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Herpes simplex virus-1 induces expression of a novel MxA isoform that enhances viral replication.

Research paper by Chia-Chi CC Ku, Xi-Bing XB Che, Mike M Reichelt, Jaya J Rajamani, Anne A Schaap-Nutt, Ke-Jung KJ Huang, Marvin H MH Sommer, Yi-Shun YS Chen, Yi-Yuan YY Chen, Ann M AM Arvin

Indexed on: 07 Jul '10Published on: 07 Jul '10Published in: Immunology & Cell Biology



Abstract

MxA is an antiviral protein induced by interferon (IFN)-α/β that is known to inhibit the replication of many RNA viruses. In these experiments, the 76-kDa MxA protein expressed in IFN-α-treated cells was shown to have antiviral activity against herpes simplex virus-1 (HSV-1), a human DNA virus. However, MxA was expressed as a 56-kDa protein in HSV-1-infected cells in the absence of IFN-α. This previously unrecognized MxA isoform was produced from an alternatively spliced MxA transcript that had a deletion of Exons 14-16 and a frame shift altering the C-terminus. The variant MxA (varMxA) isoform was associated with HSV-1 regulatory proteins and virions in nuclear replication compartments. varMxA expression enhanced HSV-1 infection as shown by a reduction in infectious virus titers from cells in which MxA had been inhibited by RNA interference and by an increase in HSV-1 titers when the 56-kDa varMxA was expressed constitutively. Thus, the human MxA gene encodes two MxA isoforms, which are expressed differentially depending on whether the stimulus is IFN-α or HSV-1. These findings show that alternative splicing of cellular mRNA can result in expression of a novel isoform of a host defense gene that supports instead of restricting viral infection.