A broad-spectrum virus- and host-targeting peptide against respiratory viruses including influenza virus and SARS-CoV-2
| dc.creator | Zhao, Hanjun | |
| dc.creator | To, Kelvin K. W. | |
| dc.creator | Sze, Kong-Hung | |
| dc.creator | Yung, Timothy Tin-Mong | |
| dc.creator | Bian, Mingjie | |
| dc.creator | Lam, Hoiyan | |
| dc.creator | Yeung, Man Lung | |
| dc.creator | Li, Cun | |
| dc.creator | Chu, Hin | |
| dc.creator | Yuen, Kwok-Yung | |
| dc.date.accessioned | 2020-09-19T16:56:22Z | |
| dc.date.available | 2020-09-19T16:56:22Z | |
| dc.date.created | 2020-08-25 | |
| dc.description.abstractenglish | The 2019 novel respiratory virus (SARS-CoV-2) causes COVID-19 with rapid global socioeconomic disruptions and disease burden to healthcare. The COVID-19 and previous emerging virus outbreaks highlight the urgent need for broad-spectrum antivirals. Here, we show that a defensin-like peptide P9R exhibited potent antiviral activity against pH-dependent viruses that require endosomal acidification for virus infection, including the enveloped pandemic A(H1N1)pdm09 virus, avian influenza A(H7N9) virus, coronaviruses (SARS-CoV-2, MERS-CoV and SARS-CoV), and the non-enveloped rhinovirus. P9R can significantly protect mice from lethal challenge by A(H1N1)pdm09 virus and shows low possibility to cause drug-resistant virus. Mechanistic studies indicate that the antiviral activity of P9R depends on the direct binding to viruses and the inhibition of virus-host endosomal acidification, which provides a proof of concept that virus-binding alkaline peptides can broadly inhibit pH-dependent viruses. These results suggest that the dual-functional virus- and host-targeting P9R can be a promising candidate for combating pH-dependent respiratory viruses. | spa |
| dc.format.extent | 10 páginas | spa |
| dc.format.mimetype | application/pdf | spa |
| dc.identifier.doi | https://doi.org/10.1038/s41467-020-17986-9 | spa |
| dc.identifier.issn | 2041-1723 | spa |
| dc.identifier.other | https://www.nature.com/articles/s41467-020-17986-9 | spa |
| dc.identifier.uri | https://hdl.handle.net/20.500.12010/13490 | |
| dc.language.iso | spa | spa |
| dc.publisher | Nature Communications | spa |
| dc.rights.accessrights | info:eu-repo/semantics/restrictedAccess | spa |
| dc.rights.local | Acceso restringido | spa |
| dc.source | reponame:Expeditio Repositorio Institucional UJTL | spa |
| dc.source | instname:Universidad de Bogotá Jorge Tadeo Lozano | spa |
| dc.subject | respiratory viruses | spa |
| dc.subject | influenza virus | spa |
| dc.subject.lemb | Síndrome respiratorio agudo grave | spa |
| dc.subject.lemb | COVID-19 | spa |
| dc.subject.lemb | SARS-CoV-2 | spa |
| dc.subject.lemb | Coronavirus | spa |
| dc.title | A broad-spectrum virus- and host-targeting peptide against respiratory viruses including influenza virus and SARS-CoV-2 | spa |
| dc.type.coar | http://purl.org/coar/resource_type/c_6501 | spa |
| dc.type.hasversion | info:eu-repo/semantics/acceptedVersion | spa |
| dc.type.local | Artículo | spa |
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