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        <datestamp>2026-09-28T17:52:10Z</datestamp>
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          <dc:title>&lt;p&gt;The low temperature-induced acyltransferase ZDHHC15a mediates palmitoylation of SVCVG.&lt;/p&gt;</dc:title>
          <dc:creator>Chen Li (54018)</dc:creator>
          <dc:creator>Yan Zhang (8098)</dc:creator>
          <dc:creator>Yujun Zhang (118792)</dc:creator>
          <dc:creator>Yan Gao (93649)</dc:creator>
          <dc:creator>Yuanan Lu (324035)</dc:creator>
          <dc:creator>Shengbo Cao (105106)</dc:creator>
          <dc:creator>Jing Ye (94291)</dc:creator>
          <dc:creator>Xueqin Liu (494581)</dc:creator>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Evolutionary Biology</dc:subject>
          <dc:subject>Environmental Sciences not elsewhere classified</dc:subject>
          <dc:subject>Ecology</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Inorganic Chemistry</dc:subject>
          <dc:subject>Science Policy</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>Virology</dc:subject>
          <dc:subject>significant economic impacts</dc:subject>
          <dc:subject>pathogenicity remain unclear</dc:subject>
          <dc:subject>modification enhances stability</dc:subject>
          <dc:subject>hold broader significance</dc:subject>
          <dc:subject>employed spring viremia</dc:subject>
          <dc:subject>competitive peptide targeting</dc:subject>
          <dc:subject>cell membrane localization</dc:subject>
          <dc:subject>20 &amp;# 176</dc:subject>
          <dc:subject>molecular mechanisms underlying</dc:subject>
          <dc:subject>affects rhabdovirus infections</dc:subject>
          <dc:subject>temperature adaptive evolution</dc:subject>
          <dc:subject>rhabdovirus prevalent</dc:subject>
          <dc:subject>mechanism underlying</dc:subject>
          <dc:subject>xlink "&gt;</dc:subject>
          <dc:subject>svcv glycoprotein</dc:subject>
          <dc:subject>svcv ),</dc:subject>
          <dc:subject>similar mechanism</dc:subject>
          <dc:subject>palmitic acid</dc:subject>
          <dc:subject>numerous rhabdoviruses</dc:subject>
          <dc:subject>high infectivity</dc:subject>
          <dc:subject>global aquaculture</dc:subject>
          <dc:subject>g protein</dc:subject>
          <dc:subject>g ).</dc:subject>
          <dc:subject>findings elucidate</dc:subject>
          <dc:subject>dependent infectivity</dc:subject>
          <dc:subject>crucial factor</dc:subject>
          <dc:subject>carp virus</dc:subject>
          <dc:subject>c ),</dc:subject>
          <dc:subject>aquatic rhabdoviruses</dc:subject>
          <dc:subject>acyltransferase zdhhc15a</dc:subject>
          <dc:description>&lt;p&gt;&lt;b&gt;(A)&lt;/b&gt; RNA interference effect on the expression of endogenous ZDHHC15a. ZF4 cells were transfected with ZDHHC15a-specific siRNA or control siRNA (NC) for 24 &lt;b&gt;h.&lt;/b&gt; The efficiency of siRNAs to inhibit the ZDHHC15a expression was detected by qRT-PCR. &lt;b&gt;(B)&lt;/b&gt; ZF4 cells were transfected with si-ZDHHC15a or si-NC for 12 h and then were transfected with the plasmid encoding SVCV G for 24 &lt;b&gt;h.&lt;/b&gt; Protein palmitoylation was examined by IP-ABE assay. The palmitoylated SVCV G and the immunoprecipitated SVCV G were blotted by HRP-streptavidin and SVCV G mAb, respectively. &lt;b&gt;(C)&lt;/b&gt; ZF4 cells were transfected with si-ZDHHC15a or si-NC for 12 h and then were transfected with the plasmid encoding SVCV G for 24 &lt;b&gt;h.&lt;/b&gt; Then, the cells were analyzed for SVCV G expression. &lt;b&gt;(D)&lt;/b&gt; ZF4 cells were infected with SVCV for 24 &lt;b&gt;h.&lt;/b&gt; The supernatant of WCL was immunoprecipitated using anti-SVCV G magnetic beads magnetic beads. Then, the precipitated proteins were analyzed by Western blotting. &lt;b&gt;(E-F)&lt;/b&gt; ZF4 cells were transfected with si-ZDHHC15a or si-NC for 12 h and then infected with SVCV(MOI = 10) for 24 &lt;b&gt;h.&lt;/b&gt; Cell samples and supernatant were collected 24 h after infection. The viral RNA abundance was detected using qRT-PCR. SVCV titers were measured by Viral plaque assay. &lt;b&gt;(G)&lt;/b&gt; Percentage survival of wild-type and &lt;i&gt;zdhhc15a&lt;/i&gt;&lt;sup&gt;-/-&lt;/sup&gt; zebrafish (n = 30) injected with 10 µl SVCV (10&lt;sup&gt;7&lt;/sup&gt;PFU/ml). Statistics of survival rate were calculated with the log-rank (Mantel-Cox). ***&lt;i&gt;p&lt;/i&gt; &lt; 0.001. &lt;b&gt;(H)&lt;/b&gt; The virus titer in tissues were detected by virus titration in zebrafish. Data was presented as mean ± SD from three independent experiments. Statistical analysis was performed using Student’s &lt;i&gt;t&lt;/i&gt;-&lt;i&gt;t&lt;/i&gt;est between different groups and the asterisk (*) indicates significant differences between groups*p &lt; 0.05, **p &lt; 0.01, ***p &lt; 0.001.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-28T17:51:51Z</dc:date>
          <dc:type>Image</dc:type>
          <dc:type>Figure</dc:type>
          <dc:identifier>10.1371/journal.ppat.1014654.g003</dc:identifier>
          <dc:relation>https://figshare.com/articles/figure/_p_The_low_temperature-induced_acyltransferase_ZDHHC15a_mediates_palmitoylation_of_SVCVG_p_/34017571</dc:relation>
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