Transcriptome analysis of response to Plasmodiophora brassicae infection in the Arabidopsis shoot and root
Abstract Background Clubroot is an important disease caused by the obligate parasite Plasmodiophora brassicae that infects the Brassicaceae. As a soil-borne pathogen, P. brassicae induces the generation of abnormal tissue in the root, resulting in the formation of galls. Root infection negatively af...
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doaj-6285a293b5ca47459a34b6eb0bc8c60e2020-11-24T23:39:04ZengBMCBMC Genomics1471-21642018-01-0119111910.1186/s12864-017-4426-7Transcriptome analysis of response to Plasmodiophora brassicae infection in the Arabidopsis shoot and rootSolmaz Irani0Brett Trost1Matthew Waldner2Naghabushana Nayidu3Jiangying Tu4Anthony J. Kusalik5Christopher D. Todd6Yangdou Wei7Peta C. Bonham-Smith8Department of Biology, University of SaskatchewanDepartment of Computer Science, University of SaskatchewanDepartment of Computer Science, University of SaskatchewanDepartment of Biology, University of SaskatchewanDepartment of Biology, University of SaskatchewanDepartment of Computer Science, University of SaskatchewanDepartment of Biology, University of SaskatchewanDepartment of Biology, University of SaskatchewanDepartment of Biology, University of SaskatchewanAbstract Background Clubroot is an important disease caused by the obligate parasite Plasmodiophora brassicae that infects the Brassicaceae. As a soil-borne pathogen, P. brassicae induces the generation of abnormal tissue in the root, resulting in the formation of galls. Root infection negatively affects the uptake of water and nutrients in host plants, severely reducing their growth and productivity. Many studies have emphasized the molecular and physiological effects of the clubroot disease on root tissues. The aim of the present study is to better understand the effect of P. brassicae on the transcriptome of both shoot and root tissues of Arabidopsis thaliana. Results Transcriptome profiling using RNA-seq was performed on both shoot and root tissues at 17, 20 and 24 days post inoculation (dpi) of A. thaliana, a model plant host for P. brassicae. The number of differentially expressed genes (DEGs) between infected and uninfected samples was larger in shoot than in root. In both shoot and root, more genes were differentially regulated at 24 dpi than the two earlier time points. Genes that were highly regulated in response to infection in both shoot and root primarily were involved in the metabolism of cell wall compounds, lipids, and shikimate pathway metabolites. Among hormone-related pathways, several jasmonic acid biosynthesis genes were upregulated in both shoot and root tissue. Genes encoding enzymes involved in cell wall modification, biosynthesis of sucrose and starch, and several classes of transcription factors were generally differently regulated in shoot and root. Conclusions These results highlight the similarities and differences in the transcriptomic response of above- and below-ground tissues of the model host Arabidopsis following P. brassicae infection. The main transcriptomic changes in root metabolism during clubroot disease progression were identified. An overview of DEGs in the shoot underlined the physiological changes in above-ground tissues following pathogen establishment and disease progression. This study provides insights into host tissue-specific molecular responses to clubroot development and may have applications in the development of clubroot markers for more effective breeding strategies.http://link.springer.com/article/10.1186/s12864-017-4426-7Arabidopsis thalianaClubrootHost-pathogen interactionPlasmodiophora brassicaeRNA-seqRoot |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Solmaz Irani Brett Trost Matthew Waldner Naghabushana Nayidu Jiangying Tu Anthony J. Kusalik Christopher D. Todd Yangdou Wei Peta C. Bonham-Smith |
spellingShingle |
Solmaz Irani Brett Trost Matthew Waldner Naghabushana Nayidu Jiangying Tu Anthony J. Kusalik Christopher D. Todd Yangdou Wei Peta C. Bonham-Smith Transcriptome analysis of response to Plasmodiophora brassicae infection in the Arabidopsis shoot and root BMC Genomics Arabidopsis thaliana Clubroot Host-pathogen interaction Plasmodiophora brassicae RNA-seq Root |
author_facet |
Solmaz Irani Brett Trost Matthew Waldner Naghabushana Nayidu Jiangying Tu Anthony J. Kusalik Christopher D. Todd Yangdou Wei Peta C. Bonham-Smith |
author_sort |
Solmaz Irani |
title |
Transcriptome analysis of response to Plasmodiophora brassicae infection in the Arabidopsis shoot and root |
title_short |
Transcriptome analysis of response to Plasmodiophora brassicae infection in the Arabidopsis shoot and root |
title_full |
Transcriptome analysis of response to Plasmodiophora brassicae infection in the Arabidopsis shoot and root |
title_fullStr |
Transcriptome analysis of response to Plasmodiophora brassicae infection in the Arabidopsis shoot and root |
title_full_unstemmed |
Transcriptome analysis of response to Plasmodiophora brassicae infection in the Arabidopsis shoot and root |
title_sort |
transcriptome analysis of response to plasmodiophora brassicae infection in the arabidopsis shoot and root |
publisher |
BMC |
series |
BMC Genomics |
issn |
1471-2164 |
publishDate |
2018-01-01 |
description |
Abstract Background Clubroot is an important disease caused by the obligate parasite Plasmodiophora brassicae that infects the Brassicaceae. As a soil-borne pathogen, P. brassicae induces the generation of abnormal tissue in the root, resulting in the formation of galls. Root infection negatively affects the uptake of water and nutrients in host plants, severely reducing their growth and productivity. Many studies have emphasized the molecular and physiological effects of the clubroot disease on root tissues. The aim of the present study is to better understand the effect of P. brassicae on the transcriptome of both shoot and root tissues of Arabidopsis thaliana. Results Transcriptome profiling using RNA-seq was performed on both shoot and root tissues at 17, 20 and 24 days post inoculation (dpi) of A. thaliana, a model plant host for P. brassicae. The number of differentially expressed genes (DEGs) between infected and uninfected samples was larger in shoot than in root. In both shoot and root, more genes were differentially regulated at 24 dpi than the two earlier time points. Genes that were highly regulated in response to infection in both shoot and root primarily were involved in the metabolism of cell wall compounds, lipids, and shikimate pathway metabolites. Among hormone-related pathways, several jasmonic acid biosynthesis genes were upregulated in both shoot and root tissue. Genes encoding enzymes involved in cell wall modification, biosynthesis of sucrose and starch, and several classes of transcription factors were generally differently regulated in shoot and root. Conclusions These results highlight the similarities and differences in the transcriptomic response of above- and below-ground tissues of the model host Arabidopsis following P. brassicae infection. The main transcriptomic changes in root metabolism during clubroot disease progression were identified. An overview of DEGs in the shoot underlined the physiological changes in above-ground tissues following pathogen establishment and disease progression. This study provides insights into host tissue-specific molecular responses to clubroot development and may have applications in the development of clubroot markers for more effective breeding strategies. |
topic |
Arabidopsis thaliana Clubroot Host-pathogen interaction Plasmodiophora brassicae RNA-seq Root |
url |
http://link.springer.com/article/10.1186/s12864-017-4426-7 |
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