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CRISPR-based tools for targeted genetic manipulation in pathogenic Sporothrix species
Sporothrix brasiliensis is an emerging fungal pathogen frequently associated with zoonotic transmission of sporotrichosis by contaminated cats. Within 25 years, the disease has spread not only throughout Brazil but now to neighboring countries in Latin America. Thermo-dimorphism, melanin, glycans, a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581184/ https://www.ncbi.nlm.nih.gov/pubmed/37707447 http://dx.doi.org/10.1128/spectrum.05078-22 |
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author | Hatinguais, Remi Leaves, Ian Brown, Gordon D. Brown, Alistair J. P. Brock, Matthias Peres da Silva, Roberta |
author_facet | Hatinguais, Remi Leaves, Ian Brown, Gordon D. Brown, Alistair J. P. Brock, Matthias Peres da Silva, Roberta |
author_sort | Hatinguais, Remi |
collection | PubMed |
description | Sporothrix brasiliensis is an emerging fungal pathogen frequently associated with zoonotic transmission of sporotrichosis by contaminated cats. Within 25 years, the disease has spread not only throughout Brazil but now to neighboring countries in Latin America. Thermo-dimorphism, melanin, glycans, adhesins, and secreted vesicles have been associated with the ability of Sporothrix species to cause disease in the mammalian host. Although certain virulence factors have been proposed as potential determinants for sporotrichosis, the scarcity of molecular tools for performing reverse genetics in Sporothrix has significantly impeded the dissection of mechanisms underlying the disease. Here, we demonstrate that PEG-mediated protoplast transformation is a powerful method for heterologous gene expression in S. brasiliensis, S. schenckii, and S. chilensis. Combined with CRISPR/Cas9 gene editing, this transformation protocol enabled the deletion of the putative DHN-melanin synthase gene pks1, which is a proposed virulence factor of Sporothrix species. To improve in locus integration of deletion constructs, we deleted the KU(80) homolog that is critical for non-homologous end-joining DNA repair. The use of Δku80 strains from S. brasiliensis enhanced homologous-directed repair during transformation resulting in increased targeted gene deletion in combination with CRISPR/Cas9. In conclusion, our CRISPR/Cas9-based transformation protocol provides an efficient tool for targeted gene manipulation in Sporothrix species. IMPORTANCE: Sporotrichosis caused by Sporothrix brasiliensis is a disease that requires long periods of treatment and is rapidly spreading across Latin America. The virulence of this fungus and the surge of atypical and more severe presentations of the disease raise the need for an understanding of the molecular mechanisms underlying sporotrichosis, as well as the development of better diagnostics and antifungal therapies. By developing molecular tools for accurate genetic manipulation in Sporothrix, this study addresses the paucity of reliable and reproducible tools for stable genetic engineering of Sporothrix species, which has represented a major obstacle for studying the virulence determinants and their roles in the establishment of sporotrichosis. |
format | Online Article Text |
id | pubmed-10581184 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-105811842023-10-18 CRISPR-based tools for targeted genetic manipulation in pathogenic Sporothrix species Hatinguais, Remi Leaves, Ian Brown, Gordon D. Brown, Alistair J. P. Brock, Matthias Peres da Silva, Roberta Microbiol Spectr Research Article Sporothrix brasiliensis is an emerging fungal pathogen frequently associated with zoonotic transmission of sporotrichosis by contaminated cats. Within 25 years, the disease has spread not only throughout Brazil but now to neighboring countries in Latin America. Thermo-dimorphism, melanin, glycans, adhesins, and secreted vesicles have been associated with the ability of Sporothrix species to cause disease in the mammalian host. Although certain virulence factors have been proposed as potential determinants for sporotrichosis, the scarcity of molecular tools for performing reverse genetics in Sporothrix has significantly impeded the dissection of mechanisms underlying the disease. Here, we demonstrate that PEG-mediated protoplast transformation is a powerful method for heterologous gene expression in S. brasiliensis, S. schenckii, and S. chilensis. Combined with CRISPR/Cas9 gene editing, this transformation protocol enabled the deletion of the putative DHN-melanin synthase gene pks1, which is a proposed virulence factor of Sporothrix species. To improve in locus integration of deletion constructs, we deleted the KU(80) homolog that is critical for non-homologous end-joining DNA repair. The use of Δku80 strains from S. brasiliensis enhanced homologous-directed repair during transformation resulting in increased targeted gene deletion in combination with CRISPR/Cas9. In conclusion, our CRISPR/Cas9-based transformation protocol provides an efficient tool for targeted gene manipulation in Sporothrix species. IMPORTANCE: Sporotrichosis caused by Sporothrix brasiliensis is a disease that requires long periods of treatment and is rapidly spreading across Latin America. The virulence of this fungus and the surge of atypical and more severe presentations of the disease raise the need for an understanding of the molecular mechanisms underlying sporotrichosis, as well as the development of better diagnostics and antifungal therapies. By developing molecular tools for accurate genetic manipulation in Sporothrix, this study addresses the paucity of reliable and reproducible tools for stable genetic engineering of Sporothrix species, which has represented a major obstacle for studying the virulence determinants and their roles in the establishment of sporotrichosis. American Society for Microbiology 2023-09-14 /pmc/articles/PMC10581184/ /pubmed/37707447 http://dx.doi.org/10.1128/spectrum.05078-22 Text en Copyright © 2023 Hatinguais et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Hatinguais, Remi Leaves, Ian Brown, Gordon D. Brown, Alistair J. P. Brock, Matthias Peres da Silva, Roberta CRISPR-based tools for targeted genetic manipulation in pathogenic Sporothrix species |
title | CRISPR-based tools for targeted genetic manipulation in pathogenic Sporothrix species |
title_full | CRISPR-based tools for targeted genetic manipulation in pathogenic Sporothrix species |
title_fullStr | CRISPR-based tools for targeted genetic manipulation in pathogenic Sporothrix species |
title_full_unstemmed | CRISPR-based tools for targeted genetic manipulation in pathogenic Sporothrix species |
title_short | CRISPR-based tools for targeted genetic manipulation in pathogenic Sporothrix species |
title_sort | crispr-based tools for targeted genetic manipulation in pathogenic sporothrix species |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581184/ https://www.ncbi.nlm.nih.gov/pubmed/37707447 http://dx.doi.org/10.1128/spectrum.05078-22 |
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