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      Gut mucosal virome alterations in ulcerative colitis

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          Abstract

          Objective

          The pathogenesis of UC relates to gut microbiota dysbiosis. We postulate that alterations in the viral community populating the intestinal mucosa play an important role in UC pathogenesis. This study aims to characterise the mucosal virome and their functions in health and UC.

          Design

          Deep metagenomics sequencing of virus-like particle preparations and bacterial 16S rRNA sequencing were performed on the rectal mucosa of 167 subjects from three different geographical regions in China (UC=91; healthy controls=76). Virome and bacteriome alterations in UC mucosa were assessed and correlated with patient metadata. We applied partition around medoids clustering algorithm and classified mucosa viral communities into two clusters, referred to as mucosal virome metacommunities 1 and 2.

          Results

          In UC, there was an expansion of mucosa viruses, particularly Caudovirales bacteriophages, and a decrease in mucosa Caudovirales diversity, richness and evenness compared with healthy controls. Altered mucosal virome correlated with intestinal inflammation. Interindividual dissimilarity between mucosal viromes was higher in UC than controls. Escherichia phage and Enterobacteria phage were more abundant in the mucosa of UC than controls. Compared with metacommunity 1, metacommunity 2 was predominated by UC subjects and displayed a significant loss of various viral species. Patients with UC showed substantial abrogation of diverse viral functions, whereas multiple viral functions, particularly functions of bacteriophages associated with host bacteria fitness and pathogenicity, were markedly enriched in UC mucosa. Intensive transkingdom correlations between mucosa viruses and bacteria were significantly depleted in UC.

          Conclusion

          We demonstrated for the first time that UC is characterised by substantial alterations of the mucosa virobiota with functional distortion. Enrichment of Caudovirales bacteriophages, increased phage/bacteria virulence functions and loss of viral-bacterial correlations in the UC mucosa highlight that mucosal virome may play an important role in UC pathogenesis.

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          Most cited references30

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          Enterotypes in the landscape of gut microbial community composition

          Population stratification is a useful approach towards a better understanding of complex biological problems in human health and well-being. The proposal that such stratification applies to the human gut microbiome, in the form of distinct community composition types, termed “enterotypes”, was met with both excitement and controversy. In view of accumulated data and re-analyses since the original work, we revisit the enterotype concept, discuss different methods of dividing up the landscape of possible microbiome configurations, and put these concepts into a functional, ecological and medical context. As enterotypes are of use in describing the gut microbial community landscape and may become relevant in clinical practice, we aim to reconcile differing views and encourage a balanced application of the concept.
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            Recapitulating adult human immune traits in laboratory mice by normalizing environment

            Our current understanding of immunology was largely defined in laboratory mice because of experimental advantages including inbred homogeneity, tools for genetic manipulation, the ability to perform kinetic tissue analyses starting with the onset of disease, and tractable models. Comparably reductionist experiments are neither technically nor ethically possible in humans. Despite revealing many fundamental principals of immunology, there is growing concern that mice fail to capture relevant aspects of the human immune system, which may account for failures to translate disease treatments from bench to bedside 1–8 . Laboratory mice live in abnormally hygienic “specific pathogen free” (SPF) barrier facilities. Here we show that the standard practice of laboratory mouse husbandry has profound effects on the immune system and that environmental changes result in better recapitulation of features of adult humans. Laboratory mice lack effector-differentiated and mucosally distributed memory T cells, which more closely resembles neonatal than adult humans. These cell populations were present in free-living barn populations of feral mice, pet store mice with diverse microbial experience, and were induced in laboratory mice after co-housing with pet store mice, suggesting a role for environment. Consequences of altering mouse housing profoundly impacted the cellular composition of the innate and adaptive immune system and resulted in global changes in blood cell gene expression patterns that more closely aligned with immune signatures of adult humans rather than neonates, altered the mouse’s resistance to infection, and impacted T cell differentiation to a de novo viral infection. These data highlight the impact of environment on the basal immune state and response to infection and suggest that restoring physiological microbial exposure in laboratory mice could provide a relevant tool for modeling immunological events in free-living organisms, including humans.
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              High-throughput clone library analysis of the mucosa-associated microbiota reveals dysbiosis and differences between inflamed and non-inflamed regions of the intestine in inflammatory bowel disease

              Background The gut microbiota is thought to play a key role in the development of the inflammatory bowel diseases Crohn's disease (CD) and ulcerative colitis (UC). Shifts in the composition of resident bacteria have been postulated to drive the chronic inflammation seen in both diseases (the "dysbiosis" hypothesis). We therefore specifically sought to compare the mucosa-associated microbiota from both inflamed and non-inflamed sites of the colon in CD and UC patients to that from non-IBD controls and to detect disease-specific profiles. Results Paired mucosal biopsies of inflamed and non-inflamed intestinal tissue from 6 CD (n = 12) and 6 UC (n = 12) patients were compared to biopsies from 5 healthy controls (n = 5) by in-depth sequencing of over 10,000 near full-length bacterial 16S rRNA genes. The results indicate that mucosal microbial diversity is reduced in IBD, particularly in CD, and that the species composition is disturbed. Firmicutes were reduced in IBD samples and there were concurrent increases in Bacteroidetes, and in CD only, Enterobacteriaceae. There were also significant differences in microbial community structure between inflamed and non-inflamed mucosal sites. However, these differences varied greatly between individuals, meaning there was no obvious bacterial signature that was positively associated with the inflamed gut. Conclusions These results may support the hypothesis that the overall dysbiosis observed in inflammatory bowel disease patients relative to non-IBD controls might to some extent be a result of the disturbed gut environment rather than the direct cause of disease. Nonetheless, the observed shifts in microbiota composition may be important factors in disease maintenance and severity.
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                Author and article information

                Journal
                Gut
                Gut
                gutjnl
                gut
                Gut
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                0017-5749
                1468-3288
                July 2019
                6 March 2019
                : 68
                : 7
                : 1169-1179
                Affiliations
                [1 ] departmentCenter for Gut Microbiota Research, Faculty of Medicine , The Chinese University of Hong Kong , Shatin, Hong Kong SAR, China
                [2 ] departmentState Key Laboratory for digestive disease, Institute of Digestive Disease, Li Ka Shing Institute of Health Science , The Chinese University of Hong Kong , Shatin, Hong Kong SAR, China
                [3 ] departmentDepartment of Medicine and Therapeutics, Faculty of Medicine , The Chinese Univetsity of Hong Kong , Shatin, Hong Kong, China
                [4 ] departmentDepartment of Gastroenterology , The General Hospital of the People’s Liberation Army , Beijing, China
                [5 ] departmentFaculty of Medicine , Zhejiang University , Hangzhou, China
                [6 ] departmentDepartment of Microbiology , The Chinese University of Hong Kong , Shatin, Hong Kong SAR, China
                [7 ] departmentDepartment of Gastroenterology, School of Medicine , Sir Run Run Shaw Hospital, Zhejiang University , Hangzhou, China
                Author notes
                [Correspondence to ] Professor Siew C Ng, Medicine and Therapeutics, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China; siewchienng@ 123456cuhk.edu.hk
                Author information
                http://orcid.org/0000-0001-9239-2416
                http://orcid.org/0000-0001-7388-2436
                http://orcid.org/0000-0002-6850-4454
                Article
                gutjnl-2018-318131
                10.1136/gutjnl-2018-318131
                6582748
                30842211
                81e0073f-0526-4c0e-aa58-41490bc346b4
                © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

                This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 17 December 2018
                : 04 February 2019
                : 15 February 2019
                Funding
                Funded by: PROCORE-France/Hong Kong Joint Research Scheme;
                Funded by: ANR/RGC Joint Research Scheme;
                Funded by: FundRef http://dx.doi.org/10.13039/100007028, Leona M. and Harry B. Helmsley Charitable Trust;
                Funded by: a seed fund for Gut Microbiome Research Microbiota Research Center, Faculty of Medicine (The Chinese University of Hong Kong).;
                Categories
                Gut Microbiota
                1506
                2312
                Original article
                Custom metadata
                unlocked

                Gastroenterology & Hepatology
                gut mucosa,virome,bacteria,virome metacommunity,ulcerative colitis
                Gastroenterology & Hepatology
                gut mucosa, virome, bacteria, virome metacommunity, ulcerative colitis

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