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Phages infecting Faecalibacterium prausnitzii belong to novel viral genera that help to decipher intestinal viromes

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Saccharomyces boulardii CNCM I-745 supplementation reduces gastrointestinal dysfunction in an animal model of IBS

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Estrous cycle and ovariectomy-induced changes in visceral pain are microbiota-dependent

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Gut microbiota modulates visceral sensitivity through calcitonin gene-related peptide (CGRP) production

Pujo, J., Palma, G. D., Lu, J. G., Galipeau, H. J., Surette, M. G., Collins, S. M., & Berčík, P. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2188874 · Cited by 43 · see citing works

Dietary Saccharomyces cerevisiae boulardii CNCM I-1079 Positively Affects Performance and Intestinal Ecosystem in Broilers during a Campylobacter jejuni Infection

Massacci, F. R., Lovito, C., Tofani, S., Tentellini, M., Genovese, D. A., de Leo, A. A. P., Papa, P., Magistrali, C. F., Manuali, E., Trabalza‐Marinucci, M., et al. (2019) · Microorganisms · doi:10.3390/microorganisms7120596 · Cited by 41 · see citing works

Bioactive Compounds in Food as a Current Therapeutic Approach to Maintain a Healthy Intestinal Epithelium

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Involvement of shared mucosal‐associated microbiota in the duodenum and rectum in diarrhea‐predominant irritable bowel syndrome

Li, G., Yang, M. J., Jin, Y. T., Li, Y., Qian, W., Xiong, H., Song, J., & Hou, X. (2017) · Journal of Gastroenterology and Hepatology · doi:10.1111/jgh.14059 · Cited by 35 · see citing works

Impact of the griffithsin anti-HIV microbicide and placebo gels on the rectal mucosal proteome and microbiome in non-human primates

Girard, L., Birse, K., Holm, J. B., Gajer, P., Humphrys, M. S., Garber, D. A., Guenthner, P. C., Noël‐Romas, L., Abou, M., McCorrister, S. J., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-26313-8 · Cited by 33 · see citing works

Bacterial modulation of visceral sensation: mediators and mechanisms

Lomax, A. E., Pradhananga, S., Sessenwein, J. L., & O’Malley, D. (2019) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00052.2019 · Cited by 35 · see citing works

Consistent Alterations of Human Fecal Microbes After Transplantation into Germ-Free Mice

Li, Y., Cao, W., Gao, N., Zhao, X., & Chen, W. (2021) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2020.06.024 · Cited by 31 · see citing works

Biodiversity and Physiological Characteristics of Novel Faecalibacterium prausnitzii Strains Isolated from Human Feces

Hu, W., Gao, W., Liu, Z., Fang, Z., Zhao, J., Zhang, H., Lu, W., & Chen, W. (2022) · Microorganisms · doi:10.3390/microorganisms10020297 · Cited by 30 · see citing works

Modulation of the Caecal Gut Microbiota of Mice by Dietary Supplement Containing Resistant Starch: Impact Is Donor-Dependent

Cherbuy, C., Bellet, D., Robert, V., Mayeur, C., Schwiertz, A., & Langella, P. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01234 · Cited by 30 · see citing works

Diet and gut microbial associations in irritable bowel syndrome according to disease subtype

Wang, Y., Ma, W., Mehta, R. S., Nguyen, L. H., Song, M., Drew, D. A., Asnicar, F., Huttenhower, C., Segata, N., Wolf, J., et al. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2262130 · Cited by 29 · see citing works

Comprehensive analysis of 84 Faecalibacterium prausnitzii strains uncovers their genetic diversity, functional characteristics, and potential risks

Bai, Z., Zhang, N., Jin, Y., Chen, L., Mao, Y., Sun, L., Fang, F., Liu, Y., Han, M., & Li, G. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.919701 · Cited by 29 · see citing works

Modulating the Gut–Muscle Axis: Increasing SCFA-Producing Gut Microbiota Commensals and Decreasing Endotoxin Production to Mitigate Cancer Cachexia

Roy, S., Bahmani, A. H. A., Davids, M., Herrema, H., & Nieuwdorp, M. (2025) · Microorganisms · doi:10.3390/microorganisms13061356 · Cited by 28 · see citing works

Stress-induced intestinal barrier dysfunction is exacerbated during diet-induced obesity

Bahlouli, W., Breton, J., Lelouard, M., L’Huillier, C., Tirelle, P., Salameh, É., Amamou, A., Atmani, K., Goichon, A., Bôle‐Feysot, C., et al. (2020) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2020.108382 · Cited by 25 · see citing works

Intestinal Microbiota Contributes to the Development of Cardiovascular Inflammation and Vasculitis in Mice

Jena, P. K., Wakita, D., Gomez, A. C., de Carvalho, T. T., Atici, A. E., Aubuchon, E. A., Narayanan, M., Lee, Y., Fishbein, M. C., Takasato, Y., et al. (2025) · Circulation Research · doi:10.1161/circresaha.124.325079 · Cited by 23 · see citing works

The Gut Microbiota and Chronic Pain

Pak, R. J., Cho, M. S., Pride, K., & Abd-Elsayed, A. A. (2024) · Current Pain and Headache Reports · doi:10.1007/s11916-024-01221-x · Cited by 23 · see citing works

Lactobacillus rhamnosus GG soluble mediators ameliorate early life stress-induced visceral hypersensitivity and changes in spinal cord gene expression

Neufeld, K. M., Strain, C., Pusceddu, M. M., Waworuntu, R. V., Manurung, S., Gross, G., Moloney, G. M., Hoban, A. E., Murphy, K., Stanton, C., et al. (2020) · Neuronal Signaling · doi:10.1042/ns20200007 · Cited by 22 · see citing works

Membrane vesicles produced by next-generation probiotics from the gut as innovative tools for human health

Abraham, L., Raise, A., Beney, L., Lapaquette, P., & Rieu, A. (2025) · Gut Microbes · doi:10.1080/19490976.2025.2552344 · Cited by 21 · see citing works

Stress induces more serious barrier dysfunction in follicle-associated epithelium than villus epithelium involving mast cells and protease-activated receptor-2

Zhang, L., Song, J., Bai, T., Qian, W., & Hou, X. (2017) · Scientific Reports · doi:10.1038/s41598-017-05064-y · Cited by 21 · see citing works

Serpin-positive Bifidobacterium breve CNCM I-5644 improves intestinal permeability in two models of irritable bowel syndrome

Torres-Maravilla, E., Holowacz, S., Delannoy, J., Lenoir, L., Jacouton, E., Gervason, S., Meynier, M., Boucard, A.-S., Carvalho, F. A., Barbut, F., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-21746-8 · Cited by 20 · see citing works

Possible relationship between the gut leaky syndrome and musculoskeletal injuries: the important role of gut microbiota as indirect modulator

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Antihyperalgesic properties of gut microbiota: Parabacteroides distasonis as a new probiotic strategy to alleviate chronic abdominal pain

Gervason, S., Méleine, M., Lolignier, S., Meynier, M., Daugey, V., Birer, A., Aissouni, Y., Berthon, J., Ardid, D., Filaire, E., et al. (2023) · Pain · doi:10.1097/j.pain.0000000000003075 · Cited by 18 · see citing works

Protease-Induced Excitation of Dorsal Root Ganglion Neurons in Response to Acute Perturbation of the Gut Microbiota Is Associated With Visceral and Somatic Hypersensitivity

Baker, C. C., Sessenwein, J. L., Wood, H. M., Yu, Y., Tsang, Q. K., Alward, T. A., Jiménez-Vargas, N. N., Omar, A. A., McDonell, A., Segal, J. P., et al. (2024) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2024.03.006 · Cited by 16 · see citing works

Fecal Proteolytic Bacteria and Staphylococcal Superantigens Are Associated With Abdominal Pain Severity in Irritable Bowel Syndrome

Quan, R., Decraecker, L., Appeltans, I., Cuende‐Estévez, M., Remoortel, S. V., Aguilera‐Lizarraga, J., Wang, Z., Hicks, G. A., Wykosky, J., McLean, P. G., et al. (2024) · The American Journal of Gastroenterology · doi:10.14309/ajg.0000000000003042 · Cited by 16 · see citing works

An unexpected connection: A narrative review of the associations between Gut Microbiome and Musculoskeletal Pain

Enrico, V. T., Vo, N. N., Methé, B. A., Morris, A., & Sowa, G. (2022) · European Spine Journal · doi:10.1007/s00586-022-07429-y · Cited by 16 · see citing works

Rodent Model of Irritable Bowel Syndrome

Wang, Y., Bi, Z., Wang, E., Sun, B., Zheng, Y., Zhong, L. L. D., & Yuan, J. (2017) · International Journal of Gastroenterology Disorders & Therapy · doi:10.15344/2393-8498/2017/131 · Cited by 15 · see citing works

Probiotics in Postoperative Pain Management

Fyntanidou, B., Amaniti, A., Soulioti, E., Zagalioti, S., Gkarmiri, S., Chorti, A. G., Loukipoudi, L., Ioannidis, A., Dalakakis, I., Menni, A.-E., et al. (2023) · Journal of Personalized Medicine · doi:10.3390/jpm13121645 · Cited by 15 · see citing works

Functional Abdominal Bloating and Gut Microbiota: An Update

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Comparative effects of α2δ-1 ligands in mouse models of colonic hypersensitivity

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Involvement of toll-like receptor 5 on mouse model of colonic hypersensitivity induced by neonatal maternal separation

Mallaret, G., Lashermes, A., Méleine, M., Boudieu, L., Barbier, J., Aissouni, Y., Gelot, A., Chassaing, B., Gewirtz, A. T., Ardid, D., et al. (2022) · World Journal of Gastroenterology · doi:10.3748/wjg.v28.i29.3903 · Cited by 13 · see citing works

Impact of gut-peripheral nervous system axis on the development of diabetic neuropathy

Mázala-de-Oliveira, T., de Sá, Y. A. P. J., & Carvalho, V. F. (2023) · Memórias do Instituto Oswaldo Cruz · doi:10.1590/0074-02760220197 · Cited by 11 · see citing works

Fermented food products for gastrointestinal health and related diseases

Meena, S. K., Reddy, B. K., & Rai, D. C. (2023) · Journal of Dairy Veterinary & Animal Research · doi:10.15406/jdvar.2023.12.00320 · Cited by 11 · see citing works

Faecalibacterium prausnitzii Is Associated with Disease Severity in MASLD but Its Supplementation Does Not Improve Diet-Induced Steatohepatitis in Mice

Münte, E., Viebahn, G., Khurana, A., Fujiki, J., Nakamura, T., Lang, S., Demir, M., Schnabl, B., & Hartmann, P. (2025) · Microorganisms · doi:10.3390/microorganisms13030675 · Cited by 11 · see citing works

Microbiome contributions to pain: a review of the preclinical literature

Pratt, M. L., Plumb, A. N., Manjrekar, A., Cardona, L. M., Chan, C. K., John, J. M., & Sadler, K. E. (2024) · Pain · doi:10.1097/j.pain.0000000000003376 · Cited by 9 · see citing works

Mechanism-Oriented Therapy of Irritable Bowel Syndrome

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Short-Term Tolerability, Safety, and Gut Microbial Composition Responses to a Multi-Strain Probiotic Supplement: An Open-Label Study in Healthy Adults.

Ryan, J. J., & Patno, N. (2021) · PubMed Central · Cited by 6 · see citing works

Gut Microbiota in Adults with Chronic Widespread Pain: A Systematic Review

Leong, P., & Shi, L. (2025) · Diseases · doi:10.3390/diseases13090299 · Cited by 5 · see citing works

Next-Generation Probiotics

Kumari, M., & Kokkiligadda, A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822909-5.00004-6 · Cited by 5 · see citing works

Consistent alterations of human fecal microbes after transplanted to germ-free micePreprint

Li, Y., Cao, W., Gao, N., Zhao, X., & Chen, W. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/495663 · Cited by 5 · see citing works

Linking Psychological Stress to Epigenetic Regulation via the Gut–Liver–Brain Axis in Irritable Bowel Syndrome and Metabolic Dysfunction-Associated Fatty Liver Disease

Crocetta, A., Giannelou, M.-A., Benfante, A., Castelli, L., & Koumbi, L. (2025) · Livers · doi:10.3390/livers5030043 · Cited by 4 · see citing works

Screening of probiotic strains to improve visceral hypersensitivity in irritable bowel syndrome by using in vitro and in vivo approaches

Torres-Maravilla, E., Carvalho, F. A., Holowacz, S., Delannoy, J., Lenoir, L., Jacouton, E., Barbut, F., Langella, P., Bermúdez‐Humarán, L. G., & Waligora‐Dupriet, A. (2024) · Beneficial Microbes · doi:10.1163/18762891-bja00006 · Cited by 5 · see citing works

Pterostilbene-mediated microbiota shifts: Implications and opportunities

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Dietary Phytonutrients in Fibromyalgia: Integrating Mechanisms, Biomarkers, and Clinical Evidence—A Narrative Review

Kahraman, T., & Ayaz, A. (2025) · Medicina · doi:10.3390/medicina61122211 · Cited by 3 · see citing works

A Comprehensive Review of Irritable Bowel Syndrome Screening Models for Drug Research and Development

Wal, A., Wal, P., Verma, N., Srivastava, A., Rai, A. K., & Kosey, S. (2022) · Pharmacophore · doi:10.51847/jc8hjh9xuf · Cited by 3 · see citing works

Complete Genome Sequences of Eight Faecalibacterium sp. Strains Isolated from Healthy Human Stool

Fraccascia, D., Chanyi, R. M., Altermann, E., Roy, N. C., Flint, S., & McNabb, W. C. (2022) · Microbiology Resource Announcements · doi:10.1128/mra.00824-22 · Cited by 3 · see citing works

Emerging therapeutic approaches for treating abdominal pain

Jiménez-Vargas, N. N., Parkar, N., Takami, K., Wood, H. M., Lomax, A. E., Reed, D. E., & Vanner, S. J. (2025) · Journal of the Canadian Association of Gastroenterology · doi:10.1093/jcag/gwaf016 · Cited by 2 · see citing works

A Narrative Hypothesis: The Important Role of Gut Microbiota in the Modulation of Effort Tolerance in Endurance Athletes

Álvarez‐Herms, J., Burtscher, M., Corbi, F., González, A., & Odriozola-Martínez, A. (2025) · Nutrients · doi:10.3390/nu17172836 · Cited by 3 · see citing works

The immunomodulatory metabolite butyrate ameliorates renal fibrosis by restoring gut barrier integrity and suppressing the TGF-β1/Smad3 pathway

Liu, G., Sun, Q., Yan, Q., Tang, F., Lai, L., & Li, X. D. (2026) · International Immunopharmacology · doi:10.1016/j.intimp.2026.116557 · Cited by 2 · see citing works

A Pilot Study on the Fecal Microbiota in Mexican Women with Gestational Diabetes Mellitus and Their Newborns

Lizárraga, D., Garcı́a-Gasca, A., García-Gasca, T., Lund, G., Guerrero, A., Peraza-Manjarrez, E., & Gómez‐Gil, B. (2024) · Diabetology · doi:10.3390/diabetology5050034 · Cited by 2 · see citing works

Exploring Screening Models for Irritable Bowel Syndrome in Drug Research and Development: A Comprehensive Review

Wal, A., Wal, P., Verma, N., Srivastava, A., Rai, A. K., & Kosey, S. (2023) · Interdisciplinary Research in Medical Sciences Specialty · doi:10.51847/wpi4h3t548 · Cited by 2 · see citing works

Separation of the effects of small intestinal microbiome-diet interactions on human gut hormone secretionPreprint

Rienzi, S. C. D., Danhof, H. A., Huerta, J., & Britton, R. A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.25.509333 · Cited by 2 · see citing works

Gut Bacteria: A Beneficial Symbiosis or a Hidden Threat? Investigating the Dual Role of Bacteria in Gastrointestinal Diseases

Soltani-Moghadam, F., Kafil, H. S., Sefidan, F. Y., Nezhadi, J., Saedi, S., Mohammadzadeh-Asl, Y., Sattarpour, S., & Rezaee, M. A. (2026) · Current Microbiology · doi:10.1007/s00284-026-05007-9 · Cited by 1 · see citing works

Management of irritable bowel syndrome in children

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Thoughts on the future of probiotic beverages

Paramithiotis, S., Syrokou, M. K., & Drosinos, E. H. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-818588-9.00022-x · Cited by 1 · see citing works

Maternal deprivation and nociception

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Impacts of Early Life Adversity on Microbiota and Immune Functioning in Individuals with Major Depressive Disorder

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Influence du microbiote sur la douleur

Gervason, S., Defaye, M., Ardid, D., Berthon, J., Altier, C., Filaire, E., & Carvalho, F. A. (2021) · Douleur et Analgésie · doi:10.3166/dea-2021-0144

Faecalibacterium prausnitzii Reduces Plasma Lipopolysaccharide and Inhibits AtherosclerosisPreprint

Yang, H.-T., Liu, J., Wu, T., Yang, Y., Wu, C.-X., Hou, X., Zheng, Y., Ma, Y., & Xie, X. (2022) · Research Square · doi:10.21203/rs.3.rs-2391124/v1

Insights into the proteome of next-generation probiotic Faecalibacterium duncaniae A2-165 through label-free proteomics approach

Américo, M. F., Rodrigues, T. V., Henry, C., da Silva, W. M., Verano-Braga, T., Azevedo, V., & Chatel, J. (2026) · BMC Microbiology · doi:10.1186/s12866-026-04814-1

Comparative Genomics of Faecalibacterium spp.

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Signalisation des "protease-activated receptors" dans les neurones sensitifs humains : implication dans le syndrome de l'intestin irritable

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Caractérisation de molécules lipidiques produites par les bactéries probiotiques Escherichia coli Nissle 1917 : rôle dans l’homéostasie intestinale

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Développement d'un modèle murin de dénutrition avec entéropathie et évaluation de molécules d'intérêt permettant de contribuer au rétablissement de la fonction de barrière intestinale

Salameh, É. (2019) · doi:10.70675/1ce7ef55ze4faz4ad9z898dz6882372a70e1

Identification de souches bactériennes à potentiel probiotique dans la diminution des hyperperméabilités intestinales et détermination de leur(s) mécanisme(s) d’action

Chamignon, C. (2020) · doi:10.70675/4a201bc9z4ec7z4ccfza054z308f73c4fdd2

Contrôle peptidergique de la douleur : modulation des voies descendantes par les systèmes relaxine.

Abboud, C. (2021) · doi:10.70675/d4d32122z1374z427ezae6dzda0f030e61ca

Exposition aux produits de peroxydation lipidique induits par l'apport nutritionnel de fer héminique des viandes : conséquences sur l'homéostasie intestinale et la susceptibilité aux maladies chroniques chez l'adulte et sa descendance

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Isolation, Identification, and Characterization of a Serine Protease with Anti-nociceptive Activity from the Gut Bacterium, Faecalibacterium prausnitziiPreprint

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The probiotic Bifidobacterium infantis 35624 displays visceral antinociceptive effects in the rat

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Tu1779 Personalized Therapy of Gastrointestinal Diseases With Symbiotic Bacteria

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Microbiota dysbiosis and mucosal hyperinnervation contribute to intestinal hyperalgesia in a mouse model of postinfectious irritable bowel syndrome

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F. prausnitzii and its supernatant increase SCFAs-producing bacteria to restore gut dysbiosis in TNBS-induced colitis

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