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Poult Sci ; 100(1): 26-38, 2021 Jan.
Article in English | MEDLINE | ID: mdl-33357689

ABSTRACT

Duck enteritis virus (DEV) multifunctional tegument protein UL13 is predicted to be a conserved herpesvirus protein kinase; however, little is known about its subcellular localization signal. In this study, through transfection of 2 predicted nuclear signals of DEV UL13 fused to enhanced green fluorescent protein, 2 bipartite nuclear localization signals (NLS) were identified. We found that ivermectin blocked the NLS-mediated nuclear import of DEV UL13, showing that the nuclear localization signal of DEV UL13 is a classical importin α- and ß-dependent process. We constructed a DEV UL13 mutant strain in which the NLS of DEV UL13 was deleted to explore whether deletion of the NLS affects viral replication. Amino acids 4 to 7 and 90 to 96 were predicted to be NLSs, further proving that nuclear import occurs via a classical importin α- and ß-dependent process. We also found that the NLS of pUL13 had no effect on DEV replication in cell culture. Our study enhances the understanding of DEV pUL13. Taken together, these results provide significant information regarding the biological function of pUL13 during DEV infection.


Subject(s)
Enteritis , Mardivirus , Nuclear Localization Signals , Protein Kinases , Animals , Antiparasitic Agents/pharmacology , Cells, Cultured , Ducks , Enteritis/physiopathology , Enteritis/veterinary , Enteritis/virology , Intracellular Space/metabolism , Intracellular Space/virology , Ivermectin/pharmacology , Mardivirus/genetics , Mardivirus/metabolism , Mutation , Nuclear Localization Signals/drug effects , Protein Kinases/genetics , Protein Kinases/metabolism , Protein Transport/drug effects , Protein Transport/genetics
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