Summary of Study ST001248

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 PR000835. The data can be accessed directly via it's Project DOI: 10.21228/M8RH65 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 IDST001248
Study TitleThe cecal and fecal metabolomes of horses before and after metronidazole administration
Study SummaryMetronidazole (15mg/kg BID PO) was given to horses (n=5) with in-dwelling cecal cannulas. The study was suspended after the fifth dose (day 3) due to adverse gastrointestinal effects. Cecal and fecal samples were obtained before and after (Days days -52, -28, -14, 0, 7, 14, 28 and 52) metronidazole administration. The metabolome was characterized by mass spectrometry-based methods. Fecal, but not cecal metabolites were affected by metronidazole. The fecal metabolites affected represented diverse metabolic pathways such as nucleic acid metabolism, secondary bile metabolism, fatty acid synthesis/degradation/elongation or metabolism and sugar metabolism.
Institute
Texas A&M University
DepartmentDepartment of Small Animal Clinical Sciences
LaboratoryGastrointestinal Laboratory
Last NameArnold
First NameCarolyn
Address4474 TAMU
Emailcarnold@cvm.tamu.edu
Phone979 845 3541
Submit Date2019-09-04
Raw Data AvailableYes
Raw Data File Type(s)cdf
Analysis Type DetailMALDI-MS
Release Date2020-03-03
Release Version1
Carolyn Arnold Carolyn Arnold
https://dx.doi.org/10.21228/M8RH65
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR000835
Project DOI:doi: 10.21228/M8RH65
Project Title:The cecal and fecal microbiomes and metabolomes of horses before and after metronidazole administration
Project Summary:Metronidazole (15mg/kg BID PO) was given to horses (n=5) with in-dwelling cecal cannulas. The study was suspended after the fifth dose (day 3) due to adverse gastrointestinal effects. Cecal and fecal samples were obtained before and after (Days days -52, -28, -14, 0, 7, 14, 28 and 52) metronidazole administration. DNA was extracted from the cecal and fecal samples, and 16S rRNA genes were sequenced. The bacterial diversity and composition of each sample was determined. Richness and evenness indices were significantly decreased by metronidazole administration in both cecal and fecal samples, but overall composition was only significantly changed in fecal samples on Day 3 (ANOSIM, p=0.008). The most dominant phyla were Bacteroidetes and Firmicutes in all groups examined. In fecal samples, significant changes at the phyla Actinobacteria, Spirochaetes, Lentisphaerae and Verrucomicrobia occurred on Day 3, which correlated with clinical signs of gastrointestinal disease. Analysis of the predicted microbial functions using PICRUSt indicated changes associated with metronidazole in fecal samples. The metabolome was characterized by mass spectrometry-based methods. Fecal, but not cecal metabolites were affected by metronidazole. The fecal metabolites affected represented diverse metabolic pathways such as nucleic acid metabolism, secondary bile metabolism, fatty acid synthesis/degradation/elongation or metabolism and sugar metabolism.
Institute:Texas A&M University
Department:Department of Small Animal Clinical Sciences
Laboratory:Gastrointestinal Laboratory
Last Name:Arnold
First Name:Carolyn
Address:4474 TAMU
Email:carnold@cvm.tamu.edu
Phone:979 845 3541
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