Gut microbiota utilize immunoglobulin A for mucosal colonization

Author:

Donaldson G. P.1ORCID,Ladinsky M. S.1ORCID,Yu K. B.1ORCID,Sanders J. G.23ORCID,Yoo B. B.1,Chou W.-C.4ORCID,Conner M. E.5ORCID,Earl A. M.4ORCID,Knight R.23ORCID,Bjorkman P. J.1ORCID,Mazmanian S. K.1ORCID

Affiliation:

1. Department of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.

2. Department of Pediatrics, University of California, San Diego, CA 92110, USA.

3. Department of Computer Science and Engineering, University of California, San Diego, CA 92093, USA.

4. Infectious Disease and Microbiome Program, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.

5. Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX 77030, USA.

Abstract

Benign colonization of the gut Microbial communities in the gut can be highly individual. What engenders this specificity? The gut characteristically produces gram quantities of immunoglobulin A (IgA) antibody, which is presumed to protect the gut from pathogen attack. Donaldson et al. engineered strains of Bacteroides fragilis , a common human commensal, to modify its surface capsule, which affects its ability to colonize the germ-free mouse gut. Capsule changes altered the capacity of IgA to bind to the different mutants. It seems that this commensal species exploits IgA sticking power specifically to give it a competitive edge and to promote its establishment in the gut. Science , this issue p. 795

Funder

National Science Foundation

National Institutes of Health

Heritage Medical Research Institute

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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