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dc.contributor.authorLowe, Patrick
dc.contributor.authorGyongyosi, Benedek
dc.contributor.authorWard, Doyle V.
dc.contributor.authorSzabo, Gyongyi
dc.date2022-08-11T08:09:19.000
dc.date.accessioned2022-08-23T16:26:34Z
dc.date.available2022-08-23T16:26:34Z
dc.date.issued2017-05-26
dc.date.submitted2017-07-20
dc.identifier.citationGut. 2017 May 26. pii: gutjnl-2016-313432. doi: 10.1136/gutjnl-2016-313432. <a href="https://doi.org/10.1136/gutjnl-2016-313432">Link to article on publisher's site</a>
dc.identifier.issn0017-5749 (Linking)
dc.identifier.doi10.1136/gutjnl-2016-313432
dc.identifier.pmid28550049
dc.identifier.urihttp://hdl.handle.net/20.500.14038/36591
dc.description<p>Full author list omitted for brevity. For the full list of authors, see article.</p>
dc.description.abstractOBJECTIVE: Alcoholic liver disease (ALD) is a global health problem with limited therapeutic options. Intestinal barrier integrity and the microbiota modulate susceptibility to ALD. Akkermansia muciniphila, a Gram-negative intestinal commensal, promotes barrier function partly by enhancing mucus production. The aim of this study was to investigate microbial alterations in ALD and to define the impact of A. muciniphila administration on the course of ALD. DESIGN: The intestinal microbiota was analysed in an unbiased approach by 16S ribosomal DNA (rDNA) sequencing in a Lieber-DeCarli ALD mouse model, and faecal A. muciniphila abundance was determined in a cohort of patients with alcoholic steatohepatitis (ASH). The impact of A. muciniphila on the development of experimental acute and chronic ALD was determined in a preventive and therapeutic setting, and intestinal barrier integrity was analysed. RESULTS: Patients with ASH exhibited a decreased abundance of faecal A. muciniphila when compared with healthy controls that indirectly correlated with hepatic disease severity. Ethanol feeding of wild-type mice resulted in a prominent decline in A. muciniphila abundance. Ethanol-induced intestinal A. muciniphila depletion could be restored by oral A. muciniphila supplementation. Furthermore, A. muciniphila administration when performed in a preventive setting decreased hepatic injury, steatosis and neutrophil infiltration. A. muciniphila also protected against ethanol-induced gut leakiness, enhanced mucus thickness and tight-junction expression. In already established ALD, A. muciniphila used therapeutically ameliorated hepatic injury and neutrophil infiltration. CONCLUSION: Ethanol exposure diminishes intestinal A. muciniphila abundance in both mice and humans and can be recovered in experimental ALD by oral supplementation. A. muciniphila promotes intestinal barrier integrity and ameliorates experimental ALD. Our data suggest that patients with ALD might benefit from A. muciniphila supplementation.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=28550049&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttps://doi.org/10.1136/gutjnl-2016-313432
dc.subjectAkkermansia muciniphila
dc.subjectalcoholic liver disease
dc.subjectalcoholic steatohepatitis
dc.subjectgut barrier
dc.subjectintestinal microbiota
dc.subjectBiochemistry
dc.subjectCell Biology
dc.subjectCellular and Molecular Physiology
dc.subjectGastroenterology
dc.subjectMolecular Biology
dc.titleRecovery of ethanol-induced Akkermansia muciniphila depletion ameliorates alcoholic liver disease
dc.typeJournal Article
dc.source.journaltitleGut
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/metnet_pubs/111
dc.identifier.contextkey10458198
html.description.abstract<p>OBJECTIVE: Alcoholic liver disease (ALD) is a global health problem with limited therapeutic options. Intestinal barrier integrity and the microbiota modulate susceptibility to ALD. Akkermansia muciniphila, a Gram-negative intestinal commensal, promotes barrier function partly by enhancing mucus production. The aim of this study was to investigate microbial alterations in ALD and to define the impact of A. muciniphila administration on the course of ALD.</p> <p>DESIGN: The intestinal microbiota was analysed in an unbiased approach by 16S ribosomal DNA (rDNA) sequencing in a Lieber-DeCarli ALD mouse model, and faecal A. muciniphila abundance was determined in a cohort of patients with alcoholic steatohepatitis (ASH). The impact of A. muciniphila on the development of experimental acute and chronic ALD was determined in a preventive and therapeutic setting, and intestinal barrier integrity was analysed.</p> <p>RESULTS: Patients with ASH exhibited a decreased abundance of faecal A. muciniphila when compared with healthy controls that indirectly correlated with hepatic disease severity. Ethanol feeding of wild-type mice resulted in a prominent decline in A. muciniphila abundance. Ethanol-induced intestinal A. muciniphila depletion could be restored by oral A. muciniphila supplementation. Furthermore, A. muciniphila administration when performed in a preventive setting decreased hepatic injury, steatosis and neutrophil infiltration. A. muciniphila also protected against ethanol-induced gut leakiness, enhanced mucus thickness and tight-junction expression. In already established ALD, A. muciniphila used therapeutically ameliorated hepatic injury and neutrophil infiltration.</p> <p>CONCLUSION: Ethanol exposure diminishes intestinal A. muciniphila abundance in both mice and humans and can be recovered in experimental ALD by oral supplementation. A. muciniphila promotes intestinal barrier integrity and ameliorates experimental ALD. Our data suggest that patients with ALD might benefit from A. muciniphila supplementation.</p>
dc.identifier.submissionpathmetnet_pubs/111
dc.contributor.departmentUMass Metabolic Network
dc.contributor.departmentDepartment of Microbiology and Physiological Systems
dc.contributor.departmentCenter for Microbiome Research
dc.contributor.departmentDepartment of Medicine, Division of Gastroenterology


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