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Nat Commun ; 9(1): 1980, 2018 05 17.
Article in English | MEDLINE | ID: mdl-29773792

ABSTRACT

The type I interferon (IFN) system plays an important role in controlling herpesvirus infections, but it is unclear which IFN-mediated effectors interfere with herpesvirus replication. Here we report that human myxovirus resistance protein B (MxB, also designated Mx2) is a potent human herpesvirus restriction factor in the context of IFN. We demonstrate that ectopic MxB expression restricts a range of herpesviruses from the Alphaherpesvirinae and Gammaherpesvirinae, including herpes simplex virus 1 and 2 (HSV-1 and HSV-2), and Kaposi's sarcoma-associated herpesvirus (KSHV). MxB restriction of HSV-1 and HSV-2 requires GTPase function, in contrast to restriction of lentiviruses. MxB inhibits the delivery of incoming HSV-1 DNA to the nucleus and the appearance of empty capsids, but not the capsid delivery to the cytoplasm or tegument dissociation from the capsid. Our study identifies MxB as a potent pan-herpesvirus restriction factor which blocks the uncoating of viral DNA from the incoming viral capsid.


Subject(s)
Herpesviridae Infections/immunology , Herpesviridae/physiology , Interferon Type I/immunology , Myxovirus Resistance Proteins/immunology , Virus Replication/immunology , Capsid/immunology , Capsid Proteins/immunology , Cell Line, Tumor , Cell Nucleus/immunology , Cell Nucleus/virology , Cytoplasm , DNA, Viral/immunology , HEK293 Cells , Herpesviridae/pathogenicity , Herpesviridae Infections/virology , Humans , Myxovirus Resistance Proteins/genetics , RNA, Small Interfering/metabolism , Virus Uncoating/immunology
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