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Role of protein-mannosyl-transferases (PMTs) in virulence of Cryptococcus neoformans

Subject Area Parasitology and Biology of Tropical Infectious Disease Pathogens
Term from 2004 to 2007
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 5426567
 
O-glycosylation, the addition of carbohydrate residues to proteins is a very important protein modification and is commonly found in all eukaryotic organisms. A wide variety of proteins is affected by O-glycosylation. In fungal organisms mainly secreted proteins and cell-membrane associated proteins are O-glycosylated while in mammals also O-glycosylated cytosolic proteins have been identified. Virulence of the opportunistic fungal pathogen Cryptococcus neoformans is mainly determined by extracellular factors such as a polysaccharide capsule, extracellular enzymes, cell-surface antigens, or melanin, a pigment deposited into the cell-wall of the organism. Therefore, O-glycosylation may have a huge impact on virulence of this organism through effects on biosynthesis, localization and function of these virulence factors. This project aims to analyze the influence of O-glycosylation on these virulence factors by characterizing the protein mannosyltransferase (PMI-) gene family of C. neoformans. This gene family, which consists of three members, PMTI, PMT2, and PMT4, encodes enzymes that catalyze the initial step of protein O-glycosylation, the addition of mannose residues to serine or threonine residues of respective target proteins. Effects of deleting PMT-genes on virulence of C neoformans will be determined by routine in vitro and in vivo assays analyzing specific virulence factors and infectivity of the pathogen, respectively.
DFG Programme Priority Programmes
 
 

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