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Microarray analysis reveals altered circulating microRNA expression in mice infected with Coxsackievirus B3
Microarray analysis reveals altered circulating microRNA expression in mice infected with Coxsackievirus B3
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Microarray analysis reveals altered circulating microRNA expression in mice infected with Coxsackievirus B3
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Microarray analysis reveals altered circulating microRNA expression in mice infected with Coxsackievirus B3
Microarray analysis reveals altered circulating microRNA expression in mice infected with Coxsackievirus B3

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Microarray analysis reveals altered circulating microRNA expression in mice infected with Coxsackievirus B3
Microarray analysis reveals altered circulating microRNA expression in mice infected with Coxsackievirus B3
Journal Article

Microarray analysis reveals altered circulating microRNA expression in mice infected with Coxsackievirus B3

2016
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Overview
Coxsackievirus B3 (CVB3) is a common causative agent in the development of inflammatory cardiomyopathy. However, whether the expression of peripheral blood microRNAs (miRNAs) is altered in this process is unknown. The present study investigated changes to miRNA expression in the peripheral blood of CVB3-infected mice. Utilizing miRNA microarray technology, differential miRNA expression was examined between normal and CVB3-infected mice. The present results suggest that specific miRNAs were differentially expressed in the peripheral blood of mice infected with CVB3, varying with infection duration. Using miRNA microarray analysis, a total of 96 and 89 differentially expressed miRNAs were identified in the peripheral blood of mice infected with CVB3 for 3 and 6 days, respectively. Quantitative polymerase chain reaction was used to validate differentially expressed miRNAs, revealing a consistency of these results with the miRNA microarray analysis results. The biological functions of the differentially expressed miRNAs were then predicted by bioinformatics analysis. The potential biological roles of differentially expressed miRNAs included hypertrophic cardiomyopathy, dilated cardiomyopathy and arrhythmogenic right ventricular cardiomyopathy. These results may provide important insights into the mechanisms responsible for the progression of CVB3 infection.