Enhanced inhibition of Avian leukosis virus subgroup J replication by multi-target miRNAs

<p>Abstract</p> <p>Background</p> <p>Avian leukosis virus (ALV) is a major infectious disease that impacts the poultry industry worldwide. Despite intensive efforts, no effective vaccine has been developed against ALV because of mutations that lead to resistant forms. T...

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Main Authors: Meng Qing-Wen, Zhang Zai-Ping, Wang Wei, Tian Jin, Xiao Zhi-Guang
Format: Article
Language:English
Published: BMC 2011-12-01
Series:Virology Journal
Subjects:
ALV
Gag
Online Access:http://www.virologyj.com/content/8/1/556
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spelling doaj-6af3854c90214c95a6484ce7765879ae2020-11-24T22:16:22ZengBMCVirology Journal1743-422X2011-12-018155610.1186/1743-422X-8-556Enhanced inhibition of Avian leukosis virus subgroup J replication by multi-target miRNAsMeng Qing-WenZhang Zai-PingWang WeiTian JinXiao Zhi-Guang<p>Abstract</p> <p>Background</p> <p>Avian leukosis virus (ALV) is a major infectious disease that impacts the poultry industry worldwide. Despite intensive efforts, no effective vaccine has been developed against ALV because of mutations that lead to resistant forms. Therefore, there is a dire need to develop antiviral agents for the treatment of ALV infections and RNA interference (RNAi) is considered an effective antiviral strategy.</p> <p>Results</p> <p>In this study, the avian leukosis virus subgroup J (ALV-J) proviral genome, including the <it>gag </it>genes, were treated as targets for RNAi. Four pairs of miRNA sequences were designed and synthesized that targeted different regions of the <it>gag </it>gene. The screened target (i.e., the <it>gag </it>genes) was shown to effectively suppress the replication of ALV-J by 19.0-77.3%. To avoid the generation of escape variants during virus infection, expression vectors of multi-target miRNAs were constructed using the multi-target serial strategy (against different regions of the <it>gag</it>, <it>pol</it>, and <it>env </it>genes). Multi-target miRNAs were shown to play a synergistic role in the inhibition of ALV-J replication, with an inhibition efficiency of viral replication ranging from 85.0-91.2%.</p> <p>Conclusion</p> <p>The strategy of multi-target miRNAs might be an effective method for inhibiting ALV replication and the acquisition of resistant mutations.</p> http://www.virologyj.com/content/8/1/556ALVmiRNAInhibitionGagMulti-target series
collection DOAJ
language English
format Article
sources DOAJ
author Meng Qing-Wen
Zhang Zai-Ping
Wang Wei
Tian Jin
Xiao Zhi-Guang
spellingShingle Meng Qing-Wen
Zhang Zai-Ping
Wang Wei
Tian Jin
Xiao Zhi-Guang
Enhanced inhibition of Avian leukosis virus subgroup J replication by multi-target miRNAs
Virology Journal
ALV
miRNA
Inhibition
Gag
Multi-target series
author_facet Meng Qing-Wen
Zhang Zai-Ping
Wang Wei
Tian Jin
Xiao Zhi-Guang
author_sort Meng Qing-Wen
title Enhanced inhibition of Avian leukosis virus subgroup J replication by multi-target miRNAs
title_short Enhanced inhibition of Avian leukosis virus subgroup J replication by multi-target miRNAs
title_full Enhanced inhibition of Avian leukosis virus subgroup J replication by multi-target miRNAs
title_fullStr Enhanced inhibition of Avian leukosis virus subgroup J replication by multi-target miRNAs
title_full_unstemmed Enhanced inhibition of Avian leukosis virus subgroup J replication by multi-target miRNAs
title_sort enhanced inhibition of avian leukosis virus subgroup j replication by multi-target mirnas
publisher BMC
series Virology Journal
issn 1743-422X
publishDate 2011-12-01
description <p>Abstract</p> <p>Background</p> <p>Avian leukosis virus (ALV) is a major infectious disease that impacts the poultry industry worldwide. Despite intensive efforts, no effective vaccine has been developed against ALV because of mutations that lead to resistant forms. Therefore, there is a dire need to develop antiviral agents for the treatment of ALV infections and RNA interference (RNAi) is considered an effective antiviral strategy.</p> <p>Results</p> <p>In this study, the avian leukosis virus subgroup J (ALV-J) proviral genome, including the <it>gag </it>genes, were treated as targets for RNAi. Four pairs of miRNA sequences were designed and synthesized that targeted different regions of the <it>gag </it>gene. The screened target (i.e., the <it>gag </it>genes) was shown to effectively suppress the replication of ALV-J by 19.0-77.3%. To avoid the generation of escape variants during virus infection, expression vectors of multi-target miRNAs were constructed using the multi-target serial strategy (against different regions of the <it>gag</it>, <it>pol</it>, and <it>env </it>genes). Multi-target miRNAs were shown to play a synergistic role in the inhibition of ALV-J replication, with an inhibition efficiency of viral replication ranging from 85.0-91.2%.</p> <p>Conclusion</p> <p>The strategy of multi-target miRNAs might be an effective method for inhibiting ALV replication and the acquisition of resistant mutations.</p>
topic ALV
miRNA
Inhibition
Gag
Multi-target series
url http://www.virologyj.com/content/8/1/556
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