Effects of dietary supplementation of polysaccharide from Agaricus blazei Murr on productive performance, egg quality, blood metabolites, intestinal morphology and microbiota of Korean quail
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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.
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.
참고문헌 (40)
- Baer J, "Laboratory animal medicine", pp.1087~1108 (2015), Elsevier
- Huss D, "Japanese quail(Coturnix japonica)as a laboratory animal model", Lab Anim(NY), 37, pp.513~519 (2008)[DOI]
- Tolik D, "Characteristics of egg parts, chemical composition and nutritive value of Japanese quail eggs–a review", Folia Biol(Krakow), 62, pp.287~292 (2014)[DOI]
- Vargas-Sánchez RD, "Use of natural ingredients in Japanese quail diet and their effect on carcass and meat quality—a review", Asian-Australas J Anim Sci, 32, pp.1641~1656 (2019)[DOI]
- Murphy EJ, "Immunomodulatory activity of β-glucan polysaccharides isolated from different species of mushroom–a potential treatment for inflammatory lung conditions", Sci Total Environ, 809, pp.152177~ (2022)[DOI]
- Liu M, "Characterization, anti-oxidation and anti-inflammation of polysaccharides by Hypsizygus marmoreus against LPS-induced toxicity on lung", Int J Biol Macromol, 111, pp.121~128 (2018)[DOI]
- Ma G, "Preparation of newly identified polysaccharide from Pleurotus eryngii and its anti-inflammation activities potential", J Food Sci, 85, pp.2822~2831 (2020)[DOI]
- Ma G, "Health benefits of edible mushroom polysaccharides and associated gut microbiota regulation", Crit Rev Food Sci Nutr, 62, pp.6646~6663 (2021)[DOI]
- O'Fallon JV, "A direct method for fatty acid methyl ester synthesis : application to wet meat tissues, oils, and feedstuffs", J Anim Sci, 85, pp.1511~1521 (2007)[DOI]
- Bancroft JD, "Theory and practice of histological techniques", pp.121~134 (2008), Elsevier
- Li R, "Effects of fungal polysaccharide on oxidative damage and TLR4 pathway to the central immune organs in cadmium intoxication in chickens", Biol Trace Elem Res, 191, pp.464~473 (2019)[DOI]
- Song Y, "Protective effect of Agaricus blazei polysaccharide against cadmium-induced damage on the testis of chicken", Biol Trace Elem Res, 184, pp.491~500 (2018)[DOI]
- Hetland 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, 2011, pp.2011, 157015~
- Williams KC, "Some factors affecting albumen quality with particular reference to Haugh unit score", Worlds Poult Sci J, 48, pp.5~16 (1992)[DOI]
- Li H, "Dietary naringin supplementation on laying performance and antioxidant capacity of Three-Yellow breeder hens during the late laying period", Poult Sci, 101, pp.102023~ (2022)[DOI]
- Hussein AS, "Effect of dietary inclusion of sugar syrup on production performance, egg quality and blood biochemical parameters in laying hens", Anim Nutr, 4, pp.59~64 (2018)[DOI]
- Attia YA, "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, 2016, pp.5, 1619~
- Li Y, "Effects of Agaricus blazei murrill polysaccharides on hyperlipidemic rats by regulation of intestinal microflora", Food Sci Nutr, 8, pp.2758~2772 (2020)[DOI]
- Jia S, "Effects of extraction methods on the antioxidant activities of polysaccharides from Agaricus blazei Murrill", Int J Biol Macromol, 62, pp.66~69 (2013)[DOI]
- Xiong X, "Differential proteome analysis along jejunal crypt-villus axis in piglets", Front Biosci(Landmark Ed), 21, pp.343~363 (2016)[DOI]
- Bai M, "Imbalanced dietary methionine-to-sulfur amino acid ratio can affect amino acid profiles, antioxidant capacity, and intestinal morphology of piglets", Anim Nutr, 6, pp.447~456 (2020)[DOI]
- Nasr MAF, "Performance, carcass traits, meat quality and amino acid profile of different Japanese quails strains", J Food Sci Technol, 54, pp.4189~4196 (2017)[DOI]
- Mirshekar R, "Supplementing flaxseed oil for long periods improved carcass quality and breast fatty acid profile in Japanese quail", Animal(Basel), 15, pp.100104~ (2021)[DOI]
- Sakamoto MI, "Performance and serum biochemical profile of Japanese quail supplemented with silymarin and contaminated with aflatoxin B1", Poult Sci, 97, pp.159~166 (2018)[DOI]
- Duan Y, "Gut microbiota mediates the protective effects of dietary β-hydroxy-β-methylbutyrate(HMB)against obesity induced by high-fat diets", FASEB J, 33, pp.10019~10033 (2019)[DOI]
- Kolátorová L, "Phytoestrogens and the intestinal microbiome", Physiol Res, 67, pp.S401~S408 (2018)[DOI]
- Williams CJ, "Oligofructose-Enriched inulin intake, gut microbiome characteristics, and the VO2Peak response to high-intensity interval training in healthy inactive adults", J Nutr, 152, pp.680~689 (2022)[DOI]
- Kiewiet MBG, "Flexibility of gut microbiota in ageing individuals during dietary fiber long-chain inulin intake", Mol Nutr Food Res, 65, pp.2000390~ (2021)[DOI]
- Ye J, "Antrodia cinnamomea polysaccharide improves liver antioxidant, anti-inflammatory capacity, and cecal flora structure of slow-growing broiler breeds challenged with lipopolysaccharide", Front Vet Sci, 9, pp.994782~ (2022)[DOI]
- Bernardshaw S, "An extract of the mushroom Agaricus blazei murill administered orally protects against systemic Streptococcus pneumoniae infection in mice", Scand J Immunol, 62, pp.393~398 (2005)[DOI]
- Kim JH, "Antimicrobial efficacy of edible mushroom extracts : assessment of fungal resistance", Appl Sci, 12, pp.4591~ (2022)[DOI]
- Geirnaert A, "Butyrate-producing bacteria supplemented in vitro to Crohn’s disease patient microbiota increased butyrate production and enhanced intestinal epithelial barrier integrity", Sci Rep, 7, pp.11450~ (2017)[DOI]
- Nielsen DSG, "Effect of butyrate and fermentation products on epithelial integrity in a mucus-secreting human colon cell line", J Funct Foods, 40, pp.9~17 (2018)[DOI]
- Ren W, "Prevotella-rich enterotype may benefit gut health in finishing pigs fed diet with a high amylose-to-amylopectin ratio", Anim Nutr, 7, pp.400~411 (2021)[DOI]
- Yeoh YK, "Prevotella species in the human gut is primarily comprised of Prevotella copri, Prevotella stercorea and related lineages", Sci Rep, 12, pp.9055~ (2022)[DOI]
- Sergeant MJ, "Extensive microbial and functional diversity within the chicken cecal microbiome", PLoS ONE, 9, pp.e91941~ (2014)[DOI]
- Weitkunat K, "Short-chain fatty acids and inulin, but not guar gum, prevent diet-induced obesity and insulin resistance through differential mechanisms in mice", Sci Rep, 7, pp.6109~ (2017)[DOI]
- Chu H, "Small metabolites, possible big changes : a microbiota-centered view of non-alcoholic fatty liver disease", Gut, 68, pp.359~370 (2019)[DOI]
- Zhou L, "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), 9, pp.516~ (2018)[DOI]
- Sun L, "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, 10, pp.1745~ (2019)[DOI]
