A Drug-Sensitive Genetic Network Masks Fungi from the Immune System

PLoS Pathogens

Robert T Wheeler¹  Gerald R Fink¹ 

[1] Whitehead Institute for Biomedical Research, Cambridge, Massachusetts, United States of America

关键词: C;    ida albicans;    Fungi;    Saccharomyces cerevisiae;    Cell walls;    Fungal pathogens;    Macrophages;    Fungal genetics;    Fungal diseases;   

DOI  :  10.1371/journal.ppat.0020035

学科分类：生物科学（综合）

来源: Public Library of Science

【 摘 要 】

Fungal pathogens can be recognized by the immune system via their β-glucan, a potent proinflammatory molecule that is present at high levels but is predominantly buried beneath a mannoprotein coat and invisible to the host. To investigate the nature and significance of “masking” this molecule, we characterized the mechanism of masking and consequences of unmasking for immune recognition. We found that the underlying β-glucan in the cell wall of Candida albicans is unmasked by subinhibitory doses of the antifungal drug caspofungin, causing the exposed fungi to elicit a stronger immune response. Using a library of bakers' yeast (Saccharomyces cerevisiae) mutants, we uncovered a conserved genetic network that is required for concealing β-glucan from the immune system and limiting the host response. Perturbation of parts of this network in the pathogen C. albicans caused unmasking of its β-glucan, leading to increased β-glucan receptor-dependent elicitation of key proinflammatory cytokines from primary mouse macrophages. By creating an anti-inflammatory barrier to mask β-glucan, opportunistic fungi may promote commensal colonization and have an increased propensity for causing disease. Targeting the widely conserved gene network required for creating and maintaining this barrier may lead to novel broad-spectrum antimycotics.

【 授权许可】

CC BY