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Immune exclusion by naturally acquired secretory IgA against pneumococcal pilus-1
Ulrike Binsker, … , Alexandria J. Hammond, Jeffrey N. Weiser
Ulrike Binsker, … , Alexandria J. Hammond, Jeffrey N. Weiser
Published November 5, 2019
Citation Information: J Clin Invest. 2020;130(2):927-941. https://doi.org/10.1172/JCI132005.
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Research Article Microbiology

Immune exclusion by naturally acquired secretory IgA against pneumococcal pilus-1

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Abstract

Successful infection by mucosal pathogens requires overcoming the mucus barrier. To better understand this key step, we performed a survey of the interactions between human respiratory mucus and the human pathogen Streptococcus pneumoniae. Pneumococcal adherence to adult human nasal fluid was seen only by isolates expressing pilus-1. Robust binding was independent of pilus-1 adhesive properties but required Fab-dependent recognition of RrgB, the pilus shaft protein, by naturally acquired secretory IgA (sIgA). Pilus-1 binding by specific sIgA led to bacterial agglutination, but adherence required interaction of agglutinated pneumococci and entrapment in mucus particles. To test the effect of these interactions in vivo, pneumococci were preincubated with human sIgA before intranasal challenge in a mouse model of colonization. sIgA treatment resulted in rapid immune exclusion of pilus-expressing pneumococci. Our findings predict that immune exclusion would select for nonpiliated isolates in individuals who acquired RrgB-specific sIgA from prior episodes of colonization with piliated strains. Accordingly, genomic data comparing isolates carried by mothers and their children showed that mothers are less likely to be colonized with pilus-expressing strains. Our study provides a specific example of immune exclusion involving naturally acquired antibody in the human host, a major factor driving pneumococcal adaptation.

Authors

Ulrike Binsker, John A. Lees, Alexandria J. Hammond, Jeffrey N. Weiser

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Figure 5

Fab-mediated binding of sIgA to pneumococcal type 1 pilus.

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Fab-mediated binding of sIgA to pneumococcal type 1 pilus.
(A and B) Con...
(A and B) Concentration-dependent binding of soluble purified sIgA to Spn. Acquisition of sIgA and serum IgA (2-fold molar ratio compared with 25 μg/mL sIgA) to type 4 Spn and isogenic mutants (A) or type 23F Spn and isogenic pilus-1–knockin mutant (B) was measured by flow cytometry using a specific FITC-labeled goat anti-human IgA1 antibody. The percentage binding of at least 3 independent experiments is shown as mean values with error bars ± SD. ****P < 0.0001 vs. WT by 2-way ANOVA followed by Tukey’s multiple comparison, n = 6–8. (C) Schematic model of cleaved sIgA treated with recombinant IgA1 protease (dashed line), generating Fabα fragments (binding analyzed in D) and Fc fragments with bound secretory component (binding analyzed in E). (D and E) Flow cytometric analysis of sIgA binding following cleavage with recombinant IgA1 protease. Binding of sIgA light chain (D) or secretory component (E) was analyzed using an anti–human κ-light chain antibody (D) or a monoclonal anti–secretory component antibody (E). Results of 3 independent experiments are illustrated as mean values with error bars ± SD. *P < 0.05, ****P < 0.001 by 1-way ANOVA followed by Tukey’s multiple comparison, n = 6. (F and G) Concentration-dependent binding of soluble human lactoferrin and serum IgG to type 4 Spn and isogenic mutants. Results of 3 independent experiments are shown as mean values with error bars ± SD; n = 6.

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