Cited by 178Gut microbiota and healthSmoking Behavior and CessationOral microbiology and periodontitis research

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Smoking Cessation Alters Intestinal Microbiota: Insights from Quantitative Investigations on Human Fecal Samples Using FISH

Biedermann, Luc, Brülisauer, Karin, Zeitz, Jonas, Frei, Pascal, Scharl, Michael, Vavricka, Stephan R., Fried, Michael, Loessner, Martin J., Rogler, Gerhard, Schuppler, Markus·2014·Inflammatory Bowel Diseases

DOI 10.1097/mib.0000000000000129

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Abstract

BACKGROUND: There has been a dramatic increase in investigations on the potential mechanistic role of the intestinal microbiota in various diseases and factors modulating intestinal microbial composition. We recently reported on intestinal microbial shifts after smoking cessation in humans. In this study, we aimed to conduct further microbial analyses and verify our previous results obtained by pyrosequencing using a direct quantitative microbial approach. METHODS: Stool samples of healthy smoking human subjects undergoing controlled smoking cessation during a 9-week observational period were analyzed and compared with 2 control groups, ongoing smoking and nonsmoking subjects. Fluorescence in situ hybridization was applied to quantify specific bacterial groups. RESULTS: Intestinal microbiota composition was substantially altered after smoking cessation as characterized by an increase in key representatives from the phyla of Firmicutes (Clostridium coccoides, Eubacterium rectale, and Clostridium leptum subgroup) and Actinobacteria (HGC bacteria and Bifidobacteria) as well as a decrease in Bacteroidetes (Prevotella spp. and Bacteroides spp.) and Proteobacteria (β- and γ-subgroup of Proteobacteria). CONCLUSIONS: As determined by fluorescence in situ hybridization, an independent direct quantitative microbial approach, we could confirm that intestinal microbiota composition in humans is influenced by smoking. The characteristics of observed microbial shifts suggest a potential mechanistic association to alterations in body weight subsequent to smoking cessation. More importantly, regarding previously described microbial hallmarks of dysbiosis in inflammatory bowel diseases, a variety of observed microbial alterations after smoking cessation deserve further consideration in view of the divergent effect of smoking on the clinical course of Crohn's disease and ulcerative colitis.

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Turnbaugh, P. J., Ley, R. E., Mahowald, M. A., Magrini, V., Mardis, E. R., & Gordon, J. I. (2006) · Nature · doi:10.1038/nature05414 · Cited by 12,444
Structure, function and diversity of the healthy human microbiome
The Human Microbiome Project Consortium (2012) · Nature · doi:10.1038/nature11234 · Cited by 11,726
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Qin, J., Li, Y., Cai, Z., Li, S., Zhu, J., Zhang, F., Liang, S., Zhang, W., Guan, Y., Shen, D., et al. (2012) · Nature · doi:10.1038/nature11450 · Cited by 6,762
The gut microbiota as an environmental factor that regulates fat storage
Bäckhed, F., Ding, H., Wang, T., Hooper, L. V., Koh, G. Y., Nagy, A., Semenkovich, C. F., & Gordon, J. I. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407076101 · Cited by 6,245
Obesity alters gut microbial ecology
Ley, R. E., Bäckhed, F., Turnbaugh, P., Lozupone, C. A., Knight, R. D., & Gordon, J. I. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504978102 · Cited by 6,176
Molecular-phylogenetic characterization of microbial community imbalances in human inflammatory bowel diseases
Frank, D. N., St. Amand, A. L., Feldman, R. A., Boedeker, E. C., Harpaz, N., & Pace, N. R. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706625104 · Cited by 4,611
Gut metagenome in European women with normal, impaired and diabetic glucose control
Karlsson, F. H., Tremaroli, V., Nookaew, I., Bergström, G., Behre, C. J., Fagerberg, B., Nielsen, J., & Bäckhed, F. (2013) · Nature · doi:10.1038/nature12198 · Cited by 3,115
A Molecular View of Microbial Diversity and the Biosphere
Pace, N. R. (1997) · Science · doi:10.1126/science.276.5313.734 · Cited by 2,797
Incomplete recovery and individualized responses of the human distal gut microbiota to repeated antibiotic perturbation
Dethlefsen, L., & Relman, D. A. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000087107 · Cited by 2,421
The pervasive effects of an antibiotic on the human gut microbiota, as revealed by deep 16S rRNA sequencing
Dethlefsen, L., Huse, S., Sogin, M. L., & Relman, D. A. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060280 · Cited by 2,361

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Bai, X., Wei, H., Liu, W., Coker, O. O., Gou, H., Liu, C., Zhao, L., Li, C., Zhou, Y., Wang, G., et al. (2022) · Gut · doi:10.1136/gutjnl-2021-325021 · Cited by 311
Association between Cigarette Smoking Status and Composition of Gut Microbiota: Population-Based Cross-Sectional Study
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Authors: Biedermann, L., Brülisauer, K., Zeitz, J., Frei, P., Scharl, M., Vavricka, S. R., Fried, M., Loessner, M. J., Rogler, G., & Schuppler, M.
Affiliations: University of Zurich (CH)
ETH Zurich (CH)
University Hospital Zurich (CH)
ORCID: Biedermann, Luc
Zeitz, Jonas
Scharl, Michael
Vavricka, Stephan R.
Loessner, Martin J.
Rogler, Gerhard
Venue: Inflammatory Bowel Diseases
Publisher: Oxford University Press (OUP)
Published: 2014-09
Volume: 20
Issue: 9
Pages: 1496-1501
ISSN: 1078-0998 (ISSN-L)
DOI: 10.1097/mib.0000000000000129
OpenAlex: W2024172588
Cited by: 178
References: 47
Citations by year: 2026: 6 · 2025: 8 · 2024: 19 · 2023: 16 · 2022: 13 · 2021: 19 · 2020: 24 · 2019: 15 · 2018: 16 · 2017: 17 · 2016: 11 · 2015: 13 · 2014: 1
FWCI: 5.74
Type: journal article
Language: en
Open access: closed
Locations: Inflammatory Bowel Diseases (publishedVersion)
PubMed (publishedVersion)
Zurich Open Repository and Archive (University of Zurich) (submittedVersion)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Smoking Behavior and Cessation
Health Sciences › Dentistry › Periodontics › Oral microbiology and periodontitis research
Keywords: smoking cessation, gut microbiota
MeSH terms: DNA, Bacterial, Feces, Humans, Intestines, Colony Count, Microbial, Oligonucleotide Probes, Smoking Cessation, In Situ Hybridization, Fluorescence, Microbiota

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Smoking Cessation Alters Intestinal Microbiota: Insights from Quantitative Investigations on Human Fecal Samples Using FISH

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