Teagasc Food Research Centre, Moorepark, Fermoy, Co, Cork, Ireland.
APC Microbiome Institute, University College Cork, Co, Cork, Ireland.
Sci Rep. 2019 Aug 23;9(1):12324. doi: 10.1038/s41598-019-48784-z.
Increasing evidence point to the relevance of intestinal disfunction and changes in the microbiome composition during chronic liver disease. More specifically, recent studies have highlighted that cholestatic diseases associate with a reduction in the microbiome diversity in patients. Still, the dynamics of the changes in the microbiome composition observed, as well as their implication in contributing to the pathogenesis of this disease remain largely undefined. Hence, experimental mouse models resembling the human pathogenesis are crucial to move forward our understanding on the mechanisms underpinning cholestatic disease and to enable the development of effective therapeutics. Our results show that the bile duct ligation (BDL) experimental model of cholestasis leads to rapid and significant changes in the microbiome diversity, with more than 100 OTUs being significantly different in faecal samples obtained from WT mice at 3 days and 7 days after BDL when compared to control animals. Changes in the microbial composition in mice after BDL included the enrichment of Akkermansia, Prevotella, Bacteroides and unclassified Ruminococcaceae in parallel with a drastic reduction of the presence of Faecalibacterium prausnitzii. In conclusion, our results support that bile duct ligation induces changes in the microbiome that partly resemble the gut microbial changes observed during human cholestatic disease.
越来越多的证据表明,在慢性肝病期间,肠道功能障碍和微生物组组成的变化与疾病相关。更具体地说,最近的研究强调,胆汁淤积性疾病与患者微生物组多样性的减少有关。然而,观察到的微生物组组成变化的动态及其对疾病发病机制的影响在很大程度上仍未得到明确界定。因此,类似于人类发病机制的实验性小鼠模型对于深入了解胆汁淤积性疾病的潜在机制以及开发有效的治疗方法至关重要。我们的研究结果表明,胆管结扎(BDL)胆汁淤积实验模型导致微生物组多样性的快速和显著变化,与对照组动物相比,WT 小鼠在 BDL 后 3 天和 7 天获得的粪便样本中,有超过 100 个 OTU 存在显著差异。BDL 后小鼠微生物组成的变化包括 Akkermansia、Prevotella、Bacteroides 和未分类的 Ruminococcaceae 的富集,同时 Faecalibacterium prausnitzii 的存在急剧减少。总之,我们的研究结果支持胆管结扎会诱导微生物组发生变化,这些变化部分类似于人类胆汁淤积性疾病中观察到的肠道微生物变化。