Cargando…
Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis
Plant diseases caused by fungi and oomycetes pose an increasing threat to food security and ecosystem health worldwide. These filamentous pathogens, while taxonomically distinct, modulate host defense responses by secreting effectors, which are typically identified based on the presence of signal pe...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4348438/ https://www.ncbi.nlm.nih.gov/pubmed/25156390 http://dx.doi.org/10.1038/ncomms5686 |
_version_ | 1782359920079798272 |
---|---|
author | Liu, Tingli Song, Tianqiao Zhang, Xiong Yuan, Hongbo Su, Liming Li, Wanlin Xu, Jing Liu, Shiheng Chen, Linlin Chen, Tianzi Zhang, Meixiang Gu, Lichuan Zhang, Baolong Dou, Daolong |
author_facet | Liu, Tingli Song, Tianqiao Zhang, Xiong Yuan, Hongbo Su, Liming Li, Wanlin Xu, Jing Liu, Shiheng Chen, Linlin Chen, Tianzi Zhang, Meixiang Gu, Lichuan Zhang, Baolong Dou, Daolong |
author_sort | Liu, Tingli |
collection | PubMed |
description | Plant diseases caused by fungi and oomycetes pose an increasing threat to food security and ecosystem health worldwide. These filamentous pathogens, while taxonomically distinct, modulate host defense responses by secreting effectors, which are typically identified based on the presence of signal peptides. Here we show that Phytophthora sojae and Verticillium dahliae secrete isochorismatases (PsIsc1 and VdIsc1, respectively) that are required for full pathogenesis. PsIsc1 and VdIsc1 can suppress salicylate-mediated innate immunity in planta and hydrolyse isochorismate in vitro. A conserved triad of catalytic residues is essential for both functions. Thus, the two proteins are isochorismatase effectors that disrupt the plant salicylate metabolism pathway by suppressing its precursor. Furthermore, these proteins lack signal peptides, but exhibit characteristics that lead to unconventional secretion. Therefore, this secretion pathway is a novel mechanism for delivering effectors and might play an important role in host–pathogen interactions. |
format | Online Article Text |
id | pubmed-4348438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43484382015-03-13 Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis Liu, Tingli Song, Tianqiao Zhang, Xiong Yuan, Hongbo Su, Liming Li, Wanlin Xu, Jing Liu, Shiheng Chen, Linlin Chen, Tianzi Zhang, Meixiang Gu, Lichuan Zhang, Baolong Dou, Daolong Nat Commun Article Plant diseases caused by fungi and oomycetes pose an increasing threat to food security and ecosystem health worldwide. These filamentous pathogens, while taxonomically distinct, modulate host defense responses by secreting effectors, which are typically identified based on the presence of signal peptides. Here we show that Phytophthora sojae and Verticillium dahliae secrete isochorismatases (PsIsc1 and VdIsc1, respectively) that are required for full pathogenesis. PsIsc1 and VdIsc1 can suppress salicylate-mediated innate immunity in planta and hydrolyse isochorismate in vitro. A conserved triad of catalytic residues is essential for both functions. Thus, the two proteins are isochorismatase effectors that disrupt the plant salicylate metabolism pathway by suppressing its precursor. Furthermore, these proteins lack signal peptides, but exhibit characteristics that lead to unconventional secretion. Therefore, this secretion pathway is a novel mechanism for delivering effectors and might play an important role in host–pathogen interactions. Nature Pub. Group 2014-08-26 /pmc/articles/PMC4348438/ /pubmed/25156390 http://dx.doi.org/10.1038/ncomms5686 Text en Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 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 Liu, Tingli Song, Tianqiao Zhang, Xiong Yuan, Hongbo Su, Liming Li, Wanlin Xu, Jing Liu, Shiheng Chen, Linlin Chen, Tianzi Zhang, Meixiang Gu, Lichuan Zhang, Baolong Dou, Daolong Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis |
title | Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis |
title_full | Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis |
title_fullStr | Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis |
title_full_unstemmed | Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis |
title_short | Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis |
title_sort | unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4348438/ https://www.ncbi.nlm.nih.gov/pubmed/25156390 http://dx.doi.org/10.1038/ncomms5686 |
work_keys_str_mv | AT liutingli unconventionallysecretedeffectorsoftwofilamentouspathogenstargetplantsalicylatebiosynthesis AT songtianqiao unconventionallysecretedeffectorsoftwofilamentouspathogenstargetplantsalicylatebiosynthesis AT zhangxiong unconventionallysecretedeffectorsoftwofilamentouspathogenstargetplantsalicylatebiosynthesis AT yuanhongbo unconventionallysecretedeffectorsoftwofilamentouspathogenstargetplantsalicylatebiosynthesis AT suliming unconventionallysecretedeffectorsoftwofilamentouspathogenstargetplantsalicylatebiosynthesis AT liwanlin unconventionallysecretedeffectorsoftwofilamentouspathogenstargetplantsalicylatebiosynthesis AT xujing unconventionallysecretedeffectorsoftwofilamentouspathogenstargetplantsalicylatebiosynthesis AT liushiheng unconventionallysecretedeffectorsoftwofilamentouspathogenstargetplantsalicylatebiosynthesis AT chenlinlin unconventionallysecretedeffectorsoftwofilamentouspathogenstargetplantsalicylatebiosynthesis AT chentianzi unconventionallysecretedeffectorsoftwofilamentouspathogenstargetplantsalicylatebiosynthesis AT zhangmeixiang unconventionallysecretedeffectorsoftwofilamentouspathogenstargetplantsalicylatebiosynthesis AT gulichuan unconventionallysecretedeffectorsoftwofilamentouspathogenstargetplantsalicylatebiosynthesis AT zhangbaolong unconventionallysecretedeffectorsoftwofilamentouspathogenstargetplantsalicylatebiosynthesis AT doudaolong unconventionallysecretedeffectorsoftwofilamentouspathogenstargetplantsalicylatebiosynthesis |