#METABOLOMICS WORKBENCH cadriano_20170802_143853_mwtab.txt DATATRACK_ID:1183 STUDY_ID:ST000881 ANALYSIS_ID:AN001437 PROJECT_ID:PR000611
VERSION             	1
CREATED_ON             	October 29, 2017, 8:18 pm
#PROJECT
PR:PROJECT_TITLE                 	Metabolomics analysis of leprosy patients with type 1 reaction
PR:PROJECT_TYPE                  	MS qualitative analysis and identification of polyunsaturated fatty acids in
PR:PROJECT_TYPE                  	retrospective serum samples of leprosy patients with type 1 reaction
PR:PROJECT_SUMMARY               	Type 1 reaction (T1R) is an acute inflammatory episode that causes severe
PR:PROJECT_SUMMARY               	neuronal damages in patients with leprosy. The factors that trigger this
PR:PROJECT_SUMMARY               	pathology is still unknown, and further studies are needed to understand T1R and
PR:PROJECT_SUMMARY               	to early prevent its start. It is well established that the host immune response
PR:PROJECT_SUMMARY               	is linked to T1R and previous studies indicated that the metabolism of the host
PR:PROJECT_SUMMARY               	also influences the adaptive immune response against M. leprae antigens.
PR:PROJECT_SUMMARY               	Therefore, metabolomics-based analyses of sera from 7 patients with and 9
PR:PROJECT_SUMMARY               	without T1R were conducted via liquid chromatography–mass spectrometry. The
PR:PROJECT_SUMMARY               	main goal of this project was to determine whether the metabolism of
PR:PROJECT_SUMMARY               	polyunsaturated fatty acids (such as eicosanoids and omega-3 fatty acids) were
PR:PROJECT_SUMMARY               	perturbed in leprosy patients with T1R.
PR:INSTITUTE                     	Colorado State University
PR:DEPARTMENT                    	Department of Microbiology, Immunology, and Pathology
PR:LABORATORY                    	Belisle
PR:LAST_NAME                     	Belisle
PR:FIRST_NAME                    	John
PR:ADDRESS                       	Rampart Road, 1682 Campus Delivery
PR:EMAIL                         	cadriano@rams.colostate.edu
PR:PHONE                         	9704819160
PR:FUNDING_SOURCE                	This work was supported by the New York Community Trust (grant to J. T. B. as
PR:FUNDING_SOURCE                	co–principle investigator [PI]), by the Heiser Foundation (grant to J. T. B.
PR:FUNDING_SOURCE                	as co-PI), and by the Brazilian Coordination for the Improvement of Higher
PR:FUNDING_SOURCE                	Education Personnel through the Science without Borders program (10546-13-8, for
PR:FUNDING_SOURCE                	the postdoctoral scholarship to C. A. M. S.).
PR:PROJECT_COMMENTS              	The institutional review boards of Colorado State University approved the use of
PR:PROJECT_COMMENTS              	sera for the reported study.
PR:PUBLICATIONS                  	J Infect Dis. 2017 Feb 1;215(3):431-439. doi: 10.1093/infdis/jiw541.
PR:CONTRIBUTORS                  	Carlos A. M. Silva, Kristofor Webb, Barbara G. Andre, Maria Angela Marques,
PR:CONTRIBUTORS                  	Fernanda Marques Carvalho, Cristiana Santos de Macedo, Roberta Olmo Pinheiro,
PR:CONTRIBUTORS                  	Euzenir Nunes Sarno, Maria Cristina Vidal Pessolani, John T. Belisle.
#STUDY
ST:STUDY_TITLE                   	Targeted metabolomics data of leprosy patients with type 1 reaction
ST:STUDY_TYPE                    	Targeted MS/MS analysis in retrospective serum samples of leprosy patients with
ST:STUDY_TYPE                    	type 1 reaction
ST:STUDY_SUMMARY                 	Targeted metabolomics-based analyses of pooled sera from 7 patients with T1R
ST:STUDY_SUMMARY                 	were conducted via LC-MS/MS.
ST:INSTITUTE                     	Colorado State University
ST:DEPARTMENT                    	Department of Microbiology, Immunology, and Pathology
ST:LABORATORY                    	Belisle
ST:LAST_NAME                     	Silva
ST:FIRST_NAME                    	Carlos
ST:ADDRESS                       	Rampart Road, 1682 Campus Delivery
ST:EMAIL                         	cadriano@rams.colostate.edu
ST:PHONE                         	9702154962
ST:NUM_GROUPS                    	02 (first group was leprosy patients with type 1 reaction, N=9; and second group
ST:NUM_GROUPS                    	was leprosy patients without type 1 reaction, N=7)
ST:TOTAL_SUBJECTS                	16
ST:NUM_MALES                     	5 (3 were leprosy patients with type 1 reaction and 2 were leprosy patients
ST:NUM_MALES                     	without type 1 reaction)
ST:NUM_FEMALES                   	11 (4 were leprosy patients with type 1 reaction and 7 were leprosy patients
ST:NUM_FEMALES                   	without type 1 reaction)
ST:STUDY_COMMENTS                	For this study we used retrospective sera samples.
ST:PUBLICATIONS                  	J Infect Dis. 2017 Feb 1;215(3):431-439. doi: 10.1093/infdis/jiw541.
#SUBJECT
SU:SUBJECT_TYPE                  	Human
SU:SUBJECT_SPECIES               	Homo sapiens
SU:TAXONOMY_ID                   	9606
SU:AGE_OR_AGE_RANGE              	13 - 66
SU:GENDER                        	Female and Male
SU:HUMAN_ETHNICITY               	Brazillian
SU:HUMAN_INCLUSION_CRITERIA      	Retrospective serum samples from leprosy patients diagnosed or not with type 1
SU:HUMAN_INCLUSION_CRITERIA      	reaction that were not receiving multidrug therapy or corticosteroid therapy at
SU:HUMAN_INCLUSION_CRITERIA      	the time of blood collection.
SU:HUMAN_EXCLUSION_CRITERIA      	Retrospective serum samples from leprosy patients that were under multidrug
SU:HUMAN_EXCLUSION_CRITERIA      	therapy and/or corticosteroid therapy at the time of blood collection were
SU:HUMAN_EXCLUSION_CRITERIA      	excluded from the study.
SU:SUBJECT_COMMENTS              	The patients exhibited borderline tuberculoid, borderline borderline and
SU:SUBJECT_COMMENTS              	borderline lepromatous forms of leprosy and was diagnosed or not with type 1
SU:SUBJECT_COMMENTS              	reaction.
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Additional sample data
SUBJECT_SAMPLE_FACTORS           	-	S1	Type 1 reaction (T1R):Yes	Gender=F; Bacillary index=-; Age=46; Serologic finding (+ or - for PGL-I)=+; clinical form of leprosy=BT
SUBJECT_SAMPLE_FACTORS           	-	S3	Type 1 reaction (T1R):Yes	Gender=F; Bacillary index=0.5; Age=27; Serologic finding (+ or - for PGL-I)=+; clinical form of leprosy=BB
SUBJECT_SAMPLE_FACTORS           	-	S5	Type 1 reaction (T1R):Yes	Gender=F; Bacillary index=0.5; Age=56; Serologic finding (+ or - for PGL-I)=+; clinical form of leprosy=BB
SUBJECT_SAMPLE_FACTORS           	-	S7	Type 1 reaction (T1R):Yes	Gender=F; Bacillary index=-; Age=32; Serologic finding (+ or - for PGL-I)=+; clinical form of leprosy=BT
SUBJECT_SAMPLE_FACTORS           	-	S8	Type 1 reaction (T1R):Yes	Gender=M; Bacillary index=-; Age=41; Serologic finding (+ or - for PGL-I)=+; clinical form of leprosy=BT
SUBJECT_SAMPLE_FACTORS           	-	S9	Type 1 reaction (T1R):Yes	Gender=M; Bacillary index=2; Age=66; Serologic finding (+ or - for PGL-I)=+; clinical form of leprosy=BL
SUBJECT_SAMPLE_FACTORS           	-	S10	Type 1 reaction (T1R):Yes	Gender=M; Bacillary index=1.5; Age=49; Serologic finding (+ or - for PGL-I)=+; clinical form of leprosy=BB
SUBJECT_SAMPLE_FACTORS           	-	S11	Type 1 reaction (T1R):No	Gender=F; Bacillary index=-; Age=65; Serologic finding (+ or - for PGL-I)=-; clinical form of leprosy=BT
SUBJECT_SAMPLE_FACTORS           	-	S12	Type 1 reaction (T1R):No	Gender=F; Bacillary index=-; Age=46; Serologic finding (+ or - for PGL-I)=-; clinical form of leprosy=BT
SUBJECT_SAMPLE_FACTORS           	-	S13	Type 1 reaction (T1R):No	Gender=F; Bacillary index=-; Age=13; Serologic finding (+ or - for PGL-I)=+; clinical form of leprosy=BT
SUBJECT_SAMPLE_FACTORS           	-	S14	Type 1 reaction (T1R):No	Gender=F; Bacillary index=-; Age=57; Serologic finding (+ or - for PGL-I)=+; clinical form of leprosy=BT
SUBJECT_SAMPLE_FACTORS           	-	S15	Type 1 reaction (T1R):No	Gender=F; Bacillary index=-; Age=15; Serologic finding (+ or - for PGL-I)=-; clinical form of leprosy=BT
SUBJECT_SAMPLE_FACTORS           	-	S16	Type 1 reaction (T1R):No	Gender=M; Bacillary index=-; Age=34; Serologic finding (+ or - for PGL-I)=-; clinical form of leprosy=BT
SUBJECT_SAMPLE_FACTORS           	-	S17	Type 1 reaction (T1R):No	Gender=F; Bacillary index=-; Age=40; Serologic finding (+ or - for PGL-I)=+; clinical form of leprosy=BT
SUBJECT_SAMPLE_FACTORS           	-	S18	Type 1 reaction (T1R):No	Gender=M; Bacillary index=-; Age=55; Serologic finding (+ or - for PGL-I)=-; clinical form of leprosy=BT
SUBJECT_SAMPLE_FACTORS           	-	S19	Type 1 reaction (T1R):No	Gender=F; Bacillary index=-; Age=64; Serologic finding (+ or - for PGL-I)=-; clinical form of leprosy=BT
#COLLECTION
CO:COLLECTION_SUMMARY            	The whole blood (10 mL) was collected in a Vacutainer tube from Becton Dickinson
CO:COLLECTION_SUMMARY            	(BD). After collection of the whole blood, it was allowed the blood to clot by
CO:COLLECTION_SUMMARY            	leaving it undisturbed at room temperature for 30 minutes. The clot was removed
CO:COLLECTION_SUMMARY            	by centrifuging at 1,000–2,000 x g for 10 minutes in a refrigerated centrifuge
CO:COLLECTION_SUMMARY            	(4 C). The resulting supernatant is designated serum. The serum samples were
CO:COLLECTION_SUMMARY            	aliquoted in 100 microliters and stored in a serum bank at -80C. These samples
CO:COLLECTION_SUMMARY            	were collected in the Leprosy Outpatient Unit (Oswaldo Cruz Foundation, Rio de
CO:COLLECTION_SUMMARY            	Janeiro, Brazil) and then they were sent in dry ice to Colorado State
CO:COLLECTION_SUMMARY            	University, where it was processed and analyzed for metabolomics. At Colorado
CO:COLLECTION_SUMMARY            	State University the samples were stored at -80C until processing.
CO:SAMPLE_TYPE                   	Serum
CO:COLLECTION_LOCATION           	Leprosy Outpatient Unit (Oswaldo Cruz Foundation, Rio de Janeiro, Brazil)
CO:COLLECTION_DURATION           	30 minutes
CO:STORAGE_CONDITIONS            	-80C
CO:ADDITIVES                     	no
CO:BLOOD_SERUM_OR_PLASMA         	Serum
#TREATMENT
TR:TREATMENT_SUMMARY             	No treatment of the patients was performed
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	Serum samples (7 serum samples from leprosy patients with T1R) were pooled prior
SP:SAMPLEPREP_SUMMARY            	the extraction. These pooled serum samples were incubated with 3 volumes of cold
SP:SAMPLEPREP_SUMMARY            	methanol (100%) for 1 hour at -20C. After this incubation, the samples were
SP:SAMPLEPREP_SUMMARY            	centrifuged for 30 minutes at 18,000 xg at 4C to clear the supernatant. The
SP:SAMPLEPREP_SUMMARY            	supernatant was then transferred and dried under vacuum. Samples were
SP:SAMPLEPREP_SUMMARY            	re-suspended in 80 μl of 50% methanol. Prior to the injections on the LC-MS
SP:SAMPLEPREP_SUMMARY            	instrument, the samples were centrifuged for 30 minutes at 18,000 xg at 4oC.
SP:SAMPLEPREP_PROTOCOL_ID        	SP000100
SP:SAMPLEPREP_PROTOCOL_FILENAME  	060613_Methanol_Serum_Extraction
SP:SAMPLEPREP_PROTOCOL_COMMENTS  	Use always nitrile gloves. Do not use gloves with powder. Use pipette tips with
SP:SAMPLEPREP_PROTOCOL_COMMENTS  	aerosol barrier.
SP:PROCESSING_METHOD             	Homogenization and solvent removal with Speed Vac
SP:PROCESSING_STORAGE_CONDITIONS 	on ice
SP:EXTRACTION_METHOD             	Cold Methanol extraction (3:1 methanol/water)
SP:EXTRACT_ENRICHMENT            	no enrichment was performed
SP:EXTRACT_CLEANUP               	Centrifugation
SP:EXTRACT_STORAGE               	-80C
SP:SAMPLE_RESUSPENSION           	50% methanol
SP:SAMPLE_DERIVATIZATION         	no derivatization process was performed
SP:SAMPLE_SPIKING                	Samples were spiked with the following commercial standards: arachidonic acid,
SP:SAMPLE_SPIKING                	docosahexaenoic acid, eicosapentaenoic acid and leukotriene B4
#CHROMATOGRAPHY
CH:CHROMATOGRAPHY_SUMMARY        	This analysis was performed only on negative mode. The solvent gradient used for
CH:CHROMATOGRAPHY_SUMMARY        	all chromatography was 2% solvent B for 3 min followed by a 15 min linear
CH:CHROMATOGRAPHY_SUMMARY        	gradient of 2% to 98% solvent B, which was held for 0.3 min. Then returned to
CH:CHROMATOGRAPHY_SUMMARY        	starting conditions over 1.2 min.
CH:CHROMATOGRAPHY_TYPE           	Reversed phase
CH:INSTRUMENT_NAME               	Agilent 1290
CH:INSTRUMENT_NAME               	quadrupole time-of-flight (Q-TOF) mass spectrometer.
CH:COLUMN_NAME                   	Waters Xbridge BEH C18 XP (100 x 2.1mm, 2.5um)
CH:COLUMN_NAME                   	Millford, MA, USA)
CH:FLOW_GRADIENT                 	0.25 mL/min
CH:FLOW_RATE                     	0.25 mL/min
CH:COLUMN_TEMPERATURE            	50C
CH:SOLVENT_A                     	89% water, 5% acetonitrile, 5% isopropanol and 1% 500 mM ammonium acetate
CH:SOLVENT_B                     	49.5% acetonitrile, 49.5% isopropanol and 1% 500 mM ammonium acetate
CH:INJECTION_TEMPERATURE         	4C
CH:SAMPLE_INJECTION              	20uL
CH:CAPILLARY_VOLTAGE             	2.8 kV
#ANALYSIS
AN:ANALYSIS_TYPE                 	MS
AN:LABORATORY_NAME               	Mycobacteria Research Laboratories
AN:OPERATOR_NAME                 	Kristofor Webb and Carlos AM Silva
AN:SOFTWARE_VERSION              	Agilent Mass Hunter Workstation Software version, Qualitative Analysis, Version
AN:SOFTWARE_VERSION              	B.05.00
AN:DATA_FORMAT                   	.d
#MS
MS:MS_COMMENTS                   	-
MS:INSTRUMENT_NAME               	Agilent 6510 QTOF
MS:INSTRUMENT_TYPE               	QTOF
MS:MS_TYPE                       	ESI
MS:ION_MODE                      	NEGATIVE
MS:CAPILLARY_VOLTAGE             	2.8kV
MS:COLLISION_ENERGY              	20eV
MS:COLLISION_GAS                 	Nitrogen
MS:DRY_GAS_FLOW                  	10 L/min
MS:DRY_GAS_TEMP                  	310C
MS:FRAGMENT_VOLTAGE              	120V
MS:NEBULIZER                     	45 psig
MS:SCANNING_RANGE                	2 spectra per second
MS:SKIMMER_VOLTAGE               	50V
MS:MS_RESULTS_FILE               	ST000881_AN001437_Results.txt	UNITS:arbitrary units
#MS_METABOLITE_DATA
MS_METABOLITE_DATA:UNITS         	MS peak area
MS_METABOLITE_DATA_START
Samples	S19	S19	S19	S18	S18	S18	S14	S14	S14	S12	S12	S12	S16	S16	S16	S11	S11	S11	S15	S15	S15	S17	S17	S17	S13	S13	S13	S10	S10	S10	S1	S1	S1	S3	S3	S3	S5	S5	S5	S7	S7	S7	S8	S8	S9	S9	S9
Factors	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):No	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes	Type 1 reaction (T1R):Yes
arachidonic acid	7299911.143	7865161.81	7936921.548	5562575.436	5537228.911	5559891.47	4680144.135	4835802.763	4816532.524	8357758.299	8862133.547	8343606.247	8418441.688	8342810.663	8312042.446	4136148.492	4025418.911	4260880.609	4233553.897	4346004.752	4203527.537	5292458.743	5121234.83	5188449.248	4479098.224	4528766.337	4419431.369	31708991.27	32862074.22	32171297.07	7718777.643	7429486.983	7396863.005	20866392.34	20688327.31	20764686.47	3481418.866	3320437.877	3410989.698	11618443.14	11451317.53	11438085.37	18047570.85	17777816.43	38371185	37472315.29	40211943.32
docosahexaenoic acid	2686477.402	2882809.909	2918531.495	2138632.78	2110494.349	2126677.293	1109918.974	1156759.048	1160184.902	1815184.813	1947984.61	1768356.609	2414648.318	2374502.446	2376769.736	1764796.054	1703935.757	1799836.869	2079716.644	2129107.69	2066720.114	1856020.532	1798867.908	1819937.346	1344961.234	1358905.61	1333346.88	10423706.86	11729078.18	11359754.35	3447777.931	3319237.391	3289928.37	6438512.579	6362206.05	6517555.083	1579765.474	1517989.64	1566183.678	3363245.455	3281245.194	3224927.67	6097781.515	5951942.001	10864616.55	11164997.78	11531546.11
eicosapentaenoic acid	648846.6632	727768.5616	744377.0623	923821.0842	895982.836	920976.3724	97437.54853	103557.6025	103139.337	870042.7675	946178.2206	832269.0022	897563.8611	897627.2845	893886.9039	1020601.157	950535.8871	1037429.957	337390.9904	327778.2676	330488.2954	381725.3189	371663.0527	371476.0546	354048.6915	359007.4749	339867.5464	12621337.18	13336485.57	12927592.16	1148844.315	1079039.972	1080763.992	2567602.737	2542341.054	2607795.945	809095.3878	756894.3451	792520.8231	1717837.072	1812159.074	1815303.276	2551800.149	2514850.163	5406129.443	5625927.864	5856024.135
leukotriene B4	94178.36922	103950.1958	NA	NA	30424.8453	35897.19797	NA	NA	NA	NA	72213.07777	64022.06455	NA	31280.61113	31468.15348	NA	23796.41231	NA	NA	NA	34383.10702	94209.2556	90014.89524	93400.19634	28021.7732	27601.6116	26461.06465	1393464.481	1521256.503	1481179.511	199025.8664	205680.5836	190631.8112	1553250.332	1551457.533	1525152.203	NA	NA	NA	1853208.387	NA	1914268.658	1861406.666	1765671.804	2281901.324	2499739.085	2580232.762
MS_METABOLITE_DATA_END
#METABOLITES
METABOLITES_START
metabolite_name	retention index	quantified m/z	PubChem ID	KEGG ID	HMDB ID
arachidonic acid		303.23	444899	C00219	HMDB01043
docosahexaenoic acid		327.23	445580	C06429	HMDB02183
eicosapentaenoic acid		301.22	446284	C06428	HMDB01999
leukotriene B4		335.22	5280492	C02165	HMDB01085
METABOLITES_END
#END