Revealing Differentially Expressed Genes and Identifying Effector Proteins of <named-content content-type="genus-species">Puccinia striiformis</named-content> f. sp. <italic toggle="yes">tritici</italic> in Response to High-Temperature Seedling Plant Resistance of Wheat Based on Transcriptome Sequencing

ABSTRACT Stripe rust, caused by Puccinia striiformis f. sp. tritici (Pst), is one of the most important diseases of wheat (Triticum aestivum L.) globally. Recently, more aggressive Pst races have evolved to acquire new virulence profiles and are adapted better to high temperature than most of the pr...

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Autores principales: Fei Tao, Yangshan Hu, Chang Su, Juan Li, Lili Guo, Xiangming Xu, Xianming Chen, Hongsheng Shang, Xiaoping Hu
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Publicado: American Society for Microbiology 2020
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spelling oai:doaj.org-article:847f4bc434614602b7a1a718e6a40d882021-11-15T15:30:15ZRevealing Differentially Expressed Genes and Identifying Effector Proteins of <named-content content-type="genus-species">Puccinia striiformis</named-content> f. sp. <italic toggle="yes">tritici</italic> in Response to High-Temperature Seedling Plant Resistance of Wheat Based on Transcriptome Sequencing10.1128/mSphere.00096-202379-5042https://doaj.org/article/847f4bc434614602b7a1a718e6a40d882020-06-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSphere.00096-20https://doaj.org/toc/2379-5042ABSTRACT Stripe rust, caused by Puccinia striiformis f. sp. tritici (Pst), is one of the most important diseases of wheat (Triticum aestivum L.) globally. Recently, more aggressive Pst races have evolved to acquire new virulence profiles and are adapted better to high temperature than most of the previous races. Breeding cultivars with durable high-temperature seedling-plant (HTSP) resistance is an important strategy for controlling stripe rust. Understanding the mechanism of wheat HTSP resistance against Pst is important for more efficient breeding to improve host resistance. In the present study, transcriptomic analysis identified 25 Pst differentially expressed genes (DEGs) that were involved in the HTSP resistance in wheat cultivar Xiaoyan6 (XY6). Functional annotation indicated that these DEGs are related to membrane proteins, mRNA binding proteins, cell membrane transporters, and synthesis of cell nitrogen compounds. Among these DEGs, a candidate effector, PstCEP1 (PSTG_13342), was identified and cloned, and its function was verified. Barley stripe mosaic virus (BSMV)-mediated host-induced gene silencing (HIGS) of PstCEP1 reduced Pst virulence. Signal peptide verification and functional testing in Nicotiana benthamiana indicated that PstCEP1 is a secreted protein and has the function of suppressing programmed cell death (PCD). PstCEP1 as a candidate effector was further supported by type three secretion system (TTSS)-mediated overexpression responding to wheat HTSP resistance via affecting the pathogen-associated molecular pattern (PAMP)-triggered immunity (PTI) and effector-triggered immunity (ETI). IMPORTANCE In the present study, we performed transcriptomic analysis to identify differentially expressed genes and effector proteins of Puccinia striiformis f. sp. tritici (Pst) in response to the high-temperature seedling-plant (HTSP) resistance in wheat. Experimental validation confirmed the function of the highest upregulated effector protein, PstCEP1. This study provides a key resource for understanding the biology and molecular basis of Pst responses to wheat HTSP resistance, and PstCEP1 may be used in future studies to understand pathogen-associated molecular pattern-triggered immunity and effector-triggered immunity processes in the Pst-wheat interaction system.Fei TaoYangshan HuChang SuJuan LiLili GuoXiangming XuXianming ChenHongsheng ShangXiaoping HuAmerican Society for MicrobiologyarticlePuccinia striiformis f. sp. triticiwheat (Triticum aestivum L.)high-temperature seedling-plant (HTSP) resistancetranscript profilingfungal effector proteinMicrobiologyQR1-502ENmSphere, Vol 5, Iss 3 (2020)
institution DOAJ
collection DOAJ
language EN
topic Puccinia striiformis f. sp. tritici
wheat (Triticum aestivum L.)
high-temperature seedling-plant (HTSP) resistance
transcript profiling
fungal effector protein
Microbiology
QR1-502
spellingShingle Puccinia striiformis f. sp. tritici
wheat (Triticum aestivum L.)
high-temperature seedling-plant (HTSP) resistance
transcript profiling
fungal effector protein
Microbiology
QR1-502
Fei Tao
Yangshan Hu
Chang Su
Juan Li
Lili Guo
Xiangming Xu
Xianming Chen
Hongsheng Shang
Xiaoping Hu
Revealing Differentially Expressed Genes and Identifying Effector Proteins of <named-content content-type="genus-species">Puccinia striiformis</named-content> f. sp. <italic toggle="yes">tritici</italic> in Response to High-Temperature Seedling Plant Resistance of Wheat Based on Transcriptome Sequencing
description ABSTRACT Stripe rust, caused by Puccinia striiformis f. sp. tritici (Pst), is one of the most important diseases of wheat (Triticum aestivum L.) globally. Recently, more aggressive Pst races have evolved to acquire new virulence profiles and are adapted better to high temperature than most of the previous races. Breeding cultivars with durable high-temperature seedling-plant (HTSP) resistance is an important strategy for controlling stripe rust. Understanding the mechanism of wheat HTSP resistance against Pst is important for more efficient breeding to improve host resistance. In the present study, transcriptomic analysis identified 25 Pst differentially expressed genes (DEGs) that were involved in the HTSP resistance in wheat cultivar Xiaoyan6 (XY6). Functional annotation indicated that these DEGs are related to membrane proteins, mRNA binding proteins, cell membrane transporters, and synthesis of cell nitrogen compounds. Among these DEGs, a candidate effector, PstCEP1 (PSTG_13342), was identified and cloned, and its function was verified. Barley stripe mosaic virus (BSMV)-mediated host-induced gene silencing (HIGS) of PstCEP1 reduced Pst virulence. Signal peptide verification and functional testing in Nicotiana benthamiana indicated that PstCEP1 is a secreted protein and has the function of suppressing programmed cell death (PCD). PstCEP1 as a candidate effector was further supported by type three secretion system (TTSS)-mediated overexpression responding to wheat HTSP resistance via affecting the pathogen-associated molecular pattern (PAMP)-triggered immunity (PTI) and effector-triggered immunity (ETI). IMPORTANCE In the present study, we performed transcriptomic analysis to identify differentially expressed genes and effector proteins of Puccinia striiformis f. sp. tritici (Pst) in response to the high-temperature seedling-plant (HTSP) resistance in wheat. Experimental validation confirmed the function of the highest upregulated effector protein, PstCEP1. This study provides a key resource for understanding the biology and molecular basis of Pst responses to wheat HTSP resistance, and PstCEP1 may be used in future studies to understand pathogen-associated molecular pattern-triggered immunity and effector-triggered immunity processes in the Pst-wheat interaction system.
format article
author Fei Tao
Yangshan Hu
Chang Su
Juan Li
Lili Guo
Xiangming Xu
Xianming Chen
Hongsheng Shang
Xiaoping Hu
author_facet Fei Tao
Yangshan Hu
Chang Su
Juan Li
Lili Guo
Xiangming Xu
Xianming Chen
Hongsheng Shang
Xiaoping Hu
author_sort Fei Tao
title Revealing Differentially Expressed Genes and Identifying Effector Proteins of <named-content content-type="genus-species">Puccinia striiformis</named-content> f. sp. <italic toggle="yes">tritici</italic> in Response to High-Temperature Seedling Plant Resistance of Wheat Based on Transcriptome Sequencing
title_short Revealing Differentially Expressed Genes and Identifying Effector Proteins of <named-content content-type="genus-species">Puccinia striiformis</named-content> f. sp. <italic toggle="yes">tritici</italic> in Response to High-Temperature Seedling Plant Resistance of Wheat Based on Transcriptome Sequencing
title_full Revealing Differentially Expressed Genes and Identifying Effector Proteins of <named-content content-type="genus-species">Puccinia striiformis</named-content> f. sp. <italic toggle="yes">tritici</italic> in Response to High-Temperature Seedling Plant Resistance of Wheat Based on Transcriptome Sequencing
title_fullStr Revealing Differentially Expressed Genes and Identifying Effector Proteins of <named-content content-type="genus-species">Puccinia striiformis</named-content> f. sp. <italic toggle="yes">tritici</italic> in Response to High-Temperature Seedling Plant Resistance of Wheat Based on Transcriptome Sequencing
title_full_unstemmed Revealing Differentially Expressed Genes and Identifying Effector Proteins of <named-content content-type="genus-species">Puccinia striiformis</named-content> f. sp. <italic toggle="yes">tritici</italic> in Response to High-Temperature Seedling Plant Resistance of Wheat Based on Transcriptome Sequencing
title_sort revealing differentially expressed genes and identifying effector proteins of <named-content content-type="genus-species">puccinia striiformis</named-content> f. sp. <italic toggle="yes">tritici</italic> in response to high-temperature seedling plant resistance of wheat based on transcriptome sequencing
publisher American Society for Microbiology
publishDate 2020
url https://doaj.org/article/847f4bc434614602b7a1a718e6a40d88
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