This study describes a sensitive (1.3 × 101 genomic copies/μL) and specific TaqMan-based qRT-PCR assay able to detect and quantify SVA RNA in porcine biological samples. The technique represents an efficient tool for the virus diagnosis and assessment of SVA load in tissues of infected animals and for epidemiological studies.
Keywords: Picornavirus infection; Quantitative PCR; Real-time RT-PCR; Seneca valley virus; Swine; Vesicular disease.
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