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The Facultative Intracellular Pathogen Candida glabrata Subverts Macrophage Cytokine Production and Phagolysosome Maturation
Open accessAbstract
Although Candida glabrata is an important human pathogenic yeast, its pathogenicity mechanisms are largely unknown. Immune evasion strategies seem to play key roles during infection, since very little inflammation is observed in mouse models. Furthermore, C. glabrata multiplies intracellularly after engulfment by macrophages. In this study, we sought to identify the strategies that enable C. glabrata to survive phagosome biogenesis and antimicrobial activities within human monocyte-derived macrophages. We show that, despite significant intracellular proliferation, macrophage damage or apoptosis was not apparent, and production of reactive oxygen species was inhibited. Additionally, with the exception of GM-CSF, levels of pro- and anti-inflammatory cytokines were only marginally increased. We demonstrate that adhesion to and internalization by macrophages occur within minutes, and recruitment of endosomal early endosomal Ag 1 and lysosomal-associated membrane protein 1 indicates phagosome maturation. However, phagosomes containing viable C. glabrata, but not heat-killed yeasts, failed to recruit cathepsin D and were only weakly acidified. This inhibition of acidification did not require fungal viability, but it had a heat-sensitive surface attribute. Therefore, C. glabrata modifies the phagosome into a nonacidified environment and multiplies until the host cells finally lyse and release the fungi. Our results suggest persistence of C. glabrata within macrophages as a possible immune evasion strategy.
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“Lastly, despite encountering iron restriction, ROS and carbon starvation, C. glabrata has equipped itself well with strategies to proliferate in macrophages, including transcriptional reconfiguration of cellular pathways [60,65,147].”
From Candida glabrata: A Lot More Than Meets the Eye (2019) · cites this paper as [65]
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In the citing paper
“C. glabrata can be engulfed by macrophages, it is highly resistant to macrophage-mediated killing and can survive and proliferate within these host cells (16).”
From Overlooked Candida glabrata petites are echinocandin tolerant, induce host inflammatory responses, and display poor in vivo fitness (2023) · cites this paper as [16]
In the citing paper
“Of note, previous studies reported an ADY2a upregulation in C. glabrata cells upon macrophage phagocytosis (Kaur et al., 2007; Seider et al., 2011).”
From Candida glabrata susceptibility to antifungals and phagocytosis is modulated by acetate (2015) · cites this paper as Seider et al., 2011
In the citing paper
“The latter includes suppression of the production of pro-inflammatory cytokine IL-1β in human THP-1 macrophages, facilitating survival in macrophages and virulence in the models of murine systemic candidiasis and Drosophila melanogaster [58,60,65,66].”
From Candida glabrata: A Lot More Than Meets the Eye (2019) · cites this paper as [65]
In the citing paper
“In accordance, macrophages did not produce TNF-α, IL-6, IL-8, IL-12, and IFN-γ pro-inflammatory cytokines, however, GM-CSF production has been reported upon C. glabrata infection [65].”
From Candida glabrata: A Lot More Than Meets the Eye (2019) · cites this paper as [65]
In the citing paper
“In accordance, macrophages did not produce TNF-α, IL-6, IL-8, IL-12, and IFN-γ pro-inflammatory cytokines, however, GM-CSF production has been reported upon C. glabrata infection [65].”
From Candida glabrata: A Lot More Than Meets the Eye (2019) · cites this paper as [65]
In the citing paper
“C. glabrata survives and replicates in human and murine macrophages without adversely affecting macrophages [60,65,147].”
From Candida glabrata: A Lot More Than Meets the Eye (2019) · cites this paper as [65]
In the citing paper
“C. glabrata is also known to impede maturation of the phagosome in macrophages [65,147], and the phosphoinositide 3-kinase subunits (CgVps15 and CgVsps34), mannosyltransferases (CgMnn10 and CgMnn11) and vesicular trafficking proteins (CgLdb17 and CgSla2) contributed to the inhibition of phagolysosomal acidification [147,149,150].”
From Candida glabrata: A Lot More Than Meets the Eye (2019) · cites this paper as [65]
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Cites
Epidemiology of Invasive Candidiasis: a Persistent Public Health Problem
Pfaller, M. A., & Diekema, D. J. (2007) · Clinical Microbiology Reviews · doi:10.1128/cmr.00029-06 · Cited by 4,174 · cited 1×
“C andida glabrata is an emerging pathogen that has become the second most frequent cause (15%) of candidiasis after Candida albicans (1, 2).”
BackgroundOhkuma, S., & Poole, B. (1978) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.75.7.3327 · Cited by 2,173
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
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
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
Gillum, A. M., Tsay, E. Y. H., & Kirsch, D. R. (1984) · Molecular and General Genetics MGG · doi:10.1007/bf00328721 · Cited by 1,253
Potential Role of Phospholipases in Virulence and Fungal Pathogenesis
Ghannoum, M. A. (2000) · Clinical Microbiology Reviews · doi:10.1128/cmr.13.1.122-143.2000 · Cited by 823
Transcriptional Response of Candida albicans 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
Phagosome maturation: aging gracefully
Vieira, O. V., Botelho, R. J., & Grinstein, S. (2002) · Biochemical Journal · doi:10.1042/bj20020691 · Cited by 696
Trends in Mortality Due to Invasive Mycotic Diseases in the United States, 1980–1997
McNeil, M. M., Nash, S. L., Hajjeh, R. A., Phelan, M. A., Conn, L. A., Plikaytis, B. D., & Warnock, D. W. (2001) · Clinical Infectious Diseases · doi:10.1086/322606 · Cited by 657
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Feldman, M. B., Vyas, J. M., & Mansour, M. K. (2018) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2018.04.008 · Cited by 27
Global Secretome Characterization of the Pathogenic Yeast Candida glabrata
Rasheed, M., Kumar, N., & Kaur, R. (2019) · Journal of Proteome Research · doi:10.1021/acs.jproteome.9b00299 · Cited by 23
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Hünniger, K., & Kurzai, O. (2018) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2018.03.021 · Cited by 25
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Beyer, R., Jandric, Z., Zutz, C., Gregori, C., Willinger, B., Jacobsen, I. D., Kovarik, P., Strauss, J., & Schüller, C. (2018) · Cellular Microbiology · doi:10.1111/cmi.12943 · Cited by 23
Plasma 1,3-β-d-glucan levels predict adverse clinical outcomes in critical illness
Kitsios, G. D., Kotok, D., Yang, H., Finkelman, M., Zhang, Y., Britton, N., Li, X., Levochkina, M. S., Wagner, A. K., Schaefer, C., et al. (2021) · JCI Insight · doi:10.1172/jci.insight.141277 · Cited by 21
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Lewis, L. E., Bain, J. M., Okai, B., Gow, N. A. R., & Erwig, L. P. (2013) · Journal of Visualized Experiments · doi:10.3791/50196 · Cited by 23
Kumar, K., Moirangthem, R., & Kaur, R. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1008620 · Cited by 21
The involvement of the Candida glabrata trehalase enzymes in stress resistance and gut colonization
Ende, M. V., Timmermans, B., Vanreppelen, G., Siscar-Lewin, S., Fischer, D., Wijnants, S., Romero, C. L., Yazdani, S., Rogiers, O., Demuyser, L., et al. (2020) · Virulence · doi:10.1080/21505594.2020.1868825 · Cited by 23
Self-citationDagher, Z., Xu, S., Negoro, P. E., Khan, N. S., Feldman, M. B., Reedy, J. L., Tam, J. M., Sykes, D. B., & Mansour, M. K. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01058 · Cited by 21
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Essig, F., Hünniger, K., Dietrich, S., Figge, M. T., & Kurzai, O. (2015) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2015.09.008 · Cited by 20
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Pountain, A. W., Collette, J. R., Farrell, W. M., & Lorenz, M. C. (2021) · mBio · doi:10.1128/mbio.03317-21 · Cited by 21
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Xu, S., Feliu, M., Lord, A. K., Lukason, D. P., Negoro, P. E., Khan, N. S., Dagher, Z., Feldman, M. B., Reedy, J. L., Steiger, S. N., et al. (2018) · Virulence · doi:10.1080/21505594.2018.1475798 · Cited by 21
Arastehfar, A., Daneshnia, F., Floyd, D. J., Jeffries, N. E., Salehi, M., Perlin, D. S., Ilkit, M., Lass-Flöerl, C., & Mansour, M. K. (2024) · mBio · doi:10.1128/mbio.00072-24 · Cited by 19
Elalouf, A., Elalouf, H., & Rosenfeld, A. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1292625 · Cited by 20
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Jandric, Z., & Schüller, C. (2011) · Future Microbiology · doi:10.2217/fmb.11.131 · Cited by 19
Brandes, S., Dietrich, S., Hünniger, K., Kurzai, O., & Figge, M. T. (2016) · Medical Image Analysis · doi:10.1016/j.media.2016.11.007 · Cited by 19
Candida glabrata meningitis and endocarditis: a late severe complication of candidemia
Colomba, C., Trizzino, M., Imburgia, C., Madonia, S., Siracusa, L., & Giammanco, A. (2014) · International Journal of Infectious Diseases · doi:10.1016/j.ijid.2014.04.032 · Cited by 18
A New Determinant of Candida glabrata Virulence: The Acetate Exporter CgDtr1
Romão, D., Cavalheiro, M., Mil-Homens, D., Santos, R., Pais, P., Costa, C., Takahashi‐Nakaguchi, A., Fialho, A., Chibana, H., & Teixeira, M. C. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00473 · Cited by 19
Predictive Virtual Infection Modeling of Fungal Immune Evasion in Human Whole Blood
Prauße, M. T. E., Lehnert, T., Timme, S., Hünniger, K., Leonhardt, I., Kurzai, O., & Figge, M. T. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00560 · Cited by 17
Human Endothelial Cells Internalize Candida parapsilosis via N-WASP-Mediated Endocytosis
Shintaku, T., Glass, K. A., Hirakawa, M. P., Longley, S. J., Bennett, R. J., Bliss, J. M., & Shaw, S. K. (2013) · Infection and Immunity · doi:10.1128/iai.00535-13 · Cited by 17
Candida glabratasurvives and replicates in human osteoblasts
Muñóz-Duarte, A. R., Castrejón-Jiménez, N. S., Baltierra‐Uribe, S. L., Pérez-Rangel, S. J., Carapia-Minero, N., Castañeda‐Sánchez, J. I., Luna‐Herrera, J., López‐Santiago, R., Rodríguez-Tovar, A. V., & García‐Pérez, B. E. (2016) · Pathogens and Disease · doi:10.1093/femspd/ftw030 · Cited by 16
Genome-Wide Response to Drugs and Stress in the Pathogenic Yeast Candida glabrata
Pais, P., Galocha, M., & Teixeira, M. C. (2019) · Progress in molecular and subcellular biology · doi:10.1007/978-3-030-13035-0_7 · Cited by 17
Timme, S., Lehnert, T., Prauße, M. T. E., Hünniger, K., Leonhardt, I., Kurzai, O., & Figge, M. T. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00667 · Cited by 15
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Sonnberger, J., Kasper, L., Lange, T., Brunke, S., & Hube, B. (2023) · Molecular Microbiology · doi:10.1111/mmi.15149 · Cited by 16
Self-citationKounatidis, 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
The yapsin family of aspartyl proteases regulate glucose homeostasis in Candida glabrata
Askari, F., Rasheed, M., & Kaur, R. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.101593 · Cited by 13
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Pérez‐Flores, G., Hernández-Silva, C., Gutiérrez‐Escobedo, G., Peñas, A. D. L., Castaño, I., Arreola, J., & Pérez‐Cornejo, P. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.11.027 · Cited by 13
Rodrigues, C. F., Correia, A., Vilanova, M., & Henriques, M. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8020142 · Cited by 15
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Ishchuk, O. P., Ahmad, K. M., Koruza, K., Bojanovič, K., Sprenger, M., Kasper, L., Brunke, S., Hube, B., Säll, T., Hellmark, T., et al. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01679 · Cited by 12
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Ma, Z., Wang, X., & Li, C. (2020) · Pharmaceutical Nanotechnology · doi:10.2174/2211738508666200910101923 · Cited by 13
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Arunachalam, D., Prajna, N. V., Lalitha, P., & Dharmalingam, K. (2021) · Infection and Immunity · doi:10.1128/iai.00794-20 · Cited by 12
Eliaš, D., Hervay, N. T., Bujdoš, M., & Gbelská, Y. (2023) · Journal of Fungi · doi:10.3390/jof9050579 · Cited by 12
Llopis-Torregrosa, V., Vaz, C., Monteoliva, L., Ryman, K., Engström, Y., Gácser, A., Gil, C., Ljungdahl, P. O., & Sychrová, H. (2019) · Scientific Reports · doi:10.1038/s41598-019-43912-1 · Cited by 11
Zhang, S., Zhao, Q., Xue, W., Li, Y., Guo, Y., Wu, X., Huo, S., Li, Y., & Li, C. (2021) · Poultry Science · doi:10.1016/j.psj.2021.01.026 · Cited by 12
Naskar, S., Prajapati, A., & Kaur, R. (2025) · FEMS Yeast Research · doi:10.1093/femsyr/foaf025 · Cited by 14
Microbe Profile: Candida glabrata – a master of deception
Granada, M., Cook, E., Sherlock, G. J., & Rosenzweig, F. (2024) · Microbiology · doi:10.1099/mic.0.001518 · Cited by 10
Pais, P., Vagueiro, S., Mil‐Homens, D., Pimenta, A. I., Viana, R., Okamoto, M., Chibana, H., Fialho, A. M., & Teixeira, M. C. (2020) · Virulence · doi:10.1080/21505594.2020.1839231 · Cited by 10
Beyda, N. D., Liao, G., Endres, B. T., Lewis, R. E., & Garey, K. W. (2015) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00624-15 · Cited by 12
Baltch, A. L., Lawrence, D. A., Ritz, W. J., Andersen, N. J., Bopp, L. H., Michelsen, P. B., Carlyn, C. J., & Smith, R. P. (2011) · Diagnostic Microbiology and Infectious Disease · doi:10.1016/j.diagmicrobio.2011.11.004 · Cited by 10
P4-ATPase subunit Cdc50 plays a role in yeast budding and cell wall integrity in Candida glabrata
Chen, K.-Z., Wang, L.-L., Liu, J., Zhao, J., Huang, S., & Xiang, M.-J. (2023) · BMC Microbiology · doi:10.1186/s12866-023-02810-3 · Cited by 9
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Kumar, K., Pareek, A., & Kaur, R. (2024) · iScience · doi:10.1016/j.isci.2024.109607 · Cited by 9
Glass, K. A., Longley, S. J., Bliss, J. M., & Shaw, S. K. (2015) · Virulence · doi:10.1080/21505594.2015.1042643 · Cited by 9
Rai, M. N., Lan, Q., Parsania, C., Rai, R., Shirgaonkar, N., Chen, R., Shen, L., Tan, K., & Wong, K. H. (2024) · eLife · doi:10.7554/elife.73832 · Cited by 10
Macrophage pyroptosis induced by Candida albicans
Zhang, F.-Y., Lian, N., & Li, M. (2024) · Pathogens and Disease · doi:10.1093/femspd/ftae003 · Cited by 11
Benchouaia, M., Ripoche, H., Sissoko, M., Thiébaut, A., Merhej, J., Delaveau, T., Fasseu, L., Benaissa, S., Lorieux, G., Jourdren, L., et al. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02689 · Cited by 8
Investigating Candida glabrata Urinary Tract Infections (UTIs) in Mice Using Bioluminescence Imaging
Schrevens, S., & Sanglard, D. (2021) · Journal of Fungi · doi:10.3390/jof7100844 · Cited by 9
Rai, M. N., Borah, S., Bairwa, G., Balusu, S., Gorityala, N., & Kaur, R. (2013) · Journal of Visualized Experiments · doi:10.3791/50625 · Cited by 8
Battu, A., Purushotham, R., Dey, P., Vamshi, S. S., & Kaur, R. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009355 · Cited by 8
Lehnert, T., Prauße, M. T. E., Hünniger, K., Praetorius, J., Kurzai, O., & Figge, M. T. (2021) · PLoS ONE · doi:10.1371/journal.pone.0249372 · Cited by 7
Kamli, M. R., Sabir, J. S. M., Malik, M. A., & Ahmad, A. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14101989 · Cited by 7
Radosa, S., Sprague, J. L., Lau, S., Tóth, R., Linde, J., Krüger, T., Sprenger, M., Kasper, L., Westermann, M., Kniemeyer, O., et al. (2021) · Cellular Microbiology · doi:10.1111/cmi.13389 · Cited by 7
Self-citationArastehfar, A. A., Daneshnia, F., Hovhannisyan, H., Cabrera, N., İlkit, M., Desai, J. V., Gabaldón, T., Shor, E., & Perlin, D. S. (2024) · FEMS Yeast Research · doi:10.1093/femsyr/foae035 · Cited by 6
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Xia, C., Liu, R., Zhang, S., Shen, J., & Wang, Z. (2025) · Diagnostic Microbiology and Infectious Disease · doi:10.1016/j.diagmicrobio.2025.116683 · Cited by 6
Sepúlveda-González, M. E., Parra-Ortega, B., Cervantes, Y. B., Hernández, G., Xicohtencatl‐Cortés, J., & Villa‐Tanaca, L. (2015) · Revista Iberoamericana de Micología · doi:10.1016/j.riam.2014.10.005 · Cited by 6
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Szabo, E. K., & MacCallum, D. M. (2013) · Virulence · doi:10.4161/viru.27046 · Cited by 6
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Roy, S., & Thompson, D. A. (2015) · FEMS Yeast Research · doi:10.1093/femsyr/fov087 · Cited by 8
Rai, M. N., Rai, R., Sethiya, P., & Parsania, C. (2023) · Research in Microbiology · doi:10.1016/j.resmic.2023.104073 · Cited by 5
Altmeier, S., & LeibundGut‐Landmann, S. (2017) · Springer eBooks · doi:10.1007/978-3-319-50842-9_2 · Cited by 5
Usher, J., Chaudhari, Y., Attah, V., Ho, H.-L., & Haynes, K. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.530915 · Cited by 5
Nasuno, R., Suzuki, S., Oiki, S., Hagiwara, D., & Takagi, H. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.825121 · Cited by 5
Belyaev, I., Marolda, A., Praetorius, J., Sarkar, A., Medyukhina, A., Hünniger, K., Kurzai, O., & Figge, M. T. (2022) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2022.05.007 · Cited by 6
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Gu, Y., Wang, H., Wang, Y.-S., Wang, L., & Jia, X.-M. (2026) · hLife · doi:10.1016/j.hlife.2025.12.008 · Cited by 5
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Ruiz‐Baca, E., Adame-Soto, P. J., Alba-Fierro, C. A., Martínez-Rocha, A. L., Pérez‐Torres, A., López-Rodríguez, A., & Romo-Lozano, Y. (2025) · Journal of Fungi · doi:10.3390/jof11060440 · Cited by 4
Castillo-Cruz, J., Palacios-Barreto, S., Mosso-Pani, M. A., Serna-Pérez, A. B., Rodríguez-Tovar, A. V., Serafín‐López, J., Castrejón-Jiménez, N. S., & García‐Pérez, B. E. (2025) · Microbial Pathogenesis · doi:10.1016/j.micpath.2025.107479 · Cited by 4
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Dupré‐Crochet, S., Erard, M., & Nüβe, O. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9424-3_18 · Cited by 4
Experimental Evolution of Candida by Serial Passaging in Host Cells
Graf, K., Hube, B., & Brunke, S. (2021) · Methods in molecular biology · doi:10.1007/978-1-0716-1182-1_10 · Cited by 4
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Arghavan, B., Sharifi, M., Shafiee, M., & Mohammadi, R. (2016) · Current Medical Mycology · doi:10.18869/acadpub.cmm.2.2.6 · Cited by 4
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Nishimura, A., Tanahashi, R., Nakagami, K., Morioka, Y., & Takagi, H. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1419530 · Cited by 3
Translation regulation promotes stress adaptation in the human fungal pathogen Candida glabrata
Rana, A., & Thakur, A. (2025) · Genetics · doi:10.1093/genetics/iyaf134 · Cited by 3
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McFadden, M. J., O’Riordan, M. X., & O’Meara, T. R. (2026) · Current Opinion in Microbiology · doi:10.1016/j.mib.2026.102710 · Cited by 3
Immunomodulatory Agents as Adjunctive Therapy for the Treatment of Resistant Candida Species
Beyda, N. D., Regen, S., Lewis, R. E., & Garey, K. W. (2013) · Current Fungal Infection Reports · doi:10.1007/s12281-013-0132-3 · Cited by 3
Jain, N., Bouklas, T., Gupta, A., Varshney, A. K., Orner, E. P., & Fries, B. C. (2015) · Infection and Immunity · doi:10.1128/iai.01046-15 · Cited by 3
Tsouris, A., Schacherer, J., & Ishchuk, O. P. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2257-5_18 · Cited by 3
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Fine-Scale Chromosomal Changes in Fungal Fitness
Fischer, D., Hube, B., & Brunke, S. (2014) · Current Fungal Infection Reports · doi:10.1007/s12281-014-0179-9 · Cited by 1
Self-citationEffect of Antifungal-Treated Host Macrophages on Candida glabrata
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Battu, A., Purushotham, R., & Kaur, R. (2021) · BIO-PROTOCOL · doi:10.21769/bioprotoc.4210 · Cited by 1
Dalai, A. K. (2011) · Cited by 1
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Viana, R., Pais, P., Cavalheiro, M., Galocha, M., & Teixeira, M. C. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819990-9.00035-4 · Cited by 1
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Self-citationfungal pathogen Candida albicans and the outcome of the host-pathogen
Okai, B., Lyall, N., & Bain, J. M. (2015)
Tóth, A. (2015) · SZTE Repository of Dissertations (University of Szeged) · doi:10.14232/phd.2592
The Epimmunity Theory: The Single Cell Defenses against Infectious and Genetic Diseases
Barghouthi, S. A. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00694
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Gilbert, A. S. (2017) · University of Birmingham Institutional Research Archive (University of Birmingham)
Radosa, S., Sprague, J. L., Tóth, R., Wolf, T., Sprenger, M., Brunke, S., Panagiotou, G., Linde, J., Gácser, A., & Hillmann, F. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/690503
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Zajta, E. (2020) · SZTE Repository of Dissertations (University of Szeged) · doi:10.14232/phd.10576
Interactions Between Intracellular Fungal Pathogens and Host Phagocytes
Case, N. T., Robbins, N., & Cowen, L. E. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00042-0
Arastehfar, A. A., Daneshnia, F., Cabrera, N., Penalva-Lopez, S., Sarathy, J. P., Zimmerman, M., Shor, E., & Perlin, D. S. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.21.513290
Dinh, T. T. H. (2020) · Chula Digiverse · doi:10.58837/chula.the.2020.309
SWI/SNF complex-mediated chromatin remodelling in Candida glabrata is vital for immune evasionPreprint
Kumar, K., Pareek, A., & Kaur, R. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.15.536997
Marcet‐Houben, M., Alvarado, M., Księżopolska, E., Saus, E., de Groot, P. W. J., & Gabaldón, T. (2022) · Figshare · doi:10.6084/m9.figshare.21303245
Metadata
- Authors
- Seider, K., Brunke, S., Schild, L., Jablonowski, N., Wilson, D., Majer, O., Barz, D., Haas, A., Kuchler, K., Schaller, M., & Hube, B.
- Affiliations
- Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI) (DE)
- Jena University Hospital (DE)
- Max Perutz Labs (AT)
- University of Bonn (DE)
- University of Tübingen (DE)
- Corresponding author
- Seider, Katja
- Brunke, Sascha
- Schild, Lydia
- Jablonowski, Nadja
- Wilson, Duncan
- Hube, Bernhard
- ORCID
- Venue
- The Journal of Immunology
- Publisher
- Oxford University Press (OUP)
- Published
- 2011-09
- Volume
- 187
- Issue
- 6
- Pages
- 3072-3086
- ISSN
- 0022-1767 (ISSN-L)
- 1550-6606
- OpenAlex
- W2124863746
- Cited by
- 220
- References
- 80
- Citations by year
- 2026: 13 · 2025: 11 · 2024: 10 · 2023: 12 · 2022: 15 · 2021: 18 · 2020: 23 · 2019: 18 · 2018: 16 · 2017: 8 · 2016: 14 · 2015: 20 · 2014: 16 · 2013: 16 · 2012: 6
- FWCI
- 9.06
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The Journal of Immunology (publishedVersion)
- PubMed (publishedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion, other-oa)
- Funders
- Deutsche Forschungsgemeinschaft (SFB 670)
- Österreichischen Akademie der Wissenschaften
- Austrian Science Fund
- Studienstiftung des Deutschen Volkes
- Center for Sepsis Control and Care
- 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 › Infectious Diseases › Fungal Infections and Studies
- Keywords
- Candida glabrata, immune evasion, cytokine production, reactive oxygen species, phagosome acidification, cathepsin D, LAMP1, GM-CSF, monocyte-derived macrophages, fungal virulence factors, host-pathogen interaction
- MeSH terms
- Candidiasis, Humans, Macrophages, Microscopy, Fluorescence, Phagosomes, Polymerase Chain Reaction, Cytokines, Apoptosis, Oligonucleotide Array Sequence Analysis, Candida glabrata, Microscopy, Electron, Transmission, Immune Evasion
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