Incorporation of therapeutically modified bacteria into gut microbiota inhibits obesity

被引:209
作者
Chen, Zhongyi [1 ,2 ]
Guo, Lilu [1 ,2 ]
Zhang, Yongqin [1 ,2 ]
Walzem, Rosemary L. [3 ]
Pendergast, Julie S. [4 ]
Printz, Richard L. [4 ]
Morris, Lindsey C. [4 ]
Matafonova, Elena [1 ,2 ]
Stien, Xavier [1 ,2 ]
Kang, Li [5 ]
Coulon, Denis [6 ,7 ]
McGuinness, Owen P. [5 ]
Niswender, Kevin D. [4 ,5 ,8 ]
Davies, Sean S. [1 ,2 ]
机构
[1] Vanderbilt Univ, Div Clin Pharmacol, Dept Med, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37232 USA
[3] Texas A&M Univ, Dept Nutr & Food Sci, College Stn, TX USA
[4] Vanderbilt Univ, Div Diabet Endocrinol & Metab, Dept Med, Nashville, TN 37232 USA
[5] Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
[6] CNRS, Bordeaux, France
[7] Univ Bordeaux, Lab Biogenese Membranaire, Bordeaux, France
[8] Tennessee Valley Healthcare Syst, Vet Adm, Nashville, TN USA
关键词
FOOD-INTAKE; RECEPTOR-ALPHA; BODY-WEIGHT; N-ACYLPHOSPHATIDYLETHANOLAMINE; ARABIDOPSIS-THALIANA; OLEOYLETHANOLAMIDE; MICE; DIET; ANTIOBESITY; MODULATION;
D O I
10.1172/JCI72517
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Metabolic disorders, including obesity, diabetes, and cardiovascular disease, are widespread in Westernized nations. Gut microbiota composition is a contributing factor to the susceptibility of an individual to the development of these disorders; therefore, altering a person's microbiota may ameliorate disease. One potential microbiome-altering strategy is the incorporation of modified bacteria that express therapeutic factors into the gut microbiota. For example, N-acylphosphatidylethanolamines (NAPEs) are precursors to the N-acylethanolamide (NAE) family of lipids, which are synthesized in the small intestine in response to feeding and reduce food intake and obesity. Here, we demonstrated that administration of engineered NAPE-expressing E. coli Nissle 1917 bacteria in drinking water for 8 weeks reduced the levels of obesity in mice fed a high-fat diet. Mice that received modified bacteria had dramatically lower food intake, adiposity, insulin resistance, and hepatosteatosis compared with mice receiving standard water or control bacteria. The protective effects conferred by NAPE-expressing bacteria persisted for at least 4 weeks after their removal from the drinking water. Moreover, administration of NAPE-expressing bacteria to TallyHo mice, a polygenic mouse model of obesity, inhibited weight gain. Our results demonstrate that incorporation of appropriately modified bacteria into the gut microbiota has potential as an effective strategy to inhibit the development of metabolic disorders.
引用
收藏
页码:3391 / 3406
页数:16
相关论文
共 76 条
[51]   Phosphatidic Acid and N-Acylphosphatidylethanolamine Form Membrane Domains in Escherichia coli Mutant Lacking Cardiolipin and Phosphatidylglycerol [J].
Mileykovskaya, Eugenia ;
Ryan, Andrea C. ;
Mo, Xi ;
Lin, Chun-Chieh ;
Khalaf, Khaled I. ;
Dowhan, William ;
Garrett, Teresa A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (05) :2990-3000
[52]   Congenital leptin deficiency is associated with severe early-onset obesity in humans [J].
Montague, CT ;
Farooqi, IS ;
Whitehead, JP ;
Soos, MA ;
Rau, H ;
Wareham, NJ ;
Sewter, CP ;
Digby, JE ;
Mohammed, SN ;
Hurst, JA ;
Cheetham, CH ;
Earley, AR ;
Barnett, AH ;
Prins, JB ;
ORahilly, S .
NATURE, 1997, 387 (6636) :903-908
[53]   Food intake is inhibited by oral oleoylethanolamide [J].
Nielsen, MJ ;
Petersen, G ;
Astrup, A ;
Hansen, HS .
JOURNAL OF LIPID RESEARCH, 2004, 45 (06) :1027-1029
[54]   Oleoylethanolamide inhibits food intake in free-feeding rats after oral administration [J].
Oveisi, F ;
Gaetani, S ;
Eng, KTP ;
Piomelli, D .
PHARMACOLOGICAL RESEARCH, 2004, 49 (05) :461-466
[55]   Modulation of nutrient sensing nuclear hormone receptors promotes weight loss through appetite suppression in mice [J].
Perreault, M. ;
Will, S. ;
Panza, D. ;
Gareski, T. ;
Harding, K. ;
Kubasiak, D. ;
Jalenak, M. ;
Gartrell, K. ;
Wang, S. ;
Bollag, G. ;
Artis, D. R. ;
Ibrahim, P. N. ;
Womack, P. ;
Lin, J. J. ;
Saiah, E. ;
Mansour, T. S. ;
Vlasuk, G. P. ;
Erbe, D. V. ;
Tobin, J. F. .
DIABETES OBESITY & METABOLISM, 2010, 12 (03) :234-245
[56]   Intestinal levels of anandamide and oleoylethanolamide in food-deprived rats are regulated through their precursors [J].
Petersen, G ;
Sorensen, C ;
Schmid, PC ;
Artmann, A ;
Tang-Christensen, M ;
Hansen, SH ;
Larsen, PJ ;
Schmid, HHO ;
Hansen, HS .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2006, 1761 (02) :143-150
[57]   Leptin receptor gene in a large cohort of massively obese subjects: No indication of the fa/fa rat mutation. Detection of an intronic variant with no association with obesity [J].
Rolland, V ;
Clement, K ;
Dugail, I ;
Guy-Grand, B ;
Basdevant, A ;
Froguel, P ;
Lavau, M .
OBESITY RESEARCH, 1998, 6 (02) :122-127
[58]   The effects of short-term overfeeding on energy expenditure and nutrient oxidation in obesity-prone and obesity-resistant individuals [J].
Schmidt, S. L. ;
Kealey, E. H. ;
Horton, T. J. ;
VonKaenel, S. ;
Bessesen, D. H. .
INTERNATIONAL JOURNAL OF OBESITY, 2013, 37 (09) :1192-1197
[59]   The Lipid Messenger OEA Links Dietary Fat Intake to Satiety [J].
Schwartz, Gary J. ;
Fu, Jin ;
Astarita, Giuseppe ;
Li, Xiaosong ;
Gaetani, Silvana ;
Campolongo, Patrizia ;
Cuomo, Vincenzo ;
Piomelli, Daniele .
CELL METABOLISM, 2008, 8 (04) :281-288
[60]   Characterization of the Hyperphagic Response to Dietary Fat in the MC4R Knockout Mouse [J].
Srisai, Dollada ;
Gillum, Matthew P. ;
Panaro, Brandon L. ;
Zhang, Xian-Man ;
Kotchabhakdi, Naiphinich ;
Shulman, Gerald I. ;
Ellacott, Kate L. J. ;
Cone, Roger D. .
ENDOCRINOLOGY, 2011, 152 (03) :890-902