Abstract
VP22, encoded by the UL49 gene of Marek's disease virus (MDV), is indispensable for virus cell-to-cell spreading. We show herein that MDV UL49 can be functionally replaced with avian and human viral orthologs. Replacement of MDV VP22 with that of avian gallid herpesvirus 3 or herpesvirus of turkey, whose residue identity with MDV is close to 60%, resulted in 73 and 131% changes in viral spreading, respectively. In contrast, VP22 replacement with human herpes simplex virus type 1 resulted in 14% plaque formation. Therefore, heterologous avian and human VP22 proteins share sufficient structural homology to support MDV cell-to-cell spreading, albeit with different efficiencies.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Alphaherpesvirinae / classification*
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Alphaherpesvirinae / genetics
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Alphaherpesvirinae / metabolism
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Alphaherpesvirinae / physiology*
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Animals
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Birds / virology
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Cells, Cultured
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Chick Embryo
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Genetic Complementation Test
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Herpesvirus 1, Human / genetics
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Herpesvirus 1, Human / metabolism
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Herpesvirus 2, Gallid / genetics
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Herpesvirus 2, Gallid / metabolism
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Herpesvirus 2, Gallid / physiology*
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Herpesvirus 3, Gallid / genetics
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Herpesvirus 3, Gallid / metabolism
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Humans
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Mardivirus / genetics
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Mardivirus / metabolism
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Sequence Homology, Amino Acid*
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Skin / cytology
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Viral Proteins* / genetics
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Viral Proteins* / metabolism
Substances
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UL49 protein, Marek's disease virus type 1
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Viral Proteins