Efficient utilization of complex N-linked glycans is a selective advantage for Bacteroides fragilis in extraintestinal infections
Bacteroides fragilis is the most common anaerobe isolated from clinical infections, and in this report we demonstrate a characteristic of the species that is critical to their success as an opportunistic pathogen. Among the Bacteroides spp. in the gut, B. fragilis has the unique ability of efficient...
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Published in: | Proceedings of the National Academy of Sciences - PNAS Vol. 111; no. 35; pp. 12901 - 12906 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
National Academy of Sciences
02-09-2014
National Acad Sciences |
Subjects: | |
Online Access: | Get full text |
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Summary: | Bacteroides fragilis is the most common anaerobe isolated from clinical infections, and in this report we demonstrate a characteristic of the species that is critical to their success as an opportunistic pathogen. Among the Bacteroides spp. in the gut, B. fragilis has the unique ability of efficiently harvesting complex N-linked glycans from the glycoproteins common to serum and serous fluid. This activity is mediated by an outer membrane protein complex designated as Don. Using the abundant serum glycoprotein transferrin as a model, it has been shown that B. fragilis alone can rapidly and efficiently deglycosylate this protein in vitro and that transferrin glycans can provide the sole source of carbon and energy for growth in defined media. We then showed that transferrin deglycosylation occurs in vivo when B. fragilis is propagated in the rat tissue cage model of extraintestinal growth, and that this ability provides a competitive advantage in vivo over strains lacking the don locus. |
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Bibliography: | http://dx.doi.org/10.1073/pnas.1407344111 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Author contributions: Y.C., E.R.R., and C.J.S. designed research; Y.C. performed research; Y.C., E.R.R., and C.J.S. analyzed data; and Y.C. and C.J.S. wrote the paper. Edited by Thomas J. Silhavy, Princeton University, Princeton, NJ, and approved July 30, 2014 (received for review April 22, 2014) |
ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.1407344111 |