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        <datestamp>2026-09-28T17:52:11Z</datestamp>
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          <dc:title>&lt;p&gt;The G protein of low-temperature-sensitive &lt;i&gt;rhabdovirus&lt;/i&gt; is palmitoylated.&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; Protein palmitoylation software CSS-palm 4.0 was used to predict the VHSV G, IHNV G, SVCV G, MSRV G palmitoylation sites. &lt;b&gt;(B)&lt;/b&gt; ZF4 cells were transfected with plasmids expressing VHSV G/WT and VHSV G(C/A) at 16 °C and subsequently mock treated (VHSV G/WT and VHSV G(C/A) groups) or treated with 50 μM 2-BP (VHSV G/WT 2-BP group). Protein palmitoylation was examined by IP-ABE assay in the presence and absence of HAM. The palmitoylated VHSV G and the immunoprecipitated VHSV G were blotted by HRP-streptavidin and His mAb, respectively. &lt;b&gt;(C)&lt;/b&gt; ZF4 cells were transfected with plasmids expressing IHNV G/WT and IHNV G(C/A) at 16 °C and subsequently mock treated (IHNV G/WT and IHNV G(C/A) groups) or treated with 50 μM 2-BP (IHNV G/WT 2-BP group). Protein palmitoylation was examined by IP-ABE assay in the presence and absence of HAM. The palmitoylated IHNV G and the immunoprecipitated IHNV G were blotted by HRP-streptavidin and His mAb, respectively. &lt;b&gt;(D-F)&lt;/b&gt; ZF4 cells were transfected with plasmids expressing VHSV G, IHNV G and MSRV G at 16 °C and 28 °C. Protein palmitoylation was examined by IP-ABE assay in the presence of HAM. The palmitoylated MSRV G, VHSV G and IHNV G and the immunoprecipitated VHSV G, IHNV G and MSRV G were blotted by HRP-streptavidin and His mAb, respectively. &lt;b&gt;(G-H)&lt;/b&gt; ZF4 cells were transfected with the plasmid encoding VHSV G for 24h at 28 °C and 16 °C. Then, the cells were stimulated with CHX (1 µg/mL) and lysed at the indicated time points (0 h, 1 h, 2 h, and 4 &lt;b&gt;h)&lt;/b&gt;. The protein levels of VHSV G in the cell lysate were measured by Western blotting. &lt;b&gt;(I-J)&lt;/b&gt; ZF4 cells were transfected with the plasmid encoding IHNV G for 24h at 28 °C and 16 °C. Then, the cells were stimulated with CHX (1 µg/mL) and lysed at the indicated time points (0 h, 1 h, 2 h, and 4 &lt;b&gt;h)&lt;/b&gt;. The protein levels of IHNV G in the cell lysate were measured by Western blotting. &lt;b&gt;(K)&lt;/b&gt; ZF4 cells were transfected with the plasmid encoding MSRV G and were then treated with Orlistat (25µM, 50 µM, and 100 µM) or DMSO for 24 h at 16 °C. The MSRV G protein levels were measured by Western blotting. &lt;b&gt;(L)&lt;/b&gt; ZF4 cells were transfected with the plasmid encoding MSRV G and were then treated with 2-BP (25µM, 50 µM, and 100 µM) or DMSO for 24 h at 16 °C. The MSRV G protein levels were measured by Western blotting. &lt;b&gt;(M-N)&lt;/b&gt; ZF4 cells were transfected with the plasmid encoding VHSV G and IHNV G and were then treated with Orlistat (25µM, 50 µM, and 100 µM) or DMSO for 24 h at 16 °C. The VHSV G and IHNV G protein levels were measured by Western blotting. &lt;b&gt;(O-P)&lt;/b&gt; ZF4 cells were transfected with the plasmid encoding VHSV G and IHNV G and were then treated with 2-BP (25µM, 50 µM, and 100 µM) or DMSO for 24 h at 16 °C. The VHSV G and IHNV G protein levels were measured by Western blotting.&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.g004</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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