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Rapid Identification of Emerging Pathogens: Coronavirus

Identifieur interne : 000E25 ( Ncbi/Merge ); précédent : 000E24; suivant : 000E26

Rapid Identification of Emerging Pathogens: Coronavirus

Auteurs : Rangarajan Sampath [États-Unis] ; Steven A. Hofstadler [États-Unis] ; Lawrence B. Blyn [États-Unis] ; Mark W. Eshoo [États-Unis] ; Thomas A. Hall [États-Unis] ; Christian Massire [États-Unis] ; Harold M. Levene [États-Unis] ; James C. Hannis [États-Unis] ; Patina M. Harrell [États-Unis] ; Benjamin Neuman [États-Unis] ; Michael J. Buchmeier [États-Unis] ; Yun Jiang [États-Unis] ; Raymond Ranken [États-Unis] ; Jared J. Drader [États-Unis] ; Vivek Samant [États-Unis] ; Richard H. Griffey [États-Unis] ; John A. Mcneil [États-Unis] ; Stanley T. Crooke [États-Unis] ; David J. Ecker [États-Unis]

Source :

RBID : PMC:3298233

Descripteurs français

English descriptors

Abstract

New surveillance approach can analyze >900 polymerase chain reactions per day.


Url:
DOI: 10.3201/eid1103.040629
PubMed: 15757550
PubMed Central: 3298233

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


Links to Exploration step

PMC:3298233

Le document en format XML

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<term>Séquence nucléotidique</term>
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<term>Coronaviridae Infections</term>
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<p>New surveillance approach can analyze >900 polymerase chain reactions per day.</p>
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<nlm:affiliation>Ibis Therapeutics, 1891 Rutherford Ct, Carlsbad, CA 92008, USA. rsampath@isisph.com</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Ibis Therapeutics, 1891 Rutherford Ct, Carlsbad, CA 92008</wicri:regionArea>
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<region type="state">Californie</region>
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<name sortKey="Hofstadler, Steven A" sort="Hofstadler, Steven A" uniqKey="Hofstadler S" first="Steven A" last="Hofstadler">Steven A. Hofstadler</name>
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<nlm:affiliation>Ibis Therapeutics, 1891 Rutherford Ct, Carlsbad, CA 92008, USA. rsampath@isisph.com</nlm:affiliation>
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<region type="state">Californie</region>
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<name sortKey="Hofstadler, Steven A" sort="Hofstadler, Steven A" uniqKey="Hofstadler S" first="Steven A" last="Hofstadler">Steven A. Hofstadler</name>
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<name sortKey="Blyn, Lawrence B" sort="Blyn, Lawrence B" uniqKey="Blyn L" first="Lawrence B" last="Blyn">Lawrence B. Blyn</name>
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<name sortKey="Eshoo, Mark W" sort="Eshoo, Mark W" uniqKey="Eshoo M" first="Mark W" last="Eshoo">Mark W. Eshoo</name>
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<name sortKey="Hall, Thomas A" sort="Hall, Thomas A" uniqKey="Hall T" first="Thomas A" last="Hall">Thomas A. Hall</name>
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<name sortKey="Massire, Christian" sort="Massire, Christian" uniqKey="Massire C" first="Christian" last="Massire">Christian Massire</name>
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<name sortKey="Harrell, Patina M" sort="Harrell, Patina M" uniqKey="Harrell P" first="Patina M" last="Harrell">Patina M. Harrell</name>
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<name sortKey="Neuman, Benjamin" sort="Neuman, Benjamin" uniqKey="Neuman B" first="Benjamin" last="Neuman">Benjamin Neuman</name>
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<term>Animals</term>
<term>Base Sequence</term>
<term>Communicable Diseases, Emerging</term>
<term>Coronaviridae (isolation & purification)</term>
<term>Coronaviridae Infections (epidemiology)</term>
<term>Coronaviridae Infections (virology)</term>
<term>Humans</term>
<term>Polymerase Chain Reaction (methods)</term>
<term>Population Surveillance</term>
<term>RNA, Viral</term>
<term>Sensitivity and Specificity</term>
<term>Spectrometry, Mass, Electrospray Ionization (methods)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>ARN viral</term>
<term>Animaux</term>
<term>Coronaviridae (isolement et purification)</term>
<term>Humains</term>
<term>Infections à Coronaviridae (virologie)</term>
<term>Infections à Coronaviridae (épidémiologie)</term>
<term>Maladies transmissibles émergentes</term>
<term>Réaction de polymérisation en chaîne ()</term>
<term>Sensibilité et spécificité</term>
<term>Spectrométrie de masse ESI ()</term>
<term>Surveillance de la population</term>
<term>Séquence nucléotidique</term>
</keywords>
<keywords scheme="MESH" type="chemical" xml:lang="en">
<term>RNA, Viral</term>
</keywords>
<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en">
<term>Coronaviridae Infections</term>
</keywords>
<keywords scheme="MESH" qualifier="isolation & purification" xml:lang="en">
<term>Coronaviridae</term>
</keywords>
<keywords scheme="MESH" qualifier="isolement et purification" xml:lang="fr">
<term>Coronaviridae</term>
</keywords>
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<term>Polymerase Chain Reaction</term>
<term>Spectrometry, Mass, Electrospray Ionization</term>
</keywords>
<keywords scheme="MESH" qualifier="virologie" xml:lang="fr">
<term>Infections à Coronaviridae</term>
</keywords>
<keywords scheme="MESH" qualifier="virology" xml:lang="en">
<term>Coronaviridae Infections</term>
</keywords>
<keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr">
<term>Infections à Coronaviridae</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Base Sequence</term>
<term>Communicable Diseases, Emerging</term>
<term>Humans</term>
<term>Population Surveillance</term>
<term>Sensitivity and Specificity</term>
</keywords>
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<term>ARN viral</term>
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<term>Humains</term>
<term>Maladies transmissibles émergentes</term>
<term>Réaction de polymérisation en chaîne</term>
<term>Sensibilité et spécificité</term>
<term>Spectrométrie de masse ESI</term>
<term>Surveillance de la population</term>
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<front>
<div type="abstract" xml:lang="en">We describe a new approach for infectious disease surveillance that facilitates rapid identification of known and emerging pathogens. The process uses broad-range polymerase chain reaction (PCR) to amplify nucleic acid targets from large groupings of organisms, electrospray ionization mass spectrometry for accurate mass measurements of PCR products, and base composition signature analysis to identify organisms in a sample. We demonstrate this principle by using 14 isolates of 9 diverse Coronavirus spp., including the severe acute respiratory syndrome-associated coronavirus (SARS-CoV). We show that this method could identify and distinguish between SARS and other known CoV, including the human CoV 229E and OC43, individually and in a mixture of all 3 human viruses. The sensitivity of detection, measured by using titered SARS-CoV spiked into human serum, was approximate, equals1 PFU/mL. This approach, applicable to the surveillance of bacterial, viral, fungal, or protozoal pathogens, is capable of automated analysis of >900 PCR reactions per day.</div>
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