Microbial metabolites in health and disease: Navigating the unknown in search of function

  1. Eugene B. Chang1
  1. From the Department of Medicine, Knapp Center for Biomedical Discovery, University of Chicago, Chicago, Illinois 60637
  1. 1 To whom correspondence should be addressed: 900 E. 57th St., Dept. of Medicine, University of Chicago, Chicago, IL 60637. Tel.: 773-702-6458; Fax: 773-702-2281; E-mail: echang{at}medicine.bsd.uchicago.edu.
  1. Edited by Ruma Banerjee

Abstract

The gut microbiota has been implicated in the development of a number of chronic gastrointestinal and systemic diseases. These include inflammatory bowel diseases, irritable bowel syndrome, and metabolic (i.e. obesity, non-alcoholic fatty liver disease, and diabetes) and neurological diseases. The advanced understanding of host-microbe interactions has largely been due to new technologies such as 16S rRNA sequencing to identify previously unknown microbial communities and, more importantly, their functional characteristics through metagenomic sequencing and other multi-omic technologies, such as metatranscriptomics, metaproteomics, and metabolomics. Given the vast array of newly acquired knowledge in the field and technological advances, it is expected that mechanisms underlying several disease states involving the interactions between microbes, their metabolites, and the host will be discovered. The identification of these mechanisms will allow for the development of more precise therapies to prevent or manage chronic disease. This review discusses the functional characterization of the microbiome, highlighting the advances in identifying bioactive microbial metabolites that have been directly linked to gastrointestinal and peripheral diseases.

Footnotes

  • This work was supported by the GI Research Foundation, Chicago, IL and National Institutes of Health Grants DK042086, DK097268, and DK102872 from NIDDK (to E. B. C.). This is the second article in the Host-Microbiome metabolic interplay Minireview series. The authors declare that they have no conflicts of interest with the contents of this article. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Table of Contents

This Article

  1. The Journal of Biological Chemistry 292, 8553-8559.
  1. All Versions of this Article:
    1. R116.752899v1
    2. 292/21/8553 (most recent)

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