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Evidencing New Roles for the Glycosyl-Transferase Cps1 in the Phytopathogenic Fungus Botrytis cinerea

The fungal cell wall occupies a central place in the interaction between fungi and their environment. This study focuses on the role of the putative polysaccharide synthase Cps1 in the physiology, development and virulence of the grey mold-causing agent Botrytis cinerea. Deletion of the Bccps1 gene...

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Autores principales: Blandenet, Matthieu, Gonçalves, Isabelle R., Rascle, Christine, Dupuy, Jean-William, Gillet, François-Xavier, Poussereau, Nathalie, Choquer, Mathias, Bruel, Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500679/
https://www.ncbi.nlm.nih.gov/pubmed/36135623
http://dx.doi.org/10.3390/jof8090899
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author Blandenet, Matthieu
Gonçalves, Isabelle R.
Rascle, Christine
Dupuy, Jean-William
Gillet, François-Xavier
Poussereau, Nathalie
Choquer, Mathias
Bruel, Christophe
author_facet Blandenet, Matthieu
Gonçalves, Isabelle R.
Rascle, Christine
Dupuy, Jean-William
Gillet, François-Xavier
Poussereau, Nathalie
Choquer, Mathias
Bruel, Christophe
author_sort Blandenet, Matthieu
collection PubMed
description The fungal cell wall occupies a central place in the interaction between fungi and their environment. This study focuses on the role of the putative polysaccharide synthase Cps1 in the physiology, development and virulence of the grey mold-causing agent Botrytis cinerea. Deletion of the Bccps1 gene does not affect the germination of the conidia (asexual spores) or the early mycelial development, but it perturbs hyphal expansion after 24 h, revealing a two-phase hyphal development that has not been reported so far. It causes a severe reduction of mycelial growth in a solid medium and modifies hyphal aggregation into pellets in liquid cultures. It strongly impairs plant penetration, plant colonization and the formation of sclerotia (survival structures). Loss of the BcCps1 protein associates with a decrease in glucans and glycoproteins in the fungus cell wall and the up-accumulation of 132 proteins in the mutant’s exoproteome, among which are fungal cell wall enzymes. This is accompanied by an increased fragility of the mutant mycelium, an increased sensitivity to some environmental stresses and a reduced adhesion to plant surface. Taken together, the results support a significant role of Cps1 in the cell wall biology of B. cinerea.
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spelling pubmed-95006792022-09-24 Evidencing New Roles for the Glycosyl-Transferase Cps1 in the Phytopathogenic Fungus Botrytis cinerea Blandenet, Matthieu Gonçalves, Isabelle R. Rascle, Christine Dupuy, Jean-William Gillet, François-Xavier Poussereau, Nathalie Choquer, Mathias Bruel, Christophe J Fungi (Basel) Article The fungal cell wall occupies a central place in the interaction between fungi and their environment. This study focuses on the role of the putative polysaccharide synthase Cps1 in the physiology, development and virulence of the grey mold-causing agent Botrytis cinerea. Deletion of the Bccps1 gene does not affect the germination of the conidia (asexual spores) or the early mycelial development, but it perturbs hyphal expansion after 24 h, revealing a two-phase hyphal development that has not been reported so far. It causes a severe reduction of mycelial growth in a solid medium and modifies hyphal aggregation into pellets in liquid cultures. It strongly impairs plant penetration, plant colonization and the formation of sclerotia (survival structures). Loss of the BcCps1 protein associates with a decrease in glucans and glycoproteins in the fungus cell wall and the up-accumulation of 132 proteins in the mutant’s exoproteome, among which are fungal cell wall enzymes. This is accompanied by an increased fragility of the mutant mycelium, an increased sensitivity to some environmental stresses and a reduced adhesion to plant surface. Taken together, the results support a significant role of Cps1 in the cell wall biology of B. cinerea. MDPI 2022-08-24 /pmc/articles/PMC9500679/ /pubmed/36135623 http://dx.doi.org/10.3390/jof8090899 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Blandenet, Matthieu
Gonçalves, Isabelle R.
Rascle, Christine
Dupuy, Jean-William
Gillet, François-Xavier
Poussereau, Nathalie
Choquer, Mathias
Bruel, Christophe
Evidencing New Roles for the Glycosyl-Transferase Cps1 in the Phytopathogenic Fungus Botrytis cinerea
title Evidencing New Roles for the Glycosyl-Transferase Cps1 in the Phytopathogenic Fungus Botrytis cinerea
title_full Evidencing New Roles for the Glycosyl-Transferase Cps1 in the Phytopathogenic Fungus Botrytis cinerea
title_fullStr Evidencing New Roles for the Glycosyl-Transferase Cps1 in the Phytopathogenic Fungus Botrytis cinerea
title_full_unstemmed Evidencing New Roles for the Glycosyl-Transferase Cps1 in the Phytopathogenic Fungus Botrytis cinerea
title_short Evidencing New Roles for the Glycosyl-Transferase Cps1 in the Phytopathogenic Fungus Botrytis cinerea
title_sort evidencing new roles for the glycosyl-transferase cps1 in the phytopathogenic fungus botrytis cinerea
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500679/
https://www.ncbi.nlm.nih.gov/pubmed/36135623
http://dx.doi.org/10.3390/jof8090899
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