A Meloidogyne incognita effector MiISE5 suppresses programmed cell death to promote parasitism in host plant

Abstract Root-knot nematodes (RKNs) are highly specialized parasites that interact with their host plants using a range of strategies. The esophageal glands are the main places where nematodes synthesize effector proteins, which play central roles in successful invasion. The Meloidogyne incognita ef...

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Autores principales: Qianqian Shi, Zhenchuan Mao, Xi Zhang, Xiaoping Zhang, Yunsheng Wang, Jian Ling, Runmao Lin, Denghui Li, Xincong Kang, Wenxian Sun, Bingyan Xie
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Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/f21f3c7d9f6e47c8824de02bacdc8cf5
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spelling oai:doaj.org-article:f21f3c7d9f6e47c8824de02bacdc8cf52021-12-02T12:32:35ZA Meloidogyne incognita effector MiISE5 suppresses programmed cell death to promote parasitism in host plant10.1038/s41598-018-24999-42045-2322https://doaj.org/article/f21f3c7d9f6e47c8824de02bacdc8cf52018-05-01T00:00:00Zhttps://doi.org/10.1038/s41598-018-24999-4https://doaj.org/toc/2045-2322Abstract Root-knot nematodes (RKNs) are highly specialized parasites that interact with their host plants using a range of strategies. The esophageal glands are the main places where nematodes synthesize effector proteins, which play central roles in successful invasion. The Meloidogyne incognita effector MiISE5 is exclusively expressed within the subventral esophageal cells and is upregulated during early parasitic stages. In this study, we show that MiISE5 can be secreted to barley cells through infectious hyphae of Magnaporthe oryzae. Transgenic Arabidopsis plants expressing MiISE5 became significantly more susceptible to M. incognita. Inversely, the tobacco rattle virus (TRV)-mediated silence of MiISE5 decreased nematode parasitism. Moreover, transient expression of MiISE5 suppressed cell death caused by Burkholderia glumae in Nicotiana benthamiana. Based on transcriptome analysis of MiISE5 transgenic sample and the wild-type (WT) sample, we obtained 261 DEGs, and the results of GO and KEGG enrichment analysis indicate that MiISE5 can interfere with various metabolic and signaling pathways, especially the JA signaling pathway, to facilitate nematode parasitism. Results from the present study suggest that MiISE5 plays an important role during the early stages of parasitism and provides evidence to decipher the molecular mechanisms underlying the manipulation of host immune defense responses by M. incognita.Qianqian ShiZhenchuan MaoXi ZhangXiaoping ZhangYunsheng WangJian LingRunmao LinDenghui LiXincong KangWenxian SunBingyan XieNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 8, Iss 1, Pp 1-12 (2018)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Qianqian Shi
Zhenchuan Mao
Xi Zhang
Xiaoping Zhang
Yunsheng Wang
Jian Ling
Runmao Lin
Denghui Li
Xincong Kang
Wenxian Sun
Bingyan Xie
A Meloidogyne incognita effector MiISE5 suppresses programmed cell death to promote parasitism in host plant
description Abstract Root-knot nematodes (RKNs) are highly specialized parasites that interact with their host plants using a range of strategies. The esophageal glands are the main places where nematodes synthesize effector proteins, which play central roles in successful invasion. The Meloidogyne incognita effector MiISE5 is exclusively expressed within the subventral esophageal cells and is upregulated during early parasitic stages. In this study, we show that MiISE5 can be secreted to barley cells through infectious hyphae of Magnaporthe oryzae. Transgenic Arabidopsis plants expressing MiISE5 became significantly more susceptible to M. incognita. Inversely, the tobacco rattle virus (TRV)-mediated silence of MiISE5 decreased nematode parasitism. Moreover, transient expression of MiISE5 suppressed cell death caused by Burkholderia glumae in Nicotiana benthamiana. Based on transcriptome analysis of MiISE5 transgenic sample and the wild-type (WT) sample, we obtained 261 DEGs, and the results of GO and KEGG enrichment analysis indicate that MiISE5 can interfere with various metabolic and signaling pathways, especially the JA signaling pathway, to facilitate nematode parasitism. Results from the present study suggest that MiISE5 plays an important role during the early stages of parasitism and provides evidence to decipher the molecular mechanisms underlying the manipulation of host immune defense responses by M. incognita.
format article
author Qianqian Shi
Zhenchuan Mao
Xi Zhang
Xiaoping Zhang
Yunsheng Wang
Jian Ling
Runmao Lin
Denghui Li
Xincong Kang
Wenxian Sun
Bingyan Xie
author_facet Qianqian Shi
Zhenchuan Mao
Xi Zhang
Xiaoping Zhang
Yunsheng Wang
Jian Ling
Runmao Lin
Denghui Li
Xincong Kang
Wenxian Sun
Bingyan Xie
author_sort Qianqian Shi
title A Meloidogyne incognita effector MiISE5 suppresses programmed cell death to promote parasitism in host plant
title_short A Meloidogyne incognita effector MiISE5 suppresses programmed cell death to promote parasitism in host plant
title_full A Meloidogyne incognita effector MiISE5 suppresses programmed cell death to promote parasitism in host plant
title_fullStr A Meloidogyne incognita effector MiISE5 suppresses programmed cell death to promote parasitism in host plant
title_full_unstemmed A Meloidogyne incognita effector MiISE5 suppresses programmed cell death to promote parasitism in host plant
title_sort meloidogyne incognita effector miise5 suppresses programmed cell death to promote parasitism in host plant
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/f21f3c7d9f6e47c8824de02bacdc8cf5
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