Polyphenols Epigallocatechin Gallate and Resveratrol, and Polyphenol-Functionalized Nanoparticles Prevent Enterovirus Infection through Clustering and Stabilization of the Viruses
Dhanik Reshamwala,
Sailee Shroff,
Olivier Sheik Amamuddy,
Valentino Laquintana,
Nunzio Denora,
Antonella Zacheo,
Vili Lampinen,
Vesa P. Hytonen,
Özlem Tastan Bishop,
Silke Krol,
Varpu Marjomäki
Affiliations
Dhanik Reshamwala
Department of Biological and Environmental Science/Nanoscience Center, University of Jyväskylä, 40014 Jyväskylä, Finland
Sailee Shroff
Department of Biological and Environmental Science/Nanoscience Center, University of Jyväskylä, 40014 Jyväskylä, Finland
Olivier Sheik Amamuddy
Research Unit in Bioinformatics (RUBi), Department of Biochemistry and Microbiology, Rhodes University, Makhanda 6140, South Africa
Valentino Laquintana
Department of Pharmacy–Pharmaceutical Sciences, University of Bari “Aldo Morro”, 70125 Bari, Italy
Nunzio Denora
Department of Pharmacy–Pharmaceutical Sciences, University of Bari “Aldo Morro”, 70125 Bari, Italy
Antonella Zacheo
Laboratory for Nanotechnology, IRCCS Istituto Tumori “Giovanni Paolo II”, 70124 Bari, Italy
Vili Lampinen
Faculty of Medicine and Health Technology, Tampere University, 33520 Tampere, Finland
Vesa P. Hytonen
Faculty of Medicine and Health Technology, Tampere University, 33520 Tampere, Finland
Özlem Tastan Bishop
Research Unit in Bioinformatics (RUBi), Department of Biochemistry and Microbiology, Rhodes University, Makhanda 6140, South Africa
Silke Krol
Laboratory for Personalized Medicine, National Institute of Gastroenterology, IRCCS “S. de Bellis” Research Hospital, 70013 Castellana Grotte, Italy
Varpu Marjomäki
Department of Biological and Environmental Science/Nanoscience Center, University of Jyväskylä, 40014 Jyväskylä, Finland
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 (107 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.