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Permanent link (DOI): https://doi.org/10.7939/R3610VX6D

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Short-chain fatty acids influence host immunity, mucus secretion and microbial community structure to reduce enteritis Open Access

Descriptions

Other title
Subject/Keyword
short-chain fatty acids
butyrate
Citrobacter rodenitum
Host response
Microbial communities
immune response
mouse model
mucus
Type of item
Thesis
Degree grantor
University of Alberta
Author or creator
Jiminez, Janelle A
Supervisor and department
Uwiera, Richard (Agricultural, Food and Nutritional Science)
Uwiera, Trina (Faculty of Medicine and Dentistry)
Inglis, Douglas (Adjunct Professor)
Examining committee member and department
Uwiera, Richard (Agricultural, Food and Nutritional Science)
Uwiera, Trina (Faculty of Medicine and Dentistry)
Inglis, Douglas (Adjunct Professor)
Guan, Leluo (Agricultural, Food and Nutritional Science)
Department
Department of Agricultural, Food, and Nutritional Science
Specialization
Animal Science
Date accepted
2016-05-11T15:07:12Z
Graduation date
2016-06
Degree
Master of Science
Degree level
Master's
Abstract
Optimal intestinal health is critical to overall host well-being, and acute and chronic enteric inflammatory diseases impart a significant detrimental impact on Canadians. The consumption of dietary fibre (DF) has long been associated with providing a health benefit to individuals, and regulatory organizations including Health Canada have legislated that scientific evidence be required to validate health claims. Short-chain fatty acids (SCFA) are produced by the microbial fermentation of DF in the colon, with acetate, propionate and butyrate being the most abundantly produced in the colon. Studies analyzing the effect of DF fermentation in pathogen-challenge models are limited. Thus, the overarching goal of this research was to determine how DFs, and in particular the by-products of DF fermentation, impact enteric inflammation and overall host health using an intestinal pathogen to incite inflammation. Two studies were conducted using Citrobacter rodentium to incite acute Th1/Th17 inflammation (i.e. enteritis). In the first study, the impact of butyrate on the host-microbiota relationship was examined in mice ± enteritis. Rectal administration of 140 mM butyrate to mice increased fecal concentrations of butyrate, and increased food consumption and weight gain in mice with enteritis. Histological scores of colonic inflammation 14 and 21 days post-infection (p.i.) were lower in infected mice administered 140 mM butyrate. In mice without enteritis, butyrate administration elevated the expression of IL-10, TGFβ, and Muc2 in comparison to mice not administered butyrate. Infected mice administered butyrate displayed elevated expression of genes necessary for pathogen clearance (i.e. IL-17A, IL-1β), and epithelial barrier repair and restoration (i.e. Relmβ, Tff3, Myd88). Butyrate supplemented to inflamed colons increased Proteobacteria and Lachnospiraceae, and reduced the abundance of Clostridiaceae species. Mice with enteritis that were administered butyrate exhibited increased accumulation of mucus in the colonic lumen and within goblet cells. In the second study, the impacts of the DFs, WB and RS on host enteric health were measured in mice ± enteritis. Diets enriched for RS increased weight gain in mice inoculated with C. rodentium compared to mice consuming a conventional control (CN) diet. Cecal and distal colonic SCFA quantities were higher in mice consuming DFs, and DF consumption increased butyrate concentrations in the distal colons of mice with enteritis. Histopathologic sores of inflammation in the proximal colon on day 14 (peak infection) and 21 p.i. (late infection) were lower in mice consuming DF-enriched diets compared to the CN diet. Consumption of WB reduced the expression of Th1/Th17 cytokines. Alternatively, the expression of bacterial recognition and response genes such as Relmβ, RegIIIγ, and TLR4 increased in mice consuming the RS-enriched diets. Furthermore, each diet selected for different bacterial communities in the cecum, proximal and distal colon, suggesting a link between DF fermentation, SCFA concentrations, and inflammation in the murine colon. Collectively, study two data indicated that the consumption of DF-rich diets ameliorate the effects of C. rodentium-induced enteritis by modifying the host microbiota to increase SCFA production, and bacterial recognition and response mechanisms to promote host health. In conclusion, SCFA are important to colonic health, and when administered directly to colons primarily influence host immunity through the activation of innate factors, while SCFA derived from DFs in diets modify the host microbiome to effectively maintain intestinal homeostasis and promote host health. Notably, this research provides foundational information to ascertain the effects of functional foods on intestinal health and host well-being.
Language
English
DOI
doi:10.7939/R3610VX6D
Rights
This thesis is made available by the University of Alberta Libraries with permission of the copyright owner solely for the purpose of private, scholarly or scientific research. This thesis, or any portion thereof, may not otherwise be copied or reproduced without the written consent of the copyright owner, except to the extent permitted by Canadian copyright law.
Citation for previous publication
Jiminez, J.A., Uwiera, T.C., Douglas Inglis, G., and Uwiera, R.R.E. (2015). Animal models to study acute and chronic intestinal inflammation in mammals. Gut Pathog 7, 1-31.

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