Mapping Interactions of Microbial Metabolites with Human G-Protein-Coupled Receptors

被引:133
作者
Colosimo, Dominic A. [1 ]
Kohn, Jeffrey A. [1 ]
Luo, Peter M. [1 ]
Piscotta, Frank J. [1 ]
Han, Sun M. [3 ]
Pickard, Amanda J. [2 ]
Rao, Arka [2 ]
Cross, Justin R. [2 ]
Cohen, Louis J. [3 ]
Brady, Sean F. [1 ]
机构
[1] Rockefeller Univ, Lab Genetically Encoded Small Mol, 1230 York Ave, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Donald B & Catherine C Marron Canc Metab Ctr, New York, NY 10065 USA
[3] Icahn Sch Med Mt Sinai, Dept Med, Div Gastroenterol, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
BRAIN ANGIOGENESIS INHIBITOR-1; GUT MICROBIOTA; NEUROMEDIN-U; ACID; FATTY; IDENTIFICATION; BIOSYNTHESIS; FERMENTATION; RECOGNITION; ENGULFMENT;
D O I
10.1016/j.chom.2019.07.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Despite evidence linking the human microbiome to health and disease, how the microbiota affects human physiology remains largely unknown. Microbiota-encoded metabolites are expected to play an integral role in human health. Therefore, assigning function to these metabolites is critical to understanding these complex interactions and developing microbiota-inspired therapies. Here, we use large-scale functional screening of molecules produced by individual members of a simplified human microbiota to identify bacterial metabolites that agonize G-protein-coupled receptors (GPCRs). Multiple metabolites, including phenylpropanoic acid, cadaverine, 9-10-methylenehexadecanoic acid, and 12-methyltetradecanoic acid, were found to interact with GPCRs associated with diverse functions within the nervous and immune systems, among others. Collectively, these metabolite-receptor pairs indicate that diverse aspects of human health are potentially modulated by structurally simple metabolites arising from primary bacterial metabolism.
引用
收藏
页码:273 / +
页数:17
相关论文
共 61 条
[1]   Deorphanization of GPR109B as a Receptor for the β-Oxidation Intermediate 3-OH-octanoic Acid and Its Role in the Regulation of Lipolysis [J].
Ahmed, Kashan ;
Tunaru, Sorin ;
Langhans, Claus-Dieter ;
Hanson, Julien ;
Michalski, Christoph W. ;
Koelker, Stefan ;
Jones, Patricia M. ;
Okun, Juergen G. ;
Offermanns, Stefan .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (33) :21928-21933
[2]   Sphingolipids from a Symbiotic Microbe Regulate Homeostasis of Host Intestinal Natural Killer T Cells [J].
An, Dingding ;
Oh, Sungwhan F. ;
Olszak, Torsten ;
Neves, Joana F. ;
Avci, Fikri Y. ;
Erturk-Hasdemir, Deniz ;
Lu, Xi ;
Zeissig, Sebastian ;
Blumberg, Richard S. ;
Kasper, Dennis L. .
CELL, 2014, 156 (1-2) :123-133
[3]   Gut Microbiota-Produced Tryptamine Activates an Epithelial G-Protein-Coupled Receptor to Increase Colonic Secretion [J].
Bhattarai, Yogesh ;
Williams, Brianna B. ;
Battaglioli, Eric J. ;
Whitaker, Weston R. ;
Till, Lisa ;
Grover, Madhusudan ;
Linden, David R. ;
Akiba, Yasutada ;
Kandimalla, Karunya K. ;
Zachos, Nicholas C. ;
Kaunitz, Jonathan D. ;
Sonnenburg, Justin L. ;
Fischbach, Michael A. ;
Farrugia, Gianrico ;
Kashyap, Purna C. .
CELL HOST & MICROBE, 2018, 23 (06) :775-+
[4]   The adhesion GPCR BAI1 mediates macrophage ROS production and microbicidal activity against Gram-negative bacteria [J].
Billings, Emily A. ;
Lee, Chang Sup ;
Owen, Katherine A. ;
D'Souza, Ryan S. ;
Ravichandran, Kodi S. ;
Casanova, James E. .
SCIENCE SIGNALING, 2016, 9 (413)
[5]   Neuromedin U and its receptors: Structure, function, and physiological roles [J].
Brighton, PJ ;
Szekeres, PG ;
Willars, GB .
PHARMACOLOGICAL REVIEWS, 2004, 56 (02) :231-248
[6]   Targeting of microbe-derived metabolites to improve human health: The next frontier for drug discovery [J].
Brown, J. Mark ;
Hazen, Stanley L. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2017, 292 (21) :8560-8568
[7]   Culturing of 'unculturable' human microbiota reveals novel taxa and extensive sporulation [J].
Browne, Hilary P. ;
Forster, Samuel C. ;
Anonye, Blessing O. ;
Kumar, Nitin ;
Neville, B. Anne ;
Stares, Mark D. ;
Goulding, David ;
Lawley, Trevor D. .
NATURE, 2016, 533 (7604) :543-+
[8]   Natural Product Libraries: Assembly, Maintenance, and Screening [J].
Butler, Mark S. ;
Fontaine, Frank ;
Cooper, Matthew A. .
PLANTA MEDICA, 2014, 80 (14) :1161-1170
[9]   Human gut microbiome: hopes, threats and promises [J].
Cani, Patrice D. .
GUT, 2018, 67 (09) :1716-1725
[10]   A Forward Chemical Genetic Screen Reveals Gut Microbiota Metabolites That Modulate Host Physiology [J].
Chen, Haiwei ;
Nwe, Phu-Khat ;
Yang, Yi ;
Rosen, Connor E. ;
Bielecka, Agata A. ;
Kuchroo, Manik ;
Cline, Gary W. ;
Kruse, Andrew C. ;
Ring, Aaron M. ;
Crawford, Jason M. ;
Palm, Noah W. .
CELL, 2019, 177 (05) :1217-+