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      A complex human gut microbiome cultured in an anaerobic intestine-on-a-chip

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          Abstract

          The diverse bacterial populations that comprise the commensal microbiome of the human intestine play a central role in health and disease. A method that sustains complex microbial communities in direct contact with living human intestinal cells and their overlying mucus layer in vitro would thus enable investigations of host–microbiome interactions. Here, we show the extended co-culture of living human intestinal epithelium with stable communities of aerobic and anaerobic human gut microbiota, enabled by a microfluidic intestine-on-a-chip that permits the control and real-time assessment of physiologically relevant oxygen gradients. When compared to aerobic co-culture conditions, the establishment of a transluminal hypoxia gradient in the chip increased intestinal barrier function and sustained a physiologically relevant level of microbial diversity, consisting of over 200 unique operational taxonomic units from 11 different genera, and of an abundance of obligate anaerobic bacteria with ratios of Firmicutes and Bacteroidetes similar to those observed in human faeces. The intestine-on-a-chip may serve as a discovery tool for the development of microbiome-related therapeutics, probiotics and nutraceuticals.

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          Most cited references39

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          Organoids as an in vitro model of human development and disease.

          The in vitro organoid model is a major technological breakthrough that has already been established as an essential tool in many basic biology and clinical applications. This near-physiological 3D model facilitates an accurate study of a range of in vivo biological processes including tissue renewal, stem cell/niche functions and tissue responses to drugs, mutation or damage. In this Review, we discuss the current achievements, challenges and potential applications of this technique.
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            Is Open Access

            Akkermansia muciniphila inversely correlates with the onset of inflammation, altered adipose tissue metabolism and metabolic disorders during obesity in mice

            Recent evidence indicates that the gut microbiota plays a key role in the pathophysiology of obesity. Indeed, diet-induced obesity (DIO) has been associated to substantial changes in gut microbiota composition in rodent models. In the context of obesity, enhanced adiposity is accompanied by low-grade inflammation of this tissue but the exact link with gut microbial community remains unknown. In this report, we studied the consequences of high-fat diet (HFD) administration on metabolic parameters and gut microbiota composition over different periods of time. We found that Akkermansia muciniphila abundance was strongly and negatively affected by age and HFD feeding and to a lower extend Bilophila wadsworthia was the only taxa following an opposite trend. Different approaches, including multifactorial analysis, showed that these changes in Akkermansia muciniphila were robustly correlated with the expression of lipid metabolism and inflammation markers in adipose tissue, as well as several circulating parameters (i.e., glucose, insulin, triglycerides, leptin) from DIO mice. Thus, our data shows the existence of a link between gut Akkermansia muciniphila abundance and adipose tissue homeostasis on the onset of obesity, thus reinforcing the beneficial role of this bacterium on metabolism.
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              Correlation between intraluminal oxygen gradient and radial partitioning of intestinal microbiota.

              The gut microbiota is a complex and densely populated community in a dynamic environment determined by host physiology. We investigated how intestinal oxygen levels affect the composition of the fecal and mucosally adherent microbiota. We used the phosphorescence quenching method and a specially designed intraluminal oxygen probe to dynamically quantify gut luminal oxygen levels in mice. 16S ribosomal RNA gene sequencing was used to characterize the microbiota in intestines of mice exposed to hyperbaric oxygen, human rectal biopsy and mucosal swab samples, and paired human stool samples. Average Po2 values in the lumen of the cecum were extremely low (<1 mm Hg). In altering oxygenation of mouse intestines, we observed that oxygen diffused from intestinal tissue and established a radial gradient that extended from the tissue interface into the lumen. Increasing tissue oxygenation with hyperbaric oxygen altered the composition of the gut microbiota in mice. In human beings, 16S ribosomal RNA gene analyses showed an increased proportion of oxygen-tolerant organisms of the Proteobacteria and Actinobacteria phyla associated with rectal mucosa, compared with feces. A consortium of asaccharolytic bacteria of the Firmicute and Bacteroidetes phyla, which primarily metabolize peptones and amino acids, was associated primarily with mucus. This could be owing to the presence of proteinaceous substrates provided by mucus and the shedding of the intestinal epithelium. In an analysis of intestinal microbiota of mice and human beings, we observed a radial gradient of microbes linked to the distribution of oxygen and nutrients provided by host tissue. Copyright © 2014 AGA Institute. Published by Elsevier Inc. All rights reserved.
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                Author and article information

                Journal
                101696896
                45929
                Nat Biomed Eng
                Nat Biomed Eng
                Nature biomedical engineering
                2157-846X
                28 May 2019
                13 May 2019
                July 2019
                13 November 2019
                : 3
                : 7
                : 520-531
                Affiliations
                [1 ]Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA
                [2 ]Department of Bioengineering and iBB - Institute for Bioengineering and Biosciences, Instituto Superior Técnico, Universidade de Lisboa, Lisboa, Portugal
                [3 ]Department of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, USA
                [4 ]Graduate Program, Department of Health Sciences and Technology, ETH Zurich, 8092 Zurich, Switzerland
                [5 ]Department of Pediatric Newborn Medicine, Brigham and Women’s Hospital, 75 Francis Street, Boston, MA 02115, USA
                [6 ]Division of Endocrinology, Boston Children’s Hospital, Boston, MA 02115, USA
                [7 ]Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA
                [8 ]Harvard Stem Cell Institute, Harvard University, Boston, MA 02139, USA
                [9 ]Vascular Biology Program and Department of Surgery, Boston Children’s Hospital and Harvard Medical School, Boston, MA 02115, USA
                [10 ]Harvard John A. Paulson School of Engineering and Applied Sciences, Cambridge, MA 02139, USA
                Author notes
                [* ]Corresponding author, don.ingber@ 123456wyss.harvard.edu
                [&]

                These authors contributed equally

                Author contributions

                S.J-F., E.L.C., F.S.G, J.M.S.C., R.N. and D.E.I. designed the research. S.J-F, E.L.C., F.S.G., B.N., C.F., A.T., A.B., B.S., and M.C. performed experiments. S.J-F., D.M.C, E.L.C., F.S.G, B.N., D.L.K., R.N. and D.E.I. analysed and interpreted the data. K.E.G helped in preparation of infant microbiota. D.T.B established and prepared human ileal organoids. S.J-F, F.S.G, E.L.C, D.M.C., and D.E.I wrote the paper with input from B.N., O.L., J.M.S.C., and R.N.. All authors reviewed, discussed and edited the manuscript.

                Article
                NIHMS1526407
                10.1038/s41551-019-0397-0
                6658209
                31086325
                d0bb0180-514f-424b-93a4-aebc02cae80e

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