Soil Bioassay for Detecting <i>Magnaporthiopsis maydis</i> Infestation Using a Hyper Susceptible Maize Hybrid
<i>Magnaporthiopsis maydis</i> is the causal agent of severe maize late wilt disease. Disease outbreak occurs at the maize flowering and fruit development stage, leading to the plugging of the plant’s water vascular system, resulting in dehydration and collapse of the infected host plant...
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MDPI AG
2020-07-01
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Online Access: | https://www.mdpi.com/2309-608X/6/3/107 |
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author | Ofir Degani Danielle Regev Shlomit Dor Onn Rabinovitz |
author_facet | Ofir Degani Danielle Regev Shlomit Dor Onn Rabinovitz |
author_sort | Ofir Degani |
collection | DOAJ |
description | <i>Magnaporthiopsis maydis</i> is the causal agent of severe maize late wilt disease. Disease outbreak occurs at the maize flowering and fruit development stage, leading to the plugging of the plant’s water vascular system, resulting in dehydration and collapse of the infected host plant. The pathogen is borne by alternative hosts, infected seeds, soil, and plant residues and gradually spreads to new areas and new countries. However, no soil assay is available today that can detect <i>M. maydis</i> infestation and study its prevalence. We recently developed a molecular quantitative Real-Time PCR (qPCR) method enabling the detection of the <i>M. maydis</i> DNA in plant tissues. Despite the technique’s high sensitivity, the direct examination of soil samples can be inconsistent. To face this challenge, the current work demonstrates the use of a soil bioassay involving the cultivation of a hyper-susceptible maize genotype (Megaton cultivar, Hazera Seeds Ltd., Berurim MP Shikmim, Israel) on inspected soils. The use of Megaton cv. may facilitate pathogen establishment and spread inside the plant’s tissues, and ease the isolation and enrichment of the pathogen from the soil. Indeed, this cultivar suffers from severe dehydration sudden death when grown in an infested field. The qPCR method was able to accurately and consistently identify and quantify the pathogen’s DNA in an in vitro seed assay after seven days, and in growth-chamber potted plants at as early as three weeks. These results now enable the use of this highly susceptible testing plant to validate the presence of the maize late wilt pathogen in infested soils and to evaluate the degree of its prevalence. |
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issn | 2309-608X |
language | English |
last_indexed | 2024-03-10T18:30:46Z |
publishDate | 2020-07-01 |
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spelling | doaj.art-98caed120bfa49f2ba532ae9387724132023-11-20T06:40:16ZengMDPI AGJournal of Fungi2309-608X2020-07-016310710.3390/jof6030107Soil Bioassay for Detecting <i>Magnaporthiopsis maydis</i> Infestation Using a Hyper Susceptible Maize HybridOfir Degani0Danielle Regev1Shlomit Dor2Onn Rabinovitz3Plant Sciences Department, Migal Galilee Research Institute, Tarshish 2, Kiryat Shmona 11016, IsraelPlant Sciences Department, Migal Galilee Research Institute, Tarshish 2, Kiryat Shmona 11016, IsraelPlant Sciences Department, Migal Galilee Research Institute, Tarshish 2, Kiryat Shmona 11016, IsraelPlant Sciences Department, Migal Galilee Research Institute, Tarshish 2, Kiryat Shmona 11016, Israel<i>Magnaporthiopsis maydis</i> is the causal agent of severe maize late wilt disease. Disease outbreak occurs at the maize flowering and fruit development stage, leading to the plugging of the plant’s water vascular system, resulting in dehydration and collapse of the infected host plant. The pathogen is borne by alternative hosts, infected seeds, soil, and plant residues and gradually spreads to new areas and new countries. However, no soil assay is available today that can detect <i>M. maydis</i> infestation and study its prevalence. We recently developed a molecular quantitative Real-Time PCR (qPCR) method enabling the detection of the <i>M. maydis</i> DNA in plant tissues. Despite the technique’s high sensitivity, the direct examination of soil samples can be inconsistent. To face this challenge, the current work demonstrates the use of a soil bioassay involving the cultivation of a hyper-susceptible maize genotype (Megaton cultivar, Hazera Seeds Ltd., Berurim MP Shikmim, Israel) on inspected soils. The use of Megaton cv. may facilitate pathogen establishment and spread inside the plant’s tissues, and ease the isolation and enrichment of the pathogen from the soil. Indeed, this cultivar suffers from severe dehydration sudden death when grown in an infested field. The qPCR method was able to accurately and consistently identify and quantify the pathogen’s DNA in an in vitro seed assay after seven days, and in growth-chamber potted plants at as early as three weeks. These results now enable the use of this highly susceptible testing plant to validate the presence of the maize late wilt pathogen in infested soils and to evaluate the degree of its prevalence.https://www.mdpi.com/2309-608X/6/3/107bioassay<i>Cephalosporium maydis</i>crop protectionfungus<i>Harpophora maydis</i>late wilt |
spellingShingle | Ofir Degani Danielle Regev Shlomit Dor Onn Rabinovitz Soil Bioassay for Detecting <i>Magnaporthiopsis maydis</i> Infestation Using a Hyper Susceptible Maize Hybrid Journal of Fungi bioassay <i>Cephalosporium maydis</i> crop protection fungus <i>Harpophora maydis</i> late wilt |
title | Soil Bioassay for Detecting <i>Magnaporthiopsis maydis</i> Infestation Using a Hyper Susceptible Maize Hybrid |
title_full | Soil Bioassay for Detecting <i>Magnaporthiopsis maydis</i> Infestation Using a Hyper Susceptible Maize Hybrid |
title_fullStr | Soil Bioassay for Detecting <i>Magnaporthiopsis maydis</i> Infestation Using a Hyper Susceptible Maize Hybrid |
title_full_unstemmed | Soil Bioassay for Detecting <i>Magnaporthiopsis maydis</i> Infestation Using a Hyper Susceptible Maize Hybrid |
title_short | Soil Bioassay for Detecting <i>Magnaporthiopsis maydis</i> Infestation Using a Hyper Susceptible Maize Hybrid |
title_sort | soil bioassay for detecting i magnaporthiopsis maydis i infestation using a hyper susceptible maize hybrid |
topic | bioassay <i>Cephalosporium maydis</i> crop protection fungus <i>Harpophora maydis</i> late wilt |
url | https://www.mdpi.com/2309-608X/6/3/107 |
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