Cargando…
Whole-genome and time-course dual RNA-Seq analyses reveal chronic pathogenicity-related gene dynamics in the ginseng rusty root rot pathogen Ilyonectria robusta
Ilyonectria robusta causes rusty root rot, the most devastating chronic disease of ginseng. Here, we for the first time report the high-quality genome of the I. robusta strain CD-56. Time-course (36 h, 72 h, and 144 h) dual RNA-Seq analysis of the infection process was performed, and many genes, inc...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994667/ https://www.ncbi.nlm.nih.gov/pubmed/32005849 http://dx.doi.org/10.1038/s41598-020-58342-7 |
_version_ | 1783493241691176960 |
---|---|
author | Guan, Yiming Chen, Meili Ma, Yingying Du, Zhenglin Yuan, Na Li, Yu Xiao, Jingfa Zhang, Yayu |
author_facet | Guan, Yiming Chen, Meili Ma, Yingying Du, Zhenglin Yuan, Na Li, Yu Xiao, Jingfa Zhang, Yayu |
author_sort | Guan, Yiming |
collection | PubMed |
description | Ilyonectria robusta causes rusty root rot, the most devastating chronic disease of ginseng. Here, we for the first time report the high-quality genome of the I. robusta strain CD-56. Time-course (36 h, 72 h, and 144 h) dual RNA-Seq analysis of the infection process was performed, and many genes, including candidate effectors, were found to be associated with the progression and success of infection. The gene expression profile of CD-56 showed a trend of initial inhibition and then gradually returned to a profile similar to that of the control. Analyses of the gene expression patterns and functions of pathogenicity-related genes, especially candidate effector genes, indicated that the stress response changed to an adaptive response during the infection process. For ginseng, gene expression patterns were highly related to physiological conditions. Specifically, the results showed that ginseng defenses were activated by CD-56 infection and persisted for at least 144 h thereafter but that the mechanisms invoked were not effective in preventing CD-56 growth. Moreover, CD-56 did not appear to fully suppress plant defenses, even in late stages after infection. Our results provide new insight into the chronic pathogenesis of CD-56 and the comprehensive and complex inducible defense responses of ginseng root to I. robusta infection. |
format | Online Article Text |
id | pubmed-6994667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69946672020-02-06 Whole-genome and time-course dual RNA-Seq analyses reveal chronic pathogenicity-related gene dynamics in the ginseng rusty root rot pathogen Ilyonectria robusta Guan, Yiming Chen, Meili Ma, Yingying Du, Zhenglin Yuan, Na Li, Yu Xiao, Jingfa Zhang, Yayu Sci Rep Article Ilyonectria robusta causes rusty root rot, the most devastating chronic disease of ginseng. Here, we for the first time report the high-quality genome of the I. robusta strain CD-56. Time-course (36 h, 72 h, and 144 h) dual RNA-Seq analysis of the infection process was performed, and many genes, including candidate effectors, were found to be associated with the progression and success of infection. The gene expression profile of CD-56 showed a trend of initial inhibition and then gradually returned to a profile similar to that of the control. Analyses of the gene expression patterns and functions of pathogenicity-related genes, especially candidate effector genes, indicated that the stress response changed to an adaptive response during the infection process. For ginseng, gene expression patterns were highly related to physiological conditions. Specifically, the results showed that ginseng defenses were activated by CD-56 infection and persisted for at least 144 h thereafter but that the mechanisms invoked were not effective in preventing CD-56 growth. Moreover, CD-56 did not appear to fully suppress plant defenses, even in late stages after infection. Our results provide new insight into the chronic pathogenesis of CD-56 and the comprehensive and complex inducible defense responses of ginseng root to I. robusta infection. Nature Publishing Group UK 2020-01-31 /pmc/articles/PMC6994667/ /pubmed/32005849 http://dx.doi.org/10.1038/s41598-020-58342-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Guan, Yiming Chen, Meili Ma, Yingying Du, Zhenglin Yuan, Na Li, Yu Xiao, Jingfa Zhang, Yayu Whole-genome and time-course dual RNA-Seq analyses reveal chronic pathogenicity-related gene dynamics in the ginseng rusty root rot pathogen Ilyonectria robusta |
title | Whole-genome and time-course dual RNA-Seq analyses reveal chronic pathogenicity-related gene dynamics in the ginseng rusty root rot pathogen Ilyonectria robusta |
title_full | Whole-genome and time-course dual RNA-Seq analyses reveal chronic pathogenicity-related gene dynamics in the ginseng rusty root rot pathogen Ilyonectria robusta |
title_fullStr | Whole-genome and time-course dual RNA-Seq analyses reveal chronic pathogenicity-related gene dynamics in the ginseng rusty root rot pathogen Ilyonectria robusta |
title_full_unstemmed | Whole-genome and time-course dual RNA-Seq analyses reveal chronic pathogenicity-related gene dynamics in the ginseng rusty root rot pathogen Ilyonectria robusta |
title_short | Whole-genome and time-course dual RNA-Seq analyses reveal chronic pathogenicity-related gene dynamics in the ginseng rusty root rot pathogen Ilyonectria robusta |
title_sort | whole-genome and time-course dual rna-seq analyses reveal chronic pathogenicity-related gene dynamics in the ginseng rusty root rot pathogen ilyonectria robusta |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994667/ https://www.ncbi.nlm.nih.gov/pubmed/32005849 http://dx.doi.org/10.1038/s41598-020-58342-7 |
work_keys_str_mv | AT guanyiming wholegenomeandtimecoursedualrnaseqanalysesrevealchronicpathogenicityrelatedgenedynamicsintheginsengrustyrootrotpathogenilyonectriarobusta AT chenmeili wholegenomeandtimecoursedualrnaseqanalysesrevealchronicpathogenicityrelatedgenedynamicsintheginsengrustyrootrotpathogenilyonectriarobusta AT mayingying wholegenomeandtimecoursedualrnaseqanalysesrevealchronicpathogenicityrelatedgenedynamicsintheginsengrustyrootrotpathogenilyonectriarobusta AT duzhenglin wholegenomeandtimecoursedualrnaseqanalysesrevealchronicpathogenicityrelatedgenedynamicsintheginsengrustyrootrotpathogenilyonectriarobusta AT yuanna wholegenomeandtimecoursedualrnaseqanalysesrevealchronicpathogenicityrelatedgenedynamicsintheginsengrustyrootrotpathogenilyonectriarobusta AT liyu wholegenomeandtimecoursedualrnaseqanalysesrevealchronicpathogenicityrelatedgenedynamicsintheginsengrustyrootrotpathogenilyonectriarobusta AT xiaojingfa wholegenomeandtimecoursedualrnaseqanalysesrevealchronicpathogenicityrelatedgenedynamicsintheginsengrustyrootrotpathogenilyonectriarobusta AT zhangyayu wholegenomeandtimecoursedualrnaseqanalysesrevealchronicpathogenicityrelatedgenedynamicsintheginsengrustyrootrotpathogenilyonectriarobusta |