Polyvalent 2D Entry Inhibitors for Pseudorabies and African Swine Fever Virus

被引:38
|
作者
Ziem, Benjamin [1 ]
Rahn, Jessica [2 ]
Donskyi, Ievgen [1 ]
Silberreis, Kim [3 ]
Cuellar, Luis [1 ]
Dernedde, Jens [3 ]
Keil, Guenther [2 ]
Mettenleiter, Thomas C. [2 ]
Haag, Rainer [1 ]
机构
[1] Freie Univ, Inst Chem & Biochem, D-14195 Berlin, Germany
[2] Friedrich Loeffler Inst, Inst Mol Virol & Cell Biol, Fed Res Inst Anim Hlth, D-17493 Greifswald, Germany
[3] Charite Univ Med Berlin, Inst Lab Med, D-13353 Berlin, Germany
关键词
African swine fever virus; polyglycerol sulfate; pseudorabies virus; thermally reduced graphene oxide; virus entry inhibitor; DENDRITIC POLYGLYCEROL SULFATES; HERPES-SIMPLEX; ANTIVIRAL ACTIVITY; WILD BOAR; IN-VITRO; ATTACHMENT; BINDING; PATHOGENESIS; PENETRATION; ENDOCYTOSIS;
D O I
10.1002/mabi.201600499
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
African swine fever virus (ASFV) is one of the most dangerous viruses for pigs and is endemic in Africa but recently also spread into the Russian Federation and the Eastern border of the EU. So far there is no vaccine or antiviral drug available to curtail the infection. Thus, control strategies based on novel inhibitors are urgently needed. Another highly relevant virus infection in pigs is Aujeszky's disease caused by the alphaherpesvirus pseudorabies virus (PrV). This article reports the synthesis and biological evaluation of novel extracellular matrix-inspired entry inhibitors based on polyglycerol sulfate-functionalized graphene sheets. The developed 2D architectures bind enveloped viruses during the adhesion process and thereby exhibit strong inhibitory effects, which are equal or better than the common standards enrofloxacin and heparin as demonstrated for ASFV and PrV. Overall, the developed polyvalent 2D entry inhibitors are nontoxic and efficient nanoarchitectures, which interact with various types of enveloped viruses. Therefore they prevent viral adhesion to the host cell and especially target viruses that rely on a heparan sulfate-dependent cell entry mechanism.
引用
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页数:9
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