Cargando…
Nitric Oxide Boosts Bemisia tabaci Performance Through the Suppression of Jasmonic Acid Signaling Pathway in Tobacco Plants
The intimate relationships between plants and insects start with herbivory, which can be traced back to approximately 420 million year ago. Like many other relationships, a plant–insect interaction can be mutualistic, commensalistic, or antagonistic. Within antagonistic relationships, plants deploy...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387647/ https://www.ncbi.nlm.nih.gov/pubmed/32792979 http://dx.doi.org/10.3389/fphys.2020.00847 |
_version_ | 1783564167914979328 |
---|---|
author | Xu, Yanan Qu, Cheng Sun, Xia Jia, Zhifei Xue, Ming Zhao, Haipeng Zhou, Xuguo |
author_facet | Xu, Yanan Qu, Cheng Sun, Xia Jia, Zhifei Xue, Ming Zhao, Haipeng Zhou, Xuguo |
author_sort | Xu, Yanan |
collection | PubMed |
description | The intimate relationships between plants and insects start with herbivory, which can be traced back to approximately 420 million year ago. Like many other relationships, a plant–insect interaction can be mutualistic, commensalistic, or antagonistic. Within antagonistic relationships, plants deploy inducible defense to insect phytophagy. Insects, however, can evade/suppress effectual plant defenses by manipulating plant defense signaling. Previously, we showed that the sweet potato whitefly, Bemisia tabaci, a global invasive insect pest, can suppress jasmonic acid (JA)-dependent defenses, thereby enhancing their performance on host plants. Given that nitric oxide (NO), a multifunctional signaling molecule, interacts closely with JA signaling pathway, we hypothesized that NO is involved in the suppression of JA defensive responses. Equipped with an integrated approach, we comprehensively examined this overarching hypothesis. We showed that: (1) tobacco plants responded to B. tabaci infestation by accumulating high levels of NO, (2) the exogenous application of sodium nitroprusside, a NO donor, in tobacco plants attracted B. tabaci adults and accelerated nymphal development, whereas plants treated with 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide (cPTIO), a NO scavenger, repelled B. tabaci adults and prolonged nymphal development, and, more importantly, (3) silencing of NO-associated protein 1, a gene associated with NO accumulation, and cPTIO application disrupted the B. tabaci-mediated suppression of JA in plants. Collectively, these results suggest that: (1) NO signaling is activated by B. tabaci infestation, (2) NO is involved in the suppression of JA-dependent plant defense, and, consequently, (3) NO improves B. tabaci performance on host plants. Our study reflects the remarkable arm race that co-evolved for millions of years between plants and insects and offers a potential novel target (nitric oxide) for the long-term sustainable management of this global invasive pest. |
format | Online Article Text |
id | pubmed-7387647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73876472020-08-12 Nitric Oxide Boosts Bemisia tabaci Performance Through the Suppression of Jasmonic Acid Signaling Pathway in Tobacco Plants Xu, Yanan Qu, Cheng Sun, Xia Jia, Zhifei Xue, Ming Zhao, Haipeng Zhou, Xuguo Front Physiol Physiology The intimate relationships between plants and insects start with herbivory, which can be traced back to approximately 420 million year ago. Like many other relationships, a plant–insect interaction can be mutualistic, commensalistic, or antagonistic. Within antagonistic relationships, plants deploy inducible defense to insect phytophagy. Insects, however, can evade/suppress effectual plant defenses by manipulating plant defense signaling. Previously, we showed that the sweet potato whitefly, Bemisia tabaci, a global invasive insect pest, can suppress jasmonic acid (JA)-dependent defenses, thereby enhancing their performance on host plants. Given that nitric oxide (NO), a multifunctional signaling molecule, interacts closely with JA signaling pathway, we hypothesized that NO is involved in the suppression of JA defensive responses. Equipped with an integrated approach, we comprehensively examined this overarching hypothesis. We showed that: (1) tobacco plants responded to B. tabaci infestation by accumulating high levels of NO, (2) the exogenous application of sodium nitroprusside, a NO donor, in tobacco plants attracted B. tabaci adults and accelerated nymphal development, whereas plants treated with 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide (cPTIO), a NO scavenger, repelled B. tabaci adults and prolonged nymphal development, and, more importantly, (3) silencing of NO-associated protein 1, a gene associated with NO accumulation, and cPTIO application disrupted the B. tabaci-mediated suppression of JA in plants. Collectively, these results suggest that: (1) NO signaling is activated by B. tabaci infestation, (2) NO is involved in the suppression of JA-dependent plant defense, and, consequently, (3) NO improves B. tabaci performance on host plants. Our study reflects the remarkable arm race that co-evolved for millions of years between plants and insects and offers a potential novel target (nitric oxide) for the long-term sustainable management of this global invasive pest. Frontiers Media S.A. 2020-07-22 /pmc/articles/PMC7387647/ /pubmed/32792979 http://dx.doi.org/10.3389/fphys.2020.00847 Text en Copyright © 2020 Xu, Qu, Sun, Jia, Xue, Zhao and Zhou. 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 | Physiology Xu, Yanan Qu, Cheng Sun, Xia Jia, Zhifei Xue, Ming Zhao, Haipeng Zhou, Xuguo Nitric Oxide Boosts Bemisia tabaci Performance Through the Suppression of Jasmonic Acid Signaling Pathway in Tobacco Plants |
title | Nitric Oxide Boosts Bemisia tabaci Performance Through the Suppression of Jasmonic Acid Signaling Pathway in Tobacco Plants |
title_full | Nitric Oxide Boosts Bemisia tabaci Performance Through the Suppression of Jasmonic Acid Signaling Pathway in Tobacco Plants |
title_fullStr | Nitric Oxide Boosts Bemisia tabaci Performance Through the Suppression of Jasmonic Acid Signaling Pathway in Tobacco Plants |
title_full_unstemmed | Nitric Oxide Boosts Bemisia tabaci Performance Through the Suppression of Jasmonic Acid Signaling Pathway in Tobacco Plants |
title_short | Nitric Oxide Boosts Bemisia tabaci Performance Through the Suppression of Jasmonic Acid Signaling Pathway in Tobacco Plants |
title_sort | nitric oxide boosts bemisia tabaci performance through the suppression of jasmonic acid signaling pathway in tobacco plants |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387647/ https://www.ncbi.nlm.nih.gov/pubmed/32792979 http://dx.doi.org/10.3389/fphys.2020.00847 |
work_keys_str_mv | AT xuyanan nitricoxideboostsbemisiatabaciperformancethroughthesuppressionofjasmonicacidsignalingpathwayintobaccoplants AT qucheng nitricoxideboostsbemisiatabaciperformancethroughthesuppressionofjasmonicacidsignalingpathwayintobaccoplants AT sunxia nitricoxideboostsbemisiatabaciperformancethroughthesuppressionofjasmonicacidsignalingpathwayintobaccoplants AT jiazhifei nitricoxideboostsbemisiatabaciperformancethroughthesuppressionofjasmonicacidsignalingpathwayintobaccoplants AT xueming nitricoxideboostsbemisiatabaciperformancethroughthesuppressionofjasmonicacidsignalingpathwayintobaccoplants AT zhaohaipeng nitricoxideboostsbemisiatabaciperformancethroughthesuppressionofjasmonicacidsignalingpathwayintobaccoplants AT zhouxuguo nitricoxideboostsbemisiatabaciperformancethroughthesuppressionofjasmonicacidsignalingpathwayintobaccoplants |