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Phytophthora infestans RXLR effectors act in concert at diverse subcellular locations to enhance host colonization
Oomycetes such as the potato blight pathogen Phytophthora infestans deliver RXLR effectors into plant cells to manipulate host processes and promote disease. Knowledge of where they localize inside host cells is important in understanding their function. Fifty-two P. infestans RXLR effectors (PiRXLR...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305197/ https://www.ncbi.nlm.nih.gov/pubmed/30329083 http://dx.doi.org/10.1093/jxb/ery360 |
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author | Wang, Shumei McLellan, Hazel Bukharova, Tatyana He, Qin Murphy, Fraser Shi, Jiayang Sun, Shaohui van Weymers, Pauline Ren, Yajuan Thilliez, Gaetan Wang, Haixia Chen, Xinwei Engelhardt, Stefan Vleeshouwers, Vivianne Gilroy, Eleanor M Whisson, Stephen C Hein, Ingo Wang, Xiaodan Tian, Zhendong Birch, Paul R J Boevink, Petra C |
author_facet | Wang, Shumei McLellan, Hazel Bukharova, Tatyana He, Qin Murphy, Fraser Shi, Jiayang Sun, Shaohui van Weymers, Pauline Ren, Yajuan Thilliez, Gaetan Wang, Haixia Chen, Xinwei Engelhardt, Stefan Vleeshouwers, Vivianne Gilroy, Eleanor M Whisson, Stephen C Hein, Ingo Wang, Xiaodan Tian, Zhendong Birch, Paul R J Boevink, Petra C |
author_sort | Wang, Shumei |
collection | PubMed |
description | Oomycetes such as the potato blight pathogen Phytophthora infestans deliver RXLR effectors into plant cells to manipulate host processes and promote disease. Knowledge of where they localize inside host cells is important in understanding their function. Fifty-two P. infestans RXLR effectors (PiRXLRs) up-regulated during early stages of infection were expressed as fluorescent protein (FP) fusions inside cells of the model host Nicotiana benthamiana. FP–PiRXLR fusions were predominantly nucleo-cytoplasmic, nuclear, or plasma membrane-associated. Some also localized to the endoplasmic reticulum, mitochondria, peroxisomes, or microtubules, suggesting diverse sites of subcellular activity. Seven of the 25 PiRXLRs examined during infection accumulated at sites of haustorium penetration, probably due to co-localization with host target processes; Pi16663 (Avr1), for example, localized to Sec5-associated mobile bodies which showed perihaustorial accumulation. Forty-five FP–RXLR fusions enhanced pathogen leaf colonization when expressed in Nicotiana benthamiana, revealing that their presence was beneficial to infection. Co-expression of PiRXLRs that target and suppress different immune pathways resulted in an additive enhancement of colonization, indicating the potential to study effector combinations using transient expression assays. We provide a broad platform of high confidence P. infestans effector candidates from which to investigate the mechanisms, singly and in combination, by which this pathogen causes disease. |
format | Online Article Text |
id | pubmed-6305197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63051972019-01-07 Phytophthora infestans RXLR effectors act in concert at diverse subcellular locations to enhance host colonization Wang, Shumei McLellan, Hazel Bukharova, Tatyana He, Qin Murphy, Fraser Shi, Jiayang Sun, Shaohui van Weymers, Pauline Ren, Yajuan Thilliez, Gaetan Wang, Haixia Chen, Xinwei Engelhardt, Stefan Vleeshouwers, Vivianne Gilroy, Eleanor M Whisson, Stephen C Hein, Ingo Wang, Xiaodan Tian, Zhendong Birch, Paul R J Boevink, Petra C J Exp Bot Research Papers Oomycetes such as the potato blight pathogen Phytophthora infestans deliver RXLR effectors into plant cells to manipulate host processes and promote disease. Knowledge of where they localize inside host cells is important in understanding their function. Fifty-two P. infestans RXLR effectors (PiRXLRs) up-regulated during early stages of infection were expressed as fluorescent protein (FP) fusions inside cells of the model host Nicotiana benthamiana. FP–PiRXLR fusions were predominantly nucleo-cytoplasmic, nuclear, or plasma membrane-associated. Some also localized to the endoplasmic reticulum, mitochondria, peroxisomes, or microtubules, suggesting diverse sites of subcellular activity. Seven of the 25 PiRXLRs examined during infection accumulated at sites of haustorium penetration, probably due to co-localization with host target processes; Pi16663 (Avr1), for example, localized to Sec5-associated mobile bodies which showed perihaustorial accumulation. Forty-five FP–RXLR fusions enhanced pathogen leaf colonization when expressed in Nicotiana benthamiana, revealing that their presence was beneficial to infection. Co-expression of PiRXLRs that target and suppress different immune pathways resulted in an additive enhancement of colonization, indicating the potential to study effector combinations using transient expression assays. We provide a broad platform of high confidence P. infestans effector candidates from which to investigate the mechanisms, singly and in combination, by which this pathogen causes disease. Oxford University Press 2019-01-01 2018-10-16 /pmc/articles/PMC6305197/ /pubmed/30329083 http://dx.doi.org/10.1093/jxb/ery360 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Papers Wang, Shumei McLellan, Hazel Bukharova, Tatyana He, Qin Murphy, Fraser Shi, Jiayang Sun, Shaohui van Weymers, Pauline Ren, Yajuan Thilliez, Gaetan Wang, Haixia Chen, Xinwei Engelhardt, Stefan Vleeshouwers, Vivianne Gilroy, Eleanor M Whisson, Stephen C Hein, Ingo Wang, Xiaodan Tian, Zhendong Birch, Paul R J Boevink, Petra C Phytophthora infestans RXLR effectors act in concert at diverse subcellular locations to enhance host colonization |
title |
Phytophthora infestans RXLR effectors act in concert at diverse subcellular locations to enhance host colonization |
title_full |
Phytophthora infestans RXLR effectors act in concert at diverse subcellular locations to enhance host colonization |
title_fullStr |
Phytophthora infestans RXLR effectors act in concert at diverse subcellular locations to enhance host colonization |
title_full_unstemmed |
Phytophthora infestans RXLR effectors act in concert at diverse subcellular locations to enhance host colonization |
title_short |
Phytophthora infestans RXLR effectors act in concert at diverse subcellular locations to enhance host colonization |
title_sort | phytophthora infestans rxlr effectors act in concert at diverse subcellular locations to enhance host colonization |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305197/ https://www.ncbi.nlm.nih.gov/pubmed/30329083 http://dx.doi.org/10.1093/jxb/ery360 |
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