Changes in glutathione-dependent redox status and mitochondrial energetic strategies are part of the adaptive response during the filamentation process in Candida albicans
Open accessAbstract
Candida albicans is an opportunist pathogen responsible for a large spectrum of infections, from superficial mycosis to systemic diseases called candidiasis. Its ability to grow in various morphological forms, such as unicellular budding yeast, filamentous pseudohyphae and hyphae, contributes to its survival in the diverse microenvironments it encounters in the host. During infection in vivo, C. albicans is faced with high levels of reactive oxygen species (ROS) generated by phagocytes, and the thiol-dependent redox status of the cells reflects their levels of oxidative stress. We investigated the role of glutathione during the transition between the yeast and hyphal forms of the pathogen, in relation to possible changes in mitochondrial bioenergetic pathways. Using various growth media and selective mutations affecting the filamentation process, we showed that C. albicans filamentation was always associated with a depletion of intracellular glutathione levels. Moreover, the induction of hypha formation resulted in general changes in thiol metabolism, including the oxidation of cell surface -SH groups and glutathione excretion. Metabolic adaptation involved tricarboxylic acid (TCA) cycle activation, acceleration of mitochondrial respiration and a redistribution of electron transfer pathways, with an increase in the contribution of the alternative oxidase and rotenone-insensitive dehydrogenase. Changes in redox status and apparent oxidative stress may be necessary to the shift to adaptive metabolic pathways, ensuring normal mitochondrial function and adenosine triphosphate (ATP) levels. The consumption of intracellular glutathione levels during the filamentation process may thus be the price paid by C. albicans for survival in the conditions encountered in the host.
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Isolated mitochondria from C. albicans are more active at 37°C compared to 30°C.
“Indeed, isolated mitochondria from C. albicans were shown to be more active at 37°C compared to 30°C [34].”
From Mitochondrial Activity and Cyr1 Are Key Regulators of Ras1 Activation of C. albicans Virulence Pathways (2015) · cites this paper as [34]
Section 3.8 (page unavailable) reports greater oxygen consumption by isolated mitochondria from filamentous cells measured at 37°C when pyruvate/malate was the electron donor. It also reports decreased consumption with NADH, so the finding does not support a general claim that the mitochondria were more active at 37°C. The comparison also changes cell form and growth conditions, not temperature alone. (LLM, conf=0.88)
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Cites
Habig, W. H., Pabst, M. J., & Jakoby, W. B. (1974) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)42083-8 · Cited by 18,394 · see citing works
Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman's reagent
Sedlak, J., & Lindsay, R. H. (1968) · Analytical Biochemistry · doi:10.1016/0003-2697(68)90092-4 · Cited by 8,092 · see citing works
Mitochondrial Dysfunction and Oxidative Stress in Neurodegenerative Diseases
Lin, M. T., & Beal, M. F. (2006) · Nature · doi:10.1038/nature05292 · Cited by 6,455 · see citing works
Meister, A., & Anderson, M. E. (1983) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.52.070183.003431 · Cited by 5,694 · see citing works
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
Isogenic strain construction and gene mapping in Candida albicans.
Fonzi, W. A., & Irwin, M. Y. (1993) · Genetics · doi:10.1093/genetics/134.3.717 · Cited by 1,695 · see citing works
Virulence factors of Candida albicans
Calderone, R. A., & Fonzi, W. A. (2001) · Trends in Microbiology · doi:10.1016/s0966-842x(01)02094-7 · Cited by 1,331 · see citing works
Odds, F. C. (1979) · Medical Entomology and Zoology · Cited by 1,297 · see citing works
Gillum, A. M., Tsay, E. Y. H., & Kirsch, D. R. (1984) · Molecular and General Genetics MGG · doi:10.1007/bf00328721 · Cited by 1,253 · 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
Quorum Sensing in the Dimorphic Fungus <i>Candida albicans</i> Is Mediated by Farnesol
Hornby, J. M., Jensen, E. C., Lisec, A. D., Tasto, J. J., Jahnke, B., Shoemaker, R., Dussault, P., & Nickerson, K. W. (2001) · Applied and Environmental Microbiology · doi:10.1128/aem.67.7.2982-2992.2001 · Cited by 983 · see citing works
Calderone, R. (2012) · ASM Press eBooks · Cited by 912 · see citing works
The distinct morphogenic states of Candida albicans
Sudbery, P., Gow, N., & Berman, J. (2004) · Trends in Microbiology · doi:10.1016/j.tim.2004.05.008 · Cited by 876 · see citing works
Lee, K. L., BUCKLEY, H. R., & Campbell, C. C. (1975) · Medical Mycology · doi:10.1080/00362177585190271 · Cited by 791 · see citing works
Suppression of Hyphal Formation in Candida albicans by Mutation of a STE12 Homolog
Liu, H., Köhler, J. R., & Fink, G. R. (1994) · Science · doi:10.1126/science.7992058 · Cited by 788 · 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
Brandt, M. E. (2002) · Emerging infectious diseases · doi:10.3201/eid0808.020059 · Cited by 646 · see citing works
Stoldt, V. R., Sonneborn, A., Leuker, C. E., & Ernst, J. F. (1997) · The EMBO Journal · doi:10.1093/emboj/16.8.1982 · Cited by 595 · see citing works
Biswas, S., Dijck, P. V., & Datta, A. (2007) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00009-06 · Cited by 516 · see citing works
Control of Filament Formation in Candida albicans by the Transcriptional Repressor TUP1
Braun, B. R., & Johnson, A. D. (1997) · Science · doi:10.1126/science.277.5322.105 · Cited by 515 · see citing works
Tyrosol is a quorum-sensing molecule in Candida albicans
Chen, H., Fujita, M., Feng, Q., Clardy, J., & Fink, G. R. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401416101 · Cited by 500 · see citing works
Redox control and oxidative stress in yeast cells
Herrero, E., Ros, J., Bellı́, G., & Cabiscol, E. (2008) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2007.12.004 · Cited by 488 · see citing works
Fradin, C., De Groot, P., MacCallum, D., Schaller, M., Klis, F., Odds, F. C., & Hube, B. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.04557.x · Cited by 455 · see citing works
Niche-specific regulation of central metabolic pathways in a fungal pathogen
Barelle, C. J., Priest, C. L., MacCallum, D. M., Gow, N. A. R., Odds, F. C., & Brown, A. J. P. (2006) · Cellular Microbiology · doi:10.1111/j.1462-5822.2005.00676.x · Cited by 336 · see citing works
Regulatory networks controlling Candida albicans morphogenesis
Brown, A. J. P., & Gow, N. A. R. (1999) · Trends in Microbiology · doi:10.1016/s0966-842x(99)01556-5 · Cited by 301 · see citing works
Life and death in a macrophage: role of the glyoxylate cycle in virulence
Lorenz, M. C., & Fink, G. R. (2002) · Eukaryotic Cell · doi:10.1128/ec.1.5.657-662.2002 · Cited by 300 · see citing works
TUP1, CPH1 and EFG1 Make Independent Contributions to Filamentation in Candida albicans
Braun, B. R., & Johnson, A. D. (2000) · Genetics · doi:10.1093/genetics/155.1.57 · Cited by 257 · see citing works
Dimorphism and virulence in Candida albicans
Mitchell, A. P. (1998) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(98)80116-1 · Cited by 256 · see citing works
A characterization of pH-regulated dimorphism in Candida albicans
Buffo, J., Herman, M. A., & Soll, D. R. (1984) · Mycopathologia · doi:10.1007/bf00436698 · Cited by 256 · see citing works
(1989) · Annals of Internal Medicine · doi:10.7326/0003-4819-111-7-624_1 · Cited by 253 · see citing works
Mavor, A., Thewes, S., & Hube, B. (2005) · Current Drug Targets · doi:10.2174/138945005774912735 · Cited by 252 · see citing works
Morphogenesis and cell cycle progression in Candida albicans
Berman, J. (2006) · Current Opinion in Microbiology · doi:10.1016/j.mib.2006.10.007 · Cited by 237 · see citing works
An overview on glutathione in versus non-conventional yeasts
Penninckx, M. J. (2002) · FEMS Yeast Research · doi:10.1016/s1567-1356(02)00081-8 · Cited by 235 · see citing works
Rapid Identification of Candida Albicans by Filamentation on Serum and Serum Substitutes
Taschdjian, C. L. (1960) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/archpedi.1960.02070030214011 · Cited by 226 · see citing works
Yeast-mycelial conversion induced by N-acetyl-D-glucosamine in Candida albicans
Simonetti, N., Strippoli, V., & Cassone, A. (1974) · Nature · doi:10.1038/250344a0 · Cited by 220 · see citing works
Candida morphogenesis and host–pathogen interactions
Whiteway, M. S., & Oberholzer, U. (2004) · Current Opinion in Microbiology · doi:10.1016/j.mib.2004.06.005 · Cited by 196 · see citing works
Candida commensalism and virulence: the evolution of phenotypic plasticity
Soll, D. R. (2002) · Acta Tropica · doi:10.1016/s0001-706x(01)00200-5 · Cited by 157 · see citing works
Lewis, L. E., Bain, J. M., Lowes, C., Gillespie, C., Rudkin, F. M., Gow, N. A. R., & Erwig, L.-P. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002578 · Cited by 150 · see citing works
Hinman, L. M., & Blass, J. P. (1981) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)69029-0 · Cited by 143 · see citing works
Germ tube growth of Candida albicans.
Gow, N. A. R. (1997) · PubMed · Cited by 130 · see citing works
Quorum sensing and Candida albicans
Kruppa, M. (2008) · Mycoses · doi:10.1111/j.1439-0507.2008.01626.x · Cited by 129 · see citing works
Westwater, C., Balish, E., & Schofield, D. A. (2005) · Eukaryotic Cell · doi:10.1128/ec.4.10.1654-1661.2005 · Cited by 127 · see citing works
Analysis of the adaptive oxidative stress response ofCandida albicans
Jamieson, D. J., Stephen, D. W. S., & ̈re, E. C. T. (1996) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1996.tb08139.x · Cited by 125 · see citing works
Characterization of the gene family encoding alternative oxidase from Candida albicans
HUH, W.-K., & KANG, S.-O. (2001) · Biochemical Journal · doi:10.1042/bj3560595 · Cited by 113 · see citing works
Reglinski, J., Hoey, S., Smith, W. E., & Sturrock, R. D. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)37763-9 · Cited by 105 · see citing works
Characterization of the mitochondrial respiratory pathways in Candida albicans
Helmerhorst, E. J., Murphy, M. P., Troxler, R. F., & Oppenheim, F. G. (2002) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/s0005-2728(02)00308-0 · Cited by 95 · see citing works
Párraga, P. G., Hernández, J. A., & Argüelles, J. C. (2003) · Yeast · doi:10.1002/yea.1029 · Cited by 94 · see citing works
Responses to hypoxia in fungal pathogens
Ernst, J. F., & Tielker, D. (2008) · Cellular Microbiology · doi:10.1111/j.1462-5822.2008.01259.x · Cited by 94 · see citing works
Auchère, F., Santos, R., Planamente, S., Lesuisse, E., & Camadro, J. (2008) · Human Molecular Genetics · doi:10.1093/hmg/ddn178 · Cited by 87 · see citing works
Self-citationPatterson, M. J., McKenzie, C. G., Smith, D. A., Dantas, A. D. S., Sherston, S., Veal, E. A., Morgan, B. A., MacCallum, D. M., Erwig, L., & Quinn, J. (2013) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5199 · Cited by 85 · see citing works
Zhu, J., Krom, B. P., Sanglard, D., Intapa, C., Dawson, C. C., Peters, B. M., Shirtliff, M. E., & Jabra‐Rizk, M. A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028830 · Cited by 83 · see citing works
Identification of the dialysable serum inducer of germ-tube formation in Candida albicans
Hudson, D. A., Sciascia, Q. L., Sanders, R. J., Norris, G. E., Edwards, P. J. B., Sullivan, P. A., & Farley, P. C. (2004) · Microbiology · doi:10.1099/mic.0.27121-0 · Cited by 82 · see citing works
Transcriptional control of cell type and morphogenesis in Candida albicans
Whiteway, M. S. (2000) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(00)00144-2 · Cited by 78 · see citing works
Ruy, F., Vercesi, A. E., & Kowaltowski, A. J. (2006) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-006-9012-7 · Cited by 74 · see citing works
Control of Dimorphism in a Biochemical Variant of Candida albicans
Mardon, D. N., Balish, E., & Phillips, A. W. (1969) · Journal of Bacteriology · doi:10.1128/jb.100.2.701-707.1969 · Cited by 72 · see citing works
Land, G. A., McDonald, W. C., STJERNHOLM, R. L., & Friedman, T. L. (1975) · Infection and Immunity · doi:10.1128/iai.11.5.1014-1023.1975 · Cited by 71 · see citing works
Molecular Cloning and Functional Expression of Alternative Oxidase from <i>Candida albicans</i>
Huh, W.-K., & Kang, S.-O. (1999) · Journal of Bacteriology · doi:10.1128/jb.181.13.4098-4102.1999 · Cited by 66 · see citing works
Activity and Toxicity of Farnesol towards Candida albicans Are Dependent on Growth Conditions
Langford, M. L., Hasim, S., Nickerson, K. W., & Atkin, A. L. (2009) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01214-09 · Cited by 66 · see citing works
Milani, G., Jarmuszkiewicz, W., Sluse-Goffart, C. M., Schreiber, A. Z., Vercesi, A. E., & Sluse, F. E. (2001) · FEBS Letters · doi:10.1016/s0014-5793(01)03060-5 · Cited by 65 · see citing works
Baek, Y., Kim, Y.-R., Yim, H., & Kang, S.-O. (2003) · FEBS Letters · doi:10.1016/s0014-5793(03)01363-2 · Cited by 64 · see citing works
Chattaway, F. W., Bishop, R. H., Holmes, M. R., Odds, F. C., & Barlow, A. (1973) · Journal of General Microbiology · doi:10.1099/00221287-75-1-97 · Cited by 62 · see citing works
Glutathione peroxidase in yeast. Presence of the enzyme and induction by oxidative conditions
Galiazzo, F., Schiesser, A., & Rotilio, G. (1987) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(87)80197-3 · Cited by 61 · see citing works
Involvement of Candida albicans NADH dehydrogenase complex I in filamentation
McDonough, J. A., Bhattacherjee, V., Sadlon, T., & Hostetter, M. K. (2002) · Fungal Genetics and Biology · doi:10.1016/s1087-1845(02)00007-5 · Cited by 61 · see citing works
AN ENZYMATIC LOCUS PARTICIPATING IN CELLULAR DIVISION OF A YEAST
Nickerson, W. J. (1954) · The Journal of General Physiology · doi:10.1085/jgp.37.4.483 · Cited by 55 · see citing works
Helmerhorst, E. J., Stan, M., Murphy, M. P., Sherman, F., & Oppenheim, F. G. (2005) · Mitochondrion · doi:10.1016/j.mito.2005.04.001 · Cited by 50 · see citing works
Chaves, G. M., Bates, S., MacCallum, D. M., & Odds, F. C. (2007) · PubMed · Cited by 49 · see citing works
Yadav, A. K., Desai, P. R., Rai, M. N., Kaur, R., Ganesan, K., & Bachhawat, A. K. (2011) · Microbiology · doi:10.1099/mic.0.045054-0 · Cited by 49 · see citing works
Bulteau, A., Planamente, S., Jornéa, L., Dürr, A., Lesuisse, E., Camadro, J., & Auchère, F. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2011.11.003 · Cited by 47 · see citing works
Self-citationRespiration, oxidative phosphorylation, and uncoupling protein in Candida albicans
Cavalheiro, R. A., Fortes, F., Borecký, J., Faustinoni, V. C., & Schreiber, A. Z. (2004) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x2004001000003 · Cited by 43 · see citing works
Involvement of Candida albicans pyruvate dehydrogenase complex protein X (Pdx1) in filamentation
Vellucci, V. F., Gygax, S. E., & Hostetter, M. K. (2007) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2006.12.003 · Cited by 40 · see citing works
Párraga, P. G., Alonso‐Monge, R., Plá, J., & Argüelles, J. C. (2010) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2010.00654.x · Cited by 37 · see citing works
Fekete, A., Emri, T., Gyetvai, Á., Gazdag, Z., Pesti, M., Varga, Z., Balla, J., Cserháti, C., Emödy, L., Gergely, L., et al. (2007) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2007.00244.x · Cited by 36 · see citing works
Changes in glutathione metabolic enzymes during yeast-to-mycelium conversion of Candida albicans
Manavathu, M., Manavathu, E. K., Gunasekaran, S., Porte, Q., & Gunasekaran, M. (1996) · Canadian Journal of Microbiology · doi:10.1139/m96-011 · Cited by 35 · see citing works
Glutathione levels during thermal induction of the yeast-to-mycelial transition in Candida albicans
Thomas, D. D. S., Klein, K., Manavathu, E. K., Dimmock, J. R., & Mutus, B. (1991) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1991.tb04371.x · Cited by 32 · see citing works
Hyphal formation of Candida albicans is controlled by electron transfer system
Watanabe, T., Ogasawara, A., Mikami, T., & Matsumoto, T. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.07.066 · Cited by 30 · see citing works
Michán, C., & Pueyo, C. (2009) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2009.00558.x · Cited by 29 · see citing works
Carbon Catabolite Control in Candida albicans: New Wrinkles in Metabolism
Lorenz, M. C. (2013) · mBio · doi:10.1128/mbio.00034-13 · Cited by 29 · see citing works
Regulatory circuitry governing morphogenesis inSaccharomyces cerevisiaeandCandida albicans
Shapiro, R. S., Ryan, O. W., Boone, C. M., & Cowen, L. E. (2012) · Cell Cycle · doi:10.4161/cc.22608 · Cited by 28 · see citing works
Mailinger, W., Baumeister, A., Reuß, M., & Rizzi, M. (1998) · Journal of Biotechnology · doi:10.1016/s0168-1656(98)00095-9 · Cited by 26 · see citing works
Párraga, P. G., Marín, F. R., Argüelles, J. C., & Hernández, J. A. (2005) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2005.01.006 · Cited by 20 · see citing works
Garcerá, A., Casas, C., & Herrero, E. (2010) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2010.00613.x · Cited by 19 · see citing works
Fekete, A., Pócsi, I., Emri, T., Gyetvai, Á., Gazdag, Z., Pesti, M., Karányi, Z., Majoros, L., Gergely, L., & Pócsi, I. (2008) · Journal of Basic Microbiology · doi:10.1002/jobm.200800114 · Cited by 11 · see citing works
Flagged first, then by citations
1 of the 83 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Grahl, N., Demers, E. G., Lindsay, A. K., Harty, C. E., Willger, S. D., Piispanen, A. E., & Hogan, D. A. (2015) · PLOS Pathogens · doi:10.1371/journal.ppat.1005133 · Cited by 111 · see citing works
System-level impact of mitochondria on fungal virulence: to metabolism and beyond
Calderone, R., Li, D., & Traven, A. (2015) · FEMS Yeast Research · doi:10.1093/femsyr/fov027 · Cited by 101 · see citing works
Wangsanut, T., & Pongpom, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231810645 · Cited by 93 · see citing works
Chang, W., Liu, J., Zhang, M., Shi, H., Zheng, S., Jin, X., Gao, Y., Wang, S., Ji, A., & Lou, H. (2018) · Nature Communications · doi:10.1038/s41467-018-07633-9 · Cited by 91 · see citing works
McCrory, C., Lenardon, M. D., & Traven, A. (2024) · Trends in Microbiology · doi:10.1016/j.tim.2024.04.004 · Cited by 68 · see citing works
Tucey, T. M., Verma-Gaur, J., Nguyen, J., Hewitt, V. L., Lo, T. L., Shingu-Vazquez, M., Robertson, A. A. B., Hill, J. R., Pettolino, F. A., Beddoe, T., et al. (2016) · mSphere · doi:10.1128/msphere.00074-16 · Cited by 66 · see citing works
“Proper mitochondrial distribution in the fila-ments could serve to power hyphal elongation, as hyphal growth depends more prominently on mitochondrial metabolism than does yeast growth (45).”
Duvenage, L., Walker, L. A., Bojarczuk, A., Johnston, S. A., MacCallum, D. M., Munro, C. A., & Gourlay, C. W. (2019) · mBio · doi:10.1128/mbio.02535-18 · Cited by 61 · see citing works
“This observation, together with previous evidence that the alternative pathway is more active in hyphal cells (64), warrants further investigation into the precise role of Aox2 in morphogenetic switching.”
She, X., Khamooshi, K., Gao, Y., Shen, Y., Lv, Y., Calderone, R., Fonzi, W., Liu, W., & Li, D. (2015) · Cellular Microbiology · doi:10.1111/cmi.12438 · Cited by 51 · 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
Face/Off: The Interchangeable Side of Candida Albicans
Cottier, F., & Hall, R. A. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2019.00471 · Cited by 47 · see citing works
Chang, C., Cai, E., Deng, Y., Mei, D., Qiu, S., Chen, B., Zhang, L., & Jiang, Z. (2018) · Environmental Microbiology · doi:10.1111/1462-2920.14496 · Cited by 43 · see citing works
Metabolism of Preimplantation Embryo Development
Kaneko, K. J. (2016) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2016.04.010 · Cited by 44 · see citing works
Fungal morphogenetic changes inside the mammalian host
Trevijano‐Contador, N., Rueda, C., & Zaragoza, Ó. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.04.008 · Cited by 40 · see citing works
Jiang, C., Li, Z., Zhang, L., Tian, Y., Dong, D., & Peng, Y. (2016) · Microbiological Research · doi:10.1016/j.micres.2016.06.003 · Cited by 34 · 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
Self-citationRole of Mitochondrial Retrograde Pathway in Regulating Ethanol-Inducible Filamentous Growth in Yeast
González, B., Mas, A., Beltran, G., Cullen, P. J., & Torija, M.-J. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00148 · Cited by 22 · see citing works
Dižová, S., Černáková, L., & Bujdáková, H. (2017) · Folia Microbiologica · doi:10.1007/s12223-017-0574-z · Cited by 21 · see citing works
Barsottini, M. R., Pires, B. A., Vieira, M. L., Pereira, J. G., Costa, P. C., Sanitá, J., Coradini, A., Mello, F., Marschalk, C., Silva, E. M., et al. (2019) · Pest Management Science · doi:10.1002/ps.5243 · Cited by 19 · see citing works
Respiration supports intraphagosomal filamentation and escape of Candida albicans from macrophages
Case, N. T., Westman, J., Hallett, M. T., Plumb, J. D., Farheen, A., Maxson, M. E., MacAlpine, J., Liston, S. D., Hube, B., Robbins, N., et al. (2023) · mBio · doi:10.1128/mbio.02745-23 · Cited by 17 · see citing works
Kwak, M., Ku, M., & Kang, S.-O. (2017) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2017.10.003 · Cited by 18 · see citing works
Ku, M., Baek, Y., Kwak, M., & Kang, S.-O. (2016) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2016.10.010 · Cited by 16 · see citing works
Barsottini, M. R. D. O., Copsey, A. C., Young, L., Baroni, R. M., Cordeiro, A. T., Pereira, G. A. G., & Moore, A. L. (2020) · Communications Biology · doi:10.1038/s42003-020-0981-6 · Cited by 16 · see citing works
Hamid, N. A. A., Abas, F., Ismail, I. S., Tham, C. L., Maulidiani, M., Mediani, A., Swarup, S., & Umashankar, S. (2019) · Food Research International · doi:10.1016/j.foodres.2019.108565 · Cited by 15 · see citing works
Castilho, D. G., Navarro, M. V., Chaves, A. F. A., Xander, P. B., & Batista, W. L. (2018) · FEMS Yeast Research · doi:10.1093/femsyr/foy007 · Cited by 14 · see citing works
Gergondey, R., Garcia, C., Serre, V., Camadro, J., & Auchère, F. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2016.04.004 · Cited by 12 · see citing works
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Божков, А. И. (2014) · American Journal of Biomedical and Life Sciences · doi:10.11648/j.ajbls.s.2014020601.12 · Cited by 11 · see citing works
Balancing act: thiol-based redox regulation drives fungal pathogenesis
Black, B., Kussat, T., & Kronstad, J. W. (2025) · Trends in Microbiology · doi:10.1016/j.tim.2025.06.003 · Cited by 10 · see citing works
Liu, Q., Wang, Y., Li, Y., Li, Y., Wang, Y., Zhou, B., & Zhou, Z. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.739159 · Cited by 8 · see citing works
Bayot, J., Martin, C., Chevreux, G., Camadro, J., & Auchère, F. (2023) · Biochemical Journal · doi:10.1042/bcj20220505 · Cited by 8 · see citing works
Self-citationAlternative Oxidase – Aid or obstacle to combat the rise of fungal pathogens?
Edrich, E. S. M., Duvenage, L., & Gourlay, C. W. (2024) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2024.149031 · Cited by 7 · see citing works
Candida albicans cells exhibit media specific proteomic profiles during induction of filamentation
Legros, V., Albanèse, V., Chevreux, G., Camadro, J., & Auchère, F. (2024) · BMC Microbiology · doi:10.1186/s12866-024-03627-4 · Cited by 7 · see citing works
Self-citationCosta, P. C. S., Barsottini, M. R. D. O., VIEIRA, M. L. L., Pires, B. A., Evangelista, J. S., Zeri, A. C. D. M., Nascimento, A. F. Z., Silva, J. S., Carazzolle, M. F., Pereira, G. A. G., et al. (2020) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2020.127903 · Cited by 7 · see citing works
Yu, J., Li, W., Xu, Y. M., & Tang, J. (2026) · Clinical Microbiology Reviews · doi:10.1128/cmr.00368-25 · Cited by 6 · see citing works
An analysis of respiratory function and mitochondrial morphology in Candida albicansPreprint
Duvenage, L., Pentland, D. R., Munro, C. A., & Gourlay, C. W. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/697516 · Cited by 5 · see citing works
Varga, J. C., Bujdák, J., & Bujdáková, H. (2025) · Journal of Fungi · doi:10.3390/jof11080582 · Cited by 3 · see citing works
Zhang, C., Zhang, N. N., Li, Z. Y., Tian, Y. T., Zhang, L. T., & Zheng, B. D. (2016) · Journal of Aquatic Food Product Technology · doi:10.1080/10498850.2015.1082525 · Cited by 3 · see citing works
Li, H., Bao, L., Deng, S., Liu, L., Cheng, J. R., Cheng, X. J., Pan, Y., Zhang, J., & Chu, W. (2021) · Scientific Reports · doi:10.1038/s41598-021-83388-6 · Cited by 3 · see citing works
Duvenage, L., Walker, L. A., Bojarczuk, A., Johnston, S. A., McCallum, D. M., Munro, C. A., & Gourlay, C. W. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/405670 · Cited by 4 · see citing works
Central Carbon Metabolism in Candida albicans Biofilms Is Altered by Dimethyl Sulfoxide
Arruda, M. F. C., Ramos, R. C. P. D. S., de Oliveira, N. S., Rosa, R. T., Campelo, P. M. S., Bianchini, L. F., Villas-Bôas, S. G., & Rosa, E. A. R. (2024) · Journal of Fungi · doi:10.3390/jof10050337 · Cited by 2 · see citing works
Novel mitochondrial-targeted alkyl chains act as fungal specific inhibitors of C. neoformans
Edrich, E. S. M., Young, L., Spencer, J., McGown, A., Moore, A. L., & Gourlay, C. W. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1505308 · Cited by 1 · see citing works
Qi, W., Roy, U., Cai, C., Acosta‐Zaldívar, M., Mascio, J., Asara, J. M., Fierro, J. F., Andrés, M. T. A., Sun, L., & Köhler, J. R. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.02.691982 · Cited by 1 · see citing works
Assessing Mitochondrial Functions in Candida albicans
Li, D., & Calderone, R. (2015) · Methods in molecular biology · doi:10.1007/978-1-4939-3052-4_5
Assessing Complex I (CI) Mitochondrial Subunit Protein Functions in Candida albicans
Li, D., She, X., & Calderone, R. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2549-1_11
Vanparis, O. (2018) · theses.fr (ABES) · doi:10.70675/9ca39a19z090cz4464zbfbcz2bea821f9091
Self-citationCascading damage to Candida albicans cells through thioredoxin reductase loss
Qi, W., Roy, U., Cai, C., Acosta‐Zaldívar, M., Mascio, J., Asara, J. M., Fierro, J. F., Andrés, M. T. A., Sun, L., & Köhler, J. R. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2615451123
- Authors
- Guedouari, H., Gergondey, R., Bourdais, A., Vanparis, O., Bulteau, A. L., Camadro, J. M., & Auchère, F.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- Université de Pau et des Pays de l'Adour (FR)
- Corresponding author
- Auchère, F.
- Venue
- Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
- Publisher
- Elsevier BV
- Published
- 2014-09
- Volume
- 1842
- Issue
- 9
- Pages
- 1855-1869
- ISSN
- 0925-4439 (ISSN-L)
- OpenAlex
- W2018502270
- Cited by
- 45
- References
- 83
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 4 · 2023: 2 · 2022: 2 · 2021: 2 · 2020: 3 · 2019: 4 · 2018: 7 · 2017: 3 · 2016: 7 · 2015: 4 · 2014: 1
- FWCI
- 2.05
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 365 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Funders
- Agence Nationale de la Recherche
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Keywords
- Candida albicans, filamentation, hyphal morphogenesis, glutathione depletion, thiol metabolism, oxidative stress, reactive oxygen species, mitochondrial respiration, TCA cycle, alternative oxidase, electron transfer pathway, ATP production, yeast-to-hypha transition
- MeSH terms
- Adaptation, Physiological, Candida albicans, Candidiasis, Electron Transport, Energy Metabolism, Fungal Proteins, Glutathione, Mitochondria, Mutation, Oxidation-Reduction, Reactive Oxygen Species, Hyphae, Metabolic Networks and Pathways
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