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    <responseDate>2026-10-15T12:54:00Z</responseDate>
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    <identifier>10.57760/sciencedb.28727</identifier>
    <datestamp>2025-08-04T11:14:54Z</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>2025-08-04</dc:date>
  <dc:title>Antiviral RNAi Restricts DNA Virus Infection in Mammals</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.28727</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Antiviral RNA interference (RNAi) is&amp;nbsp;an established&amp;nbsp;component of mammalian innate immunity, primarily recognized for targeting&amp;nbsp;RNA viruses. However, whether mammalian RNAi&amp;nbsp;can&amp;nbsp;restrict&amp;nbsp;DNA virus infection remains unclear. In this study, we uncover that double-stranded DNA (dsDNA) viruses&amp;mdash;poxviruses, including Vaccinia virus (VACV) and Monkeypox virus (MPXV),&amp;nbsp;trigger antiviral RNAi in mammalian cells. During poxvirus infection, viral dsRNAs&amp;nbsp;are derived from bidirectional transcription of the viral DNA genome and elicit&amp;nbsp;Dicer-dependent production of viral siRNAs&amp;nbsp;(vsiRNAs), which predominantly&amp;nbsp;locate&amp;nbsp;to&amp;nbsp;the inverted terminal repeat (ITR)&amp;nbsp;regions at the termini&amp;nbsp;of the poxvirus genome. Depletion of Dicer or mutagenic inactivation of AGO2&amp;rsquo;s RNA slicing activity enhances the replication of VACV and MPXV. Moreover, sequestration of ITR-derived vsiRNAs by sponge decoys increases VACV replication, attributable to the role of these vsiRNAs in inhibiting the resolution of viral concatemeric DNA genomes into mature monomers. Furthermore, AGO2-deficient cells exhibit more sensitivity to VACV infection compared to STING- or MAVS-deficient cells, suggesting that RNAi is the primary antiviral response in restricting VACV infection in mammalian cells. In VACV-infected mice, Dicer conditional knockout exacerbates disease severity, manifested by increased mortality, exacerbated pulmonary pathology&amp;nbsp;and elevated viral loads. Additionally, treatment with enoxacin, an RNAi enhancer, suppresses&amp;nbsp;VACV replication in an RNAi-dependent manner both in vitro and in vivo. Together, our&amp;nbsp;findings provide evidence for the functional relevance of RNAi in counteracting DNA viruses in mammals and discover an unprecedented role of vsiRNAs&amp;nbsp;involved in poxvirus genome replication.</dc:description>
  <dc:subject>Antiviral RN Ai; Poxvirus; vsiRNA</dc:subject>
  <dc:creator>Yang Qiu</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc-sa/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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