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A novel peptide with potent and broad-spectrum antiviral activities against multiple respiratory viruses.

Identifieur interne : 001247 ( PubMed/Corpus ); précédent : 001246; suivant : 001248

A novel peptide with potent and broad-spectrum antiviral activities against multiple respiratory viruses.

Auteurs : Hanjun Zhao ; Jie Zhou ; Ke Zhang ; Hin Chu ; Dabin Liu ; Vincent Kwok-Man Poon ; Chris Chung-Sing Chan ; Ho-Chuen Leung ; Ng Fai ; Yong-Ping Lin ; Anna Jin-Xia Zhang ; Dong-Yan Jin ; Kwok-Yung Yuen ; Bo-Jian Zheng

Source :

RBID : pubmed:26911565

English descriptors

Abstract

A safe, potent and broad-spectrum antiviral is urgently needed to combat emerging respiratory viruses. In light of the broad antiviral activity of β-defensins, we tested the antiviral activity of 11 peptides derived from mouse β-defensin-4 and found that a short peptide, P9, exhibited potent and broad-spectrum antiviral effects against multiple respiratory viruses in vitro and in vivo, including influenza A virus H1N1, H3N2, H5N1, H7N7, H7N9, SARS-CoV and MERS-CoV. The antiviral activity of P9 was attributed to its high-affinity binding to viral glycoproteins, as well as the abundance of basic amino acids in its composition. After binding viral particles through viral surface glycoproteins, P9 entered into cells together with the viruses via endocytosis and prevented endosomal acidification, which blocked membrane fusion and subsequent viral RNA release. This study has paved the avenue for developing new prophylactic and therapeutic agents with broad-spectrum antiviral activities.

DOI: 10.1038/srep22008
PubMed: 26911565

Links to Exploration step

pubmed:26911565

Le document en format XML

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<div type="abstract" xml:lang="en">A safe, potent and broad-spectrum antiviral is urgently needed to combat emerging respiratory viruses. In light of the broad antiviral activity of β-defensins, we tested the antiviral activity of 11 peptides derived from mouse β-defensin-4 and found that a short peptide, P9, exhibited potent and broad-spectrum antiviral effects against multiple respiratory viruses in vitro and in vivo, including influenza A virus H1N1, H3N2, H5N1, H7N7, H7N9, SARS-CoV and MERS-CoV. The antiviral activity of P9 was attributed to its high-affinity binding to viral glycoproteins, as well as the abundance of basic amino acids in its composition. After binding viral particles through viral surface glycoproteins, P9 entered into cells together with the viruses via endocytosis and prevented endosomal acidification, which blocked membrane fusion and subsequent viral RNA release. This study has paved the avenue for developing new prophylactic and therapeutic agents with broad-spectrum antiviral activities. </div>
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