Opsonic Antibodies to Enterococcus faecalis Strain 12030 Are Directed against Lipoteichoic Acid

• Published in: Infection and Immunity 2006-10, Vol.74 (10), p.5703-5712
• Main Authors: Theilacker, Christian, Kaczynski, Zbigniew, Kropec, Andrea, Fabretti, Francesca, Sange, Tatjana, Holst, Otto, Huebner, Johannes
• Format: Article
• Language: English
• Subjects: Animals; Antibodies, Bacterial - immunology; Antibody Specificity; Antigens, Bacterial - immunology; Bacterial Capsules - immunology; Bacteriology; Biological and medical sciences; Carbohydrate Sequence; Enterococcus faecalis; Enterococcus faecalis - chemistry; Enterococcus faecalis - immunology; Fundamental and applied biological sciences. Psychology; Host Response and Inflammation; Immune Sera - immunology; Immunodominant Epitopes - immunology; Lipopolysaccharides - immunology; Lipopolysaccharides - isolation & purification; Microbiology; Miscellaneous; Molecular Sequence Data; Opsonin Proteins - immunology; Polysaccharides, Bacterial - immunology; Rabbits; Teichoic Acids - immunology; Teichoic Acids - isolation & purification
• ISSN: 0019-9567; 1098-5522
• DOI: 10.1128/IAI.00570-06

A teichoic acid (TA)-like polysaccharide in Enterococcus faecalis has previously been shown to induce opsonic antibodies that protect against bacteremia after active and passive immunization. Here we present new data providing a corrected structure of the antigen and the epitope against which the opsonic antibodies are directed. Capsular polysaccharide isolated from E. faecalis strain 12030 by enzymatic digestion of peptidoglycan and chromatography (enzyme-TA) was compared with lipoteichoic acid (LTA) extracted using butanol and purified by hydrophobic-interaction chromatography (BuOH-LTA). Structural determinations were carried out by chemical analysis and nuclear magnetic resonance spectroscopy. Antibody specificity was assessed by enzyme-linked immunosorbent assay and the opsonophagocytosis assay. After alanine ester hydrolysis, there was structural identity between enzyme-TA and BuOH-LTA of the TA-parts of the two molecules. The basic enterococcal LTA structure was confirmed: 1,3-poly(glycerol phosphate) nonstoichiometrically substituted at position C-2 of the glycerol residues with D-Ala and kojibiose. We also detected a novel substituent at position C-2, [D-Ala[rightward arrow]6]-α-D-Glcp-(1[rightward arrow]2-[D-Ala[rightward arrow]6]-α-D-Glcp-1[rightward arrow]). Antiserum raised against enzyme-TA bound equally well to BuOH-LTA and dealanylated BuOH-LTA as to the originally described enzyme-TA antigen. BuOH-LTA was a potent inhibitor of opsonophagocytic killing by the antiserum to enzyme-TA. Immunization with antibiotic-killed whole bacterial cells did not induce a significant proportion of antibodies directed against alanylated epitopes on the TA, and opsonic activity was inhibited completely by both alanylated and dealanylated BuOH-LTA. In summary, the E. faecalis strain 12030 enzyme-TA is structurally and immunologically identical to dealanylated LTA. Opsonic antibodies to E. faecalis 12030 are directed predominantly to nonalanylated epitopes on the LTA molecule.