Summary of Study ST002345

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 PR001505. The data can be accessed directly via it's Project DOI: 10.21228/M85717 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 IDST002345
Study TitleStress-Induced Mucosal Layer Disruption Drives Gut Dysbiosis and Depressive-like Behaviors
Study SummaryDepression is a common mental health condition with a large social and economic impact. While depression etiology is multifactorial, chronic stress is a well-accepted contributor to disease onset. In addition, depression is associated with altered gut microbial signatures that can be replicated in animal models. While targeted restoration of the microbiome has been shown to reduce depressive-like behaviors in mice, the complexity and diversity of the human microbiome has complicated therapeutic intervention in patients. To circumvent these limitations, there is a critical need for identifying pathways responsible for microbiome dysbiosis. Here, for the first time, we identify the changes in host physiology that induce microbiome dysbiosis. Specifically, we show that a component of mucosal layer, the transmembrane protein mucin 13, can regulate microbiome composition. Using a model of chronic stress to induce behavioral and microbial changes in mice, we show a significant reduction in mucin 13 expression across the intestines that occurs independently of the microbiome. Furthermore, deleting Muc13 leads to gut dysbiosis, and baseline behavioral changes normally observed after stress exposure. Together, these results validate the hypothesis that mucosal layer disruption is an initiating event in stress-induced dysbiosis and offer mucin 13 as a potential new therapeutic target for microbiome dysbiosis in stress-induced depression. For the first time, our data provide an upstream and conserved target for treating microbiome dysbiosis, a result with sweeping implications for diseases presenting with microbial alterations.
Institute
University of Virginia
Last NameRivet-Noor
First NameCourtney
Address409 Lane Road, Charlottsville, Virginia, 22903, USA
Emailcrr4tz@virginia.edu
Phone434-243-1903
Submit Date2022-11-10
Num Groups2
Total Subjects23
Num Males23
Raw Data AvailableYes
Raw Data File Type(s)raw(Thermo)
Analysis Type DetailLC-MS
Release Date2022-11-28
Release Version1
Courtney Rivet-Noor Courtney Rivet-Noor
https://dx.doi.org/10.21228/M85717
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Factors:

Subject type: Mammal; Subject species: Mus musculus (Factor headings shown in green)

mb_sample_id local_sample_id Group
SA235359Cal4_BCTL
SA235360Cal4_ACTL
SA235361Cal5_ACTL
SA235362Cal5_BCTL
SA235363blank1CTL
SA235364Cal3_ACTL
SA235365Cal3_BCTL
SA235366Cal2_BCTL
SA235367blank3CTL
SA235368blank2CTL
SA235369Cal1_ACTL
SA235370blank4CTL
SA235371Cal1_BCTL
SA235372Cal2_ACTL
SA235373Naive_238Naïve
SA235374Naive_239Naïve
SA235375Naive_248Naïve
SA235376Naive_249Naïve
SA235377Naive_247Naïve
SA235378Naive_231Naïve
SA235379Naive_237Naïve
SA235380Naive_227Naïve
SA235381Naive_226Naïve
SA235382Naive_229Naïve
SA235383Naive_230Naïve
SA235384Stress_244Stress
SA235385Stress_245Stress
SA235386Stress_246Stress
SA235387Stress_243Stress
SA235388Stress_233Stress
SA235389Stress_240Stress
SA235390Stress_234Stress
SA235391Stress_232Stress
SA235392Stress_235Stress
SA235393Stress_236Stress
SA235394Stress_241Stress
SA235395Stress_242Stress
Showing results 1 to 37 of 37
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