Analysis of miRNAs Involved in Mouse Brain Damage upon Enterovirus 71 Infection

Front Cell Infect Microbiol. 2017 Apr 19:7:133. doi: 10.3389/fcimb.2017.00133. eCollection 2017.

Abstract

Enterovirus 71 (EV71) infects the central nervous system (CNS) and causes brainstem encephalitis in children. MiRNAs have been found to play various functions in EV71 infection in human cell lines. To identify potential miRNAs involved in the inflammatory injury in CNS, our study, for the first time, performed a miRNA microarray assay in vivo using EV71 infected mice brains. Twenty differentially expressed miRNAs were identified (four up- and 16 down-regulated) and confirmed by qRT-PCR. The target genes of these miRNAs were analyzed using KEGG (Kyoto Encyclopedia of Genes and Genomes) analysis, revealing that the miRNAs were mainly involved in the regulation of inflammation and neural system function. MiR-150-5p, -3082-5p, -3473a, -468-3p, -669n, -721, -709, and -5107-5p that regulate MAPK and chemokine signaling were all down-regulated, which might result in increased cytokine production. In addition, miR-3473a could also regulate focal adhesion and leukocyte trans-endothelial migration, suggesting a role in virus-induced blood-brain barrier disruption. The miRNAs and pathways identified in this study could help to understand the intricate interactions between EV71 and the brain injury, offering new insight for the future research of the molecular mechanism of EV71 induced brainstem encephalitis.

Keywords: brain; brainstem encephalitis; central nervous system; enterovirus 71 (EV71); inflammation; miRNA; neural system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood-Brain Barrier
  • Brain / pathology
  • Brain / virology*
  • Brain Injuries / pathology*
  • Brain Injuries / virology
  • Cell Line
  • Central Nervous System / pathology
  • Central Nervous System / virology
  • Chemokines / metabolism
  • Cytokines / metabolism
  • Down-Regulation
  • Enterovirus A, Human / genetics
  • Enterovirus A, Human / pathogenicity*
  • Enterovirus Infections
  • Gene Expression Profiling
  • Humans
  • Inflammation
  • Mice
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • MicroRNAs / pharmacology*
  • Mitogen-Activated Protein Kinase Kinases / metabolism
  • Real-Time Polymerase Chain Reaction
  • Survival Rate

Substances

  • Chemokines
  • Cytokines
  • MicroRNAs
  • Mitogen-Activated Protein Kinase Kinases