#METABOLOMICS WORKBENCH kenanazam_20171201_105755_mwtab.txt DATATRACK_ID:1272 STUDY_ID:ST000906 ANALYSIS_ID:AN001473 PROJECT_ID:PR000629
VERSION             	1
CREATED_ON             	December 1, 2017, 11:00 am
#PROJECT
PR:PROJECT_TITLE                 	Murine vitamin A deficiency results in a hypermetabolic state and alterations in
PR:PROJECT_TITLE                 	bacterial community structure and metabolism
PR:PROJECT_SUMMARY               	Vitamin A deficiency (A-) is a significant public health problem. To better
PR:PROJECT_SUMMARY               	understand how vitamin A status influences gut microbiota and host metabolism,
PR:PROJECT_SUMMARY               	we systematically analyzed urine, cecum, serum, and liver samples from vitamin A
PR:PROJECT_SUMMARY               	sufficient (A+) and A- mice using 1H NMR-based metabolomics, quantitative
PR:PROJECT_SUMMARY               	(q)PCR, and 16S rRNA gene sequencing coupled with multivariate data analysis.
PR:PROJECT_SUMMARY               	The microbiota in the cecum of A- mice showed compositional as well as
PR:PROJECT_SUMMARY               	functional shifts compared to the microbiota from A+ mice. Targeted 1H NMR
PR:PROJECT_SUMMARY               	analyses revealed significant changes in microbial metabolite concentrations
PR:PROJECT_SUMMARY               	including higher butyrate and hippurate and decreased acetate and
PR:PROJECT_SUMMARY               	4-hydroxyphenylacetate in A+ relative to A- mice. Bacterial butyrate-producing
PR:PROJECT_SUMMARY               	genes including butyryl-CoA:acetate CoA-transferase and butyrate kinase were
PR:PROJECT_SUMMARY               	significantly higher in bacteria from A+ versus bacteria from A- mice. A - mice
PR:PROJECT_SUMMARY               	had disturbances in multiple metabolic pathways including alterations in energy
PR:PROJECT_SUMMARY               	metabolism (hyperglycemia, glycogenesis, TCA cycle, and lipoprotein
PR:PROJECT_SUMMARY               	biosynthesis) and the A- host showed metabolites indicative of a hypermetabolic
PR:PROJECT_SUMMARY               	state (higher levels of amino acids and nucleic acids). A- mice had
PR:PROJECT_SUMMARY               	hyperglycemia, liver dysfunction, changes in bacterial metabolism, and altered
PR:PROJECT_SUMMARY               	gut microbial communities. Moreover, integrative analyses indicated a strong
PR:PROJECT_SUMMARY               	correlation between gut microbiota and host energy metabolism pathways in the
PR:PROJECT_SUMMARY               	liver. Vitamin A regulates the microbiota, bacterial metabolism and the effects
PR:PROJECT_SUMMARY               	of vitamin A on the microbiota results in alterations to host metabolism.
PR:INSTITUTE                     	The Pennsylvania State University (Penn State)
PR:LAST_NAME                     	Nichols
PR:FIRST_NAME                    	Robert
PR:ADDRESS                       	101 Life science building, University Park, State college, PA, 16803
PR:EMAIL                         	rgn5011@psu.edu
PR:PHONE                         	7247662694
#STUDY
ST:STUDY_TITLE                   	Murine vitamin A deficiency results in a hypermetabolic state and alterations in
ST:STUDY_TITLE                   	bacterial community structure and metabolism. (Serum)
ST:STUDY_SUMMARY                 	Vitamin A deficiency (A-) is a significant public health problem. To better
ST:STUDY_SUMMARY                 	understand how vitamin A status influences gut microbiota and host metabolism,
ST:STUDY_SUMMARY                 	we systematically analyzed urine, cecum, serum, and liver samples from vitamin A
ST:STUDY_SUMMARY                 	sufficient (A+) and A- mice using 1H NMR-based metabolomics, quantitative
ST:STUDY_SUMMARY                 	(q)PCR, and 16S rRNA gene sequencing coupled with multivariate data analysis.
ST:STUDY_SUMMARY                 	The microbiota in the cecum of A- mice showed compositional as well as
ST:STUDY_SUMMARY                 	functional shifts compared to the microbiota from A+ mice. Targeted 1H NMR
ST:STUDY_SUMMARY                 	analyses revealed significant changes in microbial metabolite concentrations
ST:STUDY_SUMMARY                 	including higher butyrate and hippurate and decreased acetate and
ST:STUDY_SUMMARY                 	4-hydroxyphenylacetate in A+ relative to A- mice. Bacterial butyrate-producing
ST:STUDY_SUMMARY                 	genes including butyryl-CoA:acetate CoA-transferase and butyrate kinase were
ST:STUDY_SUMMARY                 	significantly higher in bacteria from A+ versus bacteria from A- mice. A - mice
ST:STUDY_SUMMARY                 	had disturbances in multiple metabolic pathways including alterations in energy
ST:STUDY_SUMMARY                 	metabolism (hyperglycemia, glycogenesis, TCA cycle, and lipoprotein
ST:STUDY_SUMMARY                 	biosynthesis) and the A- host showed metabolites indicative of a hypermetabolic
ST:STUDY_SUMMARY                 	state (higher levels of amino acids and nucleic acids). A- mice had
ST:STUDY_SUMMARY                 	hyperglycemia, liver dysfunction, changes in bacterial metabolism, and altered
ST:STUDY_SUMMARY                 	gut microbial communities. Moreover, integrative analyses indicated a strong
ST:STUDY_SUMMARY                 	correlation between gut microbiota and host energy metabolism pathways in the
ST:STUDY_SUMMARY                 	liver. Vitamin A regulates the microbiota, bacterial metabolism and the effects
ST:STUDY_SUMMARY                 	of vitamin A on the microbiota results in alterations to host metabolism.
ST:INSTITUTE                     	Pennsylvania State University
ST:LAST_NAME                     	Nichols
ST:FIRST_NAME                    	Robert
ST:ADDRESS                       	101 Life science building, University park, PA, 16803
ST:EMAIL                         	rgn5011@psu.edu
ST:PHONE                         	17247662694
#SUBJECT
SU:SUBJECT_TYPE                  	mouse
SU:SUBJECT_SPECIES               	Mus musculus
SU:TAXONOMY_ID                   	10090
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Additional sample data
SUBJECT_SAMPLE_FACTORS           	Vit A sufficient	C1	Treatment:Control	Genotype=Wild-Type
SUBJECT_SAMPLE_FACTORS           	Vit A sufficient	C2	Treatment:Control	Genotype=Wild-Type
SUBJECT_SAMPLE_FACTORS           	Vit A sufficient	C3	Treatment:Control	Genotype=Wild-Type
SUBJECT_SAMPLE_FACTORS           	Vit A sufficient	C4	Treatment:Control	Genotype=Wild-Type
SUBJECT_SAMPLE_FACTORS           	Vit A sufficient	C5	Treatment:Control	Genotype=Wild-Type
SUBJECT_SAMPLE_FACTORS           	Vit A sufficient	C6	Treatment:Control	Genotype=Wild-Type
SUBJECT_SAMPLE_FACTORS           	Vit A deficient	T1	Treatment:Vit-A deficient food	Genotype=Wild-Type
SUBJECT_SAMPLE_FACTORS           	Vit A deficient	T2	Treatment:Vit-A deficient food	Genotype=Wild-Type
SUBJECT_SAMPLE_FACTORS           	Vit A deficient	T3	Treatment:Vit-A deficient food	Genotype=Wild-Type
SUBJECT_SAMPLE_FACTORS           	Vit A deficient	T4	Treatment:Vit-A deficient food	Genotype=Wild-Type
SUBJECT_SAMPLE_FACTORS           	Vit A deficient	T5	Treatment:Vit-A deficient food	Genotype=Wild-Type
SUBJECT_SAMPLE_FACTORS           	Vit A deficient	T6	Treatment:Vit-A deficient food	Genotype=Wild-Type
#COLLECTION
CO:COLLECTION_SUMMARY            	Serum
#TREATMENT
TR:TREATMENT_SUMMARY             	Twelve male litters were weaned at 3 wks and continuously fed the vitamin A
TR:TREATMENT_SUMMARY             	sufficient diet, vitamin A deficient diet, or the vitamin A deficient diet,
TR:TREATMENT_SUMMARY             	supplemented with retenoic acid until the end of the experiment.
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	The NMR sample prep for the urine, liver, cecal contents and serum are attached.
#CHROMATOGRAPHY
CH:CHROMATOGRAPHY_TYPE           	-
CH:INSTRUMENT_NAME               	-
CH:COLUMN_NAME                   	-
#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        	600 Mhz
#NMR_METABOLITE_DATA
NMR_METABOLITE_DATA:UNITS        	total peak intensity per metabolite
NMR_METABOLITE_DATA_START
Samples	C1	C2	C3	C4	C5	C6	T1	T2	T3	T4	T5	T6
Factors	Treatment:Control	Treatment:Control	Treatment:Control	Treatment:Control	Treatment:Control	Treatment:Control	Treatment:Vit-A deficient food	Treatment:Vit-A deficient food	Treatment:Vit-A deficient food	Treatment:Vit-A deficient food	Treatment:Vit-A deficient food	Treatment:Vit-A deficient food
glucose	0.00736627	0.01099377	0.00687083	0.00574036	0.00534264	0.00657361	0.01348922	0.01009273	0.01339732	0.01676166	0.01186162	0.01272616
lactate	0.13160623	0.11402565	0.11572843	0.11224188	0.17798374	0.12502879	0.1131474	0.14323522	0.12897283	0.11381006	0.13022178	0.11731133
lipid	0.02666239	0.02532021	0.02642352	0.02793512	0.01575683	0.02876491	0.0262228	0.02448511	0.02282556	0.02137423	0.02434821	0.02562265
3HB	0.0100286	0.00936996	0.01838309	0.00968054	0.01014632	0.01062563	0.00930723	0.00962347	0.00733673	0.0078065	0.00924269	0.0094074
succinate	0.00631077	0.00594153	0.00548456	0.00379321	0.00877321	0.00532515	0.00763939	0.00652655	0.00848384	0.00725546	0.00740122	0.00732611
citrate	1.27612514	2.24772338	3.26003745	4.25189108	5.35874898	6.27155838	7.24394925	8.27633062	9.2589361	10.23629082	11.26425409	12.25200473
BCAA	0.02540082	0.02232446	0.02265889	0.02521564	0.03452689	0.02644779	0.0196275	0.0217893	0.02094926	0.01770276	0.02134803	0.02082119
alanine	0.00801592	0.00709805	0.00791986	0.00763138	0.01431239	0.0079317	0.00620099	0.00695503	0.00734723	0.00585893	0.00706451	0.00716367
glutamine	0.0066234	0.00579623	0.00668324	0.00653609	0.01152248	0.00661839	0.00546885	0.00553881	0.00464099	0.00559544	0.00594521	0.00584208
histidine	0.00040757	0.00034709	0.00032819	0.00044205	0.00061586	0.00038745	0.00033178	0.00037454	0.00032688	0.00031059	0.00038918	0.00033998
tyrosine	0.00092292	0.00063317	0.00070308	0.00075709	0.00203103	0.000814	0.00071819	0.00097258	0.00074966	0.00060077	0.00082622	0.00068839
phe	0.00337552	0.00304378	0.00301162	0.00334335	0.00409671	0.00326308	0.00261467	0.0032374	0.00272321	0.00245075	0.00292399	0.00268554
NMR_METABOLITE_DATA_END
#METABOLITES
METABOLITES_START
metabolite_name
glucose
lactate
lipid
3HB
succinate
citrate
BCAA
alanine
glutamine
histidine
tyrosine
phe
METABOLITES_END
#END