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      Modulation of gut mucosal microbiota as a mechanism of probiotics‐based adjunctive therapy for ulcerative colitis

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          Abstract

          Ulcerative colitis is a chronic colon inflammatory disease, the probiotics might alleviate UC symptoms by modulating the gut mucosal microbiota, our research has provided new insights into the mechanism of symptom alleviation in UC by applying probiotics‐based adjunctive treatment.

          Summary

          This was a pilot study aiming to evaluate the effects of probiotics as adjunctive treatment for ulcerative colitis (UC). Twenty‐five active patients with UC were assigned to the probiotic ( n = 12) and placebo ( n = 13) groups. The probiotic group received mesalazine (60 mg kg −1 day −1) and oral probiotics (containing Lactobacillus casei Zhang, Lactobacillus plantarum P‐8 and Bifidobacterium animalis subsp . lactis V9) twice daily for 12 weeks, while the placebo group received the same amounts of mesalazine and placebo. The clinical outcomes were assessed. The gut mucosal microbiota was profiled by PacBio single‐molecule, real‐time (SMRT) sequencing of the full‐length 16S rRNA of biopsy samples obtained by colonoscopy. A significantly greater magnitude of reduction was observed in the UC disease activity index (UCDAI) in the probiotic group compared with the placebo group ( P = 0.043), accompanying by a higher remission rate (91.67% for probiotic‐receivers versus 69.23% for placebo‐receivers, P = 0.034). The probiotics could protect from diminishing of the microbiota diversity and richness. Moreover, the gut mucosal microbiota of the probiotic‐receivers had significantly more beneficial bacteria like Eubacterium ramulus ( P < 0.05), Pediococcus pentosaceus ( P < 0.05), Bacteroides fragilis ( P = 0.02) and Weissella cibaria ( P = 0.04). Additionally, the relative abundances of the beneficial bacteria correlated significantly but negatively with the UCDAI score, suggesting that the probiotics might alleviate UC symptoms by modulating the gut mucosal microbiota. Our research has provided new insights into the mechanism of symptom alleviation in UC by applying probiotic‐based adjunctive treatment.

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          Most cited references31

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          A review of activity indices and efficacy end points for clinical trials of medical therapy in adults with ulcerative colitis.

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            The ribosomal database project (RDP-II): introducing myRDP space and quality controlled public data

            Substantial new features have been implemented at the Ribosomal Database Project in response to the increased importance of high-throughput rRNA sequence analysis in microbial ecology and related disciplines. The most important changes include quality analysis, including chimera detection, for all available rRNA sequences and the introduction of myRDP Space, a new web component designed to help researchers place their own data in context with the RDP's data. In addition, new video tutorials describe how to use RDP features. Details about RDP data and analytical functions can be found at the RDP-II website ().
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              Structural Remodeling of the Human Colonic Mesenchyme in Inflammatory Bowel Disease

              Summary Intestinal mesenchymal cells play essential roles in epithelial homeostasis, matrix remodeling, immunity, and inflammation. But the extent of heterogeneity within the colonic mesenchyme in these processes remains unknown. Using unbiased single-cell profiling of over 16,500 colonic mesenchymal cells, we reveal four subsets of fibroblasts expressing divergent transcriptional regulators and functional pathways, in addition to pericytes and myofibroblasts. We identified a niche population located in proximity to epithelial crypts expressing SOX6, F3 (CD142), and WNT genes essential for colonic epithelial stem cell function. In colitis, we observed dysregulation of this niche and emergence of an activated mesenchymal population. This subset expressed TNF superfamily member 14 (TNFSF14), fibroblastic reticular cell-associated genes, IL-33, and Lysyl oxidases. Further, it induced factors that impaired epithelial proliferation and maturation and contributed to oxidative stress and disease severity in vivo. Our work defines how the colonic mesenchyme remodels to fuel inflammation and barrier dysfunction in IBD.
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                Author and article information

                Contributors
                doctorzxf@126.com
                hepingdd@vip.sina.com
                Journal
                Microb Biotechnol
                Microb Biotechnol
                10.1111/(ISSN)1751-7915
                MBT2
                Microbial Biotechnology
                John Wiley and Sons Inc. (Hoboken )
                1751-7915
                23 September 2020
                November 2020
                : 13
                : 6 ( doiID: 10.1111/mbt2.v13.6 )
                : 2032-2043
                Affiliations
                [ 1 ] The Affiliated Hospital of Inner Mongolia Medical University Hohhot 010050 China
                [ 2 ] Key Laboratory of Dairy Biotechnology and Engineering, Ministry of Education P. R. C. Key Laboratory of Dairy Products Processing Ministry of Agriculture and Rural Affairs P. R. C. Inner Mongolia Agricultural University Hohhot 010018 China
                [ 3 ] China‐Japan Friendship Hospital Beijing 100029 China
                Author notes
                [*] [* ] For correspondence. *E‐mail doctorzxf@ 123456126.com ; Tel. +86‐15901102199; Fax +86‐15901102199. **E‐mail hepingdd@ 123456vip.sina.com ; Tel. 86‐0471‐4319940; Fax 86‐0471‐4305357.

                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0002-1966-4398
                Article
                MBT213661
                10.1111/1751-7915.13661
                7533322
                32969200
                003752ea-a2db-43d9-9a27-8cb7230b8521
                © 2020 The Authors. Microbial Biotechnology published by Society for Applied Microbiology and John Wiley & Sons Ltd

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 23 April 2020
                : 07 August 2020
                : 17 August 2020
                Page count
                Figures: 5, Tables: 3, Pages: 12, Words: 7353
                Funding
                Funded by: National Natural Science Foundation of China , open-funder-registry 10.13039/501100001809;
                Award ID: 31720103911
                Funded by: Inner Mongolia Science & Technology Major Projects
                Award ID: ZDZX2018018
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                November 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.9.1 mode:remove_FC converted:05.10.2020

                Biotechnology
                Biotechnology

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