The Severity of Nonalcoholic Fatty Liver Disease Is Associated With Gut Dysbiosis and Shift in the Metabolic Function of the Gut Microbiota

被引:1187
作者
Boursier, Jerome [1 ,2 ]
Mueller, Olaf [3 ]
Barret, Matthieu [4 ]
Machado, Mariana [5 ]
Fizanne, Lionel [2 ]
Araujo-Perez, Felix [6 ]
Guy, Cynthia D. [7 ]
Seed, Patrick C. [3 ,6 ]
Rawls, John F. [3 ]
David, Lawrence A. [3 ]
Hunault, Gilles [2 ]
Oberti, Frederic [1 ,2 ]
Cales, Paul [1 ,2 ]
Diehl, Anna Mae [5 ]
机构
[1] Univ Hosp, Hepatogastroenterol Dept, Angers, France
[2] LUNAM Univ, SFR 4208, UPRES 3859, HIFIH Lab, Angers, France
[3] Duke Univ, Med Ctr, Ctr Genom Microbial Syst, Dept Mol Genet & Microbiol, Durham, NC USA
[4] INRA, Inst Rech Hort & Semences UMR1345, QUA SAV SFR4207, Beaucouze, France
[5] Duke Univ, Med Ctr, Dept Med, Div Gastroenterol, Durham, NC 27710 USA
[6] Duke Univ, Med Ctr, Dept Pediat, Durham, NC 27710 USA
[7] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
基金
美国国家卫生研究院;
关键词
INTESTINAL MICROBIOTA; STEATOHEPATITIS; DIET; FIBROSIS; OBESITY; ACID; MICE; METAANALYSIS; DEGRADATION; CONTRIBUTES;
D O I
10.1002/hep.28356
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Several animal studies have emphasized the role of gut microbiota in nonalcoholic fatty liver disease (NAFLD). However, data about gut dysbiosis in human NAFLD remain scarce in the literature, especially studies including the whole spectrum of NAFLD lesions. We aimed to evaluate the association between gut dysbiosis and severe NAFLD lesions, that is, nonalcoholic steatohepatitis (NASH) and fibrosis, in a well-characterized population of adult NAFLD. Fifty-seven patients with biopsy-proven NAFLD were enrolled. Taxonomic composition of gut microbiota was determined using 16S ribosomal RNA gene sequencing of stool samples. Thirty patients had F0/F1 fibrosis stage at liver biopsy (10 with NASH), and 27 patients had significant F >= 2 fibrosis (25 with NASH). Bacteroides abundance was significantly increased in NASH and F >= 2 patients, whereas Prevotella abundance was decreased. Ruminococcus abundance was significantly higher in F >= 2 patients. By multivariate analysis, Bacteroides abundance was independently associated with NASH and Ruminococcus with F >= 2 fibrosis. Stratification according to the abundance of these two bacteria generated three patient subgroups with increasing severity of NAFLD lesions. Based on imputed metagenomic profiles, Kyoto Encyclopedia of Genes and Genomes pathways significantly related to NASH and fibrosis F >= 2 were mostly related to carbohydrate, lipid, and amino acid metabolism. Conclusion: NAFLD severity associates with gut dysbiosis and a shift in metabolic function of the gut microbiota. We identified Bacteroides as independently associated with NASH and Ruminococcus with significant fibrosis. Thus, gut microbiota analysis adds information to classical predictors of NAFLD severity and suggests novel metabolic targets for pre-/probiotics therapies.
引用
收藏
页码:764 / 775
页数:12
相关论文
共 51 条
[31]   A metagenome-wide association study of gut microbiota in type 2 diabetes [J].
Qin, Junjie ;
Li, Yingrui ;
Cai, Zhiming ;
Li, Shenghui ;
Zhu, Jianfeng ;
Zhang, Fan ;
Liang, Suisha ;
Zhang, Wenwei ;
Guan, Yuanlin ;
Shen, Dongqian ;
Peng, Yangqing ;
Zhang, Dongya ;
Jie, Zhuye ;
Wu, Wenxian ;
Qin, Youwen ;
Xue, Wenbin ;
Li, Junhua ;
Han, Lingchuan ;
Lu, Donghui ;
Wu, Peixian ;
Dai, Yali ;
Sun, Xiaojuan ;
Li, Zesong ;
Tang, Aifa ;
Zhong, Shilong ;
Li, Xiaoping ;
Chen, Weineng ;
Xu, Ran ;
Wang, Mingbang ;
Feng, Qiang ;
Gong, Meihua ;
Yu, Jing ;
Zhang, Yanyan ;
Zhang, Ming ;
Hansen, Torben ;
Sanchez, Gaston ;
Raes, Jeroen ;
Falony, Gwen ;
Okuda, Shujiro ;
Almeida, Mathieu ;
LeChatelier, Emmanuelle ;
Renault, Pierre ;
Pons, Nicolas ;
Batto, Jean-Michel ;
Zhang, Zhaoxi ;
Chen, Hua ;
Yang, Ruifu ;
Zheng, Weimou ;
Li, Songgang ;
Yang, Huanming .
NATURE, 2012, 490 (7418) :55-60
[32]  
Sanyal Arun J, 2011, Hepatology, V54, P344, DOI 10.1002/hep.24376
[33]   Key questions to guide a better understanding of host-commensal microbiota interactions in intestinal inflammation [J].
Sartor, R. B. .
MUCOSAL IMMUNOLOGY, 2011, 4 (02) :127-132
[34]   Interactions Between the Intestinal Microbiome and Liver Diseases [J].
Schnabl, Bernd ;
Brenner, David A. .
GASTROENTEROLOGY, 2014, 146 (06) :1513-1524
[35]   Manipulating the gut microbiota to maintain health and treat disease [J].
Scott, Karen P. ;
Antoine, Jean-Michel ;
Midtvedt, Tore ;
van Hemert, Saskia .
MICROBIAL ECOLOGY IN HEALTH AND DISEASE, 2015, 26
[36]   Metagenomic biomarker discovery and explanation [J].
Segata, Nicola ;
Izard, Jacques ;
Waldron, Levi ;
Gevers, Dirk ;
Miropolsky, Larisa ;
Garrett, Wendy S. ;
Huttenhower, Curtis .
GENOME BIOLOGY, 2011, 12 (06)
[37]   Fibrosis Progression in Nonalcoholic Fatty Liver vs Nonalcoholic Steatohepatitis: A Systematic Review and Meta-analysis of Paired-Biopsy Studies [J].
Singh, Siddharth ;
Allen, Alina M. ;
Wang, Zhen ;
Prokop, Larry J. ;
Murad, Mohammad H. ;
Loomba, Rohit .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2015, 13 (04) :643-+
[38]   Meta-Analysis of the Influence of I148M Variant of Patatin-Like Phospholipase Domain Containing 3 Gene (PNPLA3) on the Susceptibility and Histological Severity of Nonalcoholic Fatty Liver Disease [J].
Sookoian, Silvia ;
Pirola, Carlos J. .
HEPATOLOGY, 2011, 53 (06) :1883-1894
[39]   An obesity-associated gut microbiome with increased capacity for energy harvest [J].
Turnbaugh, Peter J. ;
Ley, Ruth E. ;
Mahowald, Michael A. ;
Magrini, Vincent ;
Mardis, Elaine R. ;
Gordon, Jeffrey I. .
NATURE, 2006, 444 (7122) :1027-1031
[40]   A core gut microbiome in obese and lean twins [J].
Turnbaugh, Peter J. ;
Hamady, Micah ;
Yatsunenko, Tanya ;
Cantarel, Brandi L. ;
Duncan, Alexis ;
Ley, Ruth E. ;
Sogin, Mitchell L. ;
Jones, William J. ;
Roe, Bruce A. ;
Affourtit, Jason P. ;
Egholm, Michael ;
Henrissat, Bernard ;
Heath, Andrew C. ;
Knight, Rob ;
Gordon, Jeffrey I. .
NATURE, 2009, 457 (7228) :480-U7