Summary of Study ST004204

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 PR002650. The data can be accessed directly via it's Project DOI: 10.21228/M83V73 This work is supported by NIH grant, U2C- DK119886. See: https://www.metabolomicsworkbench.org/about/howtocite.php

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Study IDST004204
Study TitleThe growth and virulence of S. aureus is inhibited by C. striatum by inhibiting its arginine biosynthesis pathway
Study SummaryBackground: Patients with chronic rhinosinusitis (CRS) exhibit signs of nasal microbiota dysbiosis, specifically manifested by an increase in the relative abundance of Staphylococcus species and a decrease in the relative abundance of Corynebacterium species. This alteration may be closely associated with the pathogenesis of CRS. Understanding how commensal bacteria interact with pathogenic bacteria can help us reconstruct the homeostasis of nasal microbiota and promote nasal health. Method and Results: We conducted an in vitro co-culture model of Staphylococcus aureus and Corynebacterium striatum. Through metabolomic analysis, we discovered that the metabolic pathways of S. aureus were downregulated considerably during co-culture, especially for the arginine biosynthesis pathway. We later conducted validation experiments involving arginine supplementation and air-liquid interface culture of human nasal epithelial cells. Conclusion: The growth and virulence of S. aureus is inhibited by C. striatum by inhibiting its arginine biosynthesis pathway.
Institute
Sun Yat-sen University
DepartmentOtorhinolaryngology, First Affiliated Hospital of Sun Yat-sen University
LaboratoryOtorhinolaryngology Institute of Sun Yat-sen University
Last NameXinyu
First NameZhang
AddressNo.74 Zhongshan Er Road
Emailzhangxy2236@mail.sysu.edu.cn
Phone+86 15920583447
Submit Date2025-09-04
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailLC-MS
Release Date2025-10-10
Release Version1
Zhang Xinyu Zhang Xinyu
https://dx.doi.org/10.21228/M83V73
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Combined analysis:

Analysis ID AN006990 AN006991
Chromatography ID CH005307 CH005307
MS ID MS006687 MS006688
Analysis type MS MS
Chromatography type Reversed phase Reversed phase
Chromatography system Thermo Vanquish Thermo Vanquish
Column Thermo Hypersil Gold aQ C18 (100x2.1mm, 1.9um) Thermo Hypersil Gold aQ C18 (100x2.1mm, 1.9um)
MS Type ESI ESI
MS instrument type Orbitrap Orbitrap
MS instrument name Thermo Q Exactive HF hybrid Orbitrap Thermo Q Exactive HF hybrid Orbitrap
Ion Mode POSITIVE NEGATIVE
Units relative abundance relative abundance

Chromatography:

Chromatography ID:CH005307
Instrument Name:Thermo Vanquish
Column Name:Thermo Hypersil Gold aQ C18 (100x2.1mm, 1.9um)
Column Temperature:40℃
Flow Gradient:0 to 1.5 min: remain 98% A(A: 0.1% formic acid) and 2% B (B: methyl alcohol) solution; 1.5 to 3 min: 98%A to 15%A, 2%B to 85%B ; 3 to 10 min: 15%A to 0%A, 85%B to 100% B; 10.1 to 12 min: remain 98%A and 2% B
Flow Rate:0.2mL/min
Solvent A:100% water; 0.1% Formic acid
Solvent B:100% Methyl alcohol
Chromatography Type:Reversed phase
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