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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Combined analysis:

Analysis ID AN004157
Analysis type MS
Chromatography type Reversed phase
Chromatography system Thermo Vanquish
Column Waters ACQUITY UPLC HSS T3 (150 x 2.1mm,1.8um)
MS Type ESI
MS instrument type QTRAP
MS instrument name Thermo Orbitrap Exploris 240
Ion Mode UNSPECIFIED
Units Peak area

MS:

MS ID:MS003904
Analysis ID:AN004157
Instrument Name:Thermo Orbitrap Exploris 240
Instrument Type:QTRAP
MS Type:ESI
MS Comments:The ionization was achieved with an electrospray ionization interface operated in positive and negative ionization mode under polarity switching. Data were processed using Compound Discoverer 3.3 (Thermo Fisher Scientific) and Skyline 21.2.
Ion Mode:UNSPECIFIED
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