Commun ication : Development and Verification of Nested PCR Assay for Detection of Tobacco rattle virus in Plant Quarantine
Tobacco rattle virus (TRV) is a plant pathogen belonging to the Group IV positive-sense single-stranded RNA viruses. TRV causes disease in various plants (e.g., potato, tomato and tobacco), for which it was classified as a controlled quarantine virus in Korea. This study aimed to develop specific pr...
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Veröffentlicht in: | Journal of bacteriology and virology 2015-03, Vol.45 (1), p.54 |
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description | Tobacco rattle virus (TRV) is a plant pathogen belonging to the Group IV positive-sense single-stranded RNA viruses. TRV causes disease in various plants (e.g., potato, tomato and tobacco), for which it was classified as a controlled quarantine virus in Korea. This study aimed to develop specific primer sets for the rapid detection of TRV. Two RT-PCR primer sets were developed for specific detection of TRV. Furthermore, nested primer sets were also developed, which is required for high sensitivity detection in plant quarantine. The RT-PCR and nested PCR products had the following sizes: set 5 (1,096→540 bp), and set 7 (878→756 bp), respectively. In addition, a modified positive-control plasmid was also developed for use as a positive control in TRV quarantine. The diagnostic system for TRV detection was verified using samples from Korean quarantine sites for the last five years (2009-2014). A total of 83 cases were detected among various import crops. This system for detection of TRV will continuously contribute to plant quarantine in the future. |
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TRV causes disease in various plants (e.g., potato, tomato and tobacco), for which it was classified as a controlled quarantine virus in Korea. This study aimed to develop specific primer sets for the rapid detection of TRV. Two RT-PCR primer sets were developed for specific detection of TRV. Furthermore, nested primer sets were also developed, which is required for high sensitivity detection in plant quarantine. The RT-PCR and nested PCR products had the following sizes: set 5 (1,096→540 bp), and set 7 (878→756 bp), respectively. In addition, a modified positive-control plasmid was also developed for use as a positive control in TRV quarantine. The diagnostic system for TRV detection was verified using samples from Korean quarantine sites for the last five years (2009-2014). A total of 83 cases were detected among various import crops. 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TRV causes disease in various plants (e.g., potato, tomato and tobacco), for which it was classified as a controlled quarantine virus in Korea. This study aimed to develop specific primer sets for the rapid detection of TRV. Two RT-PCR primer sets were developed for specific detection of TRV. Furthermore, nested primer sets were also developed, which is required for high sensitivity detection in plant quarantine. The RT-PCR and nested PCR products had the following sizes: set 5 (1,096→540 bp), and set 7 (878→756 bp), respectively. In addition, a modified positive-control plasmid was also developed for use as a positive control in TRV quarantine. The diagnostic system for TRV detection was verified using samples from Korean quarantine sites for the last five years (2009-2014). A total of 83 cases were detected among various import crops. This system for detection of TRV will continuously contribute to plant quarantine in the future.</description><subject>Nested PCR</subject><subject>Quarantine</subject><subject>Tobacco rattle virus</subject><issn>1598-2467</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp9jLsOgkAQRbfQRHx8gc38AIksCmhnUGNl1BBbMsKQrMKu2VlMjD8vhbZWpzj33J7wgsUy8eU8igdiyHybzaJAJtIT79Q0TatBFeiU0bCCDT2pNo-GtAPUJVzIquqnTQUHYkclHNMzrJnxBZWxXeSo-C0yc8WiMGDRuZrgqWzLoDQca-w-Ty3ajkrTWPQrrJkmX47EdLfN0r1_V8z5w6oG7SsPw0DKOAj_2w9-iUe1</recordid><startdate>20150331</startdate><enddate>20150331</enddate><creator>Si Won Lee</creator><creator>Jin Young Lee</creator><creator>Yong Gil Shin</creator><creator>Su Heon Lee</creator><creator>Tae Young Ahn</creator><general>대한바이러스학회</general><scope>HZB</scope><scope>Q5X</scope></search><sort><creationdate>20150331</creationdate><title>Commun ication : Development and Verification of Nested PCR Assay for Detection of Tobacco rattle virus in Plant Quarantine</title><author>Si Won Lee ; Jin Young Lee ; Yong Gil Shin ; Su Heon Lee ; Tae Young Ahn</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kiss_primary_33122713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2015</creationdate><topic>Nested PCR</topic><topic>Quarantine</topic><topic>Tobacco rattle virus</topic><toplevel>online_resources</toplevel><creatorcontrib>Si Won Lee</creatorcontrib><creatorcontrib>Jin Young Lee</creatorcontrib><creatorcontrib>Yong Gil Shin</creatorcontrib><creatorcontrib>Su Heon Lee</creatorcontrib><creatorcontrib>Tae Young Ahn</creatorcontrib><collection>Korean Studies Information Service System (KISS)</collection><collection>Korean Studies Information Service System (KISS) B-Type</collection><jtitle>Journal of bacteriology and virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Si Won Lee</au><au>Jin Young Lee</au><au>Yong Gil Shin</au><au>Su Heon Lee</au><au>Tae Young Ahn</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Commun ication : Development and Verification of Nested PCR Assay for Detection of Tobacco rattle virus in Plant Quarantine</atitle><jtitle>Journal of bacteriology and virology</jtitle><addtitle>Journal of Bacteriology and Virology</addtitle><date>2015-03-31</date><risdate>2015</risdate><volume>45</volume><issue>1</issue><spage>54</spage><pages>54-</pages><issn>1598-2467</issn><abstract>Tobacco rattle virus (TRV) is a plant pathogen belonging to the Group IV positive-sense single-stranded RNA viruses. TRV causes disease in various plants (e.g., potato, tomato and tobacco), for which it was classified as a controlled quarantine virus in Korea. This study aimed to develop specific primer sets for the rapid detection of TRV. Two RT-PCR primer sets were developed for specific detection of TRV. Furthermore, nested primer sets were also developed, which is required for high sensitivity detection in plant quarantine. The RT-PCR and nested PCR products had the following sizes: set 5 (1,096→540 bp), and set 7 (878→756 bp), respectively. In addition, a modified positive-control plasmid was also developed for use as a positive control in TRV quarantine. The diagnostic system for TRV detection was verified using samples from Korean quarantine sites for the last five years (2009-2014). A total of 83 cases were detected among various import crops. This system for detection of TRV will continuously contribute to plant quarantine in the future.</abstract><pub>대한바이러스학회</pub><tpages>8</tpages></addata></record> |
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source | KoreaMed Synapse; KoreaMed Open Access |
subjects | Nested PCR Quarantine Tobacco rattle virus |
title | Commun ication : Development and Verification of Nested PCR Assay for Detection of Tobacco rattle virus in Plant Quarantine |
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