Department of Animal Science, The University of Tennessee, 2506, River Drive, Knoxville, USA.
APC Microbiome Ireland, University College Cork, Cork, Ireland.
Sci Rep. 2020 Mar 18;10(1):4941. doi: 10.1038/s41598-020-61723-7.
Gut microbial enzymes, bile salt hydrolases (BSHs) are the gateway enzymes for bile acid (BA) modification in the gut. This activity is a promising target for developing innovative non-antibiotic growth promoters to enhance animal production and health. Compelling evidence has shown that inhibition of BSH activity should enhance weight gain by altering the BA pool, host signalling and lipid metabolism. We recently identified a panel of promising BSH inhibitors. Here, we address the potential of them as alternative, effective, non-antibiotic feed additives, for commercial application, to promote animal growth using a chicken model. In this study, the in vivo efficacy of three BSH inhibitors (caffeic acid phenethylester, riboflavin, carnosic acid) were evaluated. 7-day old chicks (10 birds/group) were either untreated or they received one of the specific BSH inhibitors (25 mg/kg body weight) via oral gavage for 17 days. The chicks in treatment groups consistently displayed higher body weight gain than the untreated chicks. Metabolomic analysis demonstrated that BSH inhibitor treatment led to significant changes in both circulating and intestinal BA signatures in support of blunted intestinal BSH activity. Consistent with this finding, liver and intestinal tissue RNA-Seq analysis showed that carnosic acid treatment significantly altered expression of genes involved in lipid and bile acid metabolism. Taken together, this study validates microbial BSH activity inhibition as an alternative target and strategy to antibiotic treatment for animal growth promotion.
肠道微生物酶,胆盐水解酶(BSHs)是肠道中胆汁酸(BA)修饰的门户酶。这种活性是开发创新型非抗生素生长促进剂以提高动物生产和健康的有前途的目标。令人信服的证据表明,抑制 BSH 活性应该通过改变 BA 池、宿主信号和脂质代谢来增强体重增加。我们最近确定了一组有前途的 BSH 抑制剂。在这里,我们研究了它们作为替代、有效、非抗生素饲料添加剂的潜力,以使用鸡模型促进动物生长。在这项研究中,评估了三种 BSH 抑制剂(咖啡酸苯乙酯、核黄素、熊果酸)的体内功效。7 日龄小鸡(每组 10 只)未经处理或通过口服灌胃接受一种特定的 BSH 抑制剂(25mg/kg 体重)17 天。治疗组的小鸡体重持续增加,高于未处理的小鸡。代谢组学分析表明,BSH 抑制剂处理导致循环和肠道 BA 特征显著变化,支持肠道 BSH 活性减弱。与这一发现一致,肝和肠道组织 RNA-Seq 分析表明,熊果酸处理显著改变了参与脂质和胆汁酸代谢的基因的表达。总之,这项研究验证了微生物 BSH 活性抑制作为抗生素治疗促进动物生长的替代目标和策略。