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    <responseDate>2026-10-13T01:23:34Z</responseDate>
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    <identifier>10.57760/sciencedb.42865</identifier>
    <datestamp>2026-07-13T14:50:43Z</datestamp>
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  <dc:date>2026-07-13</dc:date>
  <dc:title>&amp;beta;-D-N4-Hydroxycytidine inhibits canine parvovirus type 2 replication through transition-biased mutagenesis</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.42865</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Canine parvovirus type 2 (CPV-2) causes severe disease in young dogs, yet no specific antiviral therapy is currently available. &amp;beta;-D-N4-hydroxycytidine (NHC) is a nucleoside analogue which can perform broad-spectrum antiviral activities against RNA viruses, but its activity against DNA viruses remains poorly characterized. Here, we evaluated the antiviral activity and potential mechanism of NHC against CPV-2 in vitro. NHC dose-dependently inhibited CPV-2a, CPV-2b, and CPV-2c replication in F81 cells with limited cytotoxicity.&amp;nbsp;</dc:description>
  <dc:subject>Canine parvovirus type 2; β-D-N4-hydroxycytidine; nucleoside analogue; antiviral activity; transition-biased mutagenesis</dc:subject>
  <dc:creator>Xili Feng</dc:creator>
  <dc:creator>Chunlin Wang</dc:creator>
  <dc:creator>Zeyu Liu</dc:creator>
  <dc:creator>Jinchao Liu</dc:creator>
  <dc:creator>Maocheng Xia</dc:creator>
  <dc:creator>Xue Bai</dc:creator>
  <dc:creator>Jianhua Zhou</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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