In vitro impact of condensed tannins on the caecal metabolites of chickens

Authors

  • Mohammed Munis Dakheel University of Baghdad, College of Veterinary Medicine, Department of Veterinary Public Health https://orcid.org/0000-0002-1938-8098
  • Mohammed Abdalmalek Ali Al-Bedhawi University of Baghdad, Institute of Genetic Engineering and Biotechnology
  • Afnan Ahmed Al-Mnaser University of Reading, Department of Food and Nutritional Sciences
  • Marina Mora-Ortiz Kings’ College London, Department of Twin Research
  • Martin John Woodward University of Reading, Department of Food and Nutritional Sciences
  • Caroline Rymer University of Reading, School of Agriculture, Policy and Development https://orcid.org/0000-0002-3535-4330

DOI:

https://doi.org/10.11606/issn.1678-4456.bjvras.2021.174733

Keywords:

Procyanidins, Prodelphinidins, 1H-NMR, Amino acids, Fatty acids, In vitro fermentation

Abstract

Tannins are a diverse group of plant phenolic compounds. Condensed tannins (CTs) represent a major subgroup of tannins and were extracted from tilia (Tilia L.) flowers and black locust (Robinia pseudoacacia) leaves. These extracts were examined for their effects on the metabolic profile of chicken caeca. By using in vitro, a nuclear magnetic resonance (1H-NMR), which was combined with multivariate statistics, the current study was applied for the first time to investigate how three different CT compositions, procyanidins (PC) and/or prodelphinidins (PD) units influenced the metabolic end-products in caecal contents of chickens. In the presence of tannins, glutamate, leucine, lysine, pyroglutamate, phenylalanine, proline, and sarcosine were significantly decreased. CT extracts significantly influenced the fermentation, increasing the concentrations of some fatty acids such as acetate, butyrate, and propionate whereas. In contrast, lactate decreased between the treatments. This study identified the key structural features of CTs that contain either high molar proportions of PD or PC, which might be useful to improve the efficiency of feed utilization in chickens.

Downloads

Download data is not yet available.

References

Amorim Franco TM, Blanchard JS. Bacterial branched-chain amino acid biosynthesis: structures, mechanisms, and drugability. Biochemistry. 2017;56(44):5849-65. https://dx.doi.org/10.1021/acs.biochem.7b00849. PMid:28977745.

Beckonert O, Keun HC, Ebbels TM, Bundy J, Holmes E, Lindon JC, Nicholson JK. Metabolic profiling, metabolomic and metabonomic procedures for NMR spectroscopy of urine, plasma, serum and tissue extracts. Nat Protoc. 2007;2(11):2692-703. https://dx.doi.org/10.1038/nprot.2007.376. PMid:18007604.

Brenes A, Viveros A, Chamorro S, Arija I. Use of polyphenol-rich grape by-products in monogastric nutrition. A review. Anim Feed Sci Technol. 2016;211:1-7. https://dx.doi.org/10.1016/j.anifeedsci.2015.09.016.

Brown RH, Mueller-Harvey I, Zeller WE, Reinhardt L, Stringano E, Gea A, Drake C, Ropiak HM, Fryganas C, Ramsay A, Hardcastle EE. Facile purification of milligram to gram quantities of condensed tannins according to mean degree of polymerization and flavan-3-ol subunit composition. J Agric Food Chem. 2017;65(36):8072-82.

Calvani R, Brasili E, Praticò G, Sciubba F, Roselli M, Finamore A, Marini F, Marzetti E, Miccheli A. Application of NMR-based metabolomics to the study of gut microbiota in obesity. J Clin Gastroenterol. 2014;48 (Suppl 1):S5-7. https://dx.doi.org/10.1097/MCG.0000000000000236. PMid:25291128.

Dakheel MM, Alkandari FA, Mueller‐Harvey I, Woodward MJ, Rymer C. Antimicrobial in vitro activities of condensed tannin extracts on avian pathogenic Escherichia coli. Lett Appl Microbiol. 2020;70(3):165-72. https://dx.doi.org/10.1111/lam.13253. PMid:31782190.

Dakheel MM. The influence of condensed tannin extracts on gut health in chickens [dissertation]. Reading: University of Reading; 2018.

Dieterle F, Ross A, Schlotterbeck G, Senn H. Probabilistic quotient normalization as robust method to account for dilution of complex biological mixtures. Application in 1H NMR metabonomics. Anal Chem. 2006;78(13):4281-90. https://dx.doi.org/10.1021/ac051632c. PMid:16808434.

Fryganas C, Drake C, Ropiak HM, Mora-Ortiz M, Smith LM, Mueller-Harvey I, Kowalczyk RM. Carbon-13 cross-polarization magic-angle spinning nuclear magnetic resonance for measuring proanthocyanidin content and procyanidin to prodelphinidin ratio in sainfoin (Onobrychis viciifolia) tissues. J Agric Food Chem. 2018;66(16):4073-81. https://dx.doi.org/10.1021/acs.jafc.8b01215. PMid:29631396.

Fuchs S, Behrends V, Bundy JG, Crisanti A, Nolan T. Phenylalanine metabolism regulates reproduction and parasite melanization in the malaria mosquito. PLoS One. 2014;9(1):e84865. https://dx.doi.org/10.1371/journal.pone.0084865. PMid:24409310.

Gea A, Stringano E, Brown RH, Mueller-Harvey I. In situ analysis and structural elucidation of sainfoin (Onobrychis viciifolia) tannins for high-throughput germplasm screening. J Agric Food Chem. 2011;59(2):495-503. https://dx.doi.org/10.1021/jf103609p. PMid:21175139.

Grabber JH, Zeller WE, Mueller-Harvey I. Acetone enhances the direct analysis of procyanidin-and prodelphinidin-based condensed tannins in Lotus species by the butanol–HCl–iron assay. J Agric Food Chem. 2013;61(11):2669-78. https://dx.doi.org/10.1021/jf304158m. PMid:23383722.

Jana A, Adak A, Haider SK, Das A, Paul T, Mondal KC, Mohapatra PK. A new strategy for improvement of tamarind seed based chicken diet after microbial detannification and assessment of its safety aspects. Acta Biol Szeged. 2015;59(1):1-9.

Le Roy CI, Mappley LJ, La Ragione RM, Woodward MJ, Claus SP. NMR-based metabolic characterization of chicken tissues and biofluids: a model for avian research. Metabolomics. 2016;12(10):157. https://dx.doi.org/10.1007/s11306-016-1105-7. PMid:27729831.

Lowry JB, McSweeney CS, Palmer B. Changing perceptions of the effect of plant phenolics on nutrient supply in the ruminant. Aust J Agric Res. 1996;47(6):829-42. https://dx.doi.org/10.1071/AR9960829.

Macfarlane GT, Macfarlane S. Bacteria, colonic fermentation, and gastrointestinal health. J AOAC Int. 2012;95(1):50-60. https://dx.doi.org/10.5740/jaoacint.SGE_Macfarlane. PMid:22468341.

Meister A. Biochemistry of the amino acids. USA: Elsevier; 2012. 485 p.

Mora-Ortiz M, Nuñez Ramos P, Oregioni A, Claus SP. NMR metabolomics identifies over 60 biomarkers associated with Type II Diabetes impairment in db/db mice. Metabolomics. 2019a;15(6):89. https://dx.doi.org/10.1007/s11306-019-1548-8. PMid:31179513.

Mora-Ortiz M, Trichard M, Oregioni A, Claus SP. Thanatometabolomics: introducing NMR-based metabolomics to identify metabolic biomarkers of the time of death. Metabolomics. 2019b;15(3):37. https://dx.doi.org/10.1007/s11306-019-1498-1. PMid:30834988.

Neis EP, Dejong CH, Rensen SS. The role of microbial amino acid metabolism in host metabolism. Nutrients. 2015;7(4):2930-46. https://dx.doi.org/10.3390/nu7042930. PMid:25894657.

Niba AT, Beal JD, Kudi AC, Brooks PH. Bacterial fermentation in the gastrointestinal tract of non-ruminants: influence of fermented feeds and fermentable carbohydrates. Trop Anim Health Prod. 2009;41(7):1393-407. https://dx.doi.org/10.1007/s11250-009-9327-6. PMid:19283504.

Quijada J, Drake C, Gaudin E, El-Korso R, Hoste H, Mueller-Harvey I. Condensed tannin changes along the digestive tract in lambs fed with sainfoin pellets or hazelnut skins. J Agric Food Chem. 2018;66(9):2136-42. https://dx.doi.org/10.1021/acs.jafc.7b05538. PMid:29424229.

Rinttilä T, Apajalahti J. Intestinal microbiota and metabolites: implications for broiler chicken health and performance. J Appl Poult Res. 2013;22(3):647-58. https://dx.doi.org/10.3382/japr.2013-00742.

Stokes DJ, Kelly AF, Gould SW, Cassar CA, Fielder MD. The withdrawal of antimicrobial treatment as a mechanism for defeating resistant microorganisms. FEMS Immunol Med Microbiol. 2008;53(3):300-5. https://dx.doi.org/10.1111/j.1574-695X.2008.00429.x. PMid:18554301.

Tjahjani S. Antimalarial activity of Garcinia mangostana L rind and its synergistic effect with artemisinin in vitro. BMC Complement Altern Med. 2017;17(1):131. https://dx.doi.org/10.1186/s12906-017-1649-8. PMid:28241761.

Zheng C, Zhang S, Ragg S, Raftery D, Vitek O. Identification and quantification of metabolites in 1H NMR spectra by Bayesian model selection. Bioinformatics. 2011;27(12):1637-44. https://dx.doi.org/10.1093/bioinformatics/btr118. PMid:21398670.

Downloads

Published

2021-07-30

Issue

Section

FULL ARTICLE

How to Cite

1.
Dakheel MM, Al-Bedhawi MAA, Al-Mnaser AA, Mora-Ortiz M, Woodward MJ, Rymer C. In vitro impact of condensed tannins on the caecal metabolites of chickens. Braz. J. Vet. Res. Anim. Sci. [Internet]. 2021 Jul. 30 [cited 2024 Dec. 4];58:e174733. Available from: https://www.revistas.usp.br/bjvras/article/view/174733