Li Peipei, Killinger Bryan A, Ensink Elizabeth, Beddows Ian, Yilmaz Ali, Lubben Noah, Lamp Jared, Schilthuis Meghan, Vega Irving E, Woltjer Randy, Pospisilik J Andrew, Brundin Patrik, Brundin Lena, Graham Stewart F, Labrie Viviane
Department of Neurodegenerative Science, Van Andel Institute, Grand Rapids, MI 49503, USA.
Department of Neurological Sciences, Rush University Medical Center, Chicago, IL 60612, USA.
Metabolites. 2021 Jan 4;11(1):29. doi: 10.3390/metabo11010029.
The gut microbiome can impact brain health and is altered in Parkinson's disease (PD). The vermiform appendix is a lymphoid tissue in the cecum implicated in the storage and regulation of the gut microbiota. We sought to determine whether the appendix microbiome is altered in PD and to analyze the biological consequences of the microbial alterations. We investigated the changes in the functional microbiota in the appendix of PD patients relative to controls ( = 12 PD, 16 C) by metatranscriptomic analysis. We found microbial dysbiosis affecting lipid metabolism, including an upregulation of bacteria responsible for secondary bile acid synthesis. We then quantitatively measure changes in bile acid abundance in PD relative to the controls in the appendix ( = 15 PD, 12 C) and ileum ( = 20 PD, 20 C). Bile acid analysis in the PD appendix reveals an increase in hydrophobic and secondary bile acids, deoxycholic acid (DCA) and lithocholic acid (LCA). Further proteomic and transcriptomic analysis in the appendix and ileum corroborated these findings, highlighting changes in the PD gut that are consistent with a disruption in bile acid control, including alterations in mediators of cholesterol homeostasis and lipid metabolism. Microbially derived toxic bile acids are heightened in PD, which suggests biliary abnormalities may play a role in PD pathogenesis.
肠道微生物群可影响大脑健康,且在帕金森病(PD)中会发生改变。阑尾是盲肠中的一种淋巴组织,与肠道微生物群的储存和调节有关。我们试图确定PD患者的阑尾微生物群是否发生改变,并分析微生物改变的生物学后果。通过宏转录组分析,我们研究了PD患者(n = 12)相对于对照组(n = 16)阑尾中功能微生物群的变化。我们发现微生物失调影响脂质代谢,包括负责次级胆汁酸合成的细菌上调。然后,我们定量测量了PD患者相对于对照组在阑尾(n = 15 PD,12 C)和回肠(n = 20 PD,20 C)中胆汁酸丰度的变化。PD阑尾中的胆汁酸分析显示疏水性和次级胆汁酸、脱氧胆酸(DCA)和石胆酸(LCA)增加。阑尾和回肠的进一步蛋白质组学和转录组学分析证实了这些发现,突出了PD肠道中与胆汁酸控制破坏一致的变化,包括胆固醇稳态和脂质代谢介质的改变。PD中微生物衍生的有毒胆汁酸升高,这表明胆汁异常可能在PD发病机制中起作用。