GPI-anchored proteins and free GPI glycolipids of procyclic form Trypanosoma brucei are nonessential for growth, are required for colonization of the tsetse fly, and are not the only components of the surface coat

• Published in: Molecular biology of the cell 2006-12, Vol.17 (12), p.5265-5274
• Main Authors: Güther, Maria Lucia Sampaio, Lee, Sylvia, Tetley, Laurence, Acosta-Serrano, Alvaro, Ferguson, Michael A J
• Format: Article
• Language: English
• Subjects: Acetylglucosamine - analogs & derivatives; Acetylglucosamine - metabolism; Amidohydrolases - metabolism; Animals; Biotinylation; Cell-Free System; Digestive System - parasitology; Flow Cytometry; Glucosamine - metabolism; Glycolipids - metabolism; Glycosylphosphatidylinositols - metabolism; Lipids - chemistry; Membrane Glycoproteins - metabolism; Mutation - genetics; Phenotype; Phosphatidylinositols - metabolism; Protozoan Proteins - chemistry; Protozoan Proteins - metabolism; Spectrometry, Mass, Electrospray Ionization; Trypanosoma brucei; Trypanosoma brucei brucei - cytology; Trypanosoma brucei brucei - growth & development; Trypanosoma brucei brucei - pathogenicity; Trypanosoma brucei brucei - ultrastructure; Tsetse Flies - parasitology
• ISSN: 1059-1524; 1939-4586; 1059-1524
• DOI: 10.1091/mbc.E06-08-0702

The procyclic form of Trypanosoma brucei exists in the midgut of the tsetse fly. The current model of its surface glycocalyx is an array of rod-like procyclin glycoproteins with glycosylphosphatidylinositol (GPI) anchors carrying sialylated poly-N-acetyllactosamine side chains interspersed with smaller sialylated poly-N-acetyllactosamine-containing free GPI glycolipids. Mutants for TbGPI12, deficient in the second step of GPI biosynthesis, were devoid of cell surface procyclins and poly-N-acetyllactosamine-containing free GPI glycolipids. This major disruption to their surface architecture severely impaired their ability to colonize tsetse fly midguts but, surprisingly, had no effect on their morphology and growth characteristics in vitro. Transmission electron microscopy showed that the mutants retained a cell surface glycocalyx. This structure, and the viability of the mutants in vitro, prompted us to look for non-GPI-anchored parasite molecules and/or the adsorption of serum components. Neither were apparent from cell surface biotinylation experiments but [3H]glucosamine biosynthetic labeling revealed a group of previously unidentified high apparent molecular weight glycoconjugates that might contribute to the surface coat. While characterizing GlcNAc-PI that accumulates in the TbGPI12 mutant, we observed inositolphosphoceramides for the first time in this organism.