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      <source-app name="Horizon">Horizon</source-app>
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      <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%">Hongjaisee, S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Kham-Kjing, N.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Musikul, P.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Daengkaokhew, W.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Kongson, N.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Guntala, R.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Jaiyapan, N.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Kline, E.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Panpradist, N.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Ngo-Giang-Huong, Nicole</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Khamduang, W.</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>A single-tube colorimetric loop-mediated isothermal amplification for rapid detection of SARS-CoV-2 RNA</title>
        <secondary-title>Diagnostics</secondary-title>
      </titles>
      <pages>3040 [8 p.]</pages>
      <keywords>
        <keyword>COVID-19</keyword>
        <keyword>SARS-CoV-2 N gene</keyword>
        <keyword>RT-LAMP</keyword>
        <keyword>hydroxynaphthol blue</keyword>
        <keyword>cresol red</keyword>
        <keyword>THAILANDE</keyword>
      </keywords>
      <dates>
        <year>2023</year>
      </dates>
      <call-num>fdi:010088768</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Diagnostics</full-title>
      </periodical>
      <accession-num>ISI:001122377400001</accession-num>
      <number>19</number>
      <electronic-resource-num>10.3390/diagnostics13193040</electronic-resource-num>
      <urls>
        <related-urls>
          <url>https://www.documentation.ird.fr/hor/fdi:010088768</url>
        </related-urls>
        <pdf-urls>
          <url>https://horizon.documentation.ird.fr/exl-doc/pleins_textes/2024-01/010088768.pdf</url>
        </pdf-urls>
      </urls>
      <volume>13</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Since SARS-CoV-2 is a highly transmissible virus, a rapid and accurate diagnostic method is necessary to prevent virus spread. We aimed to develop and evaluate a new rapid colorimetric reverse transcription loop--mediated isothermal amplification (RT-LAMP) assay for SARS-CoV-2 detection in a single closed tube. Nasopharyngeal and throat swabs collected from at-risk individuals testing for SARS-CoV-2 were used to assess the sensitivity and specificity of a new RT-LAMP assay against a commercial qRT-PCR assay. Total RNA extracts were submitted to the RT-LAMP reaction under optimal conditions and amplified at 65 degrees C for 30 min using three sets of specific primers targeting the nucleocapsid gene. The reaction was detected using two different indicator dyes, hydroxynaphthol blue (HNB) and cresol red. A total of 82 samples were used for detection with HNB and 94 samples with cresol red, and results were compared with the qRT-PCR assay. The sensitivity of the RT-LAMP-based HNB assay was 92.1% and the specificity was 93.2%. The sensitivity of the RT-LAMP-based cresol red assay was 80.3%, and the specificity was 97%. This colorimetric feature makes this assay highly accessible, low-cost, and user-friendly, which can be deployed for massive scale-up and rapid diagnosis of SARS-CoV-2 infection, particularly in low-resource settings.</abstract>
      <custom6>020 ; 052</custom6>
      <custom1>UR224</custom1>
      <custom7>Thaïlande</custom7>
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