Metagenomic and metabolomic analyses unveil dysbiosis of gut microbiota in chronic heart failure patients

被引:365
作者
Cui, Xiao [1 ,2 ]
Ye, Lei [3 ]
Li, Jing [4 ]
Jin, Ling [1 ,2 ]
Wang, Wenjie [1 ,2 ]
Li, Shuangyue [1 ,2 ]
Bao, Minghui [4 ]
Wu, Shouling [5 ]
Li, Lifeng [3 ]
Geng, Bin [1 ,2 ]
Zhou, Xin [6 ]
Zhang, Jian [1 ,2 ]
Cai, Jun [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Natl Ctr Cardiovasc Dis, State Key Lab Cardiovasc Dis, Fuwai Hosp, Beijing 100037, Peoples R China
[2] Peking Union Med Coll, Beijing 100037, Peoples R China
[3] Novogene Bioinformat Inst, Beijing 100000, Peoples R China
[4] Capital Med Univ, Beijing Chao Yang Hosp, Dept Cardiol, Beijing 100020, Peoples R China
[5] Hebei Union Univ, Kailuan Gen Hosp, Dept Cardiol, Tangshan 063000, Peoples R China
[6] Pingjin Hosp, Tianjin Key Lab Cardiovasc Remodeling & Target Org, Heart Ctr, Tianjin 300162, Peoples R China
基金
中国国家自然科学基金;
关键词
TRIMETHYLAMINE-N-OXIDE; FECAL MICROBIOTA; CONTRIBUTES; HEALTH; ACID; EPIDEMIOLOGY; INFLAMMATION; DIVERSITY; MORTALITY; IMMUNITY;
D O I
10.1038/s41598-017-18756-2
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
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Previous studies suggested a possible gut microbiota dysbiosis in chronic heart failure (CHF). However, direct evidence was lacking. In this study, we investigated the composition and metabolic patterns of gut microbiota in CHF patients to provide direct evidence and comprehensive understanding of gut microbiota dysbiosis in CHF. We enrolled 53 CHF patients and 41 controls. Metagenomic analyses of faecal samples and metabolomic analyses of faecal and plasma samples were then performed. We found that the composition of gut microbiota in CHF was significantly different from controls. Faecalibacterium prausnitzii decrease and Ruminococcus gnavus increase were the essential characteristics in CHF patients' gut microbiota. We also observed an imbalance of gut microbes involved in the metabolism of protective metabolites such as butyrate and harmful metabolites such as trimethylamine N-oxide in CHF patients. Metabolic features of both faecal and plasma samples from CHF patients also significantly changed. Moreover, alterations in faecal and plasma metabolic patterns correlated with gut microbiota dysbiosis in CHF. Taken together, we found that CHF was associated with distinct gut microbiota dysbiosis and pinpointed the specific core bacteria imbalance in CHF, along with correlations between changes in certain metabolites and gut microbes.
引用
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页数:15
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