The gut microbiota and metabolic disease: current understanding and future perspectives

被引:261
作者
Arora, T. [1 ,2 ]
Backhed, F. [1 ,2 ,3 ]
机构
[1] Univ Gothenburg, Wallenberg Lab, Gothenburg, Sweden
[2] Univ Gothenburg, Sahlgrenska Ctr Cardiovasc & Metab Res, Dept Mol & Clin Med, Inst Med, Gothenburg, Sweden
[3] Univ Copenhagen, Fac Hlth Sci, Sect Metab Receptol & Enteroendocrinol, Novo Nordisk Fdn Ctr Basic Metab Res, Copenhagen, Denmark
基金
瑞典研究理事会; 欧洲研究理事会;
关键词
diet; germ-free; microbiome; microbiota; obesity; type; 2; diabetes; HIGH-FAT-DIET; BILE-ACID METABOLISM; ADIPOSE-TISSUE; DIFFERENTIAL ADAPTATION; INTESTINAL MICROBIOTA; PEPTIDE-1; SECRETION; INDUCED OBESITY; BODY HABITATS; DELIVERY MODE; WEIGHT-LOSS;
D O I
10.1111/joim.12508
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The human gut microbiota has been studied for more than a century. However, of nonculture-based techniques exploiting next-generation sequencing for analysing the microbiota, development has renewed research within the field during the past decade. The observation that the gut microbiota, as an environmental factor, contributes to adiposity has further increased interest in the field. The human microbiota is affected by the diet, and macronutrients serve as substrates for many microbially produced metabolites, such as short-chain fatty acids and bile acids, that may modulate host metabolism. Obesity predisposes towards type 2 diabetes and cardiovascular disease. Recently, it has been established that levels of butyrate-producing bacteria are reduced in patients with type 2 diabetes, whereas levels of Lactobacillus sp. are increased. Recent data suggest that the reduced levels of butyrate-producing bacteria might be causally linked to type 2 diabetes. Bariatric surgery, which promotes long-term weight loss and diabetes remission, alters the gut microbiota in both mice and humans. Furthermore, by transferring the microbiota from post-bariatric surgery patients to mice, it has been demonstrated that an altered microbiota may contribute to the improved metabolic phenotype following this intervention. Thus, greater understanding of alterations of the gut microbiota, in combination with dietary patterns, may provide insights into how the gut microbiota contributes to disease progression and whether it can be exploited as a novel diagnostic, prognostic and therapeutic target.
引用
收藏
页码:339 / 349
页数:11
相关论文
共 104 条
[61]
Recognition and Degradation of Plant Cell Wall Polysaccharides by Two Human Gut Symbionts [J].
Martens, Eric C. ;
Lowe, Elisabeth C. ;
Chiang, Herbert ;
Pudlo, Nicholas A. ;
Wu, Meng ;
McNulty, Nathan P. ;
Abbott, D. Wade ;
Henrissat, Bernard ;
Gilbert, Harry J. ;
Bolam, David N. ;
Gordon, Jeffrey I. .
PLOS BIOLOGY, 2011, 9 (12)
[63]
Experimental Endotoxemia Induces Adipose Inflammation and Insulin Resistance in Humans [J].
Mehta, Nehal N. ;
McGillicuddy, Fiona C. ;
Anderson, Paul D. ;
Hinkle, Christine C. ;
Shah, Rachana ;
Pruscino, Leticia ;
Tabita-Martinez, Jennifer ;
Sellers, Kim F. ;
Rickels, Michael R. ;
Reilly, Muredach P. .
DIABETES, 2010, 59 (01) :172-181
[64]
Gut microbiota modulation with norfloxacin and ampicillin enhances glucose tolerance in mice [J].
Membrez, Mathieu ;
Blancher, Florence ;
Jaquet, Muriel ;
Bibiloni, Rodrigo ;
Cani, Patrice D. ;
Burcelin, Remy G. ;
Corthesy, Irene ;
Mace, Katherine ;
Chou, Chieh Jason .
FASEB JOURNAL, 2008, 22 (07) :2416-2426
[65]
Diet Drives Convergence in Gut Microbiome Functions Across Mammalian Phylogeny and Within Humans [J].
Muegge, Brian D. ;
Kuczynski, Justin ;
Knights, Dan ;
Clemente, Jose C. ;
Gonzalez, Antonio ;
Fontana, Luigi ;
Henrissat, Bernard ;
Knight, Rob ;
Gordon, Jeffrey I. .
SCIENCE, 2011, 332 (6032) :970-974
[66]
Increased gut hormones and insulin sensitivity index following a 3-d intervention with a barley kernel-based product: a randomised cross-over study in healthy middle-aged subjects [J].
Nilsson, Anne C. ;
Johansson-Boll, Elin V. ;
Bjorck, Inger M. E. .
BRITISH JOURNAL OF NUTRITION, 2015, 114 (06) :899-907
[67]
Changes of hepatic lipid mediators associated with intake of high-fat diet for 12 weeks in endotoxemic rats using LC-ESI-MS/MS [J].
Nishiokada, Aya ;
Miyoshi, Makoto ;
Fujiwara, Mayu ;
Aoyama-Ishikawa, Michiko ;
Maeshige, Noriaki ;
Takahashi, Michiko ;
Hamada, Yasuhiro ;
Usami, Yu ;
Honda, Mie ;
Arita, Makoto ;
Usami, Makoto .
CLINICAL NUTRITION, 2015, 34 (04) :685-693
[68]
Detection of diverse bacterial signatures in atherosclerotic lesions of patients with coronary heart disease [J].
Ott, SJ ;
El Mokhtari, NE ;
Musfeldt, M ;
Hellmig, S ;
Freitag, S ;
Rehman, A ;
Kühbacher, T ;
Nikolaus, S ;
Namsolleck, P ;
Blaut, M ;
Hampe, J ;
Sahly, H ;
Reinecke, A ;
Haake, N ;
Günther, R ;
Krüger, D ;
Lins, M ;
Herrmann, G ;
Fölsch, UR ;
Simon, R ;
Schreiber, S .
CIRCULATION, 2006, 113 (07) :929-937
[69]
Diet, microbiota, and microbial metabolites in colon cancer risk in rural Africans and African Americans [J].
Ou, Junhai ;
Carbonero, Franck ;
Zoetendal, Erwin G. ;
DeLany, James P. ;
Wang, Mei ;
Newton, Keith ;
Gaskins, H. Rex ;
O'Keefe, Stephen J. D. .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2013, 98 (01) :111-120
[70]
The composition and metabolic activity of child gut microbiota demonstrate differential adaptation to varied nutrient loads in an in vitro model of colonic fermentation [J].
Payne, Amanda N. ;
Chassard, Christophe ;
Banz, Yannick ;
Lacroix, Christophe .
FEMS MICROBIOLOGY ECOLOGY, 2012, 80 (03) :608-623