A method for quantitation of apoplast hydration in Arabidopsis leaves reveals water-soaking activity of effectors of Pseudomonas syringae during biotrophy

Abstract The plant apoplast has a crucial role in photosynthesis and respiration due to its vital function in gas exchange and transpiration. The apoplast is also a dynamic environment that participates in many ion and nutrient transport processes via plasma membrane-localized proteins. Furthermore,...

Full description

Bibliographic Details
Main Authors: Gayani Ekanayake, Reid Gohmann, David Mackey
Format: Article
Language:English
Published: Nature Portfolio 2022-11-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-022-22472-x
_version_ 1828309966661877760
author Gayani Ekanayake
Reid Gohmann
David Mackey
author_facet Gayani Ekanayake
Reid Gohmann
David Mackey
author_sort Gayani Ekanayake
collection DOAJ
description Abstract The plant apoplast has a crucial role in photosynthesis and respiration due to its vital function in gas exchange and transpiration. The apoplast is also a dynamic environment that participates in many ion and nutrient transport processes via plasma membrane-localized proteins. Furthermore, diverse microbes colonize the plant apoplast, including the hemibiotrophic bacterial pathogen, Pseudomonas syringae pv. tomato (Pto) strain DC3000. Pto DC3000 initiates pathogenesis upon moving through stomata into the apoplast and then proliferating to high levels. Here we developed a centrifugation-based method to isolate and quantify the apoplast fluid in Arabidopsis leaves, without significantly damaging the tissue. We applied the simple apoplast extraction method to demonstrate that the Pto DC3000 type III bacterial effectors AvrE1 and HopM1 induce hydration of the Arabidopsis apoplast in advance of macroscopic water-soaking, disruption of host cell integrity, and disease progression. Finally, we demonstrate the utility of the apoplast extraction method for isolation of bacteria proliferating in the apoplast.
first_indexed 2024-04-13T15:36:45Z
format Article
id doaj.art-7aae4a21188e4439ae061bae95ea7839
institution Directory Open Access Journal
issn 2045-2322
language English
last_indexed 2024-04-13T15:36:45Z
publishDate 2022-11-01
publisher Nature Portfolio
record_format Article
series Scientific Reports
spelling doaj.art-7aae4a21188e4439ae061bae95ea78392022-12-22T02:41:15ZengNature PortfolioScientific Reports2045-23222022-11-0112111110.1038/s41598-022-22472-xA method for quantitation of apoplast hydration in Arabidopsis leaves reveals water-soaking activity of effectors of Pseudomonas syringae during biotrophyGayani Ekanayake0Reid Gohmann1David Mackey2Department of Horticulture and Crop Science, The Ohio State UniversityDepartment of Horticulture and Crop Science, The Ohio State UniversityDepartment of Horticulture and Crop Science, The Ohio State UniversityAbstract The plant apoplast has a crucial role in photosynthesis and respiration due to its vital function in gas exchange and transpiration. The apoplast is also a dynamic environment that participates in many ion and nutrient transport processes via plasma membrane-localized proteins. Furthermore, diverse microbes colonize the plant apoplast, including the hemibiotrophic bacterial pathogen, Pseudomonas syringae pv. tomato (Pto) strain DC3000. Pto DC3000 initiates pathogenesis upon moving through stomata into the apoplast and then proliferating to high levels. Here we developed a centrifugation-based method to isolate and quantify the apoplast fluid in Arabidopsis leaves, without significantly damaging the tissue. We applied the simple apoplast extraction method to demonstrate that the Pto DC3000 type III bacterial effectors AvrE1 and HopM1 induce hydration of the Arabidopsis apoplast in advance of macroscopic water-soaking, disruption of host cell integrity, and disease progression. Finally, we demonstrate the utility of the apoplast extraction method for isolation of bacteria proliferating in the apoplast.https://doi.org/10.1038/s41598-022-22472-x
spellingShingle Gayani Ekanayake
Reid Gohmann
David Mackey
A method for quantitation of apoplast hydration in Arabidopsis leaves reveals water-soaking activity of effectors of Pseudomonas syringae during biotrophy
Scientific Reports
title A method for quantitation of apoplast hydration in Arabidopsis leaves reveals water-soaking activity of effectors of Pseudomonas syringae during biotrophy
title_full A method for quantitation of apoplast hydration in Arabidopsis leaves reveals water-soaking activity of effectors of Pseudomonas syringae during biotrophy
title_fullStr A method for quantitation of apoplast hydration in Arabidopsis leaves reveals water-soaking activity of effectors of Pseudomonas syringae during biotrophy
title_full_unstemmed A method for quantitation of apoplast hydration in Arabidopsis leaves reveals water-soaking activity of effectors of Pseudomonas syringae during biotrophy
title_short A method for quantitation of apoplast hydration in Arabidopsis leaves reveals water-soaking activity of effectors of Pseudomonas syringae during biotrophy
title_sort method for quantitation of apoplast hydration in arabidopsis leaves reveals water soaking activity of effectors of pseudomonas syringae during biotrophy
url https://doi.org/10.1038/s41598-022-22472-x
work_keys_str_mv AT gayaniekanayake amethodforquantitationofapoplasthydrationinarabidopsisleavesrevealswatersoakingactivityofeffectorsofpseudomonassyringaeduringbiotrophy
AT reidgohmann amethodforquantitationofapoplasthydrationinarabidopsisleavesrevealswatersoakingactivityofeffectorsofpseudomonassyringaeduringbiotrophy
AT davidmackey amethodforquantitationofapoplasthydrationinarabidopsisleavesrevealswatersoakingactivityofeffectorsofpseudomonassyringaeduringbiotrophy
AT gayaniekanayake methodforquantitationofapoplasthydrationinarabidopsisleavesrevealswatersoakingactivityofeffectorsofpseudomonassyringaeduringbiotrophy
AT reidgohmann methodforquantitationofapoplasthydrationinarabidopsisleavesrevealswatersoakingactivityofeffectorsofpseudomonassyringaeduringbiotrophy
AT davidmackey methodforquantitationofapoplasthydrationinarabidopsisleavesrevealswatersoakingactivityofeffectorsofpseudomonassyringaeduringbiotrophy