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Different viral effectors suppress hormone-mediated antiviral immunity of rice coordinated by OsNPR1

Salicylic acid (SA) and jasmonic acid (JA) are plant hormones that typically act antagonistically in dicotyledonous plants and SA and JA signaling is often manipulated by pathogens. However, in monocotyledonous plants, the detailed SA-JA interplay in response to pathogen invasion remains elusive. He...

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Autores principales: Zhang, Hehong, Wang, Fengmin, Song, Weiqi, Yang, Zihang, Li, Lulu, Ma, Qiang, Tan, Xiaoxiang, Wei, Zhongyan, Li, Yanjun, Li, Junmin, Yan, Fei, Chen, Jianping, Sun, Zongtao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213043/
https://www.ncbi.nlm.nih.gov/pubmed/37230965
http://dx.doi.org/10.1038/s41467-023-38805-x
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author Zhang, Hehong
Wang, Fengmin
Song, Weiqi
Yang, Zihang
Li, Lulu
Ma, Qiang
Tan, Xiaoxiang
Wei, Zhongyan
Li, Yanjun
Li, Junmin
Yan, Fei
Chen, Jianping
Sun, Zongtao
author_facet Zhang, Hehong
Wang, Fengmin
Song, Weiqi
Yang, Zihang
Li, Lulu
Ma, Qiang
Tan, Xiaoxiang
Wei, Zhongyan
Li, Yanjun
Li, Junmin
Yan, Fei
Chen, Jianping
Sun, Zongtao
author_sort Zhang, Hehong
collection PubMed
description Salicylic acid (SA) and jasmonic acid (JA) are plant hormones that typically act antagonistically in dicotyledonous plants and SA and JA signaling is often manipulated by pathogens. However, in monocotyledonous plants, the detailed SA-JA interplay in response to pathogen invasion remains elusive. Here, we show that different types of viral pathogen can disrupt synergistic antiviral immunity mediated by SA and JA via OsNPR1 in the monocot rice. The P2 protein of rice stripe virus, a negative-stranded RNA virus in the genus Tenuivirus, promotes OsNPR1 degradation by enhancing the association of OsNPR1 and OsCUL3a. OsNPR1 activates JA signaling by disrupting the OsJAZ-OsMYC complex and boosting the transcriptional activation activity of OsMYC2 to cooperatively modulate rice antiviral immunity. Unrelated viral proteins from different rice viruses also interfere with the OsNPR1-mediated SA-JA interplay to facilitate viral pathogenicity, suggesting that this may be a more general strategy in monocot plants. Overall, our findings highlight that distinct viral proteins convergently obstruct JA-SA crosstalk to facilitate viral infection in monocot rice.
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spelling pubmed-102130432023-05-27 Different viral effectors suppress hormone-mediated antiviral immunity of rice coordinated by OsNPR1 Zhang, Hehong Wang, Fengmin Song, Weiqi Yang, Zihang Li, Lulu Ma, Qiang Tan, Xiaoxiang Wei, Zhongyan Li, Yanjun Li, Junmin Yan, Fei Chen, Jianping Sun, Zongtao Nat Commun Article Salicylic acid (SA) and jasmonic acid (JA) are plant hormones that typically act antagonistically in dicotyledonous plants and SA and JA signaling is often manipulated by pathogens. However, in monocotyledonous plants, the detailed SA-JA interplay in response to pathogen invasion remains elusive. Here, we show that different types of viral pathogen can disrupt synergistic antiviral immunity mediated by SA and JA via OsNPR1 in the monocot rice. The P2 protein of rice stripe virus, a negative-stranded RNA virus in the genus Tenuivirus, promotes OsNPR1 degradation by enhancing the association of OsNPR1 and OsCUL3a. OsNPR1 activates JA signaling by disrupting the OsJAZ-OsMYC complex and boosting the transcriptional activation activity of OsMYC2 to cooperatively modulate rice antiviral immunity. Unrelated viral proteins from different rice viruses also interfere with the OsNPR1-mediated SA-JA interplay to facilitate viral pathogenicity, suggesting that this may be a more general strategy in monocot plants. Overall, our findings highlight that distinct viral proteins convergently obstruct JA-SA crosstalk to facilitate viral infection in monocot rice. Nature Publishing Group UK 2023-05-25 /pmc/articles/PMC10213043/ /pubmed/37230965 http://dx.doi.org/10.1038/s41467-023-38805-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhang, Hehong
Wang, Fengmin
Song, Weiqi
Yang, Zihang
Li, Lulu
Ma, Qiang
Tan, Xiaoxiang
Wei, Zhongyan
Li, Yanjun
Li, Junmin
Yan, Fei
Chen, Jianping
Sun, Zongtao
Different viral effectors suppress hormone-mediated antiviral immunity of rice coordinated by OsNPR1
title Different viral effectors suppress hormone-mediated antiviral immunity of rice coordinated by OsNPR1
title_full Different viral effectors suppress hormone-mediated antiviral immunity of rice coordinated by OsNPR1
title_fullStr Different viral effectors suppress hormone-mediated antiviral immunity of rice coordinated by OsNPR1
title_full_unstemmed Different viral effectors suppress hormone-mediated antiviral immunity of rice coordinated by OsNPR1
title_short Different viral effectors suppress hormone-mediated antiviral immunity of rice coordinated by OsNPR1
title_sort different viral effectors suppress hormone-mediated antiviral immunity of rice coordinated by osnpr1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213043/
https://www.ncbi.nlm.nih.gov/pubmed/37230965
http://dx.doi.org/10.1038/s41467-023-38805-x
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