A Human and Rhesus Macaque Interferon-Stimulated Gene Screen Shows That Over-Expression of ARHGEF3/XPLN Inhibits Replication of Hepatitis C Virus and Other Flavivirids.

Bibliographic Details
Title: A Human and Rhesus Macaque Interferon-Stimulated Gene Screen Shows That Over-Expression of ARHGEF3/XPLN Inhibits Replication of Hepatitis C Virus and Other Flavivirids.
Authors: Bamford, Connor G. G.1,2 (AUTHOR) c.bamford@qub.ac.uk, Aranday-Cortes, Elihu1 (AUTHOR) elihu.aranday-cortes@glasgow.ac.uk, Sanchez-Velazquez, Ricardo1,3 (AUTHOR) ricardo.sanchez@biontech.de, Mullan, Catrina1 (AUTHOR) c.mullan.1@research.gla.ac.uk, Kohl, Alain1 (AUTHOR) alain.kohl@glasgow.ac.uk, Patel, Arvind H.1 (AUTHOR) arvind.patel@glasgow.ac.uk, Wilson, Sam J.1 (AUTHOR) sam.wilson@glasgow.ac.uk, McLauchlan, John1 (AUTHOR) john.mclauchlan@glasgow.ac.uk
Source: Viruses (1999-4915). Aug2022, Vol. 14 Issue 8, p1655-1655. 18p.
Subject Terms: *MACAQUES, *RHESUS monkeys, *GUANINE nucleotide exchange factors, *HEPATITIS C virus, *SIMIAN immunodeficiency virus, *YELLOW fever, *ZIKA virus
Abstract: Natural hepatitis C virus (HCV) infection is restricted to humans, whereas other primates such as rhesus macaques are non-permissive for infection. To identify human and rhesus macaque genes that differ or share the ability to inhibit HCV replication, we conducted a medium-throughput screen of lentivirus-expressed host genes that disrupt replication of HCV subgenomic replicon RNA expressing secreted Gaussia luciferase. A combined total of >800 interferon-stimulated genes (ISGs) were screened. Our findings confirmed established anti-HCV ISGs, such as IRF1, PKR and DDX60. Novel species–specific inhibitors were also identified and independently validated. Using a cell-based system that recapitulates productive HCV infection, we identified that over-expression of the 'Rho Guanine Nucleotide Exchange Factor 3' gene (ARHGEF3) from both species inhibits full-length virus replication. Additionally, replication of two mosquito-borne flaviviruses, yellow fever virus (YFV) and Zika virus (ZIKV), were also reduced in cell lines over-expressing ARHGEF3 compared to controls. In conclusion, we ascribe novel antiviral activity to the cellular gene ARHGEF3 that inhibits replication of HCV and other important human viral pathogens belonging to the Flaviviridae, and which is conserved between humans and rhesus macaques. [ABSTRACT FROM AUTHOR]
Copyright of Viruses (1999-4915) is the property of MDPI and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Academic Search Complete
More Details
ISSN:19994915
DOI:10.3390/v14081655
Published in:Viruses (1999-4915)
Language:English