Comparative proteomic analysis of host responses to Plasmodiophora brassicae infection in susceptible and resistant Brassica oleracea
Clubroot disease, caused by Plasmodiophora brassicae , is one of the most devastating diseases affecting members of the Brassicaceae family. It is difficult to control by chemical or cultural means, and the molecular mechanisms underlying interactions with Brassica oleracea (cabbage) remain poorly u...
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Published in | Plant biotechnology reports Vol. 14; no. 3; pp. 263 - 274 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Singapore
Springer Singapore
01.06.2020
Springer Nature B.V 한국식물생명공학회 |
Subjects | |
Online Access | Get full text |
ISSN | 1863-5466 1863-5474 |
DOI | 10.1007/s11816-020-00596-8 |
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Abstract | Clubroot disease, caused by
Plasmodiophora brassicae
, is one of the most devastating diseases affecting members of the Brassicaceae family. It is difficult to control by chemical or cultural means, and the molecular mechanisms underlying interactions with
Brassica oleracea
(cabbage) remain poorly understood. Herein, we used a proteomic approach to investigate
B. oleracea–P. brassicae
interactions during the early phases of infection in above-ground tissues. Proteins were isolated from the aerial parts of clubroot-susceptible (CT-18) and -resistant (YCR) cabbage cultivars at 5 days after inoculation with
P. brassicae
or buffer (mock) and resolved by sodium dodecyl sulphate–polyacrylamide gel electrophoresis and two-dimensional gel electrophoresis. A total of 24 differentially modulated proteins were identified in at least two biological replicates, and exhibited altered expression between mock and
P. brassicae
treatments and/or in the different cabbage cultivars. Most of the identified proteins are involved in oxidative stress, abscisic acid (ABA) metabolism, glucose-mediated signalling and responses to stimuli. Resistant YCR plants harboured an increased abundance of ABA-responsive protein, fructose-bisphosphate aldolase and glucose sensor interaction protein compared with CT-18 plants in both mock and
P. brassicae
-treated samples, suggesting that they may mediate basal defences against
P. brassicae
infection in YCR. Specifically, we observed that susceptible (CT-18) plants expressed higher levels of cobalamin-independent methionine synthase than YCR, which may enhance susceptibility of the host. Further investigation of the identified proteins will likely facilitate the identification of key molecular determinants, potentially improving clubroot disease resistance in future cabbage crop species. |
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AbstractList | Clubroot disease, caused by Plasmodiophora brassicae, is one of the most devastating diseases affecting members of the Brassicaceae family. It is difficult to control by chemical or cultural means, and the molecular mechanisms underlying interactions with Brassica oleracea (cabbage) remain poorly understood. Herein, we used a proteomic approach to investigate B. oleracea–P. brassicae interactions during the early phases of infection in above-ground tissues. Proteins were isolated from the aerial parts of clubroot-susceptible (CT-18) and -resistant (YCR) cabbage cultivars at 5 days after inoculation with P. brassicae or buffer (mock) and resolved by sodium dodecyl sulphate–polyacrylamide gel electrophoresis and two-dimensional gel electrophoresis. A total of 24 differentially modulated proteins were identified in at least two biological replicates, and exhibited altered expression between mock and P. brassicae treatments and/or in the different cabbage cultivars. Most of the identified proteins are involved in oxidative stress, abscisic acid (ABA) metabolism, glucose-mediated signalling and responses to stimuli. Resistant YCR plants harboured an increased abundance of ABA-responsive protein, fructose-bisphosphate aldolase and glucose sensor interaction protein compared with CT-18 plants in both mock and P. brassicae-treated samples, suggesting that they may mediate basal defences against P. brassicae infection in YCR. Specifically, we observed that susceptible (CT-18) plants expressed higher levels of cobalamin-independent methionine synthase than YCR, which may enhance susceptibility of the host. Further investigation of the identified proteins will likely facilitate the identification of key molecular determinants, potentially improving clubroot disease resistance in future cabbage crop species. Clubroot disease, caused by Plasmodiophora brassicae , is one of the most devastating diseases affecting members of the Brassicaceae family. It is difficult to control by chemical or cultural means, and the molecular mechanisms underlying interactions with Brassica oleracea (cabbage) remain poorly understood. Herein, we used a proteomic approach to investigate B. oleracea–P. brassicae interactions during the early phases of infection in above-ground tissues. Proteins were isolated from the aerial parts of clubroot-susceptible (CT-18) and -resistant (YCR) cabbage cultivars at 5 days after inoculation with P. brassicae or buffer (mock) and resolved by sodium dodecyl sulphate–polyacrylamide gel electrophoresis and two-dimensional gel electrophoresis. A total of 24 differentially modulated proteins were identified in at least two biological replicates, and exhibited altered expression between mock and P. brassicae treatments and/or in the different cabbage cultivars. Most of the identified proteins are involved in oxidative stress, abscisic acid (ABA) metabolism, glucose-mediated signalling and responses to stimuli. Resistant YCR plants harboured an increased abundance of ABA-responsive protein, fructose-bisphosphate aldolase and glucose sensor interaction protein compared with CT-18 plants in both mock and P. brassicae -treated samples, suggesting that they may mediate basal defences against P. brassicae infection in YCR. Specifically, we observed that susceptible (CT-18) plants expressed higher levels of cobalamin-independent methionine synthase than YCR, which may enhance susceptibility of the host. Further investigation of the identified proteins will likely facilitate the identification of key molecular determinants, potentially improving clubroot disease resistance in future cabbage crop species. Clubroot disease, caused by Plasmodiophora brassicae, is one of the most devastating diseases affecting members of the Brassicaceae family. It is difficult to control by chemical or cultural means, and the molecular mechanisms underlying interactions with Brassica oleracea (cabbage) remain poorly understood. Herein, we used a proteomic approach to investigate B. oleracea–P. brassicae interactions during the early phases of infection in above-ground tissues. Proteins were isolated from the aerial parts of clubroot-susceptible (CT-18) and -resistant (YCR) cabbage cultivars at 5 days after inoculation with P. brassicae or buffer (mock) and resolved by sodium dodecyl sulphate–polyacrylamide gel electrophoresis and two-dimensional gel electrophoresis. A total of 24 differentially modulated proteins were identified in at least two biological replicates, and exhibited altered expression between mock and P. brassicae treatments and/or in the different cabbage cultivars. Most of the identified proteins are involved in oxidative stress, abscisic acid (ABA) metabolism, glucose-mediated signalling and responses to stimuli. Resistant YCR plants harboured an increased abundance of ABA-responsive protein, fructose-bisphosphate aldolase and glucose sensor interaction protein compared with CT-18 plants in both mock and P. brassicae-treated samples, suggesting that they may mediate basal defences against P. brassicae infection in YCR. Specifically, we observed that susceptible (CT-18) plants expressed higher levels of cobalamin-independent methionine synthase than YCR, which may enhance susceptibility of the host. Further investigation of the identified proteins will likely facilitate the identification of key molecular determinants, potentially improving clubroot disease resistance in future cabbage crop species. KCI Citation Count: 0 |
Author | Kim, Sun Tae Cho, Hye Sun Moon, Jae Sun Kwon, Suk-Yoon Moon, Ju Yeon Kim, Hyun-Soon Choi, Gyung Ja Park, Jeong Mee |
Author_xml | – sequence: 1 givenname: Ju Yeon surname: Moon fullname: Moon, Ju Yeon organization: Plant Systems Engineering Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Department of Biosystems and Bioengineering, KRIBB School of Biotechnology, Korea University of Science and Technology (UST) – sequence: 2 givenname: Sun Tae surname: Kim fullname: Kim, Sun Tae organization: Department of Plant Bioscience, Pusan National University – sequence: 3 givenname: Gyung Ja surname: Choi fullname: Choi, Gyung Ja organization: Center for Eco-Friendly New Materials, Korea Research Institute of Chemical Technology (KRICT) – sequence: 4 givenname: Suk-Yoon surname: Kwon fullname: Kwon, Suk-Yoon organization: Plant Systems Engineering Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Department of Biosystems and Bioengineering, KRIBB School of Biotechnology, Korea University of Science and Technology (UST) – sequence: 5 givenname: Hye Sun surname: Cho fullname: Cho, Hye Sun organization: Plant Systems Engineering Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Department of Biosystems and Bioengineering, KRIBB School of Biotechnology, Korea University of Science and Technology (UST) – sequence: 6 givenname: Hyun-Soon surname: Kim fullname: Kim, Hyun-Soon organization: Plant Systems Engineering Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Department of Biosystems and Bioengineering, KRIBB School of Biotechnology, Korea University of Science and Technology (UST) – sequence: 7 givenname: Jae Sun surname: Moon fullname: Moon, Jae Sun organization: Plant Systems Engineering Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Department of Biosystems and Bioengineering, KRIBB School of Biotechnology, Korea University of Science and Technology (UST) – sequence: 8 givenname: Jeong Mee orcidid: 0000-0002-3344-7875 surname: Park fullname: Park, Jeong Mee email: jmpark@kribb.re.kr organization: Plant Systems Engineering Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Department of Biosystems and Bioengineering, KRIBB School of Biotechnology, Korea University of Science and Technology (UST) |
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CitedBy_id | crossref_primary_10_1021_acs_jproteome_2c00684 crossref_primary_10_3390_ijms23116293 crossref_primary_10_48130_vegres_0024_0021 crossref_primary_10_3390_genes12111784 crossref_primary_10_3390_ijms23169280 crossref_primary_10_3389_fpls_2022_1037633 crossref_primary_10_3390_ijms21218381 crossref_primary_10_3390_plants9101336 |
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Snippet | Clubroot disease, caused by
Plasmodiophora brassicae
, is one of the most devastating diseases affecting members of the Brassicaceae family. It is difficult to... Clubroot disease, caused by Plasmodiophora brassicae, is one of the most devastating diseases affecting members of the Brassicaceae family. It is difficult to... |
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SubjectTerms | 5-Methyltetrahydrofolate-homocysteine S-methyltransferase Abscisic acid Agriculture Aldolase Biomedical and Life Sciences Biotechnology Brassica Brassica oleracea cabbage Cell Biology Clubroot crops Cultivars Disease resistance Electrophoresis Fructose Fructose-bisphosphate aldolase Gel electrophoresis Glucose Glucose metabolism Infections Inoculation Life Sciences metabolism Methionine methionine synthase Molecular modelling Original Article Oxidative stress Plant Biochemistry Plant Sciences Plant tissues Plasmodiophora brassicae Polyacrylamide polyacrylamide gel electrophoresis Proteins proteomics Sodium dodecyl sulfate Sodium lauryl sulfate two-dimensional gel electrophoresis Vitamin B12 농학 |
Title | Comparative proteomic analysis of host responses to Plasmodiophora brassicae infection in susceptible and resistant Brassica oleracea |
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