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Putative Core Transcription Factors Affecting Virulence in Aspergillus flavus during Infection of Maize

Aspergillus flavus is an opportunistic pathogen responsible for millions of dollars in crop losses annually and negative health impacts on crop consumers globally. A. flavus strains have the potential to produce aflatoxin and other toxic secondary metabolites, which often increase during plant colon...

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Autores principales: Gilbert, Matthew K., Mack, Brian M., Lebar, Matthew D., Chang, Perng-Kuang, Gross, Stephanie R., Sweany, Rebecca R., Cary, Jeffrey W., Rajasekaran, Kanniah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9861280/
https://www.ncbi.nlm.nih.gov/pubmed/36675939
http://dx.doi.org/10.3390/jof9010118
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author Gilbert, Matthew K.
Mack, Brian M.
Lebar, Matthew D.
Chang, Perng-Kuang
Gross, Stephanie R.
Sweany, Rebecca R.
Cary, Jeffrey W.
Rajasekaran, Kanniah
author_facet Gilbert, Matthew K.
Mack, Brian M.
Lebar, Matthew D.
Chang, Perng-Kuang
Gross, Stephanie R.
Sweany, Rebecca R.
Cary, Jeffrey W.
Rajasekaran, Kanniah
author_sort Gilbert, Matthew K.
collection PubMed
description Aspergillus flavus is an opportunistic pathogen responsible for millions of dollars in crop losses annually and negative health impacts on crop consumers globally. A. flavus strains have the potential to produce aflatoxin and other toxic secondary metabolites, which often increase during plant colonization. To mitigate the impacts of this international issue, we employ a range of strategies to directly impact fungal physiology, growth and development, thus requiring knowledge on the underlying molecular mechanisms driving these processes. Here we utilize RNA-sequencing data that are obtained from in situ assays, whereby Zea mays kernels are inoculated with A. flavus strains, to select transcription factors putatively driving virulence-related gene networks. We demonstrate, through growth, sporulation, oxidative stress-response and aflatoxin/CPA analysis, that three A. flavus strains with knockout mutations for the putative transcription factors AFLA_089270, AFLA_112760, and AFLA_031450 demonstrate characteristics such as reduced growth capacity and decreased aflatoxin/CPA accumulation in kernels consistent with decreased fungal pathogenicity. Furthermore, AFLA_089270, also known as HacA, eliminates CPA production and impacts the fungus’s capacity to respond to highly oxidative conditions, indicating an impact on plant colonization. Taken together, these data provide a sound foundation for elucidating the downstream molecular pathways potentially contributing to fungal virulence.
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spelling pubmed-98612802023-01-22 Putative Core Transcription Factors Affecting Virulence in Aspergillus flavus during Infection of Maize Gilbert, Matthew K. Mack, Brian M. Lebar, Matthew D. Chang, Perng-Kuang Gross, Stephanie R. Sweany, Rebecca R. Cary, Jeffrey W. Rajasekaran, Kanniah J Fungi (Basel) Article Aspergillus flavus is an opportunistic pathogen responsible for millions of dollars in crop losses annually and negative health impacts on crop consumers globally. A. flavus strains have the potential to produce aflatoxin and other toxic secondary metabolites, which often increase during plant colonization. To mitigate the impacts of this international issue, we employ a range of strategies to directly impact fungal physiology, growth and development, thus requiring knowledge on the underlying molecular mechanisms driving these processes. Here we utilize RNA-sequencing data that are obtained from in situ assays, whereby Zea mays kernels are inoculated with A. flavus strains, to select transcription factors putatively driving virulence-related gene networks. We demonstrate, through growth, sporulation, oxidative stress-response and aflatoxin/CPA analysis, that three A. flavus strains with knockout mutations for the putative transcription factors AFLA_089270, AFLA_112760, and AFLA_031450 demonstrate characteristics such as reduced growth capacity and decreased aflatoxin/CPA accumulation in kernels consistent with decreased fungal pathogenicity. Furthermore, AFLA_089270, also known as HacA, eliminates CPA production and impacts the fungus’s capacity to respond to highly oxidative conditions, indicating an impact on plant colonization. Taken together, these data provide a sound foundation for elucidating the downstream molecular pathways potentially contributing to fungal virulence. MDPI 2023-01-14 /pmc/articles/PMC9861280/ /pubmed/36675939 http://dx.doi.org/10.3390/jof9010118 Text en © 2023 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
Gilbert, Matthew K.
Mack, Brian M.
Lebar, Matthew D.
Chang, Perng-Kuang
Gross, Stephanie R.
Sweany, Rebecca R.
Cary, Jeffrey W.
Rajasekaran, Kanniah
Putative Core Transcription Factors Affecting Virulence in Aspergillus flavus during Infection of Maize
title Putative Core Transcription Factors Affecting Virulence in Aspergillus flavus during Infection of Maize
title_full Putative Core Transcription Factors Affecting Virulence in Aspergillus flavus during Infection of Maize
title_fullStr Putative Core Transcription Factors Affecting Virulence in Aspergillus flavus during Infection of Maize
title_full_unstemmed Putative Core Transcription Factors Affecting Virulence in Aspergillus flavus during Infection of Maize
title_short Putative Core Transcription Factors Affecting Virulence in Aspergillus flavus during Infection of Maize
title_sort putative core transcription factors affecting virulence in aspergillus flavus during infection of maize
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9861280/
https://www.ncbi.nlm.nih.gov/pubmed/36675939
http://dx.doi.org/10.3390/jof9010118
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