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6-methylmercaptopurine riboside, a thiopurine nucleoside with antiviral activity against canine distemper virus in vitro

Authors :
Otávio Valério de Carvalho
Daniele Mendes Félix
Claudia de Camargo Tozato
Juliana Lopes Rangel Fietto
Márcia Rogéria de Almeida
Gustavo Costa Bressan
Lindomar José Pena
Abelardo Silva-Júnior
Source :
Virology Journal, Vol 14, Iss 1, Pp 1-8 (2017)
Publication Year :
2017
Publisher :
BMC, 2017.

Abstract

Abstract Background Canine distemper (CD) is a widespread infectious disease that can severely impact a variety of species in the order Carnivora, as well as non-carnivore species such as non-human primates. Despite large-scale vaccination campaigns, several fatal outbreaks have been reported in wild and domestic carnivore populations. This, in association with expansion of the disease host range and the development of vaccine-escape strains, has contributed to an increased demand for therapeutic strategies synergizing with vaccine programs for effectively controlling canine distemper. 6-methylmercaptopurine riboside (6MMPr) is a modified thiopurine nucleoside with known antiviral properties against certain RNA viruses. Methods We tested the inhibitory effects of 6MMPr against a wild-type CDV strain infection in cell culture. We measured infectious particle production and viral RNA levels in treated and untreated CDV-infected cells. Ribavirin (RIB) was used as a positive control. Results Here, we report for the first time the antiviral effects of 6MMPr against canine distemper virus (CDV) in vitro. 6MMPr was able to reduce viral RNA levels and to inhibit the production of infectious CDV particles. The therapeutic selectivity of 6MMPr was approximately six times higher than that of ribavirin. Conclusion Our results indicate that 6MMPr has high anti-CDV potential and warrants further testing against other paramyxoviruses, as well as clinical testing of the compound against CDV.

Details

Language :
English
ISSN :
1743422X
Volume :
14
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Virology Journal
Publication Type :
Academic Journal
Accession number :
edsdoj.67cc998094f44e25b8e33d78c92596df
Document Type :
article
Full Text :
https://doi.org/10.1186/s12985-017-0785-6