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Development of high-throughput methods to screen disease caused by Rhizoctonia solani AG 2-1 in oilseed rape

BACKGROUND: Rhizoctonia solani (Kühn) is a soil-borne, necrotrophic fungus causing damping off, root rot and stem canker in many cultivated plants worldwide. Oilseed rape (OSR, Brassica napus) is the primary host for anastomosis group (AG) 2-1 of R. solani causing pre- and post-emergence damping-off...

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Autores principales: Drizou, Fryni, Graham, Neil S., Bruce, Toby J. A., Ray, Rumiana V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450255/
https://www.ncbi.nlm.nih.gov/pubmed/28572833
http://dx.doi.org/10.1186/s13007-017-0195-1
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author Drizou, Fryni
Graham, Neil S.
Bruce, Toby J. A.
Ray, Rumiana V.
author_facet Drizou, Fryni
Graham, Neil S.
Bruce, Toby J. A.
Ray, Rumiana V.
author_sort Drizou, Fryni
collection PubMed
description BACKGROUND: Rhizoctonia solani (Kühn) is a soil-borne, necrotrophic fungus causing damping off, root rot and stem canker in many cultivated plants worldwide. Oilseed rape (OSR, Brassica napus) is the primary host for anastomosis group (AG) 2-1 of R. solani causing pre- and post-emergence damping-off resulting in death of seedlings and impaired crop establishment. Presently, there are no known resistant OSR genotypes and the main methods for disease control are fungicide seed treatments and cultural practices. The identification of sources of resistance for crop breeding is essential for sustainable management of the disease. However, a high-throughput, reliable screening method for resistance traits is required. The aim of this work was to develop a low cost, rapid screening method for disease phenotyping and identification of resistance traits. RESULTS: Four growth systems were developed and tested: (1) nutrient media plates, (2) compost trays, (3) light expanded clay aggregate (LECA) trays, and (4) a hydroponic pouch and wick system. Seedlings were inoculated with virulent AG 2-1 to cause damping-off disease and grown for a period of 4–10 days. Visual disease assessments were carried out or disease was estimated through image analysis using ImageJ. CONCLUSION: Inoculation of LECA was the most suitable method for phenotyping disease caused by R. solani AG 2-1 as it enabled the detection of differences in disease severity among OSR genotypes within a short time period whilst allowing measurements to be conducted on whole plants. This system is expected to facilitate identification of resistant germplasm.
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spelling pubmed-54502552017-06-01 Development of high-throughput methods to screen disease caused by Rhizoctonia solani AG 2-1 in oilseed rape Drizou, Fryni Graham, Neil S. Bruce, Toby J. A. Ray, Rumiana V. Plant Methods Methodology BACKGROUND: Rhizoctonia solani (Kühn) is a soil-borne, necrotrophic fungus causing damping off, root rot and stem canker in many cultivated plants worldwide. Oilseed rape (OSR, Brassica napus) is the primary host for anastomosis group (AG) 2-1 of R. solani causing pre- and post-emergence damping-off resulting in death of seedlings and impaired crop establishment. Presently, there are no known resistant OSR genotypes and the main methods for disease control are fungicide seed treatments and cultural practices. The identification of sources of resistance for crop breeding is essential for sustainable management of the disease. However, a high-throughput, reliable screening method for resistance traits is required. The aim of this work was to develop a low cost, rapid screening method for disease phenotyping and identification of resistance traits. RESULTS: Four growth systems were developed and tested: (1) nutrient media plates, (2) compost trays, (3) light expanded clay aggregate (LECA) trays, and (4) a hydroponic pouch and wick system. Seedlings were inoculated with virulent AG 2-1 to cause damping-off disease and grown for a period of 4–10 days. Visual disease assessments were carried out or disease was estimated through image analysis using ImageJ. CONCLUSION: Inoculation of LECA was the most suitable method for phenotyping disease caused by R. solani AG 2-1 as it enabled the detection of differences in disease severity among OSR genotypes within a short time period whilst allowing measurements to be conducted on whole plants. This system is expected to facilitate identification of resistant germplasm. BioMed Central 2017-05-30 /pmc/articles/PMC5450255/ /pubmed/28572833 http://dx.doi.org/10.1186/s13007-017-0195-1 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology
Drizou, Fryni
Graham, Neil S.
Bruce, Toby J. A.
Ray, Rumiana V.
Development of high-throughput methods to screen disease caused by Rhizoctonia solani AG 2-1 in oilseed rape
title Development of high-throughput methods to screen disease caused by Rhizoctonia solani AG 2-1 in oilseed rape
title_full Development of high-throughput methods to screen disease caused by Rhizoctonia solani AG 2-1 in oilseed rape
title_fullStr Development of high-throughput methods to screen disease caused by Rhizoctonia solani AG 2-1 in oilseed rape
title_full_unstemmed Development of high-throughput methods to screen disease caused by Rhizoctonia solani AG 2-1 in oilseed rape
title_short Development of high-throughput methods to screen disease caused by Rhizoctonia solani AG 2-1 in oilseed rape
title_sort development of high-throughput methods to screen disease caused by rhizoctonia solani ag 2-1 in oilseed rape
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450255/
https://www.ncbi.nlm.nih.gov/pubmed/28572833
http://dx.doi.org/10.1186/s13007-017-0195-1
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