#METABOLOMICS WORKBENCH jburgess_20160309_070157 DATATRACK_ID:551 STUDY_ID:ST000365 ANALYSIS_ID:AN000598
VERSION                          	1
CREATED_ON                       	08-09-2023
#PROJECT
PR:PROJECT_TITLE                 	Zebrafish Metabolomics: Model for Environmental Metal Toxicity
PR:PROJECT_SUMMARY               	This metabolomics seed project will test the hypothesis that zebrafish can
PR:PROJECT_SUMMARY               	provide mechanistic insights into the human health effects of developmental
PR:PROJECT_SUMMARY               	exposure to Cd and Pb. We will use broad spectrum metabolomics of zebrafish
PR:PROJECT_SUMMARY               	larvae after exposure to Cd, Pb, and Cd and Pb compared to controls. Activity
PR:PROJECT_SUMMARY               	observed at 5 days post fertilization is will be used to determine if there is a
PR:PROJECT_SUMMARY               	correlation between biological pathways implicated by these metabolic profiles
PR:PROJECT_SUMMARY               	and cardiovascular, metabolic (obesity), and neurological phenotypes. The
PR:PROJECT_SUMMARY               	behavioral phenotypes have been quantified in zebrafish previously and have been
PR:PROJECT_SUMMARY               	measured in the Newborn Epigenetic STudy (NEST), a NIH-funded project that is
PR:PROJECT_SUMMARY               	investigating how environmental exposures and nutrition, in the womb and during
PR:PROJECT_SUMMARY               	childhood, affect how genes work and how these exposures developed into obesity
PR:PROJECT_SUMMARY               	and other diseases, disorders, and conditions. The results from this study will
PR:PROJECT_SUMMARY               	demonstrate the power of using zebrafish as a model for mechanism discovery in
PR:PROJECT_SUMMARY               	exposure using metabolomics to advance understanding of early life exposure to
PR:PROJECT_SUMMARY               	Cd and Pb and serve as preliminary data for opportunities.
PR:INSTITUTE                     	North Carolina State University
PR:LAST_NAME                     	Mattingly
PR:FIRST_NAME                    	Carolyn
PR:ADDRESS                       	142 David Clark Labs, Raleigh, NC 27695-7617
PR:EMAIL                         	cjmattin@ncsu.edu
PR:PHONE                         	919-515-2024
PR:DOI                           	http://dx.doi.org/10.21228/M8JW2K
#STUDY
ST:STUDY_TITLE                   	Zebrafish Metabolomics: Model for Environmental Metal Toxicity
ST:STUDY_SUMMARY                 	This metabolomics seed project will test the hypothesis that zebrafish can
ST:STUDY_SUMMARY                 	provide mechanistic insights into the human health effects of developmental
ST:STUDY_SUMMARY                 	exposure to Cd and Pb. We will use broad spectrum metabolomics of zebrafish
ST:STUDY_SUMMARY                 	larvae after exposure to Cd, Pb, and Cd and Pb compared to controls. Activity
ST:STUDY_SUMMARY                 	observed at 5 days post fertilization is will be used to determine if there is a
ST:STUDY_SUMMARY                 	correlation between biological pathways implicated by these metabolic profiles
ST:STUDY_SUMMARY                 	and cardiovascular, metabolic (obesity), and neurological phenotypes. The
ST:STUDY_SUMMARY                 	behavioral phenotypes have been quantified in zebrafish previously and have been
ST:STUDY_SUMMARY                 	measured in the Newborn Epigenetic STudy (NEST), a NIH-funded project that is
ST:STUDY_SUMMARY                 	investigating how environmental exposures and nutrition, in the womb and during
ST:STUDY_SUMMARY                 	childhood, affect how genes work and how these exposures developed into obesity
ST:STUDY_SUMMARY                 	and other diseases, disorders, and conditions. The results from this study will
ST:STUDY_SUMMARY                 	demonstrate the power of using zebrafish as a model for mechanism discovery in
ST:STUDY_SUMMARY                 	exposure using metabolomics to advance understanding of early life exposure to
ST:STUDY_SUMMARY                 	Cd and Pb and serve as preliminary data for opportunities.
ST:INSTITUTE                     	University of North Carolina
ST:DEPARTMENT                    	Discovery Sciences
ST:LABORATORY                    	Sumner Lab
ST:LAST_NAME                     	Sumner
ST:FIRST_NAME                    	Susan
ST:ADDRESS                       	Eastern Regional Comprehensive Metabolomics Resource Core, UNC Nutrition
ST:ADDRESS                       	Research Institute, 500 Laureate Way, Kannapolis, NC, 28081
ST:EMAIL                         	susan_sumner
 @unc.edu
ST:PHONE                         	704-250-5066
ST:SUBMIT_DATE                   	2016-03-09
#SUBJECT
SU:SUBJECT_TYPE                  	Zebrafish
SU:SUBJECT_SPECIES               	Danio rerio
SU:TAXONOMY_ID                   	7955
SU:SPECIES_GROUP                 	Fish
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Additional sample data
SUBJECT_SAMPLE_FACTORS           	-	CM_CdPool_1	Metal Exposure:Cd | Exposure Level:-	
SUBJECT_SAMPLE_FACTORS           	-	CM_CdPool_2	Metal Exposure:Cd | Exposure Level:-	
SUBJECT_SAMPLE_FACTORS           	-	CM_CdPool_3	Metal Exposure:Cd | Exposure Level:-	
SUBJECT_SAMPLE_FACTORS           	-	CM_Cdhigh_1	Metal Exposure:Cd | Exposure Level:high (1000 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_Cdhigh_2	Metal Exposure:Cd | Exposure Level:high (1000 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_Cdhigh_3	Metal Exposure:Cd | Exposure Level:high (1000 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_Cdlow_1	Metal Exposure:Cd | Exposure Level:low (10 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_Cdlow_2	Metal Exposure:Cd | Exposure Level:low (10 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_Cdlow_3	Metal Exposure:Cd | Exposure Level:low (10 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_Cdmid_1	Metal Exposure:Cd | Exposure Level:mid (100 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_Cdmid_2	Metal Exposure:Cd | Exposure Level:mid (100 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_Cdmid_3	Metal Exposure:Cd | Exposure Level:mid (100 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_CdPbPool_1	Metal Exposure:Cd+Pb | Exposure Level:-	
SUBJECT_SAMPLE_FACTORS           	-	CM_CdPbPool_2	Metal Exposure:Cd+Pb | Exposure Level:-	
SUBJECT_SAMPLE_FACTORS           	-	CM_CdPbPool_3-R	Metal Exposure:Cd+Pb | Exposure Level:-	
SUBJECT_SAMPLE_FACTORS           	-	CM_TotalPool_1	Metal Exposure:CD+Pb | Exposure Level:-	
SUBJECT_SAMPLE_FACTORS           	-	CM_TotalPool_2	Metal Exposure:CD+Pb | Exposure Level:-	
SUBJECT_SAMPLE_FACTORS           	-	CM_TotalPool_3	Metal Exposure:CD+Pb | Exposure Level:-	
SUBJECT_SAMPLE_FACTORS           	-	CM_CdPbhigh_1	Metal Exposure:Cd+Pb | Exposure Level:high (1000 ppb Cd and 1000 ppb Pb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_CdPbhigh_2	Metal Exposure:Cd+Pb | Exposure Level:high (1000 ppb Cd and 1000 ppb Pb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_CdPbhigh_3	Metal Exposure:Cd+Pb | Exposure Level:high (1000 ppb Cd and 1000 ppb Pb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_CdPblow_1	Metal Exposure:Cd+Pb | Exposure Level:low (10 ppb Cd and 10 ppb Pb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_CdPblow_2	Metal Exposure:Cd+Pb | Exposure Level:low (10 ppb Cd and 10 ppb Pb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_CdPblow_3	Metal Exposure:Cd+Pb | Exposure Level:low (10 ppb Cd and 10 ppb Pb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_CdPBmid_1	Metal Exposure:Cd+Pb | Exposure Level:mid (100 ppb Cd and 100 ppb Pb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_CdPBmid_2	Metal Exposure:Cd+Pb | Exposure Level:mid (100 ppb Cd and 100 ppb Pb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_CdPBmid_3	Metal Exposure:Cd+Pb | Exposure Level:mid (100 ppb Cd and 100 ppb Pb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_NoExpPool_1	Metal Exposure:control | Exposure Level:-	
SUBJECT_SAMPLE_FACTORS           	-	CM_NoExpPool_2	Metal Exposure:control | Exposure Level:-	
SUBJECT_SAMPLE_FACTORS           	-	CM_NoExpPool_3	Metal Exposure:control | Exposure Level:-	
SUBJECT_SAMPLE_FACTORS           	-	CM_NoExp_1	Metal Exposure:control | Exposure Level:No	
SUBJECT_SAMPLE_FACTORS           	-	CM_NoExp_2	Metal Exposure:control | Exposure Level:No	
SUBJECT_SAMPLE_FACTORS           	-	CM_NoExp_3	Metal Exposure:control | Exposure Level:No	
SUBJECT_SAMPLE_FACTORS           	-	CM_PbPool_1	Metal Exposure:Pb | Exposure Level:-	
SUBJECT_SAMPLE_FACTORS           	-	CM_PbPool_2	Metal Exposure:Pb | Exposure Level:-	
SUBJECT_SAMPLE_FACTORS           	-	CM_PbPool_3-R	Metal Exposure:Pb | Exposure Level:-	
SUBJECT_SAMPLE_FACTORS           	-	CM_Pbhigh_1	Metal Exposure:Pb | Exposure Level:high (1000 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_Pbhigh_2	Metal Exposure:Pb | Exposure Level:high (1000 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_Pbhigh_3	Metal Exposure:Pb | Exposure Level:high (1000 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_Pblow_1	Metal Exposure:Pb | Exposure Level:low (10 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_Pblow_2	Metal Exposure:Pb | Exposure Level:low (10 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_Pblow_3	Metal Exposure:Pb | Exposure Level:low (10 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_Pbmid_1	Metal Exposure:Pb | Exposure Level:mid (100 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_Pbmid_2	Metal Exposure:Pb | Exposure Level:mid (100 ppb)	
SUBJECT_SAMPLE_FACTORS           	-	CM_Pbmid_3	Metal Exposure:Pb | Exposure Level:mid (100 ppb)	
#COLLECTION
CO:COLLECTION_SUMMARY            	The larvae were collected at 48 hours post fertilization (hpf).
CO:SAMPLE_TYPE                   	Fish larvae
#TREATMENT
TR:TREATMENT_SUMMARY             	Zebrafish larvae were exposured to Cd (10, 100, and 1000 ppb), Pb (10, 100, and
TR:TREATMENT_SUMMARY             	1000 ppb), and Cd and Pb (10 ppb Cd and 10 ppb Pb, 100 ppb Cd and 100 ppb Pb,
TR:TREATMENT_SUMMARY             	and 1000 ppb Cd and 1000 ppb Pb) and compared to controls. The exposure period
TR:TREATMENT_SUMMARY             	was between 6-48 hours post fertilization (hpf). The larvae were collected at 48
TR:TREATMENT_SUMMARY             	hpf.
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	Pools with 40 larvae each were washed and snap frozen before being shipped to
SP:SAMPLEPREP_SUMMARY            	the NIH RTI-RCMRC on dry ice and immediately stored at -80 °C after being
SP:SAMPLEPREP_SUMMARY            	logged in for metabolomics analysis. A total of 30 study samples were
SP:SAMPLEPREP_SUMMARY            	lyophilized overnight for sample preparation. Each sample was mixed with 750 μl
SP:SAMPLEPREP_SUMMARY            	of methanol, vortexed, and centrifuged. 300 μl of the supernatant were used for
SP:SAMPLEPREP_SUMMARY            	the study samples, phenotypic pools were created using 350 μl of each phenotype
SP:SAMPLEPREP_SUMMARY            	and a total study pool was created by mixing 35 μl from each sample. Three
SP:SAMPLEPREP_SUMMARY            	aliquots were created from each pool for a total of 15 pooled samples. All
SP:SAMPLEPREP_SUMMARY            	samples were dried in vacuum overnight. Each sample was reconstituted with 250
SP:SAMPLEPREP_SUMMARY            	μl of 0.5 mM phosphate buffer (pH 7.5) and 25 μl of d-DSS/Chenomx as an
SP:SAMPLEPREP_SUMMARY            	internal standard. The tubes were vortexed for 2 min on a multi-tube vortexer
SP:SAMPLEPREP_SUMMARY            	and centrifuged at 16,000 rcf for 10 min. A 200 µl aliquot of the supernatant
SP:SAMPLEPREP_SUMMARY            	was transferred into pre-labeled 3 mm (4”) NMR tubes for data acquisition on a
SP:SAMPLEPREP_SUMMARY            	700 MHz spectrometer. 1H NMR spectra of zebrafish extraction samples were
SP:SAMPLEPREP_SUMMARY            	acquired on a Bruker 700 MHz NMR spectrometer (located at David H. Murdock
SP:SAMPLEPREP_SUMMARY            	Research Institute, Kannapolis, NC, USA) using a 5 mm cryogenically cooled ATMA
SP:SAMPLEPREP_SUMMARY            	inverse probe and ambient temperature of 25 ℃. A 1D NOESY presaturation pulse
SP:SAMPLEPREP_SUMMARY            	sequence (noesypr1d, [recycle delay (RD)-90°-t1-90°-tm-90°-acquire free
SP:SAMPLEPREP_SUMMARY            	induction decay (FID) was used for data acquisition. For each sample 32
SP:SAMPLEPREP_SUMMARY            	transients were collected into 65k data points using a spectral width of 17.17
SP:SAMPLEPREP_SUMMARY            	ppm, 2 s relaxation delay, 100 ms mixing time, and an acquisition time of 3.9 s
SP:SAMPLEPREP_SUMMARY            	per FID. The water resonance was suppressed using resonance irradiation during
SP:SAMPLEPREP_SUMMARY            	the relaxation delay and mixing time. NMR spectra were processed using TopSpin
SP:SAMPLEPREP_SUMMARY            	3.2 software (Bruker-Biospin, Germany). Spectra were zero filled, and Fourier
SP:SAMPLEPREP_SUMMARY            	transformed after exponential multiplication with line broadening factor of 0.5.
SP:SAMPLEPREP_SUMMARY            	Phase and baseline of the spectra were manually corrected for each spectrum.
SP:SAMPLEPREP_SUMMARY            	Spectra were referenced internally to the DSS-d6 signal. The quality of each NMR
SP:SAMPLEPREP_SUMMARY            	spectrum was assessed for the level of noise and alignment of identified
SP:SAMPLEPREP_SUMMARY            	markers. Spectra were assessed for missing data and underwent quality checks.
#CHROMATOGRAPHY
#ANALYSIS
AN:ANALYSIS_TYPE                 	NMR
#NMR
NM:INSTRUMENT_NAME               	Bruker Avance III
NM:INSTRUMENT_TYPE               	FT-NMR
NM:NMR_EXPERIMENT_TYPE           	1D 1H
NM:SPECTROMETER_FREQUENCY        	700 MHz
#NMR_BINNED_DATA
NMR_BINNED_DATA_START
Bin range(ppm)	CM_CdPool_1	CM_CdPool_2	CM_CdPool_3	CM_Cdhigh_1	CM_Cdhigh_2	CM_Cdhigh_3	CM_Cdlow_1	CM_Cdlow_2	CM_Cdlow_3	CM_Cdmid_1	CM_Cdmid_2	CM_Cdmid_3	CM_CdPbPool_1	CM_CdPbPool_2	CM_CdPbPool_3-R	CM_TotalPool_1	CM_TotalPool_2	CM_TotalPool_3	CM_CdPbhigh_1	CM_CdPbhigh_2	CM_CdPbhigh_3	CM_CdPblow_1	CM_CdPblow_2	CM_CdPblow_3	CM_CdPBmid_1	CM_CdPBmid_2	CM_CdPBmid_3	CM_NoExpPool_1	CM_NoExpPool_2	CM_NoExpPool_3	CM_NoExp_1	CM_NoExp_2	CM_NoExp_3	CM_PbPool_1	CM_PbPool_2	CM_PbPool_3-R	CM_Pbhigh_1	CM_Pbhigh_2	CM_Pbhigh_3	CM_Pblow_1	CM_Pblow_2	CM_Pblow_3	CM_Pbmid_1	CM_Pbmid_2	CM_Pbmid_3
NMR_BINNED_DATA_END
#END