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New Insights of Transcriptional Regulator AflR in Aspergillus flavus Physiology

Aspergillus flavus aflR, a gene encoding a Zn(II)(2)Cys(6) DNA-binding domain, is an important transcriptional regulator of the aflatoxin biosynthesis gene cluster. Our previous results of Gene ontology (GO) analysis for the binding sites of AflR in A. flavus suggest that AflR may play an integrativ...

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Autores principales: Wang, Peng, Xu, Jia, Chang, Perng-Kuang, Liu, Zhemin, Kong, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791188/
https://www.ncbi.nlm.nih.gov/pubmed/35080432
http://dx.doi.org/10.1128/spectrum.00791-21
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author Wang, Peng
Xu, Jia
Chang, Perng-Kuang
Liu, Zhemin
Kong, Qing
author_facet Wang, Peng
Xu, Jia
Chang, Perng-Kuang
Liu, Zhemin
Kong, Qing
author_sort Wang, Peng
collection PubMed
description Aspergillus flavus aflR, a gene encoding a Zn(II)(2)Cys(6) DNA-binding domain, is an important transcriptional regulator of the aflatoxin biosynthesis gene cluster. Our previous results of Gene ontology (GO) analysis for the binding sites of AflR in A. flavus suggest that AflR may play an integrative regulatory role. In this study the ΔaflR and overexpression (OE) strains based on the well-established double-crossover recombinational technique were constructed to investigate the integrative function of the aflR gene in A. flavus. The disruption of aflR severely affected the aflatoxin biosynthetic pathway, resulting in a significant decrease in aflatoxin production. The aflatoxin B(1) (AFB(1)) of the ΔaflR strain was 180 ng/mL and aflatoxin B(2) (AFB(2)) was 2.95 ng/mL on YES medium for 5 days, which was 1/1,000 of that produced by the wild-type strain (WT). In addition, the ΔaflR strain produced relatively sparse conidia and a very small number of sclerotia. On the seventh day, the sclerotia yield on each plate of the WT and OE strains exceeded 1,000, while the sclerotial formation of the ΔaflR strain was not detected until 14 days. However, the biosynthesis of cyclopiazonic acid (CPA) was not affected by aflR gene disruption. Transcriptomic analysis of the ΔaflR strain grown on potato dextrose agar (PDA) plates at 0 h, 24 h, and 72 h showed that expression of clustering genes involved in the biosynthesis of aflatoxin was significantly downregulated. Meanwhile, the ΔaflR strain compared with the WT strain showed significant expression differences in genes involved in spore germination, sclerotial development, and carbohydrate metabolism compared to the WT. The results demonstrated that the A. flavus aflR gene also played a positive role in the fungal growth and development in addition to aflatoxin biosynthesis. IMPORTANCE Past studies of the A. flavus aflR gene and its orthologues in related Aspergillus species were solely focused on their roles in secondary metabolism. In this study, we used the ΔaflR and OE strains to demonstrate the role of aflR in growth and development of A. flavus. For the first time, we confirmed that the ΔaflR strain also was defective in production of conidia and sclerotia, asexual propagules of A. flavus. Our transcriptomic analysis further showed that genes involved in spore germination, sclerotial development, aflatoxin biosynssssthesis, and carbohydrate metabolism exhibited significant differences in the ΔaflR strain compared with the WT strain. Our study indicates that AflR not only plays an important role in regulating aflatoxin synthesis but also in playing a positive role in the conidial formation and sclerotial development in A. flavus. This study reveals the critical and positive role of the aflR gene in fungal growth and development, and provides a theoretical basis for the genetic studies of other aspergilli.
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spelling pubmed-87911882022-02-09 New Insights of Transcriptional Regulator AflR in Aspergillus flavus Physiology Wang, Peng Xu, Jia Chang, Perng-Kuang Liu, Zhemin Kong, Qing Microbiol Spectr Research Article Aspergillus flavus aflR, a gene encoding a Zn(II)(2)Cys(6) DNA-binding domain, is an important transcriptional regulator of the aflatoxin biosynthesis gene cluster. Our previous results of Gene ontology (GO) analysis for the binding sites of AflR in A. flavus suggest that AflR may play an integrative regulatory role. In this study the ΔaflR and overexpression (OE) strains based on the well-established double-crossover recombinational technique were constructed to investigate the integrative function of the aflR gene in A. flavus. The disruption of aflR severely affected the aflatoxin biosynthetic pathway, resulting in a significant decrease in aflatoxin production. The aflatoxin B(1) (AFB(1)) of the ΔaflR strain was 180 ng/mL and aflatoxin B(2) (AFB(2)) was 2.95 ng/mL on YES medium for 5 days, which was 1/1,000 of that produced by the wild-type strain (WT). In addition, the ΔaflR strain produced relatively sparse conidia and a very small number of sclerotia. On the seventh day, the sclerotia yield on each plate of the WT and OE strains exceeded 1,000, while the sclerotial formation of the ΔaflR strain was not detected until 14 days. However, the biosynthesis of cyclopiazonic acid (CPA) was not affected by aflR gene disruption. Transcriptomic analysis of the ΔaflR strain grown on potato dextrose agar (PDA) plates at 0 h, 24 h, and 72 h showed that expression of clustering genes involved in the biosynthesis of aflatoxin was significantly downregulated. Meanwhile, the ΔaflR strain compared with the WT strain showed significant expression differences in genes involved in spore germination, sclerotial development, and carbohydrate metabolism compared to the WT. The results demonstrated that the A. flavus aflR gene also played a positive role in the fungal growth and development in addition to aflatoxin biosynthesis. IMPORTANCE Past studies of the A. flavus aflR gene and its orthologues in related Aspergillus species were solely focused on their roles in secondary metabolism. In this study, we used the ΔaflR and OE strains to demonstrate the role of aflR in growth and development of A. flavus. For the first time, we confirmed that the ΔaflR strain also was defective in production of conidia and sclerotia, asexual propagules of A. flavus. Our transcriptomic analysis further showed that genes involved in spore germination, sclerotial development, aflatoxin biosynssssthesis, and carbohydrate metabolism exhibited significant differences in the ΔaflR strain compared with the WT strain. Our study indicates that AflR not only plays an important role in regulating aflatoxin synthesis but also in playing a positive role in the conidial formation and sclerotial development in A. flavus. This study reveals the critical and positive role of the aflR gene in fungal growth and development, and provides a theoretical basis for the genetic studies of other aspergilli. American Society for Microbiology 2022-01-26 /pmc/articles/PMC8791188/ /pubmed/35080432 http://dx.doi.org/10.1128/spectrum.00791-21 Text en Copyright © 2022 Wang 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
Wang, Peng
Xu, Jia
Chang, Perng-Kuang
Liu, Zhemin
Kong, Qing
New Insights of Transcriptional Regulator AflR in Aspergillus flavus Physiology
title New Insights of Transcriptional Regulator AflR in Aspergillus flavus Physiology
title_full New Insights of Transcriptional Regulator AflR in Aspergillus flavus Physiology
title_fullStr New Insights of Transcriptional Regulator AflR in Aspergillus flavus Physiology
title_full_unstemmed New Insights of Transcriptional Regulator AflR in Aspergillus flavus Physiology
title_short New Insights of Transcriptional Regulator AflR in Aspergillus flavus Physiology
title_sort new insights of transcriptional regulator aflr in aspergillus flavus physiology
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791188/
https://www.ncbi.nlm.nih.gov/pubmed/35080432
http://dx.doi.org/10.1128/spectrum.00791-21
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