#METABOLOMICS WORKBENCH sdhungana_20140606_9260131_mwtab.txt DATATRACK_ID:105 3. BECK_Urine-Genetic_HILIC MetaData and Analytical Metadata.xlsm DATATRACK_ID:105 STUDY_ID:ST000071 ANALYSIS_ID:AN000112
VERSION                          	1
CREATED_ON                       	03-03-2022
#PROJECT
PR:PROJECT_TITLE                 	Metabolomic profiling of influenza: a 2009 pandemic H1N1 influenza in lean and
PR:PROJECT_TITLE                 	obese mice
PR:PROJECT_TYPE                  	Effects and role of obesity on the severity of influenza
PR:PROJECT_SUMMARY               	During the 2009 H1N1 influenza pandemic outbreak, obese individuals were
PR:PROJECT_SUMMARY               	reported to be at greater risk for morbidity and mortality from pandemic
PR:PROJECT_SUMMARY               	infection. However, the mechanisms contributing to greater influenza severity in
PR:PROJECT_SUMMARY               	infected obese individuals remain unclear. Given that one in ten individuals is
PR:PROJECT_SUMMARY               	obese, and worldwide influenza outbreaks are a consistent public health burden,
PR:PROJECT_SUMMARY               	garnering a better understanding of the pathways and mechanisms contributing to
PR:PROJECT_SUMMARY               	greater influenza severity in the obese is essential for limiting influenza
PR:PROJECT_SUMMARY               	infection mortality in this at-risk population. Closely paralleling pH1N1
PR:PROJECT_SUMMARY               	infection outcome in humans, obese mice exhibit increased morbidity and
PR:PROJECT_SUMMARY               	mortality following pH1N1 infection. In mice, obesity impairs the function of
PR:PROJECT_SUMMARY               	natural killer cells, dendritic cells, macrophage, B cells and memory T cells.
PR:PROJECT_SUMMARY               	Further, several analyses of lung antiviral responses revealed that obese mice
PR:PROJECT_SUMMARY               	have greater lung damage, lung immune cell infiltration and impaired lung
PR:PROJECT_SUMMARY               	healing after infection. Nevertheless, it remains unclear how altered immune
PR:PROJECT_SUMMARY               	cell function contributes to greater lung damage and increased infection
PR:PROJECT_SUMMARY               	severity in obese mice. Metabolomics will be used to dissect the metabolic
PR:PROJECT_SUMMARY               	consequences of obesity on the immune response to pH1N1 infection. We will
PR:PROJECT_SUMMARY               	compare metabolic profiles of lung-specific and peripheral samples from
PR:PROJECT_SUMMARY               	uninfected and infected lean and obese mice during early and late phases of
PR:PROJECT_SUMMARY               	influenza immunity.
PR:INSTITUTE                     	University of North Carolina at Chapel Hill
PR:DEPARTMENT                    	Department of Nutrition
PR:LAST_NAME                     	Beck
PR:FIRST_NAME                    	Melinda
PR:ADDRESS                       	2303 MHRB, CB #7461, UNC, Chapel Hill NC 27599
PR:EMAIL                         	melinda_beck@unc.edu
PR:PHONE                         	919-966-6809
PR:DOI                           	http://dx.doi.org/10.21228/M8QG6H
#STUDY
ST:STUDY_TITLE                   	Metabolomic profiling of influenza: a 2009 pandemic H1N1 influenza in lean and
ST:STUDY_TITLE                   	obese mice (via Urine)
ST:INSTITUTE                     	University of North Carolina
ST:DEPARTMENT                    	Systems and Translational 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                   	2014-06-14
#SUBJECT
SU:SUBJECT_TYPE                  	Animal
SU:SUBJECT_SPECIES               	Mus musculus
SU:TAXONOMY_ID                   	10090
SU:GENOTYPE_STRAIN               	C57BL/6J
SU:AGE_OR_AGE_RANGE              	approx. 15-16 weeks
SU:GENDER                        	male and female
SU:ANIMAL_ANIMAL_SUPPLIER        	The Jackson Laboratory
SU:ANIMAL_FEED                   	high fat, low fat or normal chow
SU:SPECIES_GROUP                 	Mammal
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Additional sample data
SUBJECT_SAMPLE_FACTORS           	-	UPALL0001	Phenotype:-- | Infection Status:-- | Sex:--	
SUBJECT_SAMPLE_FACTORS           	-	UPALL0002	Phenotype:-- | Infection Status:-- | Sex:--	
SUBJECT_SAMPLE_FACTORS           	-	UPALL0003	Phenotype:-- | Infection Status:-- | Sex:--	
SUBJECT_SAMPLE_FACTORS           	-	LUI2_67 	Phenotype:lean | Infection Status:D2 Infected | Sex:f	
SUBJECT_SAMPLE_FACTORS           	-	LUI2_68 	Phenotype:lean | Infection Status:D2 Infected | Sex:f	
SUBJECT_SAMPLE_FACTORS           	-	LUI2_92 	Phenotype:lean | Infection Status:D2 Infected | Sex:f	
SUBJECT_SAMPLE_FACTORS           	-	65	Phenotype:lean | Infection Status:D8 infected | Sex:m	
SUBJECT_SAMPLE_FACTORS           	-	86	Phenotype:lean | Infection Status:D8 infected | Sex:m	
SUBJECT_SAMPLE_FACTORS           	-	94	Phenotype:lean | Infection Status:D8 infected | Sex:m	
SUBJECT_SAMPLE_FACTORS           	-	LUC_67 	Phenotype:lean | Infection Status:uninfected | Sex:f	
SUBJECT_SAMPLE_FACTORS           	-	LUC_68 	Phenotype:lean | Infection Status:uninfected | Sex:f	
SUBJECT_SAMPLE_FACTORS           	-	LUC_92 	Phenotype:lean | Infection Status:uninfected | Sex:f	
SUBJECT_SAMPLE_FACTORS           	-	36	Phenotype:lean | Infection Status:uninfected | Sex:m	
SUBJECT_SAMPLE_FACTORS           	-	47	Phenotype:lean | Infection Status:uninfected | Sex:m	
SUBJECT_SAMPLE_FACTORS           	-	51	Phenotype:lean | Infection Status:uninfected | Sex:m	
SUBJECT_SAMPLE_FACTORS           	-	OUI2_74 	Phenotype:obese | Infection Status:D2 Infected | Sex:f	
SUBJECT_SAMPLE_FACTORS           	-	OUI2_75 	Phenotype:obese | Infection Status:D2 Infected | Sex:f	
SUBJECT_SAMPLE_FACTORS           	-	OUI2_91 	Phenotype:obese | Infection Status:D2 Infected | Sex:f	
SUBJECT_SAMPLE_FACTORS           	-	109	Phenotype:obese | Infection Status:D8 infected | Sex:m	
SUBJECT_SAMPLE_FACTORS           	-	88	Phenotype:obese | Infection Status:D8 infected | Sex:m	
SUBJECT_SAMPLE_FACTORS           	-	OUC_74 	Phenotype:obese | Infection Status:uninfected | Sex:f	
SUBJECT_SAMPLE_FACTORS           	-	OUC_75 	Phenotype:obese | Infection Status:uninfected | Sex:f	
SUBJECT_SAMPLE_FACTORS           	-	OUC_91 	Phenotype:obese | Infection Status:uninfected | Sex:f	
SUBJECT_SAMPLE_FACTORS           	-	35	Phenotype:obese | Infection Status:uninfected | Sex:m	
SUBJECT_SAMPLE_FACTORS           	-	53	Phenotype:obese | Infection Status:uninfected | Sex:m	
#COLLECTION
CO:SAMPLE_TYPE                   	Tissue
CO:STORAGE_CONDITIONS            	-80
#TREATMENT
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	Samples were homogenized on a baed beater at1750rpm in 10uL of 50:50
SP:SAMPLEPREP_SUMMARY            	acetonitrile:water per 1 mg of tissue using washed ceramic beads. Extraction was
SP:SAMPLEPREP_SUMMARY            	performed using acetonitrile. Samples were dried down  and reconstituted in
SP:SAMPLEPREP_SUMMARY            	100uL of 95:5 water:methanol.
SP:SAMPLEPREP_PROTOCOL_FILENAME  	RTI_BECK_Urine-Genetic_HILIC_Metabolomics_Procedure.docx
SP:PROCESSING_METHOD             	Homogenization
SP:EXTRACTION_METHOD             	Acetonitrile
SP:EXTRACT_STORAGE               	-80 C
SP:SAMPLE_RESUSPENSION           	95:5 Water:Methanol
SP:SAMPLE_SPIKING                	L-Tryptophan-d5
SP:ORGAN                         	Lung
#CHROMATOGRAPHY
CH:INSTRUMENT_NAME               	Waters Acquity
CH:COLUMN_NAME                   	Waters Acquity BEH Amide (150 x 2.1mm, 1.7um)
CH:COLUMN_PRESSURE               	6000-10000
CH:COLUMN_TEMPERATURE            	40 C
CH:FLOW_GRADIENT                 	Time(min) Flow Rate %A %B: 1. Initial 0.400 99.0 1.0; 2. 1.00 0.400 99.0 1.0; 3.
CH:FLOW_GRADIENT                 	12.00 0.400 1.0 99.0; 4. 14.00 0.400 1.0 99.0; 5. 15.00 0.400 99.0 1.0; 6. 19.00
CH:FLOW_GRADIENT                 	0.400 99.0 1.0
CH:FLOW_RATE                     	0.4 mL/min
CH:INJECTION_TEMPERATURE         	8 C
CH:INTERNAL_STANDARD             	L-Tryptophan-d5
CH:SOLVENT_A                     	10mM ammonium acetate in 95/5 acetonitrile/water with 0.1% formic acid
CH:SOLVENT_B                     	10mM ammonium acetate in 50/50 acetonitrile/water with 0.1% formic acid
CH:ANALYTICAL_TIME               	19 min
CH:WEAK_WASH_SOLVENT_NAME        	5%MeOH
CH:WEAK_WASH_VOLUME              	1000 uL
CH:STRONG_WASH_SOLVENT_NAME      	80%MeOH
CH:STRONG_WASH_VOLUME            	1000 uL
CH:TARGET_SAMPLE_TEMPERATURE     	8 C
CH:SAMPLE_LOOP_SIZE              	10 uL
CH:SAMPLE_SYRINGE_SIZE           	100 uL
CH:RANDOMIZATION_ORDER           	Yes
CH:CHROMATOGRAPHY_TYPE           	HILIC
#ANALYSIS
AN:LABORATORY_NAME               	RTI
AN:ANALYSIS_TYPE                 	MS
AN:ACQUISITION_DATE              	41656
AN:SOFTWARE_VERSION              	MassLynx 4.1
AN:OPERATOR_NAME                 	Suraj Dhungana, Darya Cheng
AN:DETECTOR_TYPE                 	TOF (negative)
#MS
MS:INSTRUMENT_NAME               	Waters Synapt G2 QTOF
MS:INSTRUMENT_TYPE               	QTOF
MS:MS_TYPE                       	ESI
MS:ION_MODE                      	NEGATIVE
MS:CAPILLARY_TEMPERATURE         	110 C
MS:CAPILLARY_VOLTAGE             	2.8 kV
MS:COLLISION_ENERGY              	4
MS:FRAGMENTATION_METHOD          	CID
MS:HELIUM_FLOW                   	180
MS:IONIZATION                    	ES-
MS:SOURCE_TEMPERATURE            	110 C
MS:DATAFORMAT                    	Continuum
MS:DESOLVATION_GAS_FLOW          	400 L/Hr
MS:DESOLVATION_TEMPERATURE       	400 C
MS:RESOLUTION_SETTING            	18000
MS:SCAN_RANGE_MOVERZ             	50-1000 m/z
MS:SCANNING_CYCLE                	1 s
MS:TUBE_LENS_VOLTAGE             	74
MS:MS_RESULTS_FILE               	ST000071_AN000112_Results.txt	UNITS:Peak area	Has m/z:Yes	Has RT:Yes	RT units:Minutes
#END