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Sensitivity of influenza viruses to zanamivir and oseltamivir: A study performed on viruses circulating in France prior to the introduction of neuraminidase inhibitors in clinical practice.

Identifieur interne : 000328 ( Hal/Checkpoint ); précédent : 000327; suivant : 000329

Sensitivity of influenza viruses to zanamivir and oseltamivir: A study performed on viruses circulating in France prior to the introduction of neuraminidase inhibitors in clinical practice.

Auteurs : O. Ferraris [France] ; N. Kessler [France] ; B. Lina [France]

Source :

RBID : Hal:hal-00124134

Descripteurs français

English descriptors

Abstract

Influenza virus neuraminidase inhibitors (NAIs) were introduced in clinical practice in various parts of the world since 1999 but were only scarcely distributed in France. Prior to the generalization of zanamivir and oseltamivir utilization in our country, we decided to test a large panel of influenza strains to establish the baseline sensitivity of these viruses to anti-neuraminidase drugs, based upon a fluorometric neuraminidase enzymatic test. Our study was performed on clinical samples collected by practitioners of the GROG network (Groupe Regional d'Observation de la Grippe) in the south of France during the 2002-2003 influenza season. Out of 355 isolates tested in the fluorometric neuraminidase activity assay, 267 isolates could be included in inhibition assay against anti-neuraminidase drugs. Differences in IC50 range were found according to the subtype and the anti-neuraminidase drug. Influenza B and A/H1N1 viruses appeared to be more sensitive to zanamivir than to oseltamivir (mean B IC50 values: 4.19 nM versus 13 nM; mean H1N1 IC50 values: 0.92 nM versus 1.34 nM), while A/H1N2 and A/H3N2 viruses were more sensitive to oseltamivir than to zanamivir (mean H3N2 IC50 values: 0.67 nM versus 2.28 nM; mean H1N2 IC50 values: 0.9 nM versus 3.09 nM). Out of 128 N2 carrying isolates, 10 isolates had zanamivir or oseltamivir IC50 values in upper limits compared to their respective data range. Sequencing of the neuraminidase of these outliers N2 highlighted several mutations, but none of them were associated with resistance to neuraminidase inhibitors.


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Hal:hal-00124134

Le document en format XML

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<p>Influenza virus neuraminidase inhibitors (NAIs) were introduced in clinical practice in various parts of the world since 1999 but were only scarcely distributed in France. Prior to the generalization of zanamivir and oseltamivir utilization in our country, we decided to test a large panel of influenza strains to establish the baseline sensitivity of these viruses to anti-neuraminidase drugs, based upon a fluorometric neuraminidase enzymatic test. Our study was performed on clinical samples collected by practitioners of the GROG network (Groupe Regional d'Observation de la Grippe) in the south of France during the 2002-2003 influenza season. Out of 355 isolates tested in the fluorometric neuraminidase activity assay, 267 isolates could be included in inhibition assay against anti-neuraminidase drugs. Differences in IC50 range were found according to the subtype and the anti-neuraminidase drug. Influenza B and A/H1N1 viruses appeared to be more sensitive to zanamivir than to oseltamivir (mean B IC50 values: 4.19 nM versus 13 nM; mean H1N1 IC50 values: 0.92 nM versus 1.34 nM), while A/H1N2 and A/H3N2 viruses were more sensitive to oseltamivir than to zanamivir (mean H3N2 IC50 values: 0.67 nM versus 2.28 nM; mean H1N2 IC50 values: 0.9 nM versus 3.09 nM). Out of 128 N2 carrying isolates, 10 isolates had zanamivir or oseltamivir IC50 values in upper limits compared to their respective data range. Sequencing of the neuraminidase of these outliers N2 highlighted several mutations, but none of them were associated with resistance to neuraminidase inhibitors.</p>
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<title xml:lang="en">Sensitivity of influenza viruses to zanamivir and oseltamivir: A study performed on viruses circulating in France prior to the introduction of neuraminidase inhibitors in clinical practice.</title>
<author role="aut">
<persName>
<forename type="first">O.</forename>
<surname>Ferraris</surname>
</persName>
<idno type="halauthorid">157038</idno>
<affiliation ref="#struct-714"></affiliation>
</author>
<author role="aut">
<persName>
<forename type="first">N.</forename>
<surname>Kessler</surname>
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<idno type="halauthorid">157039</idno>
<affiliation ref="#struct-714"></affiliation>
</author>
<author role="crp">
<persName>
<forename type="first">B.</forename>
<surname>Lina</surname>
</persName>
<email type="md5">81f057579f916a025a06ac7e970cd6e7</email>
<email type="domain">univ-lyon1.fr</email>
<idno type="halauthorid">155024</idno>
<affiliation ref="#struct-714"></affiliation>
</author>
<editor role="depositor">
<persName>
<forename>Bertrand</forename>
<surname>Rollin</surname>
</persName>
<email type="md5">1ff0c1caec49e1592b1fefa6c10f3e2d</email>
<email type="domain">sante.univ-lyon1.fr</email>
</editor>
<funder>We are grateful to J. Jolly, S. Paquier, G. Cartet, and G. Burfin for technical assistance. This work is performed in part with the support of the 6 framework Program in the NoE VIRGIL.</funder>
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<edition n="v1" type="current">
<date type="whenSubmitted">2007-01-12 14:05:02</date>
<date type="whenModified">2019-11-21 02:06:12</date>
<date type="whenReleased">2007-01-12 14:05:02</date>
<date type="whenProduced">2005</date>
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<forename>Bertrand</forename>
<surname>Rollin</surname>
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<email type="domain">sante.univ-lyon1.fr</email>
</name>
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<idno type="halId">hal-00124134</idno>
<idno type="halUri">https://hal.archives-ouvertes.fr/hal-00124134</idno>
<idno type="halBibtex">ferraris:hal-00124134</idno>
<idno type="halRefHtml">Antiviral Research, Elsevier Masson, 2005, sous presse, pp.43-48</idno>
<idno type="halRef">Antiviral Research, Elsevier Masson, 2005, sous presse, pp.43-48</idno>
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<seriesStmt>
<idno type="stamp" n="CNRS">CNRS - Centre national de la recherche scientifique</idno>
<idno type="stamp" n="UNIV-LYON1">Université Claude Bernard - Lyon I</idno>
<idno type="stamp" n="UDL">UDL</idno>
<idno type="stamp" n="UNIV-LYON">Université de Lyon</idno>
</seriesStmt>
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<note type="popular" n="0">No</note>
<note type="peer" n="1">Yes</note>
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<analytic>
<title xml:lang="en">Sensitivity of influenza viruses to zanamivir and oseltamivir: A study performed on viruses circulating in France prior to the introduction of neuraminidase inhibitors in clinical practice.</title>
<author role="aut">
<persName>
<forename type="first">O.</forename>
<surname>Ferraris</surname>
</persName>
<idno type="halauthorid">157038</idno>
<affiliation ref="#struct-714"></affiliation>
</author>
<author role="aut">
<persName>
<forename type="first">N.</forename>
<surname>Kessler</surname>
</persName>
<idno type="halauthorid">157039</idno>
<affiliation ref="#struct-714"></affiliation>
</author>
<author role="crp">
<persName>
<forename type="first">B.</forename>
<surname>Lina</surname>
</persName>
<email type="md5">81f057579f916a025a06ac7e970cd6e7</email>
<email type="domain">univ-lyon1.fr</email>
<idno type="halauthorid">155024</idno>
<affiliation ref="#struct-714"></affiliation>
</author>
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<monogr>
<idno type="halJournalId" status="VALID">10572</idno>
<idno type="issn">0166-3542</idno>
<title level="j">Antiviral Research</title>
<imprint>
<publisher>Elsevier Masson</publisher>
<biblScope unit="volume">sous presse</biblScope>
<biblScope unit="pp">43–48</biblScope>
<date type="datePub">2005</date>
</imprint>
</monogr>
<idno type="pubmed">16125799</idno>
</biblStruct>
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<langUsage>
<language ident="en">English</language>
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<textClass>
<keywords scheme="author">
<term xml:lang="en">Acetamides/*pharmacology</term>
<term xml:lang="en">Enzyme Inhibitors/*pharmacology</term>
<term xml:lang="en">France</term>
<term xml:lang="en">Guanidines/*pharmacology</term>
<term xml:lang="en">Humans</term>
<term xml:lang="en">Influenza A Virus</term>
<term xml:lang="en">H1N1 Subtype/drug effects/enzymology</term>
<term xml:lang="en">H3N2 Subtype/drug effects/growth & development</term>
<term xml:lang="en">Influenza A virus/*drug effects/enzymology</term>
<term xml:lang="en">Influenza B virus/*drug effects/enzymology</term>
<term xml:lang="en">Influenza</term>
<term xml:lang="en">Human/virology</term>
<term xml:lang="en">Neuraminidase/antagonists & inhibitors/*drug effects</term>
<term xml:lang="en">Oseltamivir</term>
<term xml:lang="en">Pyrans/*pharmacology</term>
<term xml:lang="en">Sialic Acids/*pharmacology</term>
<term xml:lang="en">Zanamivir</term>
</keywords>
<classCode scheme="classification">OCIS 000.1430</classCode>
<classCode scheme="halDomain" n="sdv.mp.vir">Life Sciences [q-bio]/Microbiology and Parasitology/Virology</classCode>
<classCode scheme="halTypology" n="ART">Journal articles</classCode>
</textClass>
<abstract xml:lang="en">
<p>Influenza virus neuraminidase inhibitors (NAIs) were introduced in clinical practice in various parts of the world since 1999 but were only scarcely distributed in France. Prior to the generalization of zanamivir and oseltamivir utilization in our country, we decided to test a large panel of influenza strains to establish the baseline sensitivity of these viruses to anti-neuraminidase drugs, based upon a fluorometric neuraminidase enzymatic test. Our study was performed on clinical samples collected by practitioners of the GROG network (Groupe Regional d'Observation de la Grippe) in the south of France during the 2002-2003 influenza season. Out of 355 isolates tested in the fluorometric neuraminidase activity assay, 267 isolates could be included in inhibition assay against anti-neuraminidase drugs. Differences in IC50 range were found according to the subtype and the anti-neuraminidase drug. Influenza B and A/H1N1 viruses appeared to be more sensitive to zanamivir than to oseltamivir (mean B IC50 values: 4.19 nM versus 13 nM; mean H1N1 IC50 values: 0.92 nM versus 1.34 nM), while A/H1N2 and A/H3N2 viruses were more sensitive to oseltamivir than to zanamivir (mean H3N2 IC50 values: 0.67 nM versus 2.28 nM; mean H1N2 IC50 values: 0.9 nM versus 3.09 nM). Out of 128 N2 carrying isolates, 10 isolates had zanamivir or oseltamivir IC50 values in upper limits compared to their respective data range. Sequencing of the neuraminidase of these outliers N2 highlighted several mutations, but none of them were associated with resistance to neuraminidase inhibitors.</p>
</abstract>
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