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Msp40 effector of root-knot nematode manipulates plant immunity to facilitate parasitism
Root-knot nematodes (RKNs) are obligate biotrophic parasites that invade plant roots and engage in prolonged and intimate relationships with their hosts. Nematode secretions, some of which have immunosuppressing activity, play essential roles in successful parasitism; however, their mechanisms of ac...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726423/ https://www.ncbi.nlm.nih.gov/pubmed/26797310 http://dx.doi.org/10.1038/srep19443 |
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author | Niu, Junhai Liu, Pei Liu, Qian Chen, Changlong Guo, Quanxin Yin, Junmei Yang, Guangsui Jian, Heng |
author_facet | Niu, Junhai Liu, Pei Liu, Qian Chen, Changlong Guo, Quanxin Yin, Junmei Yang, Guangsui Jian, Heng |
author_sort | Niu, Junhai |
collection | PubMed |
description | Root-knot nematodes (RKNs) are obligate biotrophic parasites that invade plant roots and engage in prolonged and intimate relationships with their hosts. Nematode secretions, some of which have immunosuppressing activity, play essential roles in successful parasitism; however, their mechanisms of action remain largely unknown. Here, we show that the RKN-specific gene MiMsp40, cloned from Meloidogyne incognita, is expressed exclusively in subventral oesophageal gland cells and is strongly upregulated during early parasitic stages. Arabidopsis plants overexpressing MiMsp40 were more susceptible to nematode infection than were wild type plants. Conversely, the host-derived MiMsp40 RNAi suppressed nematode parasitism and/or reproduction. Moreover, overexpression of MiMsp40 in plants suppressed the deposition of callose and the expression of marker genes for bacterial elicitor elf18-triggered immunity. Transient expression of MiMsp40 prevented Bax-triggered defence-related programmed cell death. Co-agroinfiltration assays indicated that MiMsp40 also suppressed macroscopic cell death triggered by MAPK cascades or by the ETI cognate elicitors R3a/Avr3a. Together, these results demonstrate that MiMsp40 is a novel Meloidogyne-specific effector that is injected into plant cells by early parasitic stages of the nematode and that plays a role in suppressing PTI and/or ETI signals to facilitate RKN parasitism. |
format | Online Article Text |
id | pubmed-4726423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47264232016-01-27 Msp40 effector of root-knot nematode manipulates plant immunity to facilitate parasitism Niu, Junhai Liu, Pei Liu, Qian Chen, Changlong Guo, Quanxin Yin, Junmei Yang, Guangsui Jian, Heng Sci Rep Article Root-knot nematodes (RKNs) are obligate biotrophic parasites that invade plant roots and engage in prolonged and intimate relationships with their hosts. Nematode secretions, some of which have immunosuppressing activity, play essential roles in successful parasitism; however, their mechanisms of action remain largely unknown. Here, we show that the RKN-specific gene MiMsp40, cloned from Meloidogyne incognita, is expressed exclusively in subventral oesophageal gland cells and is strongly upregulated during early parasitic stages. Arabidopsis plants overexpressing MiMsp40 were more susceptible to nematode infection than were wild type plants. Conversely, the host-derived MiMsp40 RNAi suppressed nematode parasitism and/or reproduction. Moreover, overexpression of MiMsp40 in plants suppressed the deposition of callose and the expression of marker genes for bacterial elicitor elf18-triggered immunity. Transient expression of MiMsp40 prevented Bax-triggered defence-related programmed cell death. Co-agroinfiltration assays indicated that MiMsp40 also suppressed macroscopic cell death triggered by MAPK cascades or by the ETI cognate elicitors R3a/Avr3a. Together, these results demonstrate that MiMsp40 is a novel Meloidogyne-specific effector that is injected into plant cells by early parasitic stages of the nematode and that plays a role in suppressing PTI and/or ETI signals to facilitate RKN parasitism. Nature Publishing Group 2016-01-22 /pmc/articles/PMC4726423/ /pubmed/26797310 http://dx.doi.org/10.1038/srep19443 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Niu, Junhai Liu, Pei Liu, Qian Chen, Changlong Guo, Quanxin Yin, Junmei Yang, Guangsui Jian, Heng Msp40 effector of root-knot nematode manipulates plant immunity to facilitate parasitism |
title | Msp40 effector of root-knot nematode manipulates plant immunity to facilitate parasitism |
title_full | Msp40 effector of root-knot nematode manipulates plant immunity to facilitate parasitism |
title_fullStr | Msp40 effector of root-knot nematode manipulates plant immunity to facilitate parasitism |
title_full_unstemmed | Msp40 effector of root-knot nematode manipulates plant immunity to facilitate parasitism |
title_short | Msp40 effector of root-knot nematode manipulates plant immunity to facilitate parasitism |
title_sort | msp40 effector of root-knot nematode manipulates plant immunity to facilitate parasitism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726423/ https://www.ncbi.nlm.nih.gov/pubmed/26797310 http://dx.doi.org/10.1038/srep19443 |
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