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Planthopper-Secreted Salivary Disulfide Isomerase Activates Immune Responses in Plants
The small brown planthopper (Laodelphax striatellus; SBPH) is a piercing-sucking insect that secretes salivary proteins into its plant host during feeding. However, the mechanisms by which these salivary proteins regulate plant defense responses remain poorly understood. Here, we identified the disu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848103/ https://www.ncbi.nlm.nih.gov/pubmed/33537052 http://dx.doi.org/10.3389/fpls.2020.622513 |
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author | Fu, Jianmei Shi, Yu Wang, Lu Zhang, Hao Li, Jing Fang, Jichao Ji, Rui |
author_facet | Fu, Jianmei Shi, Yu Wang, Lu Zhang, Hao Li, Jing Fang, Jichao Ji, Rui |
author_sort | Fu, Jianmei |
collection | PubMed |
description | The small brown planthopper (Laodelphax striatellus; SBPH) is a piercing-sucking insect that secretes salivary proteins into its plant host during feeding. However, the mechanisms by which these salivary proteins regulate plant defense responses remain poorly understood. Here, we identified the disulfide isomerase (LsPDI1) in the SBPH salivary proteome. LsPDI1 was highly expressed in the SBPH salivary glands and secreted into rice plants during feeding. Transient in planta LsPDI1 expression in the absence of signal peptide induced reactive oxygen species (ROS) burst, cell death, callose deposition, and jasmonic acid (JA) signaling pathway. Deletion mutant analysis revealed that either the a-b-b’ or the b-b’-a’ domains in LsPDI1 are required to induce cell death in plants. LsPDI1 and its orthologs were highly conserved among various planthopper species and strongly induced ROS burst and cell death in plants. Transient in Nicotiana benthamiana LsPDI1 expression impaired the performance of Spodoptera frugiperda and Myzus persicae on host plants. Hence, LsPDI1 is an important salivary elicitor that enhances plant resistance to insects by inducing the calcium, ROS, and JA signaling pathways. The findings of this study provide novel insights into the molecular mechanisms underlying plant-insect interactions. |
format | Online Article Text |
id | pubmed-7848103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78481032021-02-02 Planthopper-Secreted Salivary Disulfide Isomerase Activates Immune Responses in Plants Fu, Jianmei Shi, Yu Wang, Lu Zhang, Hao Li, Jing Fang, Jichao Ji, Rui Front Plant Sci Plant Science The small brown planthopper (Laodelphax striatellus; SBPH) is a piercing-sucking insect that secretes salivary proteins into its plant host during feeding. However, the mechanisms by which these salivary proteins regulate plant defense responses remain poorly understood. Here, we identified the disulfide isomerase (LsPDI1) in the SBPH salivary proteome. LsPDI1 was highly expressed in the SBPH salivary glands and secreted into rice plants during feeding. Transient in planta LsPDI1 expression in the absence of signal peptide induced reactive oxygen species (ROS) burst, cell death, callose deposition, and jasmonic acid (JA) signaling pathway. Deletion mutant analysis revealed that either the a-b-b’ or the b-b’-a’ domains in LsPDI1 are required to induce cell death in plants. LsPDI1 and its orthologs were highly conserved among various planthopper species and strongly induced ROS burst and cell death in plants. Transient in Nicotiana benthamiana LsPDI1 expression impaired the performance of Spodoptera frugiperda and Myzus persicae on host plants. Hence, LsPDI1 is an important salivary elicitor that enhances plant resistance to insects by inducing the calcium, ROS, and JA signaling pathways. The findings of this study provide novel insights into the molecular mechanisms underlying plant-insect interactions. Frontiers Media S.A. 2021-01-18 /pmc/articles/PMC7848103/ /pubmed/33537052 http://dx.doi.org/10.3389/fpls.2020.622513 Text en Copyright © 2021 Fu, Shi, Wang, Zhang, Li, Fang and Ji. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Fu, Jianmei Shi, Yu Wang, Lu Zhang, Hao Li, Jing Fang, Jichao Ji, Rui Planthopper-Secreted Salivary Disulfide Isomerase Activates Immune Responses in Plants |
title | Planthopper-Secreted Salivary Disulfide Isomerase Activates Immune Responses in Plants |
title_full | Planthopper-Secreted Salivary Disulfide Isomerase Activates Immune Responses in Plants |
title_fullStr | Planthopper-Secreted Salivary Disulfide Isomerase Activates Immune Responses in Plants |
title_full_unstemmed | Planthopper-Secreted Salivary Disulfide Isomerase Activates Immune Responses in Plants |
title_short | Planthopper-Secreted Salivary Disulfide Isomerase Activates Immune Responses in Plants |
title_sort | planthopper-secreted salivary disulfide isomerase activates immune responses in plants |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848103/ https://www.ncbi.nlm.nih.gov/pubmed/33537052 http://dx.doi.org/10.3389/fpls.2020.622513 |
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