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Effects of dietary supplementation of polysaccharide from Agaricus blazei Murr on productive performance, egg quality, blood metabolites, intestinal morphology and microbiota of Korean quail

  • Liang Hong (Tianjin Key Laboratory of Agricultural Animal Breeding and Healthy Husbandry, College of Animal Science and Veterinary Medicine, Tianjin Agricultural University) ;
  • Zheng Ma (Tianjin Key Laboratory of Agricultural Animal Breeding and Healthy Husbandry, College of Animal Science and Veterinary Medicine, Tianjin Agricultural University) ;
  • Xueyi Jing (Tianjin Key Laboratory of Agricultural Animal Breeding and Healthy Husbandry, College of Animal Science and Veterinary Medicine, Tianjin Agricultural University) ;
  • Hua Yang (Tianjin Key Laboratory of Agricultural Animal Breeding and Healthy Husbandry, College of Animal Science and Veterinary Medicine, Tianjin Agricultural University) ;
  • Jifei Ma (Tianjin Key Laboratory of Agricultural Animal Breeding and Healthy Husbandry, College of Animal Science and Veterinary Medicine, Tianjin Agricultural University) ;
  • Lei Pu (Tianjin Key Laboratory of Agricultural Animal Breeding and Healthy Husbandry, College of Animal Science and Veterinary Medicine, Tianjin Agricultural University) ;
  • Jianbin Zhang (Tianjin Key Laboratory of Agricultural Animal Breeding and Healthy Husbandry, College of Animal Science and Veterinary Medicine, Tianjin Agricultural University)
  • Received : 2023.10.24
  • Accepted : 2024.02.08
  • Published : 2024.08.01

Abstract

Objective: This study aimed to investigate the effects of dietary supplementation with Agaricus blazei polysaccharide (ABP) at varying concentrations on the performance, egg quality, blood biochemistry, intestinal morphology, and microflora of quail. Methods: The study involved a total of 2,700 Korean quails, which were randomly divided into three groups. The measured variables encompassed productive performance, egg parameters, carcass parameters, serum metabolites, immune response parameters, antioxidative properties, and gut microbiome. Results: The addition of ABP did not have a significant effect on average daily feed intake. However, it was found to increase the average daily egg weight and egg production rate, reduce the feed-egg ratio. There were no significant impacts on egg quality measures such as egg shape index, egg yolk index and color, egg yolk and protein content. However, ABP supplementation significantly increased the Hough unit (p<0.01) and decreased the rate of unqualified eggs (p<0.01). Regarding serum parameters, the inclusion led to an increase in total protein concentration (p<0.05) and a reduction in low-density lipoprotein cholesterol (p<0.05). There were no significant effects observed on immune indicators such as immunoglobulin A (IgA) and IgM. ABP supplementation increased the levels of serum antioxidant indicators, including glutathione peroxidase, total superoxide dismutase (p<0.05), and total antioxidant capacity colorimeter (p<0.05). Furthermore, ABP supplementation significantly elevated the intramuscular fatty acid content in quail meat. Additionally, ABP supplementation demonstrated a significant improvement in the diversity of gut microbiota and induced alterations in the composition of the gut microbiota. Conclusion: The findings of this study indicate that dietary supplementation of ABP enhanced production performance and antioxidant capacity while increasing the levels of polyunsaturated fatty acids in quail muscle.

Keywords

References

  1. Baer J, Lansford R, Cheng K. Japanese quail as a laboratory animal model. In: Fox JG, Anderson LC, Otto GM, Pritchett-Corning KR, Whary MT, editors. 3rd ed. Laboratory animal medicine. Philadelphia, USA: Elsevier; 2015. pp. 1087-108. https://doi.org/10.1016/B978-0-12-409527-4.00022-5 
  2. Huss D, Poynter G, Lansford R. Japanese quail (Coturnix japonica) as a laboratory animal model. Lab Anim (NY) 2008;37:513-9. https://doi.org/10.1038/laban1108-513 
  3. Tolik D, Poawska E, Charuta A, Nowaczewski S, Cooper R. Characteristics of egg parts, chemical composition and nutritive value of Japanese quail eggs-a review. Folia Biol (Krakow) 2014;62:287-92. https://doi.org/10.3409/fb62_4.287 
  4. Vargas-Sanchez RD, Ibarra-Arias FJ, del Mar Torres-Martinez B, Sanchez-Escalante A, Torrescano-Urrutia GR. Use of natural ingredients in Japanese quail diet and their effect on carcass and meat quality-a review. Asian-Australas J Anim Sci 2019;32:1641-56. https://doi.org/10.5713/ajas.18.0800 
  5. Murphy EJ, Rezoagli E, Pogue R, et al. Immunomodulatory activity of β-glucan polysaccharides isolated from different species of mushroom-a potential treatment for inflammatory lung conditions. Sci Total Environ 2022;809:152177. https://doi.org/10.1016/j.scitotenv.2021.152177 
  6. Liu M, Li S, Wang X, et al. Characterization, anti-oxidation and anti-inflammation of polysaccharides by Hypsizygus marmoreus against LPS-induced toxicity on lung. Int J Biol Macromol 2018;111:121-8. https://doi.org/10.1016/j.ijbiomac.2018.01.010 
  7. Ma G, Kimatu BM, Yang W, et al. Preparation of newly identified polysaccharide from Pleurotus eryngii and its anti-inflammation activities potential. J Food Sci 2020;85:2822-31. https://doi.org/10.1111/1750-3841.15375 
  8. Ma G, Du H, Hu Q, Yang W, Pei F, Xiao H. Health benefits of edible mushroom polysaccharides and associated gut microbiota regulation. Crit Rev Food Sci Nutr 2021;62:664663. https://doi.org/10.1080/10408398.2021.1903385 
  9. O'Fallon JV, Busboom JR, Nelson ML, Gaskins CT. A direct method for fatty acid methyl ester synthesis: application to wet meat tissues, oils, and feedstuffs. J Anim Sci 2007;85:1511-21. https://doi.org/10.2527/jas.2006-491 
  10. Bancroft JD, Gamble M. Theory and practice of histological techniques. Philadelphia, PA, USA: Elsevier; 2008. pp. 121-34. https://doi.org/10.1016/B978-0-443-10279-0.50016-6 
  11. Li R, Zhang L, Tang Z, et al. Effects of fungal polysaccharide on oxidative damage and TLR4 pathway to the central immune organs in cadmium intoxication in chickens. Biol Trace Elem Res 2019;191:464-73. https://doi.org/10.1007/s12011-0181627-0 
  12. Song Y, Zhang R, Wang H, Yan Y, Ming G. Protective effect of Agaricus blazei polysaccharide against cadmium-induced damage on the testis of chicken. Biol Trace Elem Res 2018;184:491-500. https://doi.org/10.1007/s12011-017-1196-7 
  13. Hetland G, Johnson E, Lyberg T, Kvalheim G. The mushroom Agaricus blazei murill elicits medicinal effects on tumor, infection, allergy, and inflammation through its modulation of innate immunity and amelioration of Th1/Th2 imbalance and inflammation. Adv Pharmacol Pharm Sci 2011;2011:157015. https://doi.org/10.1155/2011/157015 
  14. Williams KC. Some factors affecting albumen quality with particular reference to Haugh unit score. Worlds Poult Sci J 1992;48:5-16. https://doi.org/10.1079/WPS19920002 
  15. Li H, Hou Y, Chen J, et al. Dietary naringin supplementation on laying performance and antioxidant capacity of Three-Yellow breeder hens during the late laying period. Poult Sci 2022;101:102023. https://doi.org/10.1016/j.psj.2022.102023 
  16. Hussein AS, Ayoub MA, Elhwetiy AY, Ghurair JA, Sulaiman M, Habib HM. Effect of dietary inclusion of sugar syrup on production performance, egg quality and blood biochemical parameters in laying hens. Anim Nutr 2018;4:59-64. https://doi.org/10.1016/j.aninu.2017.11.001 
  17. Attia YA, Abd El-Hamid AEHE, Abedalla AA, et al. Laying performance, digestibility and plasma hormones in laying hens exposed to chronic heat stress as affected by betaine, vitamin C, and/or vitamin E supplementation. Springerplus 2016;5:1619. https://doi.org/10.1186/s40064-016-3304-0 
  18. Li Y, Lu X, Li X, et al. Effects of Agaricus blazei murrill polysaccharides on hyperlipidemic rats by regulation of intestinal microflora. Food Sci Nutr 2020;8:2758-72. https://doi.org/10.1002/fsn3.1568 
  19. Jia S, Li F, Liu Y, et al. Effects of extraction methods on the antioxidant activities of polysaccharides from Agaricus blazei Murrill. Int J Biol Macromol 2013;62:66-9. https://doi.org/10.1016/j.ijbiomac.2013.08.031 
  20. Xiong X, Yang H, Hu X, et al. Differential proteome analysis along jejunal crypt-villus axis in piglets. Front Biosci (Landmark Ed) 2016;21:343-63. https://doi.org/10.2741/4392 
  21. Bai M, Wang L, Liu H, et al. Imbalanced dietary methionine-to-sulfur amino acid ratio can affect amino acid profiles, antioxidant capacity, and intestinal morphology of piglets. Anim Nutr 2020;6:447-56. https://doi.org/10.1016/j.aninu.2020.03.009 
  22. Nasr MAF, Ali E-SM, Hussein MA. Performance, carcass traits, meat quality and amino acid profile of different Japanese quails strains. J Food Sci Technol 2017;54:4189-96. https://doi.org/10.1007/s13197-017-2881-4 
  23. Mirshekar R, Dastar B, Shargh MS. Supplementing flaxseed oil for long periods improved carcass quality and breast fatty acid profile in Japanese quail. Animal (Basel) 2021;15:100104. https://doi.org/10.1016/j.animal.2020.100104 
  24. Sakamoto MI, Murakami AE, Fernandes AM, Ospina-Rojas IC, Nunes KC, Hirata AK. Performance and serum biochemical profile of Japanese quail supplemented with silymarin and contaminated with aflatoxin B1. Poult Sci 2018;97:159-66. https://doi.org/10.3382/ps/pex277 
  25. Duan Y, Zhong Y, Xiao H, et al. Gut microbiota mediates the protective effects of dietary α-hydroxy-α-methylbutyrate (HMB) against obesity induced by high-fat diets. FASEB J 2019;33:10019-33. https://doi.org/10.1096/fj.201900665RR 
  26. Kolatorova L, Lapcak O, Starka L. Phytoestrogens and the intestinal microbiome. Physiol Res 2018;67:S401-8. https://doi.org/10.33549/physiolres.934022 
  27. Williams CJ, Torquati L, Li Z, et al. Oligofructose-Enriched inulin intake, gut microbiome characteristics, and the VO2 Peak response to high-intensity interval training in healthy inactive adults. J Nutr 2022;152:680-9. https://doi.org/10.1093/jn/nxab426 
  28. Kiewiet MBG, Elderman ME, El Aidy S, et al. Flexibility of gut microbiota in ageing individuals during dietary fiber long-chain inulin intake. Mol Nutr Food Res 2021;65:2000390. https://doi.org/10.1002/mnfr.202000390 
  29. Ye J, Zhang C, Fan Q, et al. Antrodia cinnamomea polysaccharide improves liver antioxidant, anti-inflammatory capacity, and cecal flora structure of slow-growing broiler breeds challenged with lipopolysaccharide. Front Vet Sci 2022;9:994782. https://doi.org/10.3389/fvets.2022.994782 
  30. Bernardshaw S, Johnson E, Hetland G. An extract of the mushroom Agaricus blazei murill administered orally protects against systemic Streptococcus pneumoniae infection in mice. Scand J Immunol 2005;62:393-8. https://doi.org/10.1111/j.1365-3083.2005.01667.x 
  31. Kim JH, Tam CC, Chan KL, et al. Antimicrobial efficacy of edible mushroom extracts: assessment of fungal resistance. Appl Sci 2022;12:4591. https://doi.org/10.3390/app12094591 
  32. Geirnaert A, Calatayud M, Grootaert C, et al. Butyrate-producing bacteria supplemented in vitro to Crohn's disease patient microbiota increased butyrate production and enhanced intestinal epithelial barrier integrity. Sci Rep 2017;7:11450. https://doi.org/10.1038/s41598-017-11734-8 
  33. Nielsen DSG, Jensen BB, Theil PK, Nielsen TS, Knudsen KEB, Purup S. Effect of butyrate and fermentation products on epithelial integrity in a mucus-secreting human colon cell line. J Funct Foods 2018;40:9-17. https://doi.org/10.1016/j.jff.2017.10.023 
  34. Ren W, Yan H, Yu B, et al. Prevotella-rich enterotype may benefit gut health in finishing pigs fed diet with a high amylose-to-amylopectin ratio. Anim Nutr 2021;7:400-11. https://doi.org/10.1016/j.aninu.2020.08.007 
  35. Yeoh YK, Sun Y, Ip LYT, et al. Prevotella species in the human gut is primarily comprised of Prevotella copri, Prevotella stercorea and related lineages. Sci Rep 2022;12:9055. https://doi.org/10.1038/s41598-022-12721-4 
  36. Sergeant MJ, Constantinidou C, Cogan TA, Bedford MR, Penn CW, Pallen MJ. Extensive microbial and functional diversity within the chicken cecal microbiome. PLoS ONE 2014;9:e91941. https://doi.org/10.1371/journal.pone.0091941 
  37. Weitkunat K, Stuhlmann C, Postel A, et al. Short-chain fatty acids and inulin, but not guar gum, prevent diet-induced obesity and insulin resistance through differential mechanisms in mice. Sci Rep 2017;7:6109. https://doi.org/10.1038/s41598017-06447-x 
  38. Chu H, Duan Y, Yang L, Schnabl B. Small metabolites, possible big changes: a microbiota-centered view of non-alcoholic fatty liver disease. Gut 2019;68:359-70. https://doi.org/10.1136/gutjnl-2018-316307 
  39. Zhou L, Xiao X, Zhang Q, et al. Improved glucose and lipid metabolism in the early life of female offspring by maternal dietary genistein is associated with alterations in the gut microbiota. Front Endocrinol (Lausanne) 2018;9:516. https://doi.org/10.3389/fendo.2018.00516 
  40. Sun L, Jia H, Li J, et al. Cecal gut microbiota and metabolites might contribute to the severity of acute myocardial ischemia by impacting the intestinal permeability, oxidative stress, and energy metabolism. Front Microbiol 2019;10:1745. https://doi.org/10.3389/fmicb.2019.01745