Gut microbiota utilize immunoglobulin A for mucosal colonization

Gregory P. Donaldson(California Institute of Technology), Mark S. Ladinsky(California Institute of Technology), Kristie B. Yu(California Institute of Technology), Jon G. Sanders(University of California San Diego), Byouengmin Yoo(California Institute of Technology), Wen‐Chi Chou(Broad Institute), Margaret E. Conner(Baylor College of Medicine), Ashlee M. Earl(Broad Institute), Rob Knight(University of California San Diego), Pamela J. Björkman(California Institute of Technology), Sarkis K. Mazmanian(California Institute of Technology)
Science
May 3, 2018
Cited by 645Open Access
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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


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