Pathways and functions of gut microbiota metabolism impacting host physiology

被引:154
作者
Krishnan, Smitha [1 ]
Alden, Nicholas [1 ]
Lee, Kyongbum [1 ]
机构
[1] Tufts Univ, Dept Chem & Biol Engn, Medford, MA 02155 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
ARYL-HYDROCARBON RECEPTOR; CHAIN FATTY-ACIDS; BACTERIA; REVEALS; CATALOG; OBESITY;
D O I
10.1016/j.copbio.2015.08.015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The bacterial populations in the human intestine impact host physiological functions through their metabolic activity. In addition to performing essential catabolic and biotransformation functions, the gut microbiota produces bioactive small molecules that mediate interactions with the host and contribute to the neurohumoral axes connecting the intestine with other parts of the body. This review discusses recent progress in characterizing the metabolic products of the gut microbiota and their biological functions, focusing on studies that investigate the responsible bacterial pathways and cognate host receptors. Several key areas are highlighted for future development: context-based analysis targeting pathways; integration of analytical approaches; metabolic modeling; and synthetic systems for in vivo manipulation of microbiota functions. Prospectively, these developments could further our mechanistic understanding of host microbiota interactions.
引用
收藏
页码:137 / 145
页数:9
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共 50 条
[1]   Critical role of gut microbiota in the production of biologically active, free catecholamines in the gut lumen of mice [J].
Asano, Yasunari ;
Hiramoto, Tetsuya ;
Nishino, Ryo ;
Aiba, Yuji ;
Kimura, Tae ;
Yoshihara, Kazufumi ;
Koga, Yasuhiro ;
Sudo, Nobuyuki .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2012, 303 (11) :G1288-G1295
[2]   The bacterial signal indole increases epithelial-cell tight-junction resistance and attenuates indicators of inflammation [J].
Bansal, Tarun ;
Alaniz, Robert C. ;
Wood, Thomas K. ;
Jayaraman, Arul .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (01) :228-233
[3]   Precision microbiome reconstitution restores bile acid mediated resistance to Clostridium difficile [J].
Buffie, Charlie G. ;
Bucci, Vanni ;
Stein, Richard R. ;
McKenney, Peter T. ;
Ling, Lilan ;
Gobourne, Asia ;
No, Daniel ;
Liu, Hui ;
Kinnebrew, Melissa ;
Viale, Agnes ;
Littmann, Eric ;
van den Brink, Marcel R. M. ;
Jenq, Robert R. ;
Taur, Ying ;
Sander, Chris ;
Cross, Justin R. ;
Toussaint, Nora C. ;
Xavier, Joao B. ;
Pamer, Eric G. .
NATURE, 2015, 517 (7533) :205-U207
[4]  
Cheng Y, 2015, DRUG METAB DISPOS
[5]   Bile acids: regulation of synthesis [J].
Chiang, John Y. L. .
JOURNAL OF LIPID RESEARCH, 2009, 50 (10) :1955-1966
[6]   Fecal Microbiota and Metabolome of Children with Autism and Pervasive Developmental Disorder Not Otherwise Specified [J].
De Angelis, Maria ;
Piccolo, Maria ;
Vannini, Lucia ;
Siragusa, Sonya ;
De Giacomo, Andrea ;
Serrazzanetti, Diana Isabella ;
Cristofori, Fernanda ;
Guerzoni, Maria Elisabetta ;
Gobbetti, Marco ;
Francavilla, Ruggiero .
PLOS ONE, 2013, 8 (10)
[7]   Faecal metabolite profiling identifies medium-chain fatty acids as discriminating compounds in IBD [J].
De Preter, Vicky ;
Machiels, Kathleen ;
Joossens, Marie ;
Arijs, Ingrid ;
Matthys, Christophe ;
Vermeire, Severine ;
Rutgeerts, Paul ;
Verbeke, Kristin .
GUT, 2015, 64 (03) :447-+
[8]   A Systematic Analysis of Biosynthetic Gene Clusters in the Human Microbiome Reveals a Common Family of Antibiotics [J].
Donia, Mohamed S. ;
Cimermancic, Peter ;
Schulze, Christopher J. ;
Brown, Laura C. Wieland ;
Martin, John ;
Mitreva, Makedonka ;
Clardy, Jon ;
Linington, Roger G. ;
Fischbach, Michael A. .
CELL, 2014, 158 (06) :1402-1414
[9]   Ability of the gut microbiota to produce PUFA-derived bacterial metabolites: Proof of concept in germ-free versus conventionalized mice [J].
Druart, Celine ;
Bindels, Laure B. ;
Schmaltz, Robert ;
Neyrinck, Audrey M. ;
Cani, Patrice D. ;
Walter, Jens ;
Ramer-Tait, Amanda E. ;
Delzenne, Nathalie M. .
MOLECULAR NUTRITION & FOOD RESEARCH, 2015, 59 (08) :1603-1613
[10]   Three-stage continuous culture system with a self-generated anaerobia to study the regionalized metabolism of the human gut microbiota [J].
Feria-Gervasio, David ;
Tottey, William ;
Gaci, Nadia ;
Alric, Monique ;
Cardot, Jean-Michel ;
Peyret, Pierre ;
Martin, Jean-Francois ;
Pujos, Estelle ;
Sebedio, Jean-Louis ;
Brugere, Jean-Francois .
JOURNAL OF MICROBIOLOGICAL METHODS, 2014, 96 :111-118