A safe and highly efficient antiviral is needed for the prophylaxis and/or treatment of viral diarrhea. We here demonstrate the in vitro antiviral activity of four 2′-C-methyl nucleoside analogues against noro-, rota-, and sapoviruses. The most potent nucleoside analogue, 7-deaza-2′-C-methyladenosine, inhibits replication of these viruses with a 50% effective concentration < 5 µM. Mechanistically, we demonstrate that the 2′-C-methyl nucleoside analogues act by inhibiting transcription of the rotavirus genome. This provides the first evidence that a single viral-diarrhea-targeted treatment can be developed through a viral-polymerase-targeting small molecule.
A single nucleoside viral polymerase inhibitor against norovirus, rotavirus, and sapovirus-induced diarrhea / J. Van Dycke, F. Arnoldi, G. Papa, J. Vandepoele, O.R. Burrone, E. Mastrangelo, D. Tarantino, E. Heylen, J. Neyts, J. Rocha-Pereira. - In: THE JOURNAL OF INFECTIOUS DISEASES. - ISSN 0022-1899. - 218:11(2018 Dec 01), pp. 1753-1758. [10.1093/infdis/jiy398]
A single nucleoside viral polymerase inhibitor against norovirus, rotavirus, and sapovirus-induced diarrhea
G. Papa;
2018
Abstract
A safe and highly efficient antiviral is needed for the prophylaxis and/or treatment of viral diarrhea. We here demonstrate the in vitro antiviral activity of four 2′-C-methyl nucleoside analogues against noro-, rota-, and sapoviruses. The most potent nucleoside analogue, 7-deaza-2′-C-methyladenosine, inhibits replication of these viruses with a 50% effective concentration < 5 µM. Mechanistically, we demonstrate that the 2′-C-methyl nucleoside analogues act by inhibiting transcription of the rotavirus genome. This provides the first evidence that a single viral-diarrhea-targeted treatment can be developed through a viral-polymerase-targeting small molecule.| File | Dimensione | Formato | |
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