| Literature DB >> 32056714 |
Gavin Golas1, Seung Jin Jang1, Nenavath Gopal Naik1, Juan D Alonso1, Bernadett Papp2, Zsolt Toth3.
Abstract
Unique among human viruses, Kaposi's sarcoma-associated herpesvirus (KSHV) encodes several homologs of cellular interferon regulatory factors (vIRFs). Since KSHV expresses multiple factors that can inhibit interferon (IFN) signaling to promote virus production, it is still unclear to what extent vIRFs contribute to these specific processes during KSHV infection. To study the function of vIRFs during viral infection, we engineered 3xFLAG-tagged-vIRF and vIRF-knockout recombinant KSHV clones, which were utilized to test vIRF expression, as well as their requirement for viral replication, virus production, and inhibition of the type I IFN pathway in different models of lytic KSHV infection. Our data show that all vIRFs can be expressed as lytic viral proteins, yet were dispensable for KSHV production and inhibition of type I IFN. Nevertheless, as vIRFs were able to suppress IFN-stimulated antiviral genes, vIRFs may still promote the KSHV lytic cycle in the presence of an ongoing antiviral response.Entities:
Keywords: BAC16; IFN signaling; Interferon-stimulated genes; KSHV; Lymphatic endothelial cells; Viral immune evasion; Viral replication; vIRFs
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Year: 2019 PMID: 32056714 PMCID: PMC7024068 DOI: 10.1016/j.virol.2019.12.011
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616