Mulberry leaf supplementation inhibits skatole deposition by regulating gut microbiota and upregulating liver cytochrome P450 1A1 expression in finishing pigs

IF 6.3
Yuqing Sun , Xiaoming Men , Tianbao Lin , Bo Deng , Shi Zhong , Jinxi Huo , Kaipeng Qin , Zhiqiang Lv , Ziwei Xu , Yougui Li
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Abstract

Skatole, a strong fecal odor substance, is generated through microbial degradation of tryptophan in the animal hindgut. It easily accumulates in adipose tissue and affects meat quality. In this study, the effect of mulberry leaf supplementation on skatole in finishing pigs was studied. In a 35-day trial, 20 finishing pigs (barrows and gilts) were fed with a basal diet or basal diet with 6% mulberry leaves. Growth performance of the pigs (n = 10) was automatically recorded by a performance-testing feeder system and 8 pigs in each treatment were slaughtered and sampled for the remaining tests. Skatole and short-chain fatty acids were detected using HPLC and gas chromatography, respectively. Fecal microbiota were analyzed using 16S rRNA gene sequencing. The metabolomics analysis of feces and serum was performed with UHPLC-MS/MS. The major cytochrome P450 (CYP) enzymes that catalyze skatole degradation in the liver were tested by using RT-PCR and Western blot. Effects of major bioactive compounds in mulberry leaves on the CYP genes were verified in the hepatic cell line HepG2 in an in vitro test (n = 3). In finishing pigs, mulberry leaf supplementation had no significant effect on the average daily gain, average daily feed intake, and feed conversion ratio (P > 0.05), but reduced skatole levels in feces, serum, and backfat (P < 0.05), and increased acetic acid levels in feces (P = 0.027). Mulberry leaf supplementation decreased the relative abundance of the skatole-producing bacteria Megasphaera and Olsenella (P < 0.05). Indole-3-acetic acid, the intermediate that is essential for skatole production, was significantly reduced in feces by mulberry leaf supplementation (P < 0.05) and was positively correlated with skatole content in feces (P = 0.004). In pigs treated with mulberry leaves, liver CYP1A1 expression was increased (P < 0.05) and was negatively correlated with skatole content in backfat (P = 0.045). The in vitro test demonstrated that mulberry leaf polyphenols and polysaccharides could directly stimulate CYP1A1 expression in hepatic cells. These findings suggest that mulberry leaf supplementation reduces skatole production and deposition in finishing pigs by regulating the gut microbiota and promoting skatole degradation in liver.

Abstract Image

添加桑叶通过调节肠道菌群和上调肝脏细胞色素P450 1A1表达抑制育肥猪粪臭素沉积
粪臭是一种强烈的粪便气味物质,是由动物后肠中色氨酸的微生物降解产生的。它很容易积聚在脂肪组织中,影响肉的品质。本试验研究了添加桑叶对育肥猪粪臭素的影响。在35 d的试验中,20头肥育猪(母猪和后备猪)分别饲喂基础饲粮或添加6%桑叶的基础饲粮。性能测试饲养系统自动记录10头猪的生长性能,每个处理屠宰8头猪,取样进行剩余试验。采用高效液相色谱法和气相色谱法分别检测粪臭素和短链脂肪酸。采用16S rRNA基因测序法分析粪便微生物群。采用UHPLC-MS/MS对粪便和血清进行代谢组学分析。采用RT-PCR和Western blot检测肝组织中催化粪臭素降解的主要细胞色素P450 (CYP)酶。体外实验(n = 3)验证了桑叶中主要生物活性化合物对肝脏细胞系HepG2 CYP基因的影响。在育肥猪中,添加桑叶对平均日增重、平均日采食量和饲料系数(P >0.05),但粪便、血清和背脂的粪臭素水平降低(P <0.05),粪便中乙酸水平升高(P = 0.027)。添加桑叶降低了产skatole细菌Megasphaera和Olsenella的相对丰度(P <0.05)。在粪便中添加桑叶显著降低了粪臭素生产所必需的中间体吲哚-3-乙酸(P <0.05),与粪便粪臭素含量呈正相关(P = 0.004)。桑叶处理的猪肝脏CYP1A1表达升高(P <0.05),与背脂肪中粪臭素含量呈负相关(P = 0.045)。体外实验表明,桑叶多酚和桑叶多糖可直接刺激肝细胞CYP1A1的表达。上述结果表明,添加桑叶可通过调节肠道菌群和促进肝脏粪臭素降解来减少育肥猪粪臭素的产生和沉积。
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来源期刊
Animal Nutrition
Animal Nutrition Animal Science and Zoology
CiteScore
9.70
自引率
0.00%
发文量
542
审稿时长
65 days
期刊介绍: Animal Nutrition encompasses the full gamut of animal nutritional sciences and reviews including, but not limited to, fundamental aspects of animal nutrition such as nutritional requirements, metabolic studies, body composition, energetics, immunology, neuroscience, microbiology, genetics and molecular and cell biology related to primarily to the nutrition of farm animals and aquatic species. More applied aspects of animal nutrition, such as the evaluation of novel ingredients, feed additives and feed safety will also be considered but it is expected that such studies will have a strong nutritional focus. Animal Nutrition is indexed in SCIE, PubMed Central, Scopus, DOAJ, etc.
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