4.6 Article

BAG3, a host cochaperone, facilitates Varicella-Zoster virus replication

Journal

JOURNAL OF VIROLOGY
Volume 81, Issue 14, Pages 7491-7503

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.00442-07

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Funding

  1. NIAID NIH HHS [AI024021, R21 AI024021, R01 AI024021] Funding Source: Medline

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Varicella-zoster virus (VZV) establishes a lifelong latent infection in the dorsal root ganglia of the host. During latency, a subset of virus-encoded regulatory proteins is detected; however, they are excluded from the nucleus. ORF29p, a single-stranded DNA binding protein, is one of these latency-associated proteins. We searched for cell proteins that interact with ORF29p and identified BAG3. BAG3, Hsp70/Hsc70, and Hsp90 colocalize with ORF29p in nuclear transcription/replication factories during lytic replication of VZV. Pharmacological intercession of Hsp90 activity with ansamycin antibiotics or depletion of BAG3 by small interfering RNA results in inhibition of virus replication. Replication in BAG3-depleted cell lines is restored by complementation with exogenous BAG3. Alteration of host chaperone activity provides a novel means of regulating virus replication.

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