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Rapid quantification of plant-powdery mildew interactions by qPCR and conidiospore counts

BACKGROUND: The powdery mildew disease represents a valuable patho-system to study the interaction between plant hosts and obligate biotrophic fungal pathogens. Numerous discoveries have been made on the basis of the quantitative evaluation of plant-powdery mildew interactions, especially in the con...

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Autores principales: Weßling, Ralf, Panstruga, Ralph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522566/
https://www.ncbi.nlm.nih.gov/pubmed/22937820
http://dx.doi.org/10.1186/1746-4811-8-35
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author Weßling, Ralf
Panstruga, Ralph
author_facet Weßling, Ralf
Panstruga, Ralph
author_sort Weßling, Ralf
collection PubMed
description BACKGROUND: The powdery mildew disease represents a valuable patho-system to study the interaction between plant hosts and obligate biotrophic fungal pathogens. Numerous discoveries have been made on the basis of the quantitative evaluation of plant-powdery mildew interactions, especially in the context of hyper-susceptible and/or resistant plant mutants. However, the presently available methods to score the pathogenic success of powdery mildew fungi are laborious and thus not well suited for medium- to high-throughput analysis. RESULTS: Here we present two new protocols that allow the rapid quantitative assessment of powdery mildew disease development. One procedure depends on quantitative polymerase chain reaction (qPCR)-based evaluation of fungal biomass, while the other relies on the quantification of fungal conidiospores. We validated both techniques using the powdery mildew pathogen Golovinomyces orontii on a set of hyper-susceptible and resistant Arabidopsis thaliana mutants and found that both cover a wide dynamic range of one to two (qPCR) and four to five (quantification of conidia) orders of magnitude, respectively. The two approaches yield reproducible results and are easy to perform without specialized equipment. CONCLUSIONS: The qPCR and spore count assays rapidly and reproducibly quantify powdery mildew pathogenesis. Our methods are performed at later stages of infection and discern mutant phenotypes accurately. The assays therefore complement currently used procedures of powdery mildew quantification and can overcome some of their limitations. In addition, they can easily be adapted to other plant-powdery mildew patho-systems.
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spelling pubmed-35225662012-12-15 Rapid quantification of plant-powdery mildew interactions by qPCR and conidiospore counts Weßling, Ralf Panstruga, Ralph Plant Methods Methodology BACKGROUND: The powdery mildew disease represents a valuable patho-system to study the interaction between plant hosts and obligate biotrophic fungal pathogens. Numerous discoveries have been made on the basis of the quantitative evaluation of plant-powdery mildew interactions, especially in the context of hyper-susceptible and/or resistant plant mutants. However, the presently available methods to score the pathogenic success of powdery mildew fungi are laborious and thus not well suited for medium- to high-throughput analysis. RESULTS: Here we present two new protocols that allow the rapid quantitative assessment of powdery mildew disease development. One procedure depends on quantitative polymerase chain reaction (qPCR)-based evaluation of fungal biomass, while the other relies on the quantification of fungal conidiospores. We validated both techniques using the powdery mildew pathogen Golovinomyces orontii on a set of hyper-susceptible and resistant Arabidopsis thaliana mutants and found that both cover a wide dynamic range of one to two (qPCR) and four to five (quantification of conidia) orders of magnitude, respectively. The two approaches yield reproducible results and are easy to perform without specialized equipment. CONCLUSIONS: The qPCR and spore count assays rapidly and reproducibly quantify powdery mildew pathogenesis. Our methods are performed at later stages of infection and discern mutant phenotypes accurately. The assays therefore complement currently used procedures of powdery mildew quantification and can overcome some of their limitations. In addition, they can easily be adapted to other plant-powdery mildew patho-systems. BioMed Central 2012-08-31 /pmc/articles/PMC3522566/ /pubmed/22937820 http://dx.doi.org/10.1186/1746-4811-8-35 Text en Copyright ©2012 Weßling and Panstruga; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology
Weßling, Ralf
Panstruga, Ralph
Rapid quantification of plant-powdery mildew interactions by qPCR and conidiospore counts
title Rapid quantification of plant-powdery mildew interactions by qPCR and conidiospore counts
title_full Rapid quantification of plant-powdery mildew interactions by qPCR and conidiospore counts
title_fullStr Rapid quantification of plant-powdery mildew interactions by qPCR and conidiospore counts
title_full_unstemmed Rapid quantification of plant-powdery mildew interactions by qPCR and conidiospore counts
title_short Rapid quantification of plant-powdery mildew interactions by qPCR and conidiospore counts
title_sort rapid quantification of plant-powdery mildew interactions by qpcr and conidiospore counts
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522566/
https://www.ncbi.nlm.nih.gov/pubmed/22937820
http://dx.doi.org/10.1186/1746-4811-8-35
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