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Candida albicans-Epithelial Interactions: Dissecting the Roles of Active Penetration, Induced Endocytosis and Host Factors on the Infection Process
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Candida albicans frequently causes superficial infections by invading and damaging epithelial cells, but may also cause systemic infections by penetrating through epithelial barriers. C. albicans is a remarkable pathogen because it can invade epithelial cells via two distinct mechanisms: induced endocytosis, analogous to facultative intracellular enteropathogenic bacteria, and active penetration, similar to plant pathogenic fungi. Here we investigated the contributions of the two invasion routes of C. albicans to epithelial invasion. Using selective cellular inhibition approaches and differential fluorescence microscopy, we demonstrate that induced endocytosis contributes considerably to the early time points of invasion, while active penetration represents the dominant epithelial invasion route. Although induced endocytosis depends mainly on Als3-E-cadherin interactions, we observed E-cadherin independent induced endocytosis. Finally, we provide evidence of a protective role for serum factors in oral infection: human serum strongly inhibited C. albicans adhesion to, invasion and damage of oral epithelial cells.
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“This result is in contrast to what has been found for Als3, which is required for both induced endocytosis and active penetration [29], and provides a likely explanation for why Hyr1 is dispensable for induction of epithelial cell damage.”
From Candida albicans stimulates formation of a multi-receptor complex that mediates epithelial cell invasion during oropharyngeal infection (2023) · cites this paper as [29]
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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
Gillum, A. M., Tsay, E. Y. H., & Kirsch, D. R. (1984) · Molecular and General Genetics MGG · doi:10.1007/bf00328721 · Cited by 1,253
Bacterial Adhesion and Entry into Host Cells
Pizarro-Cerdá, J., & Cossart, P. (2006) · Cell · doi:10.1016/j.cell.2006.02.012 · Cited by 977 · cited 1×
“Bacteria, on the other hand, cannot actively penetrate host cells, but have developed several strategies to cause uptake by induced endocytosis [25,26].”
BackgroundOn the Trail of a Cereal Killer: Exploring the Biology of Magnaporthe grisea
Talbot, N. J. (2003) · Annual Review of Microbiology · doi:10.1146/annurev.micro.57.030502.090957 · Cited by 956
STUDIES ON THE PROPAGATION IN VITRO OF POLIOMYELITIS VIRUSES
Scherer, W. F., Syverton, J. T., & Gey, G. O. (1953) · Journal of Experimental Medicine · doi:10.1084/jem.97.5.695 · Cited by 856
Als3 Is a Candida albicans Invasin That Binds to Cadherins and Induces Endocytosis by Host Cells
Phan, Q. T., Myers, C. L., Fu, Y., Sheppard, D. C., Yeaman, M. R., Welch, W. H., Ibrahim, A. S., Edwards, J. E., & Filler, S. G. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050064 · Cited by 641
Candida albicans Cell Wall Proteins
Chaffin, W. L. (2008) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00032-07 · Cited by 515
Cellular interactions of Candida albicans with human oral epithelial cells and enterocytes
Dalle, F., Wächtler, B., L’Ollivier, C., Holland, G., Bannert, N., Wilson, D., Labruère, C., Bonnin, A., & Hube, B. (2009) · Cellular Microbiology · doi:10.1111/j.1462-5822.2009.01394.x · Cited by 371
Self-citationSundstrom, P. (2002) · Cellular Microbiology · doi:10.1046/j.1462-5822.2002.00206.x · Cited by 336
Malaria Parasite Development in the Mosquito and Infection of the Mammalian Host
Aly, A. S. I., Vaughan, A. M., & Kappe, S. H. I. (2009) · Annual Review of Microbiology · doi:10.1146/annurev.micro.091208.073403 · Cited by 317
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Candida albicans pathogenicity mechanisms
Mayer, F. L., Wilson, D., & Hube, B. (2013) · Virulence · doi:10.4161/viru.22913 · Cited by 1,848
Self-citationCandidalysin is a fungal peptide toxin critical for mucosal infection
Moyes, D. L., Wilson, D., Richardson, J. P., Mogavero, S., Tang, S. X., Wernecke, J., Hoefs, S., Gratacap, R. L., Robbins, J., Runglall, M., et al. (2016) · Nature · doi:10.1038/nature17625 · Cited by 928
Self-citationCandida albicans cell-type switching and functional plasticity in the mammalian host
Noble, S. M., Gianetti, B. A., & Witchley, J. N. (2016) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2016.157 · Cited by 548
Santos, G. C. D. O., Vasconcelos, C. C., Lopes, A. J. O., Cartágenes, M. D. S. D. S., Filho, A. K. D. B., do Nascimento, F. R. F., Ramos, R. M., Pires, E. R. R. B., de Andrade, M. S., Rocha, F. M. G., et al. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01351 · Cited by 381
d’Enfert, C., Kaune, A.-K., Alaban, L. R., Chakraborty, S., Cole, N. L., Delavy, M., Kosmala, D., Marsaux, B., Fróis-Martins, R., Morelli, M., et al. (2020) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaa060 · Cited by 377
Self-citationDadar, M., Tiwari, R., Karthik, K., Chakraborty, S., Shahali, Y., & Dhama, K. (2018) · Microbial Pathogenesis · doi:10.1016/j.micpath.2018.02.028 · Cited by 349
The Candida Pathogenic Species ComplexPreprint
Turner, S. A., & Butler, G. (2014) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a019778 · Cited by 351
Candidiasis: Predisposing Factors, Prevention, Diagnosis and Alternative Treatment
Martins, N. A., Ferreira, I. C. F. R., Barros, L., Silva, S. M., & Henriques, M. (2014) · Mycopathologia · doi:10.1007/s11046-014-9749-1 · Cited by 293
Two unlike cousins: Candida albicans and C . glabrata infection strategies
Brunke, S., & Hube, B. (2013) · Cellular Microbiology · doi:10.1111/cmi.12091 · Cited by 239
Self-citationHoefs, S., Mogavero, S., & Hube, B. (2016) · The Journal of Microbiology · doi:10.1007/s12275-016-5514-0 · Cited by 251
Self-citationHoyer, L. L., & Cota, E. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00280 · Cited by 229
Molecular mechanisms of mucormycosis—The bitter and the sweet
Baldin, C., & Ibrahim, A. S. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006408 · Cited by 217
Candida albicans-Induced Epithelial Damage Mediates Translocation through Intestinal Barriers
Allert, S., Förster, T. M., Svensson, C.-M., Richardson, J. P., Pawlik, T., Hebecker, B., Rudolphi, S., Juraschitz, M., Schaller, M., Blagojevic, M., et al. (2018) · mBio · doi:10.1128/mbio.00915-18 · Cited by 208
Self-citationFreires, I. A., Murata, R. M., Furletti, V. F., Sartoratto, A., de Alencar, S. M., Figueira, G. M., Rodrigues, J. A. D. O., Duarte, M. C. T., & Rosalen, P. L. (2014) · PLoS ONE · doi:10.1371/journal.pone.0099086 · Cited by 201
Polke, M., Hube, B., & Jacobsen, I. D. (2015) · Advances in applied microbiology · doi:10.1016/bs.aambs.2014.12.002 · Cited by 205
Self-citationCandida albicans and Candida glabrata : global priority pathogens
Katsipoulaki, M., Stappers, M. H. T., Malavia-Jones, D., Brunke, S., Hube, B., & Gow, N. A. R. (2024) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00021-23 · Cited by 180
Self-citationCandida albicans–epithelial interactions and induction of mucosal innate immunity
Naglik, J. R., König, A., Hube, B., & Gaffen, S. L. (2017) · Current Opinion in Microbiology · doi:10.1016/j.mib.2017.10.030 · Cited by 173
Self-citationInteraction of Candida Species with the Skin
Kühbacher, A., Burger‐Kentischer, A., & Rupp, S. (2017) · Microorganisms · doi:10.3390/microorganisms5020032 · Cited by 170
Bertuzzi, M., Schrettl, M., Alcazar-Fuoli, L., Cairns, T. C., Muñoz, A., Walker, L. A., Herbst, S., Safari, M., Cheverton, A. M., Chen, D., et al. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1004413 · Cited by 158
Activity of phenolic compounds from plant origin against Candida species
Martins, N. A., Barros, L., Henriques, M., Silva, S. M., & Ferreira, I. C. F. R. (2015) · Industrial Crops and Products · doi:10.1016/j.indcrop.2015.05.067 · Cited by 138
Signaling pathways bridging microbial-triggered inflammation and cancer
Kipanyula, M. J., Etet, P. F. S., Vecchio, L., Farahna, M., Nukenine, E. N., & Kamdje, A. H. N. (2012) · Cellular Signalling · doi:10.1016/j.cellsig.2012.10.014 · Cited by 120
The Postbiotic Activity of Lactobacillus paracasei 28.4 Against Candida auris
Rossoni, R. D., de Barros, P. P., Mendonça, I. D. C., Medina, R. P., Silva, D. H. S., Fuchs, B. B., Junqueira, J. C., & Mylonakis, E. E. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00397 · Cited by 118
Candida albicans Hyphae: From Growth Initiation to Invasion
Desai, J. (2018) · Journal of Fungi · doi:10.3390/jof4010010 · Cited by 117
The Missing Link between Candida albicans Hyphal Morphogenesis and Host Cell Damage
Wilson, D., Naglik, J. R., & Hube, B. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1005867 · Cited by 122
Self-citationDermatomycoses and inflammation: The adaptive balance between growth, damage, and survival
Hube, B., Hay, R. J., Brasch, J., Veraldi, S., & Schaller, M. (2015) · Journal de Mycologie Médicale · doi:10.1016/j.mycmed.2014.11.002 · Cited by 118
Self-citationXu, H., Sobue, T., Bertolini, M., Thompson, A. K., & Dongari‐Bagtzoglou, A. I. (2016) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiw201 · Cited by 111
Oropharyngeal Candidiasis: Fungal Invasion and Epithelial Cell Responses
Swidergall, M., & Filler, S. G. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006056 · Cited by 114
Virulence factors in fungal pathogens of man
Brunke, S., Mogavero, S., Kasper, L., & Hube, B. (2016) · Current Opinion in Microbiology · doi:10.1016/j.mib.2016.05.010 · Cited by 113
Self-citationCandida–Epithelial Interactions
Richardson, J., Ho, J., & Naglik, J. R. (2018) · Journal of Fungi · doi:10.3390/jof4010022 · Cited by 108
Pellón, A., Nasab, S. D. S., & Moyes, D. L. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00081 · Cited by 97
Host–Pathogen Interactions during Female Genital Tract Infections
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Self-citationPathogenicity mechanisms and host response during oral Candida albicans infections
Hebecker, B., Naglik, J. R., Hube, B., & Jacobsen, I. D. (2014) · Expert Review of Anti-infective Therapy · doi:10.1586/14787210.2014.916210 · Cited by 95
Self-citation“ Candida Albicans Interactions With The Host: Crossing The Intestinal Epithelial Barrier”
Basmaciyan, L., Bon, F., Paradis, T., Lapaquette, P., & Dalle, F. (2019) · Tissue Barriers · doi:10.1080/21688370.2019.1612661 · Cited by 89
Self-citationArdizzoni, A., Wheeler, R. T., & Pericolini, E. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.692491 · Cited by 89
Host Cell Invasion by Medically Important FungiPreprint
Sheppard, D. C., & Filler, S. G. (2014) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a019687 · Cited by 94
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Ibe, C., & Munro, C. A. (2021) · Journal of Fungi · doi:10.3390/jof7090739 · Cited by 88
Krause, J., Geginat, G., & Tammer, I. (2015) · PLoS ONE · doi:10.1371/journal.pone.0135404 · Cited by 81
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Yang, W., Yan, L., Wu, C., Zhao, X., & Tang, J. (2014) · Microbiological Research · doi:10.1016/j.micres.2014.02.013 · Cited by 79
Activation of EphA2-EGFR signaling in oral epithelial cells by Candida albicans virulence factors
Swidergall, M., Solis, N. V., Millet, N., Huang, M. Y., Lin, J., Phan, Q. T., Lazarus, M. D., Wang, Z., Yeaman, M. R., Mitchell, A. P., et al. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009221 · Cited by 82
Ahmed, N., Mahmood, M. S., Ullah, M. A., Araf, Y., Rahaman, T. I., Moin, A. T., & Hosen, M. J. (2022) · Current Microbiology · doi:10.1007/s00284-022-02824-6 · Cited by 79
Chin, V. K., Lee, T. Y., Basir, R., & Chong, P. P. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17101643 · Cited by 83
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Dutton, L. C., Nobbs, A. H., Jepson, K., Jepson, M. A., Vickerman, M. M., Aqeel Alawfi, S., Munro, C. A., Lamont, R. J., & Jenkinson, H. F. (2014) · mBio · doi:10.1128/mbio.00911-14 · Cited by 75
Adherence of Candida sp. to host tissues and cells as one of its pathogenicity features.
Modrzewska, B., & Kurnatowski, P. (2015) · PubMed · Cited by 74
Cells under pressure: how yeast cells respond to mechanical forces
Mishra, R., Minc, N., & Peter, M. (2022) · Trends in Microbiology · doi:10.1016/j.tim.2021.11.006 · Cited by 78
Moonlighting Proteins at the Candidal Cell Surface
Satała, D., Karkowska‐Kuleta, J., Zelazna, A., Rąpała‐Kozik, M., & Kozik, A. (2020) · Microorganisms · doi:10.3390/microorganisms8071046 · Cited by 71
Mogavero, S., Sauer, F. M., Brunke, S., Allert, S., Schulz, D., Wisgott, S., Jablonowski, N., Elshafee, O., Krüger, T., Kniemeyer, O., et al. (2021) · Cellular Microbiology · doi:10.1111/cmi.13378 · Cited by 74
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The Role of Host and Fungal Factors in the Commensal-to-Pathogen Transition of Candida albicans
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Candida innate immunity at the mucosa
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Lemberg, C., Vicente, K. M. D. S., Fróis-Martins, R., Altmeier, S., Tran, V. D. T., Mertens, S., Amorim-Vaz, S., Rai, L. S., d’Enfert, C., Pagni, M., et al. (2022) · PLoS Pathogens · doi:10.1371/journal.ppat.1010012 · Cited by 63
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Badiee, P., Badali, H., Boekhout, T., Diba, K., Moghadam, A. G., Hosseininasab, A., Jafarian, H., Mohammadi, R., Mirhendi, H., Najafzadeh, M. J., et al. (2017) · BMC Infectious Diseases · doi:10.1186/s12879-017-2825-7 · Cited by 56
Goyer, M., Loiselet, A., Bon, F., L’Ollivier, C., Laue, M. M., Holland, G., Bonnin, A., & Dalle, F. (2016) · PLoS ONE · doi:10.1371/journal.pone.0149159 · Cited by 61
Self-citationIrfan, M. A., Alam, S., Manzoor, N., & Abid, M. (2017) · PLoS ONE · doi:10.1371/journal.pone.0175710 · Cited by 52
Satała, D., Satała, G., Karkowska‐Kuleta, J., Bukowski, M., Kluza, A., Rąpała‐Kozik, M., & Kozik, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21217843 · Cited by 51
Mech, F., Wilson, D., Lehnert, T., Hube, B., & Figge, M. T. (2013) · Cytometry Part A · doi:10.1002/cyto.a.22418 · Cited by 50
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Zolin, G. V. S., da Fonseca, F. H., Zambom, C. R., & Garrido, S. S. (2021) · Biomolecules · doi:10.3390/biom11081209 · Cited by 47
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Böhringer, M., Pohlers, S., Schulze, S., Albrecht-Eckardt, D., Piegsa, J., Weber, M., Martin, R., Hünniger, K., Linde, J., Guthke, R., et al. (2016) · Cellular Microbiology · doi:10.1111/cmi.12566 · Cited by 45
Maza, P. K., Bonfim‐Melo, A., Padovan, A. C. B., Mortara, R. A., Orikaza, C. M., Ramos, L. M. D., Moura, T. R., Soriani, F. M., Almeida, R. S., Suzuki, É., et al. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01235 · Cited by 49
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Self-citationLachat, J., Pascault, A., Thibaut, D., Borgne, R. L., Verbavatz, J., & Weiner, A. (2022) · Nature Communications · doi:10.1038/s41467-022-31237-z · Cited by 44
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Monteiro, C. D. A., & dos Santos, J. R. A. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.87302 · Cited by 40
Chegini, Z., Didehdar, M., Khoshbayan, A., Rajaeih, S., Salehi, M., & Shariati, A. (2020) · Mycoses · doi:10.1111/myc.13187 · Cited by 38
Hammad, N., ELBadawy, N. E., Refaie, A. N., Ghramh, H. A., & Kady, L. M. A. (2018) · BioMed Research International · doi:10.1155/2018/7648152 · Cited by 38
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Gratacap, R. L., Scherer, A. K., Seman, B. G., & Wheeler, R. T. (2017) · Infection and Immunity · doi:10.1128/iai.00276-17 · Cited by 34
Jung, P., Mischo, C. E., Gunaratnam, G., Spengler, C., Becker, S. L., Hube, B., Jacobs, K., & Bischoff, M. (2020) · Virulence · doi:10.1080/21505594.2020.1836902 · Cited by 35
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Metadata
- Authors
- Wächtler, B., Citiulo, F., Jablonowski, N., Förster, S., Dalle, F., Schaller, M., Wilson, D., & Hube, B.
- Affiliations
- Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI) (DE)
- University of Tübingen (DE)
- Corresponding author
- Hube, Bernhard
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2012-05-14
- Volume
- 7
- Issue
- 5
- Pages
- e36952
- ISSN
- 1932-6203 (ISSN-L)
- PMC
- PMC3351431
- OpenAlex
- W1995203663
- Cited by
- 250
- References
- 45
- Citations by year
- 2026: 11 · 2025: 19 · 2024: 19 · 2023: 29 · 2022: 23 · 2021: 25 · 2020: 21 · 2019: 15 · 2018: 19 · 2017: 17 · 2016: 12 · 2015: 11 · 2014: 15 · 2013: 10 · 2012: 4
- FWCI
- 8.87
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- PLoS ONE (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Aberdeen University Research Archive (Aberdeen University) (submittedVersion)
- HAL (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- Deutsche Forschungsgemeinschaft (Hu528/10, SPP1160)
- Bundesministerium für Bildung und Forschung (0315901B)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Health Sciences › Medicine › Infectious Diseases › Fungal Infections and Studies
- Keywords
- Candida albicans, epithelial invasion, ALS3, E-cadherin, oral epithelial cells, serum factors, fungal adhesion, host-pathogen interaction, oral candidiasis
- MeSH terms
- Blood Physiological Phenomena, Candida albicans, Candidiasis, Oral, Cell Adhesion, Cell Line, Endocytosis, Epithelial Cells, Fungal Proteins, Humans, Mouth Mucosa, Cadherins, Microscopy, Electron, Transmission, Host-Pathogen Interactions
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