Summary of Study ST000882

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR000611. The data can be accessed directly via it's Project DOI: 10.21228/M8XQ41 This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST000882
Study TitleUntargeted metabolomics data of leprosy patients with type 1 reaction
Study TypeUntargeted MS qualitative analysis in retrospective serum samples of leprosy patients with type 1 reaction
Study SummaryUntargeted metabolomics-based analyses of sera from 7 patients with and 9 without T1R were conducted via liquid chromatography–mass spectrometry.
Institute
Colorado State University
DepartmentDepartment of Microbiology, Immunology, and Pathology
LaboratoryBelisle
Last NameSilva
First NameCarlos
AddressRampart Road, 1682 Campus Delivery
Emailcadriano@rams.colostate.edu
Phone9702154962
Submit Date2017-06-19
Num Groups2
Total Subjects16
Num Males5
Num Females11
Study Comments2 groups (first group was leprosy patients with type 1 reaction, N=9; and second group was leprosy patients without type 1 reaction, N=7) 5 males (3 were leprosy patients with type 1 reaction and 2 were leprosy patients without type 1 reaction), 11 females (4 were leprosy patients with type 1 reaction and 7 were leprosy patients without type 1 reaction). For this study we used retrospective sera samples.
PublicationsJ Infect Dis. 2017 Feb 1;215(3):431-439. doi: 10.1093/infdis/jiw541.
Raw Data AvailableYes
Raw Data File Type(s)d
Analysis Type DetailLC-MS
Release Date2017-06-19
Release Version1
Carlos Silva Carlos Silva
https://dx.doi.org/10.21228/M8XQ41
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR000611
Project DOI:doi: 10.21228/M8XQ41
Project Title:Metabolomics analysis of leprosy patients with type 1 reaction
Project Type:MS qualitative analysis and identification of polyunsaturated fatty acids in retrospective serum samples of leprosy patients with type 1 reaction
Project Summary:Type 1 reaction (T1R) is an acute inflammatory episode that causes severe neuronal damages in patients with leprosy. The factors that trigger this pathology is still unknown, and further studies are needed to understand T1R and to early prevent its start. It is well established that the host immune response is linked to T1R and previous studies indicated that the metabolism of the host also influences the adaptive immune response against M. leprae antigens. Therefore, metabolomics-based analyses of sera from 7 patients with and 9 without T1R were conducted via liquid chromatography–mass spectrometry. The main goal of this project was to determine whether the metabolism of polyunsaturated fatty acids (such as eicosanoids and omega-3 fatty acids) were perturbed in leprosy patients with T1R.
Institute:Colorado State University
Department:Department of Microbiology, Immunology, and Pathology
Laboratory:Belisle
Last Name:Belisle
First Name:John
Address:Rampart Road, 1682 Campus Delivery
Email:cadriano@rams.colostate.edu
Phone:9704819160
Funding Source:This work was supported by the New York Community Trust (grant to J. T. B. as co–principle investigator [PI]), by the Heiser Foundation (grant to J. T. B. as co-PI), and by the Brazilian Coordination for the Improvement of Higher Education Personnel through the Science without Borders program (10546-13-8, for the postdoctoral scholarship to C. A. M. S.).
Project Comments:The institutional review boards of Colorado State University approved the use of sera for the reported study.
Publications:J Infect Dis. 2017 Feb 1;215(3):431-439. doi: 10.1093/infdis/jiw541.
Contributors:Carlos A. M. Silva, Kristofor Webb, Barbara G. Andre, Maria Angela Marques, Fernanda Marques Carvalho, Cristiana Santos de Macedo, Roberta Olmo Pinheiro, Euzenir Nunes Sarno, Maria Cristina Vidal Pessolani, John T. Belisle.

Subject:

Subject ID:SU000916
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606
Age Or Age Range:13 - 66
Gender:Female and Male
Human Inclusion Criteria:Retrospective serum samples from leprosy patients diagnosed or not with type 1 reaction that were not receiving multidrug therapy or corticosteroid therapy at the time of blood collection.
Human Exclusion Criteria:Retrospective serum samples from leprosy patients that were under multidrug therapy and/or corticosteroid therapy at the time of blood collection were excluded from the study.
Subject Comments:The patients exhibited borderline tuberculoid, borderline borderline and borderline lepromatous forms of leprosy and was diagnosed or not with type 1 reaction.

Factors:

Subject type: Human; Subject species: Homo sapiens (Factor headings shown in green)

mb_sample_id local_sample_id Type 1 reaction (T1R)
SA051152S15No
SA051153S14No
SA051154S16No
SA051155S18No
SA051156S19No
SA051157S13No
SA051158S17No
SA051159S12No
SA051160S11No
SA051161S5Yes
SA051162S3Yes
SA051163S7Yes
SA051164S9Yes
SA051165S10Yes
SA051166S1Yes
SA051167S8Yes
Showing results 1 to 16 of 16

Collection:

Collection ID:CO000910
Collection Summary:The whole blood (10 mL) was collected in a Vacutainer tube from Becton Dickinson (BD). After collection of the whole blood, it was allowed the blood to clot by leaving it undisturbed at room temperature for 30 minutes. The clot was removed by centrifuging at 1,000–2,000 x g for 10 minutes in a refrigerated centrifuge (4 C). The resulting supernatant is designated serum. The serum samples were aliquoted in 100 microliters and stored in a serum bank at -80C. These samples were collected in the Leprosy Outpatient Unit (Oswaldo Cruz Foundation, Rio de Janeiro, Brazil) and then they were sent in dry ice to Colorado State University, where it was processed and analyzed for metabolomics. At Colorado State University the samples were stored at -80C until processing.
Sample Type:Blood
Storage Conditions:-80C
Blood Serum Or Plasma:serum

Treatment:

Treatment ID:TR000930
Treatment Summary:No treatment of the patients was performed

Sample Preparation:

Sampleprep ID:SP000923
Sampleprep Summary:The retrospective serum samples (80 microliters[ul]) were incubated with 3 volumes of cold methanol (100%) for 1 hour at -20C. After this incubation, the samples were centrifuged for 30 minutes at 18,000 xg at 4C to clear the supernatant. The supernatant was then transferred and dried under vacuum. Samples were re-suspended in 80 μl of 50% methanol. Prior to the injections on the LC-MS instrument, the samples were centrifuged for 30 minutes at 18,000 xg at 4oC.
Sampleprep Protocol ID:SP000100
Sampleprep Protocol Filename:060613_Methanol_Serum_Extraction
Sampleprep Protocol Comments:Use always nitrile gloves. Do not use gloves with powder. Use pipette tips with aerosol barrier.
Processing Storage Conditions:-80C
Extraction Method:Methanol extraction
Extract Cleanup:Centrifugation
Extract Storage:-80C
Sample Resuspension:50% methanol
Sample Derivatization:no derivatization process was performed

Combined analysis:

Analysis ID AN001438 AN001439
Analysis type MS MS
Chromatography type Reversed phase Reversed phase
Chromatography system Agilent 1290 Agilent 1290
Column Waters Xbridge BEH C18 XP (100 x 2.1mm,2.5um) Waters Xbridge BEH C18 XP (100 x 2.1mm,2.5um)
MS Type ESI ESI
MS instrument type TOF TOF
MS instrument name Agilent 6224 TOF Agilent 6224 TOF
Ion Mode NEGATIVE POSITIVE
Units Peak area Peak area

Chromatography:

Chromatography ID:CH001009
Chromatography Summary:This was used for negative mode. The solvent gradient used for all chromatography was 2% solvent B for 3 min followed by a 15 min linear gradient of 2% to 98% solvent B, which was held for 0.3 min. Then returned to starting conditions over 1.2 min. Triplicate LC-MS injections were made of each sample and the order of sample injection (including triplicates) was randomized.
Instrument Name:Agilent 1290
Column Name:Waters Xbridge BEH C18 XP (100 x 2.1mm,2.5um)
Column Temperature:50C
Flow Gradient:0.25 mL/min
Flow Rate:0.25 mL/min
Injection Temperature:4C
Sample Injection:20uL
Solvent A:89% water/5% acetonitrile/5% isopropanol; 5 mM ammonium acetate
Solvent B:50% acetonitrile/50% isopropanol; 5 mM ammonium acetate
Capillary Voltage:2.8 kV
Chromatography Type:Reversed phase
  
Chromatography ID:CH001010
Chromatography Summary:This was used for positive mode. The solvent gradient used for all chromatography was 2% solvent B for 3 min followed by a 15 min linear gradient of 2% to 98% solvent B, which was held for 0.3 min. Then returned to starting conditions over 1.2 min. Triplicate LC-MS injections were made of each sample and the order of sample injection (including triplicates) was randomized.
Instrument Name:Agilent 1290
Column Name:Waters Xbridge BEH C18 XP (100 x 2.1mm,2.5um)
Column Temperature:50C
Flow Gradient:0.25 mL/min
Flow Rate:0.25 mL/min
Injection Temperature:4C
Sample Injection:20uL
Solvent A:95% water/5% acetonitrile; 0.1% formic acid
Solvent B:95% acetonitrile/5% water; 0.1% formic acid
Capillary Voltage:4.0kV
Chromatography Type:Reversed phase

MS:

MS ID:MS001328
Analysis ID:AN001438
Instrument Name:Agilent 6224 TOF
Instrument Type:TOF
MS Type:ESI
Ion Mode:NEGATIVE
Capillary Voltage:2.8kV
Dry Gas Flow:5 L/min
Dry Gas Temp:310C
Fragment Voltage:120V
Nebulizer:20 psig
Scanning Range:2 spectra per second
Skimmer Voltage:50V
  
MS ID:MS001329
Analysis ID:AN001439
Instrument Name:Agilent 6224 TOF
Instrument Type:TOF
MS Type:ESI
Ion Mode:POSITIVE
Capillary Voltage:4.0kV
Dry Gas Flow:5 L/min
Dry Gas Temp:310C
Fragment Voltage:120V
Nebulizer:20 psig
Scanning Range:2 spectra per second
Skimmer Voltage:50V
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