Effects of bowel preparation on the human gut microbiome and metabolome
Large bowel preparation may cause a substantial change in the gut microbiota and metabolites. Here, we included a bowel prep group and a no-procedure control group and evaluated the effects of bowel prep on the stability of the gut microbiome and metabolome as well as on recovery. Gut microbiota and...
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Published in | Scientific reports Vol. 9; no. 1; p. 4042 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
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Language | English |
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Nature Publishing Group UK
11.03.2019
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Abstract | Large bowel preparation may cause a substantial change in the gut microbiota and metabolites. Here, we included a bowel prep group and a no-procedure control group and evaluated the effects of bowel prep on the stability of the gut microbiome and metabolome as well as on recovery. Gut microbiota and metabolome compositions were analyzed by 16S rRNA sequencing and capillary electrophoresis time-of-flight mass spectrometry, respectively. Analysis of coefficients at the genus and species level and weighted UniFrac distance showed that, compared with controls, microbiota composition was significantly reduced immediately after the prep but not at 14 days after it. For the gut metabolome profiles, correlation coefficients between before and immediately after the prep were significantly lower than those between before and 14 days after prep and were not significantly different compared with those for between-subject differences. Thirty-two metabolites were significantly changed before and immediately after the prep, but these metabolites recovered within 14 days. In conclusion, bowel preparation has a profound effect on the gut microbiome and metabolome, but the overall composition recovers to baseline within 14 days. To properly conduct studies of the human gut microbiome and metabolome, fecal sampling should be avoided immediately after bowel prep. |
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AbstractList | Large bowel preparation may cause a substantial change in the gut microbiota and metabolites. Here, we included a bowel prep group and a no-procedure control group and evaluated the effects of bowel prep on the stability of the gut microbiome and metabolome as well as on recovery. Gut microbiota and metabolome compositions were analyzed by 16S rRNA sequencing and capillary electrophoresis time-of-flight mass spectrometry, respectively. Analysis of coefficients at the genus and species level and weighted UniFrac distance showed that, compared with controls, microbiota composition was significantly reduced immediately after the prep but not at 14 days after it. For the gut metabolome profiles, correlation coefficients between before and immediately after the prep were significantly lower than those between before and 14 days after prep and were not significantly different compared with those for between-subject differences. Thirty-two metabolites were significantly changed before and immediately after the prep, but these metabolites recovered within 14 days. In conclusion, bowel preparation has a profound effect on the gut microbiome and metabolome, but the overall composition recovers to baseline within 14 days. To properly conduct studies of the human gut microbiome and metabolome, fecal sampling should be avoided immediately after bowel prep. Large bowel preparation may cause a substantial change in the gut microbiota and metabolites. Here, we included a bowel prep group and a no-procedure control group and evaluated the effects of bowel prep on the stability of the gut microbiome and metabolome as well as on recovery. Gut microbiota and metabolome compositions were analyzed by 16S rRNA sequencing and capillary electrophoresis time-of-flight mass spectrometry, respectively. Analysis of coefficients at the genus and species level and weighted UniFrac distance showed that, compared with controls, microbiota composition was significantly reduced immediately after the prep but not at 14 days after it. For the gut metabolome profiles, correlation coefficients between before and immediately after the prep were significantly lower than those between before and 14 days after prep and were not significantly different compared with those for between-subject differences. Thirty-two metabolites were significantly changed before and immediately after the prep, but these metabolites recovered within 14 days. In conclusion, bowel preparation has a profound effect on the gut microbiome and metabolome, but the overall composition recovers to baseline within 14 days. To properly conduct studies of the human gut microbiome and metabolome, fecal sampling should be avoided immediately after bowel prep.Large bowel preparation may cause a substantial change in the gut microbiota and metabolites. Here, we included a bowel prep group and a no-procedure control group and evaluated the effects of bowel prep on the stability of the gut microbiome and metabolome as well as on recovery. Gut microbiota and metabolome compositions were analyzed by 16S rRNA sequencing and capillary electrophoresis time-of-flight mass spectrometry, respectively. Analysis of coefficients at the genus and species level and weighted UniFrac distance showed that, compared with controls, microbiota composition was significantly reduced immediately after the prep but not at 14 days after it. For the gut metabolome profiles, correlation coefficients between before and immediately after the prep were significantly lower than those between before and 14 days after prep and were not significantly different compared with those for between-subject differences. Thirty-two metabolites were significantly changed before and immediately after the prep, but these metabolites recovered within 14 days. In conclusion, bowel preparation has a profound effect on the gut microbiome and metabolome, but the overall composition recovers to baseline within 14 days. To properly conduct studies of the human gut microbiome and metabolome, fecal sampling should be avoided immediately after bowel prep. |
ArticleNumber | 4042 |
Author | Hisada, Yuya Ohsugi, Mitsuru Tohya, Mari Tsujimoto, Tetsuro Uemura, Naomi Yanagisawa, Naohiro Shimomura, Akira Hattori, Masahira Akiyama, Junichi Takeuchi, Fumihiko Fukuda, Shinji Mizokami, Masashi Imbe, Koh Miyoshi-Akiyama, Tohru Suda, Wataru Nishijima, Suguru Nagata, Naoyoshi Nakamura, Tomoka Watanabe, Kazuhiro |
Author_xml | – sequence: 1 givenname: Naoyoshi surname: Nagata fullname: Nagata, Naoyoshi email: nnagata_ncgm@yahoo.co.jp organization: Department of Gastroenterology and Hepatology, National Center for Global Health and Medicine – sequence: 2 givenname: Mari surname: Tohya fullname: Tohya, Mari organization: Pathogenic Microbe Laboratory, Research Institute, National Center for Global Health and Medicine, Department of Microbiology, Juntendo University School of Medicine – sequence: 3 givenname: Shinji surname: Fukuda fullname: Fukuda, Shinji organization: Institute for Advanced Biosciences, Keio University, Intestinal Microbiota Project, Kanagawa Institute of Industrial Science and Technology, Transborder Medical Research Center, University of Tsukuba, PRESTO, Japan Science and Technology Agency – sequence: 4 givenname: Wataru surname: Suda fullname: Suda, Wataru organization: RIKEN Center for Integrative Medical Sciences – sequence: 5 givenname: Suguru surname: Nishijima fullname: Nishijima, Suguru organization: Computational Bio-Big Data Open Innovation Lab., National Institute of Advanced Science and Technology, Graduate School of Advanced Science and Engineering, Waseda University – sequence: 6 givenname: Fumihiko orcidid: 0000-0003-3185-5661 surname: Takeuchi fullname: Takeuchi, Fumihiko organization: Department of Gene Diagnostics and Therapeutics, National Center for Global Health and Medicine – sequence: 7 givenname: Mitsuru surname: Ohsugi fullname: Ohsugi, Mitsuru organization: Department of Diabetes, Endocrinology, and Metabolism, Center Hospital, National Center for Global Health and Medicine – sequence: 8 givenname: Tetsuro surname: Tsujimoto fullname: Tsujimoto, Tetsuro organization: Department of Diabetes, Endocrinology, and Metabolism, Center Hospital, National Center for Global Health and Medicine – sequence: 9 givenname: Tomoka surname: Nakamura fullname: Nakamura, Tomoka organization: Department of Diabetes, Endocrinology, and Metabolism, Center Hospital, National Center for Global Health and Medicine – sequence: 10 givenname: Akira surname: Shimomura fullname: Shimomura, Akira organization: Department of Gastroenterology and Hepatology, National Center for Global Health and Medicine – sequence: 11 givenname: Naohiro surname: Yanagisawa fullname: Yanagisawa, Naohiro organization: Department of Gastroenterology and Hepatology, National Center for Global Health and Medicine – sequence: 12 givenname: Yuya surname: Hisada fullname: Hisada, Yuya organization: Department of Gastroenterology and Hepatology, National Center for Global Health and Medicine – sequence: 13 givenname: Kazuhiro surname: Watanabe fullname: Watanabe, Kazuhiro organization: Department of Gastroenterology and Hepatology, National Center for Global Health and Medicine – sequence: 14 givenname: Koh surname: Imbe fullname: Imbe, Koh organization: Department of Gastroenterology and Hepatology, National Center for Global Health and Medicine – sequence: 15 givenname: Junichi surname: Akiyama fullname: Akiyama, Junichi organization: Department of Gastroenterology and Hepatology, National Center for Global Health and Medicine – sequence: 16 givenname: Masashi surname: Mizokami fullname: Mizokami, Masashi organization: Department of Gastroenterology and Hepatology, National Center for Global Health and Medicine, Kohnodai Hospital – sequence: 17 givenname: Tohru surname: Miyoshi-Akiyama fullname: Miyoshi-Akiyama, Tohru organization: Pathogenic Microbe Laboratory, Research Institute, National Center for Global Health and Medicine – sequence: 18 givenname: Naomi surname: Uemura fullname: Uemura, Naomi organization: Department of Gastroenterology and Hepatology, National Center for Global Health and Medicine, Kohnodai Hospital – sequence: 19 givenname: Masahira surname: Hattori fullname: Hattori, Masahira organization: Graduate School of Advanced Science and Engineering, Waseda University, RIKEN Center for Integrative Medical Sciences |
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References_xml | – reference: ASGE Standards of Practice Committee et al. Bowel preparation before colonoscopy. Gastrointest. Endosc. 81, 781–794 (2015). – reference: TropiniCTransient Osmotic Perturbation Causes Long-Term Alteration to the Gut MicrobiotaCell201817317421754.e171:CAS:528:DC%2BC1cXhtFGjsrrK10.1016/j.cell.2018.05.008 – reference: ShobarRMThe Effects of Bowel Preparation on Microbiota-Related Metrics Differ in Health and in Inflammatory Bowel Disease and for the Mucosal and Luminal Microbiota CompartmentsClin. Transl. Gastroenterol.20167e1431:CAS:528:DC%2BC28Xis1alu7o%3D10.1038/ctg.2015.54 – reference: NishimotoYHigh stability of faecal microbiome composition in guanidine thiocyanate solution at room temperature and robustness during colonoscopyGut2016651574157510.1136/gutjnl-2016-311937 – reference: KimSWRobustness of gut microbiota of healthy adults in response to probiotic intervention revealed by high-throughput pyrosequencingDNA Res.2013202412531:CAS:528:DC%2BC3sXpvVyhsr4%3D10.1093/dnares/dst006 – reference: Nagao-KitamotoHFunctional Characterization of Inflammatory Bowel Disease-Associated Gut Dysbiosis in Gnotobiotic MiceCell. Mol. Gastroenterol. Hepatol.2016246848110.1016/j.jcmgh.2016.02.003 – reference: SawayaSMicrosatellite tandem repeats are abundant in human promoters and are associated with regulatory elementsPLoS One20138e547102013PLoSO...854710S1:CAS:528:DC%2BC3sXivFGqsLY%3D10.1371/journal.pone.0054710 – reference: GorkiewiczGAlterations in the colonic microbiota in response to osmotic diarrheaPLoS One20138e558172013PLoSO...855817G1:CAS:528:DC%2BC3sXjtVKgsbs%3D10.1371/journal.pone.0055817 – reference: JalankaJEffects of bowel cleansing on the intestinal microbiotaGut2015641562156810.1136/gutjnl-2014-307240 – reference: van den Berg, R. A., Hoefsloot, H. C., Westerhuis, J. A., Smilde, A. K. & van der Werf, M. J. Centering, scaling, and transformations: improving the biological information content of metabolomics data. BMC Genomics7, 142-2164-7-142 (2006). – reference: HarrellLStandard colonic lavage alters the natural state of mucosal-associated microbiota in the human colonPLoS One20127e325452012PLoSO...732545H1:CAS:528:DC%2BC38Xjs1ehsLs%3D10.1371/journal.pone.0032545 – reference: DragoLToscanoMDe GrandiRCasiniVPaceFPersisting changes of intestinal microbiota after bowel lavage and colonoscopyEur. J. Gastroenterol. Hepatol.20162853253710.1097/MEG.0000000000000581 – reference: FouhyFThe effects of freezing on faecal microbiota as determined using MiSeq sequencing and culture-based investigationsPLoS One201510e011935510.1371/journal.pone.0119355 – reference: LozuponeCLladserMEKnightsDStombaughJKnightRUniFrac: an effective distance metric for microbial community comparisonISME J.2011516917210.1038/ismej.2010.133 – reference: O’BrienCLAllisonGEGrimpenFPavliPImpact of colonoscopy bowel preparation on intestinal microbiotaPLoS One20138e628152013PLoSO...862815O10.1371/journal.pone.0062815 – reference: DohmotoMPreparation for colonoscopy using 1,000 ml Magcorol P isotonic solution in the absence of dietary restrictions or use of purgatives on the preceding dayRev. Gastroenterol. Peru20072737638118183279 – reference: RooksMGGarrettWSGut microbiota, metabolites and host immunityNat. Rev. Immunol.2016163413521:CAS:528:DC%2BC28Xoslyqs7k%3D10.1038/nri.2016.42 – reference: ShibagakiNAging-related changes in the diversity of women’s skin microbiomes associated with oral bacteriaSci. Rep.2017710567-01710834-92017NatSR...710567S10.1038/s41598-017-10834-9 – volume: 8 start-page: e55817 year: 2013 ident: 40182_CR3 publication-title: PLoS One doi: 10.1371/journal.pone.0055817 – volume: 28 start-page: 532 year: 2016 ident: 40182_CR5 publication-title: Eur. J. Gastroenterol. Hepatol. doi: 10.1097/MEG.0000000000000581 – volume: 27 start-page: 376 year: 2007 ident: 40182_CR14 publication-title: Rev. Gastroenterol. Peru – volume: 65 start-page: 1574 year: 2016 ident: 40182_CR8 publication-title: Gut doi: 10.1136/gutjnl-2016-311937 – volume: 10 start-page: e0119355 year: 2015 ident: 40182_CR12 publication-title: PLoS One doi: 10.1371/journal.pone.0119355 – volume: 2 start-page: 468 year: 2016 ident: 40182_CR15 publication-title: Cell. Mol. Gastroenterol. 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Snippet | Large bowel preparation may cause a substantial change in the gut microbiota and metabolites. Here, we included a bowel prep group and a no-procedure control... |
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SubjectTerms | 45 631/326 631/326/107 692/4020/1394 692/4020/2741/2135 82 82/58 Capillary electrophoresis Correlation coefficient Digestive system Feces - microbiology Gastrointestinal Microbiome - genetics Gut microbiota Humanities and Social Sciences Humans Intestinal microflora Intestine Mass Spectrometry Mass spectroscopy Metabolites Metabolome - genetics Metabolomics Microbiomes Microbiota Microbiota - genetics multidisciplinary RNA, Ribosomal, 16S - genetics rRNA 16S Science Science (multidisciplinary) |
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Title | Effects of bowel preparation on the human gut microbiome and metabolome |
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