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dc.contributor.authorChen, Hui-Meien_US
dc.contributor.authorChen, Chung-Chuen_US
dc.contributor.authorChen, Chien-Chien_US
dc.contributor.authorWang, Shen-Chihen_US
dc.contributor.authorWang, Chun-Linen_US
dc.contributor.authorHuang, Chien-Hsunen_US
dc.contributor.authorLiou, Jong-Shianen_US
dc.contributor.authorLiu, Ta-Weien_US
dc.contributor.authorPeng, Hwei-Lingen_US
dc.contributor.authorLin, Feng-Maoen_US
dc.contributor.authorLiu, Chia-Yuanen_US
dc.contributor.authorWeng, Shun-Longen_US
dc.contributor.authorCheng, Chieh-Jenen_US
dc.contributor.authorHung, Yi-Fangen_US
dc.contributor.authorLiao, Chii-Cherngen_US
dc.contributor.authorHuang, Hsien-Daen_US
dc.date.accessioned2019-04-02T06:00:57Z-
dc.date.available2019-04-02T06:00:57Z-
dc.date.issued2018-12-31en_US
dc.identifier.issn1471-2164en_US
dc.identifier.urihttp://dx.doi.org/10.1186/s12864-018-5285-6en_US
dc.identifier.urihttp://hdl.handle.net/11536/148655-
dc.description.abstractBackgroundHuman gut microbiome has an essential role in human health and disease. Although the major dominant microbiota within individuals have been reported, the change of gut microbiome caused by external factors, such as antibiotic use and bowel cleansing, remains unclear. We conducted this study to investigate the change of gut microbiome in overweight male adults after bowel preparation, where none of the participants had been diagnosed with any systemic diseases.MethodsA total of 20 overweight, male Taiwanese adults were recruited, and all participants were omnivorous. The participants provided fecal samples and blood samples at three time points: prior to bowel preparation, 7days after colonoscopy, and 28days after colonoscopy. The microbiota composition in fecal samples was analyzed using 16S ribosome RNA gene amplicon sequencing.ResultsOur results demonstrated that the relative abundance of the most dominant bacteria hardly changed from prior to bowel preparation to 28days after colonoscopy. Using the ratio of Prevotella to the sum of Prevotella and Bacteroides in the fecal samples at baseline, the participants were separated into two groups. The fecal samples of the Type 1 group was Bacteroides-dominant, and that of the Type 2 group was Prevotella-dominant with a noticeable presence Bacteroides. Bulleidia appears more in the Type 1 fecal samples, while Akkermensia appears more in the Type 2 fecal samples. Of each type, the gut microbial diversity differed slightly among the three collection times. Additionally, the Type 2 fecal microbiota was temporarily susceptible to bowel cleansing. Predictive functional analysis of microbial community reveals that their activities for the mineral absorption metabolism and arachidonic acid metabolism differed significantly between the two types. Depending on their fecal type, the variance of triglycerides and C-reactive protein also differed between the two types of participants.ConclusionsDepending upon the fecal type, the microbial diversity and the predictive functional modules of microbial community differed significantly after bowel preparation. In addition, blood biochemical markers presented somewhat associated with fecal type. Therefore, our results might provide some insights as to how knowledge of the microbial community could be used to promote health through personalized clinical treatment.en_US
dc.language.isoen_USen_US
dc.subjectGut microbiomeen_US
dc.subjectOverweighten_US
dc.subjectBowel preparationen_US
dc.subjectHigh-throughput sequencingen_US
dc.subjectBacteroidesen_US
dc.subjectPreovotellaen_US
dc.titleGut microbiome changes in overweight male adults following bowel preparationen_US
dc.typeArticleen_US
dc.identifier.doi10.1186/s12864-018-5285-6en_US
dc.identifier.journalBMC GENOMICSen_US
dc.citation.volume19en_US
dc.citation.issue10en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.department生物資訊及系統生物研究所zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.contributor.departmentInstitude of Bioinformatics and Systems Biologyen_US
dc.identifier.wosnumberWOS:000454632500014en_US
dc.citation.woscount0en_US
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