PXD048985 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | impacts of resistant starch fermentation in ex vivo microbiomes of pediatric IBD patients |
| Description | Interindividual variability in responses to prebiotic fibers is an obstacle to improving health via microbiome modulation. Recent advances in ex vivo screening have enabled the personalized selection of prebiotics. This approach, when integrated with meta-omic analyses, hold the potential to unveil microbial factors underlying interindividual variability. Furthermore, most prebiotic-based therapies target butyrate production, a process which is dysregulated in conditions like inflammatory bowel disease (IBD). Other metabolites and functional pathways are rarely considered as targets of microbiome modulation. We conducted high-throughput microbiome culturing using stool samples obtained from 15 pediatric IBD patients with a panel of 9 different resistant starches. After an 18 h culture, we performed meta-omic analyses (16S metagenomics, semi-targeted metabolomics, and shotgun metaproteomics) to examine changes to the microbiomes. Parallel group-level and individual-level analyses revealed starch- and individual-specific changes in fermentation, taxonomic diversity, and functional output. Microbiome responses principally differed by proteins involved in amino acid and nucleic acid metabolism, the metabolite uridine, and Clostridia. We also highlight individualized resistant starch-driven increases in reportedly anti-inflammatory metabolites, such as alpha-ketoglutaric acid, and preferential production of acetate over butyrate. Our ex vivo findings reinforce recent calls to individualize prebiotic therapies, particularly in clinically relevant populations. We present evidence to reconceptualize the beneficial properties of prebiotics to include fermentation by-products beyond butyrate. |
| HostingRepository | PRIDE |
| AnnounceDate | 2026-09-07 |
| AnnouncementXML | Submission_2026-09-06_16:55:58.642.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Zhibin Ning |
| SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606; scientific name: Bacteria; NCBI TaxID: NCBITaxon:2; |
| ModificationList | acetylated residue; iodoacetamide derivatized residue |
| Instrument | Orbitrap Exploris 480 |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2024-01-29 11:17:48 | ID requested | |
| ⏵ 1 | 2026-09-06 16:55:59 | announced | |
Publication List
| 10.1038/s41522-026-01003-w; |
| Dobranowski P, Duan H, Butcher J, Mayne J, Figeys D, Mack DR, Stintzi A, Individual variability shapes ex vivo responses to resistant starch in inflammatory bowel disease derived microbiomes. NPJ Biofilms Microbiomes, 12(1):(2026) [pubmed] |
Keyword List
| submitter keyword: IBD,resistant starch, microbiomes |
Contact List
| Daniel Figeys |
| contact affiliation | School of Pharmaceutical Sciences, Faculty of Medicine, University of Ottawa |
| contact email | dfigeys@uottawa.ca |
| lab head | |
| Zhibin Ning |
| contact affiliation | research associate |
| contact email | ningzhibin@gmail.com |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
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| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD048985
- Label: PRIDE project
- Name: impacts of resistant starch fermentation in ex vivo microbiomes of pediatric IBD patients