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Use of consensus sequences for the design of high density resequencing microarrays: the influenza virus paradigm

Identifieur interne : 000D84 ( Main/Exploration ); précédent : 000D83; suivant : 000D85

Use of consensus sequences for the design of high density resequencing microarrays: the influenza virus paradigm

Auteurs : India Leclercq [France] ; Nicolas Berthet [France] ; Christophe Batéjat [France] ; Claudine Rousseaux [France] ; Philip Dickinson [États-Unis] ; Iain Old [France] ; Katherine Kong [États-Unis] ; Giulia Kennedy [États-Unis] ; Stewart Cole [Suisse] ; Jean-Claude Manuguerra [France]

Source :

RBID : Hal:pasteur-00670619

Abstract

Background
A resequencing microarray called PathogenID v2.0 has been developed and used to explore various strategies of sequence selection for its design. The part dedicated to influenza viruses was based on consensus sequences specific for one gene generated from global alignments of a large number of influenza virus sequences available in databanks.
Results
For each HA (H1, H2, H3, H5, H7 and H9) and NA (N1, N2 and N7) molecular type chosen to be tested, 1 to 3 consensus sequences were computed and tiled on the microarray. A total of 12 influenza virus samples from different host origins (humans, pigs, horses and birds) and isolated over a period of about 50 years were used in this study. Influenza viruses were correctly identified, and in most cases with the accurate information of the time of their emergence.
Conclusions
PathogenID v2.0 microarray demonstrated its ability to type and subtype influenza viruses, often to the level of viral variants, with a minimum number of tiled sequences. This validated the strategy of using consensus sequences, which do not exist in nature, for our microarray design. The versatility, rapidity and high discriminatory power of the PathogenID v2.0 microarray could prove critical to detect and identify viral genome reassortment events resulting in a novel virus with epidemic or pandemic potential and therefore assist health authorities to make efficient decisions about patient treatment and outbreak management.


Url:
DOI: 10.1186/1471-2164-11-586


Affiliations:


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


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<name sortKey="Dickinson, Philip" sort="Dickinson, Philip" uniqKey="Dickinson P" first="Philip" last="Dickinson">Philip Dickinson</name>
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<orgName>Affymetrix</orgName>
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<address>
<addrLine>3420 Central Expressway Santa Clara, CA 95051 Phone (toll-free in US): +1-888-362-2447 Phone: +1-408-731-5000 Fax: +1-408-731-5380</addrLine>
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<country key="FR"></country>
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<country>États-Unis</country>
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<author>
<name sortKey="Old, Iain" sort="Old, Iain" uniqKey="Old I" first="Iain" last="Old">Iain Old</name>
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<idno type="IdRef">027936643</idno>
<idno type="ISNI">0000 0001 2353 6535</idno>
<orgName>Institut Pasteur [Paris]</orgName>
<date type="start">1887-06-04</date>
<desc>
<address>
<addrLine>25-28, rue du docteur Roux, 75724 Paris cedex 15</addrLine>
<country key="FR"></country>
</address>
<ref type="url">https://www.pasteur.fr</ref>
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</hal:affiliation>
<country>France</country>
</affiliation>
</author>
<author>
<name sortKey="Kong, Katherine" sort="Kong, Katherine" uniqKey="Kong K" first="Katherine" last="Kong">Katherine Kong</name>
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<orgName>Affymetrix</orgName>
<desc>
<address>
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<name sortKey="Kennedy, Giulia" sort="Kennedy, Giulia" uniqKey="Kennedy G" first="Giulia" last="Kennedy">Giulia Kennedy</name>
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<orgName>Affymetrix</orgName>
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<country>États-Unis</country>
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</author>
<author>
<name sortKey="Cole, Stewart" sort="Cole, Stewart" uniqKey="Cole S" first="Stewart" last="Cole">Stewart Cole</name>
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<hal:affiliation type="laboratory" xml:id="struct-184585" status="INCOMING">
<orgName>Global Health Institute</orgName>
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<address>
<addrLine>Global Health Institute, Ecole Polytechnique Fédérale de Lausanne, Station 19, CH-1015 Lausanne, Switzerland</addrLine>
<country key="CH"></country>
</address>
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<orgName>Ecole Polytechnique Fédérale de Lausanne</orgName>
<orgName type="acronym">EPFL</orgName>
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<address>
<addrLine>CH-1015 Lausanne, Switzerland </addrLine>
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</address>
<ref type="url">https://www.epfl.ch</ref>
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<country>Suisse</country>
<placeName>
<settlement type="city">Lausanne</settlement>
<region nuts="3" type="region">Canton de Vaud</region>
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<author>
<name sortKey="Manuguerra, Jean Claude" sort="Manuguerra, Jean Claude" uniqKey="Manuguerra J" first="Jean-Claude" last="Manuguerra">Jean-Claude Manuguerra</name>
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<orgName>Cellule d'Intervention Biologique d'Urgence</orgName>
<orgName type="acronym">CIBU</orgName>
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<address>
<addrLine>Département Infection et Epidémiologie, 25-28 rue du Docteur Roux F-75724 Paris Cedex 15</addrLine>
<country key="FR"></country>
</address>
<ref type="url">https://research.pasteur.fr/en/nrc/laboratory-for-urgence-response-to-biological-threats/</ref>
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<idno type="IdRef">027936643</idno>
<idno type="ISNI">0000 0001 2353 6535</idno>
<orgName>Institut Pasteur [Paris]</orgName>
<date type="start">1887-06-04</date>
<desc>
<address>
<addrLine>25-28, rue du docteur Roux, 75724 Paris cedex 15</addrLine>
<country key="FR"></country>
</address>
<ref type="url">https://www.pasteur.fr</ref>
</desc>
</org>
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</tutelles>
</hal:affiliation>
<country>France</country>
</affiliation>
</author>
</analytic>
<idno type="DOI">10.1186/1471-2164-11-586</idno>
<series>
<title level="j">BMC Genomics</title>
<idno type="ISSN">1471-2164</idno>
<imprint>
<date type="datePub">2010</date>
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<front>
<div type="abstract" xml:lang="en">
<p>Background
A resequencing microarray called PathogenID v2.0 has been developed and used to explore various strategies of sequence selection for its design. The part dedicated to influenza viruses was based on consensus sequences specific for one gene generated from global alignments of a large number of influenza virus sequences available in databanks.
Results
For each HA (H1, H2, H3, H5, H7 and H9) and NA (N1, N2 and N7) molecular type chosen to be tested, 1 to 3 consensus sequences were computed and tiled on the microarray. A total of 12 influenza virus samples from different host origins (humans, pigs, horses and birds) and isolated over a period of about 50 years were used in this study. Influenza viruses were correctly identified, and in most cases with the accurate information of the time of their emergence.
Conclusions
PathogenID v2.0 microarray demonstrated its ability to type and subtype influenza viruses, often to the level of viral variants, with a minimum number of tiled sequences. This validated the strategy of using consensus sequences, which do not exist in nature, for our microarray design. The versatility, rapidity and high discriminatory power of the PathogenID v2.0 microarray could prove critical to detect and identify viral genome reassortment events resulting in a novel virus with epidemic or pandemic potential and therefore assist health authorities to make efficient decisions about patient treatment and outbreak management.</p>
</div>
</front>
</TEI>
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<list>
<country>
<li>France</li>
<li>Suisse</li>
<li>États-Unis</li>
</country>
<region>
<li>Canton de Vaud</li>
</region>
<settlement>
<li>Lausanne</li>
</settlement>
<orgName>
<li>École polytechnique fédérale de Lausanne</li>
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<noRegion>
<name sortKey="Leclercq, India" sort="Leclercq, India" uniqKey="Leclercq I" first="India" last="Leclercq">India Leclercq</name>
</noRegion>
<name sortKey="Batejat, Christophe" sort="Batejat, Christophe" uniqKey="Batejat C" first="Christophe" last="Batéjat">Christophe Batéjat</name>
<name sortKey="Berthet, Nicolas" sort="Berthet, Nicolas" uniqKey="Berthet N" first="Nicolas" last="Berthet">Nicolas Berthet</name>
<name sortKey="Manuguerra, Jean Claude" sort="Manuguerra, Jean Claude" uniqKey="Manuguerra J" first="Jean-Claude" last="Manuguerra">Jean-Claude Manuguerra</name>
<name sortKey="Old, Iain" sort="Old, Iain" uniqKey="Old I" first="Iain" last="Old">Iain Old</name>
<name sortKey="Rousseaux, Claudine" sort="Rousseaux, Claudine" uniqKey="Rousseaux C" first="Claudine" last="Rousseaux">Claudine Rousseaux</name>
</country>
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<noRegion>
<name sortKey="Dickinson, Philip" sort="Dickinson, Philip" uniqKey="Dickinson P" first="Philip" last="Dickinson">Philip Dickinson</name>
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<name sortKey="Kennedy, Giulia" sort="Kennedy, Giulia" uniqKey="Kennedy G" first="Giulia" last="Kennedy">Giulia Kennedy</name>
<name sortKey="Kong, Katherine" sort="Kong, Katherine" uniqKey="Kong K" first="Katherine" last="Kong">Katherine Kong</name>
</country>
<country name="Suisse">
<region name="Canton de Vaud">
<name sortKey="Cole, Stewart" sort="Cole, Stewart" uniqKey="Cole S" first="Stewart" last="Cole">Stewart Cole</name>
</region>
</country>
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</record>

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