Abscisic Acid Interacts Antagonistically with Salicylic Acid Signaling Pathway in Rice–Magnaporthe grisea Interaction
Plant hormones play pivotal signaling roles in plant–pathogen interactions. Here, we report characterization of an antagonistic interaction of abscisic acid (ABA) with salicylic acid (SA) signaling pathways in the rice–Magnaporthe grisea interaction. Exogenous application of ABA drastically compromi...
Main Authors: | , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
The American Phytopathological Society
2010-06-01
|
Series: | Molecular Plant-Microbe Interactions |
Online Access: | https://apsjournals.apsnet.org/doi/10.1094/MPMI-23-6-0791 |
_version_ | 1818915240407990272 |
---|---|
author | Chang-Jie Jiang Masaki Shimono Shoji Sugano Mikiko Kojima Katsumi Yazawa Riichiro Yoshida Haruhiko Inoue Nagao Hayashi Hitoshi Sakakibara Hiroshi Takatsuji |
author_facet | Chang-Jie Jiang Masaki Shimono Shoji Sugano Mikiko Kojima Katsumi Yazawa Riichiro Yoshida Haruhiko Inoue Nagao Hayashi Hitoshi Sakakibara Hiroshi Takatsuji |
author_sort | Chang-Jie Jiang |
collection | DOAJ |
description | Plant hormones play pivotal signaling roles in plant–pathogen interactions. Here, we report characterization of an antagonistic interaction of abscisic acid (ABA) with salicylic acid (SA) signaling pathways in the rice–Magnaporthe grisea interaction. Exogenous application of ABA drastically compromised the rice resistance to both compatible and incompatible M. grisea strains, indicating that ABA negatively regulates both basal and resistance gene–mediated blast resistance. ABA markedly suppressed the transcriptional upregulation of WRKY45 and OsNPR1, the two key components of the SA signaling pathway in rice, induced by SA or benzothiadiazole or by blast infection. Overexpression of OsNPR1 or WRKY45 largely negated the enhancement of blast susceptibility by ABA, suggesting that ABA acts upstream of WRKY45 and OsNPR1 in the rice SA pathway. ABA-responsive genes were induced during blast infection in a pattern reciprocal to those of WRKY45 and OsPR1b in the compatible rice–blast interaction but only marginally in the incompatible one. These results suggest that the balance of SA and ABA signaling is an important determinant for the outcome of the rice–M. grisea interaction. ABA was detected in hyphae and conidia of M. grisea as well as in culture media, implying that blast-fungus-derived ABA could play a role in triggering ABA signaling at host infection sites. |
first_indexed | 2024-12-19T23:59:08Z |
format | Article |
id | doaj.art-afb3d9dcae944d9a99a3b2998f6631ad |
institution | Directory Open Access Journal |
issn | 0894-0282 1943-7706 |
language | English |
last_indexed | 2024-12-19T23:59:08Z |
publishDate | 2010-06-01 |
publisher | The American Phytopathological Society |
record_format | Article |
series | Molecular Plant-Microbe Interactions |
spelling | doaj.art-afb3d9dcae944d9a99a3b2998f6631ad2022-12-21T20:00:54ZengThe American Phytopathological SocietyMolecular Plant-Microbe Interactions0894-02821943-77062010-06-0123679179810.1094/MPMI-23-6-0791Abscisic Acid Interacts Antagonistically with Salicylic Acid Signaling Pathway in Rice–Magnaporthe grisea InteractionChang-Jie JiangMasaki ShimonoShoji SuganoMikiko KojimaKatsumi YazawaRiichiro YoshidaHaruhiko InoueNagao HayashiHitoshi SakakibaraHiroshi TakatsujiPlant hormones play pivotal signaling roles in plant–pathogen interactions. Here, we report characterization of an antagonistic interaction of abscisic acid (ABA) with salicylic acid (SA) signaling pathways in the rice–Magnaporthe grisea interaction. Exogenous application of ABA drastically compromised the rice resistance to both compatible and incompatible M. grisea strains, indicating that ABA negatively regulates both basal and resistance gene–mediated blast resistance. ABA markedly suppressed the transcriptional upregulation of WRKY45 and OsNPR1, the two key components of the SA signaling pathway in rice, induced by SA or benzothiadiazole or by blast infection. Overexpression of OsNPR1 or WRKY45 largely negated the enhancement of blast susceptibility by ABA, suggesting that ABA acts upstream of WRKY45 and OsNPR1 in the rice SA pathway. ABA-responsive genes were induced during blast infection in a pattern reciprocal to those of WRKY45 and OsPR1b in the compatible rice–blast interaction but only marginally in the incompatible one. These results suggest that the balance of SA and ABA signaling is an important determinant for the outcome of the rice–M. grisea interaction. ABA was detected in hyphae and conidia of M. grisea as well as in culture media, implying that blast-fungus-derived ABA could play a role in triggering ABA signaling at host infection sites.https://apsjournals.apsnet.org/doi/10.1094/MPMI-23-6-0791 |
spellingShingle | Chang-Jie Jiang Masaki Shimono Shoji Sugano Mikiko Kojima Katsumi Yazawa Riichiro Yoshida Haruhiko Inoue Nagao Hayashi Hitoshi Sakakibara Hiroshi Takatsuji Abscisic Acid Interacts Antagonistically with Salicylic Acid Signaling Pathway in Rice–Magnaporthe grisea Interaction Molecular Plant-Microbe Interactions |
title | Abscisic Acid Interacts Antagonistically with Salicylic Acid Signaling Pathway in Rice–Magnaporthe grisea Interaction |
title_full | Abscisic Acid Interacts Antagonistically with Salicylic Acid Signaling Pathway in Rice–Magnaporthe grisea Interaction |
title_fullStr | Abscisic Acid Interacts Antagonistically with Salicylic Acid Signaling Pathway in Rice–Magnaporthe grisea Interaction |
title_full_unstemmed | Abscisic Acid Interacts Antagonistically with Salicylic Acid Signaling Pathway in Rice–Magnaporthe grisea Interaction |
title_short | Abscisic Acid Interacts Antagonistically with Salicylic Acid Signaling Pathway in Rice–Magnaporthe grisea Interaction |
title_sort | abscisic acid interacts antagonistically with salicylic acid signaling pathway in rice magnaporthe grisea interaction |
url | https://apsjournals.apsnet.org/doi/10.1094/MPMI-23-6-0791 |
work_keys_str_mv | AT changjiejiang abscisicacidinteractsantagonisticallywithsalicylicacidsignalingpathwayinricemagnaporthegriseainteraction AT masakishimono abscisicacidinteractsantagonisticallywithsalicylicacidsignalingpathwayinricemagnaporthegriseainteraction AT shojisugano abscisicacidinteractsantagonisticallywithsalicylicacidsignalingpathwayinricemagnaporthegriseainteraction AT mikikokojima abscisicacidinteractsantagonisticallywithsalicylicacidsignalingpathwayinricemagnaporthegriseainteraction AT katsumiyazawa abscisicacidinteractsantagonisticallywithsalicylicacidsignalingpathwayinricemagnaporthegriseainteraction AT riichiroyoshida abscisicacidinteractsantagonisticallywithsalicylicacidsignalingpathwayinricemagnaporthegriseainteraction AT haruhikoinoue abscisicacidinteractsantagonisticallywithsalicylicacidsignalingpathwayinricemagnaporthegriseainteraction AT nagaohayashi abscisicacidinteractsantagonisticallywithsalicylicacidsignalingpathwayinricemagnaporthegriseainteraction AT hitoshisakakibara abscisicacidinteractsantagonisticallywithsalicylicacidsignalingpathwayinricemagnaporthegriseainteraction AT hiroshitakatsuji abscisicacidinteractsantagonisticallywithsalicylicacidsignalingpathwayinricemagnaporthegriseainteraction |