Abstract

Human enterovirus 71 (HEV71) has emerged as the leading cause of viral encephalitis in children in most Asian countries. The roles of host miRNAs in the neurological pathogenesis of HEV71 infection remain unknown. In the present study, comprehensive miRNA expression profiling in HEV71-infected human neuroblastoma SH-SY5Y cells was performed using the Affymetrix Gene Chip microarray assay and was validated using real-time RT-PCR. Among the 69 differentially expressed miRNAs, miR-1246 was specifically induced by HEV71 infection in human neuroblastoma cells, but inhibition of miR-1246 failed to affect HEV71 replication. Parallel mRNA and microRNA profiling based on the 35 K Human Genome Array identified 182 differentially regulated genes. Target prediction of miR-1246 and network modeling revealed 14 potential target genes involved in cell death and cell signaling. Finally, a combined analysis of the results from mRNA profiling and miR-1246 target predication led to the identification of disc-large homolog 3 (DLG3), which is associated with neurological disorders, for further validation. Sequence alignment and luciferase reporter assay showed that miR-1246 directly bound with the 3′-UTR of DLG3 gene. Down-regulation of miR-1246 induced significant changes in DLG3 expression levels in HEV71-infected SHSY5Y cells. Together, these results suggested that miR-1246 might play a role in neurological pathogenesis of HEV71 by regulating DLG3 gene in infected cells. These findings provide new information on the miRNA and mRNA profiles of HEV71-infected neuroblastoma cells. The biological significance of miR-1246 and DLG3 during the course of HEV71 infection deserves further investigation.

Highlights

  • Human enterovirus71 (HEV71) is a single-stranded, positivesense RNA virus belonging to the genus Enterovirus, family Picornaviridae[1,2]

  • SH-SY5Y cells were infected with HEV71 at an multiplicity of infection (MOI) of 1, and the infected cells were harvested after 6 and 12 hpi

  • The expression levels of miR-125a significantly decreased, while miR320b and miR-1246 significantly increased at 6 and 12 hpi; No significant change was observed for miR-1268 at either time points. These results were in agreement with the microarray analysis. These results strongly indicated that miR-1246 was significantly up-regulated in HEV71-infected SH-SY5Y cells

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Summary

Introduction

Human enterovirus (HEV71) is a single-stranded, positivesense RNA virus belonging to the genus Enterovirus, family Picornaviridae[1,2]. HEV71 has been identified as one of the leading pathogensof hand-foot-and-mouthdisease (HFMD) and is associated with encephalitis, meningitis, and neurological complications, even death, in infants and young children. Previous studies have provided rigorous radiological or histopathological evidence regarding the induction of paralysis via the infection and destruction of the anterior horn motor neurons of the spinal cord [4,5]. Some cases of HEV71-mediated paralysis may induce acute flaccid paralysis by several mechanisms, leading to the virus-mediated destruction of anterior horn motor neurons [6,7]. Other studies in cynomolgus macaques demonstrated that the development of paralytic disease following HEV71 infection was associated with inflammatory infiltrates in the spinal cord and medulla oblongata [10,11]. HEV71 viral antigen has been found in neurons following immunocytochemical staining [12,13]

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