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A Lytic Polysaccharide Monooxygenase-like protein functions in fungal copper import and meningitis

Infection by the fungal pathogen Cryptococcus neoformans causes lethal meningitis, primarily in immune-compromised individuals. Colonization of the brain by C. neoformans is dependent on copper (Cu) acquisition from the host, which drives critical virulence mechanisms. While C. neoformans Cu(+) impo...

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Detalles Bibliográficos
Autores principales: Garcia-Santamarina, Sarela, Probst, Corinna, Festa, Richard A., Ding, Chen, Smith, Aaron D., Conklin, Steven E., Brander, Søren, Kinch, Lisa N., Grishin, Nick V., Franz, Katherine J., Riggs-Gelasco, Pamela, Leggio, Leila Lo, Johansen, Katja Salomon, Thiele, Dennis J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036007/
https://www.ncbi.nlm.nih.gov/pubmed/31932719
http://dx.doi.org/10.1038/s41589-019-0437-9
Descripción
Sumario:Infection by the fungal pathogen Cryptococcus neoformans causes lethal meningitis, primarily in immune-compromised individuals. Colonization of the brain by C. neoformans is dependent on copper (Cu) acquisition from the host, which drives critical virulence mechanisms. While C. neoformans Cu(+) import and virulence are dependent on the Ctr1 and Ctr4 proteins, little is known concerning extracellular Cu ligands that participate in this process. We identified a C. neoformans gene, BIM1, strongly induced during Cu limitation and which encodes a protein related to Lytic Polysaccharide Monooxygenases (LPMOs). Surprisingly, bim1 mutants are Cu deficient and Bim1 function in Cu accumulation depends upon Cu(2+) coordination and cell surface association via a GPI anchor. Bim1 participates in Cu uptake in concert with Ctr1 and expression of this pathway drives brain colonization in mouse infection models. These studies demonstrate a new role for LPMO-like proteins as a critical factor for Cu acquisition in fungal meningitis.