Summary of Study ST000030
This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR000025. The data can be accessed directly via it's Project DOI: 10.21228/M8201W This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
Study ID | ST000030 |
Study Title | Metabolomics Involved in Early Life Antibiotic Exposures(TranSTAT-Liver) |
Study Type | Metabolomics |
Study Summary | In the TranSTAT sub-study, a total of 18 samples from 8 week old, female Swiss webster mice; comprised of 6 serum samples, 6 cecal content samples and 6 liver tissue samples were analyzed. Three mice/matrix were inoculated with cecal contents from STAT mice and 3 mice/matrix were inoculated with cecal contents from Control mice. The mice were housed with conventional bedding and fed a high fat diet. |
Institute | University of North Carolina |
Department | Systems and Translational Sciences |
Laboratory | Sumner Lab |
Last Name | Sumner |
First Name | Susan |
Address | Eastern Regional Comprehensive Metabolomics Resource Core, UNC Nutrition Research Institute, 500 Laureate Way, Kannapolis, NC, 28081 |
susan_sumner @unc.edu | |
Phone | 704-250-5066 |
Submit Date | 2014-03-14 |
Num Groups | 2 |
Total Subjects | 6 |
Study Comments | TranSTAT_Liver Study |
Raw Data Available | Yes |
Uploaded File Size | 400K approx |
Analysis Type Detail | NMR |
Release Date | 2015-03-14 |
Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Project:
Project ID: | PR000025 |
Project DOI: | doi: 10.21228/M8201W |
Project Title: | Metabolomics Involved in Early Life Antibiotic Exposures |
Project Type: | Obesity modeling of antibiotic exposure |
Project Summary: | The project Metabolomics Involved in Early Life Antibiotic Exposures profiled a total of 90 samples from five sub-studies (DuraSTAT, TranSTAT, NOD, EstroSTAT and VG STAT) which included a total of four sample matrices (urine, serum, liver tissue and cecal contents). Within each sub-study, there were three sample matrices except for VG STAT, for which there was only two. For each matrix type within each sub-study 6 samples were analyzed for a total of 18 samples per sub-study (9 of each in VG STAT), the samples were equally divided into STAT/PAT-treated (sub-therapeutic antibiotic treatment (STAT) and therapeutic dose-pulsed antibiotic treatment (PAT)) collected at various time-points versus untreated Controls for each matrix. |
Institute: | New York University |
Department: | School of Medicine |
Laboratory: | Blaser Laboratory |
Last Name: | Blaser |
First Name: | Martin |
Address: | 550 First Avenue, BCD 690, New York, NY 10016 |
Email: | Martin.Blaser@nyumc.org |
Publications: | Cho I, Blaser MJ. The human microbiome: at the interface of health and disease. Nature Reviews. Genetics 2012; 13; 260-270 |
Subject:
Subject ID: | SU000047 |
Subject Type: | Animal |
Subject Species: | Mus musculus |
Taxonomy ID: | 10090 |
Genotype Strain: | Swiss Webster Mice |
Gender: | Female |
Animal Animal Supplier: | Taconic |
Animal Housing: | Conventional |
Animal Feed: | High Fat Diet |
Species Group: | Mammals |
Factors:
Subject type: Animal; Subject species: Mus musculus (Factor headings shown in green)
mb_sample_id | local_sample_id | Treatment Group |
---|---|---|
SA001643 | LTC001 | Control |
SA001644 | LTC005 | Control |
SA001645 | LTC003 | Control |
SA001646 | LPL102 | Pooled QC |
SA001647 | LPL103 | Pooled QC |
SA001648 | LPL101 | Pooled QC |
SA001649 | LPL202 | Pooled QC |
SA001650 | LPL203 | Pooled QC |
SA001651 | LPL201 | Pooled QC |
SA001652 | LTS008 | STAT |
SA001653 | LTS002 | STAT |
SA001654 | LTS005 | STAT |
Showing results 1 to 12 of 12 |
Collection:
Collection ID: | CO000030 |
Collection Summary: | - |
Sample Type: | liver |
Collection Time: | 8 weeks |
Treatment:
Treatment ID: | TR000048 |
Treatment Summary: | Three mice were inoculated with cecal contents from STAT mice and 3 mice were inoculated with cecal contents from control mice. STAT = sub-therapeutic antibiotic treatment. |
Treatment Route: | cecal transfer |
Sample Preparation:
Sampleprep ID: | SP000043 |
Sampleprep Summary: | Frozen liver samples were weighed (50-100 mg) into labeled homogenizer bead tubes. Cold acetonitrile:water (50%) was added to tissue based on weight to make 1 mg/mL homogenates. The samples were extracted and homogenized on a Spex Geno/Grinder for two 45 second pulses at 1750 rpm. Samples were centrifuged at 12000 rcf for 5 min. Liver supernatants were transferred into BSI-labeled tubes. A 500 μL aliquot/sample was transferred into a second set of BSI-labeled tubes for further processing. To make pooled samples, a 300 μL aliquot of selected TranSTAT liver supernatants was combined in a 2 mL tube and used for QC samples in DuraSTAT, TranSTAT, EstroSTAT and NOD sub-studies. Additionally, a 200 μL aliquot of selected VG STAT liver supernatants was combined in a separate 2 mL tube and used as QC samples in the VG STAT sub-study. Three 500 μL aliquots were transferred into BSI-labeled tubes for each set of Pooled QC samples. All samples were then dried on an Eppendorf rotaVap (V-AL setting) at 30°C until dry and stored at -80 °C. On the second day of processing, 630 μL of D2O was added into each dried liver extract tube. Chenomx Internal Standard solution (Chenomx ISTD, Edmonton, Alberta, Canada) contains 5mM 4,4-dimethyl-4-silapentane-1-sulfonic acid (DSS, Chemical Shift Indicator), 100 mM Imidazole (pH indicator), and 0.2% NaN3 (to inhibit bacterial growth) was added (70 µl), and the samples were vortexed on a multi-tube vortexer for 10 minutes at speed 5. Tubes were then centrifuged at 12000 rcf for 5 minutes and a 600 μL aliquot of the supernatant was transferred into 5mm NMR tubes (Wilmad LabGlass, New Jersey, USA) which were kept on ice until data acquisition. |
Sampleprep Protocol Filename: | TranSTAT_Liver_Metabolomics_Procedure.docx |
Analysis:
Analysis ID: | AN000050 |
Laboratory Name: | RTI/ DHHMRI |
Analysis Type: | NMR |
Analysis Comments: | NMR (700 MHz) |
Acquisition Date: | 41527 |
Software Version: | Top Spin 3.2 |
Operator Name: | Wimal Pathmasiri/ Kevin Knagge/ Jason Winnikie |
Randomization Order: | yes |
Detector Type: | NMR |
Data Format: | NMR |
Chromatography ID: | CH000031 |
Num Factors: | 3 |
NMR:
NMR ID: | NM000012 |
Analysis ID: | AN000050 |
Instrument Name: | Bruker Avance III |
Instrument Type: | FT-NMR |
NMR Experiment Type: | 1D 1H |
Field Frequency Lock: | Deuterium |
Standard Concentration: | 0.5mM |
Spectrometer Frequency: | 700 MHz |
NMR Probe: | cyrogenically cooled ATMA inverse probe |
NMR Solvent: | D2O |
NMR Tube Size: | 5mm x 4inch |
Shimming Method: | topshim |
Pulse Sequence: | noesypr1d |
Water Suppression: | presat |
Pulse Width: | 14.84 us |
Power Level: | 25.704w |
Receiver Gain: | 10 |
Offset Frequency: | 3293 Hz |
Chemical Shift Ref Cpd: | DSS |
Temperature: | 298.1 K |
Number Of Scans: | 64 |
Dummy Scans: | 4 |
Acquisition Time: | 2.3243434 |
Relaxation Delay: | 2 s |
Spectral Width: | 20.1358 |
Num Data Points Acquired: | 65536 |
Real Data Points: | 65536 |
Line Broadening: | 0.5 |
Zero Filling: | yes |
Apodization: | lorentzian |
Baseline Correction Method: | polynomial |
Chemical Shift Ref Std: | DSS |