Abstract

Viral infections cause profound alterations in host cells. Here, we explore the interactions between proteins of the Alphavirus Sindbis and host factors during the course of mammalian cell infection. Using a mutant virus expressing the viral nsP3 protein tagged with green fluorescent protein (GFP) we directly observed nsP3 localization and isolated nsP3-interacting proteins at various times after infection. These results revealed that host factor recruitment to nsP3-containing complexes was time dependent, with a specific early and persistent recruitment of G3BP and a later recruitment of 14-3-3 proteins. Expression of GFP-tagged G3BP allowed reciprocal isolation of nsP3 in Sindbis infected cells, as well as the identification of novel G3BP-interacting proteins in both uninfected and infected cells. Note-worthy interactions include nuclear pore complex components whose interactions with G3BP were reduced upon Sindbis infection. This suggests that G3BP is a nuclear transport factor, as hypothesized previously, and that viral infection may alter RNA transport. Immunoelectron microscopy showed that a portion of Sindbis nsP3 is localized at the nuclear envelope, suggesting a possible site of G3BP recruitment to nsP3-containing complexes. Our results demonstrate the utility of using a standard GFP tag to both track viral protein localization and elucidate specific viral-host interactions over time in infected mammalian cells.

Highlights

  • The wide range of diseases caused by viruses is a reflection of their diverse interactions with host organisms and manipulation of cellular processes

  • Sequences encoding proteins involved in RNA replication, the nonstructural proteins,3 are located in the 5Ј twothirds of the viral genome, while the virion structural proteins are encoded by the 3Ј end of the genome

  • The stress granules identified by T-cell intracellular antigen-1 (TIA-1) staining after alphavirus infection are likely not the same structures as the cytoplasmic aggregates of nsP3 identified by us and others [34], since we did not identify TIA-1 in the nsP3 and G3BP containing complexes and TIA-1 did not co-localize with nsP3-green fluorescent protein (GFP) and G3BP

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Summary

Introduction

The wide range of diseases caused by viruses is a reflection of their diverse interactions with host organisms and manipulation of cellular processes. Using a mutant virus expressing the viral nsP3 protein tagged with green fluorescent protein (GFP) we directly observed nsP3 localization and isolated nsP3-interacting proteins at various times after infection. Our results demonstrate the utility of using a standard GFP tag to both track viral protein localization and elucidate specific viral-host interactions over time in infected mammalian cells.

Results
Conclusion
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