Structure of the N-linked oligosaccharide of the main diagnostic antigen of the pathogenic fungus Paracoccidiodes brasiliensis

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Abstract
The major diagnostic antigen of Paracoccidioides brasiliensis is the exocellularly secreted 43,000 Da glycoprotein (gp43) which contains a single N-linked oligosaccharide chain. This oligosaccharide, although poorly immunogenic in man, is responsible for the cross-reactivity of the gp43 with sera from patients with histoplasmosis, and may have a role in fungal virulence. It contains a neutral highmannose core (Man7GlcNAc2) to which a (1→6)-linked α-D-Manp chain of variable length, substituted at the 2-O positions by single α-D-Manp residues, is attached. A terminal unit of β-D-galactofuranose is (1→6)-linked to one of the (1→2)-linked mannosyl residues, either in the C or in the A arm of the oligosaccharide. The heterogeneity of the oligosaccharide is determined by the different sizes of the A arm and the sites of insertion of the β-galactofuranosyl unit. The complete structure was determined by methylation analysis, 1H-NMR, mass spectrometry, acetolysis and mannosidase degradation. Electrospray mass spectrometry showed that the oligosaccharide comprises several subtypes ranging from Hex18GlcNAc2 to Hex10GlcNAc2 which accounts for the diffuse migration of the gp43 in polyacrylamide gels. The average size of the most frequent subtype is Hex13.6GlcNAc2. Dilute acid treatment to remove β-D-Galf reduced the molecular masses of the majority of the subtypes by a single sugar unit.

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