A secondary bile acid from microbiota metabolism attenuates ileitis and bile acid reduction in subclinical necrotic enteritis in chickens

被引:22
|
作者
Bansal, Mohit [1 ]
Fu, Ying [1 ,2 ]
Alrubaye, Bilal [1 ,2 ]
Abraha, Mussie [1 ]
Almansour, Ayidh [1 ,2 ]
Gupta, Anamika [1 ]
Liyanage, Rohana [3 ]
Wang, Hong [1 ]
Hargis, Billy [1 ]
Sun, Xiaolun [1 ,2 ,3 ]
机构
[1] Univ Arkansas, Ctr Excellence Poultry Sci, 1260 W Maple St O409, Fayetteville, AR 72701 USA
[2] Univ Arkansas, CEMB, Fayetteville, AR 72701 USA
[3] Univ Arkansas, Dept Chem, Fayetteville, AR 72701 USA
基金
美国食品与农业研究所;
关键词
Bile acid; Chicken; Clostridium perfringens; Deoxycholic acid; Intestinal inflammation; Necrotic enteritis; CLOSTRIDIUM-PERFRINGENS STRAINS; NEGATIVE FEEDBACK-REGULATION; BROILER-CHICKENS; MALABSORPTION; INFECTIONS; PATHOLOGY;
D O I
10.1186/s40104-020-00441-6
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Background Clostridium perfringens-induced chicken necrotic enteritis (NE) is responsible for substantial economic losses worldwide annually. Recently, as a result of antibiotic growth promoter prohibition, the prevalence of NE in chickens has reemerged. This study was aimed to reduce NE through titrating dietary deoxycholic acid (DCA) as an effective antimicrobial alternative. Materials and methods Day-old broiler chicks were assigned to six groups and fed diets supplemented with 0 (basal diet), 0.8, 1.0 and 1.5 g/kg (on top of basal diet) DCA. The birds were challenged with Eimeria maxima (20,000 oocysts/bird) at d 18 and C. perfringens (10(9) CFU/bird per day) at d 23, 24, and 25 to induce NE. The birds were sacrificed at d 26 when ileal tissue and digesta were collected for analyzing histopathology, mRNA accumulation and C. perfringens colonization by real-time PCR, targeted metabolomics of bile acids, fluorescence in situ hybridization (FISH), or terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay. Results At the cellular level, birds infected with E. maxima and C. perfringens developed subclinical NE and showed shortening villi, crypt hyperplasia and immune cell infiltration in ileum. Dietary DCA alleviated the NE-induced ileal inflammation in a dose-dependent manner compared to NE control birds. Consistent with the increased histopathological scores, subclinical NE birds suffered body weight gain reduction compared to the uninfected birds, an effect attenuated with increased doses of dietary DCA. At the molecular level, the highest dose of DCA at 1.5 g/kg reduced C. perfringens luminal colonization compared to NE birds using PCR and FISH. Furthermore, the dietary DCA reduced subclinical NE-induced intestinal inflammatory gene expression and cell apoptosis using PCR and TUNEL assays. Upon further examining ileal bile acid pool through targeted metabolomics, subclinical NE reduced the total bile acid level in ileal digesta compared to uninfected birds. Notably, dietary DCA increased total bile acid and DCA levels in a dose-dependent manner compared to NE birds. Conclusion These results indicate that DCA attenuates NE-induced intestinal inflammation and bile acid reduction and could be an effective antimicrobial alternative against the intestinal disease.
引用
收藏
页数:10
相关论文
共 50 条
  • [41] Microbiota-accessible fiber activates short-chain fatty acid and bile acid metabolism to improve intestinal mucus barrier in broiler chickens
    Yang, Jiantao
    Qin, Kailong
    Sun, Yanpeng
    Yang, Xiaojun
    MICROBIOLOGY SPECTRUM, 2024, 12 (01):
  • [42] Tauroursodeoxycholic Acid Improves Nonalcoholic Fatty Liver Disease by Regulating Gut Microbiota and Bile Acid Metabolism
    Wang, Huan
    Guo, Yi
    Han, Weiting
    Liang, Meng
    Xiao, Xiao
    Jiang, Xiaowen
    Yu, Wenhui
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2024, 72 (36) : 20194 - 20210
  • [43] L-Theanine regulates lipid metabolism by modulating gut microbiota and bile acid metabolism
    Xu, Wei
    Kong, Yingying
    Zhang, Tuo
    Gong, Zhihua
    Xiao, Wenjun
    JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, 2023, 103 (03) : 1283 - 1293
  • [44] Amuc attenuates high-fat diet-induced metabolic disorders linked to the regulation of fatty acid metabolism, bile acid metabolism, and the gut microbiota in mice
    Song, Zhuan
    Chen, Jingqing
    Ji, Yun
    Yang, Qing
    Chen, Yinfeng
    Wang, Fengchao
    Wu, Zhenlong
    INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2023, 242
  • [45] Impact of Gut Microbiota-Mediated Bile Acid Metabolism on the Solubilization Capacity of Bile Salt Micelles and Drug Solubility
    Enright, Elaine F.
    Joyce, Susan A.
    Gahan, Cormac G. M.
    Griffin, Brendan T.
    MOLECULAR PHARMACEUTICS, 2017, 14 (04) : 1251 - 1263
  • [46] Heat stress-induced dysbiosis of the gut microbiota impairs spermatogenesis by regulating secondary bile acid metabolism in the gut
    He, Guitian
    Zhang, Boqi
    Yi, Kangle
    Chen, Tong
    Shen, Caomeihui
    Cao, Maosheng
    Wang, Nan
    Zong, Jinxin
    Wang, Yueying
    Liu, Kening
    Chang, Fuqiang
    Chen, Xue
    Chen, Lu
    Luo, Yuxin
    Meng, Yang
    Li, Chunjin
    Zhou, Xu
    SCIENCE OF THE TOTAL ENVIRONMENT, 2024, 937
  • [47] Polysaccharides from Enteromorpha prolifera alleviate hypercholesterolemia via modulating the gut microbiota and bile acid metabolism
    Yang, Changwei
    Huang, Shiying
    Lin, Zaigang
    Chen, Hui
    Xu, Caihong
    Lin, Yiqi
    Sun, Huiyu
    Huang, Fang
    Lin, Dai
    Guo, Fuchuan
    FOOD & FUNCTION, 2022, 13 (23) : 12194 - 12207
  • [48] Aryl hydrocarbon receptor attenuates cholestatic liver injury by regulating bile acid metabolism
    Han, Qi
    Yan, Xuzhen
    Wang, Likai
    Zhang, Ning
    Zhang, Wen
    Li, Hong
    Chen, Wei
    You, Hong
    Yang, Aiting
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2023, 682 : 259 - 265
  • [49] Sex Matters: From Bile Acid Metabolism to Liver Cancer
    Chauhan, Sachin Kumar Singh
    Heinrich, Bernd
    CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY, 2024, 17 (05): : 877 - 878
  • [50] Regulation of Bile Acid Metabolism: New Insights From Inside
    Quintero, Pablo
    Arrese, Marco
    HEPATOLOGY, 2013, 58 (05) : 1850 - 1853