| Literature DB >> 28704649 |
Marta Wlodarska1, Chengwei Luo2, Raivo Kolde3, Eva d'Hennezel4, John W Annand4, Cortney E Heim1, Philipp Krastel5, Esther K Schmitt5, Abdifatah S Omar6, Elizabeth A Creasey3, Ashley L Garner6, Sina Mohammadi4, Daniel J O'Connell6, Sahar Abubucker4, Timothy D Arthur6, Eric A Franzosa7, Curtis Huttenhower7, Leon O Murphy4, Henry J Haiser4, Hera Vlamakis6, Jeffrey A Porter4, Ramnik J Xavier8.
Abstract
Host factors in the intestine help select for bacteria that promote health. Certain commensals can utilize mucins as an energy source, thus promoting their colonization. However, health conditions such as inflammatory bowel disease (IBD) are associated with a reduced mucus layer, potentially leading to dysbiosis associated with this disease. We characterize the capability of commensal species to cleave and transport mucin-associated monosaccharides and identify several Clostridiales members that utilize intestinal mucins. One such mucin utilizer, Peptostreptococcus russellii, reduces susceptibility to epithelial injury in mice. Several Peptostreptococcus species contain a gene cluster enabling production of the tryptophan metabolite indoleacrylic acid (IA), which promotes intestinal epithelial barrier function and mitigates inflammatory responses. Furthermore, metagenomic analysis of human stool samples reveals that the genetic capability of microbes to utilize mucins and metabolize tryptophan is diminished in IBD patients. Our data suggest that stimulating IA production could promote anti-inflammatory responses and have therapeutic benefits.Entities:
Keywords: Muc2; Peptostreptococcus; indoleacrylic acid; indolepropionic acid; mucus; organoid
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Year: 2017 PMID: 28704649 PMCID: PMC5672633 DOI: 10.1016/j.chom.2017.06.007
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023