Multiplex Reverse Transcription (RT) High-Fidelity PCR Protocol for the Detection of Six Viruses that Cause Potato Tuber Necrosis
Viruses that cause necrotic symptoms in potato tubers can be difficult to distinguish based on symptoms and frequently require multiple molecular tests to identify the pathogen. In this study, a multiplex RT PCR high fidelity PCR protocol was developed using previously validated primers that could a...
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Veröffentlicht in: | American journal of potato research 2015-08, Vol.92 (4), p.536-540 |
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creator | Cating, Robert A Funke, Cassandra N Kaur, Navneet Hamm, Philip B Frost, Ken E |
description | Viruses that cause necrotic symptoms in potato tubers can be difficult to distinguish based on symptoms and frequently require multiple molecular tests to identify the pathogen. In this study, a multiplex RT PCR high fidelity PCR protocol was developed using previously validated primers that could accurately detect six important potato viruses and detect multiple viruses in a single sample simultaneously. To test the protocol, 53 tubers previously tested using conventional PCR were retested using this multiplex protocol and blindly evaluated. In every case, the multiplex PCR results were consistent with previous findings. In addition, the multiplex PCR protocol also detected several mixed infections that were previously undetected. The results demonstrate that this technique could be a valuable assay not only for diagnostic laboratories, but also for seed certification and regulatory agency laboratories to diagnose the virus(es) that may be present in tubers with surface or internal necrotic symptoms. |
doi_str_mv | 10.1007/s12230-015-9457-5 |
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In this study, a multiplex RT PCR high fidelity PCR protocol was developed using previously validated primers that could accurately detect six important potato viruses and detect multiple viruses in a single sample simultaneously. To test the protocol, 53 tubers previously tested using conventional PCR were retested using this multiplex protocol and blindly evaluated. In every case, the multiplex PCR results were consistent with previous findings. In addition, the multiplex PCR protocol also detected several mixed infections that were previously undetected. The results demonstrate that this technique could be a valuable assay not only for diagnostic laboratories, but also for seed certification and regulatory agency laboratories to diagnose the virus(es) that may be present in tubers with surface or internal necrotic symptoms.</description><identifier>ISSN: 1099-209X</identifier><identifier>EISSN: 1874-9380</identifier><identifier>DOI: 10.1007/s12230-015-9457-5</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Agriculture ; Biomedical and Life Sciences ; Life Sciences ; mixed infection ; necrosis ; pathogens ; Plant Breeding/Biotechnology ; Plant Genetics and Genomics ; Plant Pathology ; Plant Sciences ; polymerase chain reaction ; Potatoes ; reverse transcription ; seed certification ; Short Communication ; tubers ; viruses</subject><ispartof>American journal of potato research, 2015-08, Vol.92 (4), p.536-540</ispartof><rights>The Potato Association of America 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c410t-894239f3b44427e8cfb49cdb0940334e7f462750ba9d45d225503e170ad92d643</citedby><cites>FETCH-LOGICAL-c410t-894239f3b44427e8cfb49cdb0940334e7f462750ba9d45d225503e170ad92d643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12230-015-9457-5$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12230-015-9457-5$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids></links><search><creatorcontrib>Cating, Robert A</creatorcontrib><creatorcontrib>Funke, Cassandra N</creatorcontrib><creatorcontrib>Kaur, Navneet</creatorcontrib><creatorcontrib>Hamm, Philip B</creatorcontrib><creatorcontrib>Frost, Ken E</creatorcontrib><title>Multiplex Reverse Transcription (RT) High-Fidelity PCR Protocol for the Detection of Six Viruses that Cause Potato Tuber Necrosis</title><title>American journal of potato research</title><addtitle>Am. J. Potato Res</addtitle><description>Viruses that cause necrotic symptoms in potato tubers can be difficult to distinguish based on symptoms and frequently require multiple molecular tests to identify the pathogen. In this study, a multiplex RT PCR high fidelity PCR protocol was developed using previously validated primers that could accurately detect six important potato viruses and detect multiple viruses in a single sample simultaneously. To test the protocol, 53 tubers previously tested using conventional PCR were retested using this multiplex protocol and blindly evaluated. In every case, the multiplex PCR results were consistent with previous findings. In addition, the multiplex PCR protocol also detected several mixed infections that were previously undetected. The results demonstrate that this technique could be a valuable assay not only for diagnostic laboratories, but also for seed certification and regulatory agency laboratories to diagnose the virus(es) that may be present in tubers with surface or internal necrotic symptoms.</description><subject>Agriculture</subject><subject>Biomedical and Life Sciences</subject><subject>Life Sciences</subject><subject>mixed infection</subject><subject>necrosis</subject><subject>pathogens</subject><subject>Plant Breeding/Biotechnology</subject><subject>Plant Genetics and Genomics</subject><subject>Plant Pathology</subject><subject>Plant Sciences</subject><subject>polymerase chain reaction</subject><subject>Potatoes</subject><subject>reverse transcription</subject><subject>seed certification</subject><subject>Short Communication</subject><subject>tubers</subject><subject>viruses</subject><issn>1099-209X</issn><issn>1874-9380</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kMtO5DAQRSPESMNjPmBWWGIDC0P51YmXqHlKzEyraRA7y0kqjVFoN7aDYMmfk0xYsGJTVVLdc6t0s-w3gyMGkB9HxrkACkxRLVVO1Ua2xYpcUi0K2Oxn0Jpy0Pc_s-0YHwE444Xayt7_dG1y6xZfyRxfMEQki2BXsQpunZxfkYP54pBcuuUDPXc1ti69kdl0TmbBJ1_5ljQ-kPSA5BQTVv8J35Ab90ruXOgixn5pE5nafiYzn2zyZNGVGMhfrIKPLu5mPxrbRvz12Xey2_OzxfSSXv-7uJqeXNNKMki00JIL3YhSSslzLKqmlLqqS9AShJCYN3LCcwWl1bVUNedKgUCWg601rydS7GT7o-86-OcOYzKPvgur_qTpVaLQIi9Ur2KjanguBmzMOrgnG94MAzMkbcakTZ-0GZI2A8NHJvba1RLDF-dvoL0Raqw3dhlcNLc3HNgEgA1ViA8te4mQ</recordid><startdate>20150801</startdate><enddate>20150801</enddate><creator>Cating, Robert A</creator><creator>Funke, Cassandra N</creator><creator>Kaur, Navneet</creator><creator>Hamm, Philip B</creator><creator>Frost, Ken E</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X2</scope><scope>7XB</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>L6V</scope><scope>M0K</scope><scope>M2O</scope><scope>M7S</scope><scope>MBDVC</scope><scope>PADUT</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>S0X</scope></search><sort><creationdate>20150801</creationdate><title>Multiplex Reverse Transcription (RT) High-Fidelity PCR Protocol for the Detection of Six Viruses that Cause Potato Tuber Necrosis</title><author>Cating, Robert A ; Funke, Cassandra N ; Kaur, Navneet ; Hamm, Philip B ; Frost, Ken E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-894239f3b44427e8cfb49cdb0940334e7f462750ba9d45d225503e170ad92d643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Agriculture</topic><topic>Biomedical and Life Sciences</topic><topic>Life Sciences</topic><topic>mixed infection</topic><topic>necrosis</topic><topic>pathogens</topic><topic>Plant Breeding/Biotechnology</topic><topic>Plant Genetics and Genomics</topic><topic>Plant Pathology</topic><topic>Plant Sciences</topic><topic>polymerase chain reaction</topic><topic>Potatoes</topic><topic>reverse transcription</topic><topic>seed certification</topic><topic>Short Communication</topic><topic>tubers</topic><topic>viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cating, Robert A</creatorcontrib><creatorcontrib>Funke, Cassandra N</creatorcontrib><creatorcontrib>Kaur, Navneet</creatorcontrib><creatorcontrib>Hamm, Philip B</creatorcontrib><creatorcontrib>Frost, Ken E</creatorcontrib><collection>AGRIS</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Agricultural Science Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection (ProQuest)</collection><collection>Natural Science Collection (ProQuest)</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Engineering Collection</collection><collection>Agricultural Science Database</collection><collection>Research Library</collection><collection>Engineering Database</collection><collection>Research Library (Corporate)</collection><collection>Research Library China</collection><collection>Environmental Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><jtitle>American journal of potato research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cating, Robert A</au><au>Funke, Cassandra N</au><au>Kaur, Navneet</au><au>Hamm, Philip B</au><au>Frost, Ken E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multiplex Reverse Transcription (RT) High-Fidelity PCR Protocol for the Detection of Six Viruses that Cause Potato Tuber Necrosis</atitle><jtitle>American journal of potato research</jtitle><stitle>Am. J. Potato Res</stitle><date>2015-08-01</date><risdate>2015</risdate><volume>92</volume><issue>4</issue><spage>536</spage><epage>540</epage><pages>536-540</pages><issn>1099-209X</issn><eissn>1874-9380</eissn><abstract>Viruses that cause necrotic symptoms in potato tubers can be difficult to distinguish based on symptoms and frequently require multiple molecular tests to identify the pathogen. In this study, a multiplex RT PCR high fidelity PCR protocol was developed using previously validated primers that could accurately detect six important potato viruses and detect multiple viruses in a single sample simultaneously. To test the protocol, 53 tubers previously tested using conventional PCR were retested using this multiplex protocol and blindly evaluated. In every case, the multiplex PCR results were consistent with previous findings. In addition, the multiplex PCR protocol also detected several mixed infections that were previously undetected. The results demonstrate that this technique could be a valuable assay not only for diagnostic laboratories, but also for seed certification and regulatory agency laboratories to diagnose the virus(es) that may be present in tubers with surface or internal necrotic symptoms.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s12230-015-9457-5</doi><tpages>5</tpages></addata></record> |
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subjects | Agriculture Biomedical and Life Sciences Life Sciences mixed infection necrosis pathogens Plant Breeding/Biotechnology Plant Genetics and Genomics Plant Pathology Plant Sciences polymerase chain reaction Potatoes reverse transcription seed certification Short Communication tubers viruses |
title | Multiplex Reverse Transcription (RT) High-Fidelity PCR Protocol for the Detection of Six Viruses that Cause Potato Tuber Necrosis |
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