Protection against West Nile virus infection in mice after inoculation with type I interferon-inducing RNA transcripts

West Nile virus (WNV) is a neurovirulent single stranded RNA mosquito-borne flavivirus, whose main natural hosts are birds, but it also infects humans and horses. Nowadays, no human vaccine is commercially available and clinical treatment is only supportive. Recently, it has been shown that RNA transcripts, mimicking structural domains in the non-coding regions (NCRs) of the foot-and mouth disease virus (FMDV) induce a potent IFN response and antiviral activity in transfected cultured cells, and also reduced mice susceptibility to FMDV. By using different transcripts combinations, administration schedules, and infecting routes and doses, we have demonstrated that these FMDV RNA transcripts protect suckling and adult mice against lethal challenge with WNV. The protective activity induced by the transcripts was systemic and dependent on the infection route and dose. These results confirm the antiviral potential of these synthetic RNAs for fighting viruses of different families relevant for human and animal health. © 2012 Rodríguez-Pulido et al.

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Main Authors: Rodríguez-Pulido, M., Martín-Acebes, M. A., Escribano Romero, Estela, Blázquez Martín, Ana Belén, Sobrino, F., Borrego, B., Sáiz, M., Saiz Calahorra, Juan Carlos
Format: artículo biblioteca
Language:English
Published: Public Library of Science 2012
Online Access:http://hdl.handle.net/20.500.12792/3841
http://hdl.handle.net/10261/292940
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spelling dig-inia-es-10261-2929402023-02-20T07:34:03Z Protection against West Nile virus infection in mice after inoculation with type I interferon-inducing RNA transcripts Rodríguez-Pulido, M. Martín-Acebes, M. A. Escribano Romero, Estela Blázquez Martín, Ana Belén Sobrino, F. Borrego, B. Sáiz, M. Saiz Calahorra, Juan Carlos West Nile virus (WNV) is a neurovirulent single stranded RNA mosquito-borne flavivirus, whose main natural hosts are birds, but it also infects humans and horses. Nowadays, no human vaccine is commercially available and clinical treatment is only supportive. Recently, it has been shown that RNA transcripts, mimicking structural domains in the non-coding regions (NCRs) of the foot-and mouth disease virus (FMDV) induce a potent IFN response and antiviral activity in transfected cultured cells, and also reduced mice susceptibility to FMDV. By using different transcripts combinations, administration schedules, and infecting routes and doses, we have demonstrated that these FMDV RNA transcripts protect suckling and adult mice against lethal challenge with WNV. The protective activity induced by the transcripts was systemic and dependent on the infection route and dose. These results confirm the antiviral potential of these synthetic RNAs for fighting viruses of different families relevant for human and animal health. © 2012 Rodríguez-Pulido et al. 2023-02-20T07:34:03Z 2023-02-20T07:34:03Z 2012 artículo PLoS ONE 7(11): e49494 (2012) http://hdl.handle.net/20.500.12792/3841 http://hdl.handle.net/10261/292940 10.1371/journal.pone.0049494 1932-6203 en open Public Library of Science
institution INIA ES
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country España
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libraryname Biblioteca del INIA España
language English
description West Nile virus (WNV) is a neurovirulent single stranded RNA mosquito-borne flavivirus, whose main natural hosts are birds, but it also infects humans and horses. Nowadays, no human vaccine is commercially available and clinical treatment is only supportive. Recently, it has been shown that RNA transcripts, mimicking structural domains in the non-coding regions (NCRs) of the foot-and mouth disease virus (FMDV) induce a potent IFN response and antiviral activity in transfected cultured cells, and also reduced mice susceptibility to FMDV. By using different transcripts combinations, administration schedules, and infecting routes and doses, we have demonstrated that these FMDV RNA transcripts protect suckling and adult mice against lethal challenge with WNV. The protective activity induced by the transcripts was systemic and dependent on the infection route and dose. These results confirm the antiviral potential of these synthetic RNAs for fighting viruses of different families relevant for human and animal health. © 2012 Rodríguez-Pulido et al.
format artículo
author Rodríguez-Pulido, M.
Martín-Acebes, M. A.
Escribano Romero, Estela
Blázquez Martín, Ana Belén
Sobrino, F.
Borrego, B.
Sáiz, M.
Saiz Calahorra, Juan Carlos
spellingShingle Rodríguez-Pulido, M.
Martín-Acebes, M. A.
Escribano Romero, Estela
Blázquez Martín, Ana Belén
Sobrino, F.
Borrego, B.
Sáiz, M.
Saiz Calahorra, Juan Carlos
Protection against West Nile virus infection in mice after inoculation with type I interferon-inducing RNA transcripts
author_facet Rodríguez-Pulido, M.
Martín-Acebes, M. A.
Escribano Romero, Estela
Blázquez Martín, Ana Belén
Sobrino, F.
Borrego, B.
Sáiz, M.
Saiz Calahorra, Juan Carlos
author_sort Rodríguez-Pulido, M.
title Protection against West Nile virus infection in mice after inoculation with type I interferon-inducing RNA transcripts
title_short Protection against West Nile virus infection in mice after inoculation with type I interferon-inducing RNA transcripts
title_full Protection against West Nile virus infection in mice after inoculation with type I interferon-inducing RNA transcripts
title_fullStr Protection against West Nile virus infection in mice after inoculation with type I interferon-inducing RNA transcripts
title_full_unstemmed Protection against West Nile virus infection in mice after inoculation with type I interferon-inducing RNA transcripts
title_sort protection against west nile virus infection in mice after inoculation with type i interferon-inducing rna transcripts
publisher Public Library of Science
publishDate 2012
url http://hdl.handle.net/20.500.12792/3841
http://hdl.handle.net/10261/292940
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