Real-time Fluorescence PCR Method for Detection of Burkholderia glumae from Rice

Burkholderia glumae causing seedling rot and grain rot of rice was listed as a plant quarantine disease of China in 2007. It's quite necessary to set up effective detection methods for the pathogen to manage further dispersal of this disease. The present study combined the real-time PCR method with...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Rice science 2009-06, Vol.16 (2), p.157-160
Hauptverfasser: Fang, Yuan, Xu, Li-hui, Tian, Wen-xiao, Huai, Yan, Yu, Shan-hong, Lou, Miao-miao, Xie, Guan-lin
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 160
container_issue 2
container_start_page 157
container_title Rice science
container_volume 16
creator Fang, Yuan
Xu, Li-hui
Tian, Wen-xiao
Huai, Yan
Yu, Shan-hong
Lou, Miao-miao
Xie, Guan-lin
description Burkholderia glumae causing seedling rot and grain rot of rice was listed as a plant quarantine disease of China in 2007. It's quite necessary to set up effective detection methods for the pathogen to manage further dispersal of this disease. The present study combined the real-time PCR method with classical PCR to increase the detecting efficiency, and to develop an accurate, rapid and sensitive method to detect the pathogen in the seed quarantine for effective management of the disease. The results showed that all the tested strains of B. glumae produced about 139 bp specific fragments by the real-time PCR and the general PCR methods, while others showed negative PCR result. The bacteria could be detected at the concentrations of 1×10^4 CFU/mL by general PCR method and at the concentrations below 100 CFU/mL by real-time fluorescence PCR method. B. glumae could be detected when the inoculated and healthy seeds were mixed with a proportion of 1:100.
doi_str_mv 10.1016/S1672-6308(08)60073-6
format Article
fullrecord <record><control><sourceid>wanfang_jour_cross</sourceid><recordid>TN_cdi_wanfang_journals_zgsdyjtb_e200902012</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cqvip_id>30957885</cqvip_id><wanfj_id>zgsdyjtb_e200902012</wanfj_id><els_id>S1672630808600736</els_id><sourcerecordid>zgsdyjtb_e200902012</sourcerecordid><originalsourceid>FETCH-LOGICAL-c372t-593895c06553b242f75fe11647efe709bff62847b7a7edb6908fc90e8acf682b3</originalsourceid><addsrcrecordid>eNqFkG9LwzAQxoMoqNOPIARfKVK9pG2SvhKdf0FRpr4OaXrZMrtG006Zn97O6Wvh4O7guXvufoTsMThmwMTJExOSJyIFdQDqUADINBFrZIspKZJMCr7e13-STbLdtlMAkQkotsjjCE2ddH6G9Kqeh4itxcYifRyO6D12k1BRFyK9wA5t50NDg6Pn8_g6CXWF0Rs6ruczg9TFMKMjb3GHbDhTt7j7mwfk5eryeXiT3D1c3w7P7hKbSt4leZGqIrcg8jwtecadzB0yJjKJDiUUpXOCq0yW0kisSlGAcrYAVMY6oXiZDsjRau-naZxpxnoa5rHpHfXXuK0W067UyAEK4MB4r85XahtD20Z0-i36mYkLzUAvIeofiHpJSPfxA7HvBuR0NYf9Kx8eo26tXwKqfOyB6Cr4fzfs_zpPQjN-9_2lpbGvzteoUyhyqVSefgMO7IQJ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Real-time Fluorescence PCR Method for Detection of Burkholderia glumae from Rice</title><source>Alma/SFX Local Collection</source><creator>Fang, Yuan ; Xu, Li-hui ; Tian, Wen-xiao ; Huai, Yan ; Yu, Shan-hong ; Lou, Miao-miao ; Xie, Guan-lin</creator><creatorcontrib>Fang, Yuan ; Xu, Li-hui ; Tian, Wen-xiao ; Huai, Yan ; Yu, Shan-hong ; Lou, Miao-miao ; Xie, Guan-lin</creatorcontrib><description>Burkholderia glumae causing seedling rot and grain rot of rice was listed as a plant quarantine disease of China in 2007. It's quite necessary to set up effective detection methods for the pathogen to manage further dispersal of this disease. The present study combined the real-time PCR method with classical PCR to increase the detecting efficiency, and to develop an accurate, rapid and sensitive method to detect the pathogen in the seed quarantine for effective management of the disease. The results showed that all the tested strains of B. glumae produced about 139 bp specific fragments by the real-time PCR and the general PCR methods, while others showed negative PCR result. The bacteria could be detected at the concentrations of 1×10^4 CFU/mL by general PCR method and at the concentrations below 100 CFU/mL by real-time fluorescence PCR method. B. glumae could be detected when the inoculated and healthy seeds were mixed with a proportion of 1:100.</description><identifier>ISSN: 1672-6308</identifier><identifier>EISSN: 1876-4762</identifier><identifier>DOI: 10.1016/S1672-6308(08)60073-6</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>bacterial grain rot ; Burkholderia glumae ; detection ; PCR扩增法 ; PCR方法 ; real-time fluorescence polymerase chain reaction ; rice ; 实时PCR ; 实时荧光PCR检测方法 ; 探测效率 ; 有效管理 ; 种子检疫</subject><ispartof>Rice science, 2009-06, Vol.16 (2), p.157-160</ispartof><rights>2009 China National Rice Research Institute</rights><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-593895c06553b242f75fe11647efe709bff62847b7a7edb6908fc90e8acf682b3</citedby><cites>FETCH-LOGICAL-c372t-593895c06553b242f75fe11647efe709bff62847b7a7edb6908fc90e8acf682b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84241A/84241A.jpg</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Fang, Yuan</creatorcontrib><creatorcontrib>Xu, Li-hui</creatorcontrib><creatorcontrib>Tian, Wen-xiao</creatorcontrib><creatorcontrib>Huai, Yan</creatorcontrib><creatorcontrib>Yu, Shan-hong</creatorcontrib><creatorcontrib>Lou, Miao-miao</creatorcontrib><creatorcontrib>Xie, Guan-lin</creatorcontrib><title>Real-time Fluorescence PCR Method for Detection of Burkholderia glumae from Rice</title><title>Rice science</title><addtitle>Rice science</addtitle><description>Burkholderia glumae causing seedling rot and grain rot of rice was listed as a plant quarantine disease of China in 2007. It's quite necessary to set up effective detection methods for the pathogen to manage further dispersal of this disease. The present study combined the real-time PCR method with classical PCR to increase the detecting efficiency, and to develop an accurate, rapid and sensitive method to detect the pathogen in the seed quarantine for effective management of the disease. The results showed that all the tested strains of B. glumae produced about 139 bp specific fragments by the real-time PCR and the general PCR methods, while others showed negative PCR result. The bacteria could be detected at the concentrations of 1×10^4 CFU/mL by general PCR method and at the concentrations below 100 CFU/mL by real-time fluorescence PCR method. B. glumae could be detected when the inoculated and healthy seeds were mixed with a proportion of 1:100.</description><subject>bacterial grain rot</subject><subject>Burkholderia glumae</subject><subject>detection</subject><subject>PCR扩增法</subject><subject>PCR方法</subject><subject>real-time fluorescence polymerase chain reaction</subject><subject>rice</subject><subject>实时PCR</subject><subject>实时荧光PCR检测方法</subject><subject>探测效率</subject><subject>有效管理</subject><subject>种子检疫</subject><issn>1672-6308</issn><issn>1876-4762</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkG9LwzAQxoMoqNOPIARfKVK9pG2SvhKdf0FRpr4OaXrZMrtG006Zn97O6Wvh4O7guXvufoTsMThmwMTJExOSJyIFdQDqUADINBFrZIspKZJMCr7e13-STbLdtlMAkQkotsjjCE2ddH6G9Kqeh4itxcYifRyO6D12k1BRFyK9wA5t50NDg6Pn8_g6CXWF0Rs6ruczg9TFMKMjb3GHbDhTt7j7mwfk5eryeXiT3D1c3w7P7hKbSt4leZGqIrcg8jwtecadzB0yJjKJDiUUpXOCq0yW0kisSlGAcrYAVMY6oXiZDsjRau-naZxpxnoa5rHpHfXXuK0W067UyAEK4MB4r85XahtD20Z0-i36mYkLzUAvIeofiHpJSPfxA7HvBuR0NYf9Kx8eo26tXwKqfOyB6Cr4fzfs_zpPQjN-9_2lpbGvzteoUyhyqVSefgMO7IQJ</recordid><startdate>20090601</startdate><enddate>20090601</enddate><creator>Fang, Yuan</creator><creator>Xu, Li-hui</creator><creator>Tian, Wen-xiao</creator><creator>Huai, Yan</creator><creator>Yu, Shan-hong</creator><creator>Lou, Miao-miao</creator><creator>Xie, Guan-lin</creator><general>Elsevier B.V</general><general>State Key Laboratory of Rice Biology/Institute of Biotechnology, Zhejiang University, Hangzhou 310029, China</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W92</scope><scope>~WA</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20090601</creationdate><title>Real-time Fluorescence PCR Method for Detection of Burkholderia glumae from Rice</title><author>Fang, Yuan ; Xu, Li-hui ; Tian, Wen-xiao ; Huai, Yan ; Yu, Shan-hong ; Lou, Miao-miao ; Xie, Guan-lin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-593895c06553b242f75fe11647efe709bff62847b7a7edb6908fc90e8acf682b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>bacterial grain rot</topic><topic>Burkholderia glumae</topic><topic>detection</topic><topic>PCR扩增法</topic><topic>PCR方法</topic><topic>real-time fluorescence polymerase chain reaction</topic><topic>rice</topic><topic>实时PCR</topic><topic>实时荧光PCR检测方法</topic><topic>探测效率</topic><topic>有效管理</topic><topic>种子检疫</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fang, Yuan</creatorcontrib><creatorcontrib>Xu, Li-hui</creatorcontrib><creatorcontrib>Tian, Wen-xiao</creatorcontrib><creatorcontrib>Huai, Yan</creatorcontrib><creatorcontrib>Yu, Shan-hong</creatorcontrib><creatorcontrib>Lou, Miao-miao</creatorcontrib><creatorcontrib>Xie, Guan-lin</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-工程技术</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>CrossRef</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Rice science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fang, Yuan</au><au>Xu, Li-hui</au><au>Tian, Wen-xiao</au><au>Huai, Yan</au><au>Yu, Shan-hong</au><au>Lou, Miao-miao</au><au>Xie, Guan-lin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Real-time Fluorescence PCR Method for Detection of Burkholderia glumae from Rice</atitle><jtitle>Rice science</jtitle><addtitle>Rice science</addtitle><date>2009-06-01</date><risdate>2009</risdate><volume>16</volume><issue>2</issue><spage>157</spage><epage>160</epage><pages>157-160</pages><issn>1672-6308</issn><eissn>1876-4762</eissn><abstract>Burkholderia glumae causing seedling rot and grain rot of rice was listed as a plant quarantine disease of China in 2007. It's quite necessary to set up effective detection methods for the pathogen to manage further dispersal of this disease. The present study combined the real-time PCR method with classical PCR to increase the detecting efficiency, and to develop an accurate, rapid and sensitive method to detect the pathogen in the seed quarantine for effective management of the disease. The results showed that all the tested strains of B. glumae produced about 139 bp specific fragments by the real-time PCR and the general PCR methods, while others showed negative PCR result. The bacteria could be detected at the concentrations of 1×10^4 CFU/mL by general PCR method and at the concentrations below 100 CFU/mL by real-time fluorescence PCR method. B. glumae could be detected when the inoculated and healthy seeds were mixed with a proportion of 1:100.</abstract><pub>Elsevier B.V</pub><doi>10.1016/S1672-6308(08)60073-6</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1672-6308
ispartof Rice science, 2009-06, Vol.16 (2), p.157-160
issn 1672-6308
1876-4762
language eng
recordid cdi_wanfang_journals_zgsdyjtb_e200902012
source Alma/SFX Local Collection
subjects bacterial grain rot
Burkholderia glumae
detection
PCR扩增法
PCR方法
real-time fluorescence polymerase chain reaction
rice
实时PCR
实时荧光PCR检测方法
探测效率
有效管理
种子检疫
title Real-time Fluorescence PCR Method for Detection of Burkholderia glumae from Rice
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T03%3A20%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wanfang_jour_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Real-time%20Fluorescence%20PCR%20Method%20for%20Detection%20of%20Burkholderia%20glumae%20from%20Rice&rft.jtitle=Rice%20science&rft.au=Fang,%20Yuan&rft.date=2009-06-01&rft.volume=16&rft.issue=2&rft.spage=157&rft.epage=160&rft.pages=157-160&rft.issn=1672-6308&rft.eissn=1876-4762&rft_id=info:doi/10.1016/S1672-6308(08)60073-6&rft_dat=%3Cwanfang_jour_cross%3Ezgsdyjtb_e200902012%3C/wanfang_jour_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_cqvip_id=30957885&rft_wanfj_id=zgsdyjtb_e200902012&rft_els_id=S1672630808600736&rfr_iscdi=true