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Effects of Adding Dietary Fiber on the Gut Microbiota, Short-Chain Fatty Acids and Metabolism of Layer Chickens

Received: 30 September 2021    Accepted: 30 October 2021    Published: 5 November 2021
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Abstract

Dietary fiber is important for the growth performance and health of chickens. However, chickens must rely on fiber-degrading bacteria to grade fiber into monosaccharides due to a lack of endogenous fiber-degrading enzymes. Some of monosaccharides are then fermented into short-chain fatty acids (SCFAs) by SCFA-producing bacteria. SCFAs further regulate the host metabolism via special G protein-coupled receptors (GPRs) such as GPR43. In recent years, more and more research has focused on the impacts of adding dietary fiber on gut microorganisms and microbial metabolites-SCFAs of chickens. However, few works have focused on SCFA receptors and their impacts on metabolism of chickens. Understanding of this would help to explore how the dietary fiber affects chickens’ metabolism via SCFAs and their receptors. Given this, three different levels (0%, 1%, and 2%) of dietary fiber–eubiotic lignocellulose were added to the feed of ISA brown hens (IBH) for 0–8 weeks, with the aim of observing the effects of adding it on the gut microbiota, SCFAs, their receptors and metabolism of chickens. The results showed that the addition of 1% significantly increased the relative abundance of SCFAs-producing bacteria Sutterella, Oscillospira and Lactobacillus panis and the production of SCFAs (P < 0.05). The primer sequences of the GPR43 and reaction conditions designed in this experiment were applied to chickens. However, because the difference of the concentration of SCFAs was not great among groups, there was no significant change in the relative expression of the GPR43 mRNA in the liver and cecum (P > 0.05), resulting in there being no significant difference among groups in the appetite metabolism indexes including glucagon-like peptide-1 (GLP-1) and peptide tyrosine-tyrosine (PYY) and glucose metabolism indexes including blood glucose and liver glycogen of chickens (P > 0.05). The addition of 1% eubiotic lignocellulose is beneficial to increase the relative abundance of some SCFA-producing bacteria and the production of SCFAs at 8 weeks. The effects of added eubiotic lignocellulose on the relative expression of GPR43 mRNA and the metabolism of chickens were slight.

Published in American Journal of Life Sciences (Volume 9, Issue 5)
DOI 10.11648/j.ajls.20210905.17
Page(s) 149-156
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Dietary Fiber, Chicken, Eubiotic Lignocellulose, SCFA, GPR43, Gut Microbiota

References
[1] A. E. Kaoutari, F. Armougom, J. I. Gordon, D. Raoult, B. Henrissat. “The abundance and variety of carbohydrate-active enzymes in the human gut microbiota,” vol. 11, Nat. Rev. Microbiol, 2013, pp. 1-9.
[2] H. J. Flint, E. A. Bayer, M. T. Rincon, R. Lamed, B. A. White, “Polysaccharide utilization by gut bacteria, potential for new insights from genomic analysis,” vol. 6, Nat. Rev. Microbiol, pp. 121-131.
[3] M. Derrien, J. E. Van Hylckama Vlieg, “Fate, activity, and impact of ingested bacteria within the human gut microbiota,” vol. 23, Trends Microbiol, 2015, pp. 354-366.
[4] W, Hilpert, P, Dimroth, “Conversion of the chemical energy of methylmalonyl-CoA decarboxylation into a Na+ gradient,” vol. 296, Nature, 1984, pp. 584-585.
[5] P, Louis, P, Young, G, Holtrop, H. J. Flint, “Diversity of human colonic butyrate-producing bacteria revealed by analysis of the butyryl-CoA: Acetate CoA-transferase gene,” vol. 12, Environ. Microbiol, 2010, pp. 304–314.
[6] A. T. Reese, R. R. Dunn, “Drivers of microbiome biodiversity: a review of general rules, feces, and ignorance,” vol. 9, Microbiology, 2018, pp. e01294-18.
[7] E. E. Canfora, J. W. Jocken, E. E. Blaak, “Short-chain fatty acids in control of body weight and insulin sensitivity,” vol. 11, Nat. Rev. Endocrinol, 2015, pp. 577-591.
[8] D. R. Donohoe, N. Garge, X. Zhang, W. Sun, T. M. O'Connell, M. K. Bunger, et al, “The microbiome and butyrate regulate energy metabolism and autophagy in the mammalian colon,” Cell Metab. vol. 13, 2011, pp. 517-526.
[9] W. E. Roediger, “Role of anaerobic bacteria in the metabolic welfare of the colonic mucosa in man,” vol. 21, Gut, 1980, pp. 793-798.
[10] I. Kimura, D. Inoue, T. Maeda, T. Hara, A. Ichimura, S. Miyauchi, et al, “Short-chain fatty acids and ketones directly regulate sympathetic nervous system via G protein coupled receptor 41 (GPR41),” vol. 108, PNAS, 2011, pp. 8030-8035.
[11] F. De Vadder, P. Kovatcheva-Datchary, D. Goncalves, J. Vinera, C. Zitoun, A. Duchampt, et al, “Microbiota-generated metabolites promote metabolic benefits via gut-brain neural circuits,” vol. 156, Cell, 2014, pp. 84-96.
[12] G. Frost, M. L. Sleeth, M. Sahuri-Arisoylu, B. Lizarbe, S. Cerdan, L. Brody, et al, “The short-chain fatty acid acetate reduces appetite via a central homeostatic mechanism,” vol. 5, Nat. Commun, 2014, pp. 1–11.
[13] T. Todesco, A. V. Rao, O. Bosello, D. J. Jenkins, “Propionate lowers blood glucose and alters lipid metabolism in healthy subjects,” vol. 54, Am. J. Clin. Nutr, 1991, pp. 860-865.
[14] A. J. Brown, S. M. Goldsworthy, A. A. Barnes, M. M. Eilert, L. Tcheang, D. Daniels, et al, “The orphan G protein-coupled receptors GPR41 and GPR43 are activated by propionate and other short chain carboxylic acids,” vol. 278, J. Biol. Chem, 2003, pp. 11312-11319.
[15] A. Kroismayr, S. A. Roberts. Eubiotic lignocellulose–a new tool for swine nutritionists. vol. 24, Int. Pig Top, 2010, pp. 23-25.
[16] T. Magoč, and S. L. Salzberg, “FLASH: fast length adjustment of short reads to improve genome assemblies,” vol. 27, Bioinformatics, 2011, pp. 2957-2963.
[17] J. G. Caporaso, J. Kuczynski, J. Stombaugh, K. Bittinger, F. D. Bushman, E. K. Costello, et al, “QIIME allows analysis of high-throughput community sequencing dat,” vol. 7, Nat. Methods, 2010, pp. 335-336.
[18] R. C. Edgar, “MUSCLE, multiple sequence alignment with high accuracy and high throughput,” vol. 32, Nucleic Acids Res, 2004, pp. 1792-1797.
[19] N. Segata, J. Izard, L. Waldron, D. Gevers, L. Miropolsky, W. S. Garrett, C. Hutten. “Metagenomic biomarker discovery and explanation.” vol. 12, Genome Biol, 2011, pp. R60.
[20] J. R. White, N, Nagarajan, and M. Pop. “Statistical methods for detecting differentially abundant features in clinical metagenomic samples.” vol. 5, PLoS Comput. Biol, 2009, pp. e1000352.
[21] L. Hou, B. Sun, Y Yang. “Effects of added dietary fiber and rearing system on the gut microbial diversity and gut health of chicken,”vol. 10, Animals, 2010, pp. 1-22.
[22] S. H. Duncan, G. L. Hold, H. J. M. Harmsen, C. S. Stewart, H. J. Flint, “Growth requirements and fermentation products of Fusobacterium prausnitzii, and a pro-posal to reclassify it as Faecalibacterium prausnitzii gen. nov., comb. nov,” vol. 52, Int. J. Syst. Evol. Microbiol, 2002, pp. 2141-2146.
[23] S. E. Pryde, S. H. Duncan, G. L. Hold, C. S. Stewart, H. J. Flint, “The microbiology of butyrate formation in the human colon,” vol. 217, FEMS Microbiol. Lett, 2002, pp. 133-139.
[24] T. Konikoff, U. Gophna. “Oscillospira: a central, enigmatic component of the human gut microbiota,” vol. 24, Trends Microbio, 2016, pp. 523-524.
[25] A. Koh, F. De Vadder, P. Kovatcheva-Datchary, F. Bäckhed. “From dietary fiber to host physiology: short-chain fatty acids as key bacterial metabolites,” vol. 165, Cell, 2016, pp. 1332-1345.
[26] C. V. Ferreira-Halder, V. S. F. Alessandra, S. S. Andrade, “Action and function of Faecalibacterium prausnitzii in health and disease,” vol. 31, Best Practice & Research Clinical Gastroenterology, 2017, pp. 643-648.
[27] L. Macia, J. Tan, A. T. Vieira, K. Leach, D. Stanley, S. Luong, et al, “Metabolite-sensing receptors GPR43 and GPR109A facilitate dietary fibre-induced gut homeostasis through regulation of the inflammasom,” vol. 6, Nat. Commun, 2015, pp. 1-15.
[28] G. Tolhurst, “Short-chain fatty acids stimulate glucagon-like peptide-1 secretion via the G-protein-coupled receptor FFAR2,” vol. 61, Diabetes, 2012, pp. 364-371.
[29] S. H. Al-Lahham, M. P. Peppelenbosch, H. Roelofsen, R. J. Vonk, K. Venema, “effects of propionic acid in humans; metabolism, potential applications and underlying mechanisms,” vol. 1801, Biochim Biophys Acta, 2010, pp. 1175-1183.
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  • APA Style

    Baosheng Sun, Linyue Hou, Yu Yang. (2021). Effects of Adding Dietary Fiber on the Gut Microbiota, Short-Chain Fatty Acids and Metabolism of Layer Chickens. American Journal of Life Sciences, 9(5), 149-156. https://doi.org/10.11648/j.ajls.20210905.17

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    ACS Style

    Baosheng Sun; Linyue Hou; Yu Yang. Effects of Adding Dietary Fiber on the Gut Microbiota, Short-Chain Fatty Acids and Metabolism of Layer Chickens. Am. J. Life Sci. 2021, 9(5), 149-156. doi: 10.11648/j.ajls.20210905.17

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    AMA Style

    Baosheng Sun, Linyue Hou, Yu Yang. Effects of Adding Dietary Fiber on the Gut Microbiota, Short-Chain Fatty Acids and Metabolism of Layer Chickens. Am J Life Sci. 2021;9(5):149-156. doi: 10.11648/j.ajls.20210905.17

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  • @article{10.11648/j.ajls.20210905.17,
      author = {Baosheng Sun and Linyue Hou and Yu Yang},
      title = {Effects of Adding Dietary Fiber on the Gut Microbiota, Short-Chain Fatty Acids and Metabolism of Layer Chickens},
      journal = {American Journal of Life Sciences},
      volume = {9},
      number = {5},
      pages = {149-156},
      doi = {10.11648/j.ajls.20210905.17},
      url = {https://doi.org/10.11648/j.ajls.20210905.17},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajls.20210905.17},
      abstract = {Dietary fiber is important for the growth performance and health of chickens. However, chickens must rely on fiber-degrading bacteria to grade fiber into monosaccharides due to a lack of endogenous fiber-degrading enzymes. Some of monosaccharides are then fermented into short-chain fatty acids (SCFAs) by SCFA-producing bacteria. SCFAs further regulate the host metabolism via special G protein-coupled receptors (GPRs) such as GPR43. In recent years, more and more research has focused on the impacts of adding dietary fiber on gut microorganisms and microbial metabolites-SCFAs of chickens. However, few works have focused on SCFA receptors and their impacts on metabolism of chickens. Understanding of this would help to explore how the dietary fiber affects chickens’ metabolism via SCFAs and their receptors. Given this, three different levels (0%, 1%, and 2%) of dietary fiber–eubiotic lignocellulose were added to the feed of ISA brown hens (IBH) for 0–8 weeks, with the aim of observing the effects of adding it on the gut microbiota, SCFAs, their receptors and metabolism of chickens. The results showed that the addition of 1% significantly increased the relative abundance of SCFAs-producing bacteria Sutterella, Oscillospira and Lactobacillus panis and the production of SCFAs (P P > 0.05), resulting in there being no significant difference among groups in the appetite metabolism indexes including glucagon-like peptide-1 (GLP-1) and peptide tyrosine-tyrosine (PYY) and glucose metabolism indexes including blood glucose and liver glycogen of chickens (P > 0.05). The addition of 1% eubiotic lignocellulose is beneficial to increase the relative abundance of some SCFA-producing bacteria and the production of SCFAs at 8 weeks. The effects of added eubiotic lignocellulose on the relative expression of GPR43 mRNA and the metabolism of chickens were slight.},
     year = {2021}
    }
    

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  • TY  - JOUR
    T1  - Effects of Adding Dietary Fiber on the Gut Microbiota, Short-Chain Fatty Acids and Metabolism of Layer Chickens
    AU  - Baosheng Sun
    AU  - Linyue Hou
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    AB  - Dietary fiber is important for the growth performance and health of chickens. However, chickens must rely on fiber-degrading bacteria to grade fiber into monosaccharides due to a lack of endogenous fiber-degrading enzymes. Some of monosaccharides are then fermented into short-chain fatty acids (SCFAs) by SCFA-producing bacteria. SCFAs further regulate the host metabolism via special G protein-coupled receptors (GPRs) such as GPR43. In recent years, more and more research has focused on the impacts of adding dietary fiber on gut microorganisms and microbial metabolites-SCFAs of chickens. However, few works have focused on SCFA receptors and their impacts on metabolism of chickens. Understanding of this would help to explore how the dietary fiber affects chickens’ metabolism via SCFAs and their receptors. Given this, three different levels (0%, 1%, and 2%) of dietary fiber–eubiotic lignocellulose were added to the feed of ISA brown hens (IBH) for 0–8 weeks, with the aim of observing the effects of adding it on the gut microbiota, SCFAs, their receptors and metabolism of chickens. The results showed that the addition of 1% significantly increased the relative abundance of SCFAs-producing bacteria Sutterella, Oscillospira and Lactobacillus panis and the production of SCFAs (P P > 0.05), resulting in there being no significant difference among groups in the appetite metabolism indexes including glucagon-like peptide-1 (GLP-1) and peptide tyrosine-tyrosine (PYY) and glucose metabolism indexes including blood glucose and liver glycogen of chickens (P > 0.05). The addition of 1% eubiotic lignocellulose is beneficial to increase the relative abundance of some SCFA-producing bacteria and the production of SCFAs at 8 weeks. The effects of added eubiotic lignocellulose on the relative expression of GPR43 mRNA and the metabolism of chickens were slight.
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Author Information
  • Laboratory of Poultry Production, College of Animal Science, Shanxi Agricultural University, Jinzhong, China

  • Laboratory of Poultry Production, College of Animal Science, Shanxi Agricultural University, Jinzhong, China

  • Laboratory of Poultry Production, College of Animal Science, Shanxi Agricultural University, Jinzhong, China

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