Polyphenols Epigallocatechin Gallate and Resveratrol, and Polyphenol-Functionalized Nanoparticles Prevent Enterovirus Infection through Clustering and Stabilization of the Viruses

被引:13
|
作者
Reshamwala, Dhanik [1 ]
Shroff, Sailee [1 ]
Sheik Amamuddy, Olivier [2 ]
Laquintana, Valentino [3 ]
Denora, Nunzio [3 ]
Zacheo, Antonella [4 ]
Lampinen, Vili [5 ]
Hytonen, Vesa P. [5 ,6 ]
Tastan Bishop, Ozlem [2 ]
Krol, Silke [7 ]
Marjomaki, Varpu [1 ]
机构
[1] Univ Jyvaskyla, Dept Biol & Environm Sci, Nanosci Ctr, Jyvaskyla 40014, Finland
[2] Rhodes Univ, Dept Biochem & Microbiol, Res Unit Bioinformat RUBi, ZA-6140 Makhanda, South Africa
[3] Univ Bari Aldo Morro, Dept Pharm Pharmaceut Sci, I-70125 Bari, Italy
[4] IRCCS Ist Tumori Giovanni Paolo II, Lab Nanotechnol, I-70124 Bari, Italy
[5] Tampere Univ, Fac Med & Hlth Technol, Tampere 33520, Finland
[6] Fimlab Labs, Tampere 33520, Finland
[7] S de Bellis Res Hosp, Natl Inst Gastroenterol, Lab Personalized Med, I-70013 Castellana Grotte, Italy
关键词
polyphenols; functionalized gold nanoparticles; antiviral efficacy; enteroviruses; stabilization; COXSACKIEVIRUS A9; SEQUENCE; BINDS; CD4; TEA;
D O I
10.3390/pharmaceutics13081182
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
To efficiently lower virus infectivity and combat virus epidemics or pandemics, it is important to discover broadly acting antivirals. Here, we investigated two naturally occurring polyphenols, Epigallocatechin gallate (EGCG) and Resveratrol (RES), and polyphenol-functionalized nanoparticles for their antiviral efficacy. Concentrations in the low micromolar range permanently inhibited the infectivity of high doses of enteroviruses (10(7) PFU/mL). Sucrose gradient separation of radiolabeled viruses, dynamic light scattering, transmission electron microscopic imaging and an in-house developed real-time fluorescence assay revealed that polyphenols prevented infection mainly through clustering of the virions into very stable assemblies. Clustering and stabilization were not compromised even in dilute virus solutions or after diluting the polyphenols-clustered virions by 50-fold. In addition, the polyphenols lowered virus binding on cells. In silico docking experiments of these molecules against 2- and 3-fold symmetry axes of the capsid, using an algorithm developed for this study, discovered five binding sites for polyphenols, out of which three were novel binding sites. Our results altogether suggest that polyphenols exert their antiviral effect through binding to multiple sites on the virion surface, leading to aggregation of the virions and preventing RNA release and reducing cell surface binding.
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页数:27
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