Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Jan-Dec;14(1):2154092.
doi: 10.1080/19490976.2022.2154092.

Stool multi-omics for the study of host-microbe interactions in inflammatory bowel disease

Affiliations
Review

Stool multi-omics for the study of host-microbe interactions in inflammatory bowel disease

Consuelo Sauceda et al. Gut Microbes. 2022 Jan-Dec.

Abstract

Inflammatory Bowel Disease (IBD) is a chronic immune-mediated inflammatory disease of the gastrointestinal tract that is a growing public burden. Gut microbes and their interactions with hosts play a crucial role in disease pathogenesis and progression. These interactions are complex, spanning multiple physiological systems and data types, making comprehensive disease assessment difficult, and often overwhelming single-omic capabilities. Stool-based multi-omics is a promising approach for characterizing host-gut microbiome interactions using deep integration of technologies such as 16S rRNA sequencing, shotgun metagenomics, meta-transcriptomics, metabolomics, and metaproteomics. The wealth of information generated through multi-omic studies is poised to usher in advancements in IBD research and precision medicine. This review highlights historical and recent findings from stool-based muti-omic studies that have contributed to unraveling IBD's complexity. Finally, we discuss common pitfalls, issues, and limitations, and how future pipelines should address them to standardize multi-omics in IBD research and beyond.

Keywords: Inflammatory bowel disease (IBD); Multi-omics; diet; gut microbes; metabolomics; metagenomics; metaproteomics; precision medicine.

PubMed Disclaimer

Conflict of interest statement

No potential conflict of interest was reported by the author(s).

Figures

Figure 1.
Figure 1.
Microbe-host multi-omic targets in healthy and diseased intestinal microenvironment. Visual representation of the integration potential of multi-omics. 1) Advancements in metagenomics have identified alterations in microbial composition in IBD patients. 2) Metabolomics profile changes in the metabolic output of hosts and microbes, including short-chain fatty acids and bile acids, both of which have been linked to IBD disease severity. 3) Genomic sequencing has facilitated the identification genes that influence the development of IBD such as mutations in NOD1/2 and IL-10 inflammatory pathways. 4) Metatranscriptomics facilitates the identification of transcriptomes as a proxy for functional output differences in IBD patients. 5) Metaproteomics characterizes changes in host and microbial stool- proteins affected by IBD with the additional ability to characterize post-translational modifications.

References

    1. Human T, Project M.. Supplementary information: structure, function, and diversity of the healthy human microbiome. Nature. 2012;486:207–18. - PMC - PubMed
    1. Dulai PS, Singh S, Vande Casteele N, Boland BS, Rivera-Nieves J, Ernst PB, Eckmann L, Barrett KE, Chang JT, Sandborn WJ. Should we divide crohn’s disease into ileum-dominant and isolated colonic diseases? Clin Gastroenterol Hepatol. 2019;17(13):2634–2643. - PMC - PubMed
    1. Papamichael K, Gils A, Rutgeerts P, Levesque BG, Vermeire S, Sandborn WJ, Vande Casteele N. Role for therapeutic drug monitoring during induction therapy with TNF antagonists in IBD: evolution in the definition and management of primary nonresponse. Inflamm Bowel Dis [Internet]. 2015;21(1):182–197. Available from: http://www.ncbi.nlm.nih.gov/pubmed/25222660 - PubMed
    1. Lakatos P-L, Lakatos L. Risk for colorectal cancer in ulcerative colitis: changes, causes and management strategies. World J Gastroenterol [Internet]. 2008;14(25):3937–3947. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18609676 - PMC - PubMed
    1. Park KT, Ehrlich OG, Allen JI, Meadows P, Szigethy EM, Henrichsen K, Kim SC, Lawton RC, Murphy SM, Regueiro M, et al. The cost of inflammatory bowel disease: an initiative from the crohn’s & colitis foundation. Inflamm Bowel Dis [Internet]. 2020;26(1):1–10. Available from: http://www.ncbi.nlm.nih.gov/pubmed/31112238 - PMC - PubMed

Substances