{
"METABOLOMICS WORKBENCH":{"STUDY_ID":"ST000030","ANALYSIS_ID":"AN000050","VERSION":"1","CREATED_ON":"10-02-2015"},

"PROJECT":{"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 J.","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","PHONE":"-"},

"STUDY":{"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":"RTI International","DEPARTMENT":"Systems and Translational Sciences (STS)","LABORATORY":"NIH Eastern Regional Comprehensive Metabolomics Resource Core (RTI RCMRC)","LAST_NAME":"Sumner","FIRST_NAME":"Susan","EMAIL":"ssumner@rti.org","NUM_GROUPS":"2","TOTAL_SUBJECTS":"6","STUDY_COMMENTS":"TranSTAT_Liver Study","PHONE":"-","ADDRESS":"-"},

"SUBJECT":{"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":"Mammal"},
"SUBJECT_SAMPLE_FACTORS":[
{
"Subject ID":"-",
"Sample ID":"LTC001",
"Factors":{"Treatment Group":"Control"}
},
{
"Subject ID":"-",
"Sample ID":"LTC003",
"Factors":{"Treatment Group":"Control"}
},
{
"Subject ID":"-",
"Sample ID":"LTC005",
"Factors":{"Treatment Group":"Control"}
},
{
"Subject ID":"-",
"Sample ID":"LPL101",
"Factors":{"Treatment Group":"Pooled QC"}
},
{
"Subject ID":"-",
"Sample ID":"LPL102",
"Factors":{"Treatment Group":"Pooled QC"}
},
{
"Subject ID":"-",
"Sample ID":"LPL103",
"Factors":{"Treatment Group":"Pooled QC"}
},
{
"Subject ID":"-",
"Sample ID":"LPL201",
"Factors":{"Treatment Group":"Pooled QC"}
},
{
"Subject ID":"-",
"Sample ID":"LPL202",
"Factors":{"Treatment Group":"Pooled QC"}
},
{
"Subject ID":"-",
"Sample ID":"LPL203",
"Factors":{"Treatment Group":"Pooled QC"}
},
{
"Subject ID":"-",
"Sample ID":"LTS002",
"Factors":{"Treatment Group":"STAT"}
},
{
"Subject ID":"-",
"Sample ID":"LTS005",
"Factors":{"Treatment Group":"STAT"}
},
{
"Subject ID":"-",
"Sample ID":"LTS008",
"Factors":{"Treatment Group":"STAT"}
}
],
"COLLECTION":{"SAMPLE_TYPE":"liver","COLLECTION_TIME":"8 weeks","COLLECTION_SUMMARY":"-"},

"TREATMENT":{"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"},

"SAMPLEPREP":{"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"},

"CHROMATOGRAPHY":{"CHROMATOGRAPHY_TYPE":"-","INSTRUMENT_NAME":"-","COLUMN_NAME":"-"},

"ANALYSIS":{"LABORATORY_NAME":"RTI/ DHHMRI","ANALYSIS_TYPE":"NMR","ACQUISITION_DATE":"41527","SOFTWARE_VERSION":"Top Spin 3.2","OPERATOR_NAME":"Wimal Pathmasiri/ Kevin Knagge/ Jason Winnikie","DETECTOR_TYPE":"NMR","DATA_FORMAT":"NMR"},

"NM":{"INSTRUMENT_TYPE":"Bruker Avance III","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","INSTRUMENT_NAME":"Bruker Avance III"},

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