Candida albicans specializations for iron homeostasis: from commensalism to virulence
Open accessAbstract
Candida albicans is a fungal commensal-pathogen that persistently associates with its mammalian hosts. Between the commensal and pathogenic lifestyles, this microorganism inhabits host niches that differ markedly in the levels of bioavailable iron. A number of recent studies have exposed C. albicans specializations for acquiring iron from specific host molecules in regions where iron is scarce, while also defending against iron-related toxicity in regions where iron occurs in surfeit. Together, these results point to a central role for iron homeostasis in the evolution of this important human pathogen.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Elevated concentrations of hepcidin increase iron sequestration by macrophages and decrease duodenal iron absorption during inflammatory reactions, thus reducing plasma iron levels.
“Elevated concentrations of hepcidin increase iron sequestration by macrophages and decrease duodenal iron absorption during inflammatory reactions and thus reduces plasma iron levels (Cassat and Skaar, 2013; Noble, 2013).”
From Iron at the Centre of Candida albicans Interactions (2018) · cites this paper as Noble, 2013
In “Mechanisms of iron acquisition in the bloodstream” (page unavailable), Noble says inflammatory responses reduce serum iron through decreased intestinal absorption and retention within reticuloendothelial cells. The passage does not identify elevated hepcidin as the cause or specify duodenal absorption and macrophages. (LLM, conf=0.86)
Experimental — accuracy not yet measuredIron ions regulate hyphal development and morphological transitions by modulating key transcription factors, including Sef1, Hap43, and Sfu1.
“They regulate hyphal development and morphological transitions by modulating key transcription factors, including Sef1, Hap43, and Sfu1 (Noble 2013; Singh et al. 2011).”
From Aloe emodin disrupts Candida albicans mitochondrial iron homeostasis against its hyphal development and oral candidiasis (2026) · cites this paper as Noble 2013
The section ‘Defense against iron excess in the gut’ describes iron-dependent regulation involving Sef1, Hap43, and Sfu1. But ‘From iron homeostasis to developmental switches’ says further experiments are needed to determine whether iron levels trigger the developmental transition; it does not establish that these factors regulate hyphal development. (LLM, conf=0.87)
Experimental — accuracy not yet measuredC. albicans has evolved a complex regulatory program for iron uptake that operates in both commensal and pathogenic states.
“Thus, C. albicans has evolved an intricate transcriptional program to regulate iron acquisition during commensal or pathogenic states [91].”
From Buried Treasure: Evolutionary Perspectives on Microbial Iron Piracy (2015) · cites this paper as [91]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Wisplinghoff, H., Bischoff, T., Tallent, S. M., Seifert, H., Wenzel, R. P., & Edmond, M. B. (2004) · Clinical Infectious Diseases · doi:10.1086/421946 · Cited by 4,496 · see citing works
Andrews, N. C. (1999) · New England Journal of Medicine · doi:10.1056/nejm199912233412607 · Cited by 2,130 · see citing works
Nosocomial Bloodstream Infections in United States Hospitals: A Three‐Year Analysis
Edmond, M. B., Wallace, S. E., McClish, D. K., Pfaller, M. A., Jones, R. N., & Wenzel, R. P. (1999) · Clinical Infectious Diseases · doi:10.1086/520192 · Cited by 1,387 · see citing works
Enterobactin: an archetype for microbial iron transport.
Raymond, K. N., Dertz, E. A., & Kim, S. S. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0630018100 · Cited by 933 · see citing works
Chemistry and biology of eukaryotic iron metabolism
Aisen, P. (2001) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/s1357-2725(01)00063-2 · Cited by 804 · see citing works
Genetics and Assembly Line Enzymology of Siderophore Biosynthesis in Bacteria
Crosa, J. H., & Walsh, C. T. (2002) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.66.2.223-249.2002 · Cited by 797 · see citing works
The Battle for Iron between Bacterial Pathogens and Their Vertebrate Hosts
Skaar, E. P. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000949 · Cited by 796 · see citing works
Zaoutis, T. E., Argon, J., Chu, J., Berlin, J. A., Walsh, T. J., & Feudtner, C. (2005) · Clinical Infectious Diseases · doi:10.1086/496922 · Cited by 784 · see citing works
Blumberg, H. M., Jarvis, W. R., Soucie, J. M., Edwards, J. E., Patterson, J. E., Pfaller, M. A., Rangel‐Frausto, M. S., Rinaldi, M. G., Saiman, L., Wiblin, R. T., et al. (2001) · Clinical Infectious Diseases · doi:10.1086/321811 · Cited by 661 · see citing works
Hajjeh, R. A., Sofair, A. N., Harrison, L. H., Lyon, G. M., Arthington-Skaggs, B. A., Mirza, S. A., Phelan, M., Morgan, J., Lee-Yang, W., Ciblak, M. A., et al. (2004) · Journal of Clinical Microbiology · doi:10.1128/jcm.42.4.1519-1527.2004 · Cited by 649 · 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
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
Critical Role of Bcr1-Dependent Adhesins in C. albicans Biofilm Formation In Vitro and In Vivo
Nobile, C. J., Andes, D. R., Nett, J. E., Smith, F. J., Yue, F., Phan, Q.-T., Edwards, J. E., Filler, S. G., & Mitchell, A. P. (2006) · PLoS Pathogens · doi:10.1371/journal.ppat.0020063 · Cited by 507 · see citing works
Komshian, S. V., Uwaydah, A. K., Sobel, J. D., & Crane, L. R. (1989) · Clinical Infectious Diseases · doi:10.1093/clinids/11.3.379 · Cited by 456 · see citing works
A Phenotypic Profile of the Candida albicans Regulatory Network
Homann, O. R., Dea, J., Noble, S. M., & Johnson, A. D. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000783 · Cited by 444 · see citing works
Self-citationRisk Factors for Hospital-Acquired Candidemia: A Matched Case-Control Study
Wey, S. B. (1989) · Archives of Internal Medicine · doi:10.1001/archinte.1989.00390100145030 · Cited by 369 · see citing works
Nutritional Immunity: Host's Attempt to Withhold Iron From Microbial Invaders
Weinberg, E. D. (1975) · JAMA · doi:10.1001/jama.1975.03240130021018 · Cited by 342 · see citing works
A High-Affinity Iron Permease Essential for <i>Candida albicans</i> Virulence
Ramanan, N., & Wang, Y. (2000) · Science · doi:10.1126/science.288.5468.1062 · Cited by 336 · cited 1× · see citing works
“Of the two ferric permeases, only Ftr1 is expressed when iron is scarce, and FTR1 is essential in a murine bloodstream infection model of virulence [34].”
Haas, H. (2003) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-003-1335-2 · Cited by 334 · see citing works
Molecular mechanisms of iron uptake in fungi
Kosman, D. J. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03368.x · Cited by 331 · see citing works
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
Chen, C., Pande, K., French, S. D., Tuch, B. B., & Noble, S. M. (2011) · Cell Host & Microbe · doi:10.1016/j.chom.2011.07.005 · Cited by 314 · see citing works
Self-citationPande, K., Chen, C., & Noble, S. M. (2013) · Nature Genetics · doi:10.1038/ng.2710 · Cited by 306 · see citing works
Self-citationRIM101-Dependent and -Independent Pathways Govern pH Responses in Candida albicans
Davis, D. A., Wilson, R. B., & Mitchell, A. P. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.3.971-978.2000 · Cited by 285 · see citing works
HapX-Mediated Adaption to Iron Starvation Is Crucial for Virulence of Aspergillus fumigatus
Schrettl, M., Beckmann, N., Varga, J., Heinekamp, T., Jacobsen, I. D., Jöchl, C., Moussa, T. A., Wang, S., Gsaller, F., Blatzer, M., et al. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1001124 · Cited by 284 · see citing works
<i>Candida</i> Species Exhibit Differential In Vitro Hemolytic Activities
Luo, G., Samaranayake, L. P., & Yau, J. Y. Y. (2001) · Journal of Clinical Microbiology · doi:10.1128/jcm.39.8.2971-2974.2001 · Cited by 282 · see citing works
Candida albicans RIM101 pH Response Pathway Is Required for Host-Pathogen Interactions
Davis, D. A., Edwards, J. E., Mitchell, A. P., & Ibrahim, A. S. (2000) · Infection and Immunity · doi:10.1128/iai.68.10.5953-5959.2000 · Cited by 276 · see citing works
P HYSIOLOGY AND M OLECULAR B IOLOGY OF D IETARY I RON A BSORPTION
Miret, S., Simpson, R. J., & McKie, A. T. (2003) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.23.011702.073139 · Cited by 269 · see citing works
Iron and activated oxygen species in biology: The basic chemistry
Pierre, J. L., & Fontecave, M. (1999) · Biometals · doi:10.1023/a:1009252919854 · Cited by 263 · see citing works
Production of a Hemolytic Factor by Candida albicans
Manns, J. M., Mosser, D. M., & Buckley, H. R. (1994) · Infection and Immunity · doi:10.1128/iai.62.11.5154-5156.1994 · Cited by 258 · see citing works
Zhao, X., Oh, S.-H., Cheng, G., Green, C. B., Nuessen, J. A., Yeater, K., Leng, R. P., Brown, A. J. P., & Hoyer, L. L. (2004) · Microbiology · doi:10.1099/mic.0.26943-0 · Cited by 254 · see citing works
Bensen, E. S., Martin, S. J., Li, M., Berman, J. G., & Davis, D. A. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04350.x · Cited by 251 · see citing works
Regulatory networks affected by iron availability in <i>Candida albicans</i>
Lan, C., Rodarte, G., Murillo, L. A., Jones, T., Davis, R. W., Dungan, J., Newport, G., & Agabian, N. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04214.x · 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
Weissman, Z., & Kornitzer, D. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04199.x · Cited by 231 · see citing works
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
Jung, W. H., Sham, A. P., White, R., & Kronstad, J. W. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040410 · Cited by 222 · 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
Regulation of reticuloendothelial iron transporter MTP1 (Slc11a3) by inflammation
Yang, F., Liu, X.-B., Quinones, M., Melby, P. C., Ghio, A., & Haile, D. J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m201485200 · Cited by 197 · see citing works
Candida albicans Als3p is required for wild-type biofilm formation on silicone elastomer surfaces.
Zhao, X.-M., Daniels, K., Oh, S.-H., Green, C. B., Yeater, K., Soll, D., & Hoyer, L. (2006) · Microbiology · doi:10.1099/mic.0.28959-0 · Cited by 188 · see citing works
Ramón, A., Porta, A., & Fonzi, W. A. (1999) · Journal of Bacteriology · doi:10.1128/jb.181.24.7524-7530.1999 · Cited by 174 · see citing works
Haas, H., Zadra, I., Stöffler, G., & Angermayr, K. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.8.4613 · Cited by 168 · see citing works
Hepcidin is the major predictor of erythrocyte iron incorporation in anemic African children
Prentice, A. M., Doherty, C. P., Abrams, S. A., Cox, S. E., Atkinson, S. H., Verhoef, H., Armitage, A. E., & Drakesmith, H. (2012) · Blood · doi:10.1182/blood-2011-11-391219 · Cited by 167 · see citing works
Chemistry for an essential biological process: the reduction of ferric iron
Pierre, J. L., Fontecave, M., & Crichton, R. R. (2002) · Biometals · doi:10.1023/a:1020259021641 · Cited by 163 · see citing works
Natural resistance, iron and infection: a challenge for clinical medicine
Bullen, J. J., Rogers, H. J., Spalding, P. B., & Ward, C. G. (2006) · Journal of Medical Microbiology · doi:10.1099/jmm.0.46386-0 · Cited by 163 · see citing works
Hsu, P.-C., Yang, C.-Y., & Lan, C.-Y. (2011) · Eukaryotic Cell · doi:10.1128/ec.00158-10 · Cited by 157 · see citing works
Jung, W. H., Saikia, S., Hu, G., Wang, J., Fung, C. K.-Y., D'Souza, C., White, R., & Kronstad, J. W. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1001209 · Cited by 155 · see citing works
Nobile, C. J., Solis, N., Myers, C. L., Fay, A. J., Deneault, J.-S., Nantel, A., Mitchell, A. P., & Filler, S. G. (2008) · Cellular Microbiology · doi:10.1111/j.1462-5822.2008.01198.x · Cited by 150 · see citing works
Reductive iron uptake by Candida albicans: role of copper, iron and the TUP1 regulator
Knight, S. A. B., Lesuisse, E., Stearman, R., Klausner, R. D., & Dancis, A. (2002) · Microbiology · doi:10.1099/00221287-148-1-29 · Cited by 145 · 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
Haemin uptake and use as an iron source by Candida albicans: role of CaHMX1-encoded haem oxygenase
Santos, R., Buisson, N., Knight, S., Dancis, A., Camadro, J.-M., & Lesuisse, E. (2003) · Microbiology · doi:10.1099/mic.0.26108-0 · Cited by 139 · see citing works
An endocytic mechanism for haemoglobin‐iron acquisition in <i>Candida albicans</i>
Weissman, Z., Shemer, R., Conibear, E., & Kornitzer, D. (2008) · Molecular Microbiology · doi:10.1111/j.1365-2958.2008.06277.x · Cited by 127 · see citing works
Microbial Inhabitants of Humans
Wilson, M. A. (2004) · Cambridge University Press eBooks · doi:10.1017/cbo9780511735080 · Cited by 126 · see citing works
Fep1, an Iron Sensor Regulating Iron Transporter Gene Expression in Schizosaccharomyces pombe
Pelletier, B., Beaudoin, J., Mukai, Y., & Labbé, S. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m202682200 · Cited by 125 · see citing works
Miethke, M. (2012) · Metallomics · doi:10.1039/c2mt20193c · Cited by 121 · see citing works
Hydroxamate siderophore production by opportunistic and systemic fungal pathogens
Holzberg, M., & Artis, W. M. (1983) · Infection and Immunity · doi:10.1128/iai.40.3.1134-1139.1983 · Cited by 118 · see citing works
Voisard, C., Wang, J., Mcevoy, J. L., Xu, P., & Leong, S. A. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.11.7091 · Cited by 116 · see citing works
Singh, R. P., Prasad, H. K., Sinha, I., Agarwal, N., & Natarajan, K. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.233569 · Cited by 113 · see citing works
Heymann, P., Ernst, J. F., & Winkelmann, G. ⁄. N. (2000) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2000.tb09108.x · Cited by 113 · 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
Baek, Y.-U., Li, M., & Davis, D. A. (2008) · Eukaryotic Cell · doi:10.1128/ec.00108-08 · Cited by 109 · see citing works
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
Hu, C.-J., Bai, C., Zheng, X.-D., Wang, Y.-M., & Wang, Y. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m204545200 · Cited by 97 · see citing works
Weissman, Z., Shemer, R., & Kornitzer, D. (2002) · Molecular Microbiology · doi:10.1046/j.1365-2958.2002.02976.x · Cited by 88 · see citing works
Zhou, L., Haas, H., & Marzluf, G. A. (1998) · Molecular and General Genetics MGG · doi:10.1007/s004380050845 · Cited by 86 · see citing works
Larson, J. A., Howie, H. L., & So, M. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04169.x · Cited by 85 · see citing works
Chen, C., & Noble, S. M. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002956 · Cited by 83 · see citing works
Self-citationSoloviev, D. A., Fonzi, W. A., Sentandreu, R., Pluskota, E., Forsyth, C. B., Yadav, S. P., & Plow, E. F. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.4.2038 · Cited by 82 · see citing works
A role for complement receptor-like molecules in iron acquisition by Candida albicans
Moors, M. A., Stull, T. L., Blank, K. J., Buckley, H. R., & Mosser, D. M. (1992) · The Journal of experimental medicine · doi:10.1084/jem.175.6.1643 · Cited by 80 · see citing works
Hammacott, J. E., Williams, P. H., & Cashmore, A. M. (2000) · Microbiology · doi:10.1099/00221287-146-4-869 · Cited by 69 · see citing works
Siderophore production by the pathogenic yeast, Candida albicans
Ismail, A., Bedell, G. W., & Lupan, D. M. (1985) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(85)90499-1 · Cited by 63 · see citing works
Chao, L. Y., Marletta, M. A., & Rine, J. (2008) · Biochemistry · doi:10.1021/bi800066s · Cited by 63 · see citing works
Zipfel, P. F., Skerka, C., Kupka, D., & Luo, S. (2011) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2011.04.010 · Cited by 63 · see citing works
Haas, H., Angermayr, K., & Stöffler, G. (1997) · Gene · doi:10.1016/s0378-1119(96)00570-7 · Cited by 57 · see citing works
Cleary, I. A., Reinhard, S. M., Miller, C. L., Murdoch, C., Thornhill, M. H., Lazzell, A. L., Monteagudo, C. C., Thomas, D. P., & Saville, S. P. (2011) · Microbiology · doi:10.1099/mic.0.046326-0 · Cited by 55 · see citing works
Ziegler, L., Terzulli, A., Gaur, R., McCarthy, R., & Kosman, D. J. (2011) · Molecular Microbiology · doi:10.1111/j.1365-2958.2011.07704.x · Cited by 53 · see citing works
Novel insight into the expression and function of the multicopper oxidases in Candida albicans
Cheng, X., Xu, N., Yu, Q., Ding, X., Qian, K., Zhao, Q., Wang, Y., Zhang, B., Xing, L., & Li, M. (2013) · Microbiology · doi:10.1099/mic.0.065268-0 · Cited by 41 · see citing works
Pelletier, B., Mercier, A., Durand, M., Peter, C., Jbel, M., Beaudoin, J., & Labbé, S. (2007) · Yeast · doi:10.1002/yea.1539 · Cited by 33 · see citing works
Miele, R., Barra, D., & di Patti, M. C. B. (2007) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2007.05.020 · Cited by 22 · see citing works
The gastrointestinal tract and its indigenous microbiota
Wilson, M. (2004) · Cambridge University Press eBooks · doi:10.1017/cbo9780511735080.008 · Cited by 9 · see citing works
Flagged first, then by citations
3 of the 83 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- [1]Odds FC Candida and Candidosis, a Review and Bibliography 2 London W.B. Saunders 1988
Cited by
Sorted by citations
The Spectrum of Fungi That Infects Humans
Kohler, J. R., Casadevall, A., & Perfect, J. (2015) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a019273 · Cited by 364 · see citing works
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
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
Fungal Strategies to Evade the Host Immune Recognition
Hernández-Chávez, M., Pérez-García, L., Niño-Vega, G., & Mora-Montes, H. (2017) · Journal of Fungi · doi:10.3390/jof3040051 · Cited by 173 · see citing works
Iron acquisition in fungal pathogens of humans
Bairwa, G., Jung, W. H., & Kronstad, J. W. (2017) · Metallomics · doi:10.1039/c6mt00301j · Cited by 151 · see citing works
Mixed consortia in bioprocesses: role of microbial interactions
Ghosh, S., Chowdhury, R., & Bhattacharya, P. (2016) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-016-7448-1 · Cited by 135 · see citing works
Iron at the Centre of Candida albicans Interactions
Fourie, R., Kuloyo, O. O., Mochochoko, B. M., Albertyn, J., & Pohl, C. H. (2018) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2018.00185 · Cited by 118 · see citing works
Li, C. X., Gleason, J. E., Zhang, S. X., Bruno, V. M., Cormack, B. P., & Culotta, V. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1513447112 · Cited by 121 · see citing works
Buried Treasure: Evolutionary Perspectives on Microbial Iron Piracy
Barber, M. F., & Elde, N. C. (2015) · Trends in Genetics · doi:10.1016/j.tig.2015.09.001 · Cited by 118 · see citing works
Amorim-Vaz, S., Tran, V. D. T., Pradervand, S., Pagni, M., Coste, A. T., & Sanglard, D. (2015) · mBio · doi:10.1128/mbio.00942-15 · Cited by 78 · see citing works
Iron–sulfur cluster signaling: The common thread in fungal iron regulation
Gupta, M., & Outten, C. E. (2020) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2020.02.008 · Cited by 70 · see citing works
Srivastava, V. K., Suneetha, K. J., & Kaur, R. (2014) · Biochemical Journal · doi:10.1042/bj20140598 · Cited by 69 · see citing works
Anticandidal Effect and Mechanisms of Monoterpenoid, Perillyl Alcohol against Candida albicans
Ansari, M. A., Fatima, Z., & Hameed, S. (2016) · PLoS ONE · doi:10.1371/journal.pone.0162465 · Cited by 66 · see citing works
Lapière, A., & Richard, M. L. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2105610 · Cited by 61 · see citing works
Copper-only superoxide dismutase enzymes and iron starvation stress in Candida fungal pathogens
Schatzman, S. S., Peterson, R. L., Teka, M., He, B., Cabelli, D. E., Cormack, B. P., & Culotta, V. C. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.011084 · Cited by 54 · see citing works
Savage, K. A., Parquet, M. D. C., Allan, D. S., Davidson, R. J., Holbein, B. E., Lilly, E. A., & Fidel, P. L. (2018) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02576-17 · Cited by 53 · see citing works
Koch, B., Barugahare, A. A., Lo, T. L., Huang, C., Schittenhelm, R. B., Powell, D. R., Beilharz, T. H., & Traven, A. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.10.080 · Cited by 50 · see citing works
Transferrin-mediated iron sequestration as a novel therapy for bacterial and fungal infections
Bruhn, K. W., & Spellberg, B. (2015) · Current Opinion in Microbiology · doi:10.1016/j.mib.2015.07.005 · Cited by 48 · see citing works
Adaptation of Candida Albicans to Commensalism in the Gut
Prieto, D., Correia, I., Plá, J., & Román, E. (2016) · Future Microbiology · doi:10.2217/fmb.16.1 · Cited by 48 · 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
Alves, V., Zamith‐Miranda, D., Frasés, S., & Nosanchuk, J. D. (2025) · Journal of Fungi · doi:10.3390/jof11020093 · Cited by 48 · see citing works
Xu, N., Dong, Y., Cheng, X., Yu, Q., Qian, K., Mao, J., Jia, C., Ding, X., Zhang, B., Chen, Y., et al. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.12.009 · Cited by 47 · see citing works
Adaptation to iron deficiency in human pathogenic fungi
Martínez‐Pastor, M. T., & Puig, S. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2020.118797 · Cited by 46 · see citing works
Znaidi, S., van Wijlick, L., Hernández-Cervantes, A., Sertour, N., Desseyn, J., Vincent, F., Atanasova, R., Gouyer, V., Munro, C. A., Bachellier‐Bassi, S., et al. (2018) · Cellular Microbiology · doi:10.1111/cmi.12890 · Cited by 45 · see citing works
Xu, N., Qian, K., Dong, Y., Chen, Y., Yu, Q., Zhang, B., Xing, L., & Li, M. (2014) · Research in Microbiology · doi:10.1016/j.resmic.2014.03.001 · Cited by 44 · see citing works
Pseudomonas phage inhibition of Candida albicans
Nazik, H., Joubert, L., Secor, P. R., Sweere, J. M., Bollyky, P. L., Sass, G., Cegelski, L., & Stevens, D. A. (2017) · Microbiology · doi:10.1099/mic.0.000539 · Cited by 44 · see citing works
Stanford, F. A., & Voigt, K. (2020) · Genes · doi:10.3390/genes11111296 · Cited by 43 · see citing works
Molecular basis of the regulation of iron homeostasis in fission and filamentous yeasts
Brault, A., Mourer, T., & Labbé, S. (2015) · IUBMB Life · doi:10.1002/iub.1441 · Cited by 37 · see citing works
The vaccines and antibodies associated with Als3p for treatment of Candida albicans infections.
Sui, X., Yan, L., & Jiang, Y.-Y. (2017) · Vaccine · doi:10.1016/j.vaccine.2017.08.082 · Cited by 31 · see citing works
Bhattarai, K., Bhattarai, K., Kabir, M. E., Bastola, R., & Baral, B. (2021) · Advances in genetics · doi:10.1016/bs.adgen.2020.11.006 · Cited by 32 · see citing works
Do, E., Cho, Y., Kim, D., Kronstad, J. W., & Jung, W. H. (2020) · Genetics · doi:10.1534/genetics.120.303270 · Cited by 32 · see citing works
Regulators of commensal and pathogenic life‐styles of an opportunistic fungus— Candida albicans
Rai, L. S., van Wijlick, L., Bougnoux, M., Bachellier‐Bassi, S., & d’Enfert, C. (2021) · Yeast · doi:10.1002/yea.3550 · Cited by 32 · see citing works
Zinc Cluster Transcription Factors Alter Virulence in Candida albicans
Issi, L., Farrer, R. A., Pastor, K., Landry, B. D., Delorey, T. M., Bell, G. W., Thompson, D. A., Cuomo, C. A., & Rao, R. P. (2016) · Genetics · doi:10.1534/genetics.116.195024 · Cited by 31 · see citing works
Large-Scale Chromosomal Changes and Associated Fitness Consequences in Pathogenic Fungi
Forche, A. (2014) · Current Fungal Infection Reports · doi:10.1007/s12281-014-0181-2 · Cited by 30 · see citing works
The regulation of iron homeostasis in the fungal human pathogen Candida glabrata
Devaux, F., & Thiébaut, A. (2019) · Microbiology · doi:10.1099/mic.0.000807 · Cited by 29 · see citing works
How much do we know about hemolytic capability of pathogenic Candida species?
Furlaneto, M. C., Góes, H. P., Perini, H. F., dos Santos, R. C., & Furlaneto-Maia, L. (2018) · Folia Microbiologica · doi:10.1007/s12223-018-0584-5 · Cited by 28 · see citing works
Chakraborty, T., Tóth, Z., Tóth, R., Vágvölgyi, C., & Gácser, A. (2020) · mSphere · doi:10.1128/msphere.00227-20 · Cited by 28 · see citing works
Padder, S. A., Ramzan, A., Tahir, I., Rehman, R. U., & Shah, A. H. (2022) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2021.1935447 · Cited by 27 · see citing works
An Immunomodulatory Peptide Confers Protection in an Experimental Candidemia Murine Model
de Freitas, C. G., Lima, S. M. D. F., Freire, M. S., Cantuária, A. P. D. C., Oliveira-Júnior, N. G., dos Santos, T. S., Folha, J. D. S., Ribeiro, S. M., Dias, S. C., Rezende, T. M. B., et al. (2017) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02518-16 · Cited by 27 · see citing works
Dong, Y., Zhang, D., Yu, Q., Zhao, Q., Xiao, C., Zhang, K., Jia, C., Chen, S., Zhang, B., Zhang, B., et al. (2017) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2017.01.021 · Cited by 26 · see citing works
Zinc and Iron Homeostasis: Target-Based Drug Screening as New Route for Antifungal Drug Development
Simm, C., & May, R. C. (2019) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2019.00181 · Cited by 26 · see citing works
Duval, C., Macabiou, C., Garcia, C., Lesuisse, E., Camadro, J., & Auchère, F. (2019) · MicrobiologyOpen · doi:10.1002/mbo3.970 · Cited by 24 · see citing works
Antivirulence and avirulence genes in human pathogenic fungi
Siscar-Lewin, S., Hube, B., & Brunke, S. (2019) · Virulence · doi:10.1080/21505594.2019.1688753 · Cited by 25 · see citing works
Assessing pH‐dependent activities of virulence factors secreted by Candida albicans
Ramos‐Pardo, A., Castro‐Álvarez, R., Quindós, G., Eraso, E., Sevillano, E., & Kaberdin, V. R. (2023) · MicrobiologyOpen · doi:10.1002/mbo3.1342 · Cited by 24 · see citing works
Klimek, K., Strubińska, J., Czernel, G., Ginalska, G., & Gagoś, M. (2016) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2016.06.022 · Cited by 23 · 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
Prieto, D., Román, E., Alonso‐Monge, R., & Plá, J. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00389 · Cited by 22 · see citing works
Romo, J. A., Zhang, H., Cai, H., Kadosh, D., Köhler, J. R., Saville, S. P., Wang, Y., & Lopez-Ribot, J. L. (2019) · mSphere · doi:10.1128/msphere.00620-19 · Cited by 20 · see citing works
Alkafeef, S. S., Lane, S., Yu, C., Zhou, T., Solis, N. V., Filler, S. G., Huang, L., & Liu, H. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1008881 · Cited by 22 · see citing works
Candida albicans requires iron to sustain hyphal growth
Luo, G., Wang, T., Zhang, J., Zhang, P., & Lu, Y. (2021) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2021.05.039 · Cited by 18 · see citing works
Overexpression approaches to advance understanding of Candida albicans
Rai, L. S., van Wijlick, L., Chauvel, M., d’Enfert, C., Legrand, M., & Bachellier‐Bassi, S. (2021) · Molecular Microbiology · doi:10.1111/mmi.14818 · Cited by 17 · see citing works
The intricate link between iron, mitochondria and azoles in Candida species
Genechten, W. V., Vergauwen, R., & Dijck, P. V. (2023) · FEBS Journal · doi:10.1111/febs.16977 · Cited by 19 · see citing works
Nair, R., Shariq, M., Dhamgaye, S., Mukhopadhyay, C. K., Shaikh, S., & Prasad, R. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2016.11.021 · Cited by 19 · see citing works
Köhler, J. R., Hube, B., Puccia, R., Casadevall, A., & Perfect, J. R. (2017) · ASM Press eBooks · doi:10.1128/9781555819583.ch39 · Cited by 16 · see citing works
Dhusia, K., Bajpai, A., & Ramteke, P. W. (2017) · Journal of Controlled Release · doi:10.1016/j.jconrel.2017.11.001 · Cited by 15 · see citing works
RetractedTUP1 -Mediated Filamentation in Candida Albicans Leads to Inability to Colonize the Mouse gut
Román, E., Huertas, B., Prieto, D., Diez‐Orejas, R., & Plá, J. (2018) · Future Microbiology · doi:10.2217/fmb-2018-0012 · Cited by 15 · see citing works
Hsu, P., Lu, T., Hung, P.-H., Jhou, Y., Amine, A. A. A., Liao, C., & Leu, J. (2021) · Molecular Biology and Evolution · doi:10.1093/molbev/msab192 · Cited by 15 · see citing works
Liu, S., Bu, Z., Zhang, X., Chen, Y., Sun, Q., Wu, F., Guo, S., Zhu, Y., & Tan, X. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.133216 · Cited by 14 · see citing works
Copper Availability Influences the Transcriptomic Response of Candida albicans to Fluconazole Stress
Hunsaker, E. W., Yu, C.-H. A., & Franz, K. J. (2021) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkab065 · Cited by 13 · see citing works
Román, E., Prieto, D., Hidalgo-Vico, S., Alonso‐Monge, R., & Plá, J. (2023) · Virulence · doi:10.1080/21505594.2023.2174294 · Cited by 13 · see citing works
Wangsanut, T., Ghosh, A. K., Metzger, P. G., Fonzi, W. A., & Rolfes, R. J. (2017) · mSphere · doi:10.1128/msphere.00161-17 · Cited by 12 · see citing works
van Wijlick, L., Znaidi, S., Hernández-Cervantes, A., Basso, V., Bachellier‐Bassi, S., & d’Enfert, C. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.960884 · Cited by 11 · see citing works
Souto, X. M., Ramos, L. S., Branquinha, M. H., & dos Santos, A. L. S. (2018) · Folia Microbiologica · doi:10.1007/s12223-018-0651-y · Cited by 11 · see citing works
Sahoo, B., Goyal, R., Dutta, S., Joshi, P., & Sanyal, K. (2025) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.5c00079 · Cited by 12 · see citing works
Fallah, S., Duncan, D., Reichl, K. D., Smith, M. J., Wang, W., Porco, J. A. J., Brown, L. E., Whitesell, L. J., Robbins, N., & Cowen, L. E. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.04095-23 · Cited by 10 · see citing works
Srivastav, M. K., Agarwal, N., Poonia, P., & Natarajan, K. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100727 · Cited by 8 · see citing works
Bypass of Dfi1 Regulation of Candida albicans Invasive Filamentation by Iron Limitation
Junier, A., Weeks, A., Alcaraz, Y., & Kumamoto, C. A. (2022) · mSphere · doi:10.1128/msphere.00779-21 · Cited by 8 · see citing works
Strain variation in the Candida albicans iron limitation response
Xiong, L., Goerlich, K., Do, E., & Mitchell, A. P. (2024) · mSphere · doi:10.1128/msphere.00372-24 · Cited by 8 · see citing works
Convergent Regulation of Candida albicans Aft2 and Czf1 in Invasive and Opaque Filamentation
Xu, N., Dong, Y., Yu, Q., Zhang, B., Zhang, M., Jia, C., Chen, Y., Zhang, B., Xing, L., & Li, M. (2015) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25146 · Cited by 8 · see citing works
The Glyoxylate Cycle Is Involved in White-Opaque Switching in Candida albicans
Hidalgo-Vico, S., Prieto, D., Alonso‐Monge, R., Román, E., & Plá, J. (2021) · Journal of Fungi · doi:10.3390/jof7070502 · Cited by 8 · see citing works
A response to iron involving carbon metabolism in the opportunistic fungal pathogen Candida albicans
Garg, R., Zhu, Z., Hernandez, F. G., Wang, Y., David, M. S., Bruno, V. M., & Culotta, V. (2025) · mSphere · doi:10.1128/msphere.00040-25 · Cited by 7 · see citing works
Insight into Virulence and Mechanisms of Amphotericin B Resistance in the Candida haemulonii Complex
Huang, Y., Su, Y., Chen, X., Xiao, M., & Xu, Y. (2024) · Journal of Fungi · doi:10.3390/jof10090615 · Cited by 7 · see citing works
Transcriptomic insights into Candida albicans adaptation to an anaerobic environment
Zeise, K. D., Erb‐Downward, J. R., & Huffnagle, G. B. (2025) · Microbiology Spectrum · doi:10.1128/spectrum.03024-24 · Cited by 7 · see citing works
Candida albicans triggers qualitative and temporal responses in gut bacteria
Wang, F., Ye, Y., Xin, C., Liu, F., Zhao, C., Xiang, L., & Song, Z. (2021) · Journal de Mycologie Médicale · doi:10.1016/j.mycmed.2021.101164 · Cited by 7 · see citing works
Kumar, A., Francis, A., Hans, S., & Thakur, A. (2024) · Springer eBooks · doi:10.1007/978-981-97-4909-6_8 · Cited by 6 · see citing works
Druseikis, M. E., Mottola, A., & Berman, J. G. (2023) · Current Clinical Microbiology Reports · doi:10.1007/s40588-023-00189-3 · Cited by 5 · see citing works
Iron Acquisition in the Pathobiology of Candida albicans
Srivastav, M. K., Nair, R., & Natarajan, K. (2017) · Springer eBooks · doi:10.1007/978-3-319-50409-4_17 · Cited by 5 · see citing works
Role of Candida albicans mating in genetic variability and adaptation to the host
Correia, I., Román, E., Prieto, D., Hidalgo-Vico, S., Alonso‐Monge, R., & Plá, J. (2019) · Fungal Biology Reviews · doi:10.1016/j.fbr.2019.06.001 · Cited by 5 · see citing works
Lenarczyk, E., Oleksiak, D., & Janeczko, M. (2025) · Molecules · doi:10.3390/molecules30132735 · Cited by 4 · see citing works
Wor1‐regulated ferroxidases contribute to pigment formation in opaque cells of Candida albicans
Dai, B., Xu, Y., Gao, N., & Chen, J. (2020) · FEBS Open Bio · doi:10.1002/2211-5463.13070 · Cited by 4 · see citing works
Metallophores: How do human pathogens withdraw metal ions from the colonized host
Kozłowski, H., Piasta, K., Hecel, A., Rowińska‐Żyrek, M., & Gumienna‐Kontecka, E. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-823144-9.00086-8 · Cited by 4 · see citing works
Candida albicans Commensalism and Human Diseases
Chen, C., & Huang, X. (2018) · Springer eBooks · doi:10.1007/978-1-4939-7534-1_10 · Cited by 4 · see citing works
Pierrehumbert, A., Ischer, F., & Coste, A. T. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00873 · Cited by 3 · see citing works
Crosstalk between iron and flavins in the opportunistic fungal pathogen Candida albicans
David, M. S., Zhu, Z., McDonald, M. R., Badiee, M., Mortimer, I. P., Leung, A. K. L., & Culotta, V. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.110396 · Cited by 3 · see citing works
Yang, Y., Liao, Q., Zhang, J., Liu, Y., Li, L., Chen, S., & Gao, M. (2025) · Food Physics · doi:10.1016/j.foodp.2025.100070 · Cited by 3 · see citing works
Hirai, K., Inukai, T., & Nakayama, H. (2016) · Medical Mycology Journal · doi:10.3314/mmj.16.007 · Cited by 2 · see citing works
Ibrišimović, M., Mehmedinović, N. I., Dedić, J., Kesić, A., Marić, S., & Šestan, A. (2017) · World Congress on Medical Physics and Biomedical Engineering, September 7 - 12, 2009, Munich, Germany · doi:10.1007/978-981-10-4166-2_110 · Cited by 2 · see citing works
Prieto, D., & Plá, J. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2549-1_17 · Cited by 2 · see citing works
Hidalgo-Vico, S., Prieto, D., Alonso‐Monge, R., Román, E., Maufrais, C., d’Enfert, C., & Plá, J. (2024) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2024.103939 · Cited by 1 · see citing works
In-vitro antifungal activity of resorcinol against human fungal pathogen Candida albicans
Ansari, M. A., Tanwar, J., Fatima, Z., & Hameed, S. (2015) · Cited by 1 · see citing works
Infection-Associated Gene Expression—The Pathogen Perspective
Fanning, S., & Mitchell, A. P. (2017) · Springer eBooks · doi:10.1007/978-3-319-50409-4_13 · Cited by 1 · see citing works
Shen, J., Zhang, C., Lin, Y., Zhang, C., Zhou, J., Zhou, Y., Gou, L., Liao, G., Zhu, Z., Cheng, L., et al. (2026) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-026-13740-1
“They regulate hyphal development and morphological transitions by modulating key transcription factors, including Sef1 , Hap43 , and Sfu1 (Noble 2013; Singh et al. 2011).”
Hirai, K., Inukai, T., & Nakayama, H. (2017) · Medical Mycology Journal · doi:10.3314/mmj.17.007
Aaron, U. U., Abbey, S., & Azuonwu, O. (2017) · Journals & Books Hosting (International Knowledge Sharing Platform)
Siderophores in Antifungal Drug Discovery: A Computational Approach
Anusuya, S., Chithiravel, V., Gunasekar, A., & Anbazhagan, V. (2021) · Fungal biology · doi:10.1007/978-3-030-53077-8_11
The Fight for Iron: A Central Theme in Host-Pathogen Interactions
Hamad, M. A. (2025) · Springer eBooks · doi:10.1007/978-981-96-1305-2_11
Riboflavin Overproduction in Yeasts and Filamentous Fungi
Ruchała, J., Fedorovych, D. V., Wojdyła, D., Dmytruk, K. V., & Sibirny, A. А. (2025) · Grand challenges in biology and biotechnology · doi:10.1007/978-3-031-74726-7_9
Bacterial suppression of intestinal fungi via activation of human gut γδ T-cellsPreprint
Mathew, L., Carlson, S., Savage, M., Pardieu, C., O’Brien, M., Crawley, E., Harrow, P., Kaune, A.-K., Devlin, E., Priest, E. L., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.17.676560
- Authors
- Noble, S. M.
- Affiliations
- University of California, San Francisco (US)
- Corresponding author
- Noble, Suzanne M
- ORCID
- Noble, Suzanne M
- Venue
- Current Opinion in Microbiology
- Publisher
- Elsevier BV
- Published
- 2013-12
- Volume
- 16
- Issue
- 6
- Pages
- 708-715
- ISSN
- 1369-5274 (ISSN-L)
- PMC
- PMC3855070
- OpenAlex
- W2093869242
- Cited by
- 104
- References
- 83
- Citations by year
- 2026: 5 · 2025: 10 · 2024: 6 · 2023: 4 · 2022: 6 · 2021: 11 · 2020: 9 · 2019: 7 · 2018: 8 · 2017: 17 · 2016: 9 · 2015: 7 · 2014: 4 · 2013: 1
- FWCI
- 0.89
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Current Opinion in Microbiology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- Burroughs Wellcome Fund
- Pew Charitable Trusts
- National Institutes of Health (R21AI099659-01)
- 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
- Candida albicans, iron homeostasis, iron acquisition, iron toxicity, commensalism, fungal virulence, host-pathogen interaction, iron starvation
- MeSH terms
- Candida albicans, Homeostasis, Iron, Symbiosis, Virulence
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review