Proteome Response of Chicken Embryo Fibroblast Cells to Recombinant H5N1 Avian Influenza Viruses with Different Neuraminidase Stalk Lengths.
Identifieur interne : 000328 ( PubMed/Corpus ); précédent : 000327; suivant : 000329Proteome Response of Chicken Embryo Fibroblast Cells to Recombinant H5N1 Avian Influenza Viruses with Different Neuraminidase Stalk Lengths.
Auteurs : Yongtao Li ; Fan Ming ; Huimin Huang ; Kelei Guo ; Huanchun Chen ; Meilin Jin ; Hongbo ZhouSource :
- Scientific reports [ 2045-2322 ] ; 2017.
English descriptors
- KwdEn :
- Animals, Chick Embryo, Chickens, Fibroblasts (metabolism), Fibroblasts (virology), Host-Pathogen Interactions, Influenza A Virus, H5N1 Subtype (drug effects), Influenza A Virus, H5N1 Subtype (genetics), Influenza A Virus, H5N1 Subtype (metabolism), Influenza A Virus, H5N1 Subtype (pathogenicity), Influenza in Birds (metabolism), Influenza in Birds (virology), Interferon-gamma (pharmacology), Neuraminidase (genetics), Protein Interaction Mapping, Protein Interaction Maps, Proteome, Proteomics (methods), Recombination, Genetic, Signal Transduction, Virus Replication.
- MESH :
- chemical , genetics : Neuraminidase.
- chemical , pharmacology : Interferon-gamma.
- drug effects : Influenza A Virus, H5N1 Subtype.
- genetics : Influenza A Virus, H5N1 Subtype.
- metabolism : Fibroblasts, Influenza A Virus, H5N1 Subtype, Influenza in Birds.
- methods : Proteomics.
- pathogenicity : Influenza A Virus, H5N1 Subtype.
- virology : Fibroblasts, Influenza in Birds.
- Animals, Chick Embryo, Chickens, Host-Pathogen Interactions, Protein Interaction Mapping, Protein Interaction Maps, Proteome, Recombination, Genetic, Signal Transduction, Virus Replication.
Abstract
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.
DOI: 10.1038/srep40698
PubMed: 28079188
Links to Exploration step
pubmed:28079188Le document en format XML
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<term>Fibroblasts (virology)</term>
<term>Host-Pathogen Interactions</term>
<term>Influenza A Virus, H5N1 Subtype (drug effects)</term>
<term>Influenza A Virus, H5N1 Subtype (genetics)</term>
<term>Influenza A Virus, H5N1 Subtype (metabolism)</term>
<term>Influenza A Virus, H5N1 Subtype (pathogenicity)</term>
<term>Influenza in Birds (metabolism)</term>
<term>Influenza in Birds (virology)</term>
<term>Interferon-gamma (pharmacology)</term>
<term>Neuraminidase (genetics)</term>
<term>Protein Interaction Mapping</term>
<term>Protein Interaction Maps</term>
<term>Proteome</term>
<term>Proteomics (methods)</term>
<term>Recombination, Genetic</term>
<term>Signal Transduction</term>
<term>Virus Replication</term>
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<front><div type="abstract" xml:lang="en">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.</div>
</front>
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<Abstract><AbstractText>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.</AbstractText>
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<AffiliationInfo><Affiliation>College of Animal Husbandry &Veterinary Science, Henan Agricultural University, Zhengzhou, 450002, P.R. China.</Affiliation>
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