Cargando…

Functional Analysis of Two Affinity cAMP Phosphodiesterases in the Nematode-Trapping Fungus Arthrobotrys oligospora

Phosphodiesterases are essential regulators of cyclic nucleotide signaling with diverse physiological functions. Two phosphodiesterases, PdeH and PdeL, have been identified from yeast and filamentous fungi. Here, the orthologs of PdeH and PdeL were characterized in a typical nematode-trapping fungus...

Descripción completa

Detalles Bibliográficos
Autores principales: Ma, Ni, Jiang, Ke-Xin, Bai, Na, Li, Dong-Ni, Zhang, Ke-Qin, Yang, Jin-Kui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026129/
https://www.ncbi.nlm.nih.gov/pubmed/35456080
http://dx.doi.org/10.3390/pathogens11040405
_version_ 1784691048580120576
author Ma, Ni
Jiang, Ke-Xin
Bai, Na
Li, Dong-Ni
Zhang, Ke-Qin
Yang, Jin-Kui
author_facet Ma, Ni
Jiang, Ke-Xin
Bai, Na
Li, Dong-Ni
Zhang, Ke-Qin
Yang, Jin-Kui
author_sort Ma, Ni
collection PubMed
description Phosphodiesterases are essential regulators of cyclic nucleotide signaling with diverse physiological functions. Two phosphodiesterases, PdeH and PdeL, have been identified from yeast and filamentous fungi. Here, the orthologs of PdeH and PdeL were characterized in a typical nematode-trapping fungus Arthrobotrys oligospora by gene disruption and phenotypic comparison. Deletion of AopdeH caused serious defects in mycelial growth, conidiation, stress response, trap formation, and nematicidal efficiency compared to the wild-type strain. In contrast, these phenotypes have no significant difference in the absence of AopdeL. In addition, deletion of AopdeH and AopdeL resulted in a remarkable increase in cAMP level during vegetative growth and trap formation, and the number of autophagosomes was decreased in ΔAopdeH and ΔAopdeL mutants, whereas their volumes considerably increased. Moreover, metabolomic analyses revealed that many metabolites were downregulated in ΔAopdeH mutant compared to their expression in the wild-type strain. Our results indicate that AoPdeH plays a crucial role in mycelial growth, conidiation, stress response, secondary metabolism, and trap formation. In contrast, AoPdeL only plays a minor role in hyphal and conidial morphology, autophagy, and trap formation in A. oligospora. This work expands the roles of phosphodiesterases and deepens the understanding of the regulation of trap formation in nematode-trapping fungi.
format Online
Article
Text
id pubmed-9026129
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-90261292022-04-23 Functional Analysis of Two Affinity cAMP Phosphodiesterases in the Nematode-Trapping Fungus Arthrobotrys oligospora Ma, Ni Jiang, Ke-Xin Bai, Na Li, Dong-Ni Zhang, Ke-Qin Yang, Jin-Kui Pathogens Article Phosphodiesterases are essential regulators of cyclic nucleotide signaling with diverse physiological functions. Two phosphodiesterases, PdeH and PdeL, have been identified from yeast and filamentous fungi. Here, the orthologs of PdeH and PdeL were characterized in a typical nematode-trapping fungus Arthrobotrys oligospora by gene disruption and phenotypic comparison. Deletion of AopdeH caused serious defects in mycelial growth, conidiation, stress response, trap formation, and nematicidal efficiency compared to the wild-type strain. In contrast, these phenotypes have no significant difference in the absence of AopdeL. In addition, deletion of AopdeH and AopdeL resulted in a remarkable increase in cAMP level during vegetative growth and trap formation, and the number of autophagosomes was decreased in ΔAopdeH and ΔAopdeL mutants, whereas their volumes considerably increased. Moreover, metabolomic analyses revealed that many metabolites were downregulated in ΔAopdeH mutant compared to their expression in the wild-type strain. Our results indicate that AoPdeH plays a crucial role in mycelial growth, conidiation, stress response, secondary metabolism, and trap formation. In contrast, AoPdeL only plays a minor role in hyphal and conidial morphology, autophagy, and trap formation in A. oligospora. This work expands the roles of phosphodiesterases and deepens the understanding of the regulation of trap formation in nematode-trapping fungi. MDPI 2022-03-26 /pmc/articles/PMC9026129/ /pubmed/35456080 http://dx.doi.org/10.3390/pathogens11040405 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
Ma, Ni
Jiang, Ke-Xin
Bai, Na
Li, Dong-Ni
Zhang, Ke-Qin
Yang, Jin-Kui
Functional Analysis of Two Affinity cAMP Phosphodiesterases in the Nematode-Trapping Fungus Arthrobotrys oligospora
title Functional Analysis of Two Affinity cAMP Phosphodiesterases in the Nematode-Trapping Fungus Arthrobotrys oligospora
title_full Functional Analysis of Two Affinity cAMP Phosphodiesterases in the Nematode-Trapping Fungus Arthrobotrys oligospora
title_fullStr Functional Analysis of Two Affinity cAMP Phosphodiesterases in the Nematode-Trapping Fungus Arthrobotrys oligospora
title_full_unstemmed Functional Analysis of Two Affinity cAMP Phosphodiesterases in the Nematode-Trapping Fungus Arthrobotrys oligospora
title_short Functional Analysis of Two Affinity cAMP Phosphodiesterases in the Nematode-Trapping Fungus Arthrobotrys oligospora
title_sort functional analysis of two affinity camp phosphodiesterases in the nematode-trapping fungus arthrobotrys oligospora
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026129/
https://www.ncbi.nlm.nih.gov/pubmed/35456080
http://dx.doi.org/10.3390/pathogens11040405
work_keys_str_mv AT mani functionalanalysisoftwoaffinitycampphosphodiesterasesinthenematodetrappingfungusarthrobotrysoligospora
AT jiangkexin functionalanalysisoftwoaffinitycampphosphodiesterasesinthenematodetrappingfungusarthrobotrysoligospora
AT baina functionalanalysisoftwoaffinitycampphosphodiesterasesinthenematodetrappingfungusarthrobotrysoligospora
AT lidongni functionalanalysisoftwoaffinitycampphosphodiesterasesinthenematodetrappingfungusarthrobotrysoligospora
AT zhangkeqin functionalanalysisoftwoaffinitycampphosphodiesterasesinthenematodetrappingfungusarthrobotrysoligospora
AT yangjinkui functionalanalysisoftwoaffinitycampphosphodiesterasesinthenematodetrappingfungusarthrobotrysoligospora