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Clavibacter michiganensis Downregulates Photosynthesis and Modifies Monolignols Metabolism Revealing a Crosstalk with Tomato Immune Responses

The gram-positive pathogenic bacterium Clavibacter michiganensis subsp. michiganensis (Cmm) causes bacterial canker disease in tomato, affecting crop yield and fruit quality. To understand how tomato plants respond, the dynamic expression profile of host genes was analyzed upon Cmm infection. Sympto...

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Autores principales: Tsitsekian, Dikran, Daras, Gerasimos, Karamanou, Konstantina, Templalexis, Dimitris, Koudounas, Konstantinos, Malliarakis, Dimitris, Koufakis, Theologos, Chatzopoulos, Dimitris, Goumas, Dimitris, Ntoukakis, Vardis, Hatzopoulos, Polydefkis, Rigas, Stamatis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8395114/
https://www.ncbi.nlm.nih.gov/pubmed/34445148
http://dx.doi.org/10.3390/ijms22168442
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author Tsitsekian, Dikran
Daras, Gerasimos
Karamanou, Konstantina
Templalexis, Dimitris
Koudounas, Konstantinos
Malliarakis, Dimitris
Koufakis, Theologos
Chatzopoulos, Dimitris
Goumas, Dimitris
Ntoukakis, Vardis
Hatzopoulos, Polydefkis
Rigas, Stamatis
author_facet Tsitsekian, Dikran
Daras, Gerasimos
Karamanou, Konstantina
Templalexis, Dimitris
Koudounas, Konstantinos
Malliarakis, Dimitris
Koufakis, Theologos
Chatzopoulos, Dimitris
Goumas, Dimitris
Ntoukakis, Vardis
Hatzopoulos, Polydefkis
Rigas, Stamatis
author_sort Tsitsekian, Dikran
collection PubMed
description The gram-positive pathogenic bacterium Clavibacter michiganensis subsp. michiganensis (Cmm) causes bacterial canker disease in tomato, affecting crop yield and fruit quality. To understand how tomato plants respond, the dynamic expression profile of host genes was analyzed upon Cmm infection. Symptoms of bacterial canker became evident from the third day. As the disease progressed, the bacterial population increased in planta, reaching the highest level at six days and remained constant till the twelfth day post inoculation. These two time points were selected for transcriptomics. A progressive down-regulation of key genes encoding for components of the photosynthetic apparatus was observed. Two temporally separated defense responses were observed, which were to an extent interdependent. During the primary response, genes of the phenylpropanoid pathway were diverted towards the synthesis of monolignols away from S-lignin. In dicots, lignin polymers mainly consist of G- and S-units, playing an important role in defense. The twist towards G-lignin enrichment is consistent with previous findings, highlighting a response to generate an early protective barrier and to achieve a tight interplay between lignin recomposition and the primary defense response mechanism. Upon progression of Cmm infection, the temporal deactivation of phenylpropanoids coincided with the upregulation of genes that belong in a secondary response mechanism, supporting an elegant reprogramming of the host transcriptome to establish a robust defense apparatus and suppress pathogen invasion. This high-throughput analysis reveals a dynamic reorganization of plant defense mechanisms upon bacterial infection to implement an array of barriers preventing pathogen invasion and spread.
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spelling pubmed-83951142021-08-28 Clavibacter michiganensis Downregulates Photosynthesis and Modifies Monolignols Metabolism Revealing a Crosstalk with Tomato Immune Responses Tsitsekian, Dikran Daras, Gerasimos Karamanou, Konstantina Templalexis, Dimitris Koudounas, Konstantinos Malliarakis, Dimitris Koufakis, Theologos Chatzopoulos, Dimitris Goumas, Dimitris Ntoukakis, Vardis Hatzopoulos, Polydefkis Rigas, Stamatis Int J Mol Sci Article The gram-positive pathogenic bacterium Clavibacter michiganensis subsp. michiganensis (Cmm) causes bacterial canker disease in tomato, affecting crop yield and fruit quality. To understand how tomato plants respond, the dynamic expression profile of host genes was analyzed upon Cmm infection. Symptoms of bacterial canker became evident from the third day. As the disease progressed, the bacterial population increased in planta, reaching the highest level at six days and remained constant till the twelfth day post inoculation. These two time points were selected for transcriptomics. A progressive down-regulation of key genes encoding for components of the photosynthetic apparatus was observed. Two temporally separated defense responses were observed, which were to an extent interdependent. During the primary response, genes of the phenylpropanoid pathway were diverted towards the synthesis of monolignols away from S-lignin. In dicots, lignin polymers mainly consist of G- and S-units, playing an important role in defense. The twist towards G-lignin enrichment is consistent with previous findings, highlighting a response to generate an early protective barrier and to achieve a tight interplay between lignin recomposition and the primary defense response mechanism. Upon progression of Cmm infection, the temporal deactivation of phenylpropanoids coincided with the upregulation of genes that belong in a secondary response mechanism, supporting an elegant reprogramming of the host transcriptome to establish a robust defense apparatus and suppress pathogen invasion. This high-throughput analysis reveals a dynamic reorganization of plant defense mechanisms upon bacterial infection to implement an array of barriers preventing pathogen invasion and spread. MDPI 2021-08-05 /pmc/articles/PMC8395114/ /pubmed/34445148 http://dx.doi.org/10.3390/ijms22168442 Text en © 2021 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
Tsitsekian, Dikran
Daras, Gerasimos
Karamanou, Konstantina
Templalexis, Dimitris
Koudounas, Konstantinos
Malliarakis, Dimitris
Koufakis, Theologos
Chatzopoulos, Dimitris
Goumas, Dimitris
Ntoukakis, Vardis
Hatzopoulos, Polydefkis
Rigas, Stamatis
Clavibacter michiganensis Downregulates Photosynthesis and Modifies Monolignols Metabolism Revealing a Crosstalk with Tomato Immune Responses
title Clavibacter michiganensis Downregulates Photosynthesis and Modifies Monolignols Metabolism Revealing a Crosstalk with Tomato Immune Responses
title_full Clavibacter michiganensis Downregulates Photosynthesis and Modifies Monolignols Metabolism Revealing a Crosstalk with Tomato Immune Responses
title_fullStr Clavibacter michiganensis Downregulates Photosynthesis and Modifies Monolignols Metabolism Revealing a Crosstalk with Tomato Immune Responses
title_full_unstemmed Clavibacter michiganensis Downregulates Photosynthesis and Modifies Monolignols Metabolism Revealing a Crosstalk with Tomato Immune Responses
title_short Clavibacter michiganensis Downregulates Photosynthesis and Modifies Monolignols Metabolism Revealing a Crosstalk with Tomato Immune Responses
title_sort clavibacter michiganensis downregulates photosynthesis and modifies monolignols metabolism revealing a crosstalk with tomato immune responses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8395114/
https://www.ncbi.nlm.nih.gov/pubmed/34445148
http://dx.doi.org/10.3390/ijms22168442
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