Summary of project PR002040

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 PR002040. The data can be accessed directly via it's Project DOI: 10.21228/M8XB94 This work is supported by NIH grant, U2C- DK119886.

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

Project ID: PR002040
Project DOI:doi: 10.21228/M8XB94
Project Title:Quantification of amoxicillin in intestinal contents of mice
Project Summary:Antibiotics cause collateral damage to resident microbes that is associated with various health risks. To-date, studies have largely focused on impacts of antibiotics on large intestinal and fecal microbiota. Here, we employ a GI-wide integrated multiomic approach to reveal that amoxicillin (AMX) treatment reduces overall bacterial abundance, bile salt hydrolase activity and unconjugated bile acids in the small intestine (SI). An accompanying loss of fatty acids and increase in acyl-carnitines in the large intestine corresponded with spatially-distinct expansions of proteobacteria. Parasuterella excrementihominis utilized fatty acid biosynthesis, becoming dominant in the SI while multiple Klebsiella species employed fatty acid oxidation during expansion in the large intestine. We subsequently demonstrate that restoration of unconjugated bile acids can mitigate losses of commensals in the large intestine while also inhibiting the expansion of Proteobacteria during AMX treatment.
Institute:Brown University
Last Name:Beekman
First Name:Chapman
Address:BMC 613, 171 Meeting Street, Providence RI 02912
Email:Chapman_Beekman@brown.edu
Phone:4018635953

Summary of all studies in project PR002040

Study IDStudy TitleSpeciesInstituteAnalysis
(* : Contains Untargted data)
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Date
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(* : Contains raw data)
ST003288 Quantification of amoxicillin in mouse intestinal contents Mus musculus Brown University MS 2024-08-05 1 49 Uploaded data (4.7G)*
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