Cargando…
A novel pine wood nematode effector, BxSCD1, suppresses plant immunity and interacts with an ethylene‐forming enzyme in pine
The plant‐parasitic nematode Bursaphelenchus xylophilus, the causal agent of pine wilt disease (PWD), causes enormous economic loss every year. Currently, little is known about the pathogenic mechanisms of PWD. Several effectors have been identified in B. xylophilus, but their functions and host tar...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518578/ https://www.ncbi.nlm.nih.gov/pubmed/34396673 http://dx.doi.org/10.1111/mpp.13121 |
_version_ | 1784584256811433984 |
---|---|
author | Wen, Tong‐Yue Wu, Xiao‐Qin Hu, Long‐Jiao Qiu, Yi‐Jun Rui, Lin Zhang, Yan Ding, Xiao‐Lei Ye, Jian‐Ren |
author_facet | Wen, Tong‐Yue Wu, Xiao‐Qin Hu, Long‐Jiao Qiu, Yi‐Jun Rui, Lin Zhang, Yan Ding, Xiao‐Lei Ye, Jian‐Ren |
author_sort | Wen, Tong‐Yue |
collection | PubMed |
description | The plant‐parasitic nematode Bursaphelenchus xylophilus, the causal agent of pine wilt disease (PWD), causes enormous economic loss every year. Currently, little is known about the pathogenic mechanisms of PWD. Several effectors have been identified in B. xylophilus, but their functions and host targets have yet to be elucidated. Here, we demonstrated that BxSCD1 suppresses cell death and inhibits B. xylophilus PAMP BxCDP1‐triggered immunity in Nicotiana benthamiana and Pinus thunbergii. BxSCD1 was transcriptionally upregulated in the early stage of B. xylophilus infection. In situ hybridization experiments showed that BxSCD1 was specifically expressed in the dorsal glands and intestine. Cysteine residues are essential for the function of BxSCD1. Transient expression of BxSCD1 in N. benthamiana revealed that it was primarily targeted to the cytoplasm and nucleus. The morbidity was significantly reduced in P. thunbergii infected with B. xylophilus when BxSCD1 was silenced. We identified 1‐aminocyclopropane‐1‐carboxylate oxidase 1, the actual ethylene‐forming enzyme, as a host target of BxSCD1 by yeast two‐hybrid and coimmunoprecipitation. Overall, this study illustrated that BxSCD1 played a critical role in the B. xylophilus–plant interaction. |
format | Online Article Text |
id | pubmed-8518578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85185782021-10-22 A novel pine wood nematode effector, BxSCD1, suppresses plant immunity and interacts with an ethylene‐forming enzyme in pine Wen, Tong‐Yue Wu, Xiao‐Qin Hu, Long‐Jiao Qiu, Yi‐Jun Rui, Lin Zhang, Yan Ding, Xiao‐Lei Ye, Jian‐Ren Mol Plant Pathol Original Articles The plant‐parasitic nematode Bursaphelenchus xylophilus, the causal agent of pine wilt disease (PWD), causes enormous economic loss every year. Currently, little is known about the pathogenic mechanisms of PWD. Several effectors have been identified in B. xylophilus, but their functions and host targets have yet to be elucidated. Here, we demonstrated that BxSCD1 suppresses cell death and inhibits B. xylophilus PAMP BxCDP1‐triggered immunity in Nicotiana benthamiana and Pinus thunbergii. BxSCD1 was transcriptionally upregulated in the early stage of B. xylophilus infection. In situ hybridization experiments showed that BxSCD1 was specifically expressed in the dorsal glands and intestine. Cysteine residues are essential for the function of BxSCD1. Transient expression of BxSCD1 in N. benthamiana revealed that it was primarily targeted to the cytoplasm and nucleus. The morbidity was significantly reduced in P. thunbergii infected with B. xylophilus when BxSCD1 was silenced. We identified 1‐aminocyclopropane‐1‐carboxylate oxidase 1, the actual ethylene‐forming enzyme, as a host target of BxSCD1 by yeast two‐hybrid and coimmunoprecipitation. Overall, this study illustrated that BxSCD1 played a critical role in the B. xylophilus–plant interaction. John Wiley and Sons Inc. 2021-08-16 /pmc/articles/PMC8518578/ /pubmed/34396673 http://dx.doi.org/10.1111/mpp.13121 Text en © 2021 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Wen, Tong‐Yue Wu, Xiao‐Qin Hu, Long‐Jiao Qiu, Yi‐Jun Rui, Lin Zhang, Yan Ding, Xiao‐Lei Ye, Jian‐Ren A novel pine wood nematode effector, BxSCD1, suppresses plant immunity and interacts with an ethylene‐forming enzyme in pine |
title | A novel pine wood nematode effector, BxSCD1, suppresses plant immunity and interacts with an ethylene‐forming enzyme in pine |
title_full | A novel pine wood nematode effector, BxSCD1, suppresses plant immunity and interacts with an ethylene‐forming enzyme in pine |
title_fullStr | A novel pine wood nematode effector, BxSCD1, suppresses plant immunity and interacts with an ethylene‐forming enzyme in pine |
title_full_unstemmed | A novel pine wood nematode effector, BxSCD1, suppresses plant immunity and interacts with an ethylene‐forming enzyme in pine |
title_short | A novel pine wood nematode effector, BxSCD1, suppresses plant immunity and interacts with an ethylene‐forming enzyme in pine |
title_sort | novel pine wood nematode effector, bxscd1, suppresses plant immunity and interacts with an ethylene‐forming enzyme in pine |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518578/ https://www.ncbi.nlm.nih.gov/pubmed/34396673 http://dx.doi.org/10.1111/mpp.13121 |
work_keys_str_mv | AT wentongyue anovelpinewoodnematodeeffectorbxscd1suppressesplantimmunityandinteractswithanethyleneformingenzymeinpine AT wuxiaoqin anovelpinewoodnematodeeffectorbxscd1suppressesplantimmunityandinteractswithanethyleneformingenzymeinpine AT hulongjiao anovelpinewoodnematodeeffectorbxscd1suppressesplantimmunityandinteractswithanethyleneformingenzymeinpine AT qiuyijun anovelpinewoodnematodeeffectorbxscd1suppressesplantimmunityandinteractswithanethyleneformingenzymeinpine AT ruilin anovelpinewoodnematodeeffectorbxscd1suppressesplantimmunityandinteractswithanethyleneformingenzymeinpine AT zhangyan anovelpinewoodnematodeeffectorbxscd1suppressesplantimmunityandinteractswithanethyleneformingenzymeinpine AT dingxiaolei anovelpinewoodnematodeeffectorbxscd1suppressesplantimmunityandinteractswithanethyleneformingenzymeinpine AT yejianren anovelpinewoodnematodeeffectorbxscd1suppressesplantimmunityandinteractswithanethyleneformingenzymeinpine AT wentongyue novelpinewoodnematodeeffectorbxscd1suppressesplantimmunityandinteractswithanethyleneformingenzymeinpine AT wuxiaoqin novelpinewoodnematodeeffectorbxscd1suppressesplantimmunityandinteractswithanethyleneformingenzymeinpine AT hulongjiao novelpinewoodnematodeeffectorbxscd1suppressesplantimmunityandinteractswithanethyleneformingenzymeinpine AT qiuyijun novelpinewoodnematodeeffectorbxscd1suppressesplantimmunityandinteractswithanethyleneformingenzymeinpine AT ruilin novelpinewoodnematodeeffectorbxscd1suppressesplantimmunityandinteractswithanethyleneformingenzymeinpine AT zhangyan novelpinewoodnematodeeffectorbxscd1suppressesplantimmunityandinteractswithanethyleneformingenzymeinpine AT dingxiaolei novelpinewoodnematodeeffectorbxscd1suppressesplantimmunityandinteractswithanethyleneformingenzymeinpine AT yejianren novelpinewoodnematodeeffectorbxscd1suppressesplantimmunityandinteractswithanethyleneformingenzymeinpine |