Detection and typing of maize streak virus and other distantly related geminiviruses of grasses by polymerase chain reaction amplification of a conserved viral sequence
Identifieur interne : 000117 ( PascalFrancis/Checkpoint ); précédent : 000116; suivant : 000118Detection and typing of maize streak virus and other distantly related geminiviruses of grasses by polymerase chain reaction amplification of a conserved viral sequence
Auteurs : E. P. Rybicki ; F. L. HughesSource :
- Journal of general virology [ 0022-1317 ] ; 1990.
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- Pascal (Inist)
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- KwdEn :
Abstract
The oligonucleotide primers used for amplifications were 17-mers which contained a number of degeneracies. An approximately 250 base pair fragment was amplified from all geminivirus-infected grass and cereal samples tested. The amplification reaction was specific, working down to a concentration of 50 fg/ml of MSV-specific plasmid-cloned DNA and with a 10-9 dilution of MSV-infected maize DNA extract
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Conserved sequence</term>
<term>Detection</term>
<term>Homology</term>
<term>Isolate</term>
<term>Maize streak virus</term>
<term>Molecular cloning</term>
<term>Molecular hybridization</term>
<term>Nucleotide sequence</term>
<term>Phylogeny</term>
<term>Phytopathogen</term>
<term>Southern blotting</term>
<term>Specificity</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Virus streak maïs</term>
<term>Séquence conservée</term>
<term>Phylogenèse</term>
<term>Isolat</term>
<term>Phytopathogène</term>
<term>Séquence nucléotide</term>
<term>Homologie</term>
<term>Spécificité</term>
<term>Clonage moléculaire</term>
<term>Hybridation moléculaire</term>
<term>Méthode Southern</term>
<term>Détection</term>
<term>Réaction chaîne polymérase</term>
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<front><div type="abstract" xml:lang="en">The oligonucleotide primers used for amplifications were 17-mers which contained a number of degeneracies. An approximately 250 base pair fragment was amplified from all geminivirus-infected grass and cereal samples tested. The amplification reaction was specific, working down to a concentration of 50 fg/ml of MSV-specific plasmid-cloned DNA and with a 10<sup>-9</sup>
dilution of MSV-infected maize DNA extract</div>
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<affiliations><list></list>
<tree><noCountry><name sortKey="Hughes, F L" sort="Hughes, F L" uniqKey="Hughes F" first="F. L." last="Hughes">F. L. Hughes</name>
<name sortKey="Rybicki, E P" sort="Rybicki, E P" uniqKey="Rybicki E" first="E. P." last="Rybicki">E. P. Rybicki</name>
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