Development and Validation of Conventional and Quantitative Polymerase Chain Reaction Assays for the Detection of Storage Rot Potato Pathogens, Phytophthora erythroseptica, Pythium ultimum and Phoma foveata
The diseases pink rot, watery wound rot and gangrene are important storage rot diseases of potato associated predominantly with Phytophthora erythroseptica (P.), Pythium ultimum (Py.) and Phoma exigua (Phoma) var. foveata respectively. Reliable molecular-based diagnostic tests are required that will...
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description | The diseases pink rot, watery wound rot and gangrene are important storage rot diseases of potato associated predominantly with Phytophthora erythroseptica (P.), Pythium ultimum (Py.) and Phoma exigua (Phoma) var. foveata respectively. Reliable molecular-based diagnostic tests are required that will not only allow unequivocal identification of symptoms but will further advance epidemiological studies of these potato diseases to increase our understanding and contribute to more effective management and control strategies to the potato industry. Primers and probes were designed in specific regions of the internal transcribed spacer (ITS) regions to develop conventional and real-time quantitative polymerase chain reaction (PCR) assays able to detect all possible fungal and oomycete pathogens causing pink rot, watery wound rot and gangrene. The specificity of each diagnostic assay was rigorously tested with over 500 fungal/oomycete plant pathogen isolates from potato and reference culture collections, and both conventional and real-time PCR methods produced similar results. In terms of sensitivity, the detection limits for real-time PCR went below ag DNA levels compared with pg DNA levels with conventional PCR. The real-time PCR assays developed to detect Phoma foveata and Py. ultimum on tubers were suitable for the comparative Ct method (ΔΔCt) of quantification using the cytochrome oxidase gene of potato as a normalizer assay; an advantage as the need for a standard curve is eliminated. Each assay detected Phoma species (var. foveata or exigua) from naturally infected tubers showing symptoms of gangrene, and P. erythroseptica or Py. ultimum were also detected following inoculation of Russet Burbank tubers. Each diagnostic assay developed could reliably detect and distinguish between the pink rot, watery wound rot and gangrene-causing potato pathogens. |
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Reliable molecular-based diagnostic tests are required that will not only allow unequivocal identification of symptoms but will further advance epidemiological studies of these potato diseases to increase our understanding and contribute to more effective management and control strategies to the potato industry. Primers and probes were designed in specific regions of the internal transcribed spacer (ITS) regions to develop conventional and real-time quantitative polymerase chain reaction (PCR) assays able to detect all possible fungal and oomycete pathogens causing pink rot, watery wound rot and gangrene. The specificity of each diagnostic assay was rigorously tested with over 500 fungal/oomycete plant pathogen isolates from potato and reference culture collections, and both conventional and real-time PCR methods produced similar results. In terms of sensitivity, the detection limits for real-time PCR went below ag DNA levels compared with pg DNA levels with conventional PCR. The real-time PCR assays developed to detect Phoma foveata and Py. ultimum on tubers were suitable for the comparative Ct method (ΔΔCt) of quantification using the cytochrome oxidase gene of potato as a normalizer assay; an advantage as the need for a standard curve is eliminated. Each assay detected Phoma species (var. foveata or exigua) from naturally infected tubers showing symptoms of gangrene, and P. erythroseptica or Py. ultimum were also detected following inoculation of Russet Burbank tubers. Each diagnostic assay developed could reliably detect and distinguish between the pink rot, watery wound rot and gangrene-causing potato pathogens.</description><identifier>ISSN: 0931-1785</identifier><identifier>EISSN: 1439-0434</identifier><identifier>DOI: 10.1111/j.1439-0434.2007.01233.x</identifier><identifier>CODEN: JPHYEB</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Publishing Ltd</publisher><subject>Biological and medical sciences ; conventional and real-time PCR ; Fundamental and applied biological sciences. Psychology ; Fungal plant pathogens ; Oomycetes ; Phoma exigua ; Phoma exigua var. foveata ; Phoma foveata ; Phytopathology. Animal pests. 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Reliable molecular-based diagnostic tests are required that will not only allow unequivocal identification of symptoms but will further advance epidemiological studies of these potato diseases to increase our understanding and contribute to more effective management and control strategies to the potato industry. Primers and probes were designed in specific regions of the internal transcribed spacer (ITS) regions to develop conventional and real-time quantitative polymerase chain reaction (PCR) assays able to detect all possible fungal and oomycete pathogens causing pink rot, watery wound rot and gangrene. The specificity of each diagnostic assay was rigorously tested with over 500 fungal/oomycete plant pathogen isolates from potato and reference culture collections, and both conventional and real-time PCR methods produced similar results. In terms of sensitivity, the detection limits for real-time PCR went below ag DNA levels compared with pg DNA levels with conventional PCR. The real-time PCR assays developed to detect Phoma foveata and Py. ultimum on tubers were suitable for the comparative Ct method (ΔΔCt) of quantification using the cytochrome oxidase gene of potato as a normalizer assay; an advantage as the need for a standard curve is eliminated. Each assay detected Phoma species (var. foveata or exigua) from naturally infected tubers showing symptoms of gangrene, and P. erythroseptica or Py. ultimum were also detected following inoculation of Russet Burbank tubers. Each diagnostic assay developed could reliably detect and distinguish between the pink rot, watery wound rot and gangrene-causing potato pathogens.</description><subject>Biological and medical sciences</subject><subject>conventional and real-time PCR</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fungal plant pathogens</subject><subject>Oomycetes</subject><subject>Phoma exigua</subject><subject>Phoma exigua var. foveata</subject><subject>Phoma foveata</subject><subject>Phytopathology. Animal pests. Plant and forest protection</subject><subject>Phytophthora</subject><subject>Phytophthora erythroseptica</subject><subject>Pythium ultimum</subject><subject>Solanum tuberosum</subject><subject>storage rot potato diseases</subject><issn>0931-1785</issn><issn>1439-0434</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqNUsGO0zAQjRBIlIVvwBc4kWLHSdwcOKy6sAWtoHRZFnGxpsmkSUniYLul-Um-iUm7LFd8GY_mvTfjeQ4CJvhU0Hm9nYpYZiGPZTyNOFdTLiIpp4cHweS-8DCY8EyKUKhZ8jh44tyW84hLzifB7wvcY2P6FjvPoCvYV2jqAnxtOmZKNjfdniqUQXMsf94BpZ4Ae2RL0wwtWnDI5hXUHVsh5EfquXMwOFYay3yF7AI95n81r72xsEG2Mp4USMqwJfjKbLBzr9iyGrzpK8otMLSDr6xx2Ps6BypSWu9atmt83VIcJ1pWpgXqtEfw8DR4VELj8NldPAtu3r39Ml-EV58u38_Pr8I84ZEMsQCZJGWS5IKDSMtEcQ5qrbDgHCEGIWNVoirWKsoyjIu4xCKL0yJN86hcA8qz4OVJt7fm5w6d123tcmwa6NDsnKbtZrR4RcDZCZjTM5zFUve2bsEOWnA9Gqi3evRJjz7p0UB9NFAfiPrirge4HJrSQpfX7h9_lioRq4xwb064X3WDw3_r6w_LxXgjfnji187j4Z4P9odOlVSJvv14qZX8vrqNvy20IPzzE74Eo2Fjaaab64gL-k8qpRPJP2DlzNg</recordid><startdate>200705</startdate><enddate>200705</enddate><creator>Cullen, D.W</creator><creator>Toth, I.K</creator><creator>Boonham, N</creator><creator>Walsh, K</creator><creator>Barker, I</creator><creator>Lees, A.K</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>200705</creationdate><title>Development and Validation of Conventional and Quantitative Polymerase Chain Reaction Assays for the Detection of Storage Rot Potato Pathogens, Phytophthora erythroseptica, Pythium ultimum and Phoma foveata</title><author>Cullen, D.W ; Toth, I.K ; Boonham, N ; Walsh, K ; Barker, I ; Lees, A.K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5023-eda355f55c10a16f5700a7b7ed00ea4a1347fe7db7299e4d4fed946d66c2fbae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Biological and medical sciences</topic><topic>conventional and real-time PCR</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fungal plant pathogens</topic><topic>Oomycetes</topic><topic>Phoma exigua</topic><topic>Phoma exigua var. foveata</topic><topic>Phoma foveata</topic><topic>Phytopathology. Animal pests. Plant and forest protection</topic><topic>Phytophthora</topic><topic>Phytophthora erythroseptica</topic><topic>Pythium ultimum</topic><topic>Solanum tuberosum</topic><topic>storage rot potato diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cullen, D.W</creatorcontrib><creatorcontrib>Toth, I.K</creatorcontrib><creatorcontrib>Boonham, N</creatorcontrib><creatorcontrib>Walsh, K</creatorcontrib><creatorcontrib>Barker, I</creatorcontrib><creatorcontrib>Lees, A.K</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of phytopathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cullen, D.W</au><au>Toth, I.K</au><au>Boonham, N</au><au>Walsh, K</au><au>Barker, I</au><au>Lees, A.K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development and Validation of Conventional and Quantitative Polymerase Chain Reaction Assays for the Detection of Storage Rot Potato Pathogens, Phytophthora erythroseptica, Pythium ultimum and Phoma foveata</atitle><jtitle>Journal of phytopathology</jtitle><date>2007-05</date><risdate>2007</risdate><volume>155</volume><issue>5</issue><spage>309</spage><epage>315</epage><pages>309-315</pages><issn>0931-1785</issn><eissn>1439-0434</eissn><coden>JPHYEB</coden><abstract>The diseases pink rot, watery wound rot and gangrene are important storage rot diseases of potato associated predominantly with Phytophthora erythroseptica (P.), Pythium ultimum (Py.) and Phoma exigua (Phoma) var. foveata respectively. Reliable molecular-based diagnostic tests are required that will not only allow unequivocal identification of symptoms but will further advance epidemiological studies of these potato diseases to increase our understanding and contribute to more effective management and control strategies to the potato industry. Primers and probes were designed in specific regions of the internal transcribed spacer (ITS) regions to develop conventional and real-time quantitative polymerase chain reaction (PCR) assays able to detect all possible fungal and oomycete pathogens causing pink rot, watery wound rot and gangrene. The specificity of each diagnostic assay was rigorously tested with over 500 fungal/oomycete plant pathogen isolates from potato and reference culture collections, and both conventional and real-time PCR methods produced similar results. In terms of sensitivity, the detection limits for real-time PCR went below ag DNA levels compared with pg DNA levels with conventional PCR. The real-time PCR assays developed to detect Phoma foveata and Py. ultimum on tubers were suitable for the comparative Ct method (ΔΔCt) of quantification using the cytochrome oxidase gene of potato as a normalizer assay; an advantage as the need for a standard curve is eliminated. Each assay detected Phoma species (var. foveata or exigua) from naturally infected tubers showing symptoms of gangrene, and P. erythroseptica or Py. ultimum were also detected following inoculation of Russet Burbank tubers. Each diagnostic assay developed could reliably detect and distinguish between the pink rot, watery wound rot and gangrene-causing potato pathogens.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Publishing Ltd</pub><doi>10.1111/j.1439-0434.2007.01233.x</doi><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences conventional and real-time PCR Fundamental and applied biological sciences. Psychology Fungal plant pathogens Oomycetes Phoma exigua Phoma exigua var. foveata Phoma foveata Phytopathology. Animal pests. Plant and forest protection Phytophthora Phytophthora erythroseptica Pythium ultimum Solanum tuberosum storage rot potato diseases |
title | Development and Validation of Conventional and Quantitative Polymerase Chain Reaction Assays for the Detection of Storage Rot Potato Pathogens, Phytophthora erythroseptica, Pythium ultimum and Phoma foveata |
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