Abstract

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 2Apro 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 (TCID50) 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 2Apro region of the EV71 genome exerted antiviral effects in vitro.

Highlights

  • Enterovirus 71 (EV 71) is a member of the human Enterovirus A species, which is classified in the genus Enterovirus within the family Picornaviridae[1]

  • To investigate whether the small interfering RNAs (siRNAs) protected RD cells from Enterovirus 71 (EV71)-induced cytopathogenicity, the morphological changes in the RD cells were observed under an inverted microscope

  • These data confirm that siRNAs directed against the 2Apro region of the EV71 genome successfully protected RD cells from the cytopathogenic effects of strain EV71-2006-52-9 infection

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Summary

Introduction

Enterovirus 71 (EV 71) is a member of the human Enterovirus A species, which is classified in the genus Enterovirus within the family Picornaviridae[1]. Its genome is a positive singlestranded RNA with a long open reading frame and is about 7.4 kb in length. The virus is nonenveloped, and the viral capsid protein consists of four structural proteins, VP1–VP4[2]. EV71 is one of the main etiological agents of hand, foot, and mouth disease (HFMD), which primarily affects infants and young children (< 6 years of age), mainly manifesting as 3–4 days of fever and vesicular exanthema on the buccal mucosa, hands, feet, and oral mucosa[3]. PLOS ONE | DOI:10.1371/journal.pone.0149470 February 17, 2016

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