Altered synthesis of genes associated with short-chain fatty acids in the gut of patients with atrial fibrillation

被引:41
作者
Zhang, Jing
Zuo, Kun
Fang, Chen
Yin, Xiandong
Liu, Xiaoqing
Zhong, Jiuchang
Li, Kuibao
Li, Jing
Xu, Li [1 ]
Yang, Xinchun [1 ]
机构
[1] Capital Med Univ, Beijing Chaoyang Hosp, Heart Ctr, 8th Gongtinanlu Rd, Beijing 100020, Peoples R China
基金
中国国家自然科学基金;
关键词
Atrial Fibrillation; Short-chain fatty acids; Gut microbiota; Metagenomics; DISEASE;
D O I
10.1186/s12864-021-07944-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background The gut microbiota provides health benefits in humans by producing short-chain fatty acids (SCFAs), whose deficiency causes multiple disorders and inflammatory diseases. However, gut bacteria producing SCFAs in patients with atrial fibrillation (AF), an arrhythmia with increasing prevalence, have not been reported. To investigate major gut microbial organisms related to SCFA synthesis, SCFAs-associated KEGG orthologues (KOs), enzymatic genes, and potential producers were examined according to metagenomic data-mining in a northern Chinese cohort comprising 50 non-AF control and 50 AF patients. Results Compared with non-AF controls, individuals with AF had marked differences in microbial genes involved in SCFA-related synthesis, including 125 KOs and 5 SCFAs-related enzymatic genes. Furthermore, there were 10 species that harbored SCFA-synthesis related enzymatic genes, and were markedly decreased in the gut of AF patients. Notably, discriminative features about SCFA-synthesis related function, including 8 KOs (K01752, K01738, K00175, K03737, K01006, K01653, K01647 and K15023), 4 genes (menI, tesB, yciA and CO dehydrogenase acetyl-CoA synthase complex) and 2 species (Coprococcus catus and Firmicutes bacterium CAG:103), were selected as key factors based on LASSO analysis. Furthermore, PLS-SEM analysis showed that 72.8 and 91.14 % of the overall effects on gut microbiota diversity and key species on AF, respectively, were mediated by the key KOs. Meanwhile, 46.31 % of the total effects of SCFA-synthesis related function on left atrial enlargement was mediated by hsCRP. Upon incorporation of clinical properties in AF, the KO score was still significantly associated with AF incidence (OR = 0.004, P = 0.001). Conclusions The current study revealed that dysbiotic gut microbiota in AF is coupled with disrupted SCFA-synthesis related genes, characterized by decreased abundances of KEGG orthologues, synthesis enzymatic genes and harboring species.
引用
收藏
页数:11
相关论文
共 36 条
[1]   Therapeutic microbes to tackle disease [J].
Ainsworth, Claire .
NATURE, 2020, 577 (7792) :S20-S22
[2]   Short-Chain Fatty Acid Propionate Protects From Hypertensive Cardiovascular Damage [J].
Bartolomaeus, Hendrik ;
Balogh, Andras ;
Yakoub, Mina ;
Homann, Susanne ;
Marko, Lajos ;
Hoeges, Sascha ;
Tsvetkov, Dmitry ;
Krannich, Alexander ;
Wundersitz, Sebastian ;
Avery, Ellen G. ;
Haase, Nadine ;
Kraeker, Kristin ;
Hering, Lydia ;
Maase, Martina ;
Kusche-Vihrog, Kristina ;
Grandoch, Maria ;
Fielitz, Jens ;
Kempa, Stefan ;
Gollasch, Maik ;
Zhumadilov, Zhaxybay ;
Kozhakhmetov, Samat ;
Kushugulova, Almagul ;
Eckardt, Kai-Uwe ;
Dechend, Ralf ;
Rump, Lars Christian ;
Forslund, Sofia K. ;
Mueller, Dominik N. ;
Stegbauer, Johannes ;
Wilck, Nicola .
CIRCULATION, 2019, 139 (11) :1407-1421
[3]   Fast and sensitive protein alignment using DIAMOND [J].
Buchfink, Benjamin ;
Xie, Chao ;
Huson, Daniel H. .
NATURE METHODS, 2015, 12 (01) :59-60
[4]  
Castella M., 2020, EUR HEART J
[5]   An engineered genetic circuit for lactose intolerance alleviation [J].
Cheng, Mingyue ;
Cheng, Zhangyu ;
Yu, Yiyan ;
Liu, Wangjie ;
Li, Ruihao ;
Guo, Zhenyi ;
Qin, Jiyue ;
Zeng, Zhi ;
Di, Lin ;
Mo, Yufeng ;
Pan, Chunxiu ;
Liang, Yuanhao ;
Li, Jinman ;
Tong, Yigang ;
Yan, Yunjun ;
Zhan, Yi ;
Ning, Kang .
BMC BIOLOGY, 2021, 19 (01) :137
[6]   SHORT CHAIN FATTY-ACIDS IN HUMAN LARGE-INTESTINE, PORTAL, HEPATIC AND VENOUS-BLOOD [J].
CUMMINGS, JH ;
POMARE, EW ;
BRANCH, WJ ;
NAYLOR, CPE ;
MACFARLANE, GT .
GUT, 1987, 28 (10) :1221-1227
[7]   Propionic Acid Shapes the Multiple Sclerosis Disease Course by an Immunomodulatory Mechanism [J].
Duscha, Alexander ;
Gisevius, Barbara ;
Hirschberg, Sarah ;
Yissachar, Nissan ;
Stangl, Gabriele, I ;
Dawin, Eva ;
Bader, Verian ;
Haase, Stefanie ;
Kaisler, Johannes ;
David, Christina ;
Schneider, Ruth ;
Troisi, Riccardo ;
Zent, Daniel ;
Hegelmaier, Tobias ;
Dokalis, Nikolaos ;
Gerstein, Sara ;
Del Mare-Roumani, Sara ;
Amidror, Sivan ;
Staszewski, Ori ;
Poschmann, Gereon ;
Stuehler, Kai ;
Hirche, Frank ;
Balogh, Andras ;
Kempa, Stefan ;
Traeger, Pascal ;
Zaiss, Mario M. ;
Holm, Jacob Bak ;
Massa, Megan G. ;
Nielsen, Henrik Bjorn ;
Faissner, Andreas ;
Lukas, Carsten ;
Gatermann, Soeren G. ;
Scholz, Markus ;
Przuntek, Horst ;
Prinz, Marco ;
Forslund, Sofia K. ;
Winklhofer, Konstanze F. ;
Mueller, Dominik N. ;
Linker, Ralf A. ;
Gold, Ralf ;
Haghikia, Aiden .
CELL, 2020, 180 (06) :1067-+
[8]   Links between diet, gut microbiota composition and gut metabolism [J].
Flint, Harry J. ;
Duncan, Sylvia H. ;
Scott, Karen P. ;
Louis, Petra .
PROCEEDINGS OF THE NUTRITION SOCIETY, 2015, 74 (01) :13-22
[9]   Microbial metabolite sensor GPR43 controls severity of experimental GVHD [J].
Fujiwara, Hideaki ;
Docampo, Melissa D. ;
Riwes, Mary ;
Peltier, Daniel ;
Toubai, Tomomi ;
Henig, Israel ;
Wu, S. Julia ;
Kim, Stephanie ;
Taylor, Austin ;
Brabbs, Stuart ;
Liu, Chen ;
Zajac, Cynthia ;
Oravecz-Wilson, Katherine ;
Sun, Yaping ;
Nunez, Gabriel ;
Levine, John E. ;
van den Brink, Marcel R. M. ;
Ferrara, James L. M. ;
Reddy, Pavan .
NATURE COMMUNICATIONS, 2018, 9
[10]   Mechanisms of disease: Acute-phase proteins and other systemic responses to inflammation [J].
Gabay, C ;
Kushner, I .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (06) :448-454