Establishment of Pathogenicity Test Method for Causing Soybean Charcoal Rot

The establishment of a laboratory assay and a greenhouse assay was conducted for evaluating the pathogenicity of Macrophomina phaseolina causing soybean charcoal rot established. In the laboratory assay, microsclerotia and hyphae were used as inoculum. In the laboratory assays using microsclerotia a...

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Main Authors: So Hyeon An, Heung Tae Kim
Format: Article
Language:English
Published: Hanrimwon Publishing Company 2023-03-01
Series:Research in Plant Disease
Subjects:
Online Access:http://www.online-rpd.org/upload/pdf/RPD-2023-29-1-1.pdf
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author So Hyeon An
Heung Tae Kim
author_facet So Hyeon An
Heung Tae Kim
author_sort So Hyeon An
collection DOAJ
description The establishment of a laboratory assay and a greenhouse assay was conducted for evaluating the pathogenicity of Macrophomina phaseolina causing soybean charcoal rot established. In the laboratory assay, microsclerotia and hyphae were used as inoculum. In the laboratory assays using microsclerotia as an inoculum, disease incidences of M. phaseolina NSW17-108 and HSM17-034 were higher at 35 o C than 25 o C. Of the two isolates NSW17-108 and HSM17-034, the disease incidence of HSM17-034 isolated from diseased sesame is higher than that of NSW17-108 isolated from diseased soybean. When the mycelia of M. phaseolina were used as an inoculum, the disease incidence of NSW17-108 and HSM17-034 at 35°C exceeded 80% even after only 5 days of inoculation. Even at 25°C, furthermore, that of HSM17-034 exceeded 80% 5 days later. In the pathogenicity assays at a greenhouse, toothpicks where microsclerotia were produced or microsclerotia harvested from potato dextrose agar medium were used as an inoculum. In all greenhouse assays, M. phaseolina NSW17-108 and HSM17-034 showed 40–60% of disease incidences 35–65 days after inoculation with the pathogen, depending on the inoculation method. Between the two isolates, the pathogenicity of HSM17-034 was stronger than that of NSW17-108, and this result was consistent with laboratory assay results. Since the laboratory and greenhouse test methods tested in this study have different advantages and disadvantages depending on each test method, it is thought that the test method that can meet the purpose of the study should be selected and used.
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spelling doaj.art-b50632c80db643db8e4432c9c5a3e28b2023-04-19T02:32:32ZengHanrimwon Publishing CompanyResearch in Plant Disease1598-22622233-91912023-03-0129111010.5423/RPD.2023.29.1.11767Establishment of Pathogenicity Test Method for Causing Soybean Charcoal RotSo Hyeon An0Heung Tae Kim1Department of Plant Medicine, College of Agriculture, Life & Environment Sciences, Chungbuk National University, Cheongju 28644, KoreaDepartment of Plant Medicine, College of Agriculture, Life & Environment Sciences, Chungbuk National University, Cheongju 28644, KoreaThe establishment of a laboratory assay and a greenhouse assay was conducted for evaluating the pathogenicity of Macrophomina phaseolina causing soybean charcoal rot established. In the laboratory assay, microsclerotia and hyphae were used as inoculum. In the laboratory assays using microsclerotia as an inoculum, disease incidences of M. phaseolina NSW17-108 and HSM17-034 were higher at 35 o C than 25 o C. Of the two isolates NSW17-108 and HSM17-034, the disease incidence of HSM17-034 isolated from diseased sesame is higher than that of NSW17-108 isolated from diseased soybean. When the mycelia of M. phaseolina were used as an inoculum, the disease incidence of NSW17-108 and HSM17-034 at 35°C exceeded 80% even after only 5 days of inoculation. Even at 25°C, furthermore, that of HSM17-034 exceeded 80% 5 days later. In the pathogenicity assays at a greenhouse, toothpicks where microsclerotia were produced or microsclerotia harvested from potato dextrose agar medium were used as an inoculum. In all greenhouse assays, M. phaseolina NSW17-108 and HSM17-034 showed 40–60% of disease incidences 35–65 days after inoculation with the pathogen, depending on the inoculation method. Between the two isolates, the pathogenicity of HSM17-034 was stronger than that of NSW17-108, and this result was consistent with laboratory assay results. Since the laboratory and greenhouse test methods tested in this study have different advantages and disadvantages depending on each test method, it is thought that the test method that can meet the purpose of the study should be selected and used.http://www.online-rpd.org/upload/pdf/RPD-2023-29-1-1.pdf pathogenicity assay in laboratory and greenhousesoybean charcoal rot
spellingShingle So Hyeon An
Heung Tae Kim
Establishment of Pathogenicity Test Method for Causing Soybean Charcoal Rot
Research in Plant Disease

pathogenicity assay in laboratory and greenhouse
soybean charcoal rot
title Establishment of Pathogenicity Test Method for Causing Soybean Charcoal Rot
title_full Establishment of Pathogenicity Test Method for Causing Soybean Charcoal Rot
title_fullStr Establishment of Pathogenicity Test Method for Causing Soybean Charcoal Rot
title_full_unstemmed Establishment of Pathogenicity Test Method for Causing Soybean Charcoal Rot
title_short Establishment of Pathogenicity Test Method for Causing Soybean Charcoal Rot
title_sort establishment of pathogenicity test method for causing soybean charcoal rot
topic
pathogenicity assay in laboratory and greenhouse
soybean charcoal rot
url http://www.online-rpd.org/upload/pdf/RPD-2023-29-1-1.pdf
work_keys_str_mv AT sohyeonan establishmentofpathogenicitytestmethodforcausingsoybeancharcoalrot
AT heungtaekim establishmentofpathogenicitytestmethodforcausingsoybeancharcoalrot