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Arabinoxylan-oligosaccharides kick-start arabinoxylan digestion in the aging broiler

While arabinoxylans (AX), an important dietary fiber fraction of wheat-based broiler diets, are known for exerting antinutritional effects in the gastrointestinal (GI) tract of broilers, the prebiotic potential of arabinoxylan-oligosaccharides (AXOS) is also well-documented. However, inconsistent pe...

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Autores principales: Bautil, A., Verspreet, J., Buyse, J., Goos, P., Bedford, M.R., Courtin, C.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7597398/
https://www.ncbi.nlm.nih.gov/pubmed/32359591
http://dx.doi.org/10.1016/j.psj.2019.12.041
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author Bautil, A.
Verspreet, J.
Buyse, J.
Goos, P.
Bedford, M.R.
Courtin, C.M.
author_facet Bautil, A.
Verspreet, J.
Buyse, J.
Goos, P.
Bedford, M.R.
Courtin, C.M.
author_sort Bautil, A.
collection PubMed
description While arabinoxylans (AX), an important dietary fiber fraction of wheat-based broiler diets, are known for exerting antinutritional effects in the gastrointestinal (GI) tract of broilers, the prebiotic potential of arabinoxylan-oligosaccharides (AXOS) is also well-documented. However, inconsistent performance responses as well as the effectiveness of low amounts of AXOS used in diets of previously conducted experiments put into question the classical prebiotic route being the sole mode of action of AXOS. The objective of this study was to investigate the effects of dietary AXOS addition on the rate of AX digestion in the gastrointestinal tract of broilers as a function of broiler age to gain more insight into the mode of action of these oligosaccharides. A feeding trial was performed on 480 one-day-old chicks (Ross 308) receiving a wheat-based diet supplemented with or without 0.50% AXOS, containing no endoxylanases. Digesta samples from ileum and caeca and fecal samples were analyzed for AX content, AX digestibility, intestinal viscosity, and microbial AX-degrading enzyme activities at 6 different ages (day 5, 10, 15, 21, 28, 35). Chicks fed from hatching with 0.50% AXOS demonstrated a higher ileal viscosity (P < 0.05). Also higher levels of AX solubilization and fermentation compared to control birds at 10 D were observed. This was noted by the higher total tract AX digestibility of water-extractable AX (WE-AX) and total AX (TOT-AX) at this age (P < 0.05). Although no significant difference in AX-degrading enzyme activities was observed among the dietary treatments, AXOS supplementation in young broilers was shown to stimulate or “kick-start” dietary AX digestion, thereby speeding up the development of a fiber-fermenting microbiome in the young broiler. This stimulation effect of AXOS could enable greater functional value to be extracted from dietary fiber in broiler feeds.
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spelling pubmed-75973982020-11-02 Arabinoxylan-oligosaccharides kick-start arabinoxylan digestion in the aging broiler Bautil, A. Verspreet, J. Buyse, J. Goos, P. Bedford, M.R. Courtin, C.M. Poult Sci Metabolism and Nutrition While arabinoxylans (AX), an important dietary fiber fraction of wheat-based broiler diets, are known for exerting antinutritional effects in the gastrointestinal (GI) tract of broilers, the prebiotic potential of arabinoxylan-oligosaccharides (AXOS) is also well-documented. However, inconsistent performance responses as well as the effectiveness of low amounts of AXOS used in diets of previously conducted experiments put into question the classical prebiotic route being the sole mode of action of AXOS. The objective of this study was to investigate the effects of dietary AXOS addition on the rate of AX digestion in the gastrointestinal tract of broilers as a function of broiler age to gain more insight into the mode of action of these oligosaccharides. A feeding trial was performed on 480 one-day-old chicks (Ross 308) receiving a wheat-based diet supplemented with or without 0.50% AXOS, containing no endoxylanases. Digesta samples from ileum and caeca and fecal samples were analyzed for AX content, AX digestibility, intestinal viscosity, and microbial AX-degrading enzyme activities at 6 different ages (day 5, 10, 15, 21, 28, 35). Chicks fed from hatching with 0.50% AXOS demonstrated a higher ileal viscosity (P < 0.05). Also higher levels of AX solubilization and fermentation compared to control birds at 10 D were observed. This was noted by the higher total tract AX digestibility of water-extractable AX (WE-AX) and total AX (TOT-AX) at this age (P < 0.05). Although no significant difference in AX-degrading enzyme activities was observed among the dietary treatments, AXOS supplementation in young broilers was shown to stimulate or “kick-start” dietary AX digestion, thereby speeding up the development of a fiber-fermenting microbiome in the young broiler. This stimulation effect of AXOS could enable greater functional value to be extracted from dietary fiber in broiler feeds. Elsevier 2020-03-24 /pmc/articles/PMC7597398/ /pubmed/32359591 http://dx.doi.org/10.1016/j.psj.2019.12.041 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Metabolism and Nutrition
Bautil, A.
Verspreet, J.
Buyse, J.
Goos, P.
Bedford, M.R.
Courtin, C.M.
Arabinoxylan-oligosaccharides kick-start arabinoxylan digestion in the aging broiler
title Arabinoxylan-oligosaccharides kick-start arabinoxylan digestion in the aging broiler
title_full Arabinoxylan-oligosaccharides kick-start arabinoxylan digestion in the aging broiler
title_fullStr Arabinoxylan-oligosaccharides kick-start arabinoxylan digestion in the aging broiler
title_full_unstemmed Arabinoxylan-oligosaccharides kick-start arabinoxylan digestion in the aging broiler
title_short Arabinoxylan-oligosaccharides kick-start arabinoxylan digestion in the aging broiler
title_sort arabinoxylan-oligosaccharides kick-start arabinoxylan digestion in the aging broiler
topic Metabolism and Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7597398/
https://www.ncbi.nlm.nih.gov/pubmed/32359591
http://dx.doi.org/10.1016/j.psj.2019.12.041
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