Comparative Characterization of G Protein α Subunits in <i>Aspergillus fumigatus</i>

Trimeric G proteins play a central role in the G protein signaling in filamentous fungi and Gα subunits are the major component of trimeric G proteins. In this study, we characterize three Gα subunits in the human pathogen <i>Aspergillus fumigatus</i>. While the deletion of <i>gpaB...

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Main Authors: Yong-Ho Choi, Na-Young Lee, Sung-Su Kim, Hee-Soo Park, Kwang-Soo Shin
Format: Article
Language:English
Published: MDPI AG 2020-04-01
Series:Pathogens
Subjects:
GT
Online Access:https://www.mdpi.com/2076-0817/9/4/272
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spelling doaj-5b76090f47ae43c1895df886983197122020-11-25T02:58:38ZengMDPI AGPathogens2076-08172020-04-01927227210.3390/pathogens9040272Comparative Characterization of G Protein α Subunits in <i>Aspergillus fumigatus</i>Yong-Ho Choi0Na-Young Lee1Sung-Su Kim2Hee-Soo Park3Kwang-Soo Shin4Department of Microbiology, Graduate School, Daejeon University, Daejeon 34520, KoreaDepartment of Microbiology, Graduate School, Daejeon University, Daejeon 34520, KoreaDepartment of Biomedical Laboratory Science, Daejeon University, Daejeon 34520, KoreaSchool of Food Science and Biotechnology, Institute of Agricultural Science and Technology, Kyungpook National University, Daegu 41566, KoreaDepartment of Microbiology, Graduate School, Daejeon University, Daejeon 34520, KoreaTrimeric G proteins play a central role in the G protein signaling in filamentous fungi and Gα subunits are the major component of trimeric G proteins. In this study, we characterize three Gα subunits in the human pathogen <i>Aspergillus fumigatus</i>. While the deletion of <i>gpaB</i> and <i>ganA</i> led to reduced colony growth, the growth of the Δ<i>gpaA</i> strain was increased in minimal media. The germination rate, conidiation, and mRNA expression of key asexual development regulators were significantly decreased by the loss of <i>gpaB</i>. In contrast, the deletion of <i>gpaA</i> resulted in increased conidiation and mRNA expression levels of key asexual regulators. The deletion of <i>gpaB</i> caused a reduction in conidial tolerance against H<sub>2</sub>O<sub>2</sub>, but not in paraquat (PQ). Moreover, the Δ<i>gpaB</i> mutant showed enhanced susceptibility against membrane targeting azole antifungal drugs and reduced production of gliotoxin (GT). The protein kinase A (PKA) activity of the Δ<i>ganA</i> strain was severely decreased and protein kinase C (PKC) activity was detected all strains at similar levels, indicating that all G protein α subunits of <i>A</i>. <i>fumigatus</i> may be a component of the cAMP/PKA signaling pathway and appear to possess the PKC signaling pathway as an alternative backup pathway to compensate for PKA depletion. Collectively, the three Gα subunits regulate growth, germination, asexual development, resistance to oxidative stress, and GT production differently <i>via</i> the PKA or PKC signaling pathway. The function of GanA of <i>A</i>. <i>fumigatus</i> was elucidated for the first time.https://www.mdpi.com/2076-0817/9/4/272<i>Aspergillus fumigatus</i>G protein α subunitsasexual developmentstress responseantifungal drugGT
collection DOAJ
language English
format Article
sources DOAJ
author Yong-Ho Choi
Na-Young Lee
Sung-Su Kim
Hee-Soo Park
Kwang-Soo Shin
spellingShingle Yong-Ho Choi
Na-Young Lee
Sung-Su Kim
Hee-Soo Park
Kwang-Soo Shin
Comparative Characterization of G Protein α Subunits in <i>Aspergillus fumigatus</i>
Pathogens
<i>Aspergillus fumigatus</i>
G protein α subunits
asexual development
stress response
antifungal drug
GT
author_facet Yong-Ho Choi
Na-Young Lee
Sung-Su Kim
Hee-Soo Park
Kwang-Soo Shin
author_sort Yong-Ho Choi
title Comparative Characterization of G Protein α Subunits in <i>Aspergillus fumigatus</i>
title_short Comparative Characterization of G Protein α Subunits in <i>Aspergillus fumigatus</i>
title_full Comparative Characterization of G Protein α Subunits in <i>Aspergillus fumigatus</i>
title_fullStr Comparative Characterization of G Protein α Subunits in <i>Aspergillus fumigatus</i>
title_full_unstemmed Comparative Characterization of G Protein α Subunits in <i>Aspergillus fumigatus</i>
title_sort comparative characterization of g protein α subunits in <i>aspergillus fumigatus</i>
publisher MDPI AG
series Pathogens
issn 2076-0817
publishDate 2020-04-01
description Trimeric G proteins play a central role in the G protein signaling in filamentous fungi and Gα subunits are the major component of trimeric G proteins. In this study, we characterize three Gα subunits in the human pathogen <i>Aspergillus fumigatus</i>. While the deletion of <i>gpaB</i> and <i>ganA</i> led to reduced colony growth, the growth of the Δ<i>gpaA</i> strain was increased in minimal media. The germination rate, conidiation, and mRNA expression of key asexual development regulators were significantly decreased by the loss of <i>gpaB</i>. In contrast, the deletion of <i>gpaA</i> resulted in increased conidiation and mRNA expression levels of key asexual regulators. The deletion of <i>gpaB</i> caused a reduction in conidial tolerance against H<sub>2</sub>O<sub>2</sub>, but not in paraquat (PQ). Moreover, the Δ<i>gpaB</i> mutant showed enhanced susceptibility against membrane targeting azole antifungal drugs and reduced production of gliotoxin (GT). The protein kinase A (PKA) activity of the Δ<i>ganA</i> strain was severely decreased and protein kinase C (PKC) activity was detected all strains at similar levels, indicating that all G protein α subunits of <i>A</i>. <i>fumigatus</i> may be a component of the cAMP/PKA signaling pathway and appear to possess the PKC signaling pathway as an alternative backup pathway to compensate for PKA depletion. Collectively, the three Gα subunits regulate growth, germination, asexual development, resistance to oxidative stress, and GT production differently <i>via</i> the PKA or PKC signaling pathway. The function of GanA of <i>A</i>. <i>fumigatus</i> was elucidated for the first time.
topic <i>Aspergillus fumigatus</i>
G protein α subunits
asexual development
stress response
antifungal drug
GT
url https://www.mdpi.com/2076-0817/9/4/272
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