tetano
Editor, Senior Moderator
Virus Genes. 2016 Jun 24. [Epub ahead of print]
[h=1]Influenza A Virus-induced expression of ISG20 inhibits viral replication by interacting with nucleoprotein.[/h] Qu H[SUP]1[/SUP], Li J[SUP]2[/SUP], Yang L[SUP]2[/SUP], Sun L[SUP]2[/SUP], Liu W[SUP]3[/SUP], He H[SUP]4[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Influenza A virus (IAV) is an important pathogen that has a wide range of hosts and represents a threat to the health of humans and several animal species. IAV infection can induce the transcription of many genes in the host. In the present study, we demonstrated for the first time that three different strains of H1N1 IAV induce the expression of an IFN-stimulated gene, ISG20. We determined the antiviral activity of ISG20 against IAV because ISG20 inhibited viral protein expression and reduced the progeny viral titer dependent upon its exonuclease activity. To elucidate the detailed mechanism of ISG20, we further demonstrated that ISG20 impairs the polymerase activity and inhibits both the replication and transcription levels of the M1 and NP genes. Notably, we identified that ISG20 colocalizes and interacts with NP during IAV infection, while exonuclease-inactive mutant ISG20 lacked association with NP, indicating that ISG20 inhibits IAV replication by interacting with NP. Together, these data provide a detailed explanation for the specific antiviral action of ISG20 and suggest that ISG20 may act as a promising antiviral drug candidate against IAV.
[h=4]KEYWORDS:[/h] Exonuclease; IFN-stimulated gene; Polymerase activity
PMID: 27342813 DOI: 10.1007/s11262-016-1366-2
[PubMed - as supplied by publisher]
[h=1]Influenza A Virus-induced expression of ISG20 inhibits viral replication by interacting with nucleoprotein.[/h] Qu H[SUP]1[/SUP], Li J[SUP]2[/SUP], Yang L[SUP]2[/SUP], Sun L[SUP]2[/SUP], Liu W[SUP]3[/SUP], He H[SUP]4[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Influenza A virus (IAV) is an important pathogen that has a wide range of hosts and represents a threat to the health of humans and several animal species. IAV infection can induce the transcription of many genes in the host. In the present study, we demonstrated for the first time that three different strains of H1N1 IAV induce the expression of an IFN-stimulated gene, ISG20. We determined the antiviral activity of ISG20 against IAV because ISG20 inhibited viral protein expression and reduced the progeny viral titer dependent upon its exonuclease activity. To elucidate the detailed mechanism of ISG20, we further demonstrated that ISG20 impairs the polymerase activity and inhibits both the replication and transcription levels of the M1 and NP genes. Notably, we identified that ISG20 colocalizes and interacts with NP during IAV infection, while exonuclease-inactive mutant ISG20 lacked association with NP, indicating that ISG20 inhibits IAV replication by interacting with NP. Together, these data provide a detailed explanation for the specific antiviral action of ISG20 and suggest that ISG20 may act as a promising antiviral drug candidate against IAV.
[h=4]KEYWORDS:[/h] Exonuclease; IFN-stimulated gene; Polymerase activity
PMID: 27342813 DOI: 10.1007/s11262-016-1366-2
[PubMed - as supplied by publisher]