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Independently evolved viral effectors convergently suppress DELLA protein SLR1-mediated broad-spectrum antiviral immunity in rice

Plant viruses adopt diverse virulence strategies to inhibit host antiviral defense. However, general antiviral defense directly targeted by different types of plant viruses have rarely been studied. Here, we show that the single rice DELLA protein, SLENDER RICE 1 (SLR1), a master negative regulator...

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Autores principales: Li, Lulu, Zhang, Hehong, Yang, Zihang, Wang, Chen, Li, Shanshan, Cao, Chen, Yao, Tongsong, Wei, Zhongyan, Li, Yanjun, Chen, Jianping, Sun, Zongtao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9663503/
https://www.ncbi.nlm.nih.gov/pubmed/36376330
http://dx.doi.org/10.1038/s41467-022-34649-z
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author Li, Lulu
Zhang, Hehong
Yang, Zihang
Wang, Chen
Li, Shanshan
Cao, Chen
Yao, Tongsong
Wei, Zhongyan
Li, Yanjun
Chen, Jianping
Sun, Zongtao
author_facet Li, Lulu
Zhang, Hehong
Yang, Zihang
Wang, Chen
Li, Shanshan
Cao, Chen
Yao, Tongsong
Wei, Zhongyan
Li, Yanjun
Chen, Jianping
Sun, Zongtao
author_sort Li, Lulu
collection PubMed
description Plant viruses adopt diverse virulence strategies to inhibit host antiviral defense. However, general antiviral defense directly targeted by different types of plant viruses have rarely been studied. Here, we show that the single rice DELLA protein, SLENDER RICE 1 (SLR1), a master negative regulator in Gibberellin (GA) signaling pathway, is targeted by several different viral effectors for facilitating viral infection. Viral proteins encoded by different types of rice viruses all directly trigger the rapid degradation of SLR1 by promoting association with the GA receptor OsGID1. SLR1-mediated broad-spectrum resistance was subverted by these independently evolved viral proteins, which all interrupted the functional crosstalk between SLR1 and jasmonic acid (JA) signaling. This decline of JA antiviral further created the advantage of viral infection. Our study reveals a common viral counter-defense strategy in which different types of viruses convergently target SLR1-mediated broad-spectrum resistance to benefit viral infection in the monocotyledonous crop rice.
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spelling pubmed-96635032022-11-15 Independently evolved viral effectors convergently suppress DELLA protein SLR1-mediated broad-spectrum antiviral immunity in rice Li, Lulu Zhang, Hehong Yang, Zihang Wang, Chen Li, Shanshan Cao, Chen Yao, Tongsong Wei, Zhongyan Li, Yanjun Chen, Jianping Sun, Zongtao Nat Commun Article Plant viruses adopt diverse virulence strategies to inhibit host antiviral defense. However, general antiviral defense directly targeted by different types of plant viruses have rarely been studied. Here, we show that the single rice DELLA protein, SLENDER RICE 1 (SLR1), a master negative regulator in Gibberellin (GA) signaling pathway, is targeted by several different viral effectors for facilitating viral infection. Viral proteins encoded by different types of rice viruses all directly trigger the rapid degradation of SLR1 by promoting association with the GA receptor OsGID1. SLR1-mediated broad-spectrum resistance was subverted by these independently evolved viral proteins, which all interrupted the functional crosstalk between SLR1 and jasmonic acid (JA) signaling. This decline of JA antiviral further created the advantage of viral infection. Our study reveals a common viral counter-defense strategy in which different types of viruses convergently target SLR1-mediated broad-spectrum resistance to benefit viral infection in the monocotyledonous crop rice. Nature Publishing Group UK 2022-11-14 /pmc/articles/PMC9663503/ /pubmed/36376330 http://dx.doi.org/10.1038/s41467-022-34649-z Text en © The Author(s) 2022 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
Li, Lulu
Zhang, Hehong
Yang, Zihang
Wang, Chen
Li, Shanshan
Cao, Chen
Yao, Tongsong
Wei, Zhongyan
Li, Yanjun
Chen, Jianping
Sun, Zongtao
Independently evolved viral effectors convergently suppress DELLA protein SLR1-mediated broad-spectrum antiviral immunity in rice
title Independently evolved viral effectors convergently suppress DELLA protein SLR1-mediated broad-spectrum antiviral immunity in rice
title_full Independently evolved viral effectors convergently suppress DELLA protein SLR1-mediated broad-spectrum antiviral immunity in rice
title_fullStr Independently evolved viral effectors convergently suppress DELLA protein SLR1-mediated broad-spectrum antiviral immunity in rice
title_full_unstemmed Independently evolved viral effectors convergently suppress DELLA protein SLR1-mediated broad-spectrum antiviral immunity in rice
title_short Independently evolved viral effectors convergently suppress DELLA protein SLR1-mediated broad-spectrum antiviral immunity in rice
title_sort independently evolved viral effectors convergently suppress della protein slr1-mediated broad-spectrum antiviral immunity in rice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9663503/
https://www.ncbi.nlm.nih.gov/pubmed/36376330
http://dx.doi.org/10.1038/s41467-022-34649-z
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