Method for diagnosing parkinson's disease through bacterial metagenome analysis
A technology for Parkinson's disease and bacteria, applied in the direction of biochemical equipment and methods, microbial measurement/testing, etc., can solve problems such as movement disorders and uncomfortable movements
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Embodiment 1
[0055] Example 1. Analysis of In vivo Absorption, Distribution and Excretion Patterns of Enterobacteria and Bacteria-Derived Extracellular Vesicles
[0056] To assess whether enterobacteria and bacterial-derived extracellular vesicles are systemically absorbed through the gastrointestinal tract, experiments were performed using the following method. More specifically, 50 μg each of fluorescently labeled intestinal bacteria and extracellular vesicles (EVs) derived from the bacteria were orally administered to the gastrointestinal tract of mice, and were administered at 0 hours, and at 5 minutes, 3 hours, and 6 hours. Fluorescence was measured after 1 hour and 12 hours. As a result of observing the whole-body images of mice, as shown in Fig. 1A, bacteria were not absorbed systemically at the time of administration, but 5 minutes after administration, EVs derived from bacteria were absorbed systemically, and 3 hours after administration, at Strong fluorescence was observed in th...
Embodiment 2
[0058] Example 2. Vesicle Isolation and DNA Extraction from Urine
[0059] To isolate extracellular vesicles from urine and extract DNA, urine was first added to a 10 ml tube, centrifuged at 3500 x g for 10 minutes at 4°C, the suspension was pelleted, and only the supernatant was collected, which was Place in a new 10ml tube. The collected supernatant was filtered with a 0.22 μm filter to remove bacteria and impurities, then placed in a central centrifugal filter (50 kD) and centrifuged at 1500 x g and 4 °C for 15 min to discard material with a size less than 50 kD , and then concentrated to 10ml. Bacteria and impurities were removed again using a 0.22 μm filter, and then the resulting concentrate was subjected to ultracentrifugation at 150,000 × g and 4 °C for 3 h by using a 90ti type rotor to remove the supernatant and the aggregated precipitate Vesicles were obtained by dissolving with phosphate buffered saline (PBS).
[0060] 100 μl of extracellular vesicles isolated fr...
Embodiment 3
[0063] Example 3. Metagenomic analysis using DNA extracted from urine
[0064]As shown in Table 2 below, DNA was extracted using the same method as in Example 2, and then subjected to PCR using the 16SrDNA primers shown in Table 1 to amplify the DNA, followed by sequencing (Illumina MiSeq sequencer). Output the results as a Standard Flow Diagram (SFF) file, and convert the SFF file to a sequence file (.fasta) and nucleotide quality score file using GS FLX software (v2.9), then determine credit ratings for reads, And parts with window (20 bps) average base call accuracy less than 99% (Phred score < 20) were removed. After removal of low-quality parts, only reads with a length of 300 bps or greater (Sickle version 1.33) were used, and for operational taxonomic unit (OTU) analysis clustering was performed using UCLUST and USEARCH according to sequence similarity. In particular, based on a sequence similarity of 94% for genera, 90% for families, 85% for orders, 80% for classes, a...
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