An efficient direct screening system for microorganisms that activate plant immune responses based on plant–microbe interactions using cultured plant cells

Abstract Microorganisms that activate plant immune responses have attracted considerable attention as potential biocontrol agents in agriculture because they could reduce agrochemical use. However, conventional methods to screen for such microorganisms using whole plants and pathogens are generally...

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Autores principales: Mari Kurokawa, Masataka Nakano, Nobutaka Kitahata, Kazuyuki Kuchitsu, Toshiki Furuya
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/5a32d1a4d0b3455cb513a520510282c4
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spelling oai:doaj.org-article:5a32d1a4d0b3455cb513a520510282c42021-12-02T18:17:53ZAn efficient direct screening system for microorganisms that activate plant immune responses based on plant–microbe interactions using cultured plant cells10.1038/s41598-021-86560-02045-2322https://doaj.org/article/5a32d1a4d0b3455cb513a520510282c42021-04-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-86560-0https://doaj.org/toc/2045-2322Abstract Microorganisms that activate plant immune responses have attracted considerable attention as potential biocontrol agents in agriculture because they could reduce agrochemical use. However, conventional methods to screen for such microorganisms using whole plants and pathogens are generally laborious and time consuming. Here, we describe a general strategy using cultured plant cells to identify microorganisms that activate plant defense responses based on plant–microbe interactions. Microbial cells were incubated with tobacco BY-2 cells, followed by treatment with cryptogein, a proteinaceous elicitor of tobacco immune responses secreted by an oomycete. Cryptogein-induced production of reactive oxygen species (ROS) in BY-2 cells served as a marker to evaluate the potential of microorganisms to activate plant defense responses. Twenty-nine bacterial strains isolated from the interior of Brassica rapa var. perviridis plants were screened, and 8 strains that enhanced cryptogein-induced ROS production in BY-2 cells were selected. Following application of these strains to the root tip of Arabidopsis seedlings, two strains, Delftia sp. BR1R-2 and Arthrobacter sp. BR2S-6, were found to induce whole-plant resistance to bacterial pathogens (Pseudomonas syringae pv. tomato DC3000 and Pectobacterium carotovora subsp. carotovora NBRC 14082). Pathogen-induced expression of plant defense-related genes (PR-1, PR-5, and PDF1.2) was enhanced by the pretreatment with strain BR1R-2. This cell–cell interaction-based platform is readily applicable to large-scale screening for microorganisms that enhance plant defense responses under various environmental conditions.Mari KurokawaMasataka NakanoNobutaka KitahataKazuyuki KuchitsuToshiki FuruyaNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Mari Kurokawa
Masataka Nakano
Nobutaka Kitahata
Kazuyuki Kuchitsu
Toshiki Furuya
An efficient direct screening system for microorganisms that activate plant immune responses based on plant–microbe interactions using cultured plant cells
description Abstract Microorganisms that activate plant immune responses have attracted considerable attention as potential biocontrol agents in agriculture because they could reduce agrochemical use. However, conventional methods to screen for such microorganisms using whole plants and pathogens are generally laborious and time consuming. Here, we describe a general strategy using cultured plant cells to identify microorganisms that activate plant defense responses based on plant–microbe interactions. Microbial cells were incubated with tobacco BY-2 cells, followed by treatment with cryptogein, a proteinaceous elicitor of tobacco immune responses secreted by an oomycete. Cryptogein-induced production of reactive oxygen species (ROS) in BY-2 cells served as a marker to evaluate the potential of microorganisms to activate plant defense responses. Twenty-nine bacterial strains isolated from the interior of Brassica rapa var. perviridis plants were screened, and 8 strains that enhanced cryptogein-induced ROS production in BY-2 cells were selected. Following application of these strains to the root tip of Arabidopsis seedlings, two strains, Delftia sp. BR1R-2 and Arthrobacter sp. BR2S-6, were found to induce whole-plant resistance to bacterial pathogens (Pseudomonas syringae pv. tomato DC3000 and Pectobacterium carotovora subsp. carotovora NBRC 14082). Pathogen-induced expression of plant defense-related genes (PR-1, PR-5, and PDF1.2) was enhanced by the pretreatment with strain BR1R-2. This cell–cell interaction-based platform is readily applicable to large-scale screening for microorganisms that enhance plant defense responses under various environmental conditions.
format article
author Mari Kurokawa
Masataka Nakano
Nobutaka Kitahata
Kazuyuki Kuchitsu
Toshiki Furuya
author_facet Mari Kurokawa
Masataka Nakano
Nobutaka Kitahata
Kazuyuki Kuchitsu
Toshiki Furuya
author_sort Mari Kurokawa
title An efficient direct screening system for microorganisms that activate plant immune responses based on plant–microbe interactions using cultured plant cells
title_short An efficient direct screening system for microorganisms that activate plant immune responses based on plant–microbe interactions using cultured plant cells
title_full An efficient direct screening system for microorganisms that activate plant immune responses based on plant–microbe interactions using cultured plant cells
title_fullStr An efficient direct screening system for microorganisms that activate plant immune responses based on plant–microbe interactions using cultured plant cells
title_full_unstemmed An efficient direct screening system for microorganisms that activate plant immune responses based on plant–microbe interactions using cultured plant cells
title_sort efficient direct screening system for microorganisms that activate plant immune responses based on plant–microbe interactions using cultured plant cells
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/5a32d1a4d0b3455cb513a520510282c4
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