Serveur d'exploration Phytophthora

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Extraction of Plant DNA by Microneedle Patch for Rapid Detection of Plant Diseases.

Identifieur interne : 000512 ( Main/Exploration ); précédent : 000511; suivant : 000513

Extraction of Plant DNA by Microneedle Patch for Rapid Detection of Plant Diseases.

Auteurs : Rajesh Paul ; Amanda C. Saville ; Jeana C. Hansel ; Yanqi Ye [États-Unis] ; Carmin Ball ; Alyssa Williams ; Xinyuan Chang [République populaire de Chine] ; Guojun Chen [États-Unis] ; Zhen Gu [États-Unis] ; Jean B. Ristaino ; Qingshan Wei

Source :

RBID : pubmed:31179687

Descripteurs français

English descriptors

Abstract

In-field molecular diagnosis of plant diseases via nucleic acid amplification is currently limited by cumbersome protocols for extracting and isolating pathogenic DNA from plant tissues. To address this challenge, a rapid plant DNA extraction method was developed using a disposable polymeric microneedle (MN) patch. By applying MN patches on plant leaves, amplification-assay-ready DNA can be extracted within a minute from different plant species. MN-extracted DNA was used for direct polymerase chain reaction amplification of plant plastid DNA without purification. Furthermore, using this patch device, extraction of plant pathogen DNA ( Phytophthora infestans) from both laboratory-inoculated and field-infected leaf samples was performed for detection of late blight disease in tomato. MN extraction achieved 100% detection rate of late blight infections for samples after 3 days of inoculation when compared to the conventional gold standard cetyltrimethylammonium bromide (CTAB)-based DNA extraction method and 100% detection rate for all blind field samples tested. This simple, cell-lysis-free, and purification-free DNA extraction method could be a transformative approach to facilitate rapid sample preparation for molecular diagnosis of various plant diseases directly in the field.

DOI: 10.1021/acsnano.9b00193
PubMed: 31179687


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<term>DNA Barcoding, Taxonomic (instrumentation)</term>
<term>DNA Barcoding, Taxonomic (methods)</term>
<term>DNA, Fungal (chemistry)</term>
<term>DNA, Fungal (genetics)</term>
<term>Lycopersicon esculentum (microbiology)</term>
<term>Metagenomics (instrumentation)</term>
<term>Metagenomics (methods)</term>
<term>Needles (MeSH)</term>
<term>Phytophthora (genetics)</term>
<term>Phytophthora (pathogenicity)</term>
<term>Plant Diseases (microbiology)</term>
<term>Plant Leaves (chemistry)</term>
<term>Plant Leaves (microbiology)</term>
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<term>ADN fongique (composition chimique)</term>
<term>ADN fongique (génétique)</term>
<term>Aiguilles (MeSH)</term>
<term>Codage à barres de l'ADN pour la taxonomie (instrumentation)</term>
<term>Codage à barres de l'ADN pour la taxonomie (méthodes)</term>
<term>Feuilles de plante (composition chimique)</term>
<term>Feuilles de plante (microbiologie)</term>
<term>Lycopersicon esculentum (microbiologie)</term>
<term>Maladies des plantes (microbiologie)</term>
<term>Métagénomique (instrumentation)</term>
<term>Métagénomique (méthodes)</term>
<term>Phytophthora (génétique)</term>
<term>Phytophthora (pathogénicité)</term>
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<term>DNA, Fungal</term>
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<term>DNA, Fungal</term>
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<keywords scheme="MESH" qualifier="chemistry" xml:lang="en">
<term>Plant Leaves</term>
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<keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr">
<term>ADN fongique</term>
<term>Feuilles de plante</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Phytophthora</term>
</keywords>
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<term>ADN fongique</term>
<term>Phytophthora</term>
</keywords>
<keywords scheme="MESH" qualifier="instrumentation" xml:lang="en">
<term>DNA Barcoding, Taxonomic</term>
<term>Metagenomics</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>DNA Barcoding, Taxonomic</term>
<term>Metagenomics</term>
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<keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr">
<term>Feuilles de plante</term>
<term>Lycopersicon esculentum</term>
<term>Maladies des plantes</term>
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<keywords scheme="MESH" qualifier="microbiology" xml:lang="en">
<term>Lycopersicon esculentum</term>
<term>Plant Diseases</term>
<term>Plant Leaves</term>
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<term>Codage à barres de l'ADN pour la taxonomie</term>
<term>Métagénomique</term>
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<term>Phytophthora</term>
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<keywords scheme="MESH" qualifier="pathogénicité" xml:lang="fr">
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<term>Needles</term>
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<term>Aiguilles</term>
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<div type="abstract" xml:lang="en">In-field molecular diagnosis of plant diseases via nucleic acid amplification is currently limited by cumbersome protocols for extracting and isolating pathogenic DNA from plant tissues. To address this challenge, a rapid plant DNA extraction method was developed using a disposable polymeric microneedle (MN) patch. By applying MN patches on plant leaves, amplification-assay-ready DNA can be extracted within a minute from different plant species. MN-extracted DNA was used for direct polymerase chain reaction amplification of plant plastid DNA without purification. Furthermore, using this patch device, extraction of plant pathogen DNA ( Phytophthora infestans) from both laboratory-inoculated and field-infected leaf samples was performed for detection of late blight disease in tomato. MN extraction achieved 100% detection rate of late blight infections for samples after 3 days of inoculation when compared to the conventional gold standard cetyltrimethylammonium bromide (CTAB)-based DNA extraction method and 100% detection rate for all blind field samples tested. This simple, cell-lysis-free, and purification-free DNA extraction method could be a transformative approach to facilitate rapid sample preparation for molecular diagnosis of various plant diseases directly in the field.</div>
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<AbstractText>In-field molecular diagnosis of plant diseases via nucleic acid amplification is currently limited by cumbersome protocols for extracting and isolating pathogenic DNA from plant tissues. To address this challenge, a rapid plant DNA extraction method was developed using a disposable polymeric microneedle (MN) patch. By applying MN patches on plant leaves, amplification-assay-ready DNA can be extracted within a minute from different plant species. MN-extracted DNA was used for direct polymerase chain reaction amplification of plant plastid DNA without purification. Furthermore, using this patch device, extraction of plant pathogen DNA ( Phytophthora infestans) from both laboratory-inoculated and field-infected leaf samples was performed for detection of late blight disease in tomato. MN extraction achieved 100% detection rate of late blight infections for samples after 3 days of inoculation when compared to the conventional gold standard cetyltrimethylammonium bromide (CTAB)-based DNA extraction method and 100% detection rate for all blind field samples tested. This simple, cell-lysis-free, and purification-free DNA extraction method could be a transformative approach to facilitate rapid sample preparation for molecular diagnosis of various plant diseases directly in the field.</AbstractText>
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<DescriptorName UI="D058893" MajorTopicYN="N">DNA Barcoding, Taxonomic</DescriptorName>
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<QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName>
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<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
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<DescriptorName UI="D018551" MajorTopicYN="N">Lycopersicon esculentum</DescriptorName>
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<DescriptorName UI="D010838" MajorTopicYN="N">Phytophthora</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
<QualifierName UI="Q000472" MajorTopicYN="N">pathogenicity</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D010935" MajorTopicYN="N">Plant Diseases</DescriptorName>
<QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName>
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<MeshHeading>
<DescriptorName UI="D018515" MajorTopicYN="N">Plant Leaves</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName>
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<Keyword MajorTopicYN="Y">DNA extraction</Keyword>
<Keyword MajorTopicYN="Y">microneedle patch</Keyword>
<Keyword MajorTopicYN="Y">nucleic acid amplification</Keyword>
<Keyword MajorTopicYN="Y">plant disease</Keyword>
<Keyword MajorTopicYN="Y">point-of-care diagnostics</Keyword>
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<settlement>
<li>Chapel Hill (Caroline du Nord)</li>
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<li>Université de Caroline du Nord à Chapel Hill</li>
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<name sortKey="Paul, Rajesh" sort="Paul, Rajesh" uniqKey="Paul R" first="Rajesh" last="Paul">Rajesh Paul</name>
<name sortKey="Ristaino, Jean B" sort="Ristaino, Jean B" uniqKey="Ristaino J" first="Jean B" last="Ristaino">Jean B. Ristaino</name>
<name sortKey="Saville, Amanda C" sort="Saville, Amanda C" uniqKey="Saville A" first="Amanda C" last="Saville">Amanda C. Saville</name>
<name sortKey="Wei, Qingshan" sort="Wei, Qingshan" uniqKey="Wei Q" first="Qingshan" last="Wei">Qingshan Wei</name>
<name sortKey="Williams, Alyssa" sort="Williams, Alyssa" uniqKey="Williams A" first="Alyssa" last="Williams">Alyssa Williams</name>
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<country name="États-Unis">
<region name="Caroline du Nord">
<name sortKey="Ye, Yanqi" sort="Ye, Yanqi" uniqKey="Ye Y" first="Yanqi" last="Ye">Yanqi Ye</name>
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<name sortKey="Chen, Guojun" sort="Chen, Guojun" uniqKey="Chen G" first="Guojun" last="Chen">Guojun Chen</name>
<name sortKey="Gu, Zhen" sort="Gu, Zhen" uniqKey="Gu Z" first="Zhen" last="Gu">Zhen Gu</name>
</country>
<country name="République populaire de Chine">
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<name sortKey="Chang, Xinyuan" sort="Chang, Xinyuan" uniqKey="Chang X" first="Xinyuan" last="Chang">Xinyuan Chang</name>
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