Cargando…

Comparative RNAseq Analysis of the Insect-Pathogenic Fungus Metarhizium anisopliae Reveals Specific Transcriptome Signatures of Filamentous and Yeast-Like Development

The fungus Metarhizium anisopliae is a facultative insect pathogen used as biological control agent of several agricultural pests worldwide. It is a dimorphic fungus that is able to display two growth morphologies, a filamentous phase with formation of hyphae and a yeast-like phase with formation of...

Descripción completa

Detalles Bibliográficos
Autores principales: Iwanicki, Natasha Sant’Anna, Júnior, Italo Delalibera, Eilenberg, Jørgen, De Fine Licht, Henrik H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341153/
https://www.ncbi.nlm.nih.gov/pubmed/32354703
http://dx.doi.org/10.1534/g3.120.401040
_version_ 1783555174581665792
author Iwanicki, Natasha Sant’Anna
Júnior, Italo Delalibera
Eilenberg, Jørgen
De Fine Licht, Henrik H.
author_facet Iwanicki, Natasha Sant’Anna
Júnior, Italo Delalibera
Eilenberg, Jørgen
De Fine Licht, Henrik H.
author_sort Iwanicki, Natasha Sant’Anna
collection PubMed
description The fungus Metarhizium anisopliae is a facultative insect pathogen used as biological control agent of several agricultural pests worldwide. It is a dimorphic fungus that is able to display two growth morphologies, a filamentous phase with formation of hyphae and a yeast-like phase with formation of single-celled blastospores. Blastospores play an important role for M. anisopliae pathogenicity during disease development. They are formed solely in the hemolymph of infected insects as a fungal strategy to quickly multiply and colonize the insect’s body. Here, we use comparative genome-wide transcriptome analyses to determine changes in gene expression between the filamentous and blastospore growth phases in vitro to characterize physiological changes and metabolic signatures associated with M. anisopliae dimorphism. Our results show a clear molecular distinction between the blastospore and mycelial phases. In total 6.4% (n = 696) out of 10,981 predicted genes in M. anisopliae were differentially expressed between the two phases with a fold-change > 4. The main physiological processes associated with up-regulated gene content in the single-celled yeast-like blastospores during liquid fermentation were oxidative stress, amino acid metabolism (catabolism and anabolism), respiration processes, transmembrane transport and production of secondary metabolites. In contrast, the up-regulated gene content in hyphae were associated with increased growth, metabolism and cell wall re-organization, which underlines the specific functions and altered growth morphology of M. anisopliae blastospores and hyphae, respectively. Our study revealed significant transcriptomic differences between the metabolism of blastospores and hyphae. These findings illustrate important aspects of fungal morphogenesis in M. anisopliae and highlight the main metabolic activities of each propagule under in vitro growth conditions.
format Online
Article
Text
id pubmed-7341153
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Genetics Society of America
record_format MEDLINE/PubMed
spelling pubmed-73411532020-07-21 Comparative RNAseq Analysis of the Insect-Pathogenic Fungus Metarhizium anisopliae Reveals Specific Transcriptome Signatures of Filamentous and Yeast-Like Development Iwanicki, Natasha Sant’Anna Júnior, Italo Delalibera Eilenberg, Jørgen De Fine Licht, Henrik H. G3 (Bethesda) Genome Report The fungus Metarhizium anisopliae is a facultative insect pathogen used as biological control agent of several agricultural pests worldwide. It is a dimorphic fungus that is able to display two growth morphologies, a filamentous phase with formation of hyphae and a yeast-like phase with formation of single-celled blastospores. Blastospores play an important role for M. anisopliae pathogenicity during disease development. They are formed solely in the hemolymph of infected insects as a fungal strategy to quickly multiply and colonize the insect’s body. Here, we use comparative genome-wide transcriptome analyses to determine changes in gene expression between the filamentous and blastospore growth phases in vitro to characterize physiological changes and metabolic signatures associated with M. anisopliae dimorphism. Our results show a clear molecular distinction between the blastospore and mycelial phases. In total 6.4% (n = 696) out of 10,981 predicted genes in M. anisopliae were differentially expressed between the two phases with a fold-change > 4. The main physiological processes associated with up-regulated gene content in the single-celled yeast-like blastospores during liquid fermentation were oxidative stress, amino acid metabolism (catabolism and anabolism), respiration processes, transmembrane transport and production of secondary metabolites. In contrast, the up-regulated gene content in hyphae were associated with increased growth, metabolism and cell wall re-organization, which underlines the specific functions and altered growth morphology of M. anisopliae blastospores and hyphae, respectively. Our study revealed significant transcriptomic differences between the metabolism of blastospores and hyphae. These findings illustrate important aspects of fungal morphogenesis in M. anisopliae and highlight the main metabolic activities of each propagule under in vitro growth conditions. Genetics Society of America 2020-04-28 /pmc/articles/PMC7341153/ /pubmed/32354703 http://dx.doi.org/10.1534/g3.120.401040 Text en Copyright © 2020 Iwanicki et al. http://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 (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genome Report
Iwanicki, Natasha Sant’Anna
Júnior, Italo Delalibera
Eilenberg, Jørgen
De Fine Licht, Henrik H.
Comparative RNAseq Analysis of the Insect-Pathogenic Fungus Metarhizium anisopliae Reveals Specific Transcriptome Signatures of Filamentous and Yeast-Like Development
title Comparative RNAseq Analysis of the Insect-Pathogenic Fungus Metarhizium anisopliae Reveals Specific Transcriptome Signatures of Filamentous and Yeast-Like Development
title_full Comparative RNAseq Analysis of the Insect-Pathogenic Fungus Metarhizium anisopliae Reveals Specific Transcriptome Signatures of Filamentous and Yeast-Like Development
title_fullStr Comparative RNAseq Analysis of the Insect-Pathogenic Fungus Metarhizium anisopliae Reveals Specific Transcriptome Signatures of Filamentous and Yeast-Like Development
title_full_unstemmed Comparative RNAseq Analysis of the Insect-Pathogenic Fungus Metarhizium anisopliae Reveals Specific Transcriptome Signatures of Filamentous and Yeast-Like Development
title_short Comparative RNAseq Analysis of the Insect-Pathogenic Fungus Metarhizium anisopliae Reveals Specific Transcriptome Signatures of Filamentous and Yeast-Like Development
title_sort comparative rnaseq analysis of the insect-pathogenic fungus metarhizium anisopliae reveals specific transcriptome signatures of filamentous and yeast-like development
topic Genome Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341153/
https://www.ncbi.nlm.nih.gov/pubmed/32354703
http://dx.doi.org/10.1534/g3.120.401040
work_keys_str_mv AT iwanickinatashasantanna comparativernaseqanalysisoftheinsectpathogenicfungusmetarhiziumanisopliaerevealsspecifictranscriptomesignaturesoffilamentousandyeastlikedevelopment
AT junioritalodelalibera comparativernaseqanalysisoftheinsectpathogenicfungusmetarhiziumanisopliaerevealsspecifictranscriptomesignaturesoffilamentousandyeastlikedevelopment
AT eilenbergjørgen comparativernaseqanalysisoftheinsectpathogenicfungusmetarhiziumanisopliaerevealsspecifictranscriptomesignaturesoffilamentousandyeastlikedevelopment
AT definelichthenrikh comparativernaseqanalysisoftheinsectpathogenicfungusmetarhiziumanisopliaerevealsspecifictranscriptomesignaturesoffilamentousandyeastlikedevelopment