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Intestinal Fungal Dysbiosis Is Associated With Visceral Hypersensitivity in Patients With Irritable Bowel Syndrome and Rats
Open accessAbstract
Background & aims Visceral hypersensitivity is one feature of irritable bowel syndrome (IBS). Bacterial dysbiosis might be involved in the activation of nociceptive sensory pathways, but there have been few studies of the role of the mycobiome (the fungal microbiome) in the development of IBS. We analyzed intestinal mycobiomes of patients with IBS and a rat model of visceral hypersensitivity.Methods We used internal transcribed spacer 1-based metabarcoding to compare fecal mycobiomes of 18 healthy volunteers with those of 39 patients with IBS (with visceral hypersensitivity or normal levels of sensitivity). We also compared the mycobiomes of Long-Evans rats separated from their mothers (hypersensitive) with non-handled (normally sensitive) rats. We investigated whether fungi can cause visceral hypersensitivity using rats exposed to fungicide (fluconazole and nystatin). The functional relevance of the gut mycobiome was confirmed in fecal transplantation experiments: adult maternally separated rats were subjected to water avoidance stress (to induce visceral hypersensitivity), then given fungicide and donor cecum content via oral gavage. Other rats subjected to water avoidance stress were given soluble β-glucans, which antagonize C-type lectin domain family 7 member A (CLEC7A or DECTIN1) signaling via spleen-associated tyrosine kinase (SYK), a SYK inhibitor to reduce visceral hypersensitivity, or vehicle (control). The sensitivity of mast cells to fungi was tested with mesenteric windows (ex vivo) and the human mast cell line HMC-1.Results α diversity (Shannon index) and mycobiome signature (stability selection) of both groups of IBS patients differed from healthy volunteers, and the mycobiome signature of hypersensitive patients differed from that of normally sensitive patients. We observed mycobiome dysbiosis in rats that had been separated from their mothers compared with non-handled rats. Administration of fungicide to hypersensitive rats reduced their visceral hypersensitivity to normal levels of sensitivity. Administration of cecal mycobiomes from rats that had been separated from their mothers (but not non-handled mycobiome) restored hypersensitivity to distension. Administration of soluble β-glucans or a SYK inhibitor reduced visceral hypersensitivity, compared with controls. Particulate β-glucan (a DECTIN-1 agonist) induced mast cell degranulation in mesenteric windows and HMC-1 cells responded to fungal antigens by release of histamine.Conclusions In an analysis of patients with IBS and controls, we associated fungal dysbiosis with IBS. In studies of rats, we found fungi to promote visceral hypersensitivity, which could be reduced by administration of fungicides, soluble β-glucans, or a SYK inhibitor. The intestinal fungi might therefore be manipulated for treatment of IBS-related visceral hypersensitivity.
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“Also neglected to date is the gut mycobiome, and there are indications that our intestinal fungi are an important component of host-microbe interactions of relevance to immune homeostasis and inflammatory disorders (Leonardi et al., 2018) and stress-related disorders such as irritable bowel syndrome (Botschuijver et al., 2017).”
From Gut reactions: Breaking down xenobiotic–microbiome interactions (2019) · cites this paper as Botschuijver et al., 2017
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Cites
The validity of the Hospital Anxiety and Depression Scale
Bjelland, I., Dahl, A. A., Haug, T. T., & Neckelmann, D. (2002) · Journal of Psychosomatic Research · doi:10.1016/s0022-3999(01)00296-3 · Cited by 9,779
Jost, L. (2006) · Oikos · doi:10.1111/j.2006.0030-1299.14714.x · Cited by 4,669
Meinshausen, N., & Bühlmann, P. (2010) · Journal of the Royal Statistical Society Series B (Statistical Methodology) · doi:10.1111/j.1467-9868.2010.00740.x · Cited by 2,463
Functional Gastrointestinal Disorders: History, Pathophysiology, Clinical Features, and Rome IV
Drossman, D. A. (2016) · Gastroenterology · doi:10.1053/j.gastro.2016.02.032 · Cited by 2,444
Global Prevalence of and Risk Factors for Irritable Bowel Syndrome: A Meta-analysis
Lovell, R. M., & Ford, A. C. (2012) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2012.02.029 · Cited by 2,155
Fungal microbiota dysbiosis in IBD
Sokol, H., Leducq, V., Aschard, H., Pham, H., Jégou, S., Landman, C., Cohen, D., Liguori, G., Bourrier, A., Nion–Larmurier, I., et al. (2016) · Gut · doi:10.1136/gutjnl-2015-310746 · Cited by 1,382
How informative is the mouse for human gut microbiota research?
Nguyen, T. L. A., Vieira-Silva, S., Liston, A., & Raes, J. (2015) · Disease Models & Mechanisms · doi:10.1242/dmm.017400 · Cited by 1,334
Dectin-1 Mediates the Biological Effects of β-Glucans
Brown, G. D., Herre, J., Williams, D. L., Willment, J. A., Marshall, A. S. J., & Gordon, S. (2003) · The Journal of Experimental Medicine · doi:10.1084/jem.20021890 · Cited by 1,209
Dectin-1 is required for β-glucan recognition and control of fungal infection
Taylor, P. R., Tsoni, S. V., Willment, J. A., Dennehy, K. M., Rosas, M., Findon, H., Haynes, K., Steele, C. H., Botto, M., Gordon, S., et al. (2006) · Nature Immunology · doi:10.1038/ni1408 · Cited by 1,185
Interactions between commensal fungi and the C-type lectin receptor Dectin-1 influence colitis
Iliev, I. D., Funari, V. A., Taylor, K. D., Nguyen, Q., Reyes, C. N., Strom, S. P., Brown, J., Becker, C. A., Fleshner, P. R., Dubinsky, M., et al. (2012) · Science · doi:10.1126/science.1221789 · Cited by 1,073
Research works printed but not linked: 1
- Dukes, 2009, A randomised double blind, placebo controlled, crossover study to evaluate the efficacy and safety of the corticotrophin releasing factor 1 (CRF1) receptor antagonist GW876008 in IBS patients, Neurogastroenterol Motil, 21, 84
Cited by
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Kootte, R. S., Levin, E., Salojärvi, J., Smits, L. P., Hartstra, A. V., Udayappan, S. D., Hermes, G., Bouter, K. E., Koopen, A. M., Holst, J. J., et al. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.09.008 · Cited by 1,039
Self-citationVu, D., Groenewald, M., de Vries, M., Gehrmann, T., Stielow, J. B., Eberhardt, U., Al‐Hatmi, A. M. S., Groenewald, J. Z., Cardinali, G., Houbraken, J. A. M. P., et al. (2018) · Studies in Mycology · doi:10.1016/j.simyco.2018.05.001 · Cited by 1,010
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Wang, R., Tang, R., Li, B., Ma, X., Schnabl, B., & Tilg, H. (2021) · Cellular & Molecular Immunology · doi:10.1038/s41423-020-00592-6 · Cited by 466
Richard, M. L., & Sokol, H. (2019) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-019-0121-2 · Cited by 428
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Chong, P. P., Chin, V. K., Looi, C. Y., Wong, W. F., Madhavan, P., & Yong, P. V. C. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01136 · Cited by 353
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Auchtung, T. A., Fofanova, T. Y., Stewart, C. J., Nash, A. K., Wong, M. C., Gesell, J. R., Auchtung, J. M., Ajami, N. J., & Petrosino, J. F. (2018) · mSphere · doi:10.1128/msphere.00092-18 · Cited by 296
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Grundy, L., Erickson, A., & Brierley, S. M. (2018) · Annual Review of Physiology · doi:10.1146/annurev-physiol-020518-114525 · Cited by 256
Wang, L., Alammar, N., Singh, R., Nanavati, J., Song, Y., Chaudhary, R., & Mullin, G. E. (2019) · Journal of the Academy of Nutrition and Dietetics · doi:10.1016/j.jand.2019.05.015 · Cited by 251
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A Review of Microbiota and Irritable Bowel Syndrome: Future in Therapies
Rodiño‐Janeiro, B. K., Vicario, M., Alonso, C., Pascua-García, R., & Santos, J. (2018) · Advances in Therapy · doi:10.1007/s12325-018-0673-5 · Cited by 223
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Bouter, K. E. C., Bakker, G. J., Levin, E., Hartstra, A. V., Kootte, R. S., Udayappan, S. D., Katiraei, S., Bahler, L., Gilijamse, P. W., Tremaroli, V., et al. (2018) · Clinical and Translational Gastroenterology · doi:10.1038/s41424-018-0025-4 · Cited by 208
Pathology of pain and its implications for therapeutic interventions
Cao, B., Xu, Q., Shi, Y., Zhao, R., Li, H., Zheng, J., Liu, F., Wan, Y., & Wei, B. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01845-w · Cited by 236
The gut microbiome and irritable bowel syndrome
Menees, S., & Chey, W. (2018) · F1000Research · doi:10.12688/f1000research.14592.1 · Cited by 159
“Recent data suggest that the community of fungi or “mycobiome” is also altered in patients with IBS and may be associated with the development of visceral hypersensitivity 20 .”
BackgroundSimpson, C. A., Mu, A., Haslam, N., Schwartz, O., & Simmons, J. G. (2020) · Journal of Affective Disorders · doi:10.1016/j.jad.2020.01.124 · Cited by 174
Vemuri, R., Shankar, E. M., Chieppa, M., Eri, R., & Kavanagh, K. (2020) · Microorganisms · doi:10.3390/microorganisms8040483 · Cited by 162
Mycobiome in the Gut: A Multiperspective Review
Chin, V. K., Yong, P. V. C., Chong, P. P., Nordin, S. A., Basir, R., & Abdullah, M. (2020) · Mediators of Inflammation · doi:10.1155/2020/9560684 · Cited by 161
Gheorghe, C. E., Ritz, N. L., Martin, J. A., Wardill, H. R., Cryan, J. F., & Clarke, G. A. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1941711 · Cited by 156
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Hoggard, M., Vesty, A., Wong, G. C., Montgomery, J. M., Fourie, C., Douglas, R. G., Biswas, K., & Taylor, M. W. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02208 · Cited by 132
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The Mycobiome: A Neglected Component in the Microbiota-Gut-Brain Axis
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The role of gut mycobiome in health and diseases
Zhang, L., Zhan, H., Xu, W., Yan, S., & Ng, S. C. (2021) · Therapeutic Advances in Gastroenterology · doi:10.1177/17562848211047130 · Cited by 118
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The Mycobiome in Health and Disease: Emerging Concepts, Methodologies and Challenges
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Krishnamurthy, H. K., Pereira, M., Bosco, J., George, J., Jayaraman, V., Krishna, K., Wang, T., Bei, K., & Rajasekaran, J. J. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1244293 · Cited by 112
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Mast cell mediation of visceral sensation and permeability in irritable bowel syndrome
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Immune activation in irritable bowel syndrome: what is the evidence?
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Stress-Induced Chronic Visceral Pain of Gastrointestinal Origin
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Altered gut bacterial–fungal interkingdom networks in patients with current depressive episode
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Mars, R. A. T., Frith, M., & Kashyap, P. (2020) · Gastroenterology · doi:10.1053/j.gastro.2020.10.058 · Cited by 53
The fecal mycobiome in patients with Irritable Bowel Syndrome
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Li, Y., Hong, G., Yang, M. J., Li, G., Jin, Y. T., Xiong, H., Qian, W., & Hou, X. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.104936 · Cited by 49
Maternal separation in rodents: a journey from gut to brain and nutritional perspectives
Rincel, M., & Darnaudéry, M. (2019) · Proceedings of The Nutrition Society · doi:10.1017/s0029665119000958 · Cited by 51
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Fecal Fungi Dysbiosis in Nonalcoholic Fatty Liver Disease
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Zhang, D., Wang, Y., Shen, S., Hou, Y., Chen, Y., & Wang, T. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1731287 · Cited by 41
Hou, Q., Huang, Y., Wang, Y., Liao, L., Zhu, Z., Zhang, W., Liu, Y., Li, P., Chen, X., & Liu, F. (2020) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2002.02059 · Cited by 39
Hong, G., Li, Y., Yang, M. J., Li, G., Qian, W., Xiong, H., Bai, T., Song, J., Zhang, L., & Hou, X. (2020) · Neurogastroenterology & Motility · doi:10.1111/nmo.13891 · Cited by 39
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Balmuș, I.-M., Ilie, O., Ciobica, A. S., Cojocariu, R.-O., Stanciu, C., Trifan, A. V., Cîmpeanu, M., CIMPEANU, C. S., & Gorgan, L. (2020) · Medicina · doi:10.3390/medicina56010038 · Cited by 34
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Fiorani, M., Vecchio, L. E. D., D’Argenio, P., Kaitsas, F., Rozera, T., Porcari, S., Gasbarrini, A., Cammarota, G., & Ianiro, G. (2023) · Expert Review of Gastroenterology & Hepatology · doi:10.1080/17474124.2023.2230865 · Cited by 32
Steinert, R. E., Rehman, A., Lima, E. S., Agamennone, V., Schuren, F. H. J., Gerö, D., Schreiner, P., Vonlanthen, R., Ismaeil, A., Tzafos, S., et al. (2020) · PLoS ONE · doi:10.1371/journal.pone.0236936 · Cited by 32
The Role of Gut Microbiome in Irritable Bowel Syndrome: Implications for Clinical Therapeutics
Zhao, Y., Zhu, S., Dong, Y., Xie, T., Chai, Z., Gao, X., Dai, Y., & Wang, X. (2024) · Biomolecules · doi:10.3390/biom14121643 · Cited by 32
Gașpar, B. S., Roşu, O. A., Enache, R. M., Profir, M., Pavelescu, L. A., & Creţoiu, S. M. (2025) · Journal of Fungi · doi:10.3390/jof11050333 · Cited by 33
Azzam, S. Z., Cayme, G. J., & Martinez, L. R. (2019) · Microbial Pathogenesis · doi:10.1016/j.micpath.2019.103942 · Cited by 26
Role of Fungal Infections in Carcinogenesis and Cancer Development; A Literature Review
Hosseini, K., Ahangari, H., Chapeland‐Leclerc, F., Ruprich‐Robert, G., Tarhriz, V., & Dilmaghani, A. (2021) · Advanced Pharmaceutical Bulletin · doi:10.34172/apb.2022.076 · Cited by 29
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Caetano, C. F., Gaspar, C., Martinez‐de‐Oliveira, J., Palmeira‐de‐Oliveira, A., & Rolo, J. (2023) · Life · doi:10.3390/life13040924 · Cited by 31
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Elaskandrany, M., Patel, R., Patel, M. M., Miller, G., Saxena, D., & Saxena, A. D. (2021) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00025.2021 · Cited by 28
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Gastrointestinal microbiota alteration induced by Mucor circinelloides in a murine model
Mueller, K. D., Zhang, H., Serrano, C. R., Billmyre, R. B., Huh, E. Y., Wiemann, P., Keller, N. P., Wang, Y., Heitman, J., & Lee, S. C. (2019) · The Journal of Microbiology · doi:10.1007/s12275-019-8682-x · Cited by 25
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Hurtado‐Lorenzo, A., Honig, G., Weaver, S. A., Larkin, P. B., & Heller, C. A. (2021) · Crohn s & Colitis 360 · doi:10.1093/crocol/otab034 · Cited by 27
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Gu, Y., Li, L., Yang, M., Liu, T., Song, X., Qin, X., Xu, X. J., Liu, J., Wang, B., & Cao, H. (2022) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2022.2058353 · Cited by 26
Ferrocino, I., Ponzo, V., Pellegrini, M., Goitre, I., Papurello, M., Franciosa, I., D’Eusebio, C., Ghigo, E., Cocolin, L., & Bo, S. (2022) · Scientific Reports · doi:10.1038/s41598-022-13438-0 · Cited by 22
Xu, L., Li, W., Lü, L., Zhang, Z., Cui, Z., Jiang, G., Wang, Y., Meng, Q., Wang, Y.-D., Liu, K., et al. (2023) · Current Microbiology · doi:10.1007/s00284-023-03480-0 · Cited by 23
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Botschuijver, S., van Diest, S. A., van Thiel, I. A. M., Saia, R. S., Strik, A. S., Yu, Z., Ferreira, D. M., Welting, O., Keszthelyi, D., Jennings, G. S., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-49096-y · Cited by 23
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Meydan, C., Afshinnekoo, E., Rickard, N., Daniels, G., Kunces, L. J., Hardy, T. M., Lili, L., Pesce, S., Jacobson, P., Mason, C. E., et al. (2020) · Precision Clinical Medicine · doi:10.1093/pcmedi/pbaa013 · Cited by 22
Ponzo, V., Ferrocino, I., Goitre, I., Pellegrini, M., Bruno, M., Astegiano, M., Cadario, G., Castellana, E., Bioletto, F., Corvaglia, M. R., et al. (2021) · Nutrients · doi:10.3390/nu13041260 · Cited by 21
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Brand, B., Stoye, N. M., Guilherme, M. D. S., Nguyen, V. T. T., Baumgärtner, J. C., Schüffler, A., Thines, E., & Endres, K. (2019) · Molecules · doi:10.3390/molecules24152776 · Cited by 20
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Losso, J. N. (2021) · Annual Review of Food Science and Technology · doi:10.1146/annurev-food-062520-090235 · Cited by 18
Mengzhu, S., Yujie, Z., Song, Y., Guo, J., Tingting, Z., Yuhang, W., Pei, L., & Jianhua, S. (2022) · PubMed Central · doi:10.19852/j.cnki.jtcm.20220719.001 · Cited by 18
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Shi, Y., Li, J., Cai, S., Zhao, H., Zhao, H., Sun, G., & Yang, Y. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1205348 · Cited by 18
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van Thiel, I. A. M., Stavrou, A. A., de Jong, A. W., Theelen, B., Davids, M., Hakvoort, T. B. M., Admiraal, I., Weert, I., Hesselink, M., Vu, D., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-09436-x · Cited by 20
Vito, M. D., Bellardi, M. G., Sanguinetti, M., Mondello, F., Girolamo, A., Barbanti, L., Garzoli, S., Sabatino, M., Ragno, R., Vitali, A., et al. (2020) · Nutrients · doi:10.3390/nu12051329 · Cited by 17
Metadata
- Authors
- Botschuijver, S., Roeselers, G., Levin, E., Jonkers, D. M., Welting, O., Heinsbroek, S. E. M., de Weerd, H. H., Boekhout, T., Fornai, M., Masclee, A. A., Schuren, F. H. J., de Jonge, W. J., Seppen, J., & van den Wijngaard, R. M.
- Affiliations
- Amsterdam UMC Location University of Amsterdam (NL)
- Netherlands Organisation for Applied Scientific Research (NL)
- Maastricht University Medical Centre (NL)
- Westerdijk Fungal Biodiversity Institute (NL)
- University of Pisa (IT)
- ORCID
- Venue
- Gastroenterology
- Publisher
- Elsevier BV
- Published
- 2017-10
- Volume
- 153
- Issue
- 4
- Pages
- 1026-1039
- ISSN
- 0016-5085 (ISSN-L)
- OpenAlex
- W2624678362
- Cited by
- 202
- References
- 50
- Citations by year
- 2026: 12 · 2025: 12 · 2024: 23 · 2023: 19 · 2022: 23 · 2021: 32 · 2020: 31 · 2019: 29 · 2018: 16 · 2017: 5
- FWCI
- 23.23
- Type
- journal article
- Language
- en
- Open access
- green
- pure.amsterdamumc.nl
- Licence
- Locations
- Gastroenterology (publishedVersion)
- PubMed (publishedVersion)
- KNAW research portal (Royal Academy of Art and Sciences (KNAW)) (publishedVersion)
- Pure Amsterdam UMC (submittedVersion, other-oa)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- CINECA IRIS Institutial research information system (University of Pisa) (submittedVersion, cc-by-nc-nd)
- Research Publications (Maastricht University) (submittedVersion)
- UvA-DARE (University of Amsterdam) (submittedVersion)
- TNO Repository (submittedVersion)
- Repository hosted by TU Delft Library (TU Delft) (submittedVersion)
- Funders
- Danone
- Topics
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Gastroenterology › Inflammatory Bowel Disease
- Keywords
- irritable bowel syndrome, visceral hypersensitivity, fungal dysbiosis, gut fungi, mast cells, Dectin-1, Syk signaling, β-glucan, fungicides, fecal microbiota transplantation, water avoidance stress, maternal separation, nociception, gut-brain axis, rats, human gut microbiome, metabarcoding
- MeSH terms
- Gastrointestinal Microbiome, Fecal Microbiota Transplantation, Syk Kinase, Adult, Animals, Antifungal Agents, Anxiety, Separation, Behavior, Animal, Cell Line, Disease Models, Animal, Feces, Female, Fungi, Humans, Hyperalgesia, Intestinal Mucosa, Intestines, Male, Mast Cells, Maternal Deprivation, Middle Aged, Pain Measurement, Cell Degranulation, Abdominal Pain, Case-Control Studies, Pain Threshold, Rats, Long-Evans, Irritable Bowel Syndrome, beta-Glucans, Protein Kinase Inhibitors, Pain Perception, Dysbiosis
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