TY - JOUR
T1 - Efficient retrograde transport of pseudorabies virus within neurons requires local protein synthesis in axons
AU - Koyuncu, Orkide O.
AU - Perlman, David H.
AU - Enquist, Lynn W.
N1 - Funding Information:
We thank Emre Koyuncu and the members of the Enquist lab, especially Andrea Granstedt, Tal Kramer, Matthew Taylor, and Ren Song, for their comments and critical reading of the manuscript. L.W.E. is supported by U.S. National Institutes of Health grant R01NS033506-18.
PY - 2013/1/16
Y1 - 2013/1/16
N2 - After replicating in epithelial cells, alphaherpesviruses such as pseudorabies virus (PRV) invade axons of peripheral nervous system neurons and undergo retrograde transport toward the distant cell bodies. Although several viral proteins engage molecular motors to facilitate transport, the initial steps and neuronal responses to infection are poorly understood. Using compartmented neuron cultures to physically separate axon infection from cell bodies, we found that PRV infection induces local protein synthesis in axons, including proteins involved in cytoskeletal remodeling, intracellular trafficking, signaling, and metabolism. This rapid translation of axonal mRNAs is required for efficient PRV retrograde transport and infection of cell bodies. Furthermore, induction of axonal damage, which also induces local protein synthesis, prior to infection reduces virion trafficking, suggesting that host damage signals and virus particles compete for retrograde transport. Thus, similar to axonal damage, virus infection induces local protein translation in axons, and viruses likely exploit this response for invasion.
AB - After replicating in epithelial cells, alphaherpesviruses such as pseudorabies virus (PRV) invade axons of peripheral nervous system neurons and undergo retrograde transport toward the distant cell bodies. Although several viral proteins engage molecular motors to facilitate transport, the initial steps and neuronal responses to infection are poorly understood. Using compartmented neuron cultures to physically separate axon infection from cell bodies, we found that PRV infection induces local protein synthesis in axons, including proteins involved in cytoskeletal remodeling, intracellular trafficking, signaling, and metabolism. This rapid translation of axonal mRNAs is required for efficient PRV retrograde transport and infection of cell bodies. Furthermore, induction of axonal damage, which also induces local protein synthesis, prior to infection reduces virion trafficking, suggesting that host damage signals and virus particles compete for retrograde transport. Thus, similar to axonal damage, virus infection induces local protein translation in axons, and viruses likely exploit this response for invasion.
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U2 - 10.1016/j.chom.2012.10.021
DO - 10.1016/j.chom.2012.10.021
M3 - Article
C2 - 23332155
AN - SCOPUS:84872576880
SN - 1931-3128
VL - 13
SP - 54
EP - 66
JO - Cell Host and Microbe
JF - Cell Host and Microbe
IS - 1
ER -