tetano
Editor, Senior Moderator
Sci Rep. 2016 Nov 21;6:35041. doi: 10.1038/srep35041.
[h=1]Suppression of Rac1 Signaling by Influenza A Virus NS1 Facilitates Viral Replication.[/h] Jiang W[SUP]1[/SUP], Sheng C[SUP]1[/SUP], Gu X[SUP]1,[/SUP][SUP]2[/SUP], Liu D[SUP]1[/SUP], Yao C[SUP]1[/SUP], Gao S[SUP]1[/SUP], Chen S[SUP]3[/SUP], Huang Y[SUP]4[/SUP], Huang W[SUP]3,[/SUP][SUP]5[/SUP], Fang M[SUP]1,[/SUP][SUP]6[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Influenza A virus (IAV) is a major human pathogen with the potential to become pandemic. IAV contains only eight RNA segments; thus, the virus must fully exploit the host cellular machinery to facilitate its own replication. In an effort to comprehensively characterize the host machinery taken over by IAV in mammalian cells, we generated stable A549 cell lines with over-expression of the viral non-structural protein (NS1) to investigate the potential host factors that might be modulated by the NS1 protein. We found that the viral NS1 protein directly interacted with cellular Rac1 and facilitated viral replication. Further research revealed that NS1 down-regulated Rac1 activity via post-translational modifications. Therefore, our results demonstrated that IAV blocked Rac1-mediated host cell signal transduction through the NS1 protein to facilitate its own replication. Our findings provide a novel insight into the mechanism of IAV replication and indicate new avenues for the development of potential therapeutic targets.
PMID: 27869202 DOI: 10.1038/srep35041
[PubMed - in process] Free full text
[h=1]Suppression of Rac1 Signaling by Influenza A Virus NS1 Facilitates Viral Replication.[/h] Jiang W[SUP]1[/SUP], Sheng C[SUP]1[/SUP], Gu X[SUP]1,[/SUP][SUP]2[/SUP], Liu D[SUP]1[/SUP], Yao C[SUP]1[/SUP], Gao S[SUP]1[/SUP], Chen S[SUP]3[/SUP], Huang Y[SUP]4[/SUP], Huang W[SUP]3,[/SUP][SUP]5[/SUP], Fang M[SUP]1,[/SUP][SUP]6[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Influenza A virus (IAV) is a major human pathogen with the potential to become pandemic. IAV contains only eight RNA segments; thus, the virus must fully exploit the host cellular machinery to facilitate its own replication. In an effort to comprehensively characterize the host machinery taken over by IAV in mammalian cells, we generated stable A549 cell lines with over-expression of the viral non-structural protein (NS1) to investigate the potential host factors that might be modulated by the NS1 protein. We found that the viral NS1 protein directly interacted with cellular Rac1 and facilitated viral replication. Further research revealed that NS1 down-regulated Rac1 activity via post-translational modifications. Therefore, our results demonstrated that IAV blocked Rac1-mediated host cell signal transduction through the NS1 protein to facilitate its own replication. Our findings provide a novel insight into the mechanism of IAV replication and indicate new avenues for the development of potential therapeutic targets.
PMID: 27869202 DOI: 10.1038/srep35041
[PubMed - in process] Free full text