Metabolic modulation: Pneumocystis phosphoglucomutase is a target influencing host recognition

被引:0
|
作者
Kottom, Theodore J. [1 ]
Carmona, Eva M. [1 ]
Lepenies, Bernd [2 ,3 ]
Limper, Andrew H. [1 ]
机构
[1] Mayo Clin, Coll Med, Dept Med & Biochem, Thorac Dis Res Unit, Rochester, MN 55905 USA
[2] Univ Vet Med Hannover, Res Ctr Emerging Infect & Zoonoses, Hannover, Germany
[3] Univ Vet Med Hannover, Inst Immunol, Hannover, Germany
来源
CELL SURFACE | 2024年 / 11卷
关键词
Pneumocystis; Phosphoglucomutase; Mannoprotein; C-type lectin receptors (CLRs); MAJOR SURFACE GLYCOPROTEIN; SACCHAROMYCES-CEREVISIAE; CARINII; RECEPTORS; MANNOSE;
D O I
10.1016/j.tcsw.2024.100123
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Herein, this manuscript explores the significance of the phosphoglucomutase (PGM) enzyme in Pneumocystis spp., focusing on its role in fungal surface mannoprotein formation. Through expression of the Pneumocystis murina Pmpgm2 in a Saccharomyces cerevisiae pgm2 Delta strain, we demonstrate restoration of binding to the mannose receptor (MR) and macrophages to wildtype yeast levels in this complemented strain. Gas Chromatography-Mass Spectroscopy (GC-MS) confirmed reduced mannose content in the pgm2 Delta yeast strain compared to the wild-type and complemented Pmpgm2 cDNA-expressing strains. This study underscores fungal PGM function in dolichol glucosyl phosphate biosynthesis, crucial for proper cell wall mannoprotein formation. Furthermore, highlighting the conservation of targetable cysteine residues across fungal pathogens, PGM inhibition maybe a potential therapeutic strategy against a broad spectrum of fungal infections.
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页数:4
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