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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 : 004A86 ( Main/Exploration ); précédent : 004A85; suivant : 004A87

Detection 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. Hughes

Source :

RBID : Pascal:91-0180790

Descripteurs français

English descriptors

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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Le document en format XML

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<term>Amino Acid Sequence</term>
<term>Base Sequence</term>
<term>Conserved sequence</term>
<term>DNA Probes</term>
<term>Detection</term>
<term>Homology</term>
<term>Isolate</term>
<term>Maize streak virus</term>
<term>Molecular Sequence Data</term>
<term>Molecular cloning</term>
<term>Molecular hybridization</term>
<term>Nucleotide sequence</term>
<term>Phylogeny</term>
<term>Phytopathogen</term>
<term>Plant Viruses (classification)</term>
<term>Plant Viruses (genetics)</term>
<term>Plasmids</term>
<term>Poaceae (microbiology)</term>
<term>Polymerase Chain Reaction</term>
<term>Sensitivity and Specificity</term>
<term>Serotyping</term>
<term>Southern blotting</term>
<term>Specificity</term>
<term>Zea mays (microbiology)</term>
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<term>Données de séquences moléculaires</term>
<term>Phylogénie</term>
<term>Plasmides</term>
<term>Poaceae (microbiologie)</term>
<term>Réaction de polymérisation en chaîne</term>
<term>Sensibilité et spécificité</term>
<term>Sondes d'ADN</term>
<term>Séquence d'acides aminés</term>
<term>Séquence nucléotidique</term>
<term>Sérotypage</term>
<term>Virus des plantes ()</term>
<term>Virus des plantes (génétique)</term>
<term>Zea mays (microbiologie)</term>
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<term>DNA Probes</term>
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<term>Plant Viruses</term>
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<term>Virus des plantes</term>
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<term>Poaceae</term>
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<term>Zea mays</term>
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<term>Amino Acid Sequence</term>
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<term>Molecular Sequence Data</term>
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<term>Sensitivity and Specificity</term>
<term>Serotyping</term>
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<term>Données de séquences moléculaires</term>
<term>Phylogénie</term>
<term>Plasmides</term>
<term>Réaction de polymérisation en chaîne</term>
<term>Sensibilité et spécificité</term>
<term>Sondes d'ADN</term>
<term>Séquence d'acides aminés</term>
<term>Séquence nucléotidique</term>
<term>Sérotypage</term>
<term>Virus des plantes</term>
<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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<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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