<?xml version="1.0" encoding="UTF-8"?>
<xml>
  <records>
    <record>
      <source-app name="Horizon">Horizon</source-app>
      <rec-number>1</rec-number>
      <foreign-keys>
        <key app="Horizon" db-id="PAR00010190">1</key>
      </foreign-keys>
      <ref-type name="Journal Article">17</ref-type>
      <work-type>ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES</work-type>
      <contributors>
        <authors>
          <author>
            <style face="normal" font="default" size="100%">Etienne, L.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Eymard-Duvernay, Sabrina</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Aghokeng Fobang, Avelin</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Butel, Christelle</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Monleau, M.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Peeters, Martine</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Single Real-Time Reverse Transcription-PCR assay for detection and quantification of genetically diverse HIV-1, SIVcpz, and SIVgor strains</title>
        <secondary-title>Journal of Clinical Microbiology</secondary-title>
      </titles>
      <pages>787-798</pages>
      <dates>
        <year>2013</year>
      </dates>
      <call-num>PAR00010190</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Journal of Clinical Microbiology</full-title>
      </periodical>
      <isbn>0095-1137</isbn>
      <accession-num>ISI:000315121700008</accession-num>
      <number>3</number>
      <electronic-resource-num>10.1128/jcm.02792-12</electronic-resource-num>
      <urls>
        <related-urls>
          <url>https://www.documentation.ird.fr/hor/PAR00010190</url>
        </related-urls>
        <pdf-urls>
          <url>https://www.documentation.ird.fr/intranet/publi/depot/2020-11-25/010080153.pdf</url>
        </pdf-urls>
      </urls>
      <volume>51</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <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>
      <custom6>052 ; 020</custom6>
      <custom1>UR233</custom1>
    </record>
  </records>
</xml>
