Cargando…

Genome‐wide gene expression dynamics of the fungal pathogen Dothistroma septosporum throughout its infection cycle of the gymnosperm host Pinus radiata

We present genome‐wide gene expression patterns as a time series through the infection cycle of the fungal pine needle blight pathogen, Dothistroma septosporum, as it invades its gymnosperm host, Pinus radiata. We determined the molecular changes at three stages of the disease cycle: epiphytic/biotr...

Descripción completa

Detalles Bibliográficos
Autores principales: Bradshaw, Rosie E., Guo, Yanan, Sim, Andre D., Kabir, M. Shahjahan, Chettri, Pranav, Ozturk, Ibrahim K., Hunziker, Lukas, Ganley, Rebecca J., Cox, Murray P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746707/
https://www.ncbi.nlm.nih.gov/pubmed/25919703
http://dx.doi.org/10.1111/mpp.12273
_version_ 1782414853863899136
author Bradshaw, Rosie E.
Guo, Yanan
Sim, Andre D.
Kabir, M. Shahjahan
Chettri, Pranav
Ozturk, Ibrahim K.
Hunziker, Lukas
Ganley, Rebecca J.
Cox, Murray P.
author_facet Bradshaw, Rosie E.
Guo, Yanan
Sim, Andre D.
Kabir, M. Shahjahan
Chettri, Pranav
Ozturk, Ibrahim K.
Hunziker, Lukas
Ganley, Rebecca J.
Cox, Murray P.
author_sort Bradshaw, Rosie E.
collection PubMed
description We present genome‐wide gene expression patterns as a time series through the infection cycle of the fungal pine needle blight pathogen, Dothistroma septosporum, as it invades its gymnosperm host, Pinus radiata. We determined the molecular changes at three stages of the disease cycle: epiphytic/biotrophic (early), initial necrosis (mid) and mature sporulating lesion (late). Over 1.7 billion combined plant and fungal reads were sequenced to obtain 3.2 million fungal‐specific reads, which comprised as little as 0.1% of the sample reads early in infection. This enriched dataset shows that the initial biotrophic stage is characterized by the up‐regulation of genes encoding fungal cell wall‐modifying enzymes and signalling proteins. Later necrotrophic stages show the up‐regulation of genes for secondary metabolism, putative effectors, oxidoreductases, transporters and starch degradation. This in‐depth through‐time transcriptomic study provides our first snapshot of the gene expression dynamics that characterize infection by this fungal pathogen in its gymnosperm host.
format Online
Article
Text
id pubmed-4746707
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-47467072016-02-26 Genome‐wide gene expression dynamics of the fungal pathogen Dothistroma septosporum throughout its infection cycle of the gymnosperm host Pinus radiata Bradshaw, Rosie E. Guo, Yanan Sim, Andre D. Kabir, M. Shahjahan Chettri, Pranav Ozturk, Ibrahim K. Hunziker, Lukas Ganley, Rebecca J. Cox, Murray P. Mol Plant Pathol Original Articles We present genome‐wide gene expression patterns as a time series through the infection cycle of the fungal pine needle blight pathogen, Dothistroma septosporum, as it invades its gymnosperm host, Pinus radiata. We determined the molecular changes at three stages of the disease cycle: epiphytic/biotrophic (early), initial necrosis (mid) and mature sporulating lesion (late). Over 1.7 billion combined plant and fungal reads were sequenced to obtain 3.2 million fungal‐specific reads, which comprised as little as 0.1% of the sample reads early in infection. This enriched dataset shows that the initial biotrophic stage is characterized by the up‐regulation of genes encoding fungal cell wall‐modifying enzymes and signalling proteins. Later necrotrophic stages show the up‐regulation of genes for secondary metabolism, putative effectors, oxidoreductases, transporters and starch degradation. This in‐depth through‐time transcriptomic study provides our first snapshot of the gene expression dynamics that characterize infection by this fungal pathogen in its gymnosperm host. John Wiley and Sons Inc. 2015-06-02 /pmc/articles/PMC4746707/ /pubmed/25919703 http://dx.doi.org/10.1111/mpp.12273 Text en © 2015 THE AUTHORS. MOLECULAR PLANT PATHOLOGY PUBLISHED BY BRITISH SOCIETY FOR PLANT PATHOLOGY AND JOHN WILEY & SONS LTD. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Bradshaw, Rosie E.
Guo, Yanan
Sim, Andre D.
Kabir, M. Shahjahan
Chettri, Pranav
Ozturk, Ibrahim K.
Hunziker, Lukas
Ganley, Rebecca J.
Cox, Murray P.
Genome‐wide gene expression dynamics of the fungal pathogen Dothistroma septosporum throughout its infection cycle of the gymnosperm host Pinus radiata
title Genome‐wide gene expression dynamics of the fungal pathogen Dothistroma septosporum throughout its infection cycle of the gymnosperm host Pinus radiata
title_full Genome‐wide gene expression dynamics of the fungal pathogen Dothistroma septosporum throughout its infection cycle of the gymnosperm host Pinus radiata
title_fullStr Genome‐wide gene expression dynamics of the fungal pathogen Dothistroma septosporum throughout its infection cycle of the gymnosperm host Pinus radiata
title_full_unstemmed Genome‐wide gene expression dynamics of the fungal pathogen Dothistroma septosporum throughout its infection cycle of the gymnosperm host Pinus radiata
title_short Genome‐wide gene expression dynamics of the fungal pathogen Dothistroma septosporum throughout its infection cycle of the gymnosperm host Pinus radiata
title_sort genome‐wide gene expression dynamics of the fungal pathogen dothistroma septosporum throughout its infection cycle of the gymnosperm host pinus radiata
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746707/
https://www.ncbi.nlm.nih.gov/pubmed/25919703
http://dx.doi.org/10.1111/mpp.12273
work_keys_str_mv AT bradshawrosiee genomewidegeneexpressiondynamicsofthefungalpathogendothistromaseptosporumthroughoutitsinfectioncycleofthegymnospermhostpinusradiata
AT guoyanan genomewidegeneexpressiondynamicsofthefungalpathogendothistromaseptosporumthroughoutitsinfectioncycleofthegymnospermhostpinusradiata
AT simandred genomewidegeneexpressiondynamicsofthefungalpathogendothistromaseptosporumthroughoutitsinfectioncycleofthegymnospermhostpinusradiata
AT kabirmshahjahan genomewidegeneexpressiondynamicsofthefungalpathogendothistromaseptosporumthroughoutitsinfectioncycleofthegymnospermhostpinusradiata
AT chettripranav genomewidegeneexpressiondynamicsofthefungalpathogendothistromaseptosporumthroughoutitsinfectioncycleofthegymnospermhostpinusradiata
AT ozturkibrahimk genomewidegeneexpressiondynamicsofthefungalpathogendothistromaseptosporumthroughoutitsinfectioncycleofthegymnospermhostpinusradiata
AT hunzikerlukas genomewidegeneexpressiondynamicsofthefungalpathogendothistromaseptosporumthroughoutitsinfectioncycleofthegymnospermhostpinusradiata
AT ganleyrebeccaj genomewidegeneexpressiondynamicsofthefungalpathogendothistromaseptosporumthroughoutitsinfectioncycleofthegymnospermhostpinusradiata
AT coxmurrayp genomewidegeneexpressiondynamicsofthefungalpathogendothistromaseptosporumthroughoutitsinfectioncycleofthegymnospermhostpinusradiata