Phosphorylation of inner core heptose is a major determinant of bacterial surface lipopolysaccharide recognition by the innate immune protein hSP-D

TL;DR

This study shows how the immune protein hSP-D recognizes bacterial lipopolysaccharides, with heptose phosphorylation playing a key role in immune evasion.

Contribution

The study reveals that heptose phosphorylation is a major determinant in bacterial LPS recognition by hSP-D.

Findings

SP-D preferentially recognizes the reducing terminal heptose (HepI) via the glyceryl group.

Heptose phosphorylation significantly affects immune recognition of bacterial LPS.

HepI O4′ phosphorylation can prevent preferred HepI recognition by hSP-D.

Abstract

The innate immune protein human surfactant protein D (SP-D) recognizes pathogens in the lungs via binding to carbohydrate surface structures. SP-D targets gram-negative bacterial lipopolysaccharide via calcium-dependent binding, preferentially to the inner core heptose (HepI). To further investigate this recognition, we have determined the high-resolution crystal structures of a trimeric recombinant fragment of human SP-D complexed with synthetic di-saccharide and trisaccharides, HepI-Kdo, HepIII-HepII-HepI, and HepII-HepI phosphorylated at either HepI or HepII, inner core lipopolysaccharide motifs common to many gram-negative bacteria. In contrast to acid-hydrolyzed lipopolysaccharide used in several previous studies, these synthetic saccharides allow the presentation of both the innermost Kdo in its natural pyranose form and heptose phosphorylation. The structures confirm the flexibility of SP-D to adopt alternative binding modes when the preferred epitope is not available, reveal a preference for recognition of the reducing terminal heptose (HepI) via the glyceryl group, indicate that a single Kdo attached to HepI does not have a significant role in ligand recognition, and provide evidence that heptose phosphorylation is a major determinant of recognition. The disaccharide with HepII O4′ phosphorylation binds via the preferred HepI glyceryl-hydroxyls, while HepI O4′ phosphorylation reveals HepII binding via the pyranose ring O3′ and O4′ hydroxyls, which would not be possible with the usual HepII O3′ link to the outer core. The ability of HepI O4′ phosphorylation to prevent preferred HepI recognition suggests a role for heptose phosphorylation in shielding the bacterial LPS inner core from immune recognition.

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