Announcement

Collapse
No announcement yet.

Peptide-Mediated Interference of PB2-eIF4G1 Interaction Inhibits Influenza A Viruses' Replication in Vitro and in Vivo

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Peptide-Mediated Interference of PB2-eIF4G1 Interaction Inhibits Influenza A Viruses' Replication in Vitro and in Vivo

    ACS Infect Dis. 2016 Jul 8;2(7):471-7. doi: 10.1021/acsinfecdis.6b00064. Epub 2016 Jun 13.
    Peptide-Mediated Interference of PB2-eIF4G1 Interaction Inhibits Influenza A Viruses' Replication in Vitro and in Vivo.

    Yuan S1, Chu H1, Ye J1, Hu M1, Singh K2, Chow BK2, Zhou J1, Zheng BJ1.
    Author information

    Abstract

    Influenza viruses are obligate parasites that hijack the host cellular system. Previous results have shown that the influenza virus PB2 subunit confers a dependence of host eukaryotic translation initiation factor 4-γ 1 (eIF4G1) for viral mRNA translation. Here, we demonstrated that peptide-mediated interference of the PB2-eIF4G1 interaction inhibited virus replication in vitro and in vivo. Remarkably, intranasal administration of the peptide provided 100% protection against lethal challenges of influenza A viruses in BALB/c mice, including H1N1, H5N1, and H7N9 influenza virus subtypes. Mapping of the PB2 protein indicated that the eIF4G1 binding sites resided within the PB2 cap-binding domain. Virtual docking analysis suggested that the inhibitory peptide associated with the conserved amino acid residues that were essential to PB2 cap-binding activity. Overall, our results identified the PB2-eIF4G1 interactive site as a druggable target for influenza therapeutics.


    KEYWORDS:

    PB2; Tat; antiviral peptide; eIF4G1; host−virus interaction; influenza virus

    PMID: 27626099 DOI: 10.1021/acsinfecdis.6b00064
    [PubMed - in process]
Working...
X