The DOI matches its Crossref record; 177 of the 177 references it cites were found in a registry or an index.
Indole as an intercellular signal in microbial communities
Open accessAbstract
Bacteria can utilize signal molecules to coordinate their behavior to survive in dynamic multispecies communities. Indole is widespread in the natural environment, as a variety of both Gram-positive and Gram-negative bacteria (to date, 85 species) produce large quantities of indole. Although it has been known for over 100 years that many bacteria produce indole, the real biological roles of this molecule are only now beginning to be unveiled. As an intercellular signal molecule, indole controls diverse aspects of bacterial physiology, such as spore formation, plasmid stability, drug resistance, biofilm formation, and virulence in indole-producing bacteria. In contrast, many non-indole-producing bacteria, plants and animals produce diverse oxygenases which may interfere with indole signaling. It appears indole plays an important role in bacterial physiology, ecological balance, and possibly human health. Here we discuss our current knowledge and perspectives on indole signaling.
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
“Several bacterial taxa can also affect tryptophan levels by direct utilization for growth or via tryptophanase expression (28, 203, 204)”
From Signalling cognition: The gut microbiota and hypothalamic-pituitary-adrenal axis (2023) · cites this paper as [203]
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
QUORUM SENSING: Cell-to-Cell Communication in Bacteria
Waters, C. M., & Bassler, B. L. (2005) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.21.012704.131001 · Cited by 3,989
Fuqua, W. C., Winans, S. C., & Greenberg, E. P. (1994) · Journal of Bacteriology · doi:10.1128/jb.176.2.269-275.1994 · Cited by 2,941
Metabolomics analysis reveals large effects of gut microflora on mammalian blood metabolites
Wikoff, W. R., Anfora, A. T., Liu, J., Schultz, P. G., Lesley, S. A., Peters, E. C., & Siuzdak, G. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812874106 · Cited by 2,677
Commensal Host-Bacterial Relationships in the Gut
Hooper, L. V., & Gordon, J. I. (2001) · Science · doi:10.1126/science.1058709 · Cited by 2,362
Attenuation of Pseudomonas aeruginosa virulence by quorum sensing inhibitors
Hentzer, M., Wu, H., Andersen, J. B., Riedel, K., Rasmussen, T. B., Bagge, N., Kumar, N., Schembri, M. A., Song, Z., Kristoffersen, P., et al. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg366 · Cited by 1,440
Microbes in Gastrointestinal Health and Disease
Neish, A. S. (2008) · Gastroenterology · doi:10.1053/j.gastro.2008.10.080 · Cited by 1,423
Schuster, M., Lostroh, P., Ogi, T., & Greenberg, E. P. (2003) · Journal of Bacteriology · doi:10.1128/jb.185.7.2066-2079.2003 · Cited by 1,127
Hentzer, M., Riedel, K., Rasmussen, T. B., Heydorn, A., Andersen, J. B., Parsek, M. R., Rice, S. A., Eberl, L., Molin, S., Høiby, N., et al. (2002) · Microbiology · doi:10.1099/00221287-148-1-87 · Cited by 1,053
How bacteria talk to each other: regulation of gene expression by quorum sensing
Bassler, B. L. (1999) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(99)00025-9 · Cited by 1,046
Cruciferous vegetables and human cancer risk: epidemiologic evidence and mechanistic basis
Higdon, J. V., Delage, B., WILLIAMS, D., & Dashwood, R. H. (2007) · Pharmacological Research · doi:10.1016/j.phrs.2007.01.009 · Cited by 1,038
Research works printed but not linked: 1
- Pittard AJ (1996) Biosynthesis of the aromatic amino acids: the tryptophan pathway. Escherichia coli and Salmonella: Cellular and Molecular Biology ( Neidhardt FC , ed), pp. 458–484. ASM Press, Washington, DC.
Cited by
Sorted by citations
Items 201–300 of 1,000
Li, D., He, R., Hou, G., Ming, W., Fan, T. T., Chen, L., Zhang, L., Jiang, W., Wang, W., Lu, Z., et al. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00268 · Cited by 65
Zhang, P., Mao, D., Gao, H., Zheng, L., Chen, Z., Gao, Y., Duan, Y., Guo, J., Luo, Y., & Ren, H. (2021) · The ISME Journal · doi:10.1038/s41396-021-01171-x · Cited by 65
Exploring AI-2-mediated interspecies communications within rumen microbial communities
Liu, X., Liu, Q., Sun, S., Sun, H., Wang, Y., Shen, X., & Zhang, L. (2022) · Microbiome · doi:10.1186/s40168-022-01367-z · Cited by 66
Mao, Z., Gao, Z., Liu, D., Liu, Z., & Wu, P. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1124704 · Cited by 68
Shaw, C. A., Hess, M., & Weimer, B. C. (2023) · Microorganisms · doi:10.3390/microorganisms11071825 · Cited by 73
Niu, B., Pan, T., Xiao, Y., Wang, H., Zhu, J., Tian, F., Lu, W., & Chen, W. (2024) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2023.2299744 · Cited by 66
Jameson, K. G., Kazmi, S. A., Ohara, T. E., Son, C., Yu, K. B., Mazdeyasnan, D., Leshan, E., Vuong, H. E., Paramo, J., Lopez-Romero, A., et al. (2024) · iScience · doi:10.1016/j.isci.2024.111699 · Cited by 88
Microbiome to Brain: Unravelling the Multidirectional Axes of Communication
Aidy, S. E., Stilling, R. M., Dinan, T. G., & Cryan, J. F. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-20215-0_15 · Cited by 65
Archaeal Persisters: Persister Cell Formation as a Stress Response in Haloferax volcanii
Megaw, J., & Gilmore, B. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01589 · Cited by 62
Parai, D., Banerjee, M., Dey, P., Chakraborty, A., Islam, E., & Mukherjee, S. K. (2018) · Biofouling · doi:10.1080/08927014.2018.1437910 · Cited by 65
Han, H., Safe, S. H., Jayaraman, A., & Chapkin, R. S. (2021) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-043020-090050 · Cited by 68
Chen, K., Wang, H., Yang, X., Tang, C., Hu, G., & Gao, Z. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2024.107483 · Cited by 71
Crépin, A., Barbey, C., Beury-Cirou, A., Hélias, V., Taupin, L., Reverchon, S., Nasser, W., Faure, D., Dufour, A., Orange, N., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035176 · Cited by 63
Ma, Q., Liu, Z., Yang, B., Dai, C., & Qu, Y. (2018) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2018.12.068 · Cited by 63
A Link between Chronic Kidney Disease and Gut Microbiota in Immunological and Nutritional Aspects
Mertowska, P., Mertowski, S., Wojnicka, J., Korona‐Głowniak, I., Grywalska, E., Błażewicz, A., & Załuska, W. (2021) · Nutrients · doi:10.3390/nu13103637 · Cited by 62
Circadian Rhythms and Melatonin Metabolism in Patients With Disorders of Gut-Brain Interactions
Fowler, S., Hoedt, E. C., Talley, N. J., Keely, S., & Burns, G. L. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.825246 · Cited by 62
The Mechanism of the Gut-Brain Axis in Regulating Food Intake
Li, S., Liu, M., Cao, S., Liu, B., Li, D., Wang, Z., Sun, H., Cui, Y., & Shi, Y. (2023) · Nutrients · doi:10.3390/nu15173728 · Cited by 70
Indole Biodegradation in Acinetobacter sp. Strain O153: Genetic and Biochemical Characterization
Sadauskas, M., Vaitekūnas, J., Gasparavičiūtė, R., & Meškys, R. (2017) · Applied and Environmental Microbiology · doi:10.1128/aem.01453-17 · Cited by 61
Seymour, B. J., Trent, B. J., Allen, B. E., Berlinberg, A. J., Tangchittsumran, J., Jubair, W. K., Chriswell, M. E., Liu, S., Ornelas, A., Stahly, A., et al. (2023) · Journal of Clinical Investigation · doi:10.1172/jci167671 · Cited by 66
Chemical signaling in biofilm-mediated biofouling
Liu, X., Zou, L., Li, B., Martino, P. D., Rittschof, D., Yang, J.-L., Maki, J. S., Liu, W., & Gu, J. (2024) · Nature Chemical Biology · doi:10.1038/s41589-024-01740-z · Cited by 61
Indole–triazole conjugates are selective inhibitors and inducers of bacterial biofilms
Minvielle, M. J., Bunders, C. A., & Melander, C. (2013) · MedChemComm · doi:10.1039/c3md00064h · Cited by 61
Indole-based novel small molecules for the modulation of bacterial signalling pathways
Biswas, N. N., Kutty, S. K., Barraud, N., Iskander, G. M., Griffith, R., Rice, S. A., Willcox, M. D. P., Black, D. S., & Kumar, N. (2014) · Organic & Biomolecular Chemistry · doi:10.1039/c4ob02096k · Cited by 61
The Impact of Gut Microbiota-Derived Metabolites in Autism Spectrum Disorders
Marzal, L. N. P., Prince, N., Bajić, D., Roussin, L., Naudon, L., Rabot, S., Garssen, J., Kraneveld, A. D., & Perez‐Pardo, P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221810052 · Cited by 67
Microbial Metabolite Regulation of Epithelial Cell-Cell Interactions and Barrier Function
Ornelas, A., Dowdell, A. S., Lee, J. S., & Colgan, S. P. (2022) · Cells · doi:10.3390/cells11060944 · Cited by 69
Human gut microbiome, diet, and mental disorders
Borrego-Ruiz, A., & Borrego, J. J. (2024) · International Microbiology · doi:10.1007/s10123-024-00518-6 · Cited by 68
Xian, W.-D., Salam, N., Li, M., Zhou, E., Yin, Y.-R., Liu, Z., Ming, Y.-Z., Zhang, X., Wu, G., Liu, L., et al. (2020) · npj Biofilms and Microbiomes · doi:10.1038/s41522-020-0131-4 · Cited by 60
Possible drugs for the treatment of bacterial infections in the future: anti-virulence drugs
Ogawara, H. (2020) · The Journal of Antibiotics · doi:10.1038/s41429-020-0344-z · Cited by 62
Gut Microbial-Derived Metabolites as Immune Modulators of T Helper 17 and Regulatory T Cells
Calvo‐Barreiro, L., Zhang, L., Abdel‐Rahman, S. A., Naik, S. P., & Gabr, M. T. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021806 · Cited by 62
Production of indigo by recombinant bacteria
Linke, J. A., Rayat, A. C. M. E., & Ward, J. M. (2023) · Bioresources and Bioprocessing · doi:10.1186/s40643-023-00626-7 · Cited by 60
Kim, J., Hong, H., Heo, A., & Park, W. (2013) · FEMS Microbiology Letters · doi:10.1111/1574-6968.12135 · Cited by 59
Postbiotic-Enabled Targeting of the Host-Microbiota-Pathogen Interface: Hints of Antibiotic Decline?
Puccetti, M., Xiroudaki, S., Ricci, M., & Giovagnoli, S. (2020) · Pharmaceutics · doi:10.3390/pharmaceutics12070624 · Cited by 59
Lai, W., Zhao, J., Xu, S., Deng, W.-F., Xu, D., Wang, M., He, F.-S., Liu, Y., Guo, Y., Ye, S.-W., et al. (2020) · Journal of Affective Disorders · doi:10.1016/j.jad.2020.09.010 · Cited by 59
Berlinberg, A. J., Regner, E. H., Stahly, A., Brar, A., Reisz, J. A., Gerich, M. E., Fennimore, B. P., Scott, F. I., Freeman, A. E., & Kuhn, K. A. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.587119 · Cited by 59
D’Onofrio, F., Renga, G., Puccetti, M., Pariano, M., Bellet, M. M., Santarelli, I., Stincardini, C., Mosci, P., Ricci, M., Giovagnoli, S., et al. (2021) · Cells · doi:10.3390/cells10071622 · Cited by 61
Huang, Z., Boekhorst, J., Fogliano, V., Capuano, E., & Wells, J. M. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.2c08953 · Cited by 62
Essential Amino Acid Metabolites as Chemical Mediators of Host-Microbe Interaction in the Gut
McCann, J. R., & Rawls, J. F. (2023) · Annual Review of Microbiology · doi:10.1146/annurev-micro-032421-111819 · Cited by 64
Wang, S., van Schooten, F., Jin, H., Jonkers, D. M. A. E., & Godschalk, R. (2023) · Nutrients · doi:10.3390/nu15132886 · Cited by 58
Wang, Q., Liang, J., Zou, Q., Wang, W., Yan, G., Guo, R., Yuan, T., Wang, Y., Liu, X., & Liu, Z. (2024) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.4c07716 · Cited by 62
Marchi, S. D., Bodelón, G., Vázquez‐Iglesias, L., Liz‐Marzán, L. M., Pérez‐Juste, J., & Pastoriza‐Santos, I. (2018) · Applied Materials Today · doi:10.1016/j.apmt.2018.12.005 · Cited by 60
Metabolite-based mutualism enhances hydrogen production in a two-species microbial consortium
Wang, S., Tang, H., Peng, F., Yu, X., Su, H., Xu, P., & Tan, T. (2019) · Communications Biology · doi:10.1038/s42003-019-0331-8 · Cited by 59
Fecal Microbiome, Metabolites, and Stem Cell Transplant Outcomes: A Single-Center Pilot Study
Galloway-Peña, J., Peterson, C. B., Malik, F., Sahasrabhojane, P. V., Shah, D. P., Brumlow, C., Carlin, L. G., Chemaly, R. F., Im, J. S., Rondón, G., et al. (2019) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofz173 · Cited by 57
Huang, Z., Boekhorst, J., Fogliano, V., Capuano, E., & Wells, J. M. (2022) · Food Chemistry · doi:10.1016/j.foodchem.2022.133801 · Cited by 58
Two diversities meet in the rhizosphere: root specialized metabolites and microbiome
Wang, X., Zhang, J., Lu, X., Bai, Y., & Wang, G. (2023) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2023.10.004 · Cited by 57
Intertwined Relationship of Mitochondrial Metabolism, Gut Microbiome and Exercise Potential
Imdad, S., Lim, W., Kim, J., & Kang, C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052679 · Cited by 60
Gasmi, L., Martínez‐Solís, M., Frattini, A., Ye, M., Collado, M. C., Turlings, T. C. J., Erb, M., & Herrero, S. (2018) · Applied and Environmental Microbiology · doi:10.1128/aem.01468-18 · Cited by 57
Gut microbiota in regulatory T cell generation and function: mechanisms and health implications
Sharma, A., Sharma, G., & Im, S. (2025) · Gut Microbes · doi:10.1080/19490976.2025.2516702 · Cited by 68
Gertsman, I., Gangoiti, J. A., Nyhan, W. L., & Barshop, B. A. (2015) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2015.01.005 · Cited by 55
Yang, Q., Julyantoro, P. G. S., Wang, Z., Lin, B., Rubin, R. A., Vora, G. J., & Defoirdt, T. (2017) · Environmental Microbiology · doi:10.1111/1462-2920.13714 · Cited by 55
Solvent dependence of cyanoindole fluorescence lifetime
Hilaire, M. R., Mukherjee, D., Troxler, T., & Gai, F. (2017) · Chemical Physics Letters · doi:10.1016/j.cplett.2017.07.038 · Cited by 55
Microbial Metabolites and Intestinal Stem Cells Tune Intestinal Homeostasis
Xing, P. Y., Pettersson, S., & Kundu, P. (2020) · PROTEOMICS · doi:10.1002/pmic.201800419 · Cited by 55
Gao, J., Yang, T., Song, B., Ma, X., Ma, Y., Lin, X., & Wang, H. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115395 · Cited by 58
Intercepting Bacterial Indole Signaling with Flustramine Derivatives
Bunders, C. A., Minvielle, M. J., Worthington, R. J., Ortiz, M. C., Cavanagh, J., & Melander, C. (2011) · Journal of the American Chemical Society · doi:10.1021/ja209836z · Cited by 54
Zhou, Q., Xie, Z., Wu, D., Liu, L., Shi, Y., Li, P., & Gu, Q. (2022) · Foods · doi:10.3390/foods11203302 · Cited by 56
Yong, C. C., Sakurai, T., Kaneko, H., Horigome, A., Mitsuyama, E., Nakajima, A., Katoh, T., Sakanaka, M., Abe, T., Xiao, J., et al. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2347728 · Cited by 55
Lee, J., Kim, Y.-G., Kim, C.-J., Lee, J.-C., Cho, M. H., & Lee, J. (2012) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-012-3881-y · Cited by 53
Active efflux in dormant bacterial cells – New insights into antibiotic persistence
Pu, Y., Ke, Y., & Bai, F. (2016) · Drug Resistance Updates · doi:10.1016/j.drup.2016.11.002 · Cited by 52
Mass Spectrometric Techniques for The Analysis of Volatile Organic Compounds Emitted from Bacteria
Ratiu, I., Ligor, T., Bocoș-Bințințan, V., & Buszewski, B. (2017) · Bioanalysis · doi:10.4155/bio-2017-0051 · Cited by 52
Developmental Signatures of Microbiota-Derived Metabolites in the Mouse Brain
Swann, J. R., Spitzer, S. O., & Heijtz, R. D. (2020) · Metabolites · doi:10.3390/metabo10050172 · Cited by 56
Hui, Y., Zhao, J., Yu, Z., Wang, Y., Qin, Y., Zhang, Y., Xing, Y., Han, M., Wang, A., Guo, S., et al. (2023) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202300218 · Cited by 53
Newer guar gum ester/chicken feather keratin interact films for tissue engineering
Das, A., Das, A., Basu, A., Datta, P., Gupta, M., & Mukherjee, A. (2021) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2021.03.034 · Cited by 51
Sun, Y., Zhang, M., Ou, Z., Meng, Y., Chen, Y., Lin, R., Hashim, J. H., Hashim, Z. B., Wieslander, G., Chen, Q., et al. (2022) · European Respiratory Journal · doi:10.1183/13993003.00260-2022 · Cited by 51
Gut microbial metabolism in Alzheimer's disease and related dementias
Kang, J. W., Vemuganti, V., Kuehn, J. F., Ulland, T. K., Rey, F. E., & Bendlin, B. B. (2024) · Neurotherapeutics · doi:10.1016/j.neurot.2024.e00470 · Cited by 53
Gut Microbiome Regulation of Gut Hormone Secretion
Chao, J. L., Coleman, R. A., Keating, D. J., & Martin, A. M. (2025) · Endocrinology · doi:10.1210/endocr/bqaf004 · Cited by 60
Kim, S.-K., Park, H. Y., & Lee, J. (2015) · Applied and Environmental Microbiology · doi:10.1128/aem.03551-14 · Cited by 50
Requirements for In Vitro Germination of Paenibacillus larvae Spores
Alvarado, I., Phui, A., Elekonich, M. M., & Abel‐Santos, E. (2012) · Journal of Bacteriology · doi:10.1128/jb.01958-12 · Cited by 50
Li, X., Yang, Q., Dierckens, K. R., Milton, D. L., & Defoirdt, T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0111801 · Cited by 50
Waclawiková, B., Bullock, A., Schwalbe, M., Aranzamendi, C., Nelemans, S. A., van Dijk, G., & Aidy, S. E. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001070 · Cited by 56
Hepatoprotective Effects of Indole, a Gut Microbial Metabolite, in Leptin-Deficient Obese Mice
Knudsen, C., Neyrinck, A. M., Leyrolle, Q., Baldin, P., Leclercq, S., Rodriguez, J., Beaumont, M., Cani, P. D., Bindels, L. B., Lanthier, N., et al. (2021) · Journal of Nutrition · doi:10.1093/jn/nxab032 · Cited by 50
Huoviala, P., Dolan, M.-J., Love, F. M., Myers, P., Frechter, S., Namiki, S., Pettersson, L., Roberts, R. J. V., Turnbull, R., Mitrevica, Z., et al. (2018) · doi:10.1101/394403 · Cited by 43
Indole Pulse Signalling Regulates the Cytoplasmic pH of E. coli in a Memory-Like Manner
Zarkan, A., Muñiz, S. E. C., Zhu, J., Nahas, K. A., Cama, J., Keyser, U. F., & Summers, D. (2019) · Scientific Reports · doi:10.1038/s41598-019-40560-3 · Cited by 48
Unveiling the biotransformation mechanism of indole in a Cupriavidus sp. strain
Qu, Y., Ma, Q., Liu, Z., Wang, W., Tang, H., Zhou, J., & Xu, P. (2017) · Molecular Microbiology · doi:10.1111/mmi.13852 · Cited by 49
Sleeping ribosomes: Bacterial signaling triggers RaiA mediated persistence to aminoglycosides
Lang, M., Krin, E., Korlowski, C., Sismeiro, O., Varet, H., Coppée, J., Mazel, D., & Baharoglu, Z. (2021) · iScience · doi:10.1016/j.isci.2021.103128 · Cited by 49
Amino Acids in Microbial Metabolism and Function
Dai, Z., Wu, Z., Zhu, W., & Wu, G. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-85686-1_7 · Cited by 50
Molecular basis of indole production catalyzed by tryptophanase in the genus Prevotella
Sasaki-Imamura, T., Yoshida, Y., Suwabe, K., Yoshimura, F., & Kato, H. (2011) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2011.02329.x · Cited by 48
Gene expression profiles of Vibrio parahaemolyticus in viable but non-culturable state
Meng, L., Alter, T., Aho, T., & Huehn, S. (2015) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiv035 · Cited by 48
Radical perfluoroalkylation – easy access to 2-perfluoroalkylindol-3-imines via electron catalysis
Leifert, D., Artiukhin, D. G., Neugebauer, J., Galstyan, A., Strassert, C. A., & Studer, A. (2016) · Chemical Communications · doi:10.1039/c6cc02284g · Cited by 48
Manoharan, R. K., Lee, J., & Lee, J. (2018) · Microbial Biotechnology · doi:10.1111/1751-7915.13268 · Cited by 47
Girard, L. (2019) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2019.1624499 · Cited by 48
Synbiotics Alleviate the Gut Indole Load and Dysbiosis in Chronic Kidney Disease
Yang, C., Chen, T.-W., Lu, W.-L., Liang, S., Huang, H., Tseng, C., & Tarng, D. (2021) · Cells · doi:10.3390/cells10010114 · Cited by 49
Bello, A. U., ZULKIFLI, I., Meng, G. Y., Awad, E. A., & Farjam, A. S. (2017) · Italian Journal of Animal Science · doi:10.1080/1828051x.2017.1340814 · Cited by 47
Simoska, O., Sans, M., Eberlin, L. S., Shear, J. B., & Stevenson, K. J. (2019) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2019.111538 · Cited by 47
Hidalgo-Romano, B., Gollihar, J., Brown, S. A., Whiteley, M., Valenzuela, E., Kaplan, H. B., Wood, T. K., & McLean, R. J. C. (2014) · Microbiology · doi:10.1099/mic.0.081729-0 · Cited by 46
Ding, L., Guo, W., & Chen, X. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-09792-1 · Cited by 46
Gossip in the gut: Quorum sensing, a new player in the host-microbiota interactions
Coquant, G., Aguanno, D., Pham, S., Grellier, N., Thenet, S., Carrière, V., Grill, J.-P., & Seksik, P. (2021) · World Journal of Gastroenterology · doi:10.3748/wjg.v27.i42.7247 · Cited by 47
Szklany, K., Wopereis, H., de Waard, C., van Wageningen, T., An, R., van Limpt, K., Knol, J., Garssen, J., Knippels, L. M. J., Belzer, C., et al. (2020) · Nutritional Neuroscience · doi:10.1080/1028415x.2019.1576362 · Cited by 46
Whitman, J. A., Doherty, L. A., Pantoja-Feliciano, I. G., Racicot, K., Anderson, D., Kensil, K., Karl, J. P., Gibson, G. R., & Soares, J. W. (2024) · Nutrients · doi:10.3390/nu16081159 · Cited by 45
Lu, S., Wang, C., Ma, J., & Wang, Y. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1456030 · Cited by 49
Ziesche, L., Bruns, H., Dogs, M., Wolter, L. A., Mann, F., Wagner‐Döbler, I., Brinkhoff, T., & Schulz, S. (2015) · ChemBioChem · doi:10.1002/cbic.201500189 · Cited by 45
Detoxification of Indole by an Indole-Induced Flavoprotein Oxygenase from Acinetobacter baumannii
Lin, G.-H., Chen, H., & Shu, H. (2015) · PLoS ONE · doi:10.1371/journal.pone.0138798 · Cited by 45
Lee, J., Kim, Y., Gupta, V. K., Manoharan, R. K., & Lee, J. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02641 · Cited by 45
Raorane, C. J., Lee, J., & Lee, J. (2020) · Biomolecules · doi:10.3390/biom10081186 · Cited by 45
Raj, V., Raorane, C. J., Lee, J., & Lee, J. (2021) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.1c12617 · Cited by 47
Multi-strain volatile profiling of pathogenic and commensal cutaneous bacteria
Fitzgerald, S., Duffy, E., Holland, L., & Morrin, A. (2020) · Scientific Reports · doi:10.1038/s41598-020-74909-w · Cited by 44
Vertical and horizontal quorum-sensing-based multicellular communications
Wu, S., Xu, C., Liu, J., Liu, C., & Qiao, J. (2021) · Trends in Microbiology · doi:10.1016/j.tim.2021.04.006 · Cited by 43
Yu, S., & Lee, Y. H. (2013) · Plant and Soil · doi:10.1007/s11104-013-1652-x · Cited by 44
Effects of Growth Surface Topography on Bacterial Signaling in Coculture Biofilms
Bhattacharjee, A., Khan, M., Kleiman, M., & Hochbaum, A. I. (2017) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.7b04223 · Cited by 44
Tseng, S., Liu, P., Lee, Y., Wu, Z., Huang, C.-C., Cheng, C., & Tung, K. (2018) · Canadian Journal of Infectious Diseases and Medical Microbiology · doi:10.1155/2018/6976897 · Cited by 44
Printable QR code paper microfluidic colorimetric assay for screening volatile biomarkers
Burklund, A., Saturley-Hall, H. K., Franchina, F. A., Hill, J. E., & Zhang, J. X. J. (2018) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2018.12.026 · Cited by 44
Song, M., Wang, S., Wang, Z., Fu, Z., Zhou, S., Cheng, H., Liang, Z., & Deng, X. (2019) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2019.01.038 · Cited by 44
Bacterial metabolism-inspired molecules to modulate antibiotic efficacy
Liu, Y., Li, R., Xiao, X., & Wang, Z. (2019) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkz230 · Cited by 44
Metadata
- Authors
- Lee, J.-H., & Lee, J.
- Affiliations
- Yeungnam University (KR)
- Corresponding author
- Lee, Jintae
- Venue
- FEMS Microbiology Reviews
- Publisher
- Oxford University Press (OUP)
- Published
- 2010-07
- Volume
- 34
- Issue
- 4
- Pages
- 426-444
- ISSN
- 0168-6445 (ISSN-L)
- 1574-6976
- OpenAlex
- W2049821596
- Cited by
- 1,059
- References
- 174
- Citations by year
- 2026: 82 · 2025: 113 · 2024: 94 · 2023: 115 · 2022: 112 · 2021: 99 · 2020: 89 · 2019: 62 · 2018: 61 · 2017: 42 · 2016: 36 · 2015: 44 · 2014: 42 · 2013: 27 · 2012: 17
- FWCI
- 1.02
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- FEMS Microbiology Reviews (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Yeungnam University
- Directorate for Education and Human Resources
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacterial biofilms and quorum sensing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Life Sciences › Immunology and Microbiology › Microbiology › Escherichia coli research studies
- Keywords
- intercellular communication, bacterial quorum sensing, microbial communities, sporulation, plasmid stability, drug resistance, biofilm formation, virulence, Gram-positive bacteria, Gram-negative bacteria
- MeSH terms
- Bacteria, Indoles, Plasmids, Virulence, Signal Transduction, Gene Expression Regulation, Bacterial, Bacterial Physiological Phenomena, Biofilms, Drug Resistance, Bacterial, Quorum Sensing
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