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The Aspergillus flavus Phosphatase CDC14 Regulates Development, Aflatoxin Biosynthesis and Pathogenicity

Reversible protein phosphorylation is known to play important roles in the regulation of various cellular processes in eukaryotes. Phosphatase-mediated dephosphorylation are integral components of cellular signal pathways by counteracting the phosphorylation action of kinases. In this study, we char...

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Autores principales: Yang, Guang, Hu, Yule, Fasoyin, Opemipo E., Yue, Yuewei, Chen, Lijie, Qiu, Yue, Wang, Xiuna, Zhuang, Zhenhong, Wang, Shihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5950752/
https://www.ncbi.nlm.nih.gov/pubmed/29868497
http://dx.doi.org/10.3389/fcimb.2018.00141
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author Yang, Guang
Hu, Yule
Fasoyin, Opemipo E.
Yue, Yuewei
Chen, Lijie
Qiu, Yue
Wang, Xiuna
Zhuang, Zhenhong
Wang, Shihua
author_facet Yang, Guang
Hu, Yule
Fasoyin, Opemipo E.
Yue, Yuewei
Chen, Lijie
Qiu, Yue
Wang, Xiuna
Zhuang, Zhenhong
Wang, Shihua
author_sort Yang, Guang
collection PubMed
description Reversible protein phosphorylation is known to play important roles in the regulation of various cellular processes in eukaryotes. Phosphatase-mediated dephosphorylation are integral components of cellular signal pathways by counteracting the phosphorylation action of kinases. In this study, we characterized the functions of CDC14, a dual-specificity phosphatase in the development, secondary metabolism and crop infection of Aspergillus flavus. Deletion of AflCDC14 resulted in a growth defect and abnormal conidium morphology. Inactivation of AflCDC14 caused defective septum and failure to generate sclerotia. Additionally, the AflCDC14 deletion mutant (ΔCDC14) displayed increased sensitivity to osmotic and cell wall integrity stresses. Importantly, it had a significant increase in aflatoxin production, which was consistent with the up-regulation of the expression levels of aflatoxin biosynthesis related genes in ΔCDC14 mutant. Furthermore, seeds infection assays suggested that AflCDC14 was crucial for virulence of A. flavus. It was also found that the activity of amylase was decreased in ΔCDC14 mutant. AflCDC14-eRFP mainly localized to the cytoplasm and vesicles during coidial germination and mycelial development stages. Taken together, these results not only reveal the importance of the CDC14 phosphatase in the regulation of development, aflatoxin biosynthesis and virulence in A. flavus, but may also provide a potential target for controlling crop infections of this fungal pathogen.
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spelling pubmed-59507522018-06-04 The Aspergillus flavus Phosphatase CDC14 Regulates Development, Aflatoxin Biosynthesis and Pathogenicity Yang, Guang Hu, Yule Fasoyin, Opemipo E. Yue, Yuewei Chen, Lijie Qiu, Yue Wang, Xiuna Zhuang, Zhenhong Wang, Shihua Front Cell Infect Microbiol Microbiology Reversible protein phosphorylation is known to play important roles in the regulation of various cellular processes in eukaryotes. Phosphatase-mediated dephosphorylation are integral components of cellular signal pathways by counteracting the phosphorylation action of kinases. In this study, we characterized the functions of CDC14, a dual-specificity phosphatase in the development, secondary metabolism and crop infection of Aspergillus flavus. Deletion of AflCDC14 resulted in a growth defect and abnormal conidium morphology. Inactivation of AflCDC14 caused defective septum and failure to generate sclerotia. Additionally, the AflCDC14 deletion mutant (ΔCDC14) displayed increased sensitivity to osmotic and cell wall integrity stresses. Importantly, it had a significant increase in aflatoxin production, which was consistent with the up-regulation of the expression levels of aflatoxin biosynthesis related genes in ΔCDC14 mutant. Furthermore, seeds infection assays suggested that AflCDC14 was crucial for virulence of A. flavus. It was also found that the activity of amylase was decreased in ΔCDC14 mutant. AflCDC14-eRFP mainly localized to the cytoplasm and vesicles during coidial germination and mycelial development stages. Taken together, these results not only reveal the importance of the CDC14 phosphatase in the regulation of development, aflatoxin biosynthesis and virulence in A. flavus, but may also provide a potential target for controlling crop infections of this fungal pathogen. Frontiers Media S.A. 2018-05-07 /pmc/articles/PMC5950752/ /pubmed/29868497 http://dx.doi.org/10.3389/fcimb.2018.00141 Text en Copyright © 2018 Yang, Hu, Fasoyin, Yue, Chen, Qiu, Wang, Zhuang and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Yang, Guang
Hu, Yule
Fasoyin, Opemipo E.
Yue, Yuewei
Chen, Lijie
Qiu, Yue
Wang, Xiuna
Zhuang, Zhenhong
Wang, Shihua
The Aspergillus flavus Phosphatase CDC14 Regulates Development, Aflatoxin Biosynthesis and Pathogenicity
title The Aspergillus flavus Phosphatase CDC14 Regulates Development, Aflatoxin Biosynthesis and Pathogenicity
title_full The Aspergillus flavus Phosphatase CDC14 Regulates Development, Aflatoxin Biosynthesis and Pathogenicity
title_fullStr The Aspergillus flavus Phosphatase CDC14 Regulates Development, Aflatoxin Biosynthesis and Pathogenicity
title_full_unstemmed The Aspergillus flavus Phosphatase CDC14 Regulates Development, Aflatoxin Biosynthesis and Pathogenicity
title_short The Aspergillus flavus Phosphatase CDC14 Regulates Development, Aflatoxin Biosynthesis and Pathogenicity
title_sort aspergillus flavus phosphatase cdc14 regulates development, aflatoxin biosynthesis and pathogenicity
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5950752/
https://www.ncbi.nlm.nih.gov/pubmed/29868497
http://dx.doi.org/10.3389/fcimb.2018.00141
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