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      <title>A single-tube colorimetric loop-mediated isothermal amplification for rapid detection of SARS-CoV-2 RNA</title>
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    <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>
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      <topic>COVID-19</topic>
      <topic>SARS-CoV-2 N gene</topic>
      <topic>RT-LAMP</topic>
      <topic>hydroxynaphthol blue</topic>
      <topic>cresol red</topic>
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      <geographic>THAILANDE</geographic>
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        <title>Diagnostics</title>
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          <number>13</number>
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          <number>19</number>
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          <list> 3040 [8 p.]</list>
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        <dateIssued>2023</dateIssued>
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    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010088768</identifier>
    <identifier type="doi">10.3390/diagnostics13193040</identifier>
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