A Diet High in Resistant Starch Modulates Microbiota Composition, SCFA Concentrations, and Gene Expression in Pig Intestine

被引:264
作者
Haenen, Danielle [1 ]
Zhang, Jing [2 ]
da Silva, Carol Souza [3 ,4 ]
Bosch, Guido [4 ]
van der Meer, Ingrid M. [5 ]
van Arkel, Jeroen [5 ]
van den Borne, Joost J. G. C. [4 ]
Gutierrez, Odette Perez [2 ]
Smidt, Hauke [2 ]
Kemp, Bas [3 ]
Muller, Michael [1 ,6 ]
Hooiveld, Guido J. E. J. [1 ,6 ]
机构
[1] Wageningen Univ, Nutr Metab & Genom Grp, Div Human Nutr, NL-6700 AP Wageningen, Netherlands
[2] Wageningen Univ, Microbiol Lab, NL-6700 AP Wageningen, Netherlands
[3] Wageningen Univ, Adaptat Physiol Grp, NL-6700 AP Wageningen, Netherlands
[4] Wageningen Univ, Anim Nutr Grp, NL-6700 AP Wageningen, Netherlands
[5] Plant Res Int, Wageningen, Netherlands
[6] Netherlands Nutrigen Ctr, Wageningen, Netherlands
关键词
CHAIN FATTY-ACIDS; GLUCAGON-LIKE PEPTIDE-1; PHYLOGENETIC MICROARRAY; GASTROINTESTINAL-TRACT; HUMAN GUT; APPETITE REGULATION; METABOLIC SYNDROME; COLONIC FUNCTION; US ADULTS; BODY-FAT;
D O I
10.3945/jn.112.169672
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Resistant starch (RS) is highly fermentable by microbiota in the colon, resulting in the production of SCFAs. RS is thought to mediate a large proportion of its health benefits, including increased satiety, through the actions of SCFAs. The aim of this study was to investigate the effects of a diet high in RS on luminal microbiota composition, luminal SCFA concentrations, and the expression of host genes involved in SCFA uptake, SCFA signaling, and satiety regulation in mucosal tissue obtained from small intestine, cecum, and colon. Twenty adult female pigs were either assigned to a digestible starch (DS) diet or a diet high in RS (34%) for a period of 2 wk. After the intervention, luminal content and mucosal scrapings were obtained for detailed molecular analysis. RS was completely degraded in the cecum. In both the cecum and colon, differences in microbiota composition were observed between DS- and RS-fed pigs. In the colon these included the stimulation of the healthy gut-associated butyrate-producing Faecalibacterium prausnitzii, whereas potentially pathogenic members of the Gammaproteobacteria, including Escherichia coli and Pseudomonas spp., were reduced in relative abundance. Cecal and colonic SCFA concentrations were significantly greater in RS-fed pigs, and cecal gene expression of monocarboxylate transporter 1 (SLC16A1) and glucagon (GCG) was induced by RS. In conclusion, our data show that RS modulates microbiota composition, SCFA concentrations, and host gene expression in pig intestine. Combined, our data provide an enhanced understanding of the interaction between diet, microbiota, and host. J. Nutr. 143: 274-283, 2013.
引用
收藏
页码:274 / 283
页数:10
相关论文
共 62 条
  • [1] Amine E, 2003, 05123054 WHO
  • [2] CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING
    BENJAMINI, Y
    HOCHBERG, Y
    [J]. JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) : 289 - 300
  • [4] Two high-amylose maize starches with different amounts of resistant starch vary in their effects on fermentation, tissue and digesta mass accretion, and bacterial populations in the large bowel of pigs
    Bird, Anthony R.
    Vuaran, Michelle
    Brown, Ian
    Topping, David L.
    [J]. BRITISH JOURNAL OF NUTRITION, 2007, 97 (01) : 134 - 144
  • [5] Short chain fatty acids exchange across the gut and liver in humans measured at surgery
    Bloemen, Johanne G.
    Venema, Koen
    de Poll, Marcel C. van
    Damink, Steven W. Olde
    Buurman, Wim A.
    Dejong, Cornelis H.
    [J]. CLINICAL NUTRITION, 2009, 28 (06) : 657 - 661
  • [6] Regulation of monocarboxylate transporter 1 (MCT1) promoter by butyrate in human intestinal epithelial cells:: Involvement of NF-κB pathway
    Borthakur, Alip
    Saksena, Seema
    Gill, Ravinder K.
    Alrefai, Waddah A.
    Ramaswamy, Krishnamurthy
    Dudeja, Pradeep K.
    [J]. JOURNAL OF CELLULAR BIOCHEMISTRY, 2008, 103 (05) : 1452 - 1463
  • [7] Genome-wide analysis of PPARα activation in murine small intestine
    Bunger, Meike
    van den Bosch, Heleen M.
    van der Meijde, Jolanda
    Kersten, Sander
    Hooiveld, Guido J. E. J.
    Muller, Michael
    [J]. PHYSIOLOGICAL GENOMICS, 2007, 30 (02) : 192 - 204
  • [8] Short-chain fatty acids modify colonic motility through nerves and polypeptide YY release in the rat
    Cherbut, C
    Ferrier, L
    Rozé, C
    Anini, Y
    Blottière, H
    Lecannu, G
    Galimiche, JP
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1998, 275 (06): : G1415 - G1422
  • [9] A role for intestinal endocrine cell-expressed g protein-coupled receptor 119 in glycemic control by enhancing glucagon-like peptide-1 and glucose-dependent insulinotropic peptide release
    Chu, Zhi-Liang
    Carroll, Chris
    Alfonso, Jean
    Gutierrez, Veronica
    He, Hongmei
    Lucman, Annette
    Pedraza, Melinda
    Mondala, Helen
    Gao, Hui
    Bagnol, Didier
    Chen, Ruoping
    Jones, Robert M.
    Behan, Dominic P.
    Leonard, James
    [J]. ENDOCRINOLOGY, 2008, 149 (05) : 2038 - 2047
  • [10] Comparative Analysis of Pyrosequencing and a Phylogenetic Microarray for Exploring Microbial Community Structures in the Human Distal Intestine
    Claesson, Marcus J.
    O'Sullivan, Orla
    Wang, Qiong
    Nikkilae, Janne
    Marchesi, Julian R.
    Smidt, Hauke
    de Vos, Willem M.
    Ross, R. Paul
    O'Toole, Paul W.
    [J]. PLOS ONE, 2009, 4 (08):