The Dynein Light Chain 8 Binding Motif of Rabies Virus Phosphoprotein Promotes Efficient Viral Transcription

Gene S Tan, Thomas Jefferson University

Abstract

Recent studies implicate that interaction between rabies virus (RV) phosphoprotein (P) and the dynein light chain 8 (LC8) as essential for its pathogenesis. Through its association with the dynein motor complex, LC8 has been suggested as a molecular factor that links the viral ribonucleoprotein (RNP) to the host cell transport system. Recent structural investigations, however, dispute this model. In order to understand the role of LC8 in RV pathogenesis, we generated recombinant RVs with or without the LC8 binding domain (LC8-BD) deleted from the RV P. Peripheral infection of adult mice showed that removal of the LC8-BD did not inhibit entry into the central nervous system (CNS), although it prevented onset of RV-induced CNS disease. However, deletion of the LC8-BD significantly attenuated viral transcription and replication in the CNS. Studies in RAG2 KO mice infected with the same recombinant RVs confirmed this finding and indicated that the adaptive immune system is not a factor in the attenuation of viral replication early in the infection. In cell culture, the deletion of the LC8-BD greatly attenuated growth on neuronal cells whereas the growth pattern on non-neuronal cells remained unchanged. However, deletion of the LC8-BD did not affect production of RV virions. We provide evidence that removal of the LC8-BD decreases primary transcription. In this study, we propose that LC8 does not play a role in the retrograde axonal transport of RV and the deletion of the LC8-BD impairs the infectivity of the virions by reducing early transcription and replication in neurons.

Subject Area

Molecular biology|Microbiology|Virology

Recommended Citation

Tan, Gene S, "The Dynein Light Chain 8 Binding Motif of Rabies Virus Phosphoprotein Promotes Efficient Viral Transcription" (2007). ETD Collection for Thomas Jefferson University. AAI3537416.
https://jdc.jefferson.edu/dissertations/AAI3537416

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