Abstract

BackgroundRabies virus (RABV) causes a fatal infection of the central nervous systems (CNS) of warm-blooded animals. Once the clinical symptoms develop, rabies is almost invariably fatal. The mechanism of RABV pathogenesis remains poorly understood. Recent studies have shown that microRNA (miRNA) plays an important role in the pathogenesis of viral infections. Our recent findings have revealed that infection with laboratory-fixed rabies virus strain can induce modulation of the microRNA profile of mouse brains. However, no previous report has evaluated the miRNA expression profile of mouse brains infected with RABV street strain.ResultsThe results of microarray analysis show that miRNA expression becomes modulated in the brains of mice infected with street RABV. Quantitative real-time PCR assay of the differentially expressed miRNAs confirmed the results of microarray assay. Functional analysis showed the differentially expressed miRNAs to be involved in many immune-related signaling pathways, such as the Jak-STAT signaling pathway, the MAPK signaling pathway, cytokine-cytokine receptor interactions, and Fc gamma R-mediated phagocytosis. The predicted expression levels of the target genes of these modulated miRNAs were found to be correlated with gene expression as measured by DNA microarray and qRT-PCR.ConclusionRABV causes significant changes in the miRNA expression profiles of infected mouse brains. Predicted target genes of the differentially expression miRNAs are associated with host immune response, which may provide important information for investigation of RABV pathogenesis and therapeutic method.

Highlights

  • Rabies virus (RABV) causes a fatal infection of the central nervous systems (CNS) of warm-blooded animals

  • The results demonstrate that the RABV Fujian strain is highly pathogenic in mice

  • We found that the expression profiles of host miRNAs in mouse brains infected by these two strains of RABVs were completely different from each other

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Summary

Introduction

Rabies virus (RABV) causes a fatal infection of the central nervous systems (CNS) of warm-blooded animals. Recent studies have shown that microRNA (miRNA) plays an important role in the pathogenesis of viral infections. Our recent findings have revealed that infection with laboratory-fixed rabies virus strain can induce modulation of the microRNA profile of mouse brains. No previous report has evaluated the miRNA expression profile of mouse brains infected with RABV street strain. The rabies virus (RABV), a member of the family Rhabdoviridae, is a highly neurotropic virus that can cause fatal infections of the central nervous systems (CNS) of warm-blooded animals [1,2]. It. MiRNA (miRNA, miR) is endogenous 22 nt RNA that negatively regulates gene expression by translational repression [4]. A recent study reported that miR-28, miR-125b, miR-150, miR223, and miR-382 inhibit replication of the human immunodeficiency virus (HIV) in CD4+ T cells [14]

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