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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...

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Autores principales: Fu, Jianmei, Shi, Yu, Wang, Lu, Zhang, Hao, Li, Jing, Fang, Jichao, Ji, Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
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.
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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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