Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.699599
Title: Elucidating the role of the mucus-associated microbiota and mucin glycosylation in inflammatory bowel disease
Author: Thursby, Elizabeth
ISNI:       0000 0004 5990 3941
Awarding Body: University of East Anglia
Current Institution: University of East Anglia
Date of Award: 2016
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Abstract:
The human gastrointestinal (GI) tract is host to a dynamic community of 1013-1014 bacteria, which mainly reside in the colonic lumen and outer mucus layer covering the GI tract. Mucins are decorated in a diverse array of O-glycans, providing nutrients and attachment sites for microbes. Dysbiosis of the microbiota, and alterations in mucin glycosylation have been associated with Inflammatory Bowel Disease (IBD). However, the causal relationship between these two factors remains unclear. Here, we employed a multidisciplinary approach to address this relationship, and the molecular mechanisms mediating these changes. Mucosal lavages and biopsies obtained from the sigmoid and ascending colon of patients were used to assess alterations in the mucosal microbiota and the glycosylation of associated mucus in ulcerative colitis (UC) patients. Secondly, in vitro growth assays and gnotobiotic mouse experiments were performed to investigate the reciprocal role of mucin-degrading bacteria in the modulation of mucin O-glycosylation. These analyses highlighted inter-patient variability, but a similar microbial composition between colonic sites. In contrast, mucin glycosylation and the expression of glycosyltransferases was regio-specific. In UC, changes in the abundances of bacterial groups, including a decrease in the A. muciniphila to R. gnavus ratio were apparent. UC mucins displayed a decrease in fucosylation, increase in sialylation, and a decrease in many complex glycan structures found in abundance in controls. In vitro growth assays suggested that UC-like mucin glycosylation impaired A. muciniphila growth, whilst R. gnavus remained unaffected, potentially explaining changes in these species in UC. Furthermore, gnotobiotic mouse experiments showed that A. muciniphila and R. gnavus were able to remodel mucin glycosylation. Our findings suggest a multifactorial dysregulation at the epithelial interface in IBD, where mucus-associated microbiota and mucin glycosylation are interdependent. It is likely that an initial disruption in either of these components drives alterations in other mucosal constituents, propagating disease and exacerbating inflammation.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.699599  DOI: Not available
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