| Literature DB >> 29235978 |
Astghik Hakobyan1, Inmaculada Galindo2, Almudena Nañez2, Erik Arabyan1, Zaven Karalyan3, Alexey A Chistov4, Philipp P Streshnev4, Vladimir A Korshun4, Covadonga Alonso2, Hovakim Zakaryan1.
Abstract
Rigid amphipathic fusion inhibitors (RAFIs) are a family of nucleoside derivatives that inhibit the infectivity of several enveloped viruses by interacting with virion envelope lipids and inhibiting fusion between viral and cellular membranes. Here we tested the antiviral activity of two RAFIs, 5-(Perylen-3-ylethynyl)-arabino-uridine (aUY11) and 5-(Perylen-3-ylethynyl)uracil-1-acetic acid (cm1UY11) against African swine fever virus (ASFV), for which no effective vaccine is available. Both compounds displayed a potent, dose-dependent inhibitory effect on ASFV infection in Vero cells. The major antiviral effect was observed when aUY11 and cm1UY11 were added at early stages of infection and maintained during the complete viral cycle. Furthermore, virucidal assay revealed a significant extracellular anti-ASFV activity for both compounds. We also found decrease in the synthesis of early and late viral proteins in Vero cells treated with cm1UY11. Finally, the inhibitory effect of aUY11 and cm1UY11 on ASFV infection in porcine alveolar macrophages was confirmed. Overall, our study has identified novel anti-ASFV compounds with potential for future therapeutic developments.Entities:
Keywords: African swine fever virus; antiviral therapy; antivirals; nucleoside analogues
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Year: 2017 PMID: 29235978 DOI: 10.1099/jgv.0.000991
Source DB: PubMed Journal: J Gen Virol ISSN: 0022-1317 Impact factor: 3.891