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Proteome Response of Chicken Embryo Fibroblast Cells to Recombinant H5N1 Avian Influenza Viruses with Different Neuraminidase Stalk Lengths

tetano

Editor, Senior Moderator
Sci Rep. 2017 Jan 12;7:40698. doi: 10.1038/srep40698.
[h=1]Proteome Response of Chicken Embryo Fibroblast Cells to Recombinant H5N1 Avian Influenza Viruses with Different Neuraminidase Stalk Lengths.[/h] Li Y[SUP]1,[/SUP][SUP]2[/SUP], Ming F[SUP]1[/SUP], Huang H[SUP]1[/SUP], Guo K[SUP]1[/SUP], Chen H[SUP]1[/SUP], Jin M[SUP]1[/SUP], Zhou H[SUP]1[/SUP].
[h=3]Author information[/h]

[h=3]Abstract[/h] The variation on neuraminidase (NA) stalk region of highly pathogenic avian influenza H5N1 virus results in virulence change in animals. In our previous studies, the special NA stalk-motif of H5N1 viruses has been demonstrated to play a significant role in the high virulence and pathogenicity in chickens. However, the molecular mechanisms underlying the pathogenicity of viruses with different NA stalk remain poorly understood. This study presents a comprehensive characterization of the proteome response of chicken cells to recombinant H5N1 virus with stalk-short NA (rNA-wt) and the stalkless NA mutant virus (rSD20). 208 proteins with differential abundance profiles were identified differentially expressed (DE), and these proteins were mainly related to stress response, transcription regulation, transport, metabolic process, cellular component and cytoskeleton. Through Ingenuity Pathways Analysis (IPA), the significant biological functions of DE proteins represented included Post-Translational Modification, Protein Folding, DNA Replication, Recombination and Repair. It was interesting to find that most DE proteins were involved in the TGF-β mediated functional network. Moreover, the specific DE proteins may play important roles in the innate immune responses and H5N1 virus replication. Our data provide important information regarding the comparable host response to H5N1 influenza virus infection with different NA stalk lengths.


PMID: 28079188 DOI: 10.1038/srep40698
[PubMed - in process] Free full text
 
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