Two unlike cousins: C andida albicans and C . glabrata infection strategies

Nonfilamentous C. albicans Mutants Are Avirulent

Lo, H.-J., Köhler, J. R., DiDomenico, B., Loebenberg, D., Cacciapuoti, A., & Fink, G. R. (1997) · Cell · doi:10.1016/s0092-8674(00)80358-x · Cited by 1,809 · see citing works

Genome evolution in yeasts

Dujon, B., Sherman, D., Fischer, G., Durrens, P., Casaregola, S., Lafontaine, I., de Montigny, J., Marck, C., Neuvéglise, C., Talla, E., et al. (2004) · Nature · doi:10.1038/nature02579 · Cited by 1,623 · see citing works

Nutritional immunity: transition metals at the pathogen–host interface

Hood, M. I., & Skaar, E. P. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2836 · Cited by 1,535 · see citing works

Candida and candidosis

Odds, F. C. (1979) · Medical Entomology and Zoology · Cited by 1,297 · see citing works

Unipolar cell divisions in the yeast S. cerevisiae lead to filamentous growth: Regulation by starvation and RAS

Gimeno, C. J., Ljungdahl, P. O., Styles, C. A., & Fink, G. R. (1992) · Cell · doi:10.1016/0092-8674(92)90079-r · Cited by 1,184 · see citing works

Dectin-1 is required for β-glucan recognition and control of fungal infection

Taylor, P. R., Tsoni, S. V., Willment, J. A., Dennehy, K. M., Rosas, M., Findon, H., Haynes, K., Steele, C. H., Botto, M., Gordon, S., et al. (2006) · Nature Immunology · doi:10.1038/ni1408 · Cited by 1,155 · see citing works

Growth of Candida albicans hyphae

Sudbery, P. E. (2011) · Nature Reviews Microbiology · doi:10.1038/nrmicro2636 · Cited by 1,110 · see citing works

Evolution of pathogenicity and sexual reproduction in eight Candida genomes

Butler, G., Rasmussen, M. D., Lin, M. F., Santos, M. A. S., Sakthikumar, S., Munro, C. A., Rheinbay, E., Grabherr, M., Forche, A., Reedy, J. L., et al. (2009) · Nature · doi:10.1038/nature08064 · Cited by 1,065 · see citing works

Dynamics of cell wall structure in Saccharomyces cerevisiae

Klis, F. M., Mol, P. C., Hellingwerf, K. J., & Brul, S. (2002) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2002.tb00613.x · Cited by 1,007 · see citing works

<i>Candida glabrata</i> : Review of Epidemiology, Pathogenesis, and Clinical Disease with Comparison to <i>C. albicans</i>

Fidel, P. L., Vazquez, J. A., & Sobel, J. D. (1999) · Clinical Microbiology Reviews · doi:10.1128/cmr.12.1.80 · Cited by 953 · see citing works

Metal Chelation and Inhibition of Bacterial Growth in Tissue Abscesses

Corbin, B. D., Seeley, E. H., Raab, A., Feldmann, J., Miller, M. R., Torres, V. J., Anderson, K. L., Dattilo, B. M., Dunman, P. M., Gerads, R., et al. (2008) · Science · doi:10.1126/science.1152449 · Cited by 857 · see citing works

Nosocomial fungal infections: epidemiology, diagnosis, and treatment

Perlroth, J., Choi, B., & Spellberg, B. (2007) · Medical Mycology · doi:10.1080/13693780701218689 · Cited by 738 · see citing works

Adhesive and mammalian transglutaminase substrate properties of Candida albicans Hwp1.

Staab, J., Bradway, S. D., Fidel, P., & Sundstrom, P. (1999) · Science · doi:10.1126/science.283.5407.1535 · Cited by 683 · see citing works

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 · see citing works

Bacterial Adhesins in Host-Microbe Interactions

Kline, K. A., Fälker, S., Dahlberg, S., Normark, S. J., & Henriques‐Normark, B. (2009) · Cell Host & Microbe · doi:10.1016/j.chom.2009.05.011 · Cited by 635 · see citing works

Nutritional immunity beyond iron: a role for manganese and zinc

Kehl-Fie, T. E., & Skaar, E. P. (2010) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2009.11.008 · Cited by 634 · see citing works

Tackling Human Fungal Infections

Brown, G. D., Denning, D. W., & Levitz, S. M. (2012) · Science · doi:10.1126/science.1222236 · Cited by 619 · see citing works

Phagosome Extrusion and Host-Cell Survival after Cryptococcus neoformans Phagocytosis by Macrophages

Alvarez, M., & Casadevall, A. (2006) · Current Biology · doi:10.1016/j.cub.2006.09.061 · Cited by 414 · see citing works

Candida albicans proteinases and host/pathogen interactions

Naglik, J., Albrecht, A., Bader, O., & Hube, B. (2004) · Cellular Microbiology · doi:10.1111/j.1462-5822.2004.00439.x · Cited by 399 · see citing works

An Adhesin of the Yeast Pathogen <i>Candida glabrata</i> Mediating Adherence to Human Epithelial Cells

Cormack, B. P., Ghori, N., & Falkow, S. (1999) · Science · doi:10.1126/science.285.5427.578 · Cited by 383 · see citing works

Evidence of a Role for Monocytes in Dissemination and Brain Invasion by<i>Cryptococcus neoformans</i>

Charlier, C., Nielsen, K., Daou, S., Brigitte, M., Chretien, F., & Dromer, F. (2009) · Infection and Immunity · doi:10.1128/iai.01065-08 · Cited by 362 · see citing works

Discovering the secrets of the<i>Candida albicans</i>agglutinin-like sequence (ALS) gene family – a sticky pursuit

Hoyer, L. L., Green, C. B., Oh, S.-H., & Zhao, X. (2008) · Medical Mycology · doi:10.1080/13693780701435317 · Cited by 356 · see citing works

MAPK, MKP1 and c-Fos Discriminate Candida albicans Yeast from Hyphae in Epithelial Cells

Moyes, D., Runglall, M., Murciano, C., Shen, C., Nayar, D., Thavaraj, S., Kohli, A., Islam, A., Mora-Montes, H., Challacombe, S., et al. (2010) · Cell Host and Microbe · doi:10.1016/j.chom.2010.08.002 · Cited by 347 · see citing works

The Hyphal-Associated Adhesin and Invasin Als3 of Candida albicans Mediates Iron Acquisition from Host Ferritin

Almeida, R. S., Brunke, S., Albrecht, A., Thewes, S., Laue, M., Edwards, J. E., Filler, S. G., & Hube, B. (2008) · PLoS Pathogens · doi:10.1371/journal.ppat.1000217 · Cited by 330 · see citing works

Copper Homeostasis at the Host-Pathogen Interface

Hodgkinson, V., & Petris, M. J. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.r111.316406 · Cited by 316 · see citing works

A family of glycosylphosphatidylinositol-linked aspartyl proteases is required for virulence of <i>Candida glabrata</i>

Kaur, R., Ma, B., & Cormack, B. P. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611195104 · Cited by 284 · see citing works

Genetics and genomics of Candida albicans biofilm formation

Nobile, C. J., & Mitchell, A. P. (2006) · Cellular Microbiology · doi:10.1111/j.1462-5822.2006.00761.x · Cited by 281 · see citing works

Mixed Candida albicans and Candida glabrata populations associated with the pathogenesis of denture stomatitis

Coco, B. J., Bagg, J., Cross, L. J., Jose, A., Cross, J., & Ramage, G. (2008) · Oral Microbiology and Immunology · doi:10.1111/j.1399-302x.2008.00439.x · Cited by 276 · see citing works

A yeast by any other name: Candida glabrata and its interaction with the host

Kaur, R., Domergue, R., Zupancic, M. L., & Cormack, B. P. (2005) · Current Opinion in Microbiology · doi:10.1016/j.mib.2005.06.012 · Cited by 271 · see citing works

From Attachment to Damage: Defined Genes of Candida albicans Mediate Adhesion, Invasion and Damage during Interaction with Oral Epithelial Cells

Wächtler, B., Wilson, D., Haedicke, K., Dalle, F., & Hube, B. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017046 · Cited by 270 · see citing works

Virulence-related surface glycoproteins in the yeast pathogen <i>Candida glabrata</i> are encoded in subtelomeric clusters and subject to <i>RAP1</i> - and <i>SIR</i> -dependent transcriptional silencing

De Las Peñas, A., Pan, S.-J., Castaño, I., Alder, J., Cregg, R., & Cormack, B. P. (2003) · Genes &amp; Development · doi:10.1101/gad.1121003 · Cited by 268 · see citing works

Candida albicans-Epithelial Interactions: Dissecting the Roles of Active Penetration, Induced Endocytosis and Host Factors on the Infection Process

Wächtler, B., Citiulo, F., Jablonowski, N., Förster, S., Dalle, F., Schaller, M., Wilson, D., & Hube, B. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036952 · Cited by 250 · see citing works

Contribution of <i>Candida albicans</i> Cell Wall Components to Recognition by and Escape from Murine Macrophages

McKenzie, C. G. J., Koser, U., Lewis, L. E., Bain, J. M., Mora-Montes, H. M., Barker, R. N., Gow, N. A. R., & Erwig, L. P. (2010) · Infection and Immunity · doi:10.1128/iai.00001-10 · Cited by 250 · see citing works

Nicotinic Acid Limitation Regulates Silencing of <i>Candida</i> Adhesins During UTI

Domergue, R., Castaño, I., De Las Peñas, A., Zupancic, M., Lockatell, V., Hebel, J. R., Johnson, D., & Cormack, B. P. (2005) · Science · doi:10.1126/science.1108640 · Cited by 249 · see citing works

Candida albicans Scavenges Host Zinc via Pra1 during Endothelial Invasion

Citiulo, F., Jacobsen, I. D., Miramón, P., Schild, L., Brunke, S., Zipfel, P., Brock, M., Hube, B., & Wilson, D. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002777 · Cited by 242 · see citing works

Candida glabrata , an Emerging Oral Opportunistic Pathogen

Li, L., Redding, S. W., & Dongari‐Bagtzoglou, A. I. (2007) · Journal of Dental Research · doi:10.1177/154405910708600304 · Cited by 238 · see citing works

The Cell Wall of the Human Pathogen <i>Candida glabrata</i> : Differential Incorporation of Novel Adhesin-Like Wall Proteins

de Groot, P. W. J., Kraneveld, E. A., Yin, Q. Y., Dekker, H. L., Groß, U., Crielaard, W., de Koster, C. G., Bader, O., Klis, F. M., & Weig, M. (2008) · Eukaryotic Cell · doi:10.1128/ec.00284-08 · Cited by 232 · see citing works

A family of <i>Candida</i> cell surface haem‐binding proteins involved in haemin and haemoglobin‐iron utilization

Weissman, Z., & Kornitzer, D. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04199.x · Cited by 231 · see citing works

The Siderophore Iron Transporter of<i>Candida albicans</i>(Sit1p/Arn1p) Mediates Uptake of Ferrichrome-Type Siderophores and Is Required for Epithelial Invasion

Heymann, P., Gerads, M., Schaller, M., Dromer, F., Winkelmann, G., & Ernst, J. F. (2002) · Infection and Immunity · doi:10.1128/iai.70.9.5246-5255.2002 · Cited by 226 · see citing works

The Role of the Gastrointestinal Tract in Hematogenous Candidiasis: From the Laboratory to the Bedside

Cole, G. T., Halawa, A. A., & Anaissie, E. J. (1996) · Clinical Infectious Diseases · doi:10.1093/clinids/22.supplement_2.s73 · Cited by 222 · see citing works

The Facultative Intracellular Pathogen <i>Candida glabrata</i> Subverts Macrophage Cytokine Production and Phagolysosome Maturation

Seider, K., Brunke, S., Schild, L., Jablonowski, N., Wilson, D., Majer, O., Barz, D., Haas, A., Kuchler, K., Schaller, M., et al. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1003730 · Cited by 220 · see citing works

Interaction of <i>Candida albicans</i> Cell Wall Als3 Protein with <i>Streptococcus gordonii</i> SspB Adhesin Promotes Development of Mixed-Species Communities

Silverman, R. J., Nobbs, A. H., Vickerman, M. M., Barbour, M. E., & Jenkinson, H. F. (2010) · Infection and Immunity · doi:10.1128/iai.00685-10 · Cited by 219 · see citing works

Recognition and Blocking of Innate Immunity Cells by Candida albicans Chitin

Mora-Montes, H. M., Netea, M. G., Ferwerda, G., Lenardon, M. D., Brown, G. D., Mistry, A. R., Kullberg, B. J., O’Callaghan, C. A., Sheth, C. C., Odds, F. C., et al. (2011) · Infection and Immunity · doi:10.1128/iai.01282-10 · Cited by 204 · see citing works

Birth of a metabolic gene cluster in yeast by adaptive gene relocation

Wong, S., & Wolfe, K. H. (2005) · Nature Genetics · doi:10.1038/ng1584 · Cited by 202 · see citing works

<i>Candida albicans</i> iron acquisition within the host

Almeida, R. S., Wilson, D., & Hube, B. (2009) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2009.00570.x · Cited by 199 · see citing works

High Resistance to Oxidative Stress in the Fungal Pathogen <i>Candida glabrata</i> Is Mediated by a Single Catalase, Cta1p, and Is Controlled by the Transcription Factors Yap1p, Skn7p, Msn2p, and Msn4p

Cuéllar-Cruz, M., Briones-Martin-del-Campo, M., Cañas-Villamar, I., Montalvo-Arredondo, J., Riego-Ruiz, L., Castaño, I., & De Las Peñas, A. (2008) · Eukaryotic Cell · doi:10.1128/ec.00011-08 · Cited by 190 · see citing works

Telomere length control and transcriptional regulation of subtelomeric adhesins in <i>Candida glabrata</i>

Castaño, I., Pan, S., Zupancic, M., Hennequin, C., Dujon, B., & Cormack, B. P. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04465.x · Cited by 188 · see citing works

EGFR and HER2 receptor kinase signaling mediate epithelial cell invasion by <i>Candida albicans</i> during oropharyngeal infection

Zhu, W., Phan, Q. T., Boontheung, P., Solis, N. V., Loo, J. A., & Filler, S. G. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1117676109 · Cited by 180 · see citing works

Interaction of pathogenic yeasts with phagocytes: survival, persistence and escape.

Seider, K., Heyken, A., Lüttich, A., Miramón, P., & Hube, B. (2010) · Current Opinion in Microbiology · doi:10.1016/j.mib.2010.05.001 · Cited by 167 · see citing works

Iron Acquisition from Transferrin by <i>Candida albicans</i> Depends on the Reductive Pathway

Knight, S. A. B., Vilaire, G., Lesuisse, E., & Dancis, A. (2005) · Infection and Immunity · doi:10.1128/iai.73.9.5482-5492.2005 · Cited by 145 · see citing works

Autophagy supports<i>Candida glabrata</i>survival during phagocytosis

Roetzer, A., Gratz, N., Kovarik, P., & Schüller, C. (2010) · Cellular Microbiology · doi:10.1111/j.1462-5822.2009.01391.x · Cited by 142 · see citing works

Infection of Human Oral Epithelia with Candida Species Induces Cytokine Expression Correlated to the Degree of Virulence

Schaller, M., Sander, C. A., Körting, H. C., Mailhammer, R., Graßl, G. A., & Hube, B. (2002) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.2002.01699.x · Cited by 139 · see citing works

Live Imaging of Disseminated Candidiasis in Zebrafish Reveals Role of Phagocyte Oxidase in Limiting Filamentous Growth

Brothers, K. M., Newman, Z. R., & Wheeler, R. T. (2011) · Eukaryotic Cell · doi:10.1128/ec.05005-11 · Cited by 134 · see citing works

<i>Candida glabrata</i>displays pseudohyphal growth

Csank, C., & Haynes, K. (2000) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2000.tb09216.x · Cited by 129 · see citing works

Developmental Regulation of an Adhesin Gene during Cellular Morphogenesis in the Fungal Pathogen Candida albicans

Argimón, S., Wishart, J. A., Leng, R. P., Macaskill, S., Mavor, A. L., Alexandris, T., Nicholls, S., Knight, A. W., Enjalbert, B., Walmsley, R. M., et al. (2007) · Eukaryotic Cell · doi:10.1128/ec.00340-06 · Cited by 129 · see citing works

Candida and Candidosis

Mackenzie, D. (1988) · Journal of Clinical Pathology · doi:10.1136/jcp.41.11.1247-c · Cited by 127 · see citing works

The Yak1p kinase controls expression of adhesins and biofilm formation in <i>Candida glabrata</i> in a Sir4p‐dependent pathway

Iraqui, I., Garcia‐Sanchez, S., Aubert, S., Dromer, F., Ghigo, J., D’Enfert, C., & Janbon, G. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04475.x · Cited by 126 · see citing works

Polymorphonuclear leukocytes (PMNs) induce protective Th1-type cytokine epithelial responses in an in vitro model of oral candidosis

Schaller, M., Boeld, U., Oberbauer, S., Hamm, G., Hube, B., & Körting, H. C. (2004) · Microbiology · doi:10.1099/mic.0.27169-0 · Cited by 112 · see citing works

Characterization of a haemolytic factor from Candida albicans

Watanabe, T., Takano, M., Murakami, M., Tanaka, H., Matsuhisa, A., Nakao, N., Mikami, T., Suzuki, M., & Matsumoto, T. (1999) · Microbiology · doi:10.1099/13500872-145-3-689 · Cited by 109 · see citing works

The many niches and strategies used by pathogenic mycobacteria for survival within host macrophages

de Chastellier, C. (2009) · Immunobiology · doi:10.1016/j.imbio.2008.12.005 · Cited by 109 · see citing works

Non-lytic expulsion/exocytosis of Candida albicans from macrophages

Bain, J. M., Lewis, L. E., Okai, B., Quinn, J., Gow, N. A. R., & Erwig, L. (2012) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2012.01.008 · Cited by 100 · see citing works

Candida glabrata Persistence in Mice Does Not Depend on Host Immunosuppression and Is Unaffected by Fungal Amino Acid Auxotrophy

Jacobsen, I. D., Brunke, S., Seider, K., Schwarzmüller, T., Firon, A., d’Enfert, C., Kuchler, K., & Hube, B. (2009) · Infection and Immunity · doi:10.1128/iai.01244-09 · Cited by 100 · see citing works

Candidaconcentrations in the vagina and their association with signs and symptoms of vaginal candidosis

Odds, F. C., Webster, C. E., Mayuranathan, P., & Simmons, P. D. (1988) · Medical Mycology · doi:10.1080/02681218880000391 · Cited by 98 · see citing works

Heme Oxygenase in Candida albicans Is Regulated by Hemoglobin and Is Necessary for Metabolism of Exogenous Heme and Hemoglobin to α-Biliverdin

Pendrak, M. L., Chao, M. P., Yan, S. S., & Roberts, D. D. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m311550200 · Cited by 97 · see citing works

Host Iron Withholding Demands Siderophore Utilization for Candida glabrata to Survive Macrophage Killing

Nevitt, T., & Thiele, D. J. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1001322 · Cited by 95 · cited 5× · see citing works

Knocking on the right door and making a comfortable home: Histoplasma capsulatum intracellular pathogenesis

Woods, J. P. (2003) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(03)00080-8 · Cited by 95 · see citing works

Autophagy in the pathogen Candida albicans

Palmer, G. E., Kelly, M. N., & Sturtevant, J. E. (2006) · Microbiology · doi:10.1099/mic.0.2006/001610-0 · Cited by 86 · see citing works

Candida albicansactively modulates intracellular membrane trafficking in mouse macrophage phagosomes

Fernández‐Arenas, E., Bleck, C. K. E., Nombela, C., Gil, C., Griffiths, G., & Diez‐Orejas, R. (2008) · Cellular Microbiology · doi:10.1111/j.1462-5822.2008.01274.x · Cited by 85 · see citing works

Recognition of Yeast by Murine Macrophages Requires Mannan but Not Glucan

Keppler‐Ross, S., Douglas, L. M., Konopka, J. B., & Dean, N. (2010) · Eukaryotic Cell · doi:10.1128/ec.00156-10 · Cited by 83 · see citing works

Candida glabrataOropharyngeal Candidiasis in Patients Receiving Radiation Treatment for Head and Neck Cancer

Redding, S. W., Kirkpatrick, W. R., Coco, B. J., Sadkowski, L. C., Fothergill, A. W., Rinaldi, M. G., Eng, T. Y., & Patterson, T. F. (2002) · Journal of Clinical Microbiology · doi:10.1128/jcm.40.5.1879-1881.2002 · Cited by 71 · see citing works

Activation of MAPK/c-Fos induced responses in oral epithelial cells is specific to Candida albicans and Candida dubliniensis hyphae

Moyes, D. L., Murciano, C., Runglall, M., Kohli, A., Islam, A., & Naglik, J. R. (2011) · Medical Microbiology and Immunology · doi:10.1007/s00430-011-0209-y · Cited by 68 · see citing works

Severe Candida spp. infections: new insights into natural immunity

van der Meer, J. W. M., van de Veerdonk, F. L., Joosten, L. A. B., Kullberg, B. J., & Netea, M. G. (2010) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2010.11.013 · Cited by 58 · see citing works

Pathogenesis of Candida albicans Infections in the Alternative Chorio-Allantoic Membrane Chicken Embryo Model Resembles Systemic Murine Infections

Jacobsen, I. D., Große, K., Berndt, A., & Hube, B. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019741 · Cited by 56 · 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

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

Heterogeneous Expression of the Virulence-Related Adhesin Epa1 between Individual Cells and Strains of the Pathogen Candida glabrata

Halliwell, S., Smith, M. C. A., Muston, P., Holland, S. L., & Avery, S. V. (2011) · Eukaryotic Cell · doi:10.1128/ec.05232-11 · Cited by 46 · see citing works

Hgc1 Mediates Dynamic Candida albicans-Endothelium Adhesion Events during Circulation

Wilson, D., & Hube, B. (2009) · Eukaryotic Cell · doi:10.1128/ec.00307-09 · Cited by 42 · see citing works

Cytotoxic and cytokine-inducing properties of Candida glabrata in single and mixed oral infection models

Li, L., Kashleva, H., & Dongari‐Bagtzoglou, A. I. (2007) · Microbial Pathogenesis · doi:10.1016/j.micpath.2006.12.003 · Cited by 40 · see citing works

Reverse transcriptase polymerase chain reaction (RT‐PCR) detection of HLP gene expression in Candida glabrata and its possible role in in vitro haemolysin production

Luo, G., Samaranayake, L. P., Cheung, B. P. K., & Tang, G. (2004) · Apmis · doi:10.1111/j.1600-0463.2004.apm11204-0509.x · 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

Game theoretical modelling of survival strategies of Candida albicans inside macrophages

Hummert, S., Hummert, C., Schroeter, A., Hube, B., & Schuster, S. (2010) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2010.01.022 · Cited by 37 · see citing works

<i>Candida glabrata</i> tryptophan‐based pigment production via the Ehrlich pathway

Brunke, S., Seider, K., Almeida, R. S., Heyken, A., Fleck, C. B., Brock, M., Barz, D., Rupp, S., & Hube, B. (2010) · Molecular Microbiology · doi:10.1111/j.1365-2958.2010.07052.x · Cited by 37 · see citing works

Candida glabrataandCandida albicans; dissimilar tissue tropism and infectivity in a gnotobiotic model of mucosal candidiasis

Westwater, C., Schofield, D. A., Nicholas, P. J., Paulling, E. E., & Balish, E. (2007) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.2007.00287.x · Cited by 28 · see citing works

Immune defence against Candida fungal infections

Netea, M. G., Joosten, L. A. B., van der Meer, J. W. M., Kullberg, B.-J., & van de Veerdonk, F. L. (2015) · Nature Reviews Immunology · doi:10.1038/nri3897 · Cited by 642 · see citing works

The<i>Candida</i>Genome Database (CGD): incorporation of Assembly 22, systematic identifiers and visualization of high throughput sequencing data

Skrzypek, M. S., Binkley, J., Binkley, G., Miyasato, S. R., Simison, M., & Sherlock, G. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkw924 · Cited by 455 · see citing works

Candida glabrata: A review of its features and resistance

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

Fungal Resistance to Echinocandins and the MDR Phenomenon in Candida glabrata

Healey, K. R., & Perlin, D. S. (2018) · Journal of Fungi · doi:10.3390/jof4030105 · Cited by 194 · see citing works

Candida glabrata: pathogenicity and resistance mechanisms for adaptation and survival

Hassan, Y., Chew, S. Y., & Than, L. T. L. (2021) · Journal of Fungi · doi:10.3390/jof7080667 · Cited by 170 · see citing works

Metabolism in fungal pathogenesis

Ene, I. V., Brunke, S., Brown, A. J. P., & Hube, B. (2014) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a019695 · Cited by 169 · see citing works

Candida albicans commensalism and pathogenicity are intertwined traits directed by a tightly knit transcriptional regulatory circuit

Pérez, J. C., Kumamoto, C. A., & Johnson, A. D. (2013) · PLoS Biology · doi:10.1371/journal.pbio.1001510 · Cited by 156 · see citing works

Candida glabrata Biofilms: How Far Have We Come?

Rodrigues, C., Rodrigues, M., Silva, S., & Henriques, M. (2017) · Journal of Fungi · doi:10.3390/jof3010011 · Cited by 129 · 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

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

The birth of a deadly yeast: tracing the evolutionary emergence of virulence traits in <i>Candida glabrata</i>

Gabaldón, T., & Carreté, L. (2016) · FEMS Yeast Research · doi:10.1093/femsyr/fov110 · Cited by 99 · see citing works

Extracellular proteinases of <i>Candida</i> species pathogenic yeasts

Rapala‐Kozik, M., Bochenska, O., Zajac, D., Karkowska‐Kuleta, J., Gogol, M., Zawrotniak, M., & Kozik, A. (2018) · Molecular Oral Microbiology · doi:10.1111/omi.12206 · Cited by 94 · see citing works

Management of recurrent vulvovaginal candidosis: Narrative review of the literature and European expert panel opinion

Donders, G., Sziller, I. O., Paavonen, J., Hay, P., de Seta, F., Bohbot, J. M., Kotarski, J., Vives, J. A., Szabo, B., Cepuliené, R., et al. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.934353 · Cited by 82 · see citing works

A systematic analysis reveals an essential role for high-affinity iron uptake system, haemolysin and CFEM domain-containing protein in iron homoeostasis and virulence in <i>Candida glabrata</i>

Srivastava, V. K., Suneetha, K. J., & Kaur, R. (2014) · Biochemical Journal · doi:10.1042/bj20140598 · Cited by 69 · see citing works

Gain-of-Function Mutations in <i>PDR1</i> , a Regulator of Antifungal Drug Resistance in Candida glabrata, Control Adherence to Host Cells

Vale-Silva, L., Ischer, F., Leibundgut-Landmann, S., & Sanglard, D. (2013) · Infection and Immunity · doi:10.1128/iai.00074-13 · Cited by 65 · see citing works

Neutrophil activation by <i>C</i> <i>andida glabrata</i> but not <i>C</i> <i>andida albicans</i> promotes fungal uptake by monocytes: <i>C. albicans</i> , <i>C. glabrata</i> and neutrophils

Duggan, S., Essig, F., Hünniger, K., Mokhtari, Z., Bauer, L., Lehnert, T., Brandes, S., Häder, A., Jacobsen, I. D., Martin, R., et al. (2015) · Cellular Microbiology · doi:10.1111/cmi.12443 · Cited by 60 · see citing works

Candida albicans at Host Barrier Sites: Pattern Recognition Receptors and Beyond

Swidergall, M. (2019) · Pathogens · doi:10.3390/pathogens8010040 · Cited by 59 · see citing works

Mechanisms involved in the triggering of neutrophil extracellular traps (NETs) by Candida glabrata during planktonic and biofilm growth

Johnson, C. J., Kernien, J. F., Hoyer, A. R., & Nett, J. E. (2017) · Scientific Reports · doi:10.1038/s41598-017-13588-6 · Cited by 58 · see citing works

Fungal resistance to echinocandins and the MDR phenomenon in Candida glabrata

Healey, K., & Perlin, D. S. (2018) · doi:10.20944/preprints201808.0306.v1 · Cited by 194 · see citing works

Aspartyl proteases in Candida glabrata are required for suppression of the host innate immune response

Rasheed, M., Battu, A., & Kaur, R. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.813741 · Cited by 51 · see citing works

Glyoxylate cycle gene ICL1 is essential for the metabolic flexibility and virulence of Candida glabrata

Chew, S. Y., Ho, K. L., Cheah, Y. K., Ng, T. S., Sandai, D., Brown, A. J. P., & Than, L. T. L. (2019) · Scientific Reports · doi:10.1038/s41598-019-39117-1 · Cited by 49 · see citing works

Plants used in folk medicine: The potential of their hydromethanolic extracts against Candida species

Martins, N., Ferreira, I. C. F. R., Barros, L., Carvalho, A. M., Henriques, M., & Silva, S. (2015) · Industrial Crops and Products · doi:10.1016/j.indcrop.2014.12.033 · Cited by 48 · see citing works

Deletion of <i>ADA2</i> Increases Antifungal Drug Susceptibility and Virulence in Candida glabrata

Yu, S.-J., Chang, Y.-L., & Chen, Y.-L. (2018) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01924-17 · Cited by 43 · see citing works

A novel hybrid iron regulation network combines features from pathogenic and nonpathogenic yeasts

Gerwien, F., Safyan, A., Wisgott, S., Hille, F., Kaemmer, P., Linde, J., Brunke, S., Kasper, L., & Hube, B. (2016) · mBio · doi:10.1128/mbio.01782-16 · Cited by 47 · see citing works

Transient mitochondria dysfunction confers fungal cross-resistance against phagocytic killing and fluconazole

Siscar-Lewin, S., Gabaldón, T., Aldejohann, A. M., Kurzai, O., Hube, B., & Brunke, S. (2021) · mBio · doi:10.1128/mbio.01128-21 · Cited by 36 · see citing works

Transcriptional profiling of Candida glabrata during phagocytosis by neutrophils and in the infected mouse spleen

Fukuda, Y., Tsai, H.-F., Myers, T. G., & Bennett, J. E. (2013) · Infection and Immunity · doi:10.1128/iai.00851-12 · Cited by 41 · see citing works

A network of paralogous stress response transcription factors in the human pathogen Candida glabrata

Merhej, J., Thiebaut, A., Blugeon, C., Pouch, J., Ali Chaouche, M. E. A., Camadro, J.-M., Le Crom, S., Lelandais, G., & Devaux, F. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00645 · Cited by 36 · see citing works

The mitogen‐activated protein kinase CgHog1 is required for iron homeostasis, adherence and virulence in <i>Candida glabrata</i>

Srivastava, V. K., Suneetha, K. J., & Kaur, R. (2015) · The FEBS Journal · doi:10.1111/febs.13264 · Cited by 33 · see citing works

The fungal pathogen Candida glabrata does not depend on surface ferric reductases for iron acquisition

Gerwien, F., Safyan, A., Wisgott, S., Brunke, S., Kasper, L., & Hube, B. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01055 · Cited by 33 · see citing works

<i>Candida glabrata</i> : new tools and technologies—expanding the toolkit

Ho, H.-L., & Haynes, K. (2015) · FEMS Yeast Research · doi:10.1093/femsyr/fov066 · Cited by 29 · see citing works

Interaction of human fibronectin with Candida glabrata epithelial adhesin 6 (Epa6)

Zajac, D., Karkowska-Kuleta, J., Bochenska, O., Rapala-Kozik, M., & Kozik, A. (2016) · Acta Biochimica Polonica · doi:10.18388/abp.2016_1328 · Cited by 26 · see citing works

Human neutrophils dump Candida glabrata after intracellular killing

Essig, F., Hünniger, K., Dietrich, S., Figge, M. T., & Kurzai, O. (2015) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2015.09.008 · Cited by 20 · see citing works

Antifungal Activity of Plant Secondary Metabolites on Candida albicans: An Updated Review

Khan, A., Moni, S. S., Ali, M., Mohan, S., Jan, H., Rasool, S., Kamal, M. A., Alshahrani, S., Halawi, M., & Alhazmi, H. A. (2023) · Current Molecular Pharmacology · doi:10.2174/1874467215666220304143332 · Cited by 17 · see citing works

In Candida glabrata, ERMES Component GEM1 Controls Mitochondrial Morphology, mtROS, and Drug Efflux Pump Expression, Resulting in Azole Susceptibility

Okamoto, M., Nakano, K., Takahashi-Nakaguchi, A., Sasamoto, K., Yamaguchi, M., Teixeira, M. C., & Chibana, H. (2023) · Journal of Fungi · doi:10.3390/jof9020240 · Cited by 11 · see citing works

Uncovering the connection between tunicamycin-induced respiratory deficiency and reduced fluconazole tolerance in Candida glabrata

Zheng, L., Dong, Y., Wang, J., Zhang, M., Xu, Y., Ma, L., & Guo, L. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1528341 · Cited by 2 · see citing works

Mucins Suppress Virulence Traits of Candida albicans

Kavanaugh, N. L., Zhang, A. Q., Nobile, C. J., Johnson, A. D., & Ribbeck, K. (2014) · mBio · doi:10.1128/mbio.01911-14 · Cited by 141 · see citing works

RESEARCH OF HUMORAL IMMUNITY AGAINST CANDIDA ALBICANS INFECTION

Fu, Y. (2002)

In vitro Antagonistic Activity of Candida albicans against Filamentous Fungi

AL‐Janabi, A. A. H. S. (2015) · Medical Mycology Open Access · doi:10.21767/2471-8521.100002 · Cited by 4 · see citing works

In vitro outcomes of quercetin on Candida albicans planktonic and biofilm cells and in vivo effects on vulvovaginal candidiasis. Evidences of its mechanisms of action

Tan, Y., Lin, Q., Yao, J., et al. (2023) · Phytomedicine · doi:10.1016/j.phymed.2023.154800 · Cited by 33 · see citing works

Лечение кандидемий, вызванных Candida albicans и Candida non-albicans, у больных с опухолями системы крови

Александровна, К. Г., Malchikova, A. O., Сергеевна, Т. К., et al. (2019) · CyberLeninK (CyberLeninka)