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siRNA Targeting the 2A(pro) Genomic Region Prevents Enterovirus 71 Replication In Vitro

Enterovirus 71 (EV71) is the most important etiological agent of hand, foot, and mouth disease (HFMD) in young children, which is associated with severe neurological complications and has caused significant mortalities in recent HFMD outbreaks in Asia. However, there is no effective antiviral therap...

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Autores principales: Liu, Haibing, Qin, Yanyan, Kong, Zhenzhen, Shao, Qixiang, Su, Zhaoliang, Wang, Shengjun, Chen, Jianguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757562/
https://www.ncbi.nlm.nih.gov/pubmed/26886455
http://dx.doi.org/10.1371/journal.pone.0149470
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author Liu, Haibing
Qin, Yanyan
Kong, Zhenzhen
Shao, Qixiang
Su, Zhaoliang
Wang, Shengjun
Chen, Jianguo
author_facet Liu, Haibing
Qin, Yanyan
Kong, Zhenzhen
Shao, Qixiang
Su, Zhaoliang
Wang, Shengjun
Chen, Jianguo
author_sort Liu, Haibing
collection PubMed
description Enterovirus 71 (EV71) is the most important etiological agent of hand, foot, and mouth disease (HFMD) in young children, which is associated with severe neurological complications and has caused significant mortalities in recent HFMD outbreaks in Asia. However, there is no effective antiviral therapy against EV71. In this study, RNA interference (RNAi) was used as an antiviral strategy to inhibit EV71 replication. Three small interfering RNAs (siRNAs) targeting the 2A(pro) region of the EV71 genome were designed and synthesized. All the siRNAs were transfected individually into rhabdomyosarcoma (RD) cells, which were then infected with strain EV71-2006-52-9. The cytopathic effects (CPEs) in the infected RD cells, cell viability, viral titer, and viral RNA and protein expression were examined to evaluate the specific viral inhibition by the siRNAs. The results of cytopathogenicity and MTT tests indicated that the RD cells transfected with the three siRNAs showed slight CPEs and significantly high viability. The 50% tissue culture infective dose (TCID(50)) values demonstrated that the viral titer of the groups treated with three siRNAs were lower than those of the control groups. qRT–PCR and western blotting revealed that the levels of viral RNA and protein in the RD cells treated with the three siRNAs were lower than those in the controls. When RD cells transfected with siRNAs were also infected with strain EV71-2008-43-16, the expression of the VP1 protein was significantly inhibited. The levels of interferon α (IFN-α) and IFN-β did not differ significantly in any group. These results suggest that siRNAs targeting the 2A(pro) region of the EV71 genome exerted antiviral effects in vitro.
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spelling pubmed-47575622016-02-26 siRNA Targeting the 2A(pro) Genomic Region Prevents Enterovirus 71 Replication In Vitro Liu, Haibing Qin, Yanyan Kong, Zhenzhen Shao, Qixiang Su, Zhaoliang Wang, Shengjun Chen, Jianguo PLoS One Research Article Enterovirus 71 (EV71) is the most important etiological agent of hand, foot, and mouth disease (HFMD) in young children, which is associated with severe neurological complications and has caused significant mortalities in recent HFMD outbreaks in Asia. However, there is no effective antiviral therapy against EV71. In this study, RNA interference (RNAi) was used as an antiviral strategy to inhibit EV71 replication. Three small interfering RNAs (siRNAs) targeting the 2A(pro) region of the EV71 genome were designed and synthesized. All the siRNAs were transfected individually into rhabdomyosarcoma (RD) cells, which were then infected with strain EV71-2006-52-9. The cytopathic effects (CPEs) in the infected RD cells, cell viability, viral titer, and viral RNA and protein expression were examined to evaluate the specific viral inhibition by the siRNAs. The results of cytopathogenicity and MTT tests indicated that the RD cells transfected with the three siRNAs showed slight CPEs and significantly high viability. The 50% tissue culture infective dose (TCID(50)) values demonstrated that the viral titer of the groups treated with three siRNAs were lower than those of the control groups. qRT–PCR and western blotting revealed that the levels of viral RNA and protein in the RD cells treated with the three siRNAs were lower than those in the controls. When RD cells transfected with siRNAs were also infected with strain EV71-2008-43-16, the expression of the VP1 protein was significantly inhibited. The levels of interferon α (IFN-α) and IFN-β did not differ significantly in any group. These results suggest that siRNAs targeting the 2A(pro) region of the EV71 genome exerted antiviral effects in vitro. Public Library of Science 2016-02-17 /pmc/articles/PMC4757562/ /pubmed/26886455 http://dx.doi.org/10.1371/journal.pone.0149470 Text en © 2016 Liu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Liu, Haibing
Qin, Yanyan
Kong, Zhenzhen
Shao, Qixiang
Su, Zhaoliang
Wang, Shengjun
Chen, Jianguo
siRNA Targeting the 2A(pro) Genomic Region Prevents Enterovirus 71 Replication In Vitro
title siRNA Targeting the 2A(pro) Genomic Region Prevents Enterovirus 71 Replication In Vitro
title_full siRNA Targeting the 2A(pro) Genomic Region Prevents Enterovirus 71 Replication In Vitro
title_fullStr siRNA Targeting the 2A(pro) Genomic Region Prevents Enterovirus 71 Replication In Vitro
title_full_unstemmed siRNA Targeting the 2A(pro) Genomic Region Prevents Enterovirus 71 Replication In Vitro
title_short siRNA Targeting the 2A(pro) Genomic Region Prevents Enterovirus 71 Replication In Vitro
title_sort sirna targeting the 2a(pro) genomic region prevents enterovirus 71 replication in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757562/
https://www.ncbi.nlm.nih.gov/pubmed/26886455
http://dx.doi.org/10.1371/journal.pone.0149470
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