Summary of Study ST003941

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 PR002470. The data can be accessed directly via it's Project DOI: 10.21228/M8C82T This work is supported by NIH grant, U2C- DK119886.

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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 IDST003941
Study TitleLipidomic analysis of Bacteroides thetaiotaomicron WT vs SPT KO (sphingolipid-deficient) outer membrane vesicles (OMVs) and whole cells.
Study SummaryWe performed a lipidomic analysis of outer membrane vesicles (OMVs) from Bacteroides thetaiotaomicron vs whole cell bacteria to understand whether there are lipids enriched in the OMVs of Bacteroides. We also utilized a sphingolipid-deficient Bacteroides thetaiotaomicron strain with a knockout of the serine palmitoyltransferase gene (spt) and compared the lipidomic signature to the wild-type strain in OMVs and whole cell bacteria. Overall we report the differences in lipids from each strain in OMVs and in whole cell bacteria and which sphingolipids are enriched in OMVs.
Institute
Broad Institute of MIT and Harvard
DepartmentIDMP
LaboratoryXavier Lab and Clish Lab
Last NameBrown
First NameEric
Address415 Main Street, Cambridge, MA, USA 02142
Emailericmichbrown@gmail.com
Phone6176826566
Submit Date2025-04-21
Study CommentsBacterial lipidomics on OMVs and whole cell bacteria on B. thetaiotaomicron WT vs SPT KO strains
Raw Data AvailableYes
Raw Data File Type(s)mzML, raw(Thermo)
Analysis Type DetailLC-MS
Release Date2025-06-05
Release Version1
Eric Brown Eric Brown
https://dx.doi.org/10.21228/M8C82T
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR002470
Project DOI:doi: 10.21228/M8C82T
Project Title:Sphingolipids promote anti-inflammatory responses of Bacteroides through the mevalonate pathway
Project Type:Bacterial lipidomics
Project Summary:A lipidomics analysis to identify sphingolipids of interest in Bacteroides thetaiotaomicron outer membrane vesicles (OMVs) and whole cell bacteria.
Institute:Broad Institute of MIT and Harvard
Department:IDMP
Laboratory:Xavier Lab and Clish Lab
Last Name:Brown
First Name:Eric
Address:415 Main Street, Cambridge, Massachusetts, 02142, USA
Email:erbrown@broadinstitute.org
Phone:6176826566
Contributors:Clary Clish, Sarah Jeanfavre, Julian Avila-Pacheco

Subject:

Subject ID:SU004077
Subject Type:Bacteria
Subject Species:Bacteroides thetaiotaomicron
Taxonomy ID:8188
Genotype Strain:Wild-type vs SPT Knockout strain

Factors:

Subject type: Bacteria; Subject species: Bacteroides thetaiotaomicron (Factor headings shown in green)

mb_sample_id local_sample_id Sample source Genotype Sample type
SA450445BTSPTWC_2Bacteria SPT KO Bacteria
SA450446BTSPTWC_1Bacteria SPT KO Bacteria
SA450447BTSPTWC_3Bacteria SPT KO Bacteria
SA450448BTWTWC_1Bacteria Wild-type Bacteria
SA450449BTWTWC_2Bacteria Wild-type Bacteria
SA450450BTWTWC_3Bacteria Wild-type Bacteria
SA450451BTSPTOMV_1OMVs SPT KO OMVs
SA450452BTSPTOMV_2OMVs SPT KO OMVs
SA450453BTSPTOMV_3OMVs SPT KO OMVs
SA450454BTWTOMV_1OMVs Wild-type OMVs
SA450455BTWTOMV_2OMVs Wild-type OMVs
SA450456BTWTOMV_3OMVs Wild-type OMVs
Showing results 1 to 12 of 12

Collection:

Collection ID:CO004070
Collection Summary:Bacteroides thetaiotaomicron wild-type or spt-knockout OMVs were collected after 2 days of culture in BHI media by ultra-centrifugation and frozen at -80 degrees until analysis. To obtain the whole cell lipidomic data, either wild-type or spt knockout Bacteroides thetaiotaomicron strains were centrifuged at 8000g for 20 min and pellets were snap frozen before analysis.
Sample Type:Bacterial cells
Storage Conditions:-80℃

Treatment:

Treatment ID:TR004086
Treatment Summary:Cells were not treated
Cell Storage:-80
Cell Media:Brain Heart Infusion Agar

Sample Preparation:

Sampleprep ID:SP004083
Sampleprep Summary:Metabolites were extracted from the samples by adding isopropanol to the OMVs or cells. The extract was then subjected to LC-MS analysis.
Processing Storage Conditions:On ice
Extract Storage:-80℃

Chromatography:

Chromatography ID:CH004919
Chromatography Summary:Solvent A - 95:5:0.1 vol/vol/vol 10 mM ammonium acetate/methanol/formic acid
Methods Filename:Lipidomic_profiling_methods_Metabolomics_Workbench_Sphingolipids.pdf
Instrument Name:Shimadzu Nexera X2
Column Name:Waters ACQUITY BEH C8 (100 x 2.1mm, 1.7um)
Column Temperature:40
Flow Gradient:The column was eluted isocratically with 80% A for 1 minute followed by a linear gradient to 80% B over 2 minutes, a linear gradient to 100% B over 7 minutes, then 3 minutes at 100% B
Flow Rate:0.45mL/min
Solvent A:95% water/5% methanol; 10 mM ammonium acetate; 0.1% formic acid
Solvent B:100% water; 0.1% formic acid
Chromatography Type:Reversed phase

Analysis:

Analysis ID:AN006477
Analysis Type:MS
Analysis Protocol File:Lipidomic_profiling_methods_Metabolomics_Workbench_Sphingolipids.pdf
Chromatography ID:CH004919
Has Mz:1
Has Rt:1
Rt Units:Seconds
Results File:ST003941_AN006477_Results.txt
Units:Intensity
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