Cited by 344Gut microbiota and healthCeliac Disease Research and ManagementProbiotics and Fermented Foods

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Effects of a gluten-free diet on gut microbiota and immune function in healthy adult human subjects

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De Palma, Giada, Nadal, Inmaculada, Collado, Maria Carmen, Sanz, Yolanda·2009·British Journal Of Nutrition

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Abstract

Diet influences the composition of the gut microbiota and host's health, particularly in patients suffering from food-related diseases. Coeliac disease (CD) is a permanent intolerance to cereal gluten proteins and the only therapy for the patients is to adhere to a life-long gluten-free diet (GFD). In the present preliminary study, the effects of a GFD on the composition and immune function of the gut microbiota were analysed in ten healthy subjects (mean age 30.3 years) over 1 month. Faecal microbiota was analysed by fluorescence in situ hybridisation (FISH) and quantitative PCR (qPCR). The ability of faecal bacteria to stimulate cytokine production by peripheral blood mononuclear cells (PBMC) was determined by ELISA. No significant differences in dietary intake were found before and after the GFD except for reductions (P = 0.001) in polysaccharides. Bifidobacterium, Clostridium lituseburense and Faecalibacterium prausnitzii proportions decreased (P = 0.007, P = 0.031 and P = 0.009, respectively) as a result of the GFD analysed by FISH. Bifidobacterium, Lactobacillus and Bifidobacterium longum counts decreased (P = 0.020, P = 0.001 and P = 0.017, respectively), while Enterobacteriaceae and Escherichia coli counts increased (P = 0.005 and P = 0.003) after the GFD assessed by qPCR. TNF-alpha, interferon-gamma, IL-10 and IL-8 production by PBMC stimulated with faecal samples was also reduced (P = 0.021, P = 0.037, P = 0.002 and P = 0.007, respectively) after the diet. Therefore, the GFD led to reductions in beneficial gut bacteria populations and the ability of faecal samples to stimulate the host's immunity. Thus, the GFD may constitute an environmental variable to be considered in treated CD patients for its possible effects on gut health.

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Combination of 16S rRNA-targeted oligonucleotide probes with flow cytometry for analyzing mixed microbial populations
Amann, R., Binder, B. J., Olson, R. J., Chisholm, S. W., Devereux, R., & Stahl, D. A. (1990) · Applied and Environmental Microbiology · doi:10.1128/aem.56.6.1919-1925.1990 · Cited by 4,049
Gluten, major histocompatibility complex, and the small intestine. A molecular and immunobiologic approach to the spectrum of gluten sensitivity ('celiac sprue').
Marsh, M. N. (1992) · PubMed · Cited by 1,985
Gluten, major histocompatibility complex, and the small intestine
Marsh, M. N. (1992) · Gastroenterology · doi:10.1016/0016-5085(92)91819-p · Cited by 1,692
Optimizing fluorescent in situ hybridization with rRNA‐targeted oligonucleotide probes for flow cytometric identification of microorganisms
Wallner, G., Amann, R., & Beisker, W. (1993) · Cytometry · doi:10.1002/cyto.990140205 · Cited by 1,227
Application of a suite of 16S rRNA-specific oligonucleotide probes designed to investigate bacteria of the phylum cytophaga-flavobacter-bacteroides in the natural environment
Manz, W., Amann, R., Ludwig, W., Vancanneyt, M., & SCHLEIFER, K. H. (1996) · Microbiology · doi:10.1099/13500872-142-5-1097 · Cited by 1,176
Variations of Bacterial Populations in Human Feces Measured by Fluorescent In Situ Hybridization with Group-Specific 16S rRNA-Targeted Oligonucleotide Probes
Franks, A. H., Harmsen, H. J. M., Raangs, G. C., Jansen, G. J., Schut, F., & Welling, G. W. (1998) · Applied and Environmental Microbiology · doi:10.1128/aem.64.9.3336-3345.1998 · Cited by 1,056
Quantitative fluorescence in situ hybridization of Bifidobacterium spp. with genus-specific 16S rRNA-targeted probes and its application in fecal samples
Langendijk-Genevaux, P. S., Schut, F., Jansen, G. J., Raangs, G. C., Kamphuis, G. R., Wilkinson, M. H. F., & Welling, G. W. (1995) · Applied and Environmental Microbiology · doi:10.1128/aem.61.8.3069-3075.1995 · Cited by 974
Coeliac disease: dissecting a complex inflammatory disorder
Sollid, L. M. (2002) · Nature reviews. Immunology · doi:10.1038/nri885 · Cited by 967
The genome sequence of Bifidobacterium longum reflects its adaptation to the human gastrointestinal tract
Schell, M. A., Karmirantzou, M., Snel, ‎., Vilanova, D., Berger, B. W., Pessi, G., Zwahlen, M.-C., Desiere, F., Peer Bork, B., Delley, M., et al. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.212527599 · Cited by 942
Development of 16S rRNA-Gene-Targeted Group-Specific Primers for the Detection and Identification of Predominant Bacteria in Human Feces
Matsuki, T., Watanabe, K., Fujimoto, J., Miyamoto, Y., Takada, T., Matsumoto, K., Oyaizu, H., & Tanaka, R. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.11.5445-5451.2002 · Cited by 663

Show all 30 references

Research works printed but not linked: 2

Farran, 2004, Tablas de Composición de Alimentos CESNID (CESNID Food Composition Tables)
Sanz, 2008, Child Nutrition and Physiology, 210

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Authors: De Palma, G., Nadal, I., Collado, M. C., & Sanz, Y.
Affiliations: Consejo Superior de Investigaciones Científicas (ES)
Corresponding author: Sanz, Yolanda
ORCID: Sanz, Yolanda
Venue: British Journal Of Nutrition
Publisher: Cambridge University Press (CUP)
Published: 2009-05-18
Volume: 102
Issue: 8
Pages: 1154-1160
ISSN: 0007-1145 (ISSN-L)
1475-2662
DOI: 10.1017/s0007114509371767
OpenAlex: W2128777474
Cited by: 344
References: 30
Citations by year: 2026: 16 · 2025: 16 · 2024: 22 · 2023: 10 · 2022: 35 · 2021: 42 · 2020: 24 · 2019: 32 · 2018: 28 · 2017: 31 · 2016: 24 · 2015: 15 · 2014: 16 · 2013: 10 · 2012: 11
FWCI: 2.93
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: www.cambridge.org/core/terms (unspecified)
Locations: British Journal Of Nutrition (publishedVersion)
PubMed (publishedVersion)
DIGITAL.CSIC (Spanish National Research Council (CSIC)) (submittedVersion)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
Health Sciences › Medicine › Gastroenterology › Celiac Disease Research and Management
Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
Keywords: gluten-free diet, gut microbiota, celiac disease, immune function, fecal bacteria, Bifidobacterium, Faecalibacterium prausnitzii, Lactobacillus, Enterobacteriaceae, Escherichia coli, cytokine production, peripheral blood mononuclear cells, dietary polysaccharides, gut health
MeSH terms: Adult, Bacteria, Energy Intake, Cells, Cultured, Feces, Female, Humans, Leukocytes, Mononuclear, Male, Polymerase Chain Reaction, Cytokines, In Situ Hybridization, Fluorescence, Diet, Gluten-Free, Young Adult

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Effects of a gluten-free diet on gut microbiota and immune function in healthy adult human subjects

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