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Role of brassinosteroid signaling in modulating Tobacco mosaic virus resistance in Nicotiana benthamiana
Plant steroid hormones, brassinosteroids (BRs), play essential roles in plant growth, development and stress responses. However, mechanisms by which BRs interfere with plant resistance to virus remain largely unclear. In this study, we used pharmacological and genetic approaches in combination with...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4738339/ https://www.ncbi.nlm.nih.gov/pubmed/26838475 http://dx.doi.org/10.1038/srep20579 |
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author | Deng, Xing-Guang Zhu, Tong Peng, Xing-Ji Xi, De-Hui Guo, Hongqing Yin, Yanhai Zhang, Da-Wei Lin, Hong-Hui |
author_facet | Deng, Xing-Guang Zhu, Tong Peng, Xing-Ji Xi, De-Hui Guo, Hongqing Yin, Yanhai Zhang, Da-Wei Lin, Hong-Hui |
author_sort | Deng, Xing-Guang |
collection | PubMed |
description | Plant steroid hormones, brassinosteroids (BRs), play essential roles in plant growth, development and stress responses. However, mechanisms by which BRs interfere with plant resistance to virus remain largely unclear. In this study, we used pharmacological and genetic approaches in combination with infection experiments to investigate the role of BRs in plant defense against Tobacco Mosaic Virus (TMV) in Nicotiana benthamiana. Exogenous applied BRs enhanced plant resistance to virus infection, while application of Bikinin (inhibitor of glycogen synthase kinase-3), which activated BR signaling, increased virus susceptibility. Silencing of NbBRI1 and NbBSK1 blocked BR-induced TMV resistance, and silencing of NbBES1/BZR1 blocked Bikinin-reduced TMV resistance. Silencing of NbMEK2, NbSIPK and NbRBOHB all compromised BR-induced virus resistance and defense-associated genes expression. Furthermore, we found MEK2-SIPK cascade activated while BES1/BZR1 inhibited RBOHB-dependent ROS production, defense gene expression and virus resistance induced by BRs. Thus, our results revealed BR signaling had two opposite effects on viral defense response. On the one hand, BRs enhanced virus resistance through MEK2-SIPK cascade and RBOHB-dependent ROS burst. On the other hand, BES1/BZR1 inhibited RBOHB-dependent ROS production and acted as an important mediator of the trade-off between growth and immunity in BR signaling. |
format | Online Article Text |
id | pubmed-4738339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47383392016-02-09 Role of brassinosteroid signaling in modulating Tobacco mosaic virus resistance in Nicotiana benthamiana Deng, Xing-Guang Zhu, Tong Peng, Xing-Ji Xi, De-Hui Guo, Hongqing Yin, Yanhai Zhang, Da-Wei Lin, Hong-Hui Sci Rep Article Plant steroid hormones, brassinosteroids (BRs), play essential roles in plant growth, development and stress responses. However, mechanisms by which BRs interfere with plant resistance to virus remain largely unclear. In this study, we used pharmacological and genetic approaches in combination with infection experiments to investigate the role of BRs in plant defense against Tobacco Mosaic Virus (TMV) in Nicotiana benthamiana. Exogenous applied BRs enhanced plant resistance to virus infection, while application of Bikinin (inhibitor of glycogen synthase kinase-3), which activated BR signaling, increased virus susceptibility. Silencing of NbBRI1 and NbBSK1 blocked BR-induced TMV resistance, and silencing of NbBES1/BZR1 blocked Bikinin-reduced TMV resistance. Silencing of NbMEK2, NbSIPK and NbRBOHB all compromised BR-induced virus resistance and defense-associated genes expression. Furthermore, we found MEK2-SIPK cascade activated while BES1/BZR1 inhibited RBOHB-dependent ROS production, defense gene expression and virus resistance induced by BRs. Thus, our results revealed BR signaling had two opposite effects on viral defense response. On the one hand, BRs enhanced virus resistance through MEK2-SIPK cascade and RBOHB-dependent ROS burst. On the other hand, BES1/BZR1 inhibited RBOHB-dependent ROS production and acted as an important mediator of the trade-off between growth and immunity in BR signaling. Nature Publishing Group 2016-02-03 /pmc/articles/PMC4738339/ /pubmed/26838475 http://dx.doi.org/10.1038/srep20579 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Deng, Xing-Guang Zhu, Tong Peng, Xing-Ji Xi, De-Hui Guo, Hongqing Yin, Yanhai Zhang, Da-Wei Lin, Hong-Hui Role of brassinosteroid signaling in modulating Tobacco mosaic virus resistance in Nicotiana benthamiana |
title | Role of brassinosteroid signaling in modulating Tobacco mosaic virus resistance in Nicotiana benthamiana |
title_full | Role of brassinosteroid signaling in modulating Tobacco mosaic virus resistance in Nicotiana benthamiana |
title_fullStr | Role of brassinosteroid signaling in modulating Tobacco mosaic virus resistance in Nicotiana benthamiana |
title_full_unstemmed | Role of brassinosteroid signaling in modulating Tobacco mosaic virus resistance in Nicotiana benthamiana |
title_short | Role of brassinosteroid signaling in modulating Tobacco mosaic virus resistance in Nicotiana benthamiana |
title_sort | role of brassinosteroid signaling in modulating tobacco mosaic virus resistance in nicotiana benthamiana |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4738339/ https://www.ncbi.nlm.nih.gov/pubmed/26838475 http://dx.doi.org/10.1038/srep20579 |
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