Cargando…

Plant Aquaporins in Infection by and Immunity Against Pathogens – A Critical Review

Plant aquaporins (AQPs) of the plasma membrane intrinsic protein (PIP) family face constant risk of hijack by pathogens aiming to infect plants. PIPs can also be involved in plant immunity against infection. This review will utilize two case studies to discuss biochemical and structural mechanisms t...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Liyuan, Chen, Lei, Dong, Hansong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546722/
https://www.ncbi.nlm.nih.gov/pubmed/31191567
http://dx.doi.org/10.3389/fpls.2019.00632
_version_ 1783423562621648896
author Zhang, Liyuan
Chen, Lei
Dong, Hansong
author_facet Zhang, Liyuan
Chen, Lei
Dong, Hansong
author_sort Zhang, Liyuan
collection PubMed
description Plant aquaporins (AQPs) of the plasma membrane intrinsic protein (PIP) family face constant risk of hijack by pathogens aiming to infect plants. PIPs can also be involved in plant immunity against infection. This review will utilize two case studies to discuss biochemical and structural mechanisms that govern the functions of PIPs in the regulation of plant infection and immunity. The first example concerns the interaction between rice Oryza sativa and the bacterial blight pathogen Xanthomonas oryzae pv. oryzae (Xoo). To infect rice, Xoo uses the type III (T3) secretion system to secrete the proteic translocator Hpa1, and Hpa1 subsequently mediates the translocation of T3 effectors secreted by this system. Once shifted from bacteria into rice cells, effectors exert virulent or avirulent effects depending on the susceptibility of the rice varieties. The translocator function of Hpa1 requires cooperation with OsPIP1;3, the rice interactor of Hpa1. This role of OsPIP1;3 is related to regulatory models of effector translocation. The regulatory models have been proposed as, translocon-dependent delivery, translocon-independent pore formation, and effector endocytosis with membrane protein/lipid trafficking. The second case study includes the interaction of Hpa1 with the H(2)O(2) transport channel AtPIP1;4, and the associated consequence for H(2)O(2) signal transduction of immunity pathways in Arabidopsis thaliana, a non-host of Xoo. H(2)O(2) is generated in the apoplast upon induction by a pathogen or microbial pattern. H(2)O(2) from this source translocates quickly into Arabidopsis cells, where it interacts with pathways of intracellular immunity to confer plant resistance against diseases. To expedite H(2)O(2) transport, AtPIP1;4 must adopt a specific conformation in a number of ways, including channel width extension through amino acid interactions and selectivity for H(2)O(2) through amino acid protonation and tautomeric reactions. Both topics will reference relevant studies, conducted on other organisms and AQPs, to highlight possible mechanisms of T3 effector translocation currently under debate, and highlight the structural basis of AtPIP1;4 in H(2)O(2) transport facilitated by gating and trafficking regulation.
format Online
Article
Text
id pubmed-6546722
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-65467222019-06-12 Plant Aquaporins in Infection by and Immunity Against Pathogens – A Critical Review Zhang, Liyuan Chen, Lei Dong, Hansong Front Plant Sci Plant Science Plant aquaporins (AQPs) of the plasma membrane intrinsic protein (PIP) family face constant risk of hijack by pathogens aiming to infect plants. PIPs can also be involved in plant immunity against infection. This review will utilize two case studies to discuss biochemical and structural mechanisms that govern the functions of PIPs in the regulation of plant infection and immunity. The first example concerns the interaction between rice Oryza sativa and the bacterial blight pathogen Xanthomonas oryzae pv. oryzae (Xoo). To infect rice, Xoo uses the type III (T3) secretion system to secrete the proteic translocator Hpa1, and Hpa1 subsequently mediates the translocation of T3 effectors secreted by this system. Once shifted from bacteria into rice cells, effectors exert virulent or avirulent effects depending on the susceptibility of the rice varieties. The translocator function of Hpa1 requires cooperation with OsPIP1;3, the rice interactor of Hpa1. This role of OsPIP1;3 is related to regulatory models of effector translocation. The regulatory models have been proposed as, translocon-dependent delivery, translocon-independent pore formation, and effector endocytosis with membrane protein/lipid trafficking. The second case study includes the interaction of Hpa1 with the H(2)O(2) transport channel AtPIP1;4, and the associated consequence for H(2)O(2) signal transduction of immunity pathways in Arabidopsis thaliana, a non-host of Xoo. H(2)O(2) is generated in the apoplast upon induction by a pathogen or microbial pattern. H(2)O(2) from this source translocates quickly into Arabidopsis cells, where it interacts with pathways of intracellular immunity to confer plant resistance against diseases. To expedite H(2)O(2) transport, AtPIP1;4 must adopt a specific conformation in a number of ways, including channel width extension through amino acid interactions and selectivity for H(2)O(2) through amino acid protonation and tautomeric reactions. Both topics will reference relevant studies, conducted on other organisms and AQPs, to highlight possible mechanisms of T3 effector translocation currently under debate, and highlight the structural basis of AtPIP1;4 in H(2)O(2) transport facilitated by gating and trafficking regulation. Frontiers Media S.A. 2019-05-28 /pmc/articles/PMC6546722/ /pubmed/31191567 http://dx.doi.org/10.3389/fpls.2019.00632 Text en Copyright © 2019 Zhang, Chen and Dong. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Zhang, Liyuan
Chen, Lei
Dong, Hansong
Plant Aquaporins in Infection by and Immunity Against Pathogens – A Critical Review
title Plant Aquaporins in Infection by and Immunity Against Pathogens – A Critical Review
title_full Plant Aquaporins in Infection by and Immunity Against Pathogens – A Critical Review
title_fullStr Plant Aquaporins in Infection by and Immunity Against Pathogens – A Critical Review
title_full_unstemmed Plant Aquaporins in Infection by and Immunity Against Pathogens – A Critical Review
title_short Plant Aquaporins in Infection by and Immunity Against Pathogens – A Critical Review
title_sort plant aquaporins in infection by and immunity against pathogens – a critical review
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546722/
https://www.ncbi.nlm.nih.gov/pubmed/31191567
http://dx.doi.org/10.3389/fpls.2019.00632
work_keys_str_mv AT zhangliyuan plantaquaporinsininfectionbyandimmunityagainstpathogensacriticalreview
AT chenlei plantaquaporinsininfectionbyandimmunityagainstpathogensacriticalreview
AT donghansong plantaquaporinsininfectionbyandimmunityagainstpathogensacriticalreview