V. N., & Michiels, J. (2011) · Journal of Medical Microbiology · doi:10.1099/jmm.0.030932-0 · Cited by 425

Mechanisms of Candida Biofilm Drug Resistance

Taff, H. T., Mitchell, K. F., Edward, J. A., & Andes, D. R. (2013) · Future Microbiology · doi:10.2217/fmb.13.101 · Cited by 422

Formation, physiology, ecology, evolution and clinical importance of bacterial persisters

den Bergh, B. V., Fauvart, M., & Michiels, J. J. (2017) · FEMS Microbiology Reviews · doi:10.1093/femsre/fux001 · Cited by 400

Bacterial persistence promotes the evolution of antibiotic resistance by increasing survival and mutation rates

Windels, E. M., Michiels, J. E., Fauvart, M., Wenseleers, T., den Bergh, B. V., & Michiels, J. J. (2019) · The ISME Journal · doi:10.1038/s41396-019-0344-9 · Cited by 380

Resistance Toward Chlorhexidine in Oral Bacteria – Is There Cause for Concern?

Cieplik, F., Jakubovics, N. S., Buchalla, W., Maisch, T., Hellwig, E., & Al-Ahmad, A. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00587 · Cited by 424

Bridging the gap between viable but non-culturable and antibiotic persistent bacteria

Ayrapetyan, M., Williams, T. C., & Oliver, J. D. (2014) · Trends in Microbiology · doi:10.1016/j.tim.2014.09.004 · Cited by 321

Concepts and Principles of Photodynamic Therapy as an Alternative Antifungal Discovery Platform

Dai, T., Fuchs, B. B., Coleman, J. J., Prates, R. A., Astrakas, C., Denis, T. G. S., Ribeiro, M. S., Mylonakis, E. E., Hamblin, M. R., & Tegos, G. P. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00120 · Cited by 304

Bacterial Persisters and Infection: Past, Present, and Progressing

Gollan, B., Grabe, G. J., Michaux, C., & Hélaine, S. (2019) · Annual Review of Microbiology · doi:10.1146/annurev-micro-020518-115650 · Cited by 287

Role of oxidative stress in persister tolerance

Wu, Y., Vulić, M., Keren, I., & Lewis, K. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00921-12 · Cited by 276

Candida albicans biofilms and polymicrobial interactions

Ponde, N. O., Lortal, L., Ramage, G., Naglik, J. R., & Richardson, J. P. (2021) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2020.1843400 · Cited by 281

Candida glabrata: A review of its features and resistance

Rodrigues, C. F., Silva, S., & Henriques, M. (2014) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-013-2009-3 · Cited by 268

Antifungal drug-resistance mechanisms in Candida biofilms

Kaur, J., & Nobile, C. J. (2022) · Current Opinion in Microbiology · doi:10.1016/j.mib.2022.102237 · Cited by 279

HipBA–promoter structures reveal the basis of heritable multidrug tolerance

Schumacher, M. A., Balani, P., Min, J., Chinnam, N. B., Hansen, S., Vulić, M., Lewis, K., & Brennan, R. G. (2015) · Nature · doi:10.1038/nature14662 · Cited by 243

Fighting bacterial persistence: Current and emerging anti-persister strategies and therapeutics

Defraine, V., Fauvart, M., & Michiels, J. (2018) · Drug Resistance Updates · doi:10.1016/j.drup.2018.03.002 · Cited by 222

Clinically prevalent mutations in Mycobacterium tuberculosis alter propionate metabolism and mediate multidrug tolerance

Hicks, N. D., Yang, J., Zhang, X., Zhao, B. T., Grad, Y. H., Liu, L., Ou, X., Chang, Z., Xia, H., Zhou, Y., et al. (2018) · Nature Microbiology · doi:10.1038/s41564-018-0218-3 · Cited by 207

Persister Cells: Molecular Mechanisms Related to Antibiotic Tolerance

Lewis, K. (2012) · Handbook of Experimental Pharmacology · doi:10.1007/978-3-642-28951-4_8 · Cited by 217

Importance of Biofilms in Urinary Tract Infections: New Therapeutic Approaches

Soto, S. M. (2014) · Advances in Biology · doi:10.1155/2014/543974 · Cited by 219

Biofilm-Associated Infections: Antibiotic Resistance and Novel Therapeutic Strategies

Sun, F., Qu, F., Yan, L., Mao, P., Xia, P., Chen, H., & Zhou, D. (2013) · Future Microbiology · doi:10.2217/fmb.13.58 · Cited by 221

Pharmacodynamics, Population Dynamics, and the Evolution of Persistence in Staphylococcus aureus

Johnson, P. J., & Levin, B. R. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003123 · Cited by 187

Strategies to Combat Multidrug-Resistant and Persistent Infectious Diseases

Pacios, O., Blasco, L., Bleriot, I., Fernández-García, L., Bardanca, M. G., Ambroa, A., Bou, G., López, M. C., & Tomás, M. (2020) · Antibiotics · doi:10.3390/antibiotics9020065 · Cited by 189

Heterogeneous bacterial persisters and engineering approaches to eliminate them

Allison, K. R., Brynildsen, M. P., & Collins, J. J. (2011) · Current Opinion in Microbiology · doi:10.1016/j.mib.2011.09.002 · Cited by 185

General Mechanisms Leading to Persister Formation and Awakening

Wilmaerts, D., Windels, E. M., Verstraeten, N., & Michiels, J. J. (2019) · Trends in Genetics · doi:10.1016/j.tig.2019.03.007 · Cited by 186

Candida Survival Strategies

Polke, M., Hube, B., & Jacobsen, I. D. (2015) · Advances in applied microbiology · doi:10.1016/bs.aambs.2014.12.002 · Cited by 205

Borrelia burgdorferi, the Causative Agent of Lyme Disease, Forms Drug-Tolerant Persister Cells

Sharma, B., Brown, A. V., Matluck, N. E., Hu, L. T., & Lewis, K. (2015) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00864-15 · Cited by 175

Anti-Candida albicans natural products, sources of new antifungal drugs: A review

Zida, A., Bamba, S., Yacouba, A., Ouedraogo-Traoré, R., & Guiguemdé, R. T. (2016) · Journal de Mycologie Médicale · doi:10.1016/j.mycmed.2016.10.002 · Cited by 182

Persister Cells in Biofilm Associated Infections

Conlon, B. P., Rowe, S. E., & Lewis, K. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-09782-4_1 · Cited by 175

Fresh Approaches to Anti-Infective Therapies

Nathan, C. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003081 · Cited by 167

Drug resistance in eukaryotic microorganisms

Fairlamb, A. H., Gow, N. A. R., Matthews, K. R., & Waters, A. P. (2016) · Nature Microbiology · doi:10.1038/nmicrobiol.2016.92 · Cited by 153

Stiffness of Cross-Linked Poly(Dimethylsiloxane) Affects Bacterial Adhesion and Antibiotic Susceptibility of Attached Cells

Song, F., & Ren, D. (2014) · Langmuir · doi:10.1021/la502029f · Cited by 150

Staphylococcus aureus Persisters Tolerant to Bactericidal Antibiotics

Lechner, S., Lewis, K., & Bertram, R. (2012) · Microbial Physiology · doi:10.1159/000342449 · Cited by 155

Efficacy of Artilysin Art-175 against Resistant and Persistent Acinetobacter baumannii

Defraine, V., Schuermans, J., Grymonprez, B., Govers, S. K., Aertsen, A., Fauvart, M., Michiels, J. J., Lavigne, R., & Briers, Y. (2016) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00285-16 · Cited by 161

Developing a New Generation of Antimicrobial and Bioactive Dental Resins

Cheng, L., Zhang, K., Zhang, N., Melo, M. A. S., Weir, M. D., Zhou, X., Bai, Y., Reynolds, M. A., & Xu, H. H. K. (2017) · Journal of Dental Research · doi:10.1177/0022034517709739 · Cited by 156

New-found fundamentals of bacterial persistence

Kint, C. I., Verstraeten, N., Fauvart, M., & Michiels, J. J. (2012) · Trends in Microbiology · doi:10.1016/j.tim.2012.08.009 · Cited by 154

High Persister Mutants in Mycobacterium tuberculosis

Torrey, H. L., Keren, I., Via, L. E., Lee, J. S., & Lewis, K. (2016) · PLoS ONE · doi:10.1371/journal.pone.0155127 · Cited by 147

Fungal persister cells: The basis for recalcitrant infections?

Wuyts, J., Van Dijck, P., & Holtappels, M. (2018) · PLOS Pathogens · doi:10.1371/journal.ppat.1007301 · Cited by 136

Targeting Phenotypically Tolerant Mycobacterium tuberculosis

Gold, B. S., & Nathan, C. (2017) · Microbiology Spectrum · doi:10.1128/microbiolspec.tbtb2-0031-2016 · Cited by 134

Methodologies for in vitro and in vivo evaluation of efficacy of antifungal and antibiofilm agents and surface coatings against fungal biofilms

Dijck, P. V., Sjollema, J., Cammue, B. P. A., Lagrou, K., Berman, J. G., d’Enfert, C., Andes, D. R., Arendrup, M. C., Brakhage, A. A., Calderone, R., et al. (2018) · Microbial Cell · doi:10.15698/mic2018.07.638 · Cited by 136

Molecular mechanisms of multiple toxin–antitoxin systems are coordinated to govern the persister phenotype

Fasani, R. A., & Savageau, M. A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1301023110 · Cited by 119

New approaches to antimicrobial discovery

Lewis, K. (2016) · Biochemical Pharmacology · doi:10.1016/j.bcp.2016.11.002 · Cited by 126

Persisters—as elusive as ever

Kaldalu, N., Hauryliuk, V., & Tenson, T. (2016) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-016-7648-8 · Cited by 109

Regulation of the Escherichia coli HipBA Toxin-Antitoxin System by Proteolysis

Hansen, S., Vulić, M., Min, J., Yen, T.-J., Schumacher, M. A., Brennan, R. G., & Lewis, K. (2012) · PLoS ONE · doi:10.1371/journal.pone.0039185 · Cited by 101

In Vitro Emergence of High Persistence upon Periodic Aminoglycoside Challenge in the ESKAPE Pathogens

Michiels, J. E., den Bergh, B. V., Verstraeten, N., Fauvart, M., & Michiels, J. J. (2016) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00757-16 · Cited by 97

Delicate metabolic control and coordinated stress response critically determine antifungal tolerance of Candida albicans biofilm persisters

Li, P., Seneviratne, C. J., Alpi, E., Vizcaino, J. A., & Jin, L. (2015) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00543-15 · Cited by 95

Aspergillus Biofilm In Vitro and In Vivo

Beauvais, A., & Latgé, J. (2015) · Microbiology Spectrum · doi:10.1128/microbiolspec.mb-0017-2015 · Cited by 102

Bacterial persisters in long-term infection: Emergence and fitness in a complex host environment

Bartell, J. A., Cameron, D. R., Mojsoska, B., Haagensen, J. A. J., Pressler, T., Sommer, L. M., Lewis, K., Molin, S., & Johansen, H. K. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1009112 · Cited by 90

A Quorum Sensing Small Volatile Molecule Promotes Antibiotic Tolerance in Bacteria

Que, Y., Hazan, R., Strobel, B., Maura, D., He, J., Kesarwani, M., Panopoulos, P., Tsurumi, A., Giddey, M., Wilhelmy, J., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080140 · Cited by 86

Bacterial persistence: Fundamentals and clinical importance

Jung, S., Ryu, C., & Kim, J. (2019) · The Journal of Microbiology · doi:10.1007/s12275-019-9218-0 · Cited by 79

Antibiotic persistence and tolerance: not just one and the same

Ronneau, S., Hill, P. W. S., & Hélaine, S. (2021) · Current Opinion in Microbiology · doi:10.1016/j.mib.2021.09.017 · Cited by 83

The vulnerable versatility of Salmonella antibiotic persisters during infection

Hill, P. W. S., Moldoveanu, A. L., Sargen, M. R., Ronneau, S., Glegola-Madejska, I., Beetham, C. M., Fisher, R. A., & Hélaine, S. (2021) · Cell Host & Microbe · doi:10.1016/j.chom.2021.10.002 · Cited by 84

Reverting Antibiotic Tolerance of Pseudomonas aeruginosa PAO1 Persister Cells by (Z)-4-bromo-5-(bromomethylene)-3-methylfuran-2(5H)-one

Pan, J., Bahar, A. A., Syed, H., & Ren, D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0045778 · Cited by 78

Identification of an Antimicrobial Agent Effective against Methicillin-Resistant Staphylococcus aureus Persisters Using a Fluorescence-Based Screening Strategy

Kim, W., Conery, A. L., Rajamuthiah, R., Fuchs, B. B., Ausubel, F. M., & Mylonakis, E. E. (2015) · PLoS ONE · doi:10.1371/journal.pone.0127640 · Cited by 75

Biofilm Formation of Candida albicans Facilitates Fungal Infiltration and Persister Cell Formation in Vaginal Candidiasis

Wu, X., Zhang, S., Li, H., Shen, L., Dong, C., Sun, Y., Chen, H., Xu, B., Zhuang, W., Deighton, M. A., et al. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01117 · Cited by 80

Survival of Bactericidal Antibiotic Treatment by a Persister Subpopulation of Listeria monocytogenes

Knudsen, G. M., Ng, Y., & Gram, L. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.02184-13 · Cited by 69

Dormancy in Cryptococcus neoformans: 60 years of accumulating evidence

Alanio, A. (2020) · Journal of Clinical Investigation · doi:10.1172/jci136223 · Cited by 62

Persistence and resistance as complementary bacterial adaptations to antibiotics

Vogwill, T., Comfort, A. C., Furió, V., & MacLean, R. C. (2016) · Journal of Evolutionary Biology · doi:10.1111/jeb.12864 · Cited by 67

Fungal Biofilms: Update on Resistance

Borghi, E., Borgo, F., & Morace, G. (2016) · Advances in experimental medicine and biology · doi:10.1007/5584_2016_7 · Cited by 69

Fungal biofilm inhibitors from a human oral microbiome-derived bacterium

Wang, X., Du, L., You, J., King, J. B., & Cichewicz, R. H. (2011) · Organic & Biomolecular Chemistry · doi:10.1039/c2ob06856g · Cited by 67

Waikialoid A Suppresses Hyphal Morphogenesis and Inhibits Biofilm Development in Pathogenic Candida albicans

Wang, X., You, J., King, J. B., Powell, D. R., & Cichewicz, R. H. (2012) · Journal of Natural Products · doi:10.1021/np2009994 · Cited by 66

The Culture Environment Influences Both Gene Regulation and Phenotypic Heterogeneity in Escherichia coli

Smith, A., Kaczmar, A., Bamford, R. A., Smith, C., Frustaci, S., Kovacs-Simon, A., O’Neill, P., Moore, K., Paszkiewicz, K. H., Titball, R. W., et al. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01739 · Cited by 67

Novel high-throughput screen against Candida albicans identifies antifungal potentiators and agents effective against biofilms

LaFleur, M. D., Lucumi, E., Napper, A. D., Diamond, S. L., & Lewis, K. (2011) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkq530 · Cited by 59

The arsenal of pathogens and antivirulence therapeutic strategies for disarming them

Hadjifrangiskou, M., & Brannon, J. R. (2016) · Drug Design Development and Therapy · doi:10.2147/dddt.s98939 · Cited by 58

Novel Glycopolymer Eradicates Antibiotic- and CCCP-Induced Persister Cells in Pseudomonas aeruginosa

Narayanaswamy, V. P., Keagy, L. L., Duris, K., Wiesmann, W. P., Loughran, A. J., Townsend, S. M., & Baker, S. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01724 · Cited by 60

Small-Molecule Suppressors of Candida albicans Biofilm Formation Synergistically Enhance the Antifungal Activity of Amphotericin B against Clinical Candida Isolates

You, J., Du, L., King, J. B., Hall, B. E., & Cichewicz, R. H. (2013) · ACS Chemical Biology · doi:10.1021/cb400009f · Cited by 60

Decline in nitrosative stress drives antibiotic persister regrowth during infection

Ronneau, S., Michaux, C., & Hélaine, S. (2023) · Cell Host & Microbe · doi:10.1016/j.chom.2023.05.002 · Cited by 58

The toxin-antitoxin systemtisB-istR1

Wagner, E. G. H., & Unoson, C. (2012) · RNA Biology · doi:10.4161/rna.22578 · Cited by 56

The Role of Proteomics in Bacterial Response to Antibiotics

Tsakou, F., Jersie-Christensen, R., Jenssen, H., & Mojsoska, B. (2020) · Pharmaceuticals · doi:10.3390/ph13090214 · Cited by 60

The Clinical Importance of Fungal Biofilms

Ramage, G., & Williams, C. (2013) · Advances in applied microbiology · doi:10.1016/b978-0-12-407673-0.00002-3 · Cited by 58

The within-host evolution of antimicrobial resistance in Mycobacterium tuberculosis

Castro, R. A. D., Borrell, S., & Gagneux, S. (2020) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaa071 · Cited by 56

Antifungal drug resistance in Candida: a special emphasis on amphotericin B

Ahmady, L., Gothwal, M., Mukkoli, M. M., & Bari, V. K. (2024) · Apmis · doi:10.1111/apm.13389 · Cited by 61

Active efflux in dormant bacterial cells – New insights into antibiotic persistence

Pu, Y., Ke, Y., & Bai, F. (2016) · Drug Resistance Updates · doi:10.1016/j.drup.2016.11.002 · Cited by 52

Nh125 Kills Methicillin-Resistant Staphylococcus Aureus Persisters by Lipid Bilayer Disruption

Kim, W., Fricke, N., Conery, A. L., Fuchs, B. B., Rajamuthiah, R., Jayamani, E., Vlahovska, P. M., Ausubel, F. M., & Mylonakis, E. E. (2016) · Future Medicinal Chemistry · doi:10.4155/fmc.15.189 · Cited by 47

Aspergillus Biofilm In Vitro and In Vivo

Beauvais, A., & Latgé, J. (2015) · ASM Press eBooks · doi:10.1128/9781555817466.ch8 · Cited by 47

Liposomal and Deoxycholate Amphotericin B Formulations: Effectiveness against Biofilm Infections of Candida spp.

Rodrigues, C. F., & Henriques, M. (2017) · Pathogens · doi:10.3390/pathogens6040062 · Cited by 48

Fitness trade‐offs explain low levels of persister cells in the opportunistic pathogen Pseudomonas aeruginosa

Stepanyan, K., Wenseleers, T., Duéñez‐Guzmán, E. A., Muratori, F. B., den Bergh, B. V., Verstraeten, N., Meester, L. D., Verstrepen, K. J., Fauvart, M., & Michiels, J. J. (2015) · Molecular Ecology · doi:10.1111/mec.13127 · Cited by 44

The Pharmaco –, Population and Evolutionary Dynamics of Multi-drug Therapy: Experiments with S. aureus and E. coli and Computer Simulations

Ankomah, P., Johnson, P. J., & Levin, B. R. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003300 · Cited by 45

Phenotypic Heterogeneity Enables Uropathogenic Escherichia coli To Evade Killing by Antibiotics and Serum Complement

Putrinš, M., Kogermann, K., Lukk, E., Lippus, M., Varik, V., & Tenson, T. (2015) · Infection and Immunity · doi:10.1128/iai.02725-14 · Cited by 45

Extreme Antibiotic Persistence via Heterogeneity-Generating Mutations Targeting Translation

Khare, A., & Tavazoie, S. (2020) · mSystems · doi:10.1128/msystems.00847-19 · Cited by 46

Biofilm formation in clinically relevant filamentous fungi: a therapeutic challenge

Roudbary, M., Vahedi‐Shahandashti, R., dos Santos, A. L. S., Mohammadi, S. R., Aslani, P., Lass‐Flörl, C., & Rodrigues, C. F. (2021) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2021.1950121 · Cited by 46

A common mechanism involving the TORC1 pathway can lead to amphotericin B-persistence in biofilm and planktonic Saccharomyces cerevisiae populations

Bojsen, R., Regenberg, B., Gresham, D., & Folkesson, A. (2016) · Scientific Reports · doi:10.1038/srep21874 · Cited by 42

A Comparative In Vitro Study of Two Denture Cleaning Techniques as an Effective Strategy for Inhibiting Candida albicans Biofilms on Denture Surfaces and Reducing Inflammation

Ramage, G., Zalewska, A., Cameron, D. A., Sherry, L., Murray, C. A., Finnegan, M. B., Loewy, Z. G., & Jagger, D. C. (2012) · Journal of Prosthodontics · doi:10.1111/j.1532-849x.2012.00865.x · Cited by 40

Fungal Biofilms: Inside Out

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