Abstract

ABSTRACTMany molecular and cell biological details of the alphaherpesvirus assembly and egress pathway remain unclear. Recently we developed a live-cell fluorescence microscopy assay of pseudorabies virus (PRV) exocytosis, based on total internal reflection fluorescence (TIRF) microscopy and a virus-encoded pH-sensitive fluorescent probe. Here, we use this assay to distinguish three classes of viral exocytosis in a nonpolarized cell type: (i) trafficking of viral glycoproteins to the plasma membrane, (ii) exocytosis of viral light particles, and (iii) exocytosis of virions. We find that viral glycoproteins traffic to the cell surface in association with constitutive secretory Rab GTPases and exhibit free diffusion into the plasma membrane after exocytosis. Similarly, both virions and light particles use these same constitutive secretory mechanisms for egress from infected cells. Furthermore, we show that viral light particles are distinct from cellular exosomes. Together, these observations shed light on viral glycoprotein trafficking steps that precede virus particle assembly and reinforce the idea that virions and light particles share a biogenesis and trafficking pathway.

Highlights

  • Many molecular and cell biological details of the alphaherpesvirus assembly and egress pathway remain unclear

  • We found that Rab6a, Rab8a, and Rab11a are associated with trafficking of viral glycoproteins to the plasma membrane (Fig. 2A to F)

  • We found that Rab6a, Rab8a, and Rab11a were dynamically associated with all three types of viral exocytosis, implicating these same constitutive secretory mechanisms in multiple steps in the virus replication cycle

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Summary

Introduction

Many molecular and cell biological details of the alphaherpesvirus assembly and egress pathway remain unclear. We find that viral glycoproteins traffic to the cell surface in association with constitutive secretory Rab GTPases and exhibit free diffusion into the plasma membrane after exocytosis Both virions and light particles use these same constitutive secretory mechanisms for egress from infected cells. In addition to assembly of infectious virions, the alphaherpesviruses produce a multitude of noninfectious “light particles,” or “L-particles” [8] These particles are similar in size to virions and contain viral tegument and membrane proteins but do not contain virus capsids or genomes. Both viral light particles and cell-derived extracellular microvesicles (i.e., exosomes) deliver biologically active molecules (e.g., proteins and RNA) between cells, their relationship remains unclear [9, 10]

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