Summary of Study ST001287

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 PR000869. The data can be accessed directly via it's Project DOI: 10.21228/M8C40P This work is supported by NIH grant, U2C- DK119886.

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Study IDST001287
Study TitleLuminal succinate in UC-HMA (human microbiota-associated) mice.
Study TypeMS analysis
Study SummaryPatients with ulcerative colitis (UC) are known to be at higher risk for Clostridium difficile (C. difficile) infection (CDI), and CDI in UC patients is recognized as a major clinical problem because it worsens UC outcome. In order to assess the role of gut dysbiosis, seen in UC patients, we have established a human microbiota-associated mouse model in which germ-free mice are colonized with gut microbiota from UC patients. Utilizing this model, we found that UC microbiota colonized HMA mice (UC-HMA mice) were susceptible to CDI. To address the mechanism by which UC-HMA mice are unable to acquire the colonization resistance against C. difficile, we analyzed the luminal metabolites in UC-HMA mice, especially in succinate which is a crucial metabolite doe the growth of C. difficile.
Institute
University of Michigan
DepartmentBiomedical Research Core Facilities
LaboratoryMetabolomics core
Last NameKachman
First NameMaureen
AddressAnn Arbor, MI
Emailmkachman@med.umich.edu
Phone734-232-0842
Submit Date2019-12-11
Num Groups63
Total Subjects3
Raw Data AvailableYes
Raw Data File Type(s)d
Analysis Type DetailLC-MS
Release Date2020-01-13
Release Version1
Maureen Kachman Maureen Kachman
https://dx.doi.org/10.21228/M8C40P
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR000869
Project DOI:doi: 10.21228/M8C40P
Project Title:Association of luminal succinate in UC-Mb mice and succinate consuming bacteria
Project Type:MS analysis
Project Summary:Measure the levels of luminal succinate in UC-Mb mice (UC-Mb colonized human gnotobiotic mise) and succinate consuming bacteria inoculated UC-Mb mice to elucidate the association between the increased abundance of succinate consuming bacteira and decreased amounts of luminal succinate in CDI-susceptible UC-Mb mice.
Institute:University of Michigan
Department:Internal Medicine-Gastroenterology
Laboratory:Kamada Lab
Last Name:Kamada
First Name:Nobuhiko
Address:Ann Arbor, MI
Email:nkamada@umich.edu
Phone:734-763-2142
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