Cholestasis induced by bile duct ligation promotes changes in the intestinal microbiome in mice

被引:43
作者
Cabrera-Rubio, Raul [1 ,2 ]
Patterson, Angela M. [3 ]
Cotter, Paul D. [1 ,2 ]
Beraza, Naiara [3 ]
机构
[1] TEAGASC, Food Res Ctr, Moorepk, Fermoy, Cork, Ireland
[2] Univ Coll Cork, APC Microbiome Inst, Cork, Ireland
[3] Norwich Res Pk, Gut Microbes & Hlth Inst Strateg Programme, Quadram Inst, Norwich, Norfolk, England
基金
英国生物技术与生命科学研究理事会;
关键词
PRIMARY SCLEROSING CHOLANGITIS; GUT MICROBIOTA; BACTERIAL TRANSLOCATION; FAECALIBACTERIUM-PRAUSNITZII; AKKERMANSIA-MUCINIPHILA; LIVER-DISEASE; COMMUNITIES; DYSBIOSIS; DISCOVERY; MUCIN-2;
D O I
10.1038/s41598-019-48784-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Increasing evidence point to the relevance of intestinal disfunction and changes in the microbiome composition during chronic liver disease. More specifically, recent studies have highlighted that cholestatic diseases associate with a reduction in the microbiome diversity in patients. Still, the dynamics of the changes in the microbiome composition observed, as well as their implication in contributing to the pathogenesis of this disease remain largely undefined. Hence, experimental mouse models resembling the human pathogenesis are crucial to move forward our understanding on the mechanisms underpinning cholestatic disease and to enable the development of effective therapeutics. Our results show that the bile duct ligation (BDL) experimental model of cholestasis leads to rapid and significant changes in the microbiome diversity, with more than 100 OTUs being significantly different in faecal samples obtained from WT mice at 3 days and 7 days after BDL when compared to control animals. Changes in the microbial composition in mice after BDL included the enrichment of Akkermansia, Prevotella, Bacteroides and unclassified Ruminococcaceae in parallel with a drastic reduction of the presence of Faecalibacterium prausnitzii. In conclusion, our results support that bile duct ligation induces changes in the microbiome that partly resemble the gut microbial changes observed during human cholestatic disease.
引用
收藏
页数:10
相关论文
共 67 条
[1]   A Re-Evaluation of the Risk Factors for the Recurrence of Primary Sclerosing Cholangitis in Liver Allografts [J].
Alabraba, Edward ;
Nightingale, Peter ;
Gunson, Bridget ;
Hubscher, Stefan ;
Olliff, Simon ;
Mirza, Darius ;
Neuberger, James .
LIVER TRANSPLANTATION, 2009, 15 (03) :330-340
[2]   Gut microbiota, tight junction protein expression, intestinal resistance, bacterial translocation and mortality following cholestasis depend on the genetic background of the host [J].
Alaish, Samuel M. ;
Smith, Alexis D. ;
Timmons, Jennifer ;
Greenspon, Jose ;
Eyvazzadeh, Daniel ;
Murphy, Ebony ;
Shea-Donahue, Terez ;
Cirimotich, Shana ;
Mongodin, Emmanuel ;
Zhao, Aiping ;
Fasano, Alessio ;
Nataro, James P. ;
Cross, Alan .
GUT MICROBES, 2013, 4 (04) :292-305
[3]  
Aronesty E., 2013, OPEN BIOINFORMATICS, V7, P1, DOI [10.2174/1875036201307010001, DOI 10.2174/1875036201307010001]
[4]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[5]   New paradigms in the treatment of hepatic cholestasis: From UDCA to FXR, PXR and beyond [J].
Beuers, Ulrich ;
Trauner, Michael ;
Jansen, Peter ;
Poupon, Raoul .
JOURNAL OF HEPATOLOGY, 2015, 62 :S25-S37
[6]   Fine-Tuning of Sirtuin 1 Expression Is Essential to Protect the Liver From Cholestatic Liver Disease [J].
Blokker, Britt A. ;
Maijo, Monica ;
Echeandia, Marta ;
Galduroz, Mikel ;
Patterson, Angela M. ;
Ten, Anna ;
Philo, Mark ;
Schungel, Rebecca ;
Gutierrez-de Juan, Virginia ;
Halilbasic, Emina ;
Fuchs, Claudia ;
Le Gall, Gwenaelle ;
Milkiewicz, Malgorzata ;
Milkiewicz, Piotr ;
Banales, Jesus M. ;
Rushbrook, Simon M. ;
Mato, Jose M. ;
Trauner, Michael ;
Mueller, Michael ;
Luz Martinez-Chantar, Maria ;
Varela-Rey, Marta ;
Beraza, Naiara .
HEPATOLOGY, 2019, 69 (02) :699-716
[7]   The Severity of Nonalcoholic Fatty Liver Disease Is Associated With Gut Dysbiosis and Shift in the Metabolic Function of the Gut Microbiota [J].
Boursier, Jerome ;
Mueller, Olaf ;
Barret, Matthieu ;
Machado, Mariana ;
Fizanne, Lionel ;
Araujo-Perez, Felix ;
Guy, Cynthia D. ;
Seed, Patrick C. ;
Rawls, John F. ;
David, Lawrence A. ;
Hunault, Gilles ;
Oberti, Frederic ;
Cales, Paul ;
Diehl, Anna Mae .
HEPATOLOGY, 2016, 63 (03) :764-775
[8]   The gut microbiome as a target for prevention and treatment of hyperglycaemia in type 2 diabetes: from current human evidence to future possibilities [J].
Brunkwall, Louise ;
Orho-Melander, Marju .
DIABETOLOGIA, 2017, 60 (06) :943-951
[9]   The epigenetic effects of butyrate: potential therapeutic implications for clinical practice [J].
Canani, Roberto Berni ;
Di Costanzo, Margherita ;
Leone, Ludovica .
CLINICAL EPIGENETICS, 2012, 4
[10]   A gut microbiome signature for cirrhosis due to nonalcoholic fatty liver disease [J].
Caussy, Cyrielle ;
Tripathi, Anupriya ;
Humphrey, Greg ;
Bassirian, Shirin ;
Singh, Seema ;
Faulkner, Claire ;
Bettencourt, Ricki ;
Rizo, Emily ;
Richards, Lisa ;
Xu, Zhenjiang Z. ;
Downes, Michael R. ;
Evans, Ronald M. ;
Brenner, David A. ;
Sirlin, Claude B. ;
Knight, Rob ;
Loomba, Rohit .
NATURE COMMUNICATIONS, 2019, 10 (1)