Sialylglycoconjugates and sialyltransferase activity in the fungus Cryptococcus neoformans

• Published in: Glycoconjugate journal 2002-03, Vol.19 (3), p.165-173
• Main Authors: Rodrigues, Marcio L, Dobroff, Andrey S S, Couceiro, José Nelson dos S S, Alviano, Celuta S, Schauer, Roland, Travassos, Luiz R
• Format: Article
• Language: English
• Subjects: Acids; Acquired Immunodeficiency Syndrome - microbiology; Animals; Blotting, Western; Chromatography, High Pressure Liquid; Cryptococcus neoformans; Cryptococcus neoformans - enzymology; Cryptococcus neoformans - metabolism; Culture Media - pharmacology; Electrophoresis, Polyacrylamide Gel; Fungi; Gammainfluenzavirus - metabolism; Glycoconjugates - metabolism; Glycolipids - chemistry; Humans; Influenza C virus; Lectins - metabolism; Limax flavus; Rabbits; Sambucus nigra; Sialic Acids - metabolism; Sialyltransferases - metabolism
• ISSN: 0282-0080; 1573-4986
• DOI: 10.1023/A:1024245606607

Cryptococcus neoformans is a fungal pathogen associated with systemic mycoses in up to 10% of AIDS patients. C. neoformans yeasts express sialic acids on the cell wall, where they play an anti-phagocytic role, and may represent a virulence factor at the initial phase of infection. Since the nature of the sialic acid-carrying components is undefined in C. neoformans, our aim in the present work was to identify sialylated molecules in this fungus and study the sialylation process. C. neoformans yeast forms were cultivated in a chemically defined medium free of sialic acids, to search for autologous sialylglycoconjugates. Sialylated glycolipids were not detected. Two glycoproteins with molecular masses of 38 and 67 kDa were recognized by Sambucus nigra agglutinin, an alpha2,6-sialic acid-specific lectin. The 67 kDa glycoprotein also interacted with Influenza C virus, but not with Limax flavus agglutinin, suggesting the presence of the 9-O-acetylated sialic acid derivative as a constituent of the oligosaccharide chains. A partially purified protein fraction from cryptococcal yeast forms was able to transfer sialic acid from CMP-Neu5Ac to both N-(acetyl-1-(14)C)-lactosamine and asialofetuin. Additional evidence for a sialyltransferase in C. neoformans was obtained through the reactivity of fungal proteins with rabbit anti-rat alpha2,6 sialyltransferase polyclonal antibody. Our results indicate that sialic acids in C. neoformans are linked to glycoproteins, which are sialylated by the action of a fungal sialyltransferase. This is the first demonstration of this biosynthetic step in pathogenic fungi.