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"PROJECT":{"PROJECT_TITLE":"Metabolomics Changes in the feces of infants exposed to arsenic","PROJECT_SUMMARY":"Exposure to arsenic (As) during the vulnerable window of fetal development and early childhood has shown significant clinical effects. In highly exposed populations, altered immunity is one of the most affected pathways and can lead to an elevated risk of infection and a pre-disposition to allergy/atopy. Since well water in the New Hampshire region has been determined to be a potential source of As exposure, this study includes mother-infant dyads living in the area, who obtain household water from private wells. This study seeks to determine if in utero and early life As exposure is related to increase occurrence of childhood: infections, allergy and atopy, and diminished vaccine response. It has been observed that the microbiome is an important mediator of immune impairment due to As exposure. Therefore, we will further investigate the relation between in utero and early life As exposure on the development of the infant intestinal microbiome in the first year of life. For this study fecal samples, from infants at risk of As exposure, were collected at 6 weeks and 12 months of age. Metabolomics data will allow for a more complete picture of the relationships between the microbiome, As exposure and immune function.","INSTITUTE":"Dartmouth College","DEPARTMENT":"Department of Epidemiology","LAST_NAME":"Margaret","FIRST_NAME":"Karagas","ADDRESS":"One Medical Center Road, 7927 HB, Rubin Building, Lebanon, NH 03756","EMAIL":"Margaret.Karagas@Dartmouth.edu","PHONE":"603-653-9010","DOI":"http://dx.doi.org/10.21228/M8H029"},

"STUDY":{"STUDY_TITLE":"Stool metabolomics in the New Hampshire Birth Cohort Study","STUDY_TYPE":"Untargeted and semi-targeted metabolomics analysis","STUDY_SUMMARY":"This is a study of data collected from fecal samples from larger New Hampshire Birth Cohort Study (NHBCS). 1H NMR metabolomic profiling of 524 infant stool samples collected at 6 week - 3 year age was performed and spectra were binned (untargeted metabolomics). A set of host-microbiome co-metabolites were library matched in individual sample spectra and their relative concentrations were determined. This study investigated associations of the functional metabolic response of the microbial milieu of the infant gut with environmental and other factors.","INSTITUTE":"University of North Carolina at Chapel Hill","DEPARTMENT":"Nutrition","LABORATORY":"Metabolomics and Exposome Laboratory, Nutrition Research Institute, UNC Chapel Hill","LAST_NAME":"Sumner","FIRST_NAME":"Susan","ADDRESS":"500 Laureate Way, Kannapolis, NC 28081","EMAIL":"susan_sumner@unc.edu","PHONE":"(919) 622-4456","SUBMIT_DATE":"2021-08-09"},

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"COLLECTION":{"COLLECTION_SUMMARY":"Infant stool samples were collected at home using provided diapers, sealed in a separate polyethylene bag and frozen in a home freezer or kept chilled until transport. Samples were transported in a cooler with ice packs and brought to the routine 6-week post-partum visit within 24 hours of collection. Stool samples remained frozen until processing where they were thawed at 4 °C. Using sterile applicators, 0.5–1 g of stool was aliquoted into trace element-free cryovial tubes and then frozen at −80 °C in a biorepository","SAMPLE_TYPE":"Feces","STORAGE_CONDITIONS":"-80℃"},

"TREATMENT":{"TREATMENT_SUMMARY":"NA"},

"SAMPLEPREP":{"SAMPLEPREP_SUMMARY":"De-identified stool aliquots were shipped on dry ice and immediately stored at -80 °C for metabolomics analysis. Samples were randomized into batches. For each batch, samples were thawed and ~150mg of stool was transferred to MagNA Lyser tubes after recording the weight, Samples were then homogenized with 50% acetonitrile in water by using the Omni Bead Disruptor (Omni International, GA, USA). Homogenized samples were centrifuged at 16000 rcf and the supernatant was separated into another tube. An aliquot (1000 uL, 100 mg equivalent of fecal mass) was transferred into Eppendorf tube and lyophilized overnight. The dried extract was reconstituted in 700 uL of NMR master mix (containing 0.2M phosphate, 0.5 mM DSS-d6, and 0.2% sodium azide), vortexed on a multitube vortexer at speed 5 for 2 min and centrifuged at 16000 rcf for 5 min. A 600 µl aliquot of the supernatant was transferred into a pre-labeled 5mm NMR tube for data acquisition on a 700 MHz spectrometer. Additionally, study pooled samples (created from randomly selected study samples) and batch pooled quality control (QC) samples were generated from supernatants of study samples and aliquots of supernatants were dried and reconstituted similar to study samples described above, and used for QC purposes.","SAMPLEPREP_PROTOCOL_FILENAME":"1. Dartmouth-Fecal Metabolomics_NMR_Batch2 Procedures","PROCESSING_STORAGE_CONDITIONS":"4℃","EXTRACTION_METHOD":"50% Acetonitrile in Water","EXTRACT_STORAGE":"-80℃","SAMPLE_RESUSPENSION":"In phosphate buffer containing D2O"},

"CHROMATOGRAPHY":[],

"ANALYSIS":{"LABORATORY_NAME":"Metabolomics and Exposome Lab at UNC Nutrition Research Institute","ANALYSIS_TYPE":"NMR","SOFTWARE_VERSION":"TopSpin 3.5","OPERATOR_NAME":"Wimal Pathmasiri","DETECTOR_TYPE":"NMR","DATA_FORMAT":"fid, 1r"},

"NM":{"INSTRUMENT_NAME":"Avance III 700 MHz NMR Spectrometer","INSTRUMENT_TYPE":"FT-NMR","NMR_EXPERIMENT_TYPE":"1D-1H","FIELD_FREQUENCY_LOCK":"3015 Hz, D2O","STANDARD_CONCENTRATION":"0.5 mM","SPECTROMETER_FREQUENCY":"700 MHz","NMR_PROBE":"CP QCI/HPCN","NMR_SOLVENT":"90% H2O, 10% D2O","NMR_TUBE_SIZE":"5 mm","SHIMMING_METHOD":"topshim","PULSE_SEQUENCE":"noesygppr1d","WATER_SUPPRESSION":"pre-saturation","PULSE_WIDTH":"14.59 us","POWER_LEVEL":"12.3 Watts","RECEIVER_GAIN":"36","OFFSET_FREQUENCY":"3290.61 Hz","PRESATURATION_POWER_LEVEL":"0.0000964 Watts","CHEMICAL_SHIFT_REF_CPD":"DSS-d6","TEMPERATURE":"25 C","NUMBER_OF_SCANS":"64","DUMMY_SCANS":"4","ACQUISITION_TIME":"3.9 seconds","RELAXATION_DELAY":"2 seconds","SPECTRAL_WIDTH":"12 ppm","NUM_DATA_POINTS_ACQUIRED":"65536","REAL_DATA_POINTS":"32768","LINE_BROADENING":"0.5 Hz","ZERO_FILLING":"Yes","APODIZATION":"Lorentzian","BASELINE_CORRECTION_METHOD":"Polynomial","CHEMICAL_SHIFT_REF_STD":"DSS-d6","BINNED_INCREMENT":"0.04ppm","BINNED_DATA_EXCLUDED_RANGE":"4.79 - 4.85 ppm (Water region)"}

}