Role of Us9 phosphorylation in axonal sorting and anterograde transport of pseudorabies virus.

Alphaherpes viruses, such as pseudorabies virus (PRV), undergo anterograde transport in neuronal axons to facilitate anterograde spread within hosts. Axonal sorting and anterograde transport of virions is dependent on the viral membrane protein Us9, which interacts with the host motor protein Kif1A...

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Main Authors: Radomir Kratchmarov, Matthew P Taylor, Lynn W Enquist
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3602541?pdf=render
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author Radomir Kratchmarov
Matthew P Taylor
Lynn W Enquist
author_facet Radomir Kratchmarov
Matthew P Taylor
Lynn W Enquist
author_sort Radomir Kratchmarov
collection DOAJ
description Alphaherpes viruses, such as pseudorabies virus (PRV), undergo anterograde transport in neuronal axons to facilitate anterograde spread within hosts. Axonal sorting and anterograde transport of virions is dependent on the viral membrane protein Us9, which interacts with the host motor protein Kif1A to direct transport. Us9-Kif1A interactions are necessary but not sufficient for these processes, indicating that additional cofactors or post-translational modifications are needed. In this study, we characterized two conserved serine phosphorylation sites (S51 and S53) in the PRV Us9 protein that are necessary for anterograde spread in vivo. We assessed the subcellular localization of phospho-Us9 subspecies during infection of neurons and found that the phospho-form is detectable on the majority, but not all, of axonal vesicles containing Us9 protein. In biochemical assays, phospho-Us9 was enriched in lipid raft membrane microdomains, though Us9 phosphorylation did not require prior lipid raft association. During infections of chambered neuronal cultures, we observed only a modest reduction in anterograde spread capacity for diserine mutant Us9, and no defect for monoserine mutants. Conversely, mutation of the kinase recognition sequence residues adjacent to the phosphorylation sites completely abrogated anterograde spread. In live-cell imaging analyses, anterograde transport of virions was reduced during infection with a recombinant PRV strain expressing GFP-tagged diserine mutant Us9. Phosphorylation was not required for Us9-Kif1A interaction, suggesting that Us9-Kif1A binding is a distinct step from the activation and/or stabilization of the transport complex. Taken together, our findings indicate that, while not essential, Us9 phosphorylation enhances Us9-Kif1A-based transport of virions in axons to modulate the overall efficiency of long-distance anterograde spread of infection.
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spelling doaj.art-efd481571ef544b8bd80a80ec8db37d22022-12-22T00:48:36ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0183e5877610.1371/journal.pone.0058776Role of Us9 phosphorylation in axonal sorting and anterograde transport of pseudorabies virus.Radomir KratchmarovMatthew P TaylorLynn W EnquistAlphaherpes viruses, such as pseudorabies virus (PRV), undergo anterograde transport in neuronal axons to facilitate anterograde spread within hosts. Axonal sorting and anterograde transport of virions is dependent on the viral membrane protein Us9, which interacts with the host motor protein Kif1A to direct transport. Us9-Kif1A interactions are necessary but not sufficient for these processes, indicating that additional cofactors or post-translational modifications are needed. In this study, we characterized two conserved serine phosphorylation sites (S51 and S53) in the PRV Us9 protein that are necessary for anterograde spread in vivo. We assessed the subcellular localization of phospho-Us9 subspecies during infection of neurons and found that the phospho-form is detectable on the majority, but not all, of axonal vesicles containing Us9 protein. In biochemical assays, phospho-Us9 was enriched in lipid raft membrane microdomains, though Us9 phosphorylation did not require prior lipid raft association. During infections of chambered neuronal cultures, we observed only a modest reduction in anterograde spread capacity for diserine mutant Us9, and no defect for monoserine mutants. Conversely, mutation of the kinase recognition sequence residues adjacent to the phosphorylation sites completely abrogated anterograde spread. In live-cell imaging analyses, anterograde transport of virions was reduced during infection with a recombinant PRV strain expressing GFP-tagged diserine mutant Us9. Phosphorylation was not required for Us9-Kif1A interaction, suggesting that Us9-Kif1A binding is a distinct step from the activation and/or stabilization of the transport complex. Taken together, our findings indicate that, while not essential, Us9 phosphorylation enhances Us9-Kif1A-based transport of virions in axons to modulate the overall efficiency of long-distance anterograde spread of infection.http://europepmc.org/articles/PMC3602541?pdf=render
spellingShingle Radomir Kratchmarov
Matthew P Taylor
Lynn W Enquist
Role of Us9 phosphorylation in axonal sorting and anterograde transport of pseudorabies virus.
PLoS ONE
title Role of Us9 phosphorylation in axonal sorting and anterograde transport of pseudorabies virus.
title_full Role of Us9 phosphorylation in axonal sorting and anterograde transport of pseudorabies virus.
title_fullStr Role of Us9 phosphorylation in axonal sorting and anterograde transport of pseudorabies virus.
title_full_unstemmed Role of Us9 phosphorylation in axonal sorting and anterograde transport of pseudorabies virus.
title_short Role of Us9 phosphorylation in axonal sorting and anterograde transport of pseudorabies virus.
title_sort role of us9 phosphorylation in axonal sorting and anterograde transport of pseudorabies virus
url http://europepmc.org/articles/PMC3602541?pdf=render
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