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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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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 |
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author | 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. |
author_facet | 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. |
author_sort | Garcia-Santamarina, Sarela |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7036007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-70360072020-07-13 A Lytic Polysaccharide Monooxygenase-like protein functions in fungal copper import and meningitis 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. Nat Chem Biol Article 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. 2020-01-13 2020-03 /pmc/articles/PMC7036007/ /pubmed/31932719 http://dx.doi.org/10.1038/s41589-019-0437-9 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article 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. A Lytic Polysaccharide Monooxygenase-like protein functions in fungal copper import and meningitis |
title | A Lytic Polysaccharide Monooxygenase-like protein functions in fungal copper import and meningitis |
title_full | A Lytic Polysaccharide Monooxygenase-like protein functions in fungal copper import and meningitis |
title_fullStr | A Lytic Polysaccharide Monooxygenase-like protein functions in fungal copper import and meningitis |
title_full_unstemmed | A Lytic Polysaccharide Monooxygenase-like protein functions in fungal copper import and meningitis |
title_short | A Lytic Polysaccharide Monooxygenase-like protein functions in fungal copper import and meningitis |
title_sort | lytic polysaccharide monooxygenase-like protein functions in fungal copper import and meningitis |
topic | Article |
url | 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 |
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