Gut microbiome dysbiosis is associated with elevated toxic bile acids in Parkinson's disease

Li, P.; Killinger, B. A.; Beddows, I.; Ensink, E.; Yilmaz, A.; Lubben, N.; Lamp, J.; Schilthuis, M.; Vega, I. E.; Britschgi, M.; Pospisilik, A. J.; Brundin, P.; Brundin, L.; Graham, S.; Labrie, V.

doi:10.1101/2020.09.26.279851

bioRxiv · 10.1101/2020.09.26.279851

Gut microbiome dysbiosis is associated with elevated toxic bile acids in Parkinson's disease

Li, P.·Killinger, B. A.·Beddows, I.·Ensink, E.·Yilmaz, A.·Lubben, N.·Lamp, J.·Schilthuis, M.·Vega, I. E.·Britschgi, M.·Pospisilik, A. J.·Brundin, P.·Brundin, L.·Graham, S.·Labrie, V.

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Abstract

The gut microbiome can impact brain health and is altered in Parkinsons disease (PD) patients. Here, we investigate changes in the functional microbiome in the appendix of PD patients relative to controls by metatranscriptomic analysis. We find microbial dysbiosis affecting lipid metabolism, particularly an upregulation of bacteria responsible for secondary bile acid synthesis. Proteomic and transcript analysis corroborates a disruption in cholesterol homeostasis and lipid catabolism. Bile acid analysis reveals an increase in microbially-derived, toxic secondary bile acids. Synucleinopathy in mice induces similar microbiome alterations to those of PD patients. The mouse model of synucleinopathy has elevated DCA and LCA. An analysis of blood markers shows evidence of biliary abnormalities early in PD, including elevated alkaline phosphatase and bilirubin. Increased bilirubin levels are also evident before PD diagnosis. In sum, microbially-derived toxic bile acids are heightened in PD and biliary changes may even precede the onset of overt motor symptoms.

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Li, P., Killinger, B. A., Beddows, I., Ensink, E., Yilmaz, A., Lubben, N., Lamp, J., Schilthuis, M., Vega, I. E., Britschgi, M., Pospisilik, A. J., Brundin, P., Brundin, L., Graham, S., Labrie, V.. 2020-09-28. Gut microbiome dysbiosis is associated with elevated toxic bile acids in Parkinson's disease. https://doi.org/10.1101/2020.09.26.279851

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