Tags

Type your tag names separated by a space and hit enter

Current understanding of microbiota- and dietary-therapies for treating inflammatory bowel disease.
J Microbiol. 2018 Mar; 56(3):189-198.JM

Abstract

Inflammatory bowel disease (IBD) is a result of chronic inflammation caused, in some part, by dysbiosis of intestinal microbiota, mainly commensal bacteria. Gut dysbiosis can be caused by multiple factors, including abnormal immune responses which might be related to genetic susceptibility, infection, western dietary habits, and administration of antibiotics. Consequently, the disease itself is characterized as having multiple causes, etiologies, and severities. Recent studies have identified >200 IBD risk loci in the host. It has been postulated that gut microbiota interact with these risk loci resulting in dysbiosis, and this subsequently leads to the development of IBD. Typical gut microbiota in IBD patients are characterized with decrease in species richness and many of the commensal, and beneficial, fecal bacteria such as Firmicutes and Bacteroidetes and an increase or bloom of Proteobacteria. However, at this time, cause and effect relationships have not been rigorously established. While treatments of IBD usually includes medications such as corticosteroids, 5-aminosalicylates, antibiotics, immunomodulators, and anti-TNF agents, restoration of gut dysbiosis seems to be a safer and more sustainable approach. Bacteriotherapies (now called microbiota therapies) and dietary interventions are effective way to modulate gut microbiota. In this review, we summarize factors involved in IBD and studies attempted to treat IBD with probiotics. We also discuss the potential use of microbiota therapies as one promising approach in treating IBD. As therapies based on the modulation of gut microbiota becomes more common, future studies should include individual gut microbiota differences to develop personalized therapy for IBD.

Authors+Show Affiliations

Subtropical/tropical Organism Gene Bank, Jeju National University, Jeju, 63243, Republic of Korea.Department of Gastroenterology, Wonkwang Digestive Disease Research Institute, Wonkwang University Sanbon Hospital, Gunpo, 15865, Republic of Korea.Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul, 06974, Republic of Korea.BioTechnology Institute, University of Minnesota, St. Paul, Minnesota, 55108, USA. Department of Soil, Water, and Climate, University of Minnesota, St. Paul, Minnesota, 55108, USA. Department of Plant and Microbial Biology, University of Minnesota, St. Paul, Minnesota, 55108, USA.Subtropical/tropical Organism Gene Bank, Jeju National University, Jeju, 63243, Republic of Korea. tatsu@jejunu.ac.kr. Faculty of Biotechnology, School of life sciences, SARI, Jeju National University, Jeju, 63243, Republic of Korea. tatsu@jejunu.ac.kr.

Pub Type(s)

Journal Article
Review

Language

eng

PubMed ID

29492876

Citation

Eom, Taekil, et al. "Current Understanding of Microbiota- and Dietary-therapies for Treating Inflammatory Bowel Disease." Journal of Microbiology (Seoul, Korea), vol. 56, no. 3, 2018, pp. 189-198.
Eom T, Kim YS, Choi CH, et al. Current understanding of microbiota- and dietary-therapies for treating inflammatory bowel disease. J Microbiol. 2018;56(3):189-198.
Eom, T., Kim, Y. S., Choi, C. H., Sadowsky, M. J., & Unno, T. (2018). Current understanding of microbiota- and dietary-therapies for treating inflammatory bowel disease. Journal of Microbiology (Seoul, Korea), 56(3), 189-198. https://doi.org/10.1007/s12275-018-8049-8
Eom T, et al. Current Understanding of Microbiota- and Dietary-therapies for Treating Inflammatory Bowel Disease. J Microbiol. 2018;56(3):189-198. PubMed PMID: 29492876.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Current understanding of microbiota- and dietary-therapies for treating inflammatory bowel disease. AU - Eom,Taekil, AU - Kim,Yong Sung, AU - Choi,Chang Hwan, AU - Sadowsky,Michael J, AU - Unno,Tatsuya, Y1 - 2018/02/28/ PY - 2018/01/27/received PY - 2018/02/11/accepted PY - 2018/02/06/revised PY - 2018/3/2/entrez PY - 2018/3/2/pubmed PY - 2018/9/22/medline KW - dysbiosis KW - gut microbiota KW - inflammatory bowel disease KW - prebiotics KW - probiotics KW - short chain fatty acids SP - 189 EP - 198 JF - Journal of microbiology (Seoul, Korea) JO - J Microbiol VL - 56 IS - 3 N2 - Inflammatory bowel disease (IBD) is a result of chronic inflammation caused, in some part, by dysbiosis of intestinal microbiota, mainly commensal bacteria. Gut dysbiosis can be caused by multiple factors, including abnormal immune responses which might be related to genetic susceptibility, infection, western dietary habits, and administration of antibiotics. Consequently, the disease itself is characterized as having multiple causes, etiologies, and severities. Recent studies have identified >200 IBD risk loci in the host. It has been postulated that gut microbiota interact with these risk loci resulting in dysbiosis, and this subsequently leads to the development of IBD. Typical gut microbiota in IBD patients are characterized with decrease in species richness and many of the commensal, and beneficial, fecal bacteria such as Firmicutes and Bacteroidetes and an increase or bloom of Proteobacteria. However, at this time, cause and effect relationships have not been rigorously established. While treatments of IBD usually includes medications such as corticosteroids, 5-aminosalicylates, antibiotics, immunomodulators, and anti-TNF agents, restoration of gut dysbiosis seems to be a safer and more sustainable approach. Bacteriotherapies (now called microbiota therapies) and dietary interventions are effective way to modulate gut microbiota. In this review, we summarize factors involved in IBD and studies attempted to treat IBD with probiotics. We also discuss the potential use of microbiota therapies as one promising approach in treating IBD. As therapies based on the modulation of gut microbiota becomes more common, future studies should include individual gut microbiota differences to develop personalized therapy for IBD. SN - 1976-3794 UR - https://www.unboundmedicine.com/medline/citation/29492876/full_citation DB - PRIME DP - Unbound Medicine ER -