<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" 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:title xml:lang="eng">CRISPR‐Enhanced RAA‐SHERLOCK Assay for Point‐of‐Care Detection of Cyprinid Herpesvirus‐3: Development, Validation and Clinical Application</dc:title>
  <dc:description xml:lang="eng">Koi herpesvirus disease (KHVD), caused by Cyprinid herpesvirus-3 (CyHV-3), poses a significant threat to global aquaculture due to its high mortality rates and economic impact. Current diagnostic methods, such as PCR, are limited by equipment dependency and procedural complexity, hindering point-of-care (POC) applications. To address this, we developed an integrated assay combining recombinase-aided amplification (RAA) with CRISPR-Cas13a-mediated SHERLOCK technology and lateral flow detection (LFD) for rapid and visual detection of CyHV-3 in clinical samples. The KHV-SHERLOCK assay targets a conserved region of the CyHV-3 thymidine kinase (TK) gene, demonstrating exceptional specificity with no cross-reactivity to related pathogens or host DNA. Sensitivity evaluations revealed a detection limit of 100 ag/μL for CyHV-3 plasmid DNA, tenfold more sensitive than the conventional PCR (1 fg/μL) assay, even in the presence of 100 ng of carp genomic DNA as background interference. Clinical validation using 50 archived samples showed 100% concordance with reference PCR results, confirming diagnostic reliability. The assay&#39;s isothermal RAA step (37°C, 40 min) and CRISPR-Cas13a detection (37°C, 1 h) enable equipment-free operation, while LFD provides unambiguous visual results within minutes. This platform merges high sensitivity with POC practicality, offering a transformative tool for field-based KHVD surveillance.</dc:description>
  <dc:language>eng</dc:language>
  <dc:type xml:lang="deu">Text</dc:type>
  <dc:type xml:lang="deu">Wissenschaftlicher Artikel</dc:type>
  <dc:rights xml:lang="ita">Open Access</dc:rights>
  <dc:format>application/pdf</dc:format>
  <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
  <dc:subject xml:lang="eng">CRISPR-Cas13a</dc:subject>
  <dc:subject xml:lang="eng">CyHV-3</dc:subject>
  <dc:subject xml:lang="eng">Lateral Flow Detection</dc:subject>
  <dc:subject xml:lang="eng">Point-of-care Diagnostics</dc:subject>
  <dc:subject xml:lang="eng">Recombinase-aided Amplification</dc:subject>
  <dc:subject xml:lang="eng">SHERLOCK</dc:subject>
  <dc:creator>Hatem Soliman</dc:creator>
  <dc:creator>Naveed Akram</dc:creator>
  <dc:creator>Mona Saleh</dc:creator>
  <dc:publisher>Wiley</dc:publisher>
  <dc:type xml:lang="ita">Documento PDF</dc:type>
  <dc:type xml:lang="ita">Articolo scientifico</dc:type>
  <dc:source xml:lang="eng">Journal of Fish Diseases</dc:source>
  <dc:type xml:lang="eng">Text</dc:type>
  <dc:type xml:lang="eng">journal article</dc:type>
  <dc:identifier>doi:10.1111/jfd.70079</dc:identifier>
  <dc:rights xml:lang="eng">© 2025 The Author(s)</dc:rights>
  <dc:rights xml:lang="eng">open access</dc:rights>
  <dc:date>2026</dc:date>
  <dc:identifier>https://phaidra.vetmeduni.ac.at/o:5395</dc:identifier>
</oai_dc:dc>