From Saccharomyces cerevisiae to Candida glabrata in a few easy steps: important adaptations for an opportunistic pathogen: Candida glabrata stress response
Open accessAbstract
The opportunistic human fungal pathogen Candida glabrata is closely related to Saccharomyces cerevisiae, yet it has evolved to survive within mammalian hosts. Which traits help C. glabrata to adapt to this different environment? Which specific responses are crucial for its survival in the host? The main differences seem to include an extended repertoire of adhesin genes, high drug resistance, an enhanced ability to sustain prolonged starvation and adaptations of the transcriptional wiring of key stress response genes. Here, we discuss the properties of C. glabrata with a focus on the differences to related fungi.
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The C. glabrata genome harbors several members of a specific gene family encoding epithelial adhesin proteins (EPA genes), which are considered a key factor in its ability to infect humans.
“The C. glabrata genome harbors several members of a specific gene family encoding epithelial adhesin proteins (EPA genes), which are considered a key factor in its ability to infect humans (Cormack and Falkow, 1999; Roetzer et al., 2011; Gabaldón et al., 2013; Vale-Silva et al., 2017).”
From Genome Comparisons of Candida glabrata Serial Clinical Isolates Reveal Patterns of Genetic Variation in Infecting Clonal Populations (2019) · cites this paper as Roetzer et al., 2011
The number of generations that occurred within the time-lapse of DSY562 and DSY565 isolation may correspond to at least 250-500 generations, taking into account 5-10 generations/d according to published data.
“The number of generations that occurred within the time-lapse of DSY562 and DSY565 isolation may correspond to at least 250–500 generations, when taking into account 5–10 generations/d according to published data (Forche et al. 2009; Roetzer et al. 2011).”
From Comparative Genomics of Two Sequential <i>Candida glabrata</i> Clinical Isolates (2017) · cites this paper as Roetzer et al. 2011
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Cites
Genomic Expression Programs in the Response of Yeast Cells to Environmental Changes
Gasch, A. P., Spellman, P. T., Kao, C. M., Carmel-Harel, O., Eisen, M. B., Storz, G., Botstein, D., & Brown, P. O. (2000) · Molecular Biology of the Cell · doi:10.1091/mbc.11.12.4241 · Cited by 4,815 · see citing works
How long do nosocomial pathogens persist on inanimate surfaces? A systematic review
Krämer, A., Schwebke, I., & Kampf, G. (2006) · BMC Infectious Diseases · doi:10.1186/1471-2334-6-130 · Cited by 2,508 · see citing works
Autophagosome formation: core machinery and adaptations
Xie, Z., & Klionsky, D. J. (2007) · Nature Cell Biology · doi:10.1038/ncb1007-1102 · Cited by 2,165 · see citing works
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
Global transcriptional responses of fission yeast to environmental stress
Chen, D., Toone, W. M., Mata, J., Lyne, R., Burns, G., Kivinen, K., Brazma, A., Jones, N., & Bähler, J. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e02-08-0499 · Cited by 796 · see citing works
Görner, W., Durchschlag, E., Martínez‐Pastor, M. T., Estruch, F., Ammerer, G., Hamilton, B., Ruis, H., & Schüller, C. (1998) · Genes & Development · doi:10.1101/gad.12.4.586 · Cited by 758 · see citing works
Self-citationNosocomial 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
Transcriptional Response of <i>Candida albicans</i> upon Internalization by Macrophages
Lorenz, M. C., Bender, J. A., & Fink, G. R. (2004) · Eukaryotic Cell · doi:10.1128/ec.3.5.1076-1087.2004 · Cited by 712 · see citing works
Stuart, L. M., & Ezekowitz, R. A. B. (2005) · Immunity · doi:10.1016/j.immuni.2005.05.002 · Cited by 667 · see citing works
Bakers' Yeast, a Model for Fungal Biofilm Formation
Reynolds, T. B., & Fink, G. R. (2001) · Science · doi:10.1126/science.291.5505.878 · Cited by 585 · see citing works
Pfaller, M. A., & Diekema, D. J. (2004) · Clinical Microbiology and Infection · doi:10.1111/j.1470-9465.2004.t01-1-00844.x · Cited by 422 · 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
Contributions of hyphae and hypha-co-regulated genes to Candida albicans virulence
Kumamoto, C. A., & Vinces, M. D. (2005) · Cellular Microbiology · doi:10.1111/j.1462-5822.2005.00616.x · Cited by 388 · see citing works
Cormack, B. P., Ghori, N., & Falkow, S. (1999) · Science · doi:10.1126/science.285.5427.578 · Cited by 383 · see citing works
Enjalbert, B., Smith, D. A., Cornell, M. J., Alam, I., Nicholls, S., Brown, A. J. P., & Quinn, J. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-06-0501 · Cited by 381 · see citing works
Alonso-Monge, R., Navarro-García, F., Molero, G., Diez-Orejas, R., Gustin, M., Pla, J., Sánchez, M., & Nombela, C. (1999) · Journal of Bacteriology · doi:10.1128/jb.181.10.3058-3068.1999 · Cited by 344 · see citing works
Stress-activated Genomic Expression Changes Serve a Preparative Role for Impending Stress in Yeast
Berry, D. B., & Gasch, A. P. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-07-0680 · Cited by 326 · see citing works
Control of pseudohyphae formation inSaccharomyces cerevisiae
Gancedo, J. M. (2001) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2001.tb00573.x · Cited by 317 · see citing works
Görner, W., Durchschlag, E., Wolf, J., Brown, E. L., Ammerer, G., Ruis, H., & Schüller, C. (2002) · The EMBO Journal · doi:10.1093/emboj/21.1.135 · Cited by 300 · see citing works
Self-citationFerrari, S., Ischer, F., Calabrese, D., Posteraro, B., Sanguinetti, M., Fadda, G., Rohde, B., Bauser, C., Bader, O., & Sanglard, D. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000268 · Cited by 295 · see citing works
Fungal—bacterial interactions: a mixed bag of mingling microbes
Wargo, M. J., & Hogan, D. A. (2006) · Current Opinion in Microbiology · doi:10.1016/j.mib.2006.06.001 · Cited by 286 · see citing works
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
Stress-induced Gene Expression inCandida albicans: Absence of a General Stress Response
Enjalbert, B., Nantel, A., & Whiteway, M. S. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e02-08-0546 · Cited by 277 · 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
De Las Peñas, A., Pan, S.-J., Castaño, I., Alder, J., Cregg, R., & Cormack, B. P. (2003) · Genes & Development · doi:10.1101/gad.1121003 · Cited by 268 · see citing works
Frohner, I. E., Bourgeois, C., Yatsyk, K., Majer, O., & Kuchler, K. (2008) · Molecular Microbiology · doi:10.1111/j.1365-2958.2008.06528.x · Cited by 267 · see citing works
Smith, D. A., Nicholls, S., Morgan, B. A., Brown, A. J. P., & Quinn, J. (2004) · Molecular Biology of the Cell · doi:10.1091/mbc.e04-03-0181 · Cited by 263 · 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
Sanglard, D., Ischer, F., & Bille, J. (2001) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.45.4.1174-1183.2001 · Cited by 247 · see citing works
Acquisition of prokaryotic genes by fungal genomes
Marcet‐Houben, M., & Gabaldón, T. (2009) · Trends in Genetics · doi:10.1016/j.tig.2009.11.007 · Cited by 241 · see citing works
Self-citationVermitsky, J., Earhart, K. D., Smith, W. L., Homayouni, R., Edlind, T. D., & Rogers, P. D. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2006.05235.x · Cited by 233 · see citing works
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
Kvaal, C. A., Lachke, S. A., Srikantha, T., Daniels, K. J., McCoy, J. W., & Soll, D. R. (1999) · Infection and Immunity · doi:10.1128/iai.67.12.6652-6662.1999 · Cited by 221 · see citing works
Hu, G., Hacham, M., Waterman, S. R., Panepinto, J. C., Shin, S., Liu, X., Gibbons, J. T., Vályi-Nagy, T., Obara, K., Jaffe, H. A., et al. (2008) · Journal of Clinical Investigation · doi:10.1172/jci32053 · Cited by 219 · see citing works
Comparative genomics of the environmental stress response in ascomycete fungi
Gasch, A. P. (2007) · Yeast · doi:10.1002/yea.1512 · Cited by 210 · see citing works
Formation of new chromosomes as a virulence mechanism in yeast <i>Candida glabrata</i>
Poláková, S., Blume, C., Zárate, J. Á., Mentel, M., Jørck-Ramberg, D., Stenderup, J., & Piškur, J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809793106 · Cited by 206 · see citing works
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
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
Cryptococcus neoformansGene Expression during Murine Macrophage Infection
Fan, W., Kraus, P. R., Boily, M.-J., & Heitman, J. (2005) · Eukaryotic Cell · doi:10.1128/ec.4.8.1420-1433.2005 · Cited by 186 · see citing works
Immune responses to commensal and environmental microbes
Pamer, E. G. (2007) · Nature Immunology · doi:10.1038/ni1526 · Cited by 169 · 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
Klionsky, D. J. (2005) · Current Biology · doi:10.1016/j.cub.2005.04.013 · Cited by 163 · see citing works
Schüller, C., Mamnun, Y. M., Mollapour, M., Krapf, G., Schuster, M., BAUER, B. E., Piper, P. W., & Kuchler, K. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e03-05-0322 · Cited by 160 · see citing works
Self-citationKvaal, C. A., Srikantha, T., & Soll, D. R. (1997) · Infection and Immunity · doi:10.1128/iai.65.11.4468-4475.1997 · Cited by 146 · 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
Self-citationNicholls, S., Straffon, M. J., Enjalbert, B., Nantel, A., Macaskill, S., Whiteway, M. S., & Brown, A. J. P. (2004) · Eukaryotic Cell · doi:10.1128/ec.3.5.1111-1123.2004 · Cited by 140 · 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
Skin Facilitates Candida albicans Mating
Lachke, S. A., Lockhart, S. R., Daniels, K. J., & Soll, D. R. (2003) · Infection and Immunity · doi:10.1128/iai.71.9.4970-4976.2003 · Cited by 127 · see citing works
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
Roetzer, A., Gregori, C., Jennings, A. M., Quintin, J., Ferrandon, D., Butler, G., Kuchler, K., Ammerer, G., & Schüller, C. (2008) · Molecular Microbiology · doi:10.1111/j.1365-2958.2008.06301.x · Cited by 124 · see citing works
Self-citationWong, S., Fares, M. A., Zimmermann, W., Butler, G., & Wolfe, K. H. (2003) · Genome biology · doi:10.1186/gb-2003-4-2-r10 · Cited by 113 · see citing works
Epidemiology of invasive fungal infection
Castón, J. J., Rivero, A., & Torre‐Cisneros, J. (2008) · International Journal of Antimicrobial Agents · doi:10.1016/s0924-8579(08)70009-8 · Cited by 105 · see citing works
Stress signalling to fungal stress-activated protein kinase pathways
Smith, D. A., Morgan, B. A., & Quinn, J. (2010) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2010.01937.x · Cited by 105 · see citing works
Phenotypic switching and filamentation in Candida glabrata
Lachke, S. A., Joly, S., Daniels, K., & Soll, D. R. (2002) · Microbiology · doi:10.1099/00221287-148-9-2661 · Cited by 103 · see citing works
Evolutionary Genomics: Yeasts Accelerate beyond BLAST
Wolfe, K. H. (2004) · Current Biology · doi:10.1016/j.cub.2004.05.015 · Cited by 89 · see citing works
Live Candida albicans Suppresses Production of Reactive Oxygen Species in Phagocytes
Wellington, M. A., Dolan, K., & Krysan, D. J. (2008) · Infection and Immunity · doi:10.1128/iai.00860-08 · Cited by 89 · see citing works
Butler, G. (2010) · Clinical Microbiology Reviews · doi:10.1128/cmr.00053-09 · Cited by 87 · 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
Marcet-Houben, M., & Gabaldón, T. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004357 · Cited by 83 · see citing works
Self-citationWhat makes pathogens pathogenic
Ehrlich, G. D., Hiller, N. L., & Hu, F. Z. (2008) · Genome biology · doi:10.1186/gb-2008-9-6-225 · Cited by 83 · see citing works
The Anatomy of Mucosal Immune Responses
Garside, P., Millington, O. R., & SMITH, K. M. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1309.002 · Cited by 76 · see citing works
Kamran, M., Calcagno, A.-M., Findon, H., Bignell, E., Jones, M. D., Warn, P., Hopkins, P., Denning, D. W., Butler, G., Rogers, T., et al. (2004) · Eukaryotic Cell · doi:10.1128/ec.3.2.546-552.2004 · Cited by 75 · see citing works
Phenotypic Switching and Mating Type Switching of <i>Candida glabrata</i> at Sites ofColonization
Brockert, P. J., Lachke, S. A., Srikantha, T., Pujol, C., Galask, R., & Soll, D. R. (2003) · Infection and Immunity · doi:10.1128/iai.71.12.7109-7118.2003 · Cited by 75 · see citing works
Retrograde regulation of multidrug resistance in Saccharomyces cerevisiae
Moye-Rowley, S. (2005) · Gene · doi:10.1016/j.gene.2005.03.019 · Cited by 74 · see citing works
Calcagno-Pizarelli, A. M., Bignell, E., Warn, P. A., Jones, M. D., Denning, D. W., Mühlschlegel, F. A., Rogers, T. R., & Haynes, K. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03755.x · Cited by 70 · see citing works
Intracellular pathogenic bacteria and fungi — a case of convergent evolution?
Bliska, J. B., & Casadevall, A. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro2049 · Cited by 65 · see citing works
Gregori, C., Schüller, C., Roetzer, A., Schwarzmüller, T., Ammerer, G., & Kuchler, K. (2007) · Eukaryotic Cell · doi:10.1128/ec.00106-07 · Cited by 57 · see citing works
Self-citationAnisimova, M. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9074-0 · Cited by 56 · see citing works
Assimilation of NAD + precursors in Candida glabrata
Ma, B., Pan, S., Zupancic, M. L., & Cormack, B. P. (2007) · Molecular Microbiology · doi:10.1111/j.1365-2958.2007.05886.x · Cited by 54 · see citing works
Early prediction of Candida glabrata fungemia in nonneutropenic critically ill patients*
Cohen, Y., Karoubi, P., Adrie, C., Gauzit, R., Marsepoil, T., Zarka, D., & Clec’h, C. (2010) · Critical Care Medicine · doi:10.1097/ccm.0b013e3181cc4734 · Cited by 48 · see citing works
MacCallum, D. M., Findon, H., Kenny, C. C., Butler, G., Haynes, K., & Odds, F. C. (2006) · Infection and Immunity · doi:10.1128/iai.00817-06 · Cited by 45 · see citing works
Expression of Candida glabrata Adhesins after Exposure to Chemical Preservatives
Mundy, R. D., & Cormack, B. P. (2009) · The Journal of Infectious Diseases · doi:10.1086/599120 · Cited by 43 · 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
Hof, H. (2009) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-009-0822-5 · Cited by 31 · see citing works
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
Impact of the transcriptional regulator, Ace2, on the Candida glabrata secretome
Stead, D., Walker, J., Holcombe, L. J., Gibbs, S. R. S., Yin, Z., Selway, L., Butler, G., Brown, A. J. P., & Haynes, K. (2009) · PROTEOMICS · doi:10.1002/pmic.200800706 · Cited by 29 · see citing works
Ma, B., Pan, S., Domergue, R., Rigby, T., Whiteway, M. S., Johnson, D., & Cormack, B. P. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.01461-08 · Cited by 29 · see citing works
Calcagno-Pizarelli, A. M., Bignell, E., Rogers, T. R., Jones, M. D., Mühlschlegel, F. A., & Haynes, K. (2005) · Medical Mycology · doi:10.1080/13693780400006088 · Cited by 25 · see citing works
Dark brown is the more virulent of the switch phenotypes of Candida glabrata
Srikantha, T., Daniels, K. J., Wu, W., Lockhart, S. R., Song, Y., Sahni, N., Ma, N., & Soll, D. R. (2008) · Microbiology · doi:10.1099/mic.0.2008/020578-0 · Cited by 24 · see citing works
Hogan, D. A., & Kolter, R. (2014) · ASM Press eBooks · doi:10.1128/9781555815776.ch19 · Cited by 8 · see citing works
Bennett, J. W., & Feibelman, T. P. (2001) · Springer eBooks · doi:10.1007/978-3-662-07334-6_13 · Cited by 8 · see citing works
Karanasios, E., & Ktistakis, N. T. (2016) · Springer eBooks · doi:10.1007/978-3-319-33145-4_4 · Cited by 2 · see citing works
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Free, S. J. (2013) · Advances in Genetics · doi:10.1016/b978-0-12-407677-8.00002-6 · Cited by 576 · see citing works
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Rodrigues, C. F., Silva, S., & Henriques, M. (2014) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-013-2009-3 · Cited by 268 · see citing works
Comparative genomics of emerging pathogens in the Candida glabrata clade.
Gabaldón, T., Martin, T., Marcet-Houben, M., Durrens, P., Bolotin-Fukuhara, M., Lespinet, O., Arnaise, S., Boisnard, S., Aguileta, G., Atanasova, R., et al. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-623 · Cited by 198 · see citing works
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Hassan, Y., Chew, S. Y., & Than, L. T. L. (2021) · Journal of Fungi · doi:10.3390/jof7080667 · Cited by 170 · see citing works
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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
Katiyar, S. K., Alastruey-Izquierdo, A., Healey, K. R., Johnson, M. E., Perlin, D. S., & Edlind, T. D. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00813-12 · Cited by 148 · see citing works
Hull, C. M., Parker, J. E., Bader, O., Weig, M., Gross, U., Warrilow, A. G. S., Kelly, D. E., & Kelly, S. L. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.06253-11 · Cited by 113 · see citing works
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Gabaldón, T., Naranjo-Ortíz, M. A., & Marcet-Houben, M. (2016) · FEMS Yeast Research · doi:10.1093/femsyr/fow064 · Cited by 105 · see citing works
Self-citationGabaldón, T., & Carreté, L. (2016) · FEMS Yeast Research · doi:10.1093/femsyr/fov110 · Cited by 99 · see citing works
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Cuéllar-Cruz, M., López-Romero, E., Villagómez-Castro, J. C., & Ruiz-Baca, E. (2012) · Future Microbiology · doi:10.2217/fmb.12.48 · Cited by 80 · see citing works
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
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
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Vale-Silva, L., Beaudoing, E., Tran, V. D. T., & Sanglard, D. (2017) · G3 Genes|Genomes|Genetics · doi:10.1534/g3.117.042887 · Cited by 61 · see citing works
Carreté, L., Ksiezopolska, E., Gómez-Molero, E., Angoulvant, A., Bader, O., Fairhead, C., & Gabaldón, T. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00112 · Cited by 58 · see citing works
Self-citationRasheed, M., Battu, A., & Kaur, R. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.813741 · Cited by 51 · 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
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Riera, M., Mogensen, E., d’Enfert, C., & Janbon, G. (2012) · Research in Microbiology · doi:10.1016/j.resmic.2012.02.005 · Cited by 43 · see citing works
Costa, C., Ribeiro, J., Miranda, I. M., Silva-Dias, A., Cavalheiro, M., Costa-de-Oliveira, S., Rodrigues, A. G., & Teixeira, M. C. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00526 · Cited by 43 · see citing works
Sorbic acid stress activates the Candida glabrata high osmolarity glycerol MAP kinase pathway
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Self-citationShor, E., Schuyler, J., & Perlin, D. S. (2019) · mBio · doi:10.1128/mbio.00120-19 · Cited by 19 · see citing works
Sharma, V., Purushotham, R., & Kaur, R. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.751529 · Cited by 22 · see citing works
Kounatidis, I., Ames, L., Mistry, R., Ho, H.-L., Haynes, K., & Ligoxygakis, P. (2018) · G3 Genes Genomes Genetics · doi:10.1534/g3.118.200182 · Cited by 13 · see citing works
Tanaka, Y., Sasaki, M., Ito, F., Aoyama, T., Sato-Okamoto, M., Takahashi-Nakaguchi, A., Chibana, H., & Shibata, N. (2018) · Fungal Biology · doi:10.1016/j.funbio.2017.09.007 · Cited by 13 · see citing works
Life-history strategies and carbon metabolism gene dosage in the<i>Nakaseomyces</i>yeasts
Legrand, J., Bolotin-Fukuhara, M., Bourgais, A., Fairhead, C., & Sicard, D. (2016) · FEMS Yeast Research · doi:10.1093/femsyr/fov112 · Cited by 8 · see citing works
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
- Authors
- Roetzer, A., Gabaldón, T., & Schüller, C.
- Affiliations
- University of Vienna (AT)
- Centre for Genomic Regulation (ES)
- Corresponding author
- Schüller, Christoph
- Venue
- FEMS Microbiology Letters
- Publisher
- Oxford University Press (OUP)
- Published
- 2010-09-16
- Volume
- 314
- Issue
- 1
- Pages
- 1-9
- ISSN
- 0378-1097 (ISSN-L)
- PMC
- PMC3015064
- OpenAlex
- W1941779326
- Cited by
- 154
- References
- 82
- Citations by year
- 2026: 11 · 2025: 8 · 2024: 7 · 2023: 11 · 2022: 10 · 2021: 8 · 2020: 7 · 2019: 12 · 2018: 11 · 2017: 4 · 2016: 16 · 2015: 14 · 2014: 13 · 2013: 11 · 2012: 9
- FWCI
- 2.86
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- FEMS Microbiology Letters (publishedVersion)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- Austrian Science Fund
- Universität Wien (I031-B)
- Ministerio de Ciencia e Innovación
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Yeasts and Rust Fungi Studies
- Keywords
- Candida glabrata, Saccharomyces cerevisiae, opportunistic fungal pathogens, host adaptation, adhesin genes, antifungal resistance, starvation resistance, fungal evolution
- MeSH terms
- Adaptation, Physiological, Animals, Candidiasis, Fungal Proteins, Humans, Phylogeny, Saccharomyces cerevisiae, Gene Expression Regulation, Fungal, Candida glabrata
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