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A novel nematode effector suppresses plant immunity by activating host reactive oxygen species‐scavenging system

Evidence is emerging that plant‐parasitic nematodes can secrete effectors to interfere with the host immune response, but it remains unknown how these effectors can conquer host immune responses. Here, we depict a novel effector, MjTTL5, that could suppress plant immune response. Immunolocalization...

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Detalles Bibliográficos
Autores principales: Lin, Borong, Zhuo, Kan, Chen, Shiyan, Hu, Lili, Sun, Longhua, Wang, Xiaohong, Zhang, Lian‐Hui, Liao, Jinling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5057313/
https://www.ncbi.nlm.nih.gov/pubmed/26484653
http://dx.doi.org/10.1111/nph.13701
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author Lin, Borong
Zhuo, Kan
Chen, Shiyan
Hu, Lili
Sun, Longhua
Wang, Xiaohong
Zhang, Lian‐Hui
Liao, Jinling
author_facet Lin, Borong
Zhuo, Kan
Chen, Shiyan
Hu, Lili
Sun, Longhua
Wang, Xiaohong
Zhang, Lian‐Hui
Liao, Jinling
author_sort Lin, Borong
collection PubMed
description Evidence is emerging that plant‐parasitic nematodes can secrete effectors to interfere with the host immune response, but it remains unknown how these effectors can conquer host immune responses. Here, we depict a novel effector, MjTTL5, that could suppress plant immune response. Immunolocalization and transcriptional analyses showed that MjTTL5 is expressed specifically within the subventral gland of Meloidogyne javanica and up‐regulated in the early parasitic stage of the nematode. Transgenic Arabidopsis lines expressing MjTTL5 were significantly more susceptible to M. javanica infection than wild‐type plants, and vice versa, in planta silencing of MjTTL5 substantially increased plant resistance to M. javanica. Yeast two‐hybrid, coimmunoprecipitation and bimolecular fluorescent complementation assays showed that MjTTL5 interacts specifically with Arabidopsis ferredoxin : thioredoxin reductase catalytic subunit (AtFTRc), a key component of host antioxidant system. The expression of AtFTRc is induced by the infection of M. javanica. Interaction between AtFTRc and MjTTL could drastically increase host reactive oxygen species‐scavenging activity, and result in suppression of plant basal defenses and attenuation of host resistance to the nematode infection. Our results demonstrate that the host ferredoxin : thioredoxin system can be exploited cunningly by M. javanica, revealing a novel mechanism utilized by plant–parasitic nematodes to subjugate plant innate immunity and thereby promoting parasitism.
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spelling pubmed-50573132016-10-19 A novel nematode effector suppresses plant immunity by activating host reactive oxygen species‐scavenging system Lin, Borong Zhuo, Kan Chen, Shiyan Hu, Lili Sun, Longhua Wang, Xiaohong Zhang, Lian‐Hui Liao, Jinling New Phytol Research Evidence is emerging that plant‐parasitic nematodes can secrete effectors to interfere with the host immune response, but it remains unknown how these effectors can conquer host immune responses. Here, we depict a novel effector, MjTTL5, that could suppress plant immune response. Immunolocalization and transcriptional analyses showed that MjTTL5 is expressed specifically within the subventral gland of Meloidogyne javanica and up‐regulated in the early parasitic stage of the nematode. Transgenic Arabidopsis lines expressing MjTTL5 were significantly more susceptible to M. javanica infection than wild‐type plants, and vice versa, in planta silencing of MjTTL5 substantially increased plant resistance to M. javanica. Yeast two‐hybrid, coimmunoprecipitation and bimolecular fluorescent complementation assays showed that MjTTL5 interacts specifically with Arabidopsis ferredoxin : thioredoxin reductase catalytic subunit (AtFTRc), a key component of host antioxidant system. The expression of AtFTRc is induced by the infection of M. javanica. Interaction between AtFTRc and MjTTL could drastically increase host reactive oxygen species‐scavenging activity, and result in suppression of plant basal defenses and attenuation of host resistance to the nematode infection. Our results demonstrate that the host ferredoxin : thioredoxin system can be exploited cunningly by M. javanica, revealing a novel mechanism utilized by plant–parasitic nematodes to subjugate plant innate immunity and thereby promoting parasitism. John Wiley and Sons Inc. 2016-02 2015-10-20 /pmc/articles/PMC5057313/ /pubmed/26484653 http://dx.doi.org/10.1111/nph.13701 Text en © 2015 The Authors. New Phytologist © 2015 New Phytologist Trust This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/3.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Lin, Borong
Zhuo, Kan
Chen, Shiyan
Hu, Lili
Sun, Longhua
Wang, Xiaohong
Zhang, Lian‐Hui
Liao, Jinling
A novel nematode effector suppresses plant immunity by activating host reactive oxygen species‐scavenging system
title A novel nematode effector suppresses plant immunity by activating host reactive oxygen species‐scavenging system
title_full A novel nematode effector suppresses plant immunity by activating host reactive oxygen species‐scavenging system
title_fullStr A novel nematode effector suppresses plant immunity by activating host reactive oxygen species‐scavenging system
title_full_unstemmed A novel nematode effector suppresses plant immunity by activating host reactive oxygen species‐scavenging system
title_short A novel nematode effector suppresses plant immunity by activating host reactive oxygen species‐scavenging system
title_sort novel nematode effector suppresses plant immunity by activating host reactive oxygen species‐scavenging system
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5057313/
https://www.ncbi.nlm.nih.gov/pubmed/26484653
http://dx.doi.org/10.1111/nph.13701
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