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Yacon (Smallanthus sonchifolius) root extracts affect laying performance, egg quality, serum biochemical parameters and intestinal microbiota in hens

  • Zhiwei Wu (College of Food and Health, College of Animal Science and Technology, Zhejiang Agriculture & Forestry University) ;
  • Qunli Liu (Hospital of Stomatology, Wuhan University) ;
  • Zhenting Ruan (College of Food and Health, College of Animal Science and Technology, Zhejiang Agriculture & Forestry University) ;
  • Liuchao Wang (College of Food and Health, College of Animal Science and Technology, Zhejiang Agriculture & Forestry University) ;
  • Jinghui Fan (Institute of Animal Husbandry, Hangzhou Academy of Agricultural Sciences) ;
  • Fei Chen (Hangzhou Xiaoshan Chicken Breeding Co., Ltd) ;
  • Zhangguo Liu (College of Food and Health, College of Animal Science and Technology, Zhejiang Agriculture & Forestry University) ;
  • Lizhi Lu (Institute of Animal Husbandry and veterinary medicine, Zhejiang Academy of Agricultural Sciences)
  • Received : 2024.02.04
  • Accepted : 2024.04.21
  • Published : 2024.10.01

Abstract

Objective: The objective of this study was to investigate the influence of yacon root extracts (YREs) on productive performance and health of laying hens. Methods: Six hundred 30-week-old Xiaoshan Chicken layers were divided into 5 groups, control group, antibiotic positive control group, and 3 YREs treatment groups. In a 9-wk feeding experiment, at the end of wk 3, 6, and 9, twenty eggs were collected from each replicate to measure egg qualities. At the end of wk 9, three hen serum samples, and 5 hen cecal content samples were collected from each replicate. Results: Compared to the control group, 0.8%, 1.6%, and 2.4% YREs treatments could increase hens' daily feed intake, and YREs supplementation affected daily feed intake in linear manner. YREs did not change egg size, but 0.8% and 2.4% YREs changed egg shape by decreasing the egg shape index and sphericity, and 0.8% YREs tended to improve the eggshell breaking strength. Diet supplemented with 1.6% YREs might decrease yolk color grade but optimize the pH of thick egg white in fresh egg; moreover, 1.6% and 2.4% YREs might be helpful for eggs to inhibit water loss during storage, and YREs supplementation affected water loss rate in linear manner. 2.4% YREs could decrease the serum lactate dehydrogenases (LDH) level, and YREs supplemental levels linearly affected serum LDH content. Finally, YREs could enrich the diversity of intestinal microbiota of hens fed with 0.8% and be beneficial for the relative abundance of phylum Bacteroidota and Halobacterota; 2.4% YREs might increase the abundance of phylum Actinobacteriota and genus Bifidobacterium, while decrease genus Bacteroides; YREs supplemental levels affected the abundance of phylum Actinobacteriota, and genera Bifidobacterium and Bacteroides in linear manner. Conclusion: Dietary supplementation with YREs could affect egg quality, protect the health of organs and exhibit prebiotic activity.

Keywords

Acknowledgement

This study was supported by the Zhejiang Science and Technology Major Program on Agricultural New Variety Breeding (Chiana; 2021C02068-10), and Agricultural and Social Development Project of Hangzhou City of China (202003A02).

References

  1. Honore SM, Grande MV, Gomez Rojas J, Sanchez SS. Smallanthus sonchifolius (Yacon) flour improves visceral adiposity and metabolic parameters in high-fat-diet-fed rats. J Obes 2018;2018:5341384. https://doi.org/10.1155/2018/5341384
  2. Caetano BFR, de Moura NA, Almeida APS, Dias MC, Sivieri K, Barbisan LF. Yacon (Smallanthus sonchifolius) as a food supplement: health-promoting benefits of fructooligosaccharides. Nutrients 2016;8:436. https://doi.org/10.3390/nu8070436
  3. Higashimura Y, Hirabayashi M, Nishikawa H, et al. Dietary intake of yacon roots (Smallanthus sonchifolius) affects gut microbiota and fecal mucin and prevents intestinal inflammation in mice. J Clin Biochem Nutr 2021;69:272-9. https://doi.org/10.3164/jcbn.20-203
  4. Misaki R, Fujiyama K, Kajiura H. Structure and biological functions of plant glycans and polysaccharides. Comp Glycoscience 2021;5:93-109. https://doi.org/10.1016/B978-0-12-819475-1.00101-2
  5. Delgado GTC, Tamashiro WM, Marostica Junior MRM, Pastore GM. Yacon (Smallanthus sonchifolius): a functional food. Plant Foods Hum Nutr 2013;68:222-8. https://doi.org/10.1007/s11130-013-0362-0
  6. Fabersani E, Grande MV, Araoz MVC, et al. Metabolic effects of goat milk yogurt supplemented with yacon flour in rats on high-fat diet. J Funct Food 2018;49: 447-57. https://doi.org/10.1016/j.jff.2018.08.042
  7. Kanmanee C, Srinual O, Punyatong M, et al. Effects of dietary supplementation with red yeast (Sporidiobolus pararoseus) on productive performance, egg quality, and duodenal cell proliferation of laying hens. Animals (Basel) 2022;12:238. https://doi.org/10.3390/ani12030238
  8. Obianwuna UE, Chang XY, Wang J, et al. Dietary fructooligosaccharides effectively facilitate the production of high-quality eggs via improving the physiological status of laying hens. Foods 2022;11:1828. https://doi.org/10.3390/foods11131828
  9. Ministry of Agriculture of China. Feeding standard of chicken (NY/T 33-2004). Beijing, China: Chinese Standard; 2004.
  10. Mohsenin NN. Physical properties of plant and animal material. New York, USA and London, UK: Gordon and Breach Press; 1970.
  11. Severa L, Nedomova S, Buchar J, Cupera J. Novel approaches in mathematical description of hen egg geometry. Int J Food Prop 2013;16:1472-82. https://doi.org/10.1080/10942912.2011.595028
  12. Wang LC, Ruan ZT, Wu ZW, et al. Geometrical characteristics of eggs from 3 poultry species. Poult Sci 2021;100:100965. https://doi.org/10.1016/j.psj.2020.12.062
  13. Eisen EJ, Bohren BB, McKean HE. The Haugh unit as a measure of egg albumen quality. Poult Sci 1962;41:1461-8. https://doi.org/10.3382/ps.0411461
  14. Funk EM. The relation of yolk index determined in natural position to the yolk index as determined after separating the yolk from the albumen. Poult Sci 1948;27:367. https://doi.org/10.3382/ps.0270367
  15. Su Y, Ge Y, Xu Z, Zhang D, Li D. The digestive and reproductive tract microbiotas and their association with body weight in laying hens. Poult Sci 2021; 100:101422. https://doi.org/10.1016/j.psj.2021.101422
  16. Stoddard MC, Yong EH, Akkaynak D, Tobias JA, Mahadevan L. Avian egg shape: form, function, and evolution. Science 2017;356:1249-54. https://doi.org/10.1126/science.aaj1945
  17. Denys S, Pieters JG, Dewettinck K. Combined CFD and experimental approach for determination of the surface heat transfer coefficient during thermal processing of eggs. J Food Sci 2003;68:943-51. https://doi.org/10.1111/j.1365-2621.2003.tb08269.x
  18. Gervais O, Nirasawa K, Vincenot CE, Nagamine Y, Moriya K. Effect of long-term selection for non-destructive deformation on egg shape in white leghorns. J Poult Sci 2016;53:249-56. https://doi.org/10.2141/jpsa.0160014
  19. Gutierrez E, Ordaz G, Perez RE, Ortiz R, Juarez A. Effect of the pigmentation, shine, weight, and shape index of the quail egg (Coturnix coturnix japonica) on the hatchability rate. J Adv Vet Anim Res 2021;8:629-34. https://doi.org/10.5455/javar.2021.h554
  20. Morgan NK, Wallace A, Bedford MR, Gonzalez-Ortiz G. Impact of fermentable fiber, xylo-oligosaccharides and xylanase on laying hen productive performance and nutrient utilization. Poult Sci 2022;101:102210. https://doi.org/10.1016/j.psj.2022.102210
  21. Peng K, Long L, Wang Y, Wang S. Effects of octacosanol extracted from rice bran on the laying performance, egg quality and blood metabolites of laying hens. Asian-Australas J Anim Sci 2016;29:1458-63. https://doi.org/10.5713/ajas.16.0287
  22. Guo XY, Kim IH. Impacts of limestone multi-particle size on production performance, egg shell quality, and egg quality in laying hens. Asian-Australas J Anim Sci 2012;25:839-44. https://doi.org/10.5713/ajas.2011.11468
  23. Topolska K, Radzki RP, Filipiak-Florkiewicz A, Bienko M, Florkiewicz A, Cieslik E. Could fructan sources in strawberry matrix be more effective as a tool for improvement of bone structure than these compounds added to diet alone? - study on osteopenic rat model. Ann Agric Environ Med 2020;27:19-28. https://doi.org/10.26444/aaem/108656
  24. Cayan H, Erener G. Effect of olive leaf (Olea europaea) powder on laying hens performance, egg quality and egg yolk cholesterol levels. Asian-Australas J Anim Sci 2015;28:538-43. https://doi.org/10.5713/ajas.14.0369
  25. Paganelli CV, Ar A, Rahn H. Diffusion-induced convective gas flow through the pores of the eggshell. J Exp Zool 1987;1:173-80.
  26. Tazawa H. Carbon dioxide transport and acid-base balance in chickens before and after hatching. In: Seymour RS, editors. Respiration and metabolism of embryonic vertebrates. Perspectives in vertebrate science, vol 3. Dordrecht, Netherlands: Springer; 1984.
  27. O'Dea EE, Fasenko GM, Feddes JJR, et al. Investigating the eggshell conductance and embryonic metabolism of modern and unselected domestic avian genetic strains at two flock ages. Poult Sci 2004;83:2059-70. https://doi.org/10.1093/ps/83.12.2059
  28. Oliveira GO, Braga CP, Fernandes AAH. Improvement of biochemical parameters in type 1 diabetic rats after the roots aqueous extract of yacon [Smallanthus sonchifolius (Poepp.& Endl.)] treatment. Food Chem Toxicol 2013;59:256-60. https://doi.org/10.1016/j.fct.2013.05.050
  29. Kim S, Jo K, Kim N, Hong KB, Suh HJ. The role of alternative sugars on endurance capacity in bal b/c mice. J Food Biochem 2020;44:e13409. https://doi.org/10.1111/jfbc.13409
  30. Whelan K. Mechanisms and effectiveness of prebiotics in modifying the gastrointestinal microbiota for the management of digestive disorders. Proc Nutr Soc 2013;72:288-98. https://doi.org/10.1017/S0029665113001262
  31. Lewin GR, Carlos C, Chevrette MG, et al. Evolution and ecology of Actinobacteria and their bioenergy applications. Annu Rev Microbiol 2016;70: 235-54. https://doi.org/10.1146/annurev-micro-102215-095748
  32. Garrido D, Ruiz-Moyano S, Kirmiz N, et al. A novel gene cluster allows preferential utilization of fucosylated milk oligosaccharides in Bifidobacterium longum subsp. longum SC596. Sci Rep 2016;6:35045. https://doi.org/10.1038/srep35045
  33. Rodriguez CI, Martiny JBH. Evolutionary relationships among bifidobacteria and their hosts and environments. BMC Genomics 2020;21:26. https://doi.org/10.1186/s12864-019-6435-1
  34. Manafi M, Hedayati M, Yari M. Aflatoxicosis and herbal detoxification: the effectiveness of thyme essence on performance parameters and antibody titers of commercial broilers fed Aflatoxin B1. Res Zool 2014;4:43-50.
  35. Medvecky M, Cejkova D, Polansky O, et al. Whole genome sequencing and function prediction of 133 gut anaerobes isolated from chicken caecum in pure cultures. BMC Genomics 2018;19:561. https://doi.org/10.1186/s12864-018-4959-4
  36. Rychlik I. Composition and function of chicken gut microbiota. Animals (Basel). 2020;10:103. https://doi.org/10.3390/ani10010103