A single siRNA suppresses fatal encephalitis induced by two different flaviviruses.

Japanese encephalitis virus (JEV) and West Nile virus (WNV) are neurotropic flaviviruses that can cause acute encephalitis with a high fatality rate. Currently there is no effective treatment for these infections.We tested RNA interference (RNAi)-based intervention to suppress lethal JE and WN encep...

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Main Authors: Priti Kumar, Sang Kyung Lee, Premlata Shankar, N Manjunath
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2006-04-01
Series:PLoS Medicine
Online Access:http://europepmc.org/articles/PMC1361782?pdf=render
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spelling doaj-856574c774ac46bcb219e73e777811402020-11-25T02:31:45ZengPublic Library of Science (PLoS)PLoS Medicine1549-12771549-16762006-04-0134e9610.1371/journal.pmed.0030096A single siRNA suppresses fatal encephalitis induced by two different flaviviruses.Priti KumarSang Kyung LeePremlata ShankarN ManjunathJapanese encephalitis virus (JEV) and West Nile virus (WNV) are neurotropic flaviviruses that can cause acute encephalitis with a high fatality rate. Currently there is no effective treatment for these infections.We tested RNA interference (RNAi)-based intervention to suppress lethal JE and WN encephalitis in mice. To induce RNAi, we used either lentivirally expressed short hairpin RNA (shRNA) or synthetic short interfering RNA (siRNA). As target, we selected the cd loop-coding sequence in domain II of the viral Envelope protein, which is highly conserved among all flaviviruses because of its essential role in membrane fusion. Using as a target a species-specific sequence in the cd loop that is conserved only among the different strains of either JEV or WNV, we could achieve specific protection against the corresponding virus. However, by targeting a cross-species conserved sequence within the cd loop, we were able to protect mice against encephalitis induced by both viruses. A single intracranial administration of lentivirally delivered shRNA or lipid-complexed siRNA before viral challenge or siRNA treatment after viral challenge was sufficient for protection against lethal encephalitis.RNAi-based intervention affords near complete protection from both JEV- and WNV- induced encephalitis in mice. Our results show, to our knowledge for the first time, that siRNA can be used as a broad-spectrum antiviral agent for treating encephalitis caused by multiple related viruses.http://europepmc.org/articles/PMC1361782?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Priti Kumar
Sang Kyung Lee
Premlata Shankar
N Manjunath
spellingShingle Priti Kumar
Sang Kyung Lee
Premlata Shankar
N Manjunath
A single siRNA suppresses fatal encephalitis induced by two different flaviviruses.
PLoS Medicine
author_facet Priti Kumar
Sang Kyung Lee
Premlata Shankar
N Manjunath
author_sort Priti Kumar
title A single siRNA suppresses fatal encephalitis induced by two different flaviviruses.
title_short A single siRNA suppresses fatal encephalitis induced by two different flaviviruses.
title_full A single siRNA suppresses fatal encephalitis induced by two different flaviviruses.
title_fullStr A single siRNA suppresses fatal encephalitis induced by two different flaviviruses.
title_full_unstemmed A single siRNA suppresses fatal encephalitis induced by two different flaviviruses.
title_sort single sirna suppresses fatal encephalitis induced by two different flaviviruses.
publisher Public Library of Science (PLoS)
series PLoS Medicine
issn 1549-1277
1549-1676
publishDate 2006-04-01
description Japanese encephalitis virus (JEV) and West Nile virus (WNV) are neurotropic flaviviruses that can cause acute encephalitis with a high fatality rate. Currently there is no effective treatment for these infections.We tested RNA interference (RNAi)-based intervention to suppress lethal JE and WN encephalitis in mice. To induce RNAi, we used either lentivirally expressed short hairpin RNA (shRNA) or synthetic short interfering RNA (siRNA). As target, we selected the cd loop-coding sequence in domain II of the viral Envelope protein, which is highly conserved among all flaviviruses because of its essential role in membrane fusion. Using as a target a species-specific sequence in the cd loop that is conserved only among the different strains of either JEV or WNV, we could achieve specific protection against the corresponding virus. However, by targeting a cross-species conserved sequence within the cd loop, we were able to protect mice against encephalitis induced by both viruses. A single intracranial administration of lentivirally delivered shRNA or lipid-complexed siRNA before viral challenge or siRNA treatment after viral challenge was sufficient for protection against lethal encephalitis.RNAi-based intervention affords near complete protection from both JEV- and WNV- induced encephalitis in mice. Our results show, to our knowledge for the first time, that siRNA can be used as a broad-spectrum antiviral agent for treating encephalitis caused by multiple related viruses.
url http://europepmc.org/articles/PMC1361782?pdf=render
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