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Candida albicans Biofilms Produce Antifungal-Tolerant Persister Cells
Open accessAbstract
Fungal pathogens form biofilms that are highly recalcitrant to antimicrobial therapy. The expression of multidrug resistance pumps in young biofilms has been linked to increased resistance to azoles, but this mechanism does not seem to underlie the resistance of mature biofilms that is a model of in vivo infection. The mechanism of drug resistance of mature biofilms remains largely unknown. We report that biofilms formed by the major human pathogen Candida albicans exhibited a strikingly biphasic killing pattern in response to two microbicidal agents, amphotericin B, a polyene antifungal, and chlorhexidine, an antiseptic, indicating that a subpopulation of highly tolerant cells, termed persisters, existed. The extent of killing with a combination of amphotericin B and chlorhexidine was similar to that observed with individually added antimicrobials. Thus, surviving persisters form a multidrug-tolerant subpopulation. Interestingly, surviving C. albicans persisters were detected only in biofilms and not in exponentially growing or stationary-phase planktonic populations. Reinoculation of cells that survived killing of the biofilm by amphotericin B produced a new biofilm with a new subpopulation of persisters. This suggests that C. albicans persisters are not mutants but phenotypic variants of the wild type. Using a stain for dead cells, rare dark cells were visible in a biofilm after amphotericin B treatment, and a bright and a dim population were physically sorted from this biofilm. Only the dim cells produced colonies, showing that this method allows the isolation of yeast persisters. Given that persisters formed only in biofilms, mutants defective in biofilm formation were examined for tolerance of amphotericin B. All of the known mutants affected in biofilm formation were able to produce normal levels of persisters. This finding indicates that attachment rather than formation of a complex biofilm architecture initiates persister formation. Bacteria produce multidrug-tolerant persister cells in both planktonic and biofilm populations, and it appears that yeasts and bacteria have evolved analogous strategies that assign the function of survival to a small part of the population. In bacteria, persisters are dormant cells. It remains to be seen whether attachment initiates dormancy that leads to the formation of fungal persisters. This study suggests that persisters may be largely responsible for the multidrug tolerance of fungal biofilms.
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“Currently, antifungal persistence is mainly identified in Candida-associated biofilms [2,32,33].”
From Antifungal persistence: Clinical relevance and mechanisms (2025) · cites this paper as [2]
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“Antifungal persistence is most commonly observed in biofilm rather than in planktonic cells [2,33,34]”
From Antifungal persistence: Clinical relevance and mechanisms (2025) · cites this paper as [2]
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“To solve these problems, live/dead staining method can be applied because of its ability to distinguish live/dead cells, which reflects the essence of persisters that survive exposure to fungicides.”
From Antifungal persistence: Clinical relevance and mechanisms (2025) · cites this paper as [2]
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“For example, C. albicans persister biofilms are recalcitrant to AmB and broad-spectrum antimicrobial agent chlorhexidine [2];”
From Antifungal persistence: Clinical relevance and mechanisms (2025) · cites this paper as [2]
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“indicating that antifungal persistence is not solely dependent on matured biofilm structure formation [2].”
From Antifungal persistence: Clinical relevance and mechanisms (2025) · cites this paper as [2]
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“However, LaFleur and colleagues first reported that the biofilm-deficient double mutant strain efg1Δ/cph1Δ did not result in the reduction of AmB-triggered persisters”
From Antifungal persistence: Clinical relevance and mechanisms (2025) · cites this paper as [2]
In the citing paper
“Inside the biofilm cell population, persister cells form a unique group that is formed randomly, phenotypically dormant, highly tolerant to antifungal drugs [164], and which is a key mechanism of resistance in chronic infections [130].”
From Candida glabrata Biofilms: How Far Have We Come? (2017) · cites this paper as [164]
In the citing paper
“A minor subset of metabolically dormant yeast cells that stochastically arise as phenotypical variants within biofilms, persister cells are extremely resistant to antifungal drugs (100).”
From Candida albicans Biofilms and Human Disease (2015) · cites this paper as [100]
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“Although we know little about the formation and roles of persister cells in C. albicans biofilms, we do know that the drug resistance of persister cells is independent of cell membrane composition and efflux pump expression; rather, it is the result of the metabolically dormant state of the cells (88, 100).”
From Candida albicans Biofilms and Human Disease (2015) · cites this paper as [100]
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Cites
Bacterial Persistence as a Phenotypic Switch
Balaban, N. Q., Merrin, J., Chait, R., Kowalik, L., & Leibler, S. (2004) · Science · doi:10.1126/science.1099390 · Cited by 2,952
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
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
Persister cells and tolerance to antimicrobials
Keren, I., Kaldalu, N., Spoering, A. L., Wang, Y., & Lewis, K. (2003) · FEMS Microbiology Letters · doi:10.1016/s0378-1097(03)00856-5 · Cited by 1,094
Self-citationCandida Infections of Medical Devices
Kojic, E. M., & Darouiche, R. O. (2004) · Clinical Microbiology Reviews · doi:10.1128/cmr.17.2.255-267.2004 · Cited by 1,055
Spoering, A. L., & Lewis, K. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.23.6746-6751.2001 · Cited by 907
Self-citationSpecialized 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
Self-citationKuhn, D. M., George, T., Chandra, J., Mukherjee, P. K., & Ghannoum, M. A. (2002) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.46.6.1773-1780.2002 · Cited by 775
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
Ramage, G., Saville, S. P., Thomas, D. P., & López-Ribot, J. L. (2005) · Eukaryotic Cell · doi:10.1128/ec.4.4.633-638.2005 · Cited by 678
Research works printed but not linked: 1
- 10.1111/j.1574-6968.2002.tb11330.x · DOI · Paper page
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Vihodceva, S., Bankovskis, V., Muter, O., & Šutka, A. (2022) · BioMetals · doi:10.1007/s10534-022-00429-x · Cited by 2
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de Andrade, A. R. C., Rezende, M. D. S., Portela, F. V. M., Pereira, L. M. G., da Silva, B. N., de Lima-Neto, R. G., Rocha, M. F. G., Sidrim, J. J. C., Castelo‐Branco, D. D. S. C. M., & Cordeiro, R. D. A. (2023) · Biofouling · doi:10.1080/08927014.2023.2256674 · Cited by 1
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Li, P., Seneviratne, C. J., & Jin, L. (2017) · Routledge eBooks · doi:10.1201/9781315120119-9 · Cited by 1
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Yadav, M., & Malvi, Y. (2019) · Fungal biology · doi:10.1007/978-3-030-18586-2_10 · Cited by 1
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Lunestad, B. T., Møretrø, T., Hegstad, K., Langsrud, S., Scheie, A. A., Kapperud, G., Lassen, J. F., Nygård, K. M., Robertson, L. J., Nesbakken, T., et al. (2010) · BIBSYS Brage (BIBSYS (Norway)) · Cited by 1
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MacCallum, D. M. (2007) · Springer eBooks · doi:10.1007/978-1-4020-6397-8_5
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Jenkinson, H. F., & Munro, C. A. (2011) · Wiley eBooks · doi:10.1128/9781555817107.ch12
de Jesus, R. S. (2013) · Americanae (AECID Library)
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Ingersol, L. J. (2014) · UNM’s Digital Repository (University of New Mexico)
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Fleur, L., & David, M. Z. (2008)
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Attavar, S. (2012) · J. Willard Marriott Library · doi:10.26053/0h-82b3-wc00
Fungal Drug Resistance: Azoles
Lopez-Ribot, J. L., & Patterson, T. F. (2009) · Humana Press eBooks · doi:10.1007/978-1-59745-180-2_26
Lopes, M. D. C. G. (2013) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
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Santos, N. C. (2013) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
In Vitro Screening of Antifungal Compounds Able to Counteract Biofilm Development
Girardot, M., & Imbert, C. (2014) · Methods in molecular biology · doi:10.1007/978-1-4939-0467-9_13
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Nett, J. E., Brooks, E. G., Cabezas‐Olcoz, J., Sánchez, H., Żarnowski, R., Marchillo, K., & Andes, D. R. (2014)
Fitch, L. E. (2015) · Digital Repository Service (Northeastern University) · doi:10.17760/d20197922
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Bojsen, R. K. (2014)
Hill, J. A. (2014) · TSpace (University of Toronto)
Gene expression patterns of encapsulated microbial cells
Fazal, Z. (2017) · Illinois Digital Environment for Access to Learning and Scholarship (University of Illinois at Urbana-Champaign)
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Zenaide-Neto, H., de Oliveira, B. T. M., Barbosa, P. S. Z., de Souza, R. L., Cavalcanti, T. G., & Vasconcelos, U. (2019) · International Journal of Advanced Engineering Research and Science · doi:10.22161/ijaers.6.3.11
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Kanematsu, H., & Barry, D. M. (2020) · Springer eBooks · doi:10.1007/978-981-15-2240-6_3
Markelova, N. N., Tutelyan, A. V., & Sedykh, N. G. (2020) · Antibiot Khimioter = Antibiotics and Chemotherapy · doi:10.37489/0235-2990-2020-65-1-2-27-32
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Rebelo, J. S., Domingues, C. P. F., Monteiro, F., Nogueira, T., & Dionísio, F. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.20.427471
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Campbell, M. (2022) · Digital Archive @ GSU · doi:10.57709/18687479
(2007) · Yeast · doi:10.1002/yea.1328
Seneviratne, C. J., Truong, T., & Wang, Y. (2017) · Routledge eBooks · doi:10.1201/9781315120119-6
Samanta, I., & Bandyopadhyay, S. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-815770-1.00026-2
Vila, T. V. M., Montelongo‐Jauregui, D., Romo, J. A., Wall, G., Pierce, C. G., & Lopez-Ribot, J. L. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-809633-8.12092-8
Candida: Biofilm formation and antifungal resistance
Sharma, S., Singh, S. M., Mane, G., Pote, S. T., Patole, M. S., & Sharma, R. K. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-99977-9.00024-7
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Hussain, M. B., Abbas, S., Raza, M., Mehmood, N., Amin, Z. S., Fatima, N., & Hamza, M. (2023) · Research Square · doi:10.21203/rs.3.rs-3088685/v1
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David, H., Nithya, K., Salian, L. S., Dandela, R., Suresh, D., Amali, A. J., & Solomon, A. P. (2025) · ACS Applied Bio Materials · doi:10.1021/acsabm.5c00559
Balasubramanian, H. K., & Osmani, S. A. (2025) · Autophagy Reports · doi:10.1080/27694127.2025.2547194
Peng, G., Weilun, X., Shulei, Q., Junmeng, Z., Pan, K., Huang, L., Zheng, D., & Zhang, X. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5413480
Peng, G., Weilun, X., Shulei, Q., Junmeng, Z., Pan, K., Huang, L., Zheng, D., & Zhang, X. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5407034
Ghosh, S., Sarkar, S., Garai, P., Maiti, A. K., Saha, N. C., & Banerjee, P. (2025) · Discover Applied Sciences · doi:10.1007/s42452-025-07493-1
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Bhairavi, V. A., Vidya, S. L., & Sathishkumar, R. (2024) · Figshare · doi:10.6084/m9.figshare.26588607
Wang, F., Liu, Q., Wu, W., Su, Y., Song, Z., & Feng, R. (2026) · Pharmaceutical Development and Technology · doi:10.1080/10837450.2026.2615155
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Dermitzaki, N., Balomenou, F., Kosmeri, C., Baltogianni, M. S., Nikolaou, A. I., Serbis, A., & Giapros, V. I. (2026) · Antibiotics · doi:10.3390/antibiotics15010073
Kumar, P., Kumar, M., Saini, A., Mohamad, S. O., Ali, B., Esquivel, B. D., Banerjee, A., White, T. C., Gaur, N. A., Shah, A. H., et al. (2026) · Journal of Fungi · doi:10.3390/jof12020094
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Imir, O. B., Druseikis, M. E., Xie, Y., Ji, Y., Holt, L. J., Berman, J. G., & Gresham, D. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.27.708532
Shathan, A., Najjar, A., Jourk, A., & Noor, S. O. (2026) · Microorganisms · doi:10.3390/microorganisms14040795
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Costa, D. (2015) · theses.fr (ABES) · doi:10.70675/a2dc41b4zc93ez4fa9za3b0z92693dea83f5
Environmental adaptation of Candida albicans : the examples of persistence and chlamydosporulation
Denega, I. (2020) · theses.fr (ABES) · doi:10.70675/748584ddzf6f4z4124z9237z56d0535d3352
Couttenier, E. (2020) · theses.fr (ABES) · doi:10.70675/402f3bf1zd527z43acz9758z57e168d6e67e
Metadata
- Authors
- LaFleur, M. D., Kumamoto, C. A., & Lewis, K.
- Affiliations
- Northeastern University (US)
- Tufts University (US)
- Corresponding author
- Lewis, Kim
- Venue
- Antimicrobial Agents and Chemotherapy
- Publisher
- American Society for Microbiology
- Published
- 2006-11
- Volume
- 50
- Issue
- 11
- Pages
- 3839-3846
- ISSN
- 0066-4804 (ISSN-L)
- 1098-6596
- PMC
- PMC1635216
- OpenAlex
- W2135493487
- Cited by
- 521
- References
- 52
- Citations by year
- 2026: 26 · 2025: 29 · 2024: 20 · 2023: 20 · 2022: 20 · 2021: 39 · 2020: 33 · 2019: 21 · 2018: 22 · 2017: 41 · 2016: 34 · 2015: 39 · 2014: 25 · 2013: 31 · 2012: 26
- FWCI
- 9.91
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Antimicrobial Agents and Chemotherapy (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- Tufts University School of Medicine
- National Institute of General Medical Sciences (R01GM061162)
- National Institute of Allergy and Infectious Diseases (AI052805, R01AI052805)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacterial biofilms and quorum sensing
- Keywords
- Candida albicans, biofilm, persister cells, antifungal tolerance, multidrug tolerance, amphotericin B, chlorhexidine, phenotypic variants, biofilm formation, cell attachment, dormancy, antifungal resistance
- MeSH terms
- Antifungal Agents, Candida albicans, Chlorhexidine, Disinfectants, Fluoresceins, Microbial Sensitivity Tests, Microscopy, Fluorescence, Phenotype, Biofilms, Drug Resistance, Multiple, Fungal
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