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Colitogenic Bacteroides thetaiotaomicron Antigens Access Host Immune Cells in a Sulfatase-Dependent Manner via Outer Membrane Vesicles
- Source :
- Cell Host & Microbe. 17(5):672-680
- Publication Year :
- 2015
- Publisher :
- Elsevier BV, 2015.
-
Abstract
- Summary Microbes interact with the host immune system via several potential mechanisms. One essential step for each mechanism is the method by which intestinal microbes or their antigens access specific host immune cells. Using genetically susceptible mice ( dnKO ) that develop spontaneous, fulminant colitis, triggered by Bacteroides thetaiotaomicron ( B. theta ), we investigated the mechanism of intestinal microbial access under conditions that stimulate colonic inflammation. B. theta antigens localized to host immune cells through outer membrane vesicles (OMVs) that harbor bacterial sulfatase activity. We deleted the anaerobic sulfatase maturating enzyme (anSME) from B. theta , which is required for post-translational activation of all B. theta sulfatase enzymes. This bacterial mutant strain did not stimulate colitis in dnKO mice. Lastly, access of B. theta OMVs to host immune cells was sulfatase dependent. These data demonstrate that bacterial OMVs and associated enzymes promote inflammatory immune stimulation in genetically susceptible hosts.
- Subjects :
- Cancer Research
Inflammation
Biology
Microbiology
Mice
Immune system
Antigen
Virology
Immunology and Microbiology(all)
medicine
Animals
Bacteroides
Colitis
Molecular Biology
chemistry.chemical_classification
Antigens, Bacterial
Secretory Vesicles
Sulfatase
medicine.disease
3. Good health
Disease Models, Animal
Enzyme
chemistry
Genes, Bacterial
Host-Pathogen Interactions
Parasitology
Sulfatases
medicine.symptom
Bacterial outer membrane
Bacteroides thetaiotaomicron
Gene Deletion
Subjects
Details
- ISSN :
- 19313128
- Volume :
- 17
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- Cell Host & Microbe
- Accession number :
- edsair.doi.dedup.....b048a4525d205f6601066c46b59ce811
- Full Text :
- https://doi.org/10.1016/j.chom.2015.04.002