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Rigid amphipathic fusion inhibitors demonstrate antiviral activity against African swine fever virus
被引:41
|作者:
Hakobyan, Astghik
[1
]
Galindo, Inmaculada
[2
]
Nanez, Almudena
[2
]
Arabyan, Erik
[1
]
Karalyan, Zaven
[3
]
Chistov, Alexey A.
[4
]
Streshnev, Philipp P.
[4
]
Korshun, Vladimir A.
[4
]
Alonso, Covadonga
[2
]
Zakaryan, Hovakim
[1
]
机构:
[1] NAS RA, Inst Mol Biol, Grp Antiviral Def Mech, Yerevan 0014, Armenia
[2] INIA, Dept Biotechnol, Inst Nacl Invest & Tecnol & Agr & Alimentaria, Ctra Coruna Km 7-5, Madrid 28040, Spain
[3] NAS RA, Inst Mol Biol, Lab Cell Biol & Virol, Yerevan 0014, Armenia
[4] Shemyakin Ovchinnikov Inst Bioorgan Chem, Miklukho Maklaya 16-10, Moscow 117997, Russia
来源:
基金:
俄罗斯基础研究基金会;
俄罗斯科学基金会;
关键词:
African swine fever virus;
antivirals;
antiviral therapy;
nucleoside analogues;
IN-VITRO;
ENVELOPED VIRUSES;
REPLICATION;
SURFACTANTS;
INFECTION;
VACCINE;
PROTEIN;
GEMINI;
AUY11;
PIGS;
D O I:
10.1099/jgv.0.000991
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
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.
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页码:148 / 156
页数:9
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