Cargando…
Two NIS1-like proteins from apple canker pathogen (Valsa mali) play distinct roles in plant recognition and pathogen virulence
Conserved effectors produced by phytopathogens play critical roles in plant-microbe interactions. NIS1-like proteins represent a newly identified family of effectors distributed in multiple fungal species. However, their biological functions in a majority of pathogenic fungi remain largely elusive a...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442039/ https://www.ncbi.nlm.nih.gov/pubmed/37676376 http://dx.doi.org/10.1007/s44154-021-00031-0 |
_version_ | 1785093499944697856 |
---|---|
author | Nie, Jiajun Zhou, Wenjing Lin, Yonghui Liu, Zhaoyang Yin, Zhiyuan Huang, Lili |
author_facet | Nie, Jiajun Zhou, Wenjing Lin, Yonghui Liu, Zhaoyang Yin, Zhiyuan Huang, Lili |
author_sort | Nie, Jiajun |
collection | PubMed |
description | Conserved effectors produced by phytopathogens play critical roles in plant-microbe interactions. NIS1-like proteins represent a newly identified family of effectors distributed in multiple fungal species. However, their biological functions in a majority of pathogenic fungi remain largely elusive and require further investigation. In this study, we characterized two NIS1-like proteins VmNIS1 and VmNIS2 from Valsa mali, the causal agent of apple Valsa canker. Both of these two proteins were predicted to be secreted. Using agroinfiltration, we found that VmNIS1 induced intense cell death, whereas VmNIS2 suppressed INF1 elicitin-triggered cell death in Nicotiana benthamiana. Treatment of N. benthamiana with VmNIS1 recombinant protein produced by Escherichia coli activated a series of immune responses and enhanced plant disease resistance against Phytophthora capsici. In contrast, VmNIS2 suppressed plant immune responses and promoted P. capsici infection when transiently expressed in N. benthamiana. Both VmNIS1 and VmNIS2 were shown to be highly induced at late stage of V. mali infection. By individually knocking out of these two genes in V. mali, however, only VmNIS2 was shown to be required for pathogen virulence as well as tolerance to oxidative stress. Notably, we further showed that C-terminal extension of VmNIS1 was essential for plant recognition and VmNIS2 may escape plant detection via sequence truncation. Our data collectively indicate that VmNIS1 and VmNIS2 play distinct roles in plant recognition and pathogen virulence, which provided new insights into the function of NIS1-like proteins in plant-microbe interactions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s44154-021-00031-0. |
format | Online Article Text |
id | pubmed-10442039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-104420392023-08-28 Two NIS1-like proteins from apple canker pathogen (Valsa mali) play distinct roles in plant recognition and pathogen virulence Nie, Jiajun Zhou, Wenjing Lin, Yonghui Liu, Zhaoyang Yin, Zhiyuan Huang, Lili Stress Biol Original Paper Conserved effectors produced by phytopathogens play critical roles in plant-microbe interactions. NIS1-like proteins represent a newly identified family of effectors distributed in multiple fungal species. However, their biological functions in a majority of pathogenic fungi remain largely elusive and require further investigation. In this study, we characterized two NIS1-like proteins VmNIS1 and VmNIS2 from Valsa mali, the causal agent of apple Valsa canker. Both of these two proteins were predicted to be secreted. Using agroinfiltration, we found that VmNIS1 induced intense cell death, whereas VmNIS2 suppressed INF1 elicitin-triggered cell death in Nicotiana benthamiana. Treatment of N. benthamiana with VmNIS1 recombinant protein produced by Escherichia coli activated a series of immune responses and enhanced plant disease resistance against Phytophthora capsici. In contrast, VmNIS2 suppressed plant immune responses and promoted P. capsici infection when transiently expressed in N. benthamiana. Both VmNIS1 and VmNIS2 were shown to be highly induced at late stage of V. mali infection. By individually knocking out of these two genes in V. mali, however, only VmNIS2 was shown to be required for pathogen virulence as well as tolerance to oxidative stress. Notably, we further showed that C-terminal extension of VmNIS1 was essential for plant recognition and VmNIS2 may escape plant detection via sequence truncation. Our data collectively indicate that VmNIS1 and VmNIS2 play distinct roles in plant recognition and pathogen virulence, which provided new insights into the function of NIS1-like proteins in plant-microbe interactions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s44154-021-00031-0. Springer Singapore 2022-01-17 /pmc/articles/PMC10442039/ /pubmed/37676376 http://dx.doi.org/10.1007/s44154-021-00031-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Paper Nie, Jiajun Zhou, Wenjing Lin, Yonghui Liu, Zhaoyang Yin, Zhiyuan Huang, Lili Two NIS1-like proteins from apple canker pathogen (Valsa mali) play distinct roles in plant recognition and pathogen virulence |
title | Two NIS1-like proteins from apple canker pathogen (Valsa mali) play distinct roles in plant recognition and pathogen virulence |
title_full | Two NIS1-like proteins from apple canker pathogen (Valsa mali) play distinct roles in plant recognition and pathogen virulence |
title_fullStr | Two NIS1-like proteins from apple canker pathogen (Valsa mali) play distinct roles in plant recognition and pathogen virulence |
title_full_unstemmed | Two NIS1-like proteins from apple canker pathogen (Valsa mali) play distinct roles in plant recognition and pathogen virulence |
title_short | Two NIS1-like proteins from apple canker pathogen (Valsa mali) play distinct roles in plant recognition and pathogen virulence |
title_sort | two nis1-like proteins from apple canker pathogen (valsa mali) play distinct roles in plant recognition and pathogen virulence |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442039/ https://www.ncbi.nlm.nih.gov/pubmed/37676376 http://dx.doi.org/10.1007/s44154-021-00031-0 |
work_keys_str_mv | AT niejiajun twonis1likeproteinsfromapplecankerpathogenvalsamaliplaydistinctrolesinplantrecognitionandpathogenvirulence AT zhouwenjing twonis1likeproteinsfromapplecankerpathogenvalsamaliplaydistinctrolesinplantrecognitionandpathogenvirulence AT linyonghui twonis1likeproteinsfromapplecankerpathogenvalsamaliplaydistinctrolesinplantrecognitionandpathogenvirulence AT liuzhaoyang twonis1likeproteinsfromapplecankerpathogenvalsamaliplaydistinctrolesinplantrecognitionandpathogenvirulence AT yinzhiyuan twonis1likeproteinsfromapplecankerpathogenvalsamaliplaydistinctrolesinplantrecognitionandpathogenvirulence AT huanglili twonis1likeproteinsfromapplecankerpathogenvalsamaliplaydistinctrolesinplantrecognitionandpathogenvirulence |