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Neofusicoccum parvum Colonization of the Grapevine Woody Stem Triggers Asynchronous Host Responses at the Site of Infection and in the Leaves

Grapevine trunk diseases cause important economic losses in vineyards worldwide. Neofusicoccum parvum, one of the most aggressive causal agents of the trunk disease Botryosphaeria dieback, colonizes cells and tissues of the grapevine wood, leading to the formation of an internal canker. Symptoms the...

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Autores principales: Massonnet, Mélanie, Figueroa-Balderas, Rosa, Galarneau, Erin R. A., Miki, Shiho, Lawrence, Daniel P., Sun, Qiang, Wallis, Christopher M., Baumgartner, Kendra, Cantu, Dario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487829/
https://www.ncbi.nlm.nih.gov/pubmed/28702038
http://dx.doi.org/10.3389/fpls.2017.01117
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author Massonnet, Mélanie
Figueroa-Balderas, Rosa
Galarneau, Erin R. A.
Miki, Shiho
Lawrence, Daniel P.
Sun, Qiang
Wallis, Christopher M.
Baumgartner, Kendra
Cantu, Dario
author_facet Massonnet, Mélanie
Figueroa-Balderas, Rosa
Galarneau, Erin R. A.
Miki, Shiho
Lawrence, Daniel P.
Sun, Qiang
Wallis, Christopher M.
Baumgartner, Kendra
Cantu, Dario
author_sort Massonnet, Mélanie
collection PubMed
description Grapevine trunk diseases cause important economic losses in vineyards worldwide. Neofusicoccum parvum, one of the most aggressive causal agents of the trunk disease Botryosphaeria dieback, colonizes cells and tissues of the grapevine wood, leading to the formation of an internal canker. Symptoms then extend to distal shoots, with wilting of leaves and bud mortality. Our aim was to characterize the transcriptional dynamics of grapevine genes in the woody stem and in the leaves during Neofusicoccum parvum colonization. Genome-wide transcriptional profiling at seven distinct time points (0, 3, and 24 hours; 2, 6, 8, and 12 weeks) showed that both stems and leaves undergo extensive transcriptomic reprogramming in response to infection of the stem. While most intense transcriptional responses were detected in the stems at 24 hours, strong responses were not detected in the leaves until the next sampling point at 2 weeks post-inoculation. Network co-expression analysis identified modules of co-expressed genes common to both organs and showed most of these genes were asynchronously modulated. The temporal shift between stem vs. leaf responses affected transcriptional modulation of genes involved in both signal perception and transduction, as well as downstream biological processes, including oxidative stress, cell wall rearrangement and cell death. Promoter analysis of the genes asynchronously modulated in stem and leaves during N. parvum colonization suggests that the temporal shift of transcriptional reprogramming between the two organs might be due to asynchronous co-regulation by common transcriptional regulators. Topology analysis of stem and leaf co-expression networks pointed to specific transcription factor-encoding genes, including WRKY and MYB, which may be associated with the observed transcriptional responses in the two organs.
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spelling pubmed-54878292017-07-12 Neofusicoccum parvum Colonization of the Grapevine Woody Stem Triggers Asynchronous Host Responses at the Site of Infection and in the Leaves Massonnet, Mélanie Figueroa-Balderas, Rosa Galarneau, Erin R. A. Miki, Shiho Lawrence, Daniel P. Sun, Qiang Wallis, Christopher M. Baumgartner, Kendra Cantu, Dario Front Plant Sci Plant Science Grapevine trunk diseases cause important economic losses in vineyards worldwide. Neofusicoccum parvum, one of the most aggressive causal agents of the trunk disease Botryosphaeria dieback, colonizes cells and tissues of the grapevine wood, leading to the formation of an internal canker. Symptoms then extend to distal shoots, with wilting of leaves and bud mortality. Our aim was to characterize the transcriptional dynamics of grapevine genes in the woody stem and in the leaves during Neofusicoccum parvum colonization. Genome-wide transcriptional profiling at seven distinct time points (0, 3, and 24 hours; 2, 6, 8, and 12 weeks) showed that both stems and leaves undergo extensive transcriptomic reprogramming in response to infection of the stem. While most intense transcriptional responses were detected in the stems at 24 hours, strong responses were not detected in the leaves until the next sampling point at 2 weeks post-inoculation. Network co-expression analysis identified modules of co-expressed genes common to both organs and showed most of these genes were asynchronously modulated. The temporal shift between stem vs. leaf responses affected transcriptional modulation of genes involved in both signal perception and transduction, as well as downstream biological processes, including oxidative stress, cell wall rearrangement and cell death. Promoter analysis of the genes asynchronously modulated in stem and leaves during N. parvum colonization suggests that the temporal shift of transcriptional reprogramming between the two organs might be due to asynchronous co-regulation by common transcriptional regulators. Topology analysis of stem and leaf co-expression networks pointed to specific transcription factor-encoding genes, including WRKY and MYB, which may be associated with the observed transcriptional responses in the two organs. Frontiers Media S.A. 2017-06-28 /pmc/articles/PMC5487829/ /pubmed/28702038 http://dx.doi.org/10.3389/fpls.2017.01117 Text en Copyright © 2017 Massonnet, Figueroa-Balderas, Galarneau, Miki, Lawrence, Sun, Wallis, Baumgartner and Cantu. http://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) or licensor 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
Massonnet, Mélanie
Figueroa-Balderas, Rosa
Galarneau, Erin R. A.
Miki, Shiho
Lawrence, Daniel P.
Sun, Qiang
Wallis, Christopher M.
Baumgartner, Kendra
Cantu, Dario
Neofusicoccum parvum Colonization of the Grapevine Woody Stem Triggers Asynchronous Host Responses at the Site of Infection and in the Leaves
title Neofusicoccum parvum Colonization of the Grapevine Woody Stem Triggers Asynchronous Host Responses at the Site of Infection and in the Leaves
title_full Neofusicoccum parvum Colonization of the Grapevine Woody Stem Triggers Asynchronous Host Responses at the Site of Infection and in the Leaves
title_fullStr Neofusicoccum parvum Colonization of the Grapevine Woody Stem Triggers Asynchronous Host Responses at the Site of Infection and in the Leaves
title_full_unstemmed Neofusicoccum parvum Colonization of the Grapevine Woody Stem Triggers Asynchronous Host Responses at the Site of Infection and in the Leaves
title_short Neofusicoccum parvum Colonization of the Grapevine Woody Stem Triggers Asynchronous Host Responses at the Site of Infection and in the Leaves
title_sort neofusicoccum parvum colonization of the grapevine woody stem triggers asynchronous host responses at the site of infection and in the leaves
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487829/
https://www.ncbi.nlm.nih.gov/pubmed/28702038
http://dx.doi.org/10.3389/fpls.2017.01117
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