Detection of several strains of the bacterium-like organism of citrus greening disease by DNA probes
Identifieur interne : 001528 ( Istex/Corpus ); précédent : 001527; suivant : 001529Detection of several strains of the bacterium-like organism of citrus greening disease by DNA probes
Auteurs : S. Villechanoux ; Monique Garnier ; Joël Renaudin ; M. BovéSource :
- Current Microbiology [ 0343-8651 ] ; 1992-02-01.
Abstract
Abstract: Greening disease of citrus is caused by a phloem-restricted, bacterium-like organism (BLO). DNA was purified from phloem tissue of periwinkle plants infected with an indian strain of the greening BLO, restricted withHindIII endonuclease, and cloned in the replicative form of bacteriophage M13mp18. By differential hybrizations involving DNA from healthy and infected periwinkle plants, we have selected three recombinant phages containing BLO DNA. The BLO DNA inserts (In-2.6, In-1.9, and In-0.6) have been purified from the viral replicative forms and used as probes. Southern and dot hybridizations have shown that In-2.6 and In-1.9 recognized all asian strains tested (strains from India, Thailand, the Philippines, Indonesia, China, and Taiwan), but not a South African strain. In-0.6 reacted only with the indian BLO strain.
Url:
DOI: 10.1007/BF01570903
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ISTEX:758ED90F1434C52AD2570DB8711E7E19A7E9B49DLe document en format XML
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Villechanoux</name><affiliation><mods:affiliation>Laboratoire de Biologie Cellulaire et Moléculaire, INRA et Université de Bordeaux, Domaine de la Grande Ferrade, B.P. 81, 33883, Villenave D'Ornon Cedex, France</mods:affiliation></affiliation></author><author><name sortKey="Garnier, Monique" sort="Garnier, Monique" uniqKey="Garnier M" first="Monique" last="Garnier">Monique Garnier</name><affiliation><mods:affiliation>Laboratoire de Biologie Cellulaire et Moléculaire, INRA et Université de Bordeaux, Domaine de la Grande Ferrade, B.P. 81, 33883, Villenave D'Ornon Cedex, France</mods:affiliation></affiliation></author><author><name sortKey="Renaudin, Joel" sort="Renaudin, Joel" uniqKey="Renaudin J" first="Joël" last="Renaudin">Joël Renaudin</name><affiliation><mods:affiliation>Laboratoire de Biologie Cellulaire et Moléculaire, INRA et Université de Bordeaux, Domaine de la Grande Ferrade, B.P. 81, 33883, Villenave D'Ornon Cedex, France</mods:affiliation></affiliation></author><author><name sortKey="Bove, M" sort="Bove, M" uniqKey="Bove M" first="M." last="Bové">M. 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DNA was purified from phloem tissue of periwinkle plants infected with an indian strain of the greening BLO, restricted withHindIII endonuclease, and cloned in the replicative form of bacteriophage M13mp18. By differential hybrizations involving DNA from healthy and infected periwinkle plants, we have selected three recombinant phages containing BLO DNA. The BLO DNA inserts (In-2.6, In-1.9, and In-0.6) have been purified from the viral replicative forms and used as probes. Southern and dot hybridizations have shown that In-2.6 and In-1.9 recognized all asian strains tested (strains from India, Thailand, the Philippines, Indonesia, China, and Taiwan), but not a South African strain. In-0.6 reacted only with the indian BLO strain.</div></front></TEI><istex><corpusName>springer</corpusName><author><json:item><name>S. Villechanoux</name><affiliations><json:string>Laboratoire de Biologie Cellulaire et Moléculaire, INRA et Université de Bordeaux, Domaine de la Grande Ferrade, B.P. 81, 33883, Villenave D'Ornon Cedex, France</json:string></affiliations></json:item><json:item><name>Dr. Monique Garnier</name><affiliations><json:string>Laboratoire de Biologie Cellulaire et Moléculaire, INRA et Université de Bordeaux, Domaine de la Grande Ferrade, B.P. 81, 33883, Villenave D'Ornon Cedex, France</json:string></affiliations></json:item><json:item><name>Joël Renaudin</name><affiliations><json:string>Laboratoire de Biologie Cellulaire et Moléculaire, INRA et Université de Bordeaux, Domaine de la Grande Ferrade, B.P. 81, 33883, Villenave D'Ornon Cedex, France</json:string></affiliations></json:item><json:item><name>Joseph M. Bové</name><affiliations><json:string>Laboratoire de Biologie Cellulaire et Moléculaire, INRA et Université de Bordeaux, Domaine de la Grande Ferrade, B.P. 81, 33883, Villenave D'Ornon Cedex, France</json:string></affiliations></json:item></author><articleId><json:string>BF01570903</json:string><json:string>Art5</json:string></articleId><language><json:string>eng</json:string></language><originalGenre><json:string>OriginalPaper</json:string></originalGenre><abstract>Abstract: Greening disease of citrus is caused by a phloem-restricted, bacterium-like organism (BLO). DNA was purified from phloem tissue of periwinkle plants infected with an indian strain of the greening BLO, restricted withHindIII endonuclease, and cloned in the replicative form of bacteriophage M13mp18. By differential hybrizations involving DNA from healthy and infected periwinkle plants, we have selected three recombinant phages containing BLO DNA. The BLO DNA inserts (In-2.6, In-1.9, and In-0.6) have been purified from the viral replicative forms and used as probes. Southern and dot hybridizations have shown that In-2.6 and In-1.9 recognized all asian strains tested (strains from India, Thailand, the Philippines, Indonesia, China, and Taiwan), but not a South African strain. 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DNA was purified from phloem tissue of periwinkle plants infected with an indian strain of the greening BLO, restricted withHindIII endonuclease, and cloned in the replicative form of bacteriophage M13mp18. By differential hybrizations involving DNA from healthy and infected periwinkle plants, we have selected three recombinant phages containing BLO DNA. The BLO DNA inserts (In-2.6, In-1.9, and In-0.6) have been purified from the viral replicative forms and used as probes. Southern and dot hybridizations have shown that In-2.6 and In-1.9 recognized all asian strains tested (strains from India, Thailand, the Philippines, Indonesia, China, and Taiwan), but not a South African strain. 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DNA was purified from phloem tissue of periwinkle plants infected with an indian strain of the greening BLO, restricted with<Emphasis Type="Italic">Hin</Emphasis>dIII endonuclease, and cloned in the replicative form of bacteriophage M13mp18.</Para><Para>By differential hybrizations involving DNA from healthy and infected periwinkle plants, we have selected three recombinant phages containing BLO DNA. The BLO DNA inserts (In-2.6, In-1.9, and In-0.6) have been purified from the viral replicative forms and used as probes. Southern and dot hybridizations have shown that In-2.6 and In-1.9 recognized all asian strains tested (strains from India, Thailand, the Philippines, Indonesia, China, and Taiwan), but not a South African strain. In-0.6 reacted only with the indian BLO strain.</Para></Abstract></ArticleHeader><NoBody></NoBody></Article></Issue></Volume></Journal></Publisher></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Detection of several strains of the bacterium-like organism of citrus greening disease by DNA probes</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Detection of several strains of the bacterium-like organism of citrus greening disease by DNA probes</title></titleInfo><name type="personal"><namePart type="given">S.</namePart><namePart type="family">Villechanoux</namePart><affiliation>Laboratoire de Biologie Cellulaire et Moléculaire, INRA et Université de Bordeaux, Domaine de la Grande Ferrade, B.P. 81, 33883, Villenave D'Ornon Cedex, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal" displayLabel="corresp"><namePart type="termsOfAddress">Dr.</namePart><namePart type="given">Monique</namePart><namePart type="family">Garnier</namePart><affiliation>Laboratoire de Biologie Cellulaire et Moléculaire, INRA et Université de Bordeaux, Domaine de la Grande Ferrade, B.P. 81, 33883, Villenave D'Ornon Cedex, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Joël</namePart><namePart type="family">Renaudin</namePart><affiliation>Laboratoire de Biologie Cellulaire et Moléculaire, INRA et Université de Bordeaux, Domaine de la Grande Ferrade, B.P. 81, 33883, Villenave D'Ornon Cedex, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Joseph</namePart><namePart type="given">M.</namePart><namePart type="family">Bové</namePart><affiliation>Laboratoire de Biologie Cellulaire et Moléculaire, INRA et Université de Bordeaux, Domaine de la Grande Ferrade, B.P. 81, 33883, Villenave D'Ornon Cedex, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="OriginalPaper"></genre><originInfo><publisher>Springer-Verlag</publisher><place><placeTerm type="text">New York</placeTerm></place><dateIssued encoding="w3cdtf">1992-02-01</dateIssued><copyrightDate encoding="w3cdtf">1992</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType></physicalDescription><abstract lang="en">Abstract: Greening disease of citrus is caused by a phloem-restricted, bacterium-like organism (BLO). DNA was purified from phloem tissue of periwinkle plants infected with an indian strain of the greening BLO, restricted withHindIII endonuclease, and cloned in the replicative form of bacteriophage M13mp18. By differential hybrizations involving DNA from healthy and infected periwinkle plants, we have selected three recombinant phages containing BLO DNA. The BLO DNA inserts (In-2.6, In-1.9, and In-0.6) have been purified from the viral replicative forms and used as probes. Southern and dot hybridizations have shown that In-2.6 and In-1.9 recognized all asian strains tested (strains from India, Thailand, the Philippines, Indonesia, China, and Taiwan), but not a South African strain. 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