Adhesins in human fungal pathogens: glue with plenty of stick.

de Groot, Piet W. J.; Bader, Oliver; de Boer, Albert D.; Weig, Michael; Chauhan, Neeraj

doi:10.1128/ec.00364-12

Cited by 319Antifungal resistance and susceptibilityFungal and yeast genetics researchFungal Infections and Studies

Adhesins in human fungal pathogens: glue with plenty of stick.

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de Groot, Piet W. J., Bader, Oliver, de Boer, Albert D., Weig, Michael, Chauhan, Neeraj·2013·Eukaryotic Cell

DOI 10.1128/ec.00364-12PMC PMC3623432

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Abstract

Understanding the pathogenesis of an infectious disease is critical for developing new methods to prevent infection and diagnose or cure disease. Adherence of microorganisms to host tissue is a prerequisite for tissue invasion and infection. Fungal cell wall adhesins involved in adherence to host tissue or abiotic medical devices are critical for colonization leading to invasion and damage of host tissue. Here, with a main focus on pathogenic Candida species, we summarize recent progress made in the field of adhesins in human fungal pathogens and underscore the importance of these proteins in establishment of fungal diseases.

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DSY562 contains 101 adhesin-like proteins, exceeding the 66 deduced in CBS138.
“According to our analysis, we proposed a list of 101 adhesin-like proteins in DSY562 (File S5 and File S6), which well exceeds the number of deduced adhesins in CBS138 (66) according to de Groot et al. (2013).”
From Comparative Genomics of Two Sequential Candida glabrata Clinical Isolates (2017) · cites this paper as de Groot et al. (2013)
Candida glabrata contains 63 ORFs with adhesin properties.
“It is estimated that C. glabrata contains 63 ORFs with adhesin properties (de Groot et al. 2013).”
From Comparative Genomics of Two Sequential Candida glabrata Clinical Isolates (2017) · cites this paper as de Groot et al. 2013
DSY562 and DSY565 each contained a large set of adhesin-like genes (101 and 107, respectively), exceeding the 63 reported adhesins in the CBS138 genome.
“DSY562 and DSY565 each contained a large set of adhesin-like genes (101 and 107, respectively), which exceed by far the number of reported adhesins (63) in the CBS138 genome.”
From Comparative Genomics of Two Sequential Candida glabrata Clinical Isolates (2017) · cites this paper as de Groot et al. 2013

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Klotz, S., Gaur, N., Lake, D., Chan, V., Rauceo, J. M., & Lipke, P. (2004) · Infection and Immunity · doi:10.1128/iai.72.4.2029-2034.2004 · Cited by 89 · see citing works
A C‐terminal EGF‐like domain governs BAD1 localization to the yeast surface and fungal adherence to phagocytes, but is dispensable in immune modulation and pathogenicity of Blastomyces dermatitidis
Brandhorst, T. T., Wüthrich, M., Finkel‐Jimenez, B., & Klein, B. S. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03415.x · Cited by 86 · see citing works
Sequence and Analysis of the Genome of the Pathogenic Yeast Candida orthopsilosis
Riccombeni, A., Vidanes, G. M., Proux‐Wéra, E., Wolfe, K. H., & Butler, G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035750 · Cited by 84 · see citing works
Expression of Transglutaminase Substrate Activity on Candida albicans Germ Tubes through a Coiled, Disulfide-bonded N-terminal Domain of Hwp1 Requires C-terminal Glycosylphosphatidylinositol Modification
Staab, J. F., Bahn, Y., Tai, C.-H., Cook, P. F., & Sundstrom, P. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m406005200 · Cited by 83 · see citing works
The Anti-Candida Vaccine Based on the Recombinant N-Terminal Domain of Als1p Is Broadly Active against Disseminated Candidiasis
Ibrahim, A., Spellberg, B., Avanesian, V., Fu, Y., & Edwards, J. (2006) · Infection and Immunity · doi:10.1128/iai.74.5.3039-3041.2006 · Cited by 83 · see citing works
FungalRV: adhesin prediction and immunoinformatics portal for human fungal pathogens
Chaudhuri, R., Ansari, F. A., Raghunandanan, M. V., & Ramachandran, S. (2011) · BMC Genomics · doi:10.1186/1471-2164-12-192 · Cited by 79 · see citing works
Sixty alleles of the ALS7 open reading frame in Candida albicans: ALS7 is a hypermutable contingency locus.Preprint
Zhang, N.-X., Harrex, A., Holland, B., Fenton, L., Cannon, R., & Schmid, J. (2003) · Genome Research · doi:10.1101/gr.1024903 · Cited by 79 · see citing works
Reducing haziness in white wine by overexpression of Saccharomyces cerevisiae genes YOL155c and YDR055w
Brown, S. L., Stockdale, V. J., Pettolino, F. A., Pocock, K. F., Lopes, M. D. B., Williams, P. J., Bacic, A., Fincher, G. B., Høj, P. B., & Waters, E. J. (2006) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-006-0606-0 · Cited by 75 · see citing works
Identification of potential cell‐surface proteins in Candida albicans and investigation of the role of a putative cell‐surface glycosidase in adhesion and virulence
Alberti‐Segui, C., Morales, A. J., Xing, H., Kessler, M. M., Willins, D. A., Weinstock, K. G., Cottarel, G., Fechtel, K., & Rogers, B. L. (2004) · Yeast · doi:10.1002/yea.1061 · Cited by 74 · see citing works
The Aspergillus fumigatus cspA Gene Encoding a Repeat-Rich Cell Wall Protein Is Important for Normal Conidial Cell Wall Architecture and Interaction with Host Cells
Levdansky, E., Kashi, O., Sharon, H., Shadkchan, Y., & Osherov, N. (2010) · Eukaryotic Cell · doi:10.1128/ec.00126-10 · Cited by 73 · see citing works
Gene Overexpression/Suppression Analysis of Candidate Virulence Factors of Candida albicans
Fu, Y., Luo, G., Spellberg, B., Edwards, J., & Ibrahim, A. (2008) · Eukaryotic Cell · doi:10.1128/ec.00445-07 · Cited by 72 · see citing works
The WI-1 Adhesin Blocks Phagocyte TNF-α Production, Imparting Pathogenicity on Blastomyces dermatitidis
Finkel-Jimenez, B., Wüthrich, M., Brandhorst, T. T., & Klein, B. S. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.4.2665 · Cited by 68 · see citing works
Structural basis for promiscuity and specificity during Candida glabrata invasion of host epithelia
Maestre-Reyna, M., Diderrich, R., Veelders, M. S., Eulenburg, G., Kalugin, V., Brückner, S., Keller, P., Rupp, S., Mösch, H.-U., & Essen, L.-O. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1207653109 · Cited by 67 · see citing works
Hwp1 and Related Adhesins Contribute to both Mating and Biofilm Formation in Candida albicans
Ene, I. V., & Bennett, R. J. (2009) · Eukaryotic Cell · doi:10.1128/ec.00245-09 · Cited by 66 · see citing works
Structure and Function of Glycosylated Tandem Repeats from Candida albicans Als Adhesins
Frank, A. T., Ramsook, C. B., Otoo, H. N., Tan, C., Soybelman, G., Rauceo, J. M., Gaur, N. K., Klotz, S. A., & Lipke, P. N. (2010) · Eukaryotic Cell · doi:10.1128/ec.00235-09 · Cited by 63 · see citing works
Identification and characterization of a laminin-binding protein of Aspergillus fumigatus: extracellular thaumatin domain protein (AfCalAp).
Upadhyay, S., Mahajan, L., Ramjee, S., Singh, Y., Basir, S., & Madan, T. (2009) · Journal of Medical Microbiology · doi:10.1099/jmm.0.005991-0 · Cited by 63 · see citing works
Active and passive immunization with rHyr1p-N protects mice against hematogenously disseminated candidiasis.
Luo, G., Ibrahim, A. S., French, S. W., Edwards, J. E., & Fu, Y. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025909 · Cited by 62 · see citing works
Adherence and Invasion Studies ofCandida albicansStrains, Using In Vitro Models of Esophageal Candidiasis
Bernhardt, J., Herman, D., Sheridan, M. J., & Calderone, R. (2001) · The Journal of Infectious Diseases · doi:10.1086/323807 · Cited by 62 · see citing works
The GPI-modified proteins Pga59 and Pga62 of Candida albicans are required for cell wall integrity
Moreno‐Ruiz, E., Ortu, G., de Groot, P. W. J., Cottier, F., Loussert-Fonta, C., Prévost, M., de Koster, C. G., Klis, F. M., Goyard, S., & d’Enfert, C. (2009) · Microbiology · doi:10.1099/mic.0.028902-0 · Cited by 62 · see citing works
Deletion ofALS5,ALS6orALS7increases adhesion ofCandida albicansto human vascular endothelial and buccal epithelial cells
Zhao, X., Oh, S.-H., & Hoyer, L. L. (2007) · Medical Mycology · doi:10.1080/13693780701377162 · Cited by 60 · see citing works
Genes Selectively Up-Regulated by Pheromone in White Cells Are Involved in Biofilm Formation in Candida albicans
Sahni, N., Song, Y., Daniels, K. J., Srikantha, T., Pujol, C., & Soll, D. R. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000601 · Cited by 59 · see citing works
RBR1 , a Novel pH-Regulated Cell Wall Gene of Candida albicans , Is Repressed by RIM101 and Activated by NRG1
Lotz, H., Sohn, K., Brunner, H., Mühlschlegel, F. A., & Rupp, S. (2004) · Eukaryotic Cell · doi:10.1128/ec.3.3.776-784.2004 · Cited by 55 · see citing works
The N‐terminal part of Als1 protein from Candida albicans specifically binds fucose‐containing glycans
Donohue, D. S., Ielasi, F., Goossens, K. V. Y., & Willaert, R. (2011) · Molecular Microbiology · doi:10.1111/j.1365-2958.2011.07676.x · Cited by 54 · see citing works
Candida glabrata Pwp7p and Aed1p are required for adherence to human endothelial cells: Candida glabrata adhesins
Desai, C., Mavrianos, J., & Chauhan, N. (2011) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2011.00743.x · Cited by 52 · see citing works
Unzipping a Functional Microbial Amyloid
Alsteens, D., Ramsook, C. B., Lipke, P. N., & Dufrêne, Y. F. (2012) · ACS Nano · doi:10.1021/nn3025699 · Cited by 51 · see citing works
Identification and differential gene expression of adhesin-like wall proteins in Candida glabrata biofilms
Kraneveld, E. A., de Soet, J. J., Deng, D. M., Dekker, H. L., de Koster, C. G., Klis, F. M., Crielaard, W., & de Groot, P. W. J. (2011) · Mycopathologia · doi:10.1007/s11046-011-9446-2 · Cited by 50 · see citing works
Insight into the Antiadhesive Effect of Yeast Wall Protein 1 of Candida albicans
Granger, B. L. (2012) · Eukaryotic Cell · doi:10.1128/ec.00026-12 · Cited by 48 · see citing works
Are we any closer to beating the biofilm: novel methods of biofilm control
Ramage, G., Culshaw, S., Jones, B., & Williams, C. (2010) · Current Opinion in Infectious Diseases · doi:10.1097/qco.0b013e32833e5850 · Cited by 47 · see citing works
Unexpected Role for a Serine/Threonine-Rich Domain in the Candida albicans Iff Protein Family
Boisramé, A., Cornu, A., Costa, G. D., & Richard, M. L. (2011) · Eukaryotic Cell · doi:10.1128/ec.05044-11 · Cited by 47 · see citing works
Pga13 in Candida albicans is localized in the cell wall and influences cell surface properties, morphogenesis and virulence
Gelis, S., de Groot, P. W. J., Castillo, L., Moragues, M. D., Sentandreu, R., Gómez, M.-M., & Valentı́n, E. (2012) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2012.01.010 · Cited by 45 · see citing works
Differences in the acid-labile component of Candida albicans mannan from hydrophobic and hydrophilic yeast cells
Masuoka, J., & Hazen, K. C. (1999) · Glycobiology · doi:10.1093/glycob/9.11.1281 · Cited by 45 · see citing works
Candida albicans Iff11, a Secreted Protein Required for Cell Wall Structure and Virulence
Bates, S., de la Rosa, J. M., MacCallum, D. M., Brown, A. J. P., Gow, N. A. R., & Odds, F. C. (2007) · Infection and Immunity · doi:10.1128/iai.00102-07 · Cited by 42 · see citing works
The Candida albicans Hwp2 is necessary for proper adhesion, biofilm formation and oxidative stress tolerance
Younes, S., Bahnan, W., Dimassi, H. I., & Khalaf, R. A. (2010) · Microbiological Research · doi:10.1016/j.micres.2010.08.004 · Cited by 39 · see citing works
The Candida glabrata adhesin Epa1p causes adhesion, phagocytosis, and cytokine secretion by innate immune cells
Kuhn, D. M., & Vyas, V. K. (2012) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2011.00785.x · Cited by 38 · see citing works
The epithelial adhesin 1 (Epa1p) from the human-pathogenic yeastCandida glabrata: structural and functional study of the carbohydrate-binding domain
Ielasi, F., Decanniere, K., & Willaert, R. (2012) · Acta Crystallographica Section D Biological Crystallography · doi:10.1107/s0907444911054898 · Cited by 38 · see citing works
The Fusarium oxysporum cell wall proteome under adhesion‐inducing conditions
Prados‐Rosales, R., Luque-Garcia, J. L., Martínez‐López, R., Gil, C., & Pietro, A. D. (2009) · PROTEOMICS · doi:10.1002/pmic.200800950 · Cited by 36 · see citing works
Disruption of the GPI Protein-Encoding Gene IFF4 of Candida albicans Results in Decreased Adherence and Virulence
Kempf, M., Cottin, J., Licznar, P., Lefrançois, C., Robert, R., & Apaire-Marchais, V. (2009) · Mycopathologia · doi:10.1007/s11046-009-9201-0 · Cited by 33 · see citing works
Megasatellites: a new class of large tandem repeats discovered in the pathogenic yeast Candida glabrata
Thierry, A., Dujon, B., & Richard, G. (2009) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-0216-y · Cited by 29 · see citing works
Characterization of Hwp2, a Candida albicans putative GPI-anchored cell wall protein necessary for invasive growth
Hayek, P., Dib, L., Yazbeck, P., Beyrouthy, B., & Khalaf, R. A. (2009) · Microbiological Research · doi:10.1016/j.micres.2009.03.006 · Cited by 27 · see citing works
Development and use of complex probes for DNA fingerprinting the infectious fungi
Lockhart, S. R., Pujol, C., Joly, S., & Soll, D. R. (2001) · Medical Mycology · doi:10.1080/mmy.39.1.1.8 · Cited by 27 · see citing works
Profiling of adhesive properties of the agglutinin-like sequence (ALS) protein family, a virulent attribute ofCandida albicans
Aoki, W., Kitahara, N., Miura, N., Morisaka, H., Kuroda, K., & Ueda, M. (2012) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.2012.00941.x · Cited by 26 · see citing works
State of differentiation defines buccal epithelial cell affinity for cross‐linking to Candida albicans Hwp1
Ponniah, G., Rollenhagen, C., Bahn, Y., Staab, J. F., & Sundstrom, P. (2007) · Journal of Oral Pathology and Medicine · doi:10.1111/j.1600-0714.2007.00565.x · Cited by 25 · see citing works
ProFASTA: A pipeline web server for fungal protein scanning with integration of cell surface prediction software
de Groot, P. W. J., & Brandt, B. W. (2012) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2011.12.009 · Cited by 23 · see citing works
Glycoconjugate structure and function in fungal cell walls
Gonzalez, M., de Groot, P. W. J., Klis, F. M., & Lipke, P. N. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-374546-0.00010-9 · Cited by 22 · see citing works
Disruption of Candida albicans IFF4 gene involves modifications of the cell electrical surface properties
Kempf, M., Apaire-Marchais, V., Saulnier, P., Licznar‐Fajardo, P., Lefrançois, C., Robert, R., & Cottin, J. (2007) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2007.03.017 · Cited by 17 · see citing works

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Candida Biofilms: Threats, Challenges, and Promising Strategies
Cavalheiro, M., & Teixeira, M. C. (2018) · Frontiers in Medicine · doi:10.3389/fmed.2018.00028 · Cited by 690 · see citing works
Oral Candidiasis: A Disease of Opportunity
Vila, T., Sultan, A. S., Montelongo-Jauregui, D., & Jabra-Rizk, M. A. (2020) · Journal of Fungi · doi:10.3390/jof6010015 · Cited by 537 · see citing works
Aspergillus fumigatus morphology and dynamic host interactions
van de Veerdonk, F. L., Gresnigt, M. S., Romani, L., Netea, M. G., & Latgé, J.-P. (2017) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2017.90 · Cited by 490 · see citing works
Pathogenesis and virulence of Candida albicans
Lopes, J. P., & Lionakis, M. S. (2021) · Virulence · doi:10.1080/21505594.2021.2019950 · Cited by 511 · see citing works
The impact of the Fungus-Host-Microbiota interplay uponCandida albicansinfections: current knowledge and new perspectives
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 351 · see citing works
Fungi that Infect Humans
Köhler, J. R., Hube, B., Puccia, R., Casadevall, A., & Perfect, J. R. (2017) · Microbiology Spectrum · doi:10.1128/microbiolspec.funk-0014-2016 · Cited by 301 · see citing works
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 · see citing works
Candida albicans Agglutinin-Like Sequence (Als) Family Vignettes: A Review of Als Protein Structure and Function
Hoyer, L., & Cota, E. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00280 · Cited by 196 · see citing works
Adaptive immune responses to Candida albicans infection
Richardson, J. P., & Moyes, D. L. (2015) · Virulence · doi:10.1080/21505594.2015.1004977 · Cited by 206 · see citing works
Adaptive immunity induces mutualism between commensal eukaryotes
Ost, K. S., O’Meara, T. R., Stephens, W. Z., Chiaro, T. R., Zhou, H., Penman, J., Bell, R. S., Catanzaro, J., Song, D., Singh, S., et al. (2021) · Nature · doi:10.1038/s41586-021-03722-w · Cited by 205 · see citing works
Divergent and Convergent Evolution of Fungal Pathogenicity
Shang, Y., Xiao, G., Zheng, P., Cen, K., Zhan, S., & Wang, C. (2016) · Genome Biology and Evolution · doi:10.1093/gbe/evw082 · Cited by 189 · see citing works
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 188 · see citing works
Biofilm formation in medically important Candida species
Malinovská, Z., Čonková, E., & Váczi, P. (2023) · Journal of Fungi · doi:10.3390/jof9100955 · Cited by 167 · see citing works
Candida auris Genetics and Emergence
Chowdhary, A., Jain, K., & Chauhan, N. (2023) · Annual Review of Microbiology · doi:10.1146/annurev-micro-032521-015858 · Cited by 158 · see citing works
Complex multicellularity in fungi: evolutionary convergence, single origin, or both?
Nagy, L. G., Kovács, G. M., & Krizsán, K. (2018) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12418 · Cited by 144 · see citing works
Mechanism of Candida pathogenesis: Revisiting the vital drivers
Mba, I. E., & Nweze, E. I. (2020) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-020-03912-w · Cited by 143 · see citing works
Interactions of Aspergillus fumigatus Conidia with Airway Epithelial Cells: A Critical Review
Croft, C. A., Culibrk, L., Moore, M. M., & Tebbutt, S. J. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00472 · Cited by 142 · see citing works
A Candida auris –specific adhesin, Scf1 , governs surface association, colonization, and virulence
Santana, D. J., Anku, J. A. E., Zhao, G., Zarnowski, R., Johnson, C. J., Hautau, H., Visser, N. D., Ibrahim, A. S., Andes, D., Nett, J. E., et al. (2023) · Science · doi:10.1126/science.adf8972 · Cited by 142 · see citing works
Candida glabrata Binding to Candida albicans Hyphae Enables Its Development in Oropharyngeal Candidiasis
Tati, S., Davidow, P., McCall, A. D., Hwang-Wong, E., Rojas, I. G., Cormack, B. P., & Edgerton, M. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1005522 · Cited by 142 · see citing works
Bloodstream infections: mechanisms of pathogenesis and opportunities for intervention
Holmes, C. L., Albin, O. R., Mobley, H. L. T., & Bachman, M. A. (2024) · Nature Reviews Microbiology · doi:10.1038/s41579-024-01105-2 · Cited by 150 · see citing works
Portrait of Candida Species Biofilm Regulatory Network Genes
Araújo, D., Henriques, M., & Silva, S. M. (2016) · Trends in Microbiology · doi:10.1016/j.tim.2016.09.004 · Cited by 135 · see citing works
Biofilms and vulvovaginal candidiasis
Rodríguez‐Cerdeira, C., Carnero-Gregorio, M., Molares-Vila, A., López-Bárcenas, A., Fabbrocini, G., Bardhi, B., Sinani, A., Sánchez-Blanco, E., Arenas, R., & Hernández‐Castro, R. (2018) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2018.11.011 · Cited by 154 · see citing works
Innocent until proven guilty: mechanisms and roles of S treptococcus– C andida interactions in oral health and disease
Xu, H., Jenkinson, H. F., & Dongari‐Bagtzoglou, A. I. (2014) · Molecular Oral Microbiology · doi:10.1111/omi.12049 · Cited by 131 · see citing works
Clade-specific chromosomal rearrangements and loss of subtelomeric adhesins in Candida auris
Muñoz, J. F., Welsh, R. M., Shea, T., Batra, D., Gade, L., Howard, D., Rowe, L. A., Meis, J. F., Litvintseva, A. P., & Cuomo, C. A. (2021) · Genetics · doi:10.1093/genetics/iyab029 · Cited by 125 · see citing works
Candida parapsilosis Virulence and Antifungal Resistance Mechanisms: A Comprehensive Review of Key Determinants
Branco, J., Miranda, I. M., & Rodrigues, A. G. (2023) · Journal of Fungi · doi:10.3390/jof9010080 · Cited by 133 · see citing works
Multispecies biofilms in fermentation: Biofilm formation, microbial interactions, and communication
Yao, S., Hao, L., Zhou, R., Jin, Y., Huang, J., & Wu, C. (2022) · Comprehensive Reviews in Food Science and Food Safety · doi:10.1111/1541-4337.12991 · Cited by 126 · see citing works
Oral Candidosis: Pathophysiology and Best Practice for Diagnosis, Classification, and Successful Management
Lu, S.-Y. (2021) · Journal of Fungi · doi:10.3390/jof7070555 · Cited by 118 · see citing works
Patterns of Genomic Variation in the Opportunistic Pathogen Candida glabrata Suggest the Existence of Mating and a Secondary Association with Humans
Carreté, L., Ksiezopolska, E., Pegueroles, C., Gómez-Molero, E., Saus, E., Iraola-Guzmán, S., Loska, D., Bader, O., Fairhead, C., & Gabaldón, T. (2018) · Current Biology · doi:10.1016/j.cub.2017.11.027 · Cited by 118 · see citing works
Cell wall-related bionumbers and bioestimates of Saccharomyces cerevisiae and Candida albicans
Klis, F. M., de Koster, C. G., & Brul, S. (2014) · Eukaryotic Cell · doi:10.1128/ec.00250-13 · Cited by 109 · see citing works
Candidalysin Crucially Contributes to Nlrp3 Inflammasome Activation by Candida albicans Hyphae
Rogiers, O., Frising, U. C., Kucharíková, S., Jabra-Rizk, M. A., van Loo, G., Van Dijck, P., & Wullaert, A. (2019) · mBio · doi:10.1128/mbio.02221-18 · Cited by 113 · see citing works
Evolutionary genomics of yeast pathogens in the Saccharomycotina
Gabaldón, T., Naranjo-Ortíz, M. A., & Marcet-Houben, M. (2016) · FEMS Yeast Research · doi:10.1093/femsyr/fow064 · Cited by 105 · see citing works
The role of Lactobacillus species in the control of Candida via biotrophic interactions
Zangl, I., Pap, I.-J., Aspöck, C., & Schüller, C. (2020) · Microbial Cell · doi:10.15698/mic2020.01.702 · Cited by 108 · see citing works
Divergent Approaches to Virulence in C. albicans and C. glabrata: Two Sides of the Same Coin
Galocha, M., Pais, P., Cavalheiro, M., Pereira, D., Viana, R., & Teixeira, M. C. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20092345 · Cited by 105 · see citing works
Adhesins in Candida glabrata
Timmermans, B., De Las Peñas, A., Castaño, I., & Van Dijck, P. (2018) · Journal of Fungi · doi:10.3390/jof4020060 · Cited by 109 · see citing works
The birth of a deadly yeast: tracing the evolutionary emergence of virulence traits in Candida glabrata
Gabaldón, T., & Carreté, L. (2016) · FEMS Yeast Research · doi:10.1093/femsyr/fov110 · Cited by 99 · see citing works
Skin Commensal FungusMalasseziaand Its Lipases
Park, M., Park, S.-M., & Jung, W. H. (2021) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2012.12048 · Cited by 100 · see citing works
Adhesins of Yeasts: Protein Structure and Interactions
Willaert, R. (2018) · Journal of Fungi · doi:10.3390/jof4040119 · Cited by 92 · see citing works
V erticillium transcription activator of adhesion V ta2 suppresses microsclerotia formation and is required for systemic infection of plant roots
Tran, V., Braus‐Stromeyer, S. A., Kusch, H., Reusche, M., Kaever, A., Kühn, A., Valerius, O., Landesfeind, M., Aßhauer, K. P., Tech, M., et al. (2014) · New Phytologist · doi:10.1111/nph.12671 · Cited by 99 · see citing works
What We Do Not Know about Fungal Cell Adhesion Molecules
Lipke, P. (2018) · Journal of Fungi · doi:10.3390/jof4020059 · Cited by 81 · see citing works
“ 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 · see citing works
Therapeutic activity of aSaccharomyces cerevisiae-based probiotic and inactivated whole yeast on vaginal candidiasis
Pericolini, E., Gabrielli, E., Ballet, N., Sabbatini, S., Roselletti, E., Decherf, A. C., Pélerin, F., Luciano, E., Perito, S., Jüsten, P., et al. (2016) · Virulence · doi:10.1080/21505594.2016.1213937 · Cited by 90 · see citing works
Host–Pathogen Interactions during Female Genital Tract Infections
Pekmezovic, M. G., Mogavero, S., Naglik, J. R., & Hube, B. (2019) · Trends in Microbiology · doi:10.1016/j.tim.2019.07.006 · Cited by 91 · see citing works
Host cell invasion by medically important fungi.Preprint
Sheppard, D., & Filler, S. (2014) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a019687 · Cited by 77 · see citing works
Natural Killer Cells in Antifungal Immunity
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Authors: de Groot, P. W. J., Bader, O., de Boer, A. D., Weig, M., & Chauhan, N.
Affiliations: Regional Center for Biomedical Research, Albacete Science and Technology Park, University of Castilla—La Mancha, Albacete, Spain
Universitätsmedizin Göttingen (DE)
Rutgers New Jersey Medical School (US)
ORCID: Bader, Oliver
Weig, Michael
Chauhan, Neeraj
Venue: Eukaryotic Cell
Publisher: American Society for Microbiology
Published: 2013-04
Volume: 12
Issue: 4
Pages: 470-481
ISSN: 1535-9778 (ISSN-L)
1535-9786
DOI: 10.1128/ec.00364-12
PMC: PMC3623432
OpenAlex: W2141294282
Cited by: 319
References: 126
Citations by year: 2026: 17 · 2025: 23 · 2024: 33 · 2023: 32 · 2022: 25 · 2021: 30 · 2020: 29 · 2019: 22 · 2018: 21 · 2017: 25 · 2016: 22 · 2015: 21 · 2014: 16 · 2013: 3
FWCI: 2.68
Type: journal article
Language: en
Open access: diamond
doi.org
Licence: journals.asm.org/non-commercial-tdm-license (tdm)
Locations: Eukaryotic Cell (publishedVersion)
Europe PMC (PubMed Central) (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Rutgers University Community Repository (Rutgers University) (submittedVersion)
GRO (submittedVersion)
University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion)
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 › Epidemiology › Fungal Infections and Studies
Keywords: fungal adhesins, Candida, fungal cell wall, microbial adhesion, medical device colonization, fungal pathogenesis, fungal virulence factors
MeSH terms: Amino Acid Sequence, Candida, Candidiasis, Cell Adhesion, Cell Wall, Fungal Proteins, Multigene Family, Humans, Membrane Glycoproteins, Molecular Sequence Data, Cell Adhesion Molecules, Gene Expression Regulation, Fungal, Protein Structure, Secondary, Protein Structure, Tertiary, Host-Pathogen Interactions

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Adhesins in human fungal pathogens: glue with plenty of stick.

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