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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Main Authors: Ofir Degani, Danielle Regev, Shlomit Dor, Onn Rabinovitz
Format: Article
Language:English
Published: MDPI AG 2020-07-01
Series:Journal of Fungi
Subjects:
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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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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