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Quantification of viable cells of Clavibacter michiganensis subsp. michiganensis using a DNA binding dye and a real‐time PCR assay
Viable cells of Clavibacter michiganensis subsp. michiganensis (CMM), the causal agent of bacterial canker of tomato, were discriminated from the dead cells by quantitative real‐time polymerase chain reaction (PCR), after the bacterial solution was treated with the DNA binding dye ethidium monoazide...
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Published in: | Plant pathology 2008-04, Vol.57 (2), p.332-337 |
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container_title | Plant pathology |
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creator | Luo, L. X. Walters, C. Bolkan, H. Liu, X. L. Li, J. Q. |
description | Viable cells of Clavibacter michiganensis subsp. michiganensis (CMM), the causal agent of bacterial canker of tomato, were discriminated from the dead cells by quantitative real‐time polymerase chain reaction (PCR), after the bacterial solution was treated with the DNA binding dye ethidium monoazide (EMA). The primers and TaqMan probe, based on the 16S‐23S rDNA spacer sequences, were highly specific for CMM at the subspecies level. The detection limit of the direct real‐time PCR was 103 colony forming units per mL (cfu mL−1) in samples and with an apparent sensitivity of 2 cfu of target cells in PCR reaction solution. Application of this method allows for selective quantification of viable cells of CMM and facilitates monitoring the pathogen in tomato seeds. |
doi_str_mv | 10.1111/j.1365-3059.2007.01736.x |
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X. ; Walters, C. ; Bolkan, H. ; Liu, X. L. ; Li, J. Q.</creator><creatorcontrib>Luo, L. X. ; Walters, C. ; Bolkan, H. ; Liu, X. L. ; Li, J. Q.</creatorcontrib><description>Viable cells of Clavibacter michiganensis subsp. michiganensis (CMM), the causal agent of bacterial canker of tomato, were discriminated from the dead cells by quantitative real‐time polymerase chain reaction (PCR), after the bacterial solution was treated with the DNA binding dye ethidium monoazide (EMA). The primers and TaqMan probe, based on the 16S‐23S rDNA spacer sequences, were highly specific for CMM at the subspecies level. The detection limit of the direct real‐time PCR was 103 colony forming units per mL (cfu mL−1) in samples and with an apparent sensitivity of 2 cfu of target cells in PCR reaction solution. Application of this method allows for selective quantification of viable cells of CMM and facilitates monitoring the pathogen in tomato seeds.</description><identifier>ISSN: 0032-0862</identifier><identifier>EISSN: 1365-3059</identifier><identifier>DOI: 10.1111/j.1365-3059.2007.01736.x</identifier><identifier>CODEN: PLPAAD</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>bacterial canker of tomato ; Bacterial plant pathogens ; Biological and medical sciences ; Clavibacter michiganensis ; ethidium monoazide ; Fundamental and applied biological sciences. Psychology ; Lycopersicon esculentum ; Phytopathology. Animal pests. Plant and forest protection ; quantitative RT‐PCR ; TaqMan probe</subject><ispartof>Plant pathology, 2008-04, Vol.57 (2), p.332-337</ispartof><rights>2007 The Authors</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4076-5b58da41ceb24cea9347d78276566398ea7acaf24ba9fbc965d72a4a557bf35e3</citedby><cites>FETCH-LOGICAL-c4076-5b58da41ceb24cea9347d78276566398ea7acaf24ba9fbc965d72a4a557bf35e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20218777$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Luo, L. 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The detection limit of the direct real‐time PCR was 103 colony forming units per mL (cfu mL−1) in samples and with an apparent sensitivity of 2 cfu of target cells in PCR reaction solution. Application of this method allows for selective quantification of viable cells of CMM and facilitates monitoring the pathogen in tomato seeds.</description><subject>bacterial canker of tomato</subject><subject>Bacterial plant pathogens</subject><subject>Biological and medical sciences</subject><subject>Clavibacter michiganensis</subject><subject>ethidium monoazide</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Lycopersicon esculentum</subject><subject>Phytopathology. Animal pests. 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Q.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantification of viable cells of Clavibacter michiganensis subsp. michiganensis using a DNA binding dye and a real‐time PCR assay</atitle><jtitle>Plant pathology</jtitle><date>2008-04</date><risdate>2008</risdate><volume>57</volume><issue>2</issue><spage>332</spage><epage>337</epage><pages>332-337</pages><issn>0032-0862</issn><eissn>1365-3059</eissn><coden>PLPAAD</coden><abstract>Viable cells of Clavibacter michiganensis subsp. michiganensis (CMM), the causal agent of bacterial canker of tomato, were discriminated from the dead cells by quantitative real‐time polymerase chain reaction (PCR), after the bacterial solution was treated with the DNA binding dye ethidium monoazide (EMA). The primers and TaqMan probe, based on the 16S‐23S rDNA spacer sequences, were highly specific for CMM at the subspecies level. The detection limit of the direct real‐time PCR was 103 colony forming units per mL (cfu mL−1) in samples and with an apparent sensitivity of 2 cfu of target cells in PCR reaction solution. Application of this method allows for selective quantification of viable cells of CMM and facilitates monitoring the pathogen in tomato seeds.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1111/j.1365-3059.2007.01736.x</doi><tpages>6</tpages></addata></record> |
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subjects | bacterial canker of tomato Bacterial plant pathogens Biological and medical sciences Clavibacter michiganensis ethidium monoazide Fundamental and applied biological sciences. Psychology Lycopersicon esculentum Phytopathology. Animal pests. Plant and forest protection quantitative RT‐PCR TaqMan probe |
title | Quantification of viable cells of Clavibacter michiganensis subsp. michiganensis using a DNA binding dye and a real‐time PCR assay |
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