Herpesviruses assimilate kinesin to produce motorized viral particles

Article

关键词: HERPES-SIMPLEX-VIRUS;    MICROTUBULE-DEPENDENT TRAFFICKING;    LENGTH INFECTIOUS CLONE;    LARGE TEGUMENT PROTEIN;    PSEUDORABIES VIRUS;    CAPSID TRANSPORT;    TYPE-1;    BINDING;    EGRESS;    IDENTIFICATIONS;   

DOI  :  10.1038/s41586-021-04106-w

来源: SCIE

【 摘 要 】

Neurotropic alphaherpesviruses initiate infection in exposed mucosal tissues and, unlike most viruses, spread rapidly to sensory and autonomic nerves where life-long latency is established(1). Recurrent infections arise sporadically from the peripheral nervous system throughout the life of the host, and invasion of the central nervous system may occur, with severe outcomes(2). These viruses directly recruit cellular motors for transport along microtubules in nerve axons, but how the motors are manipulated to deliver the virus to neuronal nuclei is not understood. Here, using herpes simplex virus type I and pseudorabies virus as model alphaherpesviruses, we show that a cellular kinesin motor is captured by virions in epithelial cells, carried between cells, and subsequently used in neurons to traffic to nuclei. Viruses assembled in the absence of kinesin are not neuroinvasive. The findings explain a critical component of the alphaherpesvirus neuroinvasive mechanism and demonstrate that these viruses assimilate a cellular protein as an essential proviral structural component. This principle of viral assimilation may prove relevant to other virus families and offers new strategies to combat infection.

【 授权许可】

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