Summary of Study ST000881

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 IDST000881
Study TitleTargeted metabolomics data of leprosy patients with type 1 reaction
Study TypeTargeted MS/MS analysis in retrospective serum samples of leprosy patients with type 1 reaction
Study SummaryTargeted metabolomics-based analyses of pooled sera from 7 patients with T1R were conducted via LC-MS/MS.
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 Date2017-08-02
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 Date2017-08-02
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:SU000915
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606
Age Or Age Range:13 - 66
Gender:Female and Male
Human Ethnicity:Brazillian
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.
Species Group:Mammals

Factors:

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

mb_sample_id local_sample_id Type 1 reaction (T1R)
SA051136S15No
SA051137S14No
SA051138S16No
SA051139S18No
SA051140S19No
SA051141S13No
SA051142S17No
SA051143S12No
SA051144S11No
SA051145S5Yes
SA051146S3Yes
SA051147S7Yes
SA051148S9Yes
SA051149S10Yes
SA051150S1Yes
SA051151S8Yes
Showing results 1 to 16 of 16

Collection:

Collection ID:CO000909
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:Serum
Collection Location:Leprosy Outpatient Unit (Oswaldo Cruz Foundation, Rio de Janeiro, Brazil)
Collection Duration:30 minutes
Storage Conditions:-80C
Additives:no
Blood Serum Or Plasma:Serum

Treatment:

Treatment ID:TR000929
Treatment Summary:No treatment of the patients was performed

Sample Preparation:

Sampleprep ID:SP000922
Sampleprep Summary:Serum samples (7 serum samples from leprosy patients with T1R) were pooled prior the extraction. These pooled serum samples 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 Method:Homogenization and solvent removal with Speed Vac
Processing Storage Conditions:on ice
Extraction Method:Cold Methanol extraction (3:1 methanol/water)
Extract Enrichment:no enrichment was performed
Extract Cleanup:Centrifugation
Extract Storage:-80C
Sample Resuspension:50% methanol
Sample Derivatization:no derivatization process was performed
Sample Spiking:Samples were spiked with the following commercial standards: arachidonic acid, docosahexaenoic acid, eicosapentaenoic acid and leukotriene B4

Combined analysis:

Analysis ID AN001437
Analysis type MS
Chromatography type Reversed phase
Chromatography system Agilent 1290
Column Waters Xbridge BEH C18 XP (100 x 2.1mm,2.5um)
MS Type ESI
MS instrument type QTOF
MS instrument name Agilent 6510 QTOF
Ion Mode NEGATIVE
Units arbitrary units

Chromatography:

Chromatography ID:CH001008
Chromatography Summary:This analysis was performed only on 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.
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

MS:

MS ID:MS001327
Analysis ID:AN001437
Instrument Name:Agilent 6510 QTOF
Instrument Type:QTOF
MS Type:ESI
Ion Mode:NEGATIVE
Capillary Voltage:2.8kV
Collision Energy:20eV
Collision Gas:Nitrogen
Dry Gas Flow:10 L/min
Dry Gas Temp:310C
Fragment Voltage:120V
Nebulizer:45 psig
Scanning Range:2 spectra per second
Skimmer Voltage:50V
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