Summary of Study ST002523

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 PR001625. The data can be accessed directly via it's Project DOI: 10.21228/M8NM7N 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 IDST002523
Study TitleCandida expansion in the human gut is associated with an ecological signature that supports growth under dysbiotic conditions
Study SummaryThe overgrowth of Candida species in the human gut is considered a prerequisite for invasive candidiasis. However, our understanding of how gut bacteria promote or restrict overgrowth of Candida species in the human gut is still limited. By integrating mycobiome and shotgun metagenomics data from stool of 75 patients at risk but with no systemic candidiasis, we revealed that bacterial communities from high Candida samples had greater metabolic potential whereas communities from low Candida had greater functional redundancy. In addition, we developed machine learning models that used only bacterial taxa or functional relative abundances to predict the levels of Candida genus and species in an external validation cohort with an area under the curve of 78.6-81.1%. Last, we proposed an intriguing mechanism for Candida species overgrowth based on a decrease in short-chain fatty acid producing-bacteria resulting in increased oxygen levels. These conditions create a metabolic niche for Candida species to use lactate as a carbon source and overtake their fungal competitors in the human gut.
Institute
Leibniz Institute for Natural Product Research and Infection Biology Hans Knöll Institute (Leibniz-HKI)
DepartmentMicrobiome Dynamics
Last NameBastian
First NameSeelbinder
AddressBeutenbergstraße 11a, Jena, Thuringia, 07745, Germany
Emailbastian.seelbinder@leibniz-hki.de
Phone+4936415321360
Submit Date2023-03-23
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailLC-MS
Release Date2023-04-12
Release Version1
Seelbinder Bastian Seelbinder Bastian
https://dx.doi.org/10.21228/M8NM7N
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Treatment:

Treatment ID:TR002635
Treatment Summary:To unfreeze samples at MS-OMICS, samples were assigned to their SpinX filters and centrifugated at 15,000 RPM for 5 minutes at 4 °C. Urine samples were then diluted 11 times in mobile phase eluent A and fortified with stable isotope labelled standards before analysis.
Treatment Compound:mobile phase eluent A
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