Xanthine Dehydrogenase Is a Modulator of Dopaminergic Neurodegeneration in Response to Bacterial Metabolite Exposure in .

Oxidative stress is a contributing factor to Parkinson's disease (PD). Considering the prevalence of sporadic PD, environmental exposures are postulated to increase reactive oxygen species and either incite or exacerbate neurodegeneration. We previously determined that exposure to the common soil bacterium, (), enhanced oxidative stress and mitochondrial dysfunction in , leading to dopaminergic (DA) neurodegeneration. Here, metabolite exposure in was followed by RNA-Seq analysis. Half of the differentially identified genes (DEGs) were associated with the transcription factor DAF-16 (FOXO), which is a key node in regulating stress response. Our DEGs were enriched for Phase I (CYP) and Phase II (UGT) detoxification genes and non-CYP Phase I enzymes associated with oxidative metabolism, including the downregulated xanthine dehydrogenase gene, -. The XDH-1 enzyme exhibits reversible interconversion to xanthine oxidase (XO) in response to calcium. metabolite exposure enhanced XO activity in . The chelation of calcium diminishes the conversion of XDH-1 to XO and results in neuroprotection from exposure, whereas CaCl supplementation enhanced neurodegeneration. These results suggest a defense mechanism that delimits the pool of XDH-1 available for interconversion to XO, and associated ROS production, in response to metabolite exposure.