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    <responseDate>2026-10-14T21:39:14Z</responseDate>
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    <header >
    <identifier>10.57760/sciencedb.16909</identifier>
    <datestamp>2024-03-15T16:49:28Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2024-03-15</dc:date>
  <dc:title>Ultrasensitive and Visual Detection of Pseudorabies Virus based on CRISPR-Cas12b</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.16909</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Aujeszky's disease (AD) is an acute infectious disease that infects pigs or other animals, resulting in significant economic losses and posing a threat to human health. Reliable and rapid detection methods are essential for the prevention and control of AD. In this study, a platform based on recombinase aided amplification (RAA) and CRISPR-Cas12b has been established, optimized, and evaluated for the rapid detection of Pseudorabies Virus (PRV). To enhance the usability and simplicity of the assay, we have developed PRV RAA-Cas12b methods for fluorescence-based detection and visualization. There was no cross-reaction with PRV Bartha-K61 strain or other common swine infectious viruses. The analytical sensitivity of the assay was determined to be 15 copies/&amp;micro;L by real-time fluorescence read-out with a 95% probability. The limit of detection (LOD) for the visual PRV RAA-Cas12b assay was 140 copies/&amp;micro;L with a 95% probability. Thirty-one clinical tissue samples were detected and compared with PRV qPCR to evaluate the diagnostic performance of the method. The diagnostic coincidence rate of the two methods was 100 %. Taking together, we established a rapid and convenient RAA-Cas12b method for the detection of wild-type PRV. This method holds a broad application prospect in the point-of-care testing (POCT).</dc:description>
  <dc:subject>CRISPR-Cas12b system; Pseudorabies virus; Recombinase aided amplification; quantitative PCR; rapid detection</dc:subject>
  <dc:creator>Haoran Kang</dc:creator>
  <dc:creator>Xintan Yang</dc:creator>
  <dc:creator>Ruijiao Jiang</dc:creator>
  <dc:creator>Peng Gao</dc:creator>
  <dc:creator>Yongning Zhang</dc:creator>
  <dc:creator>Zhou Lei</dc:creator>
  <dc:creator>Xinna Ge</dc:creator>
  <dc:creator>Jun Han</dc:creator>
  <dc:creator>Xin Guo</dc:creator>
  <dc:creator>Hanchun Yang</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://opendatacommons.org/licenses/pddl/1-0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
</oai_dc:dc>

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