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Tissue-specific transcriptome responses to Fusarium head blight and Fusarium root rot

Fusarium head blight (FHB) and Fusarium root rot (FRR) are important diseases of small-grain cereals caused by Fusarium species. While host response to FHB has been subject to extensive study, very little is known about response to FRR and the transcriptome responses of FHB and FRR have not been tho...

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Autores principales: Haidoulis, John Francis, Nicholson, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637937/
https://www.ncbi.nlm.nih.gov/pubmed/36352885
http://dx.doi.org/10.3389/fpls.2022.1025161
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author Haidoulis, John Francis
Nicholson, Paul
author_facet Haidoulis, John Francis
Nicholson, Paul
author_sort Haidoulis, John Francis
collection PubMed
description Fusarium head blight (FHB) and Fusarium root rot (FRR) are important diseases of small-grain cereals caused by Fusarium species. While host response to FHB has been subject to extensive study, very little is known about response to FRR and the transcriptome responses of FHB and FRR have not been thoroughly compared. Brachypodium distachyon (Bd) is an effective model for investigating host responses to both FHB and FRR. In this study the transcriptome response of Bd to F. graminearum (Fg) infection of heads and roots was investigated. An RNA-seq analysis was performed on both Bd FHB and FRR during the early infection. Additionally, an RNA-seq analysis was performed on in vitro samples of Fg for comparison with Fg gene expression in planta. Differential gene expression and gene-list enrichment analyses were used to compare FHB and FRR transcriptome responses in both Bd and Fg. Differential expression of selected genes was confirmed using RT-qPCR. Most genes associated with receptor signalling, cell-wall modification, oxidative stress metabolism, and cytokinin and auxin biosynthesis and signalling genes were generally upregulated in FHB or were downregulated in FRR. In contrast, Bd genes involved in jasmonic acid and ethylene biosynthesis and signalling, and antimicrobial production were similarly differentially expressed in both tissues in response to infection. A transcriptome analysis of predicted Fg effectors with the same infected material revealed elevated expression of core tissue-independent genes including cell-wall degradation enzymes and the gene cluster for DON production but also several tissue-dependent genes including those for aurofusarin production and cutin degradation. This evidence suggests that Fg modulates its transcriptome to different tissues of the same host.
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spelling pubmed-96379372022-11-08 Tissue-specific transcriptome responses to Fusarium head blight and Fusarium root rot Haidoulis, John Francis Nicholson, Paul Front Plant Sci Plant Science Fusarium head blight (FHB) and Fusarium root rot (FRR) are important diseases of small-grain cereals caused by Fusarium species. While host response to FHB has been subject to extensive study, very little is known about response to FRR and the transcriptome responses of FHB and FRR have not been thoroughly compared. Brachypodium distachyon (Bd) is an effective model for investigating host responses to both FHB and FRR. In this study the transcriptome response of Bd to F. graminearum (Fg) infection of heads and roots was investigated. An RNA-seq analysis was performed on both Bd FHB and FRR during the early infection. Additionally, an RNA-seq analysis was performed on in vitro samples of Fg for comparison with Fg gene expression in planta. Differential gene expression and gene-list enrichment analyses were used to compare FHB and FRR transcriptome responses in both Bd and Fg. Differential expression of selected genes was confirmed using RT-qPCR. Most genes associated with receptor signalling, cell-wall modification, oxidative stress metabolism, and cytokinin and auxin biosynthesis and signalling genes were generally upregulated in FHB or were downregulated in FRR. In contrast, Bd genes involved in jasmonic acid and ethylene biosynthesis and signalling, and antimicrobial production were similarly differentially expressed in both tissues in response to infection. A transcriptome analysis of predicted Fg effectors with the same infected material revealed elevated expression of core tissue-independent genes including cell-wall degradation enzymes and the gene cluster for DON production but also several tissue-dependent genes including those for aurofusarin production and cutin degradation. This evidence suggests that Fg modulates its transcriptome to different tissues of the same host. Frontiers Media S.A. 2022-10-24 /pmc/articles/PMC9637937/ /pubmed/36352885 http://dx.doi.org/10.3389/fpls.2022.1025161 Text en Copyright © 2022 Haidoulis and Nicholson https://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(s) 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 Plant Science
Haidoulis, John Francis
Nicholson, Paul
Tissue-specific transcriptome responses to Fusarium head blight and Fusarium root rot
title Tissue-specific transcriptome responses to Fusarium head blight and Fusarium root rot
title_full Tissue-specific transcriptome responses to Fusarium head blight and Fusarium root rot
title_fullStr Tissue-specific transcriptome responses to Fusarium head blight and Fusarium root rot
title_full_unstemmed Tissue-specific transcriptome responses to Fusarium head blight and Fusarium root rot
title_short Tissue-specific transcriptome responses to Fusarium head blight and Fusarium root rot
title_sort tissue-specific transcriptome responses to fusarium head blight and fusarium root rot
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637937/
https://www.ncbi.nlm.nih.gov/pubmed/36352885
http://dx.doi.org/10.3389/fpls.2022.1025161
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