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Construction of varicella-zoster virus recombinants from parent Oka cosmids and demonstration that ORF65 protein is dispensable for infection of human skin and T cells in the SCID-hu mouse model
Authors:Niizuma Takahiro  Zerboni Leigh  Sommer Marvin H  Ito Hideki  Hinchliffe Stewart  Arvin Ann M
Affiliation:Department of Pediatrics, Stanford University School of Medicine, Stanford, California 94305, USA.
Abstract:We generated an ORF65 deletion mutant by using a cosmid system constructed from the genome of a low-passage clinical isolate (P-Oka). Using the SCID-hu mouse model, we demonstrated that the ORF65 protein is dispensable for viral replication in skin and T cells, which are critical host cell targets during primary varicella-zoster virus infection.
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