Journal
EMBO REPORTS
Volume 16, Issue 2, Pages 164-177Publisher
WILEY
DOI: 10.15252/embr.201439263
Keywords
Bacteria; Colon; Intestine; MUC2; Mucus
Categories
Funding
- Swedish Research Council [7461, 21027, 22220-01-5]
- Swedish Cancer Foundation
- Knut and Alice Wallenberg Foundation
- IngaBritt and Arne Lundberg Foundation
- Sahlgren's University Hospital (LUA-ALF)
- Wilhelm and Martina Lundgren's Foundation
- Assar Gabrielsson's foundation
- Clas Groschinskys foundation
- Torsten och Ragnar Soderbergs Stiftelser
- Sahlgrenska Academy
- National Institute of Allergy and Infectious Diseases [U01AI095473, U01AI095776-03:9006862]
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Two C57BL/6 mice colonies maintained in two rooms of the same specific pathogen-free (SPF) facility were found to have different gut microbiota and a mucus phenotype that was specific for each colony. The thickness and growth of the colon mucus were similar in the two colonies. However, one colony had mucus that was impenetrable to bacteria or beads the size of bacteria-which is comparable to what we observed in free-living wild mice-whereas the other colony had an inner mucus layer penetrable to bacteria and beads. The different properties of the mucus depended on the microbiota, as they were transmissible by transfer of caecal microbiota to germ-free mice. Mice with an impenetrable mucus layer had increased amounts of Erysipelotrichi, whereas mice with a penetrable mucus layer had higher levels of Proteobacteria and TM7 bacteria in the distal colon mucus. Thus, our study shows that bacteria and their community structure affect mucus barrier properties in ways that can have implications for health and disease. It also highlights that genetically identical animals housed in the same facility can have rather distinct microbiotas and barrier structures.
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