Development of real-time PCR assays for the detection and differentiation of Australian and European ranaviruses.

Serious systemic disease in fish and amphibians is associated with the ranaviruses, epizootic haernatopoietic necrosis virus (EHNV) and Bohle iridovirus (BIV) in Australia, and European sheattish virus (ESV) and European catfish virus (ECV) in Europe. EHNV, ESV and ECV are recognized causative agents of the OlE (Office International des Epizooties) notifiable systemic necrotizing iridovirus syndrome and are currently identified by proteinbased assays, none of which are able to rapidly identify the specific agents. The aim of this study was to develop T aqMan real-time PCR assays that differentiated these viruses using nucleotide sequence variation in two ranavirus genes. A conserved probe representing 100% sequence homology was used as a reference for virus-specific probes. The virus-specific probes produced a similar signal level to the conserved probe while those probes binding to non-target viral DNA produced an altered fluorescent curve. The pattern of probe binding was characteristic for each virus. Sensitivity, specificity and dynamic range of the assay were assessed. The test is currently useful as a research and initial screening tool, with the potential to become a sensitive and specific method for detection and differentiation of ranaviruses with further development