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The Protective Role of Commensal Gut Microbes and Their Metabolites Against Bacterial Pathogens

Abstract

Multidrug-resistant microorganisms have become a major public health concern around the world. The gut microbiome is a gold mine for bioactive compounds that protect the human body from pathogens. We used a multi-omics approach that integrated whole-genome sequencing (WGS) of 74 commensal gut microbiome isolates with metabolome analysis to discover their metabolic interaction with and other antibiotic-resistant pathogens. We evaluated differences in the functional potential of these selected isolates based on WGS annotation profiles. Furthermore, the top altered metabolites in co-culture supernatants of selected commensal gut microbiome isolates were identified including a series of dipeptides and examined for their ability to prevent the growth of various antibiotic-resistant bacteria. Our results provide compelling evidence that the gut microbiome produces metabolites, including the compound class of dipeptides that can potentially be applied for anti-infection medication, especially against antibiotic-resistant pathogens. Our established pipeline for the discovery and validation of bioactive metabolites from the gut microbiome as novel candidates for multidrug-resistant infections represents a new avenue for the discovery of antimicrobial lead structures.

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References
1.
Jacobson A, Lam L, Rajendram M, Tamburini F, Honeycutt J, Pham T . A Gut Commensal-Produced Metabolite Mediates Colonization Resistance to Salmonella Infection. Cell Host Microbe. 2018; 24(2):296-307.e7. PMC: 6223613. DOI: 10.1016/j.chom.2018.07.002. View

2.
McMurdie P, Holmes S . phyloseq: an R package for reproducible interactive analysis and graphics of microbiome census data. PLoS One. 2013; 8(4):e61217. PMC: 3632530. DOI: 10.1371/journal.pone.0061217. View

3.
Yang J, Wright S, Hamblin M, McCloskey D, Alcantar M, Schrubbers L . A White-Box Machine Learning Approach for Revealing Antibiotic Mechanisms of Action. Cell. 2019; 177(6):1649-1661.e9. PMC: 6545570. DOI: 10.1016/j.cell.2019.04.016. View

4.
Ramirez J, Guarner F, Bustos Fernandez L, Maruy A, Sdepanian V, Cohen H . Antibiotics as Major Disruptors of Gut Microbiota. Front Cell Infect Microbiol. 2020; 10:572912. PMC: 7732679. DOI: 10.3389/fcimb.2020.572912. View

5.
Hu Y, Hugerth L, Bengtsson C, Alisjahbana A, Seifert M, Kamal A . Bacteriophages Synergize with the Gut Microbial Community To Combat . mSystems. 2018; 3(5). PMC: 6172775. DOI: 10.1128/mSystems.00119-18. View