The DOI matches its Crossref record; 33 of the 33 references it cites were found in a registry or an index.
Quorum Sensing in the Dimorphic Fungus Candida albicans Is Mediated by Farnesol
Open accessAbstract
The inoculum size effect in the dimorphic fungus Candida albicans results from production of an extracellular quorum-sensing molecule (QSM). This molecule prevents mycelial development in both a growth morphology assay and a differentiation assay using three chemically distinct triggers for germ tube formation (GTF): L-proline, N-acetylglucosamine, and serum (either pig or fetal bovine). In all cases, the presence of QSM prevents the yeast-to-mycelium conversion, resulting in actively budding yeasts without influencing cellular growth rates. QSM exhibits general cross-reactivity within C. albicans in that supernatants from strain A72 are active on five other strains of C. albicans and vice versa. The QSM excreted by C. albicans is farnesol (C(15)H(26)O; molecular weight, 222.37). QSM is extracellular, and is produced continuously during growth and over a temperature range from 23 to 43 degrees C, in amounts roughly proportional to the CFU/milliliter. Production is not dependent on the type of carbon source nor nitrogen source or on the chemical nature of the growth medium. Both commercial mixed isomer and (E,E)-farnesol exhibited QSM activity (the ability to prevent GTF) at a level sufficient to account for all the QSM activity present in C. albicans supernatants, i.e., 50% GTF at ca. 30 to 35 microM. Nerolidol was ca. two times less active than farnesol. Neither geraniol (C(10)), geranylgeraniol (C(20)), nor farnesyl pyrophosphate had any QSM activity.
Overview
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
Verification
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?
In the citing paper
“In the biofilm environment, Candida species cells have the ability to communicate with each other via quorum sensing (via numerous signalling molecules), which is directly dependent on the cell density [148].”
From Candida glabrata Biofilms: How Far Have We Come? (2017) · cites this paper as [148]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Handbook of Microbiological Media
Atlas, R. M., & Atlas, R. M. (2004) · CRC Press eBooks · doi:10.1201/9781420039726 · Cited by 2,162
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
Lee, K. L., BUCKLEY, H. R., & Campbell, C. C. (1975) · Medical Mycology · doi:10.1080/00362177585190271 · Cited by 791
Shaw, P. D., Ping, G., Daly, S. L., Cha, C., Cronan, J. E., RINEHART, K. L. J., & Farrand, S. K. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.12.6036 · Cited by 748
Cha, C., Gao, P. H., Chen, Y.-C., Shaw, P. D., & Farrand, S. K. (1998) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.1998.11.11.1119 · Cited by 618
Brown‐Borg, H. M. (1995) · Tissue and Cell · doi:10.1016/s0040-8166(05)80072-2 · Cited by 511
Evidence for Mating of the "Asexual" Yeast Candida albicans in a Mammalian Host
Hull, C. M., Raisner, R. M., & Johnson, A. D. (2000) · Science · doi:10.1126/science.289.5477.307 · Cited by 465
Induction of Mating in Candida albicans by Construction of MTL a and MTL α Strains
Magee, B. B., & Magee, P. T. (2000) · Science · doi:10.1126/science.289.5477.310 · Cited by 443
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 300
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
Research works printed but not linked: 3
- Coscia C. J. (1984) Handbook of chromatography: terpenoids. (CRC Press Boca Raton Fla).
- Griffin D. H. (1994) Fungal physiology (Wiley-Liss New York N. Y) 2nd ed.
- Lisec A. D. (1998) Quorum sensing in Candida albicans: partial purification of two extracellular candidate molecules. M.S. thesis. (University of Nebraska Lincoln).
Cited by
Sorted by citations
Items 301–400 of 982
In vitro and in vivo Effect of Exogenous Farnesol Exposure Against Candida auris
Nagy, F., Vitális, E., Jakab, Á., Borman, A. M., Forgács, L., Tóth, Z., Majoros, L., & Kovács, R. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.00957 · Cited by 56
Impact of linoleic acid supplementation on lovastatin production in Aspergillus terreus cultures
Sorrentino, F., Roy, I., & Keshavarz, T. (2010) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-010-2722-0 · Cited by 58
Candida albicans induces early apoptosis followed by secondary necrosis in oral epithelial cells
Villar, C. C., & Zhao, X. R. (2010) · Molecular Oral Microbiology · doi:10.1111/j.2041-1014.2010.00577.x · Cited by 59
Quorum Sensing and Quorum Quenching with a Focus on Cariogenic and Periodontopathic Oral Biofilms
Wright, P. P., & Ramachandra, S. S. (2022) · Microorganisms · doi:10.3390/microorganisms10091783 · Cited by 65
Sensing the environment: Response of Candida albicans to the X factor
Cottier, F., & Mühlschlegel, F. A. (2009) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2009.01564.x · Cited by 56
Torres, M., Dessaux, Y., & Llamas, I. (2019) · Marine Drugs · doi:10.3390/md17030191 · Cited by 56
Lin, C.-J., & Chen, Y.-L. (2018) · Journal of Fungi · doi:10.3390/jof4020068 · Cited by 55
The Clinical Importance of Fungal Biofilms
Ramage, G., & Williams, C. (2013) · Advances in applied microbiology · doi:10.1016/b978-0-12-407673-0.00002-3 · Cited by 58
Yajima, A. (2014) · Tetrahedron Letters · doi:10.1016/j.tetlet.2014.03.051 · Cited by 55
Quorum sensing as a method for improving sclerotiorin production in Penicillium sclerotiorum
Raina, S., Odell, M., & Keshavarz, T. (2010) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2010.04.009 · Cited by 54
Chang, W., Li, Y., Zhang, L., Cheng, A., & Lou, H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0041624 · Cited by 54
Zawrotniak, M., Wojtalik, K., & Rąpała‐Kozik, M. (2019) · Cells · doi:10.3390/cells8121611 · Cited by 54
Natural antimicrobials in food safety and quality
(2011) · CABI eBooks · doi:10.1079/9781845937690.0000 · Cited by 55
Cell Signals, Cell Contacts, and the Organization of Yeast Communities
Honigberg, S. M. (2011) · Eukaryotic Cell · doi:10.1128/ec.00313-10 · Cited by 53
González, B., Vázquez, J., Cullen, P. J., Mas, A., Beltran, G., & Torija, M.-J. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00670 · Cited by 52
Quorum Sensing: Not Just a Bridge Between Bacteria
Liu, D., Lu, Y., Li, Z., Pang, X., & Gao, X. (2025) · MicrobiologyOpen · doi:10.1002/mbo3.70016 · Cited by 60
Krist, S., Banovac, D., Tabanca, N., Wedge, D. E., Gochev, V., Wanner, J., Erich, S., & Jirovetz, L. (2015) · Natural Product Communications · doi:10.1177/1934578x1501000133 · Cited by 52
Zhang, L., Chang, W., Sun, B., Groh, M., Speicher, A., & Lou, H. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028953 · Cited by 52
Langford, M. L., Hargarten, J. C., Patefield, K. D., Marta, E., Blankenship, J. R., Fanning, S., Nickerson, K. W., & Atkin, A. L. (2013) · Eukaryotic Cell · doi:10.1128/ec.00311-12 · Cited by 53
Self-citationKostoulias, X., Murray, G. L., Cerqueira, G. M., Kong, J. B., Bantun, F., Mylonakis, E. E., Khoo, C. A., & Peleg, A. Y. (2015) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01540-15 · Cited by 51
The Metacaspase (Mca1p) has a Dual Role in Farnesol-induced Apoptosis in Candida albicans
Léger, T., Garcia, C., Ounissi, M., Lelandais, G., & Camadro, J. (2014) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m114.041210 · Cited by 51
Kovács, R., Bozó, A., Gesztelyi, R., Domán, M., Kardos, G., Nagy, F., Tóth, Z., & Majoros, L. (2016) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2016.01.007 · Cited by 51
Linking Quorum Sensing Regulation and Biofilm Formation by Candida albicans
Deveau, A., & Hogan, D. A. (2010) · Methods in molecular biology · doi:10.1007/978-1-60761-971-0_16 · Cited by 51
Décanis, N., Savignac, K., & Rouabhia, M. (2009) · Cytokine · doi:10.1016/j.cyto.2008.11.011 · Cited by 50
Mech, F., Wilson, D., Lehnert, T., Hube, B., & Figge, M. T. (2013) · Cytometry Part A · doi:10.1002/cyto.a.22418 · Cited by 50
Berretta, A. A., de Castro, P. A., Cavalheiro, A. H., Fortes, V. S., Bom, V. L. P., Nascimento, A. P., Marquele‐Oliveira, F., Pedrazzi, V., Ramalho, L. N. Z., & Goldman, G. H. (2013) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2013/641480 · Cited by 50
Microbial Quorum-Sensing Molecules Induce Acrosome Loss and Cell Death in Human Spermatozoa
Rennemeier, C., Frambach, T., Hennicke, F., Dietl, J., & Staib, P. (2009) · Infection and Immunity · doi:10.1128/iai.00586-09 · Cited by 50
Vila, T. V. M., Kong, E. F., Ibrahim, A., Piepenbrink, K. H., Shetty, A. C., McCracken, C. L., Bruno, V. M., & Jabra‐Rizk, M. A. (2019) · Virulence · doi:10.1080/21505594.2019.1635418 · Cited by 51
Barot, T. D., Rawtani, D., Kulkarni, P., Hussain, C. M., & Satyaprasad, A. (2020) · Journal of the mechanical behavior of biomedical materials/Journal of mechanical behavior of biomedical materials · doi:10.1016/j.jmbbm.2020.103675 · Cited by 50
Quorum Sensing: Alcohols in a Social Situation
Hogan, D. A. (2006) · Current Biology · doi:10.1016/j.cub.2006.05.035 · Cited by 50
Neutrophil Extracellular Traps in Candida albicans Infection
He, Y., Liu, J., Chen, Y., Yan, L., & Wu, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.913028 · Cited by 50
Candida albicans in Multispecies Oral Communities; A Keystone Commensal?
Janus, M. M., Willems, H. M. E., & Krom, B. P. (2016) · Advances in experimental medicine and biology · doi:10.1007/5584_2016_5 · Cited by 49
Abrogation of pathogenic attributes in drug resistant Candida auris strains by farnesol
Srivastava, V., & Ahmad, A. (2020) · PLoS ONE · doi:10.1371/journal.pone.0233102 · Cited by 50
Smolarz, M., Zawrotniak, M., Satała, D., & Rąpała‐Kozik, M. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.681030 · Cited by 50
Influence of farnesol on the morphogenesis of Aspergillus niger
Lorek, J., Pöggeler, S., Weide, M. R., Breves, R., & Bockmühl, D. P. (2008) · Journal of Basic Microbiology · doi:10.1002/jobm.200700292 · Cited by 49
Abe, S., Rumi, T., Iijima, R., Yamada, T., Maruyama, N., Hisajima, T., Abe, Y., Oshima, H., & Yamazaki, M. (2009) · Microbiology and Immunology · doi:10.1111/j.1348-0421.2009.00128.x · Cited by 48
Is quorum sensing involved in lovastatin production in the filamentous fungus Aspergillus terreus?
Raina, S., Vizio, D. D., Palonen, E. K., Odell, M., Brandt, A. M., Soini, J. T., & Keshavarz, T. (2012) · Process Biochemistry · doi:10.1016/j.procbio.2012.02.021 · Cited by 48
The Effects of Farnesol on Staphylococcus aureus Biofilms and Osteoblasts
Unnanuntana, A., Bonsignore, L. A., Shirtliff, M. E., & Greenfield, E. M. (2009) · Journal of Bone and Joint Surgery · doi:10.2106/jbjs.h.01699 · Cited by 48
Signal exchange and integration during self-fusion in filamentous fungi
Fleißner, A., & Herzog, S. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.03.016 · Cited by 52
Formulations for Pulmonary Administration of Anticancer Agents to Treat Lung Malignancies
Carvalho, T. C., Carvalho, S. R., & McConville, J. T. (2011) · Journal of Aerosol Medicine and Pulmonary Drug Delivery · doi:10.1089/jamp.2009.0794 · Cited by 47
Wendland, J., & Walther, A. (2011) · G3 Genes Genomes Genetics · doi:10.1534/g3.111.001032 · Cited by 47
Hogan, D. A., & Mühlschlegel, F. A. (2011) · Current Opinion in Microbiology · doi:10.1016/j.mib.2011.09.014 · Cited by 47
Lipid Signaling in Pathogenic Fungi
Rhome, R. M., & Poeta, M. D. (2009) · Annual Review of Microbiology · doi:10.1146/annurev.micro.091208.073431 · Cited by 44
Effect of quorum-sensing molecule 2-phenylethanol and ARO genes on Saccharomyces cerevisiae biofilm
Zhang, D., Wang, F., Yu, Y., Ding, S., Chen, T., Sun, W., Liang, C., Yu, B., Ying, H., Liu, D., et al. (2021) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-021-11280-4 · Cited by 47
Uppuluri, P., Mekala, S., & Chaffin, W. L. (2007) · Yeast · doi:10.1002/yea.1501 · Cited by 45
A clash of quorum sensing vs quorum sensing inhibitors: an overview and risk of resistance
Patel, R., Soni, M., Soyantar, B., Shivangi, S., Sutariya, S., Saraf, M. S., & Goswami, D. (2023) · Archives of Microbiology · doi:10.1007/s00203-023-03442-x · Cited by 47
Ghosh, S., Howe, N., Volk, K., Tati, S., Nickerson, K. W., & Petro, T. M. (2010) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.2010.00717.x · Cited by 51
Self-citationIkeda, R., Saito, F., Matsuo, M., Kurokawa, K., Sekimizu, K., Yamaguchi, M., & Kawamoto, S. (2007) · Journal of Bacteriology · doi:10.1128/jb.00412-07 · Cited by 46
Guedouari, H., Gergondey, R., Bourdais, A., Vanparis, O., Bulteau, A. L., Camadro, J. M., & Auchère, F. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2014.07.006 · Cited by 45
The complex roles of NADPH oxidases in fungal infection
Hogan, D. A., & Wheeler, R. T. (2014) · Cellular Microbiology · doi:10.1111/cmi.12320 · Cited by 44
Polymicrobial community‐acquired pneumonia: An emerging entity
Cillóniz, C., Čivljak, R., Nicolini, A., & Torres, A. (2015) · Respirology · doi:10.1111/resp.12663 · Cited by 46
Colabardini, A. C., de Castro, P. A., de Gouvêa, P. F., Savoldi, M., Malavazi, I., Goldman, M. H. S., & Goldman, G. H. (2010) · Molecular Microbiology · doi:10.1111/j.1365-2958.2010.07403.x · Cited by 45
The effect of cinnamaldehyde on the growth and the morphology of Candida albicans
Taguchi, Y., Hasumi, Y., Abe, S., & Nishiyama, Y. (2013) · Medical Molecular Morphology · doi:10.1007/s00795-012-0001-0 · Cited by 45
Thewes, S., Moran, G. P., Magee, B. B., Schaller, M., Sullivan, D. J., & Hube, B. (2008) · BMC Microbiology · doi:10.1186/1471-2180-8-187 · Cited by 46
Two 2[5H]-Furanones as Possible Signaling Molecules inLactobacillus helveticus
Ndagijimana, M., Vallicelli, M., Cocconcelli, P. S., Cappa, F., Patrignani, F., Lanciotti, R., & Guerzoni, M. E. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.00363-06 · Cited by 45
Boucias, D. G., Liu, S., Meagher, R. L., & Baniszewski, J. A. (2016) · Journal of Invertebrate Pathology · doi:10.1016/j.jip.2016.03.013 · Cited by 45
Midkiff, J., Borochoff-Porte, N., White, D., & Johnson, D. I. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025395 · Cited by 44
Biofilm formation in clinically relevant filamentous fungi: a therapeutic challenge
Roudbary, M., Vahedi‐Shahandashti, R., dos Santos, A. L. S., Mohammadi, S. R., Aslani, P., Lass‐Flörl, C., & Rodrigues, C. F. (2021) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2021.1950121 · Cited by 46
Tooth-Binding Micelles for Dental Caries Prevention
Chen, F., Liu, X.-M., Rice, K. C., Li, X., Yu, F., Reinhardt, R. A., Bayles, K. W., & Wang, D. (2009) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00387-09 · Cited by 44
Hyphal development in Candida albicans from different cell states
Su, C., Yu, J., & Lü, Y. (2018) · Current Genetics · doi:10.1007/s00294-018-0845-5 · Cited by 44
Effect of farnesol on Candida dubliniensis morphogenesis
Henriques, M., Martins, M. I. B. C., Azeredo, J., & de Oliveira, R. P. S. (2006) · Letters in Applied Microbiology · doi:10.1111/j.1472-765x.2006.02044.x · Cited by 44
Abdel-Rhman, S. H., El-Mahdy, A. M., & El‐Mowafy, M. (2015) · BioMed Research International · doi:10.1155/2015/456463 · Cited by 43
A functional link between hyphal maintenance and quorum sensing in Candida albicans
Polke, M., Sprenger, M., Scherlach, K., Albán‐Proaño, M. C., Martin, R., Hertweck, C., Hube, B., & Jacobsen, I. D. (2016) · Molecular Microbiology · doi:10.1111/mmi.13526 · Cited by 46
Sensing of the Microbial Neighborhood by Candida albicans
Mallick, E. M., & Bennett, R. J. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003661 · Cited by 47
Shareck, J., Nantel, A., & Belhumeur, P. (2011) · Eukaryotic Cell · doi:10.1128/ec.00305-10 · Cited by 41
Décanis, N., Tazi, N., Correia, A., Vilanova, M., & Rouabhia, M. (2011) · The Open Microbiology Journal · doi:10.2174/1874285801105010119 · Cited by 43
Emerging and future strategies in the management of recalcitrant Candida auris
Bandara, N., & Samaranayake, L. P. (2022) · Medical Mycology · doi:10.1093/mmy/myac008 · Cited by 42
Su, Y., & Ding, T. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2252780 · Cited by 42
Candida albicans: Molecular interactions with Pseudomonas aeruginosa and Staphylococcus aureus
Lindsay, A. K., & Hogan, D. A. (2014) · Fungal Biology Reviews · doi:10.1016/j.fbr.2014.10.002 · Cited by 45
Safari, M., Amache, R., Esmaeilishirazifard, E., & Keshavarz, T. (2014) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-014-5518-9 · Cited by 42
Zouari, S., Ketata, M., Boudhrioua, N. M., & Ammar, E. (2012) · Industrial Crops and Products · doi:10.1016/j.indcrop.2012.04.020 · Cited by 41
Murata, H., Ohta, A., Yamada, A., Narimatsu, M., & Futamura, N. (2005) · Mycorrhiza · doi:10.1007/s00572-005-0358-1 · Cited by 43
Lagree, K., & Mitchell, A. P. (2017) · Microbiology Spectrum · doi:10.1128/microbiolspec.funk-0024-2016 · Cited by 41
Fungal diseases: Oral dysbiosis in susceptible hosts
Villar, C. C., & Dongari‐Bagtzoglou, A. I. (2021) · Periodontology 2000 · doi:10.1111/prd.12378 · Cited by 44
A roadmap to understanding diversity and function of coral reef-associated fungi
Roik, A., Reverter, M., & Pogoreutz, C. (2022) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuac028 · Cited by 43
Stratford, M., Steels, H., Nebe‐von‐Caron, G., Avery, S. V., Novodvorska, M., & Archer, D. B. (2014) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2014.04.017 · Cited by 40
Interkingdom signaling in plant-microbe interactions
Kan, J., Fang, R., & Jia, Y. (2017) · Science China Life Sciences · doi:10.1007/s11427-017-9092-3 · Cited by 40
The architecture of a mixed fungal–bacterial biofilm is modulated by quorum‐sensing signals
Ruiz, A., Herráez, M., Costa‐Gutierrez, S. B., Molina‐Henares, M. A., Martı́nez, M. J., Espinosa‐Urgel, M., & Barriuso, J. (2021) · Environmental Microbiology · doi:10.1111/1462-2920.15444 · Cited by 41
Berrocal, A., Navarrete, J., Oviedo, C., & Nickerson, K. W. (2012) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2012.05317.x · Cited by 40
Self-citationQuenching and quorum sensing in bacterial bio-films
Kameswaran, S., Gujjala, S., Zhang, S., Kondeti, S., Mahalingam, S., Manjunatha, B., & Ramesh, B. (2023) · Research in Microbiology · doi:10.1016/j.resmic.2023.104085 · Cited by 39
Prunuske, A. J., Waltner, J. K., Kuhn, P., Gu, B., & Craig, E. A. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1119184109 · Cited by 39
Quorum sensing in African trypanosomes
Rojas, F., & Matthews, K. R. (2019) · Current Opinion in Microbiology · doi:10.1016/j.mib.2019.07.001 · Cited by 39
Satała, D., Gonzalez‐Gonzalez, M., Smolarz, M., Surowiec, M., Kulig, K., Wronowska, E., Zawrotniak, M., Kozik, A., Rąpała‐Kozik, M., & Karkowska‐Kuleta, J. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.765942 · Cited by 40
Microbial production of farnesol (FOH): Current states and beyond
Wang, C., Kim, J., Choi, E., & Kim, S.-W. (2011) · Process Biochemistry · doi:10.1016/j.procbio.2011.02.020 · Cited by 39
Madrera, R. R., & Valles, B. S. (2011) · Journal of Food Science · doi:10.1111/j.1750-3841.2011.02406.x · Cited by 39
Care, A., Vousden, K. A., Binley, K. M., Radcliffe, P. A., Trevethick, J., Mannazzu, I., & Sudbery, P. E. (2004) · Genetics · doi:10.1534/genetics.166.2.707 · Cited by 39
Biofouling in Membrane Bioreactors—Mitigation and Current Status: a Review
Maddela, N. R., Aransiola, S. A., Zhang, S., & Prasad, R. (2022) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-022-04262-3 · Cited by 38
Shanmughapriya, S., Sornakumari, H., Lency, A., Kavitha, S., & Natarajaseenivasan, K. (2014) · Medical Mycology · doi:10.1093/mmy/myu046 · Cited by 38
Brilhante, R. S. N., de Lima, R. A. C., Caetano, É. P., Leite, J. J. G., Castelo‐Branco, D. D. S. C. M., Ribeiro, J. F., Bandeira, T. D. J. P. G., Cordeiro, R. D. A., Monteiro, A. J., Sidrim, J. J. C., et al. (2013) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02457-12 · Cited by 38
Effect of tyrosol on adhesion ofCandida albicansandCandida glabratato acrylic surfaces
Monteiro, D. R., Feresin, L. P., Arias, L. S., Barão, V. A. R., Barbosa, D. B., & Delbem, A. C. B. (2015) · Medical Mycology · doi:10.1093/mmy/myv052 · Cited by 38
Costa, A. C. B. P., Pereira, C. A., Freire, F., Junqueira, J. C., & Jorge, A. O. C. (2013) · Mycoses · doi:10.1111/myc.12092 · Cited by 38
Doing, G., Koeppen, K., Occhipinti, P., Harty, C. E., & Hogan, D. A. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1008783 · Cited by 35
Morphology Regulatory Metabolites from Arthrobotrys oligospora
Zhang, H., Tan, J.-L., Wei, L.-X., Wang, Y., Chuan-ping, Z., Wu, D.-K., Zhu, C., Zhang, Y., Zhang, K., & Niu, X. (2012) · Journal of Natural Products · doi:10.1021/np300342w · Cited by 38
Biologically Active Fluorescent Farnesol Analogs
Shchepin, R. V., Dumitru, ., Nickerson, K. W., Lund, M., & Dussault, P. H. (2005) · Chemistry & Biology · doi:10.1016/j.chembiol.2005.04.008 · Cited by 38
Self-citationTashiro, M., Kimura, S., Tateda, K., Saga, T., Ohno, A., Ishii, Y., Izumikawa, K., Tashiro, T., Kohno, S., & Yamaguchi, K. (2012) · Medical Mycology · doi:10.3109/13693786.2011.610037 · Cited by 36
Yeast biofilms on abiotic surfaces: Adhesion factors and control methods
Alonso, V. P. P., Lemos, J. G., & do Nascimento, M. D. S. (2023) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2023.110265 · Cited by 39
Truman, J. W., Riddiford, L. M., Konopová, B., Nouzová, M., Noriega, F. G., & Herko, M. (2023) · eLife · doi:10.7554/elife.92643 · Cited by 38
de Rossi, B. P., Garcia, C. A., Alcaraz, E. S., & Franco, M. A. (2014) · Revista Argentina de Microbiología · doi:10.1016/s0325-7541(14)70084-7 · Cited by 37
Nagy, G., Hennig, G. W., Petrényi, K., Kovacs, L., Pócsi, I., Dombrádi, V., & Bánfalvi, G. (2014) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-014-5696-5 · Cited by 37
Bozó, A., Domán, M., Majoros, L., Kardos, G., Varga, I., & Kovács, R. (2016) · The Journal of Microbiology · doi:10.1007/s12275-016-6298-y · Cited by 35
Metadata
- Authors
- Hornby, J. M., Jensen, E. C., Lisec, A. D., Tasto, J. J., Jahnke, B., Shoemaker, R., Dussault, P., & Nickerson, K. W.
- Affiliations
- University of Nebraska–Lincoln (US)
- College of Saint Benedict and Saint John's University (US)
- Venue
- Applied and Environmental Microbiology
- Publisher
- American Society for Microbiology
- Published
- 2001-07
- Volume
- 67
- Issue
- 7
- Pages
- 2982-2992
- ISSN
- 0099-2240 (ISSN-L)
- 1098-5336
- PMC
- PMC92970
- OpenAlex
- W2144677145
- Cited by
- 983
- References
- 33
- Citations by year
- 2026: 23 · 2025: 30 · 2024: 32 · 2023: 51 · 2022: 42 · 2021: 59 · 2020: 46 · 2019: 48 · 2018: 42 · 2017: 60 · 2016: 40 · 2015: 51 · 2014: 45 · 2013: 42 · 2012: 50
- FWCI
- 10.29
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Applied and Environmental Microbiology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Lincoln (University of Nebraska) (submittedVersion)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacterial biofilms and quorum sensing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Keywords
- quorum sensing, Candida albicans, farnesol, dimorphic fungi, germ tube formation, mycelial development, extracellular signaling molecules, inoculum size effect, nerolidol, geranylgeraniol, geraniol, farnesyl pyrophosphate
- MeSH terms
- Candida albicans, Chromatography, High Pressure Liquid, Chromatography, Thin Layer, Culture Media, Farnesol, Hot Temperature, Gas Chromatography-Mass Spectrometry, Gene Expression Regulation, Fungal
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