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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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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AT chantalemccabe newtoolsforcharacterizingearlybrownstemrotdiseaseresistancesignalinginsoybean AT michelleagraham newtoolsforcharacterizingearlybrownstemrotdiseaseresistancesignalinginsoybean |
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