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Updated: May 22, 2026

An Integrated Workflow of Identification and Quantification on FDR Control-Based Untargeted Metabolome
Published on: September 20, 2022
Glucuronidation metabolomic fingerprinting to map host-microbe metabolism
Nina R Boyle1, Josh J Sekela2, Mingxun Wang3
1Huck Institutes of the Life Sciences, Pennsylvania State University, University Park, PA, USA.
Microbial activity significantly alters the body's glucuronidation, compressing the colonic glucuronidome and expanding urinary glucuronidome diversity. This host-microbe interaction impacts drug metabolism and biomarker discovery.
Area of Science:
- Metabolomics
- Microbiome research
- Host-microbe interactions
Background:
- Glucuronidation is a key detoxification pathway.
- Gastrointestinal microbial beta-glucuronidase (GUS) activity can regenerate metabolites from glucuronidated forms.
- The impact of host-microbe interactions on the glucuronidome is poorly understood.
Purpose of the Study:
- To map the glucuronidome in various biological samples.
- To understand how microbial colonization and GUS activity shape the glucuronidome.
- To develop a resource for analyzing the glucuronidome.
Main Methods:
- Untargeted LC-MS/MS metabolomics was used to profile the glucuronidome.
- Pattern-filtering data science approaches were employed.
- Samples were analyzed from gnotobiotic and conventional mice, as well as humans.
Main Results:
- Microbial colonization and GUS activity compress the colonic glucuronidome.
- Urinary glucuronidome diversity is expanded by microbial activity, indicating compartmental redistribution.
- A glucuronidation fingerprint resource was created, revealing metabolite diversity.
Conclusions:
- Microbial activity reshapes systemic glucuronidation, impacting drug metabolism and biomarker discovery.
- A scalable analytical framework for studying the glucuronidome was established.
- This work provides mechanistic insights into host-microbe interactions affecting metabolite pools.
Related Concept Videos
Phase II Reactions: Glucuronidation
Drug Metabolism: Phase II Reactions
Pharmacogenetics of Drug Metabolism: Overview
Pharmacogenetics of Phase II Enzymes: N-acetyltransferase, Thiopurine S-methyltransferase, UDP-glucuronosyltransferase

