New tools for characterizing early brown stem rot disease resistance signaling in soybean

Abstract Brown stem rot (BSR) reduces soybean [Glycine max (L.) Merr.] yield by up to 38%. The BSR causal agent is Phialophora gregata f. sp. sojae, a slow‐growing, necrotrophic fungus whose life cycle includes latent and pathogenic phases, each lasting several weeks. Brown stem rot foliar symptoms...

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Main Authors: Chantal E. McCabe, Michelle A. Graham
Format: Article
Language:English
Published: Wiley 2020-11-01
Series:The Plant Genome
Online Access:https://doi.org/10.1002/tpg2.20037
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spelling doaj-55daf0e69b9d479da801b08d67662a0a2020-11-25T04:11:20ZengWileyThe Plant Genome1940-33722020-11-01133n/an/a10.1002/tpg2.20037New tools for characterizing early brown stem rot disease resistance signaling in soybeanChantal E. McCabe0Michelle A. Graham1USDA–ARS Corn Insects and Crop Genetics Research Unit Ames IA 50011‐1010 USAUSDA–ARS Corn Insects and Crop Genetics Research Unit Ames IA 50011‐1010 USAAbstract Brown stem rot (BSR) reduces soybean [Glycine max (L.) Merr.] yield by up to 38%. The BSR causal agent is Phialophora gregata f. sp. sojae, a slow‐growing, necrotrophic fungus whose life cycle includes latent and pathogenic phases, each lasting several weeks. Brown stem rot foliar symptoms are often misdiagnosed as other soybean diseases or nutrient stress, making BSR resistance especially difficult to phenotype. To shed light on the genes and networks contributing to P. gregata resistance, we conducted RNA sequencing (RNA‐seq) of a resistant genotype (PI 437970, Rbs3). Leaf, stem, and root tissues were collected 12, 24, and 36 h after stab inoculation with P. gregata, or mock infection, in the plant stem. By using multiple tissues and time points, we could see that leaves, stems, and roots use the same defense pathways. Our analyses suggest that P. gregata induces a biphasic defense response, with pathogen‐associated molecular pattern (PAMP) triggered immunity observed in leaves at 12 and 24 h after infection (HAI) and effector triggered immunity detected at 36 h after infection in the stems. Gene networks associated with defense, photosynthesis, nutrient homeostasis, DNA replication, and growth are the hallmarks of resistance to P. gregata. While P. gregata is a slow‐growing pathogen, our results demonstrate that pathogen recognition occurs hours after infection. By exploiting the genes and networks described here, we will be able to develop novel diagnostic tools to facilitate breeding and screening for BSR resistance.https://doi.org/10.1002/tpg2.20037
collection DOAJ
language English
format Article
sources DOAJ
author Chantal E. McCabe
Michelle A. Graham
spellingShingle Chantal E. McCabe
Michelle A. Graham
New tools for characterizing early brown stem rot disease resistance signaling in soybean
The Plant Genome
author_facet Chantal E. McCabe
Michelle A. Graham
author_sort Chantal E. McCabe
title New tools for characterizing early brown stem rot disease resistance signaling in soybean
title_short New tools for characterizing early brown stem rot disease resistance signaling in soybean
title_full New tools for characterizing early brown stem rot disease resistance signaling in soybean
title_fullStr New tools for characterizing early brown stem rot disease resistance signaling in soybean
title_full_unstemmed New tools for characterizing early brown stem rot disease resistance signaling in soybean
title_sort new tools for characterizing early brown stem rot disease resistance signaling in soybean
publisher Wiley
series The Plant Genome
issn 1940-3372
publishDate 2020-11-01
description Abstract Brown stem rot (BSR) reduces soybean [Glycine max (L.) Merr.] yield by up to 38%. The BSR causal agent is Phialophora gregata f. sp. sojae, a slow‐growing, necrotrophic fungus whose life cycle includes latent and pathogenic phases, each lasting several weeks. Brown stem rot foliar symptoms are often misdiagnosed as other soybean diseases or nutrient stress, making BSR resistance especially difficult to phenotype. To shed light on the genes and networks contributing to P. gregata resistance, we conducted RNA sequencing (RNA‐seq) of a resistant genotype (PI 437970, Rbs3). Leaf, stem, and root tissues were collected 12, 24, and 36 h after stab inoculation with P. gregata, or mock infection, in the plant stem. By using multiple tissues and time points, we could see that leaves, stems, and roots use the same defense pathways. Our analyses suggest that P. gregata induces a biphasic defense response, with pathogen‐associated molecular pattern (PAMP) triggered immunity observed in leaves at 12 and 24 h after infection (HAI) and effector triggered immunity detected at 36 h after infection in the stems. Gene networks associated with defense, photosynthesis, nutrient homeostasis, DNA replication, and growth are the hallmarks of resistance to P. gregata. While P. gregata is a slow‐growing pathogen, our results demonstrate that pathogen recognition occurs hours after infection. By exploiting the genes and networks described here, we will be able to develop novel diagnostic tools to facilitate breeding and screening for BSR resistance.
url https://doi.org/10.1002/tpg2.20037
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