Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
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
_version_ 1783382512112762880
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
work_keys_str_mv AT wangshumei phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT mclellanhazel phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT bukharovatatyana phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT heqin phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT murphyfraser phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT shijiayang phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT sunshaohui phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT vanweymerspauline phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT renyajuan phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT thilliezgaetan phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT wanghaixia phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT chenxinwei phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT engelhardtstefan phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT vleeshouwersvivianne phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT gilroyeleanorm phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT whissonstephenc phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT heiningo phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT wangxiaodan phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT tianzhendong phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT birchpaulrj phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization
AT boevinkpetrac phytophthorainfestansrxlreffectorsactinconcertatdiversesubcellularlocationstoenhancehostcolonization