Comparative Evaluations of the Pathogenesis of Candida auris Phenotypes and Candida albicans Using Clinically Relevant Murine Models of Infections
Open accessAbstract
The newly emerged Candida species C. auris has been associated with an exponential rise in invasive disease in health care facilities worldwide with a mortality rate approaching 60%. C. auris exhibits a high level of transmissibility, multidrug resistance, and persistence in hospital environments, yet little is known about its pathogenesis largely due to limited data from animal studies. We used clinically relevant murine models of infection to comparatively evaluate the host niche-specific pathogenic potential of C. auris and C. albicans . Findings demonstrated that C. auris adheres more avidly, forming robust biofilms on catheters implanted in mice. However, although C. auris adhered to oral tissue ex vivo , it failed to colonize the oral cavity in vivo . In contrast, in the intraperitoneal infection model, C. auris persisted longer in the peritoneal cavity and kidneys. Understanding the host-pathogen factors contributing to the rise of C. auris as a nosocomial pathogen is critical for controlling the spread of this species.
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C. auris persisted longer than C. albicans in kidneys of infected mice.
“In addition, C. auris persisted longer than C. albicans in kidneys of infected mice (26).”
From Differential skin immune responses in mice intradermally infected with <i>Candida auris</i> and <i>Candida albicans</i> (2023) · cites this paper as [26]
Candida auris has an extraordinary resistance profile to antifungals.
“One of the major phenotypic distinctions between other Candida species and C. auris is its extraordinary resistance profile to antifungals [5–7].”
From Lansoprazole interferes with fungal respiration and acts synergistically with amphotericin B against multidrug-resistant <i>Candida auris</i> (2024) · cites this paper as [6]
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Antibiotic resistance threats in the United States, 2019
(U.S.), C. F. D. C. A. P. (2019) · doi:10.15620/cdc:82532 · Cited by 5,782 · see citing works
Satoh, K., Makimura, K., Hasumi, Y., Nishiyama, Y., Uchida, K., & Yamaguchi, H. (2009) · Microbiology and Immunology · doi:10.1111/j.1348-0421.2008.00083.x · Cited by 1,381 · 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
First hospital outbreak of the globally emerging Candida auris in a European hospital
Schelenz, S., Hagen, F., Rhodes, J. L., Abdolrasouli, A., Chowdhary, A., Hall, A., Ryan, L., Shackleton, J., Trimlett, R., Meis, J. F., et al. (2016) · Antimicrobial Resistance & Infection Control · doi:10.1186/s13756-016-0132-5 · Cited by 768 · see citing works
Chowdhary, A., Sharma, C., & Meis, J. F. (2017) · PLOS Pathogens · doi:10.1371/journal.ppat.1006290 · Cited by 750 · see citing works
Oral Candidiasis: A Disease of Opportunity
Vila, T., Sultan, A. S., Montelongo-Jauregui, D., & Jabra-Rizk, M. A. (2020) · Journal of Fungi · doi:10.3390/jof6010015 · Cited by 537 · see citing works
Self-citationFirst Three Reported Cases of Nosocomial Fungemia Caused by Candida auris
Lee, W. G., Shin, J. H., Uh, Y., Kang, M. G., Kim, S. H., Park, K. H., & Jang, H. (2011) · Journal of Clinical Microbiology · doi:10.1128/jcm.00319-11 · Cited by 524 · see citing works
A <i>Candida auris</i> Outbreak and Its Control in an Intensive Care Setting
Eyre, D. W., Sheppard, A. E., Madder, H., Moir, I., Moroney, R., Quan, T. P., Griffiths, D., George, S., Butcher, L., Morgan, M., et al. (2018) · New England Journal of Medicine · doi:10.1056/nejmoa1714373 · Cited by 517 · see citing works
On the emergence of Candida auris: climate change, azoles, swamps, and birds
Casadevall, A., Kontoyiannis, D. P., & Robert, V. (2019) · mBio · doi:10.1128/mbio.01397-19 · Cited by 515 · see citing works
Dispersion as an Important Step in the Candida albicans Biofilm Developmental Cycle
Uppuluri, P., Chaturvedi, A. K., Srinivasan, A., Banerjee, M., Ramasubramaniam, A. K., Köhler, J. R., Kadosh, D., & Lopez-Ribot, J. L. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000828 · Cited by 432 · see citing works
<i>Candida auris</i> : The recent emergence of a multidrug-resistant fungal pathogen
Forsberg, K., Woodworth, K., Walters, M., Berkow, E. L., Jackson, B., Chiller, T., & Vallabhaneni, S. (2019) · Medical Mycology · doi:10.1093/mmy/myy054 · Cited by 421 · see citing works
Biofilm-Forming Capability of Highly Virulent, Multidrug-Resistant <i>Candida auris</i>
Sherry, L., Ramage, G., Kean, R., Borman, A., Johnson, E. M., Richardson, M. D., & Rautemaa-Richardson, R. (2017) · Emerging Infectious Diseases · doi:10.3201/eid2302.161320 · Cited by 420 · see citing works
Larkin, E., Hager, C., Chandra, J., Mukherjee, P. K., Retuerto, M., Salem, I., Long, L., Isham, N., Kovanda, L., Borroto-Esoda, K., et al. (2017) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02396-16 · Cited by 395 · see citing works
Ruiz‐Gaitán, A., Moret, A. M., Tasias‐Pitarch, M., Aleixandre‐López, A. I., Martínez‐Morel, H., Calabuig, E., Salavert‐Lletí, M., Ramírez, P., López‐Hontangas, J. L., Hagen, F., et al. (2018) · Mycoses · doi:10.1111/myc.12781 · Cited by 343 · see citing works
Borman, A. M., Szekely, A., & Johnson, E. M. (2016) · mSphere · doi:10.1128/msphere.00189-16 · Cited by 333 · see citing works
Sekyere, J. O. (2018) · MicrobiologyOpen · doi:10.1002/mbo3.578 · Cited by 307 · see citing works
Schlecht, L. M., Peters, B. M., Krom, B. P., Freiberg, J. A., Hänsch, G. M., Filler, S. G., Jabra‐Rizk, M. A., & Shirtliff, M. E. (2014) · Microbiology · doi:10.1099/mic.0.083485-0 · Cited by 282 · see citing works
Self-citationGenetic Basis of<i>Candida</i>Biofilm Resistance Due to Drug‐Sequestering Matrix Glucan
Nett, J. E., Sanchez, H., Cain, M. T., & Andes, D. R. (2010) · The Journal of Infectious Diseases · doi:10.1086/651200 · Cited by 250 · see citing works
Review on Antifungal Resistance Mechanisms in the Emerging Pathogen Candida auris
Chaabane, F., Graf, A., Jequier, L., & Coste, A. T. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.02788 · Cited by 223 · see citing works
Kean, R., Delaney, C., Sherry, L., Borman, A., Johnson, E. M., Richardson, M. D., Rautemaa-Richardson, R., Williams, C., & Ramage, G. (2018) · mSphere · doi:10.1128/msphere.00334-18 · Cited by 220 · see citing works
Candida auris and multidrug resistance: Defining the new normal
Lockhart, S. R. (2019) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2019.103243 · Cited by 205 · see citing works
Mouse model of oropharyngeal candidiasis
Solis, N. V., & Filler, S. G. (2012) · Nature Protocols · doi:10.1038/nprot.2012.011 · Cited by 195 · see citing works
Community participation in biofilm matrix assembly and function
Mitchell, K. F., Zarnowski, R., Sanchez, H., Edward, J. A., Reinicke, E. L., Nett, J. E., Mitchell, A. P., & Andes, D. R. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1421437112 · Cited by 183 · see citing works
Candida albicans Pathogenesis: Fitting within the Host-Microbe Damage Response Framework
Jabra‐Rizk, M. A., Kong, E. F., Tsui, C., Nguyen, M. H., Clancy, C. J., Fidel, P. L., & Noverr, M. C. (2016) · Infection and Immunity · doi:10.1128/iai.00469-16 · Cited by 183 · see citing works
Self-citationYue, H., Bing, J., Zheng, Q., Zhang, Y., Hu, T., Du, H., Wang, H., & Huang, G. (2018) · Emerging Microbes & Infections · doi:10.1038/s41426-018-0187-x · Cited by 176 · see citing works
On the Origins of a Species: What Might Explain the Rise of Candida auris?
Jackson, B. R., Chow, N. A., Forsberg, K., Litvintseva, A. P., Lockhart, S. R., Welsh, R. M., Vallabhaneni, S., & Chiller, T. M. (2019) · Journal of Fungi · doi:10.3390/jof5030058 · Cited by 165 · see citing works
The NDV-3A vaccine protects mice from multidrug resistant Candida auris infection
Singh, S., Uppuluri, P., Mamouei, Z., Alqarihi, A., Elhassan, H., French, S., Lockhart, S. R., Chiller, T., Edwards, J. E., & Ibrahim, A. S. (2019) · PLOS Pathogens · doi:10.1371/journal.ppat.1007460 · Cited by 162 · see citing works
Candida auris Forms High-Burden Biofilms in Skin Niche Conditions and on Porcine Skin
Horton, M. V., Johnson, C. J., Kernien, J. F., Patel, T. D., Lam, B. C., Cheong, J. Z. A., Meudt, J. J., Shanmuganayagam, D., Kalan, L. R., & Nett, J. E. (2020) · mSphere · doi:10.1128/msphere.00910-19 · Cited by 159 · see citing works
Emerging fungal pathogen Candida auris evades neutrophil attack
Johnson, C. J., Davis, J. M., Huttenlocher, A., Kernien, J. F., & Nett, J. E. (2018) · mBio · doi:10.1128/mbio.01403-18 · Cited by 157 · see citing works
Candida albicans-Staphylococcus aureus Polymicrobial Peritonitis Modulates Host Innate Immunity
Peters, B. M., & Noverr, M. C. (2013) · Infection and Immunity · doi:10.1128/iai.00265-13 · Cited by 152 · see citing works
Kim, S. H., Iyer, K. R., Pardeshi, L., Muñoz, J. F., Robbins, N., Cuomo, C. A., Wong, K. H., & Cowen, L. E. (2019) · mBio · doi:10.1128/mbio.02529-18 · Cited by 136 · see citing works
Navarro-Arias, M. J., Hernández-Chávez, M. J., García-Carnero, L. C., Amezcua-Hernández, D. G., Lozoya‐Pérez, N. E., Estrada-Mata, E., Martínez-Duncker, I., Franco, B., & Mora-Montes, H. M. (2019) · Infection and Drug Resistance · doi:10.2147/idr.s197531 · Cited by 136 · see citing works
Candida auris: Epidemiology, risk factors, virulence, resistance, and therapeutic options
Sardi, J. D. C. O., Silva, D. R., Mendes‐Giannini, M. J. S., & Rosalen, P. L. (2018) · Microbial Pathogenesis · doi:10.1016/j.micpath.2018.09.014 · Cited by 132 · see citing works
Conserved Role for Biofilm Matrix Polysaccharides in <i>Candida auris</i> Drug Resistance
Dominguez, E. G., Zarnowski, R., Choy, H. L., Zhao, M., Sanchez, H., Nett, J. E., & Andes, D. R. (2019) · mSphere · doi:10.1128/mspheredirect.00680-18 · Cited by 132 · see citing works
Szekely, A., Borman, A. M., & Johnson, E. M. (2019) · Journal of Clinical Microbiology · doi:10.1128/jcm.02055-18 · Cited by 125 · see citing works
Candida auris: What Have We Learned About Its Mechanisms of Pathogenicity?
Rossato, L., & Colombo, A. L. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.03081 · Cited by 121 · see citing works
Hog1 regulates stress tolerance and virulence in the emerging fungal pathogen Candida auris
Day, A. M., McNiff, M. M., da Silva Dantas, A., Gow, N. A. R., & Quinn, J. (2018) · mSphere · doi:10.1128/msphere.00506-18 · Cited by 116 · see citing works
Lara, H. H., Ixtepan-Turrent, L., Jose Yacaman, M., & Lopez-Ribot, J. (2020) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.9b20708 · Cited by 116 · see citing works
Nobbs, A. H., Vickerman, M. M., & Jenkinson, H. F. (2010) · Eukaryotic Cell · doi:10.1128/ec.00103-10 · Cited by 112 · see citing works
Forgács, L., Borman, A. M., Prépost, E., Tóth, Z., Kardos, G., Kovács, R., Szekely, A., Nagy, F., Kovacs, I., & Majoros, L. (2020) · Emerging Microbes & Infections · doi:10.1080/22221751.2020.1771218 · Cited by 107 · see citing works
Bravo Ruiz, G., Ross, Z. K., Gow, N. A. R., & Lorenz, A. (2020) · mSphere · doi:10.1128/msphere.00151-20 · Cited by 101 · see citing works
de Jong, A. W., & Hagen, F. (2019) · Mycopathologia · doi:10.1007/s11046-019-00351-w · Cited by 98 · see citing works
Hager, C. L., Larkin, E. L., Long, L. A., & Ghannoum, M. A. (2018) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dky153 · Cited by 95 · see citing works
Kumar, D., Banerjee, T., Pratap, C. B., & Tilak, R. (2015) · The Journal of Infection in Developing Countries · doi:10.3855/jidc.4582 · Cited by 90 · see citing works
Wall, G., Chaturvedi, A. K., Wormley, F. L., Wiederhold, N. P., Patterson, H. P., Patterson, T. F., & Lopez-Ribot, J. L. (2018) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01084-18 · Cited by 89 · see citing works
Biofilm formation by <i>Candida auris</i> isolated from colonising sites and candidemia cases
Singh, R., Kaur, M., Chakrabarti, A., Shankarnarayan, S. A., & Rudramurthy, S. M. (2019) · Mycoses · doi:10.1111/myc.12947 · Cited by 86 · see citing works
Candida auris Phenotypic Heterogeneity Determines Pathogenicity <i>In Vitro</i>
Brown, J. L., Delaney, C., Short, B., Butcher, M. C., McKloud, E., Williams, C., Kean, R., & Ramage, G. (2020) · mSphere · doi:10.1128/msphere.00371-20 · Cited by 76 · see citing works
Pathirana, R. U., Friedman, J., Norris, H. L., Salvatori, O., McCall, A. D., Kay, J. G., & Edgerton, M. (2017) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01872-17 · Cited by 70 · see citing works
Candida auris: An emerging pathogen “incognito”?
Nett, J. E. (2019) · PLOS Pathogens · doi:10.1371/journal.ppat.1007638 · Cited by 69 · see citing works
Candida auris: a comparison between planktonic and biofilm susceptibility to antifungal drugs
Romera, D., Aguilera-Correa, J. J., Gadea, I., Viñuela-Sandoval, L., García‐Rodríguez, J., & Esteban, J. (2019) · Journal of Medical Microbiology · doi:10.1099/jmm.0.001036 · Cited by 68 · see citing works
Lockhart, S. R., Jackson, B. R., Vallabhaneni, S., Ostrosky-Zeichner, L., Pappas, P. G., & Chiller, T. (2017) · Journal of Clinical Microbiology · doi:10.1128/jcm.01355-17 · Cited by 61 · see citing works
Kong, E. F., Tsui, C., Boyce, H. J., Ibrahim, A., Hoag, S. W., Karlsson, A. J., Meiller, T. F., & Jabra‐Rizk, M. A. (2015) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02624-15 · Cited by 51 · see citing works
Self-citationImpact of Candida auris Infection in a Neutropenic Murine Model
Torres, S. R., Pichowicz, A., Torres-Velez, F., Song, R., Singh, N., Lasek-Nesselquist, E., & De Jesus, M. (2020) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01625-19 · Cited by 45 · see citing works
Candida auris Biofilm Colonization on Skin Niche Conditions
Uppuluri, P. (2020) · mSphere · doi:10.1128/msphere.00972-19 · Cited by 29 · see citing works
Kucharíková, S., Velde, G. V., Himmelreich, U., & Dijck, P. V. (2015) · Journal of Visualized Experiments · doi:10.3791/52239 · Cited by 26 · see citing works
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Santana, D. J., Anku, J. A. E., Zhao, G., Zarnowski, R., Johnson, C. J., Hautau, H., Visser, N. D., Ibrahim, A. S., Andes, D., Nett, J. E., et al. (2023) · Science · doi:10.1126/science.adf8972 · Cited by 142 · see citing works
Vila, T. V. M., Kong, E. F., Montelongo‐Jauregui, D., Dijck, P. V., Shetty, A. C., McCracken, C. L., Bruno, V. M., & Jabra‐Rizk, M. A. (2021) · Virulence · doi:10.1080/21505594.2021.1894834 · Cited by 89 · see citing works
Self-citationMechanisms of pathogenicity for the emerging fungus Candida auris
Horton, M. V., Holt, A. M., & Nett, J. E. (2023) · PLOS Pathogens · doi:10.1371/journal.ppat.1011843 · Cited by 67 · see citing works
The many faces of Candida auris: Phenotypic and strain variation in an emerging pathogen
Santana, D. J., Zhao, G., & O’Meara, T. R. (2024) · PLOS Pathogens · doi:10.1371/journal.ppat.1012011 · Cited by 62 · see citing works
Wang, T. W., Sofras, D., Montelongo-Jauregui, D., Paiva, T. O., Carolus, H., Dufrêne, Y. F., Alfaifi, A. A., McCracken, C., Bruno, V. M., Van Dijck, P., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-53588-5 · Cited by 47 · see citing works
Self-citationPiatti, G., Sartini, M., Cusato, C., & Schito, A. M. (2021) · Journal of Hospital Infection · doi:10.1016/j.jhin.2021.11.004 · Cited by 38 · see citing works
Overview about Candida auris: What's up 12 years after its first description?
Désoubeaux, G., Coste, A. T., Imbert, C., & Hennequin, C. (2022) · Journal de Mycologie Médicale · doi:10.1016/j.mycmed.2022.101248 · Cited by 38 · see citing works
Zhao, G., Lyu, J., Veniaminova, N. A., Zarnowski, R., Mattos, E., Johnson, C. J., Quintanilla, D., Hautau, H., Hold, L. A., Xu, B., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60876-1 · Cited by 32 · see citing works
“C. auris is knownforits ability to adhereto synthetic surfaces,posing a signi fi cant threat to patients with indwelling devices, such as catheters 11,12,29,47 .”
Datta, A., Das, D., Nett, J. E., Vyas, J. M., Lionakis, M. S., & Thangamani, S. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.02215-23 · Cited by 30 · see citing works
“albicans in kidneys of infected mice (26).”
Uniqueness of Candida auris cell wall in morphogenesis, virulence, resistance, and immune evasion
Dakalbab, S., Hamdy, R., Holigová, P., Abuzaid, E. J., Abu-Qiyas, A., Lashine, Y., Mohammad, M. G., & Soliman, S. S. M. (2024) · Microbiological Research · doi:10.1016/j.micres.2024.127797 · Cited by 27 · see citing works
Farooqi, J. Q., Niamatullah, H., Irfan, S., Zafar, A., Malik, F. R., & Jabeen, K. (2021) · Clinical Microbiology and Infection · doi:10.1016/j.cmi.2021.05.031 · Cited by 21 · see citing works
Cruz, R., & Wuest, W. M. (2023) · Tetrahedron · doi:10.1016/j.tet.2023.133268 · Cited by 19 · see citing works
Innate immune response to Candida auris
Holt, A. M., & Nett, J. E. (2024) · Current Opinion in Microbiology · doi:10.1016/j.mib.2024.102510 · Cited by 18 · see citing works
Candida auris biofilm: a review on model to mechanism conservation
Khari, A., Biswas, B., Gangwar, G., Thakur, A., & Puria, R. (2023) · Expert Review of Anti-infective Therapy · doi:10.1080/14787210.2023.2179036 · Cited by 18 · see citing works
Das, D., HogenEsch, H., & Thangamani, S. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1123200 · Cited by 18 · see citing works
Mikulska, M., Ullah, N., Magnasco, L., Codda, G., Bartalucci, C., Miletich, F., Sepulcri, C., Willison, E., Vena, A., Giacobbe, D. R., et al. (2024) · Clinical Microbiology and Infection · doi:10.1016/j.cmi.2024.02.012 · Cited by 18 · see citing works
Salama, E. A., Elgammal, Y., Wijeratne, A., Lanman, N. A., Utturkar, S. M., Farhangian, A., Li, J., Meunier, B., Hazbun, T. R., & Seleem, M. N. (2024) · Emerging Microbes & Infections · doi:10.1080/22221751.2024.2322649 · Cited by 16 · see citing works
Identification of Candida auris by PCR and assessment of biofilm formation by crystal violet assay
Singh, P., Srivastava, S., Malhotra, R., & Mathur, P. (2023) · Indian Journal of Medical Microbiology · doi:10.1016/j.ijmmb.2023.100421 · Cited by 14 · see citing works
Ionescu, S. G., Luchian, I. A., Dămian, C., Goriuc, A., Porumb‐Andrese, E., Popa, C. G., Cobzaru, R. G., Ripa, C. V., & Ursu, R. G. (2024) · Current Issues in Molecular Biology · doi:10.3390/cimb46060362 · Cited by 13 · see citing works
Characterization of susceptibility patterns and adaptability of the newly emerged Candida auris
Semenya, M. D., Aladejana, A. E., & Ndlovu, S. I. (2024) · International Microbiology · doi:10.1007/s10123-024-00563-1 · Cited by 14 · see citing works
Enablers of Candida auris persistence on medical devices and their mode of eradication.
Nwachukwu, K. C., Nwarunma, E., Uchenna, C. D., & Ugbogu, O. C. (2023) · PubMed Central · doi:10.18502/cmm.2023.150673 · Cited by 10 · see citing works
Li, X., Gong, Y., Lin, X., Lin, Q., Luo, J., Yu, T., Xu, J., Chen, L., Xu, L., & Hu, Y. (2022) · The Journal of Microbiology · doi:10.1007/s12275-022-1663-5 · Cited by 10 · see citing works
Miranda, V., Laarej, K., & Cavaliere, C. (2026) · Cells · doi:10.3390/cells15010082 · Cited by 10 · see citing works
Shinohara, T., Wada, A., Abe, M., Nakayama, N., Nagi, M., & Miyazaki, Y. (2023) · JAC-Antimicrobial Resistance · doi:10.1093/jacamr/dlad155 · Cited by 8 · see citing works
Yang, B., Vaisvil, B., Schmitt, D. P., Collins, J., Young, E. M., Kapatral, V., & Rao, R. P. (2024) · Infection and Immunity · doi:10.1128/iai.00103-24 · Cited by 7 · see citing works
Towns, K. A., Datta, A., & Thangamani, S. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.00127-24 · Cited by 7 · see citing works
Does Candida auris colonize the oral cavity? A retrospective institutional experience
Alfaifi, A. A., Brooks, J. K., Jabra‐Rizk, M. A., Meiller, T. F., & Sultan, A. S. (2023) · Oral Diseases · doi:10.1111/odi.14720 · Cited by 7 · see citing works
Self-citationPathogenicity and virulence of Candida auris
Phan-Canh, T., Seiser, S., Chauhan, M., Kuchler, K., Chauhan, N., & Elbe‐Bürger, A. (2026) · Virulence · doi:10.1080/21505594.2026.2707827 · Cited by 6 · see citing works
A Human Ex Vivo Skin Model to Study Candida auris Biofilms
Corzo-León, D., Mark, C., MacCallum, D. M., & Munro, C. A. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2417-3_21 · Cited by 6 · see citing works
HIV protease inhibitors restore amphotericin B activity against Candida
Elgammal, Y., Salama, E. A., & Seleem, M. N. (2025) · PLoS ONE · doi:10.1371/journal.pone.0324080 · Cited by 5 · see citing works
In Vivo Evolution of Candida auris Multidrug Resistance in a Patient Receiving Antifungal Treatment
Wang, T. W., Putnam, N. E., Johnson, J. K., & Jabra‐Rizk, M. A. (2025) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiaf394 · Cited by 3 · see citing works
Self-citationAnti-virulence and anti-efflux pump activity of synthetic defensins and histatin in Candida auris
Shaban, S., Patel, M., & Ahmad, A. (2025) · Microbial Pathogenesis · doi:10.1016/j.micpath.2025.107644 · Cited by 3 · see citing works
Candida auris adhesins, specifically Als3, a key target to understand and mitigate
Lashine, Y., Hamdy, R., Dakalbab, S., Lazreg, I. K., Aldhaheri, F., Chin, S.-P., Hashim, N., & Soliman, S. S. M. (2025) · Mycologia · doi:10.1080/00275514.2025.2536345 · Cited by 3 · see citing works
C. elegans as a tractable infection model for the emerging fungal pathogen Candida auris
Martinez, M., Cruz, M. R., Garsin, D. A., & Lorenz, M. C. (2026) · Microbiology Spectrum · doi:10.1128/spectrum.03156-25 · Cited by 3 · see citing works
Vaccaro, A., Cooper, J. F., Rodríguez, A. V., Badali, H., Kean, R., Ramage, G., & Lopez-Ribot, J. L. (2026) · Journal of Fungi · doi:10.3390/jof12040247 · Cited by 3 · see citing works
Therapeutic potential of biosynthesized Ag/AgO NPs against Candida albicans and Candida auris
Alsagaby, R. A. S., Ansari, M. A., Alsulami, E. M. A., & Rehman, S. (2025) · Microbial Pathogenesis · doi:10.1016/j.micpath.2025.107935 · Cited by 2 · see citing works
Zainal, M., Sarmin, N. ‘. M., Ibrahim, M. J., Cirillo, N., Dashper, S. G., & Arzmi, M. H. (2025) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2025.106478 · Cited by 2 · see citing works
Frolov, N. A., Seferyan, M. A., Detusheva, E. V., Son, E., Kolmakov, I. G., & Vereshchagin, A. N. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262412098 · Cited by 2 · see citing works
Araujo, G. S., de Jesus, I. C. T. A., da Costa, P. C. Q. G., Marques, K. K. G., Gonçalves, J. C. R., & de Castro, R. D. (2026) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2026.106572 · Cited by 3 · see citing works
Isolamento e perfil de resistência de Candida spp. de animais domésticos e selvagens
Cândido, S. L., Menezes, I. D. G., Nakazato, L., Morgado, T. O., Ludwig, A., Santúrio, J. M., & Dutra, V. (2021) · Research Society and Development · doi:10.33448/rsd-v10i10.18541 · Cited by 2 · see citing works
Zhao, G., Lyu, J., Veniaminova, N. A., Zarnowski, R., Mattos, E., Johnson, C. J., Quintanilla, D., Hautau, H., Hold, L. A., Xu, B., et al. (2025) · doi:10.1101/2025.02.13.637978 · Cited by 2 · see citing works
Ramage, G., Kean, R., Mackay, W. G., Vaccaro, A., Lopez-Ribot, J. L., & Howe, M. H. (2025) · Springer series on biofilms · doi:10.1007/978-3-031-93315-8_7 · Cited by 1 · see citing works
Nebeluk, N., & Doub, J. B. (2025) · Infectious Disease Reports · doi:10.3390/idr17060144 · Cited by 1 · see citing works
Giammarino, A., Verdolini, L., Mussin, J. E., Radocchia, G., Rojas, F. D., Giusiano, G., & Angiolella, L. (2026) · Microorganisms · doi:10.3390/microorganisms14010188 · Cited by 1 · see citing works
From Oral Candidiasis to Candidemia: A Review of Superficial to Invasive Progression
Jerez, J. R., Ambrosio, M. V., Fernandes, M. E. O., & Mima, E. G. D. O. (2026) · MicrobiologyOpen · doi:10.1002/mbo3.70353 · Cited by 1 · see citing works
Alves, M., Ricardo, E., & Costa‐de‐Oliveira, S. (2026) · Journal of Fungi · doi:10.3390/jof12080603 · Cited by 1 · see citing works
CANDIDA AURIS: IMMINENCE OF A NEW PANDEMIC?
Chaves, Á. G., da Costa, V. M., & Brito, M. D. V. (2021) · RECIMA21 - Revista Científica Multidisciplinar · doi:10.47820/recima21.v2i4.287 · Cited by 3 · see citing works
Inabuy, F. S., Ramona, Y., Darmayasa, I. B. G., Teriyani, N. M., Ariwathi, N. L. P., & Shetty, K. (2025) · Microbiology and Biotechnology Letters · doi:10.48022/mbl.2501.01001 · Cited by 1 · see citing works
COMPARAÇÃO DE TRÊS TÉCNICAS DE DIAGNÓSTICO DA DOENÇA DE HIRSCHSPRUNG
Lopes, C. C. C., Bertuci, J. V. F., Lopes, E. B., Lopes, L. C., Barros, V. D. S., Zanatta, L., dos Santos, D. L., da Costa, M. M., Dias, T. G., Adami, E. R., et al. (2021) · doi:10.22533/at.ed.77221091111
Alzheimer’s disease, dementia, aging, and COVID-19
Paley, E. L. (2023) · Elsevier eBooks · doi:10.1016/b978-0-443-19122-0.00021-2
Do farnesol and tyrosol production in Candidozyma auris biofilms reflect virulence potential?
dos Santos, M. M., Moure, H. S., Ferreira, M. J. P., & Ishida, K. (2025) · Virulence · doi:10.1080/21505594.2025.2561832
Zhang, D., XiaoXing, L., Zhao, X., Yan, Z., Wang, W., & Dai, G. (2026) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2026.2655675
Kumari, S., Rain, Z., Prakash, P., Tilak, R., & Singh, A. K. (2026) · Scientific Reports · doi:10.1038/s41598-026-57636-6
Zainal, M., Ibrahim, M. J., Sarmin, N. ‘. M., Ismail, S., Cirillo, N., Dashper, S. G., & Arzmi, M. H. (2026) · Biofouling · doi:10.1080/08927014.2026.2688203
Hang, S., Jiang, B., Li, W., Xu, X., Xu, L., Xiong, J., Jiang, Y., & Lu, H. (2026) · Biochemical Pharmacology · doi:10.1016/j.bcp.2026.118302
He, J., Wang, Q., Sun, B., Velkov, T., Shen, J., Jiang, H., & Dai, C. (2026) · ACS Omega · doi:10.1021/acsomega.6c05321
Soni, A., Vrzoňová, R., Paulovičová, L., Bzducha‐Wróbel, A., & Farkaš, P. (2026) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2026.154672
Candidozyma auris ( Candida auris ) as a harbinger of novel fungal pathogens
Schuh, C., & Gokhale, C. S. (2026) · mSphere · doi:10.1128/msphere.00109-26
- Authors
- Vila, T., Montelongo-Jauregui, D., Ahmed, H., Puthran, T., Sultan, A. S., & Jabra-Rizk, M. A.
- Affiliations
- University of Maryland, Baltimore (US)
- Department of Oncology and Diagnostic Sciences, School of Dentistry, University of Maryland, Baltimore, Maryland, USA
- Venue
- mSphere
- Publisher
- American Society for Microbiology
- Published
- 2020-08-26
- Volume
- 5
- Issue
- 4
- ISSN
- 2379-5042 (ISSN-L)
- PMC
- PMC7407074
- OpenAlex
- W3047582300
- Cited by
- 58
- References
- 55
- Citations by year
- 2026: 15 · 2025: 13 · 2024: 10 · 2023: 11 · 2022: 3 · 2021: 6
- FWCI
- 0.66
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- mSphere (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- HHS | National Institutes of Health (R01AI130170)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Health Sciences › Medicine › Epidemiology › Fungal Infections and Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Yeasts and Rust Fungi Studies
- Keywords
- Candida auris, Candida albicans, fungal pathogenesis, mouse infection model, biofilm formation, catheter-related infection, oral colonization, peritoneal infection, kidney colonization, nosocomial fungal infections, host-pathogen interaction, multidrug resistance
- MeSH terms
- Animals, Candida, Candida albicans, Candidiasis, Disease Models, Animal, Female, Mice, Inbred C57BL, Phenotype, Virulence, Biofilms, Microscopy, Confocal, Microscopy, Electron, Transmission, Mice, Host-Pathogen Interactions
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