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    <titleInfo>
      <title>Single Real-Time Reverse Transcription-PCR assay for detection and quantification of genetically diverse HIV-1, SIVcpz, and SIVgor strains</title>
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    <name type="personnal">
      <namePart type="family">Etienne</namePart>
      <namePart type="given">L.</namePart>
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    <name type="personnal">
      <namePart type="family">Eymard-Duvernay</namePart>
      <namePart type="given">Sabrina</namePart>
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        <roleTerm type="text">auteur</roleTerm>
        <roleTerm type="code" authority="marcrelator">aut</roleTerm>
      </role>
      <affiliation>IRD</affiliation>
    </name>
    <name type="personnal">
      <namePart type="family">Aghokeng Fobang</namePart>
      <namePart type="given">Avelin</namePart>
      <role>
        <roleTerm type="text">auteur</roleTerm>
        <roleTerm type="code" authority="marcrelator">aut</roleTerm>
      </role>
      <affiliation>IRD</affiliation>
    </name>
    <name type="personnal">
      <namePart type="family">Butel</namePart>
      <namePart type="given">Christelle</namePart>
      <role>
        <roleTerm type="text">auteur</roleTerm>
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    <name type="personnal">
      <namePart type="family">Monleau</namePart>
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        <roleTerm type="text">auteur</roleTerm>
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    <name type="personnal">
      <namePart type="family">Peeters</namePart>
      <namePart type="given">Martine</namePart>
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    <abstract>Although antiretroviral treatment availability has improved, the virological monitoring of patients remains largely uneven across regions. In addition, viral quantification tests are suffering from human immunodeficiency virus type 1 (HIV-1) genetic diversity, fueled by the emergence of new recombinants and of lentiviruses from nonhuman primates. We developed a real-time reverse transcription-PCR (RT-PCR) assay that is relatively inexpensive and able to detect and quantify all circulating forms of HIV-1 and its simian immunodeficiency virus (SIV) precursors, SIVcpz and SIVgor. Primers and a probe were designed to detect all variants of the HIV-1/SIVcpz/SIVgor lineage. HIV-1 M plasma (n = 190; 1.68 to 7.78 log(10) copies/ml) representing eight subtypes, nine circulating recombinant forms, and 21 unique recombinant forms were tested. The mean PCR efficiency was 99%, with low coefficients of intra-and interassay variation (&lt;5%) and a limit of quantification of &lt;2.50 log(10) copies/ml, with a 200-mu l plasma volume. On the studied range, the specificity and the analytical sensitivity were 100 and 97.4%, respectively. The viral loads were highly correlated (r = 0.95, P &lt; 0.0001) with the reference method (generic HIV assay; Biocentric) and had no systematic difference, irrespective of genotype. Furthermore, 22 HIV-1 O plasmas were screened and were better quantified compared to the gold-standard RealTime HIV-1 assay (Abbott), including four samples that were only quantified by our assay. Finally, we could quantify SIVcpzPtt and SIVcpzPts from chimpanzee plasma (n = 5) and amplify SIVcpz and SIVgor from feces. Thus, the newly developed real-time RT-PCR assay detects and quantifies strains from the HIV-1/SIVcpz/SIVgor lineage, including a wide diversity of group M strains and HIV-1 O. It can therefore be useful in geographical areas of high HIV diversity and at risk for the emergence of new HIV variants.</abstract>
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    <classification authority="local">052</classification>
    <classification authority="local">020</classification>
    <relatedItem type="host">
      <titleInfo>
        <title>Journal of Clinical Microbiology</title>
      </titleInfo>
      <part>
        <detail type="volume">
          <number>51</number>
        </detail>
        <detail type="volume">
          <number>3</number>
        </detail>
        <extent unit="pages">
          <list> 787-798</list>
        </extent>
      </part>
      <originInfo>
        <dateIssued>2013</dateIssued>
      </originInfo>
      <identifier type="issn">0095-1137</identifier>
    </relatedItem>
    <identifier type="uri">https://www.documentation.ird.fr/hor/PAR00010190</identifier>
    <identifier type="doi">10.1128/jcm.02792-12</identifier>
    <identifier type="issn">0095-1137</identifier>
    <location>
      <shelfLocator>[F B010080153]</shelfLocator>
      <url usage="primary display" access="object in context">https://www.documentation.ird.fr/hor/PAR00010190</url>
      <url access="row object">https://www.documentation.ird.fr/intranet/publi/depot/2020-11-25/010080153.pdf</url>
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    <accessCondition type="restriction access" displayLabel="Accès réservé">Accès réservé (Intranet de l'IRD)</accessCondition>
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      <recordCreationDate encoding="w3cdtf">2013-04-02</recordCreationDate>
      <recordChangeDate encoding="w3cdtf">2020-12-08</recordChangeDate>
      <recordIdentifier>PAR00010190</recordIdentifier>
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        <languageTerm authority="iso639-2b">fre</languageTerm>
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