Cryptococcus neoformans Copper Detoxification Machinery Is Critical for Fungal Virulence

被引:153
作者
Ding, Chen [1 ]
Festa, Richard A. [1 ]
Chen, Ying-Lien [2 ]
Espart, Anna [3 ]
Palacios, Oscar [4 ]
Espin, Jordi [4 ]
Capdevila, Merce [4 ]
Atrian, Silvia [3 ]
Heitman, Joseph [1 ,2 ]
Thiele, Dennis J. [1 ]
机构
[1] Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA
[2] Duke Univ, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
[3] Univ Barcelona, Dept Genet, E-08028 Barcelona, Spain
[4] Univ Autonoma Barcelona, Dept Quim, Barcelona 08193, Spain
关键词
IRON-SULFUR CLUSTERS; P-TYPE ATPASE; CANDIDA-ALBICANS; MYCOBACTERIUM-TUBERCULOSIS; SACCHAROMYCES-CEREVISIAE; MOLECULAR CHARACTERIZATION; YEAST METALLOTHIONEIN; NUTRITIONAL IMMUNITY; SELECTABLE MARKER; MAMMALIAN HOSTS;
D O I
10.1016/j.chom.2013.02.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Copper (Cu) is an essential metal that is toxic at high concentrations. Thus, pathogens often rely on host Cu for growth, but host cells can hyperaccumulate Cu to exert antimicrobial effects. The human fungal pathogen Cryptococcus neoformans encodes many Cu-responsive genes, but their role in infection is unclear. We determined that pulmonary C. neoformans infection results in Cu-specific induction of genes encoding the Cu-detoxifying metallothionein (Cmt) proteins. Mutant strains lacking CMTs or expressing Cmt variants defective in Cu-coordination exhibit severely attenuated virulence and reduced pulmonary colonization. Consistent with the upregulation of Cmt proteins, C. neoformans pulmonary infection results in increased serum Cu concentrations and increases and decreases alveolar macrophage expression of the Cu importer (Ctr1) and ATP7A, a transporter implicated in phagosomal Cu compartmentalization, respectively. These studies indicate that the host mobilizes Cu as an innate antifungal defense but C. neoformans senses and neutralizes toxic Cu to promote infection.
引用
收藏
页码:265 / 276
页数:12
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