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Enzymatic hydrolysis of fumonisins in the gastrointestinal tract of broiler chickens

Fumonisins (FB) are among the most frequently detected mycotoxins in feedstuffs and finished feed, and recent data suggest that the functions of the gastrointestinal tract (GIT) in poultry species might be compromised at doses ranging from 10 to 20 mg/kg, close to field incidences and below the US a...

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Autores principales: Grenier, B, Schwartz-Zimmermann, H E, Gruber-Dorninger, C, Dohnal, I, Aleschko, M, Schatzmayr, G, Moll, W D, Applegate, T J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850661/
https://www.ncbi.nlm.nih.gov/pubmed/29053869
http://dx.doi.org/10.3382/ps/pex280
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author Grenier, B
Schwartz-Zimmermann, H E
Gruber-Dorninger, C
Dohnal, I
Aleschko, M
Schatzmayr, G
Moll, W D
Applegate, T J
author_facet Grenier, B
Schwartz-Zimmermann, H E
Gruber-Dorninger, C
Dohnal, I
Aleschko, M
Schatzmayr, G
Moll, W D
Applegate, T J
author_sort Grenier, B
collection PubMed
description Fumonisins (FB) are among the most frequently detected mycotoxins in feedstuffs and finished feed, and recent data suggest that the functions of the gastrointestinal tract (GIT) in poultry species might be compromised at doses ranging from 10 to 20 mg/kg, close to field incidences and below the US and EU guidelines. Strategies are therefore necessary to reduce the exposure of poultry to FB. In the present study, we assessed the efficacy of fumonisin esterase FumD (EC 3.1.1.87, commercial name FUMzyme(®)) to cleave the tricarballylic acid side chains of FB, leading to the formation of non-toxic hydrolyzed fumonisins in the GIT of broiler chickens. Broiler chickens were fed for 14 d (7 to 21 d of age) 3 different diets (6 birds/cage, 6 cages/diet), i) control feed (negative control group), ii) feed contaminated with 10 mg FB/kg (FB group), and iii) feed contaminated with 10 mg FB/kg and supplemented with 100 units of FUMzyme(®)/kg (FB+FUMzyme(®) group). To determine the degree of reduction of FB in the GIT, 2 characteristics were analyzed. First, the sphinganine-to-sphingosine ratio in the serum and liver was determined as a biomarker of effect for exposure to FB. Second, the concentration of fumonisin B(1) and its hydrolyzed forms was evaluated in the gizzard, the proximal and distal parts of the small intestine, and the excreta. Significantly reduced sphinganine-to-sphingosine ratios in the serum and liver of the FB+FUMzyme(®) group (serum: 0.15 ± 0.01; liver: 0.17 ± 0.01) compared to the FB group (serum: 0.20 ± 0.01; liver: 0.29 ± 0.03) proved that supplementation of broiler feed with FUMzyme(®) was effective in partially counteracting the toxic effect of dietary FB. Likewise, FB concentrations in digesta and excreta were significantly reduced in the FB+FUMzyme(®) group compared to the FB group (P < 0.05; up to 75%). FUMzyme(®) furthermore partially counteracted FB-induced up-regulation of cytokine gene expression (IL-8 and IL-10) in the jejunum. The FB group showed significantly higher gene expression of IL-8 and IL-10 compared to the negative control group (IL-8: fold change = 2.9 ± 1.1, P < 0.05; IL-10: fold change = 3.6 ± 1.4, P < 0.05), whereas IL-8 and IL-10 mRNA levels were not significantly different in the FB+FUMzyme(®)((®)) group compared to the other 2 groups. In conclusion, FUMzyme(®) is suitable to detoxify FB in chickens and maintain gut functions.
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spelling pubmed-58506612018-03-23 Enzymatic hydrolysis of fumonisins in the gastrointestinal tract of broiler chickens Grenier, B Schwartz-Zimmermann, H E Gruber-Dorninger, C Dohnal, I Aleschko, M Schatzmayr, G Moll, W D Applegate, T J Poult Sci Metabolism and Nutrition Fumonisins (FB) are among the most frequently detected mycotoxins in feedstuffs and finished feed, and recent data suggest that the functions of the gastrointestinal tract (GIT) in poultry species might be compromised at doses ranging from 10 to 20 mg/kg, close to field incidences and below the US and EU guidelines. Strategies are therefore necessary to reduce the exposure of poultry to FB. In the present study, we assessed the efficacy of fumonisin esterase FumD (EC 3.1.1.87, commercial name FUMzyme(®)) to cleave the tricarballylic acid side chains of FB, leading to the formation of non-toxic hydrolyzed fumonisins in the GIT of broiler chickens. Broiler chickens were fed for 14 d (7 to 21 d of age) 3 different diets (6 birds/cage, 6 cages/diet), i) control feed (negative control group), ii) feed contaminated with 10 mg FB/kg (FB group), and iii) feed contaminated with 10 mg FB/kg and supplemented with 100 units of FUMzyme(®)/kg (FB+FUMzyme(®) group). To determine the degree of reduction of FB in the GIT, 2 characteristics were analyzed. First, the sphinganine-to-sphingosine ratio in the serum and liver was determined as a biomarker of effect for exposure to FB. Second, the concentration of fumonisin B(1) and its hydrolyzed forms was evaluated in the gizzard, the proximal and distal parts of the small intestine, and the excreta. Significantly reduced sphinganine-to-sphingosine ratios in the serum and liver of the FB+FUMzyme(®) group (serum: 0.15 ± 0.01; liver: 0.17 ± 0.01) compared to the FB group (serum: 0.20 ± 0.01; liver: 0.29 ± 0.03) proved that supplementation of broiler feed with FUMzyme(®) was effective in partially counteracting the toxic effect of dietary FB. Likewise, FB concentrations in digesta and excreta were significantly reduced in the FB+FUMzyme(®) group compared to the FB group (P < 0.05; up to 75%). FUMzyme(®) furthermore partially counteracted FB-induced up-regulation of cytokine gene expression (IL-8 and IL-10) in the jejunum. The FB group showed significantly higher gene expression of IL-8 and IL-10 compared to the negative control group (IL-8: fold change = 2.9 ± 1.1, P < 0.05; IL-10: fold change = 3.6 ± 1.4, P < 0.05), whereas IL-8 and IL-10 mRNA levels were not significantly different in the FB+FUMzyme(®)((®)) group compared to the other 2 groups. In conclusion, FUMzyme(®) is suitable to detoxify FB in chickens and maintain gut functions. Oxford University Press 2017-12 2017-10-05 /pmc/articles/PMC5850661/ /pubmed/29053869 http://dx.doi.org/10.3382/ps/pex280 Text en © The Author 2017. Published by Oxford University Press on behalf of Poultry Science Association. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com.
spellingShingle Metabolism and Nutrition
Grenier, B
Schwartz-Zimmermann, H E
Gruber-Dorninger, C
Dohnal, I
Aleschko, M
Schatzmayr, G
Moll, W D
Applegate, T J
Enzymatic hydrolysis of fumonisins in the gastrointestinal tract of broiler chickens
title Enzymatic hydrolysis of fumonisins in the gastrointestinal tract of broiler chickens
title_full Enzymatic hydrolysis of fumonisins in the gastrointestinal tract of broiler chickens
title_fullStr Enzymatic hydrolysis of fumonisins in the gastrointestinal tract of broiler chickens
title_full_unstemmed Enzymatic hydrolysis of fumonisins in the gastrointestinal tract of broiler chickens
title_short Enzymatic hydrolysis of fumonisins in the gastrointestinal tract of broiler chickens
title_sort enzymatic hydrolysis of fumonisins in the gastrointestinal tract of broiler chickens
topic Metabolism and Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850661/
https://www.ncbi.nlm.nih.gov/pubmed/29053869
http://dx.doi.org/10.3382/ps/pex280
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